Skip to main content
Journal of Evidence-based Complementary & Alternative Medicine logoLink to Journal of Evidence-based Complementary & Alternative Medicine
. 2017 Jul 13;22(4):824–839. doi: 10.1177/2156587217717413

Investigating Chemical Composition and Indications of Hydrosol Soft Drinks (Aromatic Waters) Used in Persian Folk Medicine for Women’s Hormonal and Reproductive Health Conditions

Azadeh Hamedi 1,2,✉, Mehdi Afifi 3, Hamed Etemadfard 1
PMCID: PMC5871293  PMID: 28701045

Abstract

Hydrosol soft drinks in Persian nutrition culture are produced as side products of the essential oil industry to be used as safe remedies for treatment of some ailments. This study investigated hydrosols for women’s hormonal health conditions. Detailed information was gathered by questionnaires. Chemical constituents of these mono- or poly-herbal hydrosols were identified after liquid/liquid extraction and gas chromatography–mass spectrometry. Hierarchical cluster and K-means analysis (SPSS software) were used to find their relevance. A literature survey was also performed. In most cases, thymol, carvacrol, and carvone were the major constituents except for dill, white horehound, willow, Moderr, and yarrow hydrosols, whose their major components were dill ether, menthol, phenethyl alcohol, linalool, or camphor. Based on clustering methods, some similarities could be found in their constituents with some exceptions. None of them have been studied scientifically before. These investigations may lead to the development of some functional drinks or even new lead components.

Keywords: essential oil, women’s reproductive disorder, distillate, aromatic waters, Aragh


Different ethnomedicinal herbal formulations have long been used by women to treat hormonal and reproductive health conditions such as premenstrual syndrome, menopausal symptoms, hormonal imbalance, infertility, or as contraceptives.1,2 In many communities, because of economic or cultural issues, herbal remedies are the most—or even the only—available therapeutics. Despite the necessity of evaluating their purity, safety, efficacy, and authenticity, herbal formulations are not currently subjected to the same regulations as conventional drugs, which is due to a lack of knowledge about their constituents.3 Another problem arises from misadministration and lack of knowledge about the side effects. For example, many herbal formulations—which may be used for other therapeutic properties or even ingested as daily food or drinks—may cause unwanted side effects for a pregnant woman or her fetus.4 Scientific investigation of safety and efficacy of herbal remedies, food, and beverages with potential effects on hormonal condition may prevent a notable number of unwanted infertility cases, abortions, or fetal abnormalities. It also can lead researchers to reach new active components as well as functional food or beverages for use as contraceptives or fertility therapeutics or supplements.5,6

In Iranian nutrition culture as well as Persian ethnomedicine aromatic waters, or Araghijat or Araghiat (plural of Aragh in Persian), are consumed as delicious daily drinks or as functional beverages. They are usually sweeten with natural sugars such as sucrose or honey. Some prepared syrup of aromatic waters can also be found in food markets containing some additives such as colors, flavoring agent, and sweeteners to improve the organoleptic properties.

Aromatic waters, which are also called floral water, distillate water, or hydrosols, are the side products of the volatile oil industry.7 During industrial hydrodistillation water is evaporated simultaneously with the essential oil of the plants. After condensation of the vapors in contact with cold vessels or tubes, the liquefied components are separated into 2 phases inside a collecting vessel, an oily phase and the aromatic water saturated with different amounts of the volatile components of the plant, which are partly or completely soluble in water.8,9 These 2 phases are then collected; the oily phase (essential oil) is usually sold to the pharmaceutical or cosmetic industry while the aromatic water, depending on its taste, potency, and biological properties, is diluted 1:8 or 1:12 with water. For marketing purposes, the aromatic waters might be distributed in big containers (250-1000 liters) for retail shops or in small sealed polyethylene terephthalate or glass containers (1-5 liters). Some are pasteurized before marketing. In traditional and folk Persian medicine, aromatic water drinks are used also for medicinal purposes to treat different conditions. Despite some adverse effects in improper applications, they are considered as safe beverages. They are mostly mono-herbal but some poly-herbal hydrosol (Aragh) can be found in the food market.10,11 Depending on the plants used to prepare each of the aromatic waters, an overall nature is considered including, hot, cold, wet, dry, or moderate. Pure essential oils are very potent or even harsh in presenting their medicinal activities and are not usually safe in oral administration. But these hydrosols have their unique aroma and composition, which is considerably different from the pure essential oil they co-distilled with. They are usually moderated and balanced by the water and their water-soluble volatile components.12,13 On the other hand, aromatic waters have additional properties not possessed by the essential oils alone.

Over 50 different types of hydrosol beverages are manufactured and marketed in Persian nutrition culture, but as far as we know, chemical composition and biological activities of many of them have not been investigated scientifically. This study was designed to investigate the chemical composition of aromatic waters and hydrosol beverages used in Persian folk medicine for women’s hormonal and reproductive health conditions. A wide range of plants are used in Persian folk medicine for these conditions, but only those plants were investigated that are used to prepare hydrosol beverages.

Materials and Methods

An Overview of Geographical Profile and Climate Variation of Field Study

Fars Province with the highest production rate for aromatic waters was selected as the field of study. Fars, or known in Old Persian as Pârsâ, is the original homeland of the ancient Persians.

The province, with area of 122 400 km2 and a population of 4.59 million people, is located in the south of Iran. There are 3 different climates in the Fars province: the highland area with moderate cold winters and mild summers; the central regions, with relatively rainy mild winter and hot dry summers; and the south to southeast region, which has cold winters with hot summers. The average temperature of Shiraz as the province administrative center is 16.8°C (ranging from 4.7°C to29.2°C).14

The geographical and climatic variation enriches the province with varieties of plants that has a huge influence on agricultural and herbal industries. Over 84 manufactories in Fars province produce different aroma water beverages with full industrial techniques (19 manufactories) or traditional (65 manufactories) equipment. These manufactories are mostly located in Meymand and Darab cities, and their products are distributed in retail markets all over the country.

Information and Sample Collection

To gather information about different aromatic beverages used in Persian folk medicine for women’s hormonal and reproductive health conditions, a field study was conducted from June 2013 to June 2014 under the supervision of a local researcher as a native guide in all visits. A suitable questionnaire was filled according to the information gathered in all visits to local manufactories or their shops. However, most popular aromatic waters with indications for women’s hormonal and reproductive system health conditions were purchased for further analysis (Table 1).

Table 1.

Plant Names and Their Medicinal Parts That Are Used to Prepare Aromatic Waters for Women’s Hormonal and Reproductive Health Conditions.

No. Aromatic Water Beverage Name Aromatic Water Name in Persian Scientific Name Family Plant Parts
Monoherbal aromatic waters
 1 Chamomile Aragh-e-Babooneh Matricaria chamomilla L. Asteraceae Flowers
 2 Dill Aragh-e-Shevid Anethum graveolens L. Apiaceae Leaf
 3 Fennel Aragh-e-Raziyaneh Foeniculum vulgare Mill. Apiaceae Seeds
 4 Ginger Aragh-e-Zanjebil Zingiber officinale Roscoe Zingiberaceae Rhizome
 5 Lemon balm Aragh-e-Badranjbooye Melissa officinalis L. Lamiaceae Leaf
 6 Parsley Aragh-e-Jafari Petroselinum crispum Mill. Apiaceae Leaf
 7 Persian cumin Aragh-e-Zireh Carum carvi L. Apiaceae Seeds
 8 Persian leek Aragh-e-Tareh Allium ampeloprasum ssp. persicum Amaryllidaceae Leaf
 9 Polygermander Aragh-e-Kalpooreh Teucrium polium L. Lamiaceae Aerial parts
 10 Persian hogweed Aragh-e-Golpar Heracleum persicum Desf. ex Fisch. Apiaceae Fruits
 11 Stinging nettle Aragh-e-Gazaneh Urtica dioica Urticaceae Aerial parts
 12 Valerian Aragh-e-Sonbolottib Valeriana officinalis L. Caprifoliaceae Aerial parts
 13 Willow Aragh-e-Beedemeshk Salix spp L. Salicaceae Catkins
 14 White horehound Aragh-e-Farasiyon Marrubium vulgare L. Lamiaceae Aerial parts
 15 Yarrow Aragh-e-Boomadaran Achillea millefolium L. Asteraceae Aerial parts
Polyherbal aromatic waters
 16 Chehelgeyah (polyherbal) Aragh-e-Chehelgeyah A mixture of:
Carum carvi L. Apiaceae Seeds
Carum copticum L. Apiaceae Seeds
Citrus aurantium L. Rutaceae Fruits peel
Glycyrrhiza glabra L. Leguminosae Root
Lavandula angustifolia Mill. Lamiaceae Aerial parts
Matricaria chamomilla L. Asteraceae Flowers
Mentha longifoilia (L.) L. Lamiaceae Leaf
Satureja hortensis L. Lamiaceae Aerial parts
Valeriana officinalis L. Caprifoliaceae Aerial parts
Zataria multiflora Boiss. Lamiaceae Aerial parts
 17 Moderr (polyherbal) Aragh-e-Moderr A mixture of:
Alhagi maurorum Medik. Leguminosae Aerial parts
Cerasus avium (L.) Moench Rosaceae Stalks
Cichorium intybus L. Asteraceae Aerial parts
Fumaria parviflora Lam. Papaveraceae Aerial parts
Marrubium vulgare Lamiaceae Aerial parts
Salix spp L. Salicaceae Leaf
Tribulus terrestris L. Zygophyllaceae Fruits
Zea mays L. Poaceae Silk
 18 Taadol (poly herbal) Aragh-e-Taadol Apium graveolens var. dulce Apiaceae Aerial parts
Juglans regia L. Juglandaceae Leaf
Olea europaea L. Oleaceae Leaf
Urtica dioica L. Urticaceae Aerial parts
Zataria multiflora Boiss. Lamiaceae Aerial parts

Phytochemical Analysis

Volatile components of each beverage sample (500 mL) were extracted with 500 mL of petroleum ether using a glass liquid/liquid extractor system during 150 minutes. Chloroform was used for liquid/liquid extraction of ginger hydrosol. In this technique, the solvent vapor was transferred to the bottom of beverage container. The liquefied vapor in the beverage traveled to the top of the beverage container due to its lower density. Meanwhile, volatile components of the sample were transferred from the aqueous phase to the petroleum ether phase. In order to increase the concentration of volatile components in the organic phase, after 150 minutes the used beverage was replaced with fresh beverage and then extracted for another 150 minutes. The volume of each extracts was decreased to approximately 10 mL at 40°C and 60 rpm using a basic rotary evaporator.15

Gas Chromatography–Mass Spectrometry

The concentrated and dehydrated extract of each ample beverage was injected to a gas chromatography–mass spectrometer for the analysis of respective volatile components. Agilent Technologies 7890 gas chromatograph with a mass detector (Agilent Technologies model 5975 C) was used in this study. The gas chromatograph was equipped with a HP-5MS capillary column (phenyl-methylsiloxan, 30 m, 0.25 mm id; Agilent Technologies 19091S-433 [60°C to 325/350°C]) and a mass spectrometer (Agilent Technologies 5975 C), which was operating in EI mode at 70 eV. The interface temperature was 280°C, and the mass range was 30 to 600 m/z. The oven was heated at a rate of 5°C/min from 60°C to 220°C and then it was held for 10 minutes at 220°C. Helium was used as the carrier gas with a flow rate of 1 mL/min. The components were identified by comparing the mass spectra and retention times with those of reference compounds, or with mass spectra in NIST or Willey libraries or in literature.16,17

Results and Discussion

Hydrosols and Their Phytochemicals

The aromatic waters soft drinks that are used for women’s hormonal and reproductive health conditions are listed in Table 1. The data were prepared according to the information gathered via questionnaires (Tables 1 and 2).

Table 2.

Aromatic Waters’ Indications for Women’s Hormonal and Reproductive Health Conditions as Well as Their Other Indications.

Aromatic Water Beverage Name Nature Indications for Women’s Hormonal and Reproductive Health Condition Other Indications Dosing
Monoherbal aromatic waters
 Chamomile Hot nature Regulating menstrual cycle Treatment of dysmenorrhea (chronic ingestion is contraindicated for pregnant women) Energizer Treatment of painful infections Treatment of phlegmatic fever Vermicide 100 mL TID, before meal
 Caraway  (Persian  cumin) Hot nature Treatment of dysmenorrhea Galactogogue Energizer Nerve tonic Cholesterol lowering Digestant Gastrointestinal tonic For body slimming 100 mL TID, after meal
 Dill Hot nature Galactogogue Menstrual inducer Antihypertension Cholesterol lowering Gastrointestinal tonic Relieve hiccups Antiasthma To treat urinary tract pain 150 mL TID, after meal
 Fennel Hot nature Galactogogue Menstrual inducer (there is a belief that ingestion during pregnancy may help newborn to have more beautiful eyes) Carminative Treatment of colic To remove phlegm Diuretic Treatment of gall stone Treatment of kidney inflammation 100 mL TID, after meal
 Ginger Hot nature Treatment of morning sickness Energizer Nerve tonic Cholesterol lowering effect Digestant Gastrointestinal tonic For body slimming Expectorant 100 mL TID, after meal
 Lemon balm Hot nature Treatment of morning sickness in pregnant women Treatment of dysmenorrhea Nerve tonic, antiseizure Antidepressant Cardiotonic, for heart failure Hypertensive Treatment of insects Bits (topical applications) 100 mL TID, after meal
 Parsley Cold nature Galactogogue Menstrual inducer Aphrodisiac Anti-arthritis Antihypertension Anti-anemia Diuretic Blood cleansing Gastrointestinal tonic Antipyretic 100 mL TID before meal
 Persian hogweed Hot nature Menstrual inducer Appetizer Digestant Carminative Diuretic Strengthening memory Relieve hiccups Antimicrobial Treatment of numbness 100 mL TID, after meal
 Persian leek Hot nature Uterus and reproductive system cleansing Thinning vaginal discharge Prevention of abortion Aphrodisiac Expectorant, antitussive For laryngitis and pharyngitis Digestant Antihemorrhoid Skin lightening 100 mL TID, after meal
 Poleygermander Hot nature Facilitate delivery (start treatment 1 month before delivery due date) Treatment of infertility (start treatment 3 month before pregnancy intention) Energetic Appetizer Liver tonic Anti-emetic Anti-asthma Antihypertension Antidiabetic Blood cleansing 100 mL TID, after meal
 Stinging nettle Hot nature Menstrual inducer Galactogogue Antihypertension Anti-atherosclerosis Antidiabetic Expectorant, anti-asthma Energizer, anti-anemia Treatment of tonsillitis and for strengthening the gums (by gargling) Treatment of prostatic hypertrophy Diuretic Hair tonic 100 mL TID, before meal
 Valerian Hot nature Treatment of dysmenorrhea Nerve tonic, antianxiety Treatment of headache 100 mL QID, before meal and bedtime
 White horehound Hot nature Treatment of ovarian and uterine cysts Treatment of breast cysts Uterus and reproductive system cleansing Thinning vaginal discharge Regulating menstrual cycle Treatment of dysmenorrhea Facilitate delivery Treatment of infertility Treatment of fibroma Prevention and treatment of lipoma mass Liver tonic Treatment of fatty liver Astringent Anti-catarrh in brain 150 mL TID, after meal (contraindicated during pregnancy and menstruation)
 Willow Cold nature Treatment of dysmenorrhea Gastrointestinal tonic Anti-epilepsy Treatment of headache Cardio-tonic Anti-pyretic Anti-dandruff (topical) 150 mL TID, before meal
 Yarrow Hot nature Regulating menstrual cycle Treatment of dysmenorrhea Blood cleansing Nerve tonic, anti-epileptic Cardio tonic Anti-hemorrhoid Antipyretic To treat muscle cramps To treat gastrointestinal inflammations 100 mL TID, after meal
Polyherbal aromatic waters
 Chehelgeyah Treatment of dysmenorrhea Digestant Gastrointestinal tonic Antidiarrhea Treatment of colic 100 mL TID, after meal
 Moderr To facilitate delivery Treatment of uterus cyst 100 mL TID, after meal
 Taadol Hot nature Treatment of dysmenorrhea Antihypertension Anti-atherosclerosis Antidiabetic Blood thinning Lipid lowering 100 mL TID, after meal

This study was designed to investigate the aromatic waters that are used in Persian folk medicine, but some of these aromatic waters and their applications listed in this article have been mentioned also in some traditional Persian manuscript such as Qarabadin-e-salehi 18 and Qarabadin-e-kabir.11 Although most current ethnopharmacological knowledge in Iran has been derived from historical Persian manuscripts,19 it seems that some also have been arisen and accepted in recent years. This might be due to impact of new research on medicinal plants extracts on the knowledge of traditional healers as well as the companies that produce such products, although as far as we know there are not much research studies to provide evidence based data on the effects of aromatic waters or to elucidate their constituents.

In ethnomedical surveys, frequency of citation can reflect a kind of cultural importance of species, which may result in more accurate and more informants’ data obtained from questionnaires.20 The frequency of citations of each hormonal and reproductive application for these beverages in all gathered questionnaires is shown in Figure 1. The higher frequency of citation can show the higher importance of an application for any of these aromatic waters. As seen in Figure 1, in all of the questionnaires (100%), fennel aromatic water was suggested to start menstruation, yarrow aromatic water to regulate menstruation, and Chehelgeyah aromatic water to treat dysmenorrhea. On the other hand, only a few informants believed that valerian aromatic water can regulate menstruation. As seen in Figure 1, most of introduced aromatic waters were believed to have indication to start menstruation. The second frequent cited application was regulation of menstruation.

Figure 1.

Figure 1.

Frequency of citations in questionnaires for women’s hormonal and reproductive health conditions.

In order to roughly investigate the popularity of these beverages, manufactories also were asked to rank them from 1 to 18 according to their mean of annual production over the past 3 years. Since these data were confidential for these manufactories, a ranking system was applied. The aromatic water with the lowest level of production was ranked 1. The manufactories ranking data represented as mean ± SD are shown in Figure 2. Among the aromatic waters that have indication for women’s hormonal and reproductive health conditions, yarrow, white horehound, Chehelgeyah, and fennel aromatic waters had higher annual production level during the past 3 years. This popularity might be because of their efficacy, the aromatic waters’ organoleptic properties such as taste and aroma, or even possible side effects during longer periods of consumptions. This might be also, due to their other applications rather than their effects on the reproductive system.

Figure 2.

Figure 2.

Ranking (1-18) of annual production level of aromatic waters in different manufactories over the past 3 years. Data are represented as mean ± SD.

The plants that are used to prepare these aromatic waters belong to 17 families. Apiaceae, Lamiaceae, and Asteraceae had a greater portion than others (Table 1).

Most of these aromatic waters are prepared from aerial parts of the plants. Different effects on women’s reproductive conditions including aphrodisiac, galactogogue, induction or regulation of menstruation, thinning vaginal discharge, cleansing reproductive system tracts, prevention of abortion, delivery induction, antitumor, treating infertility, and treating morning sickness were mentioned for these aromatic waters. Most of these beverages were believed to have hot nature.

Other indications rather than women’s hormonal and reproductive health were also mentioned for these beverages, which are summarized in Table 2. As mentioned in the introduction, aromatic waters’ aroma and compositions are considerably irrelevant to the pure volatile oil they were co-distilled with. As far as we know, the chemical constituents of most of these aromatic waters have not been investigated scientifically. This study determined constituents of these aromatic waters by gas chromatography–mass spectrometry after liquid-liquid extraction. As seen in Table 3, which shows the results of gas chromatography–mass spectrometry analysis, thymol is major or second major component except for dill, white horehound, willow, Moderr, and yarrow aromatic waters, whose major constituents are dill ether, menthol, phenethyl alcohol, linalool, or camphor. Carvacrol was also detected in all of these aromatic waters except for Taadol.

Table 3.

Aromatic Water Constituents Resulting From Gas Chromatography–Mass Spectrometry Analysis.

Monoherbal Polyherbal
Chamomile Dill Fennel Ginger Lemon balm Parsley Persian leek Stinging nettle Valerian Willow White horehound Yarrow Chehelgeyah Moderr Taadol
cis-Anethole 5.93 0.53 12.47 — 0.94 — — — — — — — 1.08 — —
trans-Anethole — — — 0.752 — — — — 1.13 — — — — — —
Anisyl methyl ketone — — 0.49 — — — — — — — — — — — —
Apiole — — — — 1.43 1.28 — — — — — — — — —
Aristolane — — — — — — — — 3.03 — — — — — —
Artemisia alcohol — — — — — — — — — — — 7.32 — — —
Benzene, 1,4-dimethoxy — — — — — — — — — 8.16 — — — — —
α-Bisabolol oxide A 18.63 — — — — — — — — — — — — — —
α-Bisabolone oxide A 9.08 — — — — — — — — — — — — — —
Borneol — — — 3.21 — — 0.481 — — — — 4.84 — — —
δ-Cadinene — — — — — — — — — 0.92 — — — — —
Bornyl acetate — — — — — — — — — — — — — — —
Camphor — — — — — — 2.183 5.91 — — — 41.88 — 3.84 —
Carvacrol 6.71 12.14 4.65 26.20 30.49 2.74 26.27 12.34 4.12 — 5.39 — 29.36 2.76 —
Carvone 8.12 9.9 14.53 3.38 3.92 — 2.257 — — — — — 0.95 6.54 15.84
Caryophyllene oxide — — — — — — — — — 0.74 — — — — —
1,8-Cineole 0.43 — 0.92 4.37 — — 0.62 4.14 — — 1.24 8.27 — 0.98 0.85
trans-Citral — — — 0.76 — — — — — — — — — — —
Citronellol — — — — — — — — — 4.78 — — — — —
Coumarin, 7-methoxy 0.57 — — — — — — — — — — — — — —
p-Cymen-8-ol — — — — — — — — — — — — — — —
Diethyl disulfide — — — — — — — 1.67 — — — — — — —
Dihydroactinolide — — — — — — — 2.47 — — — — — 0.59 —
Dihydro carveol — — — — 0.72 — — — — — — — — — 8.93
neo-Dihydro carveol 1.33 — 2.17 — — — — — — — — — — — —
cis-Dihydro carvone — 1.32 — — — — 0.54 — — — — — — — 5.76
trans-Dihydro carvone 2.18 0.66 1.72 0.761 1.23 — — — — — — 0.64 — 1.44 —
Dill apiole 0.35 5.96 — — — — 3.375 — — — — — — 22.48 —
Dill ether — 40.91 — — — 1.56 4.783 — — — — — — — —
Durenol — — — — — — — — — — — — — — —
β-Eudesmol — — — — — — — — — 0.67 — 0.52 — — —
Eugenol — 0.91 — — — — — — — 20.43 — 0.62 — 1.06 —
Farnesyl acetate c — — — — — — — — — 0.48 — — — — —
Fenchone — — 13.22 1.05 — — 0.978 — — — — — — — —
Geraniol — — — 2.57 — — — — — — — — — — —
p-Vinyl guaiacol — — — — — — — — — — — — — 1.34 —
Hexadecanoic acid — — — — — 2.16 — 18.09 — — — — — — —
β-Humulene — — — — — — — — — — 1.143 — — — —
trans-Isolimonene — — — — — — — — — — — — — — —
trans-Jasmone — — — — — — — — — — — 0.64 — — —
Linalool 0.38 — — 1.64 0.92 — — 2.31 — — — — 1.22 26.69 —
cis-Linalool oxide (furanoid) — — — — — — — 4.61 — — — — — — —
trans-Linalool oxide (furanoid) — — — — — — — 4.17 — — — — — — —
Menthol — 3.8 — 0.839 — — — — — — 36.27 — 1.79 — —
Menthone — 2.41 — — — — 0.67 — — — 16.16 — — — —
Iso-Menthone — 0.82 — — — — — — — — 6.06 — — — —
Methyl eugenol — — — — — — — — — 1.2 — 1.13 — — —
Methyl hexadecanoate — — — — 4.58 — — — 4.33 — — — — — —
Methyl jasmonate — — — — — — — — — — — — — — —
Methyl octadecanoate — — — — 0.57 — — 3.23 — — — — — — —
Myristicin — — — — — 34 — — — 3.54 — — — — —
Nerol — — — 2.955 — — — — — — — — — — —
Phenethyl alcohol — — — — — — — — — 55.78 — — — — —
Pinocarvone — — — — — — — — — — — — — — —
Piperitenone 5.74 — 0.81 — — — — — — — — — — — 0.76
Piperitenone oxide — — — — — — — — — — — — — — —
Piperitone — — — — — — — — — — — — — — —
Pulegone 3.1 0.57 4.77 2.209 2.56 0.99 — 1.93 — 1.07 0.48 — — — 6.13
Sabina ketone — — — — — — — — — — — — — — —
γ-Terpinene — — — — — — — — — 1.16 — — — — —
Terpinen-4-ol — 0.56 0.45 0.58 0.89 — — — — — 0.838 2.02 0.85 — 0.49
α-Terpineol 0.36 — — 1.675 1.11 — — — — — — — — — —
Terpinolene — — 1.15 — — — — — — — — 0.47 — — —
β-Thujone — — — — — — — — — — — — — — —
trans-Thujone — — — — — — — — — — — 3.16 — — —
Thymol 34.35 19.49 42.2 41.455 46.97 56.6 56.944 27.28 8.45 0.63 14.55 0.52 64.74 8.25 44.98
Thymol ethanoate — — — — — — — — — — — — — — 13.8
Toluene, 2,3-dimethoxy — — — — — — — — — — 1.043 — — — —
Verbenone — — — — — — — — — — — 1.97 — — —
m-Xylene 0.44 — — — — — — — — — — — — — —
o-Xylene — — — — — — — — — — 1.16 — — 0.93 —
p-Xylene — — — — — — — — — — 5.53 0.482 — 5.95 —
Yomogi alcohol — — — — — — — — — — — 19.36 — — —

According to both hierarchical cluster analysis and K-means, all the aromatic waters that contain thymol as the major constituent make a cluster that includes some subcultures (Figure 3, Table 4). Lemon balm, Persian leek, Chehelgeyah, and ginger aromatic waters make a distinct subcluster. The reason behind the observed similarities between these aromatic waters based on clustering analysis was the presence of comparable amounts of thymol (41.45% to 64.74%) and carvacrol (26.20% to 30.49%) in these aromatic waters. The certain similarity of fennel, Taadol, and chamomile was also seen by hierarchical cluster analysis, which might be due to the presence of comparable amounts of thymol as the major constituent (42.20%, 44.98%, and 34.35%), carvone (14.53%, 15.84%, and 8.12%), and carvacrol (6.71%, 4.12%, and 4.65%) in these 3 aromatic waters.

Figure 3.

Figure 3.

Cluster analysis of aromatic waters’ constituents based on hierarchical cluster analysis. The aromatic waters are the following: 1, chamomile; 2, lemon balm; 3, yarrow; 4, Chehelgeyah; 5, white horehound; 6, stinging nettle; 7, parsley; 8, Moderr; 9, fennel; 10, dill; 11, valerian; 12, Taadol; 13, willow; 14, Persian leek; and 15, ginger.

Table 4.

Analysis of the Aromatic Waters’ Constituents Based on K-Means by SPSS Software (10 Epochs of Training).

Aromatic Waters’ Name Class
Dill I
Chamomile, stinging nettle, fennel, valerian, Taadol II
Yarrow III
Lemon balm, Chehelgeyah, Persian leek, ginger IV
White horehound V
Willow VI
Parsley VII
Moderr VIII

In contrast to other aromatic waters, thymol was fond in zero or trace amount in willow and yarrow aromatic waters. Their major constituents are also completely different from others, and they were clustered at distinct groups.

Based on clustering methods applied in this study, although some similarities could be found, composition of white horehound, Moderr, willow, and yarrow aromatic waters revealed more differences than others. The main components of these aromatic waters were menthol (36.27%, white horehound), linalool (26.69%, Moderr), camphor (41.88, yarrow), and phenethyl alcohol (55.73%, willow).

Literature Survey

We could not find any reports on chemical constituents of aromatic waters of the mentioned plants in Table 1. Thus, it was not possible to compare the results, but the major components of the reported essential oils are summarized in Table 5.

Table 5.

Profile of Essential Oils Reported in Literature for the Plants Used to Prepare Aromatic Waters With Indications for Women’s Hormonal and Reproductive Health Conditions.

Plant Name Profile of Essential Oils Reported in Literature for Plants Used to Prepare Monoherbal Aromatic Waters References
Chamomile Bisabolol oxide A and B, bisabolon oxide A, (E)-β-farnesene, α-bisabolol, chamazulene 23
α-Bisabolol, chamazulene, farnesene and a-pinene, bisabolol oxides A and B 24
Dill Carvone, trans-dihydrocarvone, dill ether, α-phellandrene, limonene 22
Fennel Limonene, β-pinene, myrcene, fenchone 25
Ginger Geranial, a-zingiberene, (E,E)-α-farnesene, neral, ar-curcumene 26–28
Lemon balm Citronellal, citral, geranial, beta-caryophyllene, beta-caryophyllene oxid, citronellal, geraniol, β-pinen 29
Parsley Myrcene, myristicin, α-pinene, β-pinene, α-phellandrene, p-mentdatriene, dillapiol, bisabolole, camphor 30
Persian cumin Thymol, o-cymene, γ-terpinen, trimethylene dichloride, β-pinene, 2-(1-cyclohexenyl) cyclohexanone, β-hellandrene 31
Carvacrol, carvone, α-pinene, limonene, γ-terpinene, linalool, carvenone, p-cymene 32
Persian leek Dipropyl disulfide, dipropyl trisulfide, methyl propyl disulfide, dimethyl disulfide, allyl methyl disulfide 21
Persian hogweed Stem oil before flowering: (E)-anethole, terpinolene, γ-terpinene, limonene 33
Stem oil at the full flowering stage: (E)-anethole, terpinolene, γ-terpinene
Seed oil: hexyl butyrate, octyl acetate, hexyl isobutyrate
Stinging nettle Neophytadiene, butyl tetradecyl ester, bis(2-ethyl hexyl) maleat, 1,2-benzen dicarboxylic acid 34
Valerian Patchoulol, α-pinene, β-humulene 35
Bornyl acetate, valerenic acid, (Z)-valernyl acetate, acetoxyvaleranone 36
White horehound 4,8,12,16-Tetramethyl heptadecan-4-olid, Germacrene D-4-ol and α-pinene, eudesmol, citronellol, citronellyl formate, germacrene D 37
Willow Salix aegyptiaca leaf: 1,4-Dimethoxybenzene, phenylethyl alcohol, carvone 38
Yarrow Sabinene, 1,8-cineole, borneol, bornyl acetate, α-pinene, β-pinene, terpinine-4-oland chamazulene 39
Plant Name Profile of Essential Oils Reported in Literature for Plants Used to Prepare Polyherbal Aromatic Waters
Chehelgeyah Persian cumin Mentioned above
Ajowan caraway Thymol, ρ-cymene, γ-terpinene 40, 41
Bigarade orange Limonene, Myrcene, Octane 42
Licorice 2-Ethoxy-1-propanol, 4-terpineol, hexanal 43
Thymol, carvacrol, (2E,4E)-decadienal, ß-caryophyllene oxide, 1a,10a-epoxyamorpha-4-ene 44
Lavender Linalool, linalyl acetate, 1,8-cineole, ocimene, terpinen-4-ol, camphor 45
Chamomile Mentioned above
Mint Piperitone oxide, menthone, isomenthone 46
Piperitone oxide, 1,8-cineole, caryophyllene oxide, piperitenone oxide 47
Summer savory γ-Terpinene, carvacrol, thymol, cymene 48, 49
Valerian Mentioned above
Saatar Thymol, carvacrol, linalool 50
Moderr Caltrop Whole plant: a-Amyrin, n-hexadecanoic acid, 9,12,15-octadecanoic acid 51
Camelthorn Leaf oil: drimenol, 9-octylheptadecane, 4-hexyl-2,5-dihydro-2,5-dioxo-3-furanacetic acid 52
Stem oil: neophytadiene, trans-ionone, 6,10,14-trimethyl-2-pentadecanone, actinidiolide 52
Cherry stalk Profile of volatile components was not found in literatures
Chicory Octane, n-nonadecane, n-hexadecane, pentadecanone 53
Corn silk cis-Terpineol, acor-4-ene (6,11-oxido), citronellol 54
2-Heptanol and geosmin 55
White horehound Eudesmol, citronellol, citronellyl formate, germacrene D 56
Willow Mentioned above
Taadol Celery Leaf: 4-Chloro-4,4-dimethyl-3-(1-imidazolyl)-valerophenone, 1-dodecanol, 9-octadecen-12-ynoic acid 57
Olive Leaf: 2-hexenal, α-farnesene, linalool 58
Stinging nettle Profile of volatile components was not found in literatures
Saatar Mentioned above
Walnut Husks: (E)-4,8-dimethyl-1,3,7-nonatriene, pinocarvone, pinocarveol, myrtenal, myrtenol, (E,E)-4,8,12-trimethyl-1,3,7,11-tridecatetraene, caryophyllene epoxide, verbenol 59
Leaf: germacrene D, methyl salicylate 60

For most of these aromatic waters including lemon balm, stinging nettle, valerian, fennel, Persian leek, ginger, and white horehound, the major components in the aromatic waters and essential oils are completely different. Different allyl sulfides were reported as the major components of the Persian leek essential oils21 but none of these components were detected in the aromatic waters in the present study. In the case of dill essential oil, the major components were reported to be phellandrene, limonene, myristicin, followed by dill ether.22 In the present study, the major compound in dill aromatic water was dill ether (40.9%), followed by thymol and carvacrol. On the other hand, the major components of parsley leaf (myristicin) and willow (phenylethyl alcohol) were similar in aromatic waters and reported essentials but their amount as well as nonmajor constituents were different (Tables 3 and 5). As was expected, comparing the results of this study on chemical composition of the aromatic waters (Table 3) with the previous reports on the plants’ essential oils (Table 5) shows that there is a significant difference between aromatic waters and essential oil components. This difference may arise from different water solubility of the volatile components. It is possible that some of these volatile components were not entered in water during the preparation procedure of aromatic waters. Also, it can be concluded that it is essential to consider different pharmacological and biological properties of the aromatic waters due to different chemical compositions compared with the pure co-distilled essential oils.

Different biological activities of the plants used to prepare the identified aromatic waters on the reproductive system or sexual hormone conditions were investigated in the literature and summarized in Table 6. We could not find any report on hormonal activity or effects on reproductive system conditions for any of the aromatic waters. But, for some of these plants including fennel, dill, chamomile, and ginger, some clinical trial have been reported on their essential oils or different extracts. Of course, we cannot compare the observed effects of the essential oils or other extracts of these plants with their aromatic waters due to differences in constituents as well as their concentrations but these reports might strengthen the hypothesis of the beneficial effects for these aromatic waters on women’s reproductive and hormonal health conditions.

Table 6.

Literature Survey on Biological Activities of Plants Used in Preparing Aromatic Waters With Indications for Women’s Hormonal and Reproductive Health Conditions.

Plant name Observed effects Plant preparation Study type Reference
Chamomile Relieving the intensity of mastalgia associated with premenstrual syndrome Capsule 100 mg Clinical trial 61
Treatment of menopausal symptoms Chewable tablets Clinical trial 62
Improving the symptoms of vaginitis Chamomile douche Clinical trial 24, 63
Treatment of polycystic ovary syndrome (PCOS) Alcoholic extract In vivo 64, 65
Pain relief effect with and without physiological doses of sex hormones Hydroalcoholic extract In vivo 66
Decrease in the serum level of estrogen Hydroalcoholic extract In vivo 67
Decline in the mean number of primary and graafian follicles Hydroalcoholic extract In vivo
Uterotonic action Aqueous extract In vitro 68
Dill Treatment of premenstrual syndrome and dysmenorrheal Aqueous extract or tea Clinical trial 61, 69–71
Reducing the pain severity in primary dysmenorrhea Dill powder Clinical trial 72
Facilitating delivery, prevention of post term pregnancy Seed infusion Clinical trial 73–75
Regulating menstrual cycle, increasing the duration of the estrous cycle Aqueous extract In vivo 76
Contractive effects on myometer, enhanced releasing of oxytocin Seed extracts In vivo 77, 78
Infertility induction Seed fractions In vivo 79–81
Estrogenic activities Ethanolic extracts In vitro 82
Fennel Treatment of primary dysmenorrhea Seed extracts Clinical trial 69, 83–87
Reducing the severity of dysmenorrhea Essential oil (oral drop) Clinical trial 88, 89
Inhibitory effect on the response of uterine to oxytocin and PGE2 Essential oil In vivo 90
Inducing folliculogenesis Alcoholic extract In vivo 91
Effects on blood sex hormones and reproductive tissues Alcoholic extract In vivo 89, 92, 93
Effects on uterine contraction Essential oil In vivo 90
Effects on fertility Alcoholic extract In vivo 94
Ginger Treatment of morning sickness during pregnancy Extract or plant powder Clinical trial 27, 95–102
Treatment of postoperative nausea and vomiting after gynecological surgery Extract or plant powder Clinical trial 103, 104
Treatment of primary dysmenorrhea Extract or plant powder Clinical trial 105–110
Effects on uterus muscles Hydroalcoholic extract In vivo 111, 112
Effects on sexual behavior and fertility Hydroalcoholic extract In vivo 113–115
Effects on the fetal development Hydroalcoholic extract In vivo 116, 117
Lemon balm Emmenagogue (stimulate menstruation) Aqueous extract In vivo 118, 119
Persian hogweed Inhibitory effects on folliculogenesis and cause infertility in females Hydroalcoholic extract In vivo 120
Testosterone level Hydroalcoholic extract In vivo 121
Persian leek Antimicrobial and antifungal effects (possibly useful for vaginosis) Hydroalcoholic extract In vitro 122, 123
Stinging nettle Anti-androgenic activity Aqueous extract Clinical trial 124
Treatment of heavy menstrual bleeding Aqueous extract Clinical trial 125
Hyperoestrogenism, gynaecomastia Aqueous extract Case report 126
Anti-proliferative activities against breast cancer cell lines (MCF-7) Aqueous extract In vitro 127
Positive effect on luteinizing hormone or testosterone level Hydroalcoholic extract In vivo 128–130
Positive effects on spermatozoa sperm parameters Hydroalcoholic extract In vivo 131
Follicular development and induction of estrus Hydroalcoholic extract In vivo 132
Valerian Improves the quality of sleep in women with menopause Hydroalcoholic Clinical trial 133
Treatment for dysmenorrhea Hydroalcoholic Clinical trial 134
Destructive effect on the ovarian tissue Hydroalcoholic extract In vivo 135
Significant decrease in zinc level in fetal brain In vivo 136
White horehound Improving hormonal parameters in PCOS Alcoholic extract In vivo 137
Estrogen like activity Phytoestrogen constituents Hypothesis 138
Yarrow Reducing fetal weight and increasing placental weight (unsafe during pregnancy) Hydroalcoholic extract In vivo 139
Estrogenic/antiestrogenic activity Aqueous extract In vivo 140
Estrogenic activity Aqueous extract from leaves In vitro 141, 142

For some of these plants mentioned in Table 6, different aqueous, ethanol, and methanol extracts or plant powders were investigated and it is not clear that if the volatile components had a role in the observed effects. On the other hand, for some others listed in Table 6, the medicinal parts that were used in these studies are different from those that are used to prepare the aromatic waters in Persian ethnomedicine. For oriental plane we could not find any related report. The present investigation was not intended to evaluate the efficacy of these aromatic waters, but high consumption of these aromatic waters in Persian folk medicine and nutrition culture might be related to their efficacy.

Conclusion

This article introduced some aromatic waters that are used for women’s reproductive and hormonal health conditions in Persian folk medicine with different popularity and market values. Almost in all investigated aromatic waters the chemical composition was remarkably different from the essential oils of the plants that were used for their preparations. Clustering these aromatic waters using SPSS software revealed that despite the differences in the plants genus, family, and the medicinal parts of the plants that are used to prepare them, some similarity can be identified in their chemical compositions. In most cases thymol, carvacrol, and carvone were the major constituents and may have a role in their biological activities.

Scientific investigation of these aromatic waters may lead to the development of some functional beverages and soft drinks as a safe way of administration of essential oils or even new lead components or therapeutic agents.

Acknowledgments

The authors want to thank Nahal Shamaeezadeh (PharmD student at Shiraz University of Medical Sciences) for assistance in some parts of the extracting procedures.

Authors’ Note: This study was part of the PharmD thesis project of Mehdi Afifi.

Author Contributions: AH wrote the draft and contributed in guidance, data collection, and revisions of the final version of the article. HE and MA contributed to data collection, analyzing data, and revising the final version of the article.

Declaration of Conflicting Interests: The authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Funding: The authors disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This study was funded by Shiraz University of Medical Sciences (Grant No. 92-01-70-7067).

Ethical Approval: This study was an experimental and laboratorial work and did not require ethical approval.

References

  • 1. Hardy ML. Herbs of special interest to women. J Am Pharm Assoc (Wash). 1999;40:234–242. [DOI] [PubMed] [Google Scholar]
  • 2. Tesch BJ. Herbs commonly used by women: an evidence-based review. Am J Obstet Gynecol. 2003;188:S44–S55. [DOI] [PubMed] [Google Scholar]
  • 3. Nordeng H, Havnen GC. Use of herbal drugs in pregnancy: a survey among 400 Norwegian women. Pharmacoepidemiol Drug Sag. 2004;13:371–380. [DOI] [PubMed] [Google Scholar]
  • 4. Ernst E. Herbal medicinal products during pregnancy: are they safe? BJOG. 2002;109:227–235. [DOI] [PubMed] [Google Scholar]
  • 5. Adams J, Sibbritt D, Lui CW. The use of complementary and alternative medicine during pregnancy: a longitudinal study of Australian women. Birth. 2011;38:200–206. [DOI] [PubMed] [Google Scholar]
  • 6. Hamedi A, Abbasi F, Khoshnoud M, et al. Reproductive toxicity of Cassia absus seeds in female rats: possible progesteronic properties of chaksine and b sitosterol. Pharm Chem J. 2015;49:220–226. [Google Scholar]
  • 7. Sağdιç O. Sensitivity of four pathogenic bacteria to Turkish thyme and oregano hydrosols. LWT Food Sci Technol. 2003;36:467–473. [Google Scholar]
  • 8. Aazza S, Lyoussi B, Miguel MG. Antioxidant activity of eight hydrosols from Morocco. Asian J Plant Sci. 2012;11(3):137–142. [Google Scholar]
  • 9. Schorr S. Bioresonance and phytotherapeutic hydrosols in healing. http://www.bioponic.com/pdfs/Bioresonance.pdf. Accessed June 16, 2017.
  • 10. Hamedi A, Moheimani SM, Sakhteman A, Etemardfard H, Moein M. An overview on indications and chemical composition of aromatic waters (hydrosols) as functional beverages in Persian nutrition culture and folk medicine for hyperlipidemia and cardiovascular conditions. J Evid Based Complementary Altern Med. 2017;22(4):544–561. doi:10.1177/2156587216686460 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11. Aghili Shirazi S. Qarabadin-e-Kabir (in Persian). Tehran, Iran: Ostad Allah Qoli Khan Qajar; 1772/1855. [Google Scholar]
  • 12. Catty S. Hydrosols: The Next Aromatherapy. Rochester, VT: Inner Traditions/Bear; 2001. [Google Scholar]
  • 13. Price L, Price S. Understanding Hydrolats: The Specific Hydrosols for Aromatherapy: A Guide for Health Professionals. London, England: Churchill Livingstone; 2004. [Google Scholar]
  • 14. Sedaghatzadeh Z, Tashakorrian V, Mobasheri M, et al. Province of Fars (in Persian). Tehran, Iran: Shabak; 2014. [Google Scholar]
  • 15. Moein M, Zarshenas MM, Delnavaz S. Chemical composition analysis of rose water samples from Iran. Pharm Biol. 2014;52:1358–1361. [DOI] [PubMed] [Google Scholar]
  • 16. Hamedi A, Mohagheghzadeh A, Rivaz S. Preliminary pharmacognostic evaluation and volatile constituent analysis of spathe of Phoenix dactylifera L. (Tarooneh). Pharmacogn J. 2013;5(2):83–86. [Google Scholar]
  • 17. Mojab F, Hamedi A, Nickavar B, et al. Hydrodistilled volatile constituents of the leaves of Daucus carota L. subsp. sativus (Hoffman.) Arcang. (Apiaceae) from Iran. J Essent Oil Bearing Plants. 2008;11:271–277. [Google Scholar]
  • 18. Heravi MG. Qarabadin-e-Salehi. Tehran, Iran: Dar-ol-khalafeh (Litograph in Persian) 1765. [Google Scholar]
  • 19. Hamedi A, Zarshenas MM, Sohrabpour M, Zargaran A. Herbal medicinal oils in traditional Persian medicine. Pharm Biol. 2013;51:1208–1218. [DOI] [PubMed] [Google Scholar]
  • 20. Heinrich M, Edwards S, Moerman DE, Leonti M. Ethnopharmacological field studies: a critical assessment of their conceptual basis and methods. J Ethnopharmacol. 2009;124:1–17. [DOI] [PubMed] [Google Scholar]
  • 21. Mnayer D, Fabiano-Tixier AS, Petitcolas E, et al. Chemical composition, antibacterial and antioxidant activities of six essentials oils from the Alliaceae family. Molecules. 2014;19:20034–20053. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22. Sharopov FS, Wink M, Gulmurodov IS, Isupov SJ, Zhang HJ, Setzer WN. Composition and bioactivity of the essential oil of Anethum graveolens L. from Tajikistan. Int J Med Aromatic Plants. 2013;3:125–130. [Google Scholar]
  • 23. Amiri S, Sharafzadeh S. Essential oil components of German chamomile cultivated in Firoozabad, Iran. Orient J Chem. 2014;30:365–367. [Google Scholar]
  • 24. Srivastava JK, Shankar E, Gupta S. Chamomile: a herbal medicine of the past with a bright future. Mol Med Rep. 2010;3:895–901. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25. El Ouariachi E, Lahhit N, Bouyanzer A, et al. Chemical composition and antioxidant activity of essential oils and solvent extracts of Foeniculum vulgare Mill. from Morocco. J Chem Pharm Res. 2014;6:743–748. [Google Scholar]
  • 26. Singh G, Kapoor IP, Singh P, de Heluani CS, de Lampasona MP, Catalan CA. Chemistry, antioxidant and antimicrobial investigations on essential oil and oleoresins of Zingiber officinale . Food Chem Toxicol. 2008;46:3295–3302. [DOI] [PubMed] [Google Scholar]
  • 27. Ali BH, Blunden G, Tanira MO, Nemmar A. Some phytochemical, pharmacological and toxicological properties of ginger (Zingiber officinale Roscoe): a review of recent research. Food Chem Toxicol. 2008;46:409–20. [DOI] [PubMed] [Google Scholar]
  • 28. Geiger JL. The essential oil of ginger, Zingiber officinale, and anaesthesia. Int J Aromatherapy. 2005;15:7–14. [Google Scholar]
  • 29. Bağdat RB, Coşge B. The essential oil of lemon balm (Melissa officinalis L.), its components and using fields. J Fac Agric OMU. 2006;21:116–121. [Google Scholar]
  • 30. Nawel O, Ahmed H. Phytochemical analysis and antimicrobial bioactivity of the Algerian parsley essential oil (Petroselinum crispum). Afr J Microbiol Res. 2014;8:1157–1169. [Google Scholar]
  • 31. Begum J, Bhuiyan MNI, Chowdhury JU, et al. Antimicrobial activity of essential oil from seeds of Carum carvi and its composition. Bangladesh J Microbiol. 2008;25(2):85–89. [Google Scholar]
  • 32. Johri R. Cuminum cyminum and Carum carvi: an update. Pharmacogn Rev. 2011;5(9):63. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33. Sefidkon F, Dabiri M, Mohammad N. Analysis of the oil of Heracleum persicum L. (seeds and stems). J Essent Oil Res. 2004;16:296–298. [Google Scholar]
  • 34. Lahigi SH, Amini K, Moradi P, et al. Investigating the chemical composition of different parts extracts of bipod nettle Urtica dioica L. in Tonekabon region. Physiology. 2011;2:337–340. [Google Scholar]
  • 35. Wang J, Zhao J, Liu H, et al. Chemical analysis and biological activity of the essential oils of two valerianaceous species from China: Nardostachys chinensis and Valeriana officinalis . Molecules. 2010;15:6411–6422. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36. Safaralie A, Fatemi S, Sefidkon F. Essential oil composition of Valeriana officinalis L. roots cultivated in Iran: comparative analysis between supercritical CO2 extraction and hydrodistillation. J Chromatogr A. 2008;1180:159–164. [DOI] [PubMed] [Google Scholar]
  • 37. Abadi A, Hassani A. Essential oil composition and antioxidant activity of Marrubium vulgare L. growing wild in Eastern Algeria. Int Lett Chem Phys Astronom. 2013;9:17–24. [Google Scholar]
  • 38. Karimi I, Hayatgheybi H, Kamalak A, et al. Chemical composition and effect of an essential oil of Salix aegyptiaca L., Salicaceae (musk willow), in hypercholesterolemic rabbit model. Rev Bras Farmacogn. 2011;21:407–414. [Google Scholar]
  • 39. Nadim M, Malik AA, Ahmad J, et al. The essential oil composition of Achillea millefolium L. cultivated under tropical condition in India. World J Agric Sci. 2011;7:561–565. [Google Scholar]
  • 40. Oroojalian F, Kasra-Kermanshahi R, Azizi M, et al. Phytochemical composition of the essential oils from three Apiaceae species and their antibacterial effects on food-borne pathogens. Food Chem. 2010;120:765–770. [Google Scholar]
  • 41. Kavoosi G, Tafsiry A, Ebdam AA, et al. Evaluation of antioxidant and antimicrobial activities of essential oils from Carum copticum seed and Ferula assafoetida latex. J Food Sci. 2013;78:T356–T361. [DOI] [PubMed] [Google Scholar]
  • 42. Moraes TM, Kushima H, Moleiro FC, et al. Effects of limonene and essential oil from Citrus aurantium on gastric mucosa: role of prostaglandins and gastric mucus secretion. Chem Biol Interact. 2009;180:499–505. [DOI] [PubMed] [Google Scholar]
  • 43. Gyawali R, Seo HY, Shim SL, et al. Effect of γ-irradiation on the volatile compounds of licorice (Glycyrrhiza uralensis Fischer). Eur Food Res Technol. 2008;226:577–582. [Google Scholar]
  • 44. Farag MA, Wessjohann LA. Volatiles profiling in medicinal licorice roots using steam distillation and solid-phase microextraction (SPME) coupled to chemometrics. J Food Sci. 2012;77:C1179–C1184. [DOI] [PubMed] [Google Scholar]
  • 45. Cavanagh H, Wilkinson J. Biological activities of lavender essential oil. Phytother Res. 2002;16:301–308. [DOI] [PubMed] [Google Scholar]
  • 46. Gulluce M, Sahin F, Sokmen M, et al. Antimicrobial and antioxidant properties of the essential oils and methanol extract from Mentha longifolia L. ssp. longifolia. Food Chem. 2007;103:1449–1456. [Google Scholar]
  • 47. Nikšić H, Bešović EK, Makarević E, et al. Chemical composition, antimicrobial and antioxidant properties of Mentha longifolia (L.) Huds. essential oil. J Health Sci. 2012;2:192–200. [Google Scholar]
  • 48. Khajeh M. Optimization of process variables for essential oil components from Satureja hortensis by supercritical fluid extraction using Box-Behnken experimental design. J Supercrit Fluids. 2011;55:944–948. [Google Scholar]
  • 49. Gursoy UK, Gursoy M, Gursoy OV, et al. Anti-biofilm properties of Satureja hortensis L. essential oil against periodontal pathogens. Anaerobe. 2009;15:164–167. [DOI] [PubMed] [Google Scholar]
  • 50. Saei-Dehkordi SS, Tajik H, Moradi M, et al. Chemical composition of essential oils in Zataria multiflora Boiss. from different parts of Iran and their radical scavenging and antimicrobial activity. Food Chem Toxicol. 2010;48:1562–1567. [DOI] [PubMed] [Google Scholar]
  • 51. Abirami P, Rajendran A. GC-MS analysis of Tribulus terrestris L. Asian J Plant Sci Res. 2011;1:13. [Google Scholar]
  • 52. Samejo M, Memon S, Bhanger M, Khan KM. Chemical composition of essential oils from Alhagi maurorum . Chem Nat Compounds. 2012;48(5). doi:10.1007/s10600-012-0417-8. [Google Scholar]
  • 53. Judžentienė A, Būdienė J. Volatile constituents from aerial parts and roots of Cichorium intybus L. (chicory) grown in Lithuania. Chemija. 2008;19(2):25–28. [Google Scholar]
  • 54. El-Ghorab A, El-Massry KF, Shibamoto T. Chemical composition of the volatile extract and antioxidant activities of the volatile and nonvolatile extracts of Egyptian corn silk (Zea mays L.). J Agric Food Chem. 2007;55:9124–9127. [DOI] [PubMed] [Google Scholar]
  • 55. Flath RA, Forrey RR, John JO, et al. Volatile components of corn silk (Zea mays L.): possible Heliothis zea (Boddie) attractants. J Agric Food Chem. 1978;26:1290–1293. [Google Scholar]
  • 56. Kadri A, Zarai Z, Békir A, et al. Chemical composition and antioxidant activity of Marrubium vulgare L. essential oil from Tunisia. Afr J Biotechnol. 2013;10:3908–3914. [Google Scholar]
  • 57. Nagella P, Ahmad A, Kim SJ, et al. Chemical composition, antioxidant activity and larvicidal effects of essential oil from leaves of Apium graveolens . Immunopharm Immunol. 2012;34:205–209. [DOI] [PubMed] [Google Scholar]
  • 58. Flamini G, Cioni PL, Morelli I. Volatiles from leaves, fruits, and virgin oil from Olea europaea Cv. Olivastra Seggianese from Italy. J Agric Food Chem. 2003;51:1382–1386. [DOI] [PubMed] [Google Scholar]
  • 59. Buttery RG, Light DM, Nam Y, et al. Volatile components of green walnut husks. J Agric Food Chem. 2000;48:2858–2861. [DOI] [PubMed] [Google Scholar]
  • 60. Farag MA. Headspace analysis of volatile compounds in leaves from the Juglandaceae (walnut) family. J Essent Oil Res. 2008;20:323–327. [Google Scholar]
  • 61. Sharifi F, Simbar M, Mojab F, Majd HA. Comparison of the effects of Matricaria chamomila (Chamomile) extract and mefenamic acid on the intensity of mastalgia associated with premenstrual syndrome. Womens Health Bull. 2014;1(2):e20042. [DOI] [PubMed] [Google Scholar]
  • 62. Kupfersztain C, Rotem C, Fagot R, et al. The immediate effect of natural plant extract, Angelica sinensis and Matricaria chamomilla (Climex) for the treatment of hot flushes during menopause. A preliminary report. Clin Exp Obstet Gynecol. 2002;30:203–206. [PubMed] [Google Scholar]
  • 63. Benetti C, Manganelli F. Clinical experiences in the pharmacological treatment of vaginitis with a camomile-extract vaginal douche. Minerva Ginecol. 1985;37:799–801. [PubMed] [Google Scholar]
  • 64. Farideh ZZ, Bagher M, Ashraf A, Akram A, Kazem M. Effects of chamomile extract on biochemical and clinical parameters in a rat model of polycystic ovary syndrome. J Reprod Infertil. 2010;11:169–174. [PMC free article] [PubMed] [Google Scholar]
  • 65. Sarmast S, Zafari Z, Minaei B, et al. Female infertility: efficacy of cammomile extracts on polycystic ovary syndrome in rat. Int J Fertil Streril. 2010;4:80. [Google Scholar]
  • 66. Kesmati M, Barfinejad N, Moghadam HF. Effect of Matricaria recutita on acute pain in the presence and absence of sex hormones. J Res Med Sci. 2007;12:190–197. [Google Scholar]
  • 67. Johari H, Sharifi E, Mardan M, et al. The effects of a hydroalcoholic extract of Matricaria chamomilla flower on the pituitary-gonadal axis and ovaries of rats. Int J Endocrinol Metab. 2011;9:330–334. [Google Scholar]
  • 68. Shipochliev T. Uterotonic action of extracts from a group of medicinal plants. Vet Med Nauki. 1980;18(4):94–98. [PubMed] [Google Scholar]
  • 69. Yazdani M, Shahrani M, Hamedi B. Comparison of fennel and chamomile extract and placebo in treatment of premenstrual syndrome and dysmenorrheal. Bimonth J Hormozgan Univ Med Sci. 2004;8(1):57–61. [Google Scholar]
  • 70. Sharifi F, Simbar M, Mojab F, et al. Comparison of the effects of Matricaria chamomila (chamomile) extract and mefenamic acid on the intensity of premenstrual syndrome. Complement Ther Clin Pract. 2014;20(1):81–88. [DOI] [PubMed] [Google Scholar]
  • 71. Jenabi E, Ebrahimzadeh S. Chamomile tea for relief of primary dysmenorrhea. Iran J Obestet Gynecol Infertil. 2010; 3(1):39–42. [Google Scholar]
  • 72. Heidarifar R, Mehran N, Heidari A, Tehran HA, Koohbor M. Effect of dill (Anethum graveolens) on the severity of primary dysmenorrhea in compared with mefenamic acid: a randomized, double-blind trial. J Res Med Sci. 2014;19:326–330. [PMC free article] [PubMed] [Google Scholar]
  • 73. Zagami SE, Golmakani N, Kabirian M, et al. Effect of dill (Anethum graveolens Linn.) seed on uterus contractions pattern in active phase of labor. Indian J Tradit Knowedge. 2012;11:602–606. [Google Scholar]
  • 74. Mirmolaee ST, Hekmatzadeh SF, Kazemnazhad A, et al. Evaluating the effects of dill (Anethum graveolens) seed on the duration of active phase and intensity of labour pain. J Herb Med. 2015;5:26–29. [Google Scholar]
  • 75. Hekmatzadeh SF, Bazarganipour F, Malekzadeh J, et al. A randomized clinical trial of the efficacy of applying a simple protocol of boiled Anethum graveolens seeds on pain intensity and duration of labor stages. Complement Ther Med. 2014;22:970–976. [DOI] [PubMed] [Google Scholar]
  • 76. Monsefi M, Ghasemi M, Bahaoddini A. The effects of Anethum graveolens L. on female reproductive system. Phytother Res. 2006;20:865–868. [DOI] [PubMed] [Google Scholar]
  • 77. Al-Snafi A. The pharmacological importance of Anethum graveolens—a review. Int J Pharm Pharm Sci. 2014;6(4):11–13. [Google Scholar]
  • 78. Gharib AM, Mard S, Farboud Y. Effect of Anethum graveolens fruit extract on rat uterus contractions. Iran J Basic Med Sci. 2005;8:263–270. [Google Scholar]
  • 79. Malihezaman M, Mojaba M, Elham H, et al. Anti-fertility effects of different fractions of Anethum graveolens L. extracts on female rats. Afr J Tradit Complement Alternat Med. 2012;9:336–341. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 80. Monsefi M, Zahmati M, Masoudi M, Javidnia K. Effects of Anethum graveolens L. on fertility in male rats. Eur J Contracept Reprod Health Care. 2011;16:488–497. [DOI] [PubMed] [Google Scholar]
  • 81. Monsefi M, Lohrasbi P, Abpaikar Z, Bakhtiari S. Anti-implantation and anti-fertility potentials of Anethum graveolens L. extracts in rats [published online April 20, 2015]. Toxicol Environ Chem. doi:10.1080/02772248.2015.1027204. [Google Scholar]
  • 82. Saeed IA, Ali L, Jabeen A, Khasawneh M, Rizvi TA, Ashraf SS. Estrogenic activities of ten medicinal herbs from the Middle East. J Chromatogr Sci. 2013;51:33–39. [DOI] [PubMed] [Google Scholar]
  • 83. Moslemi L, Bekhradi R, Galini Moghaddam T, et al. Comparative effect of fennel extract on the intensity of primary dysmenorrhea. Afr J Pharm Pharmacol. 2012;6:1770–1773. [Google Scholar]
  • 84. Delaran M, Jafari F. The effect of fennel on the pre-menstrual syndrome. Knowledge Health. 2011;6(1):1–6. [Google Scholar]
  • 85. Moslemi L, Aghamohammadi A, Bekhradi R, et al. The comparison of vitamin E and fennel extract on duration of pain in primary dysmenorrhea. Knowledge Health. 2012;7(2):61–64. [Google Scholar]
  • 86. Asti P, Delfan B, Masudi M, et al. Ibuprofen versus fennel for the relief of postpartum pain: a randomized controlled trial. J Fam Plann Reprod Health Care. 201;5(2):65. [Google Scholar]
  • 87. Delaram M, Kheiri S, Hodjati MR. Comparing the effects of echinophora-platyloba, fennel and placebo on pre-menstrual syndrome. J Reprod Infertil. 2011;12:221–226. [PMC free article] [PubMed] [Google Scholar]
  • 88. Bokaie M, Farajkhoda T, Enjezab B, et al. Oral fennel (Foeniculum vulgare) drop effect on primary dysmenorrhea: effectiveness of herbal drug. Iran J Nurs Midwifery Res. 2013;18(2):128. [PMC free article] [PubMed] [Google Scholar]
  • 89. Mirabolghasemi G, Alizadeh F. The effect of hydroalcoholic extract of fennel (Foeniculum vulgare) seed on serum levels of sexual hormones in female Wistar rats with polycystic ovarian syndrome (PCOS). AMUJ. 2014;17(5):70–78. [Google Scholar]
  • 90. Ostad S, Soodi M, Shariffzadeh M, et al. The effect of fennel essential oil on uterine contraction as a model for dysmenorrhea, pharmacology and toxicology study. J Ethnopharmacol. 2001;76:299–304. [DOI] [PubMed] [Google Scholar]
  • 91. Khazaei M, Montaseri A, Khazaei MR, Khanahmadi M. Study of Foeniculum vulgare effect on folliculogenesis in female mice. Int J Fertil Steril. 2011;5:122–127. [PMC free article] [PubMed] [Google Scholar]
  • 92. Dehghani F, Panjehshahin M, Mirzaee Z, et al. Effect of Foeniculum vulgare organic extract on blood sex hormones and reproductive tissues of male rats. J Appl Anim Res. 2005;27(1):17–20. [Google Scholar]
  • 93. Sadeghpour N, Khaki AA, Najafpour A, et al. Study of Foeniculum vulgare (fennel) seed extract effects on serum level of estrogen, progesterone and prolactin in mouse. Crescent J Med Biol Sci. 2015;2(1):23–27. [Google Scholar]
  • 94. Fallah H, Kianbakht S. Study on effects of chicory (Cichorium intybus L.), fennel (Foeniculum vulgare Mill.) and dill (Anethum graveolens L.) on fertility and neonatal gender in rats. J Med Plant. 2012;11(9):192–196. [Google Scholar]
  • 95. Ernst E, Pittler M. Efficacy of ginger for nausea and vomiting: a systematic review of randomized clinical trials. Br J Anaesth. 2000;84:367–371. [DOI] [PubMed] [Google Scholar]
  • 96. Keating A, Chez RA. Ginger syrup as an antiemetic in early pregnancy. Altern Ther Health Med. 2002;8(5):89–91. [PubMed] [Google Scholar]
  • 97. Vutyavanich T, Kraisarin T, Ruangsri RA. Ginger for nausea and vomiting in pregnancy: randomized, double-masked, placebo-controlled trial. Obstet Gynecol. 2001;97:577–582. [DOI] [PubMed] [Google Scholar]
  • 98. Smith C, Crowther C, Willson K, Hotham N, McMillian V. A randomized controlled trial of ginger to treat nausea and vomiting in pregnancy. Obstet Gynecol. 2004;103:639–645. [DOI] [PubMed] [Google Scholar]
  • 99. Borrelli F, Capasso R, Aviello G, et al. Effectiveness and safety of ginger in the treatment of pregnancy-induced nausea and vomiting. Obstet Gynecol. 2005;105:849–856. [DOI] [PubMed] [Google Scholar]
  • 100. Bryer E. A literature review of the effectiveness of ginger in alleviating mild-to-moderate nausea and vomiting of pregnancy. J Midwifery Womens Health. 2005;50(1):e1–e3. [DOI] [PubMed] [Google Scholar]
  • 101. Pongrojpaw D, Somprasit C, Chanthasenanont A. A randomized comparison of ginger and dimenhydrinate in the treatment of nausea and vomiting in pregnancy. J Med Assoc Thai. 2007;90:1703–1709. [PubMed] [Google Scholar]
  • 102. Choi J, Han J, Ahn H, et al. Assessment of fetal and neonatal outcomes in the offspring of women who had been treated with dried ginger (Zingiberis rhizoma siccus) for a variety of illnesses during pregnancy. J Obstet Gynecol. 2015;35:125–130. [DOI] [PubMed] [Google Scholar]
  • 103. Bone M, Wilkinson D, Young J, et al. Ginger root—a new antiemetic. The effect of ginger root on postoperative nausea and vomiting after major gynaecological surgery. Anaesthesia. 1990;45:669–671. [DOI] [PubMed] [Google Scholar]
  • 104. Kalava A, Darji SJ, Kalstein A, et al. Efficacy of ginger on intraoperative and postoperative nausea and vomiting in elective cesarean section patients. Eur J Obstet Gynecol Reprod Biol. 2013;169:184–188. [DOI] [PubMed] [Google Scholar]
  • 105. Ozgoli G, Goli M, Moattar F. Comparison of effects of ginger, mefenamic acid, and ibuprofen on pain in women with primary dysmenorrhea. J Altern Complement Med. 2009;15:129–132. [DOI] [PubMed] [Google Scholar]
  • 106. Rahnama P, Montazeri A, Huseini HF, et al. Effect of Zingiber officinale R. rhizomes (ginger) on pain relief in primary dysmenorrhea: a placebo randomized trial. BMC Complement Altern Med. 2012;12:92. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 107. Kashefi F, Khajehei M, Tabatabaeichehr M, et al. Comparison of the effect of ginger and zinc sulfate on primary dysmenorrhea: a placebo-controlled randomized trial. Pain Manag Nurs. 2014;15:826–833. [DOI] [PubMed] [Google Scholar]
  • 108. Kashefi F, Khajehei M, Alavinia M, et al. Effect of ginger (Zingiber officinale) on heavy menstrual bleeding: a placebo-controlled, randomized clinical trial. Phytother Res. 2015;29:114–119. [DOI] [PubMed] [Google Scholar]
  • 109. Daily JW, Zhang X, Kim DS, et al. Efficacy of ginger for alleviating the symptoms of primary dysmenorrhea: a systematic review and meta-analysis of randomized clinical trials. Pain Med. 2015;16:2243–2255. [DOI] [PubMed] [Google Scholar]
  • 110. Shirvani MA, Motahari-Tabari N, Alipour A. The effect of mefenamic acid and ginger on pain relief in primary dysmenorrhea: a randomized clinical trial. Arch Gynecol Obstet. 2015;291:1277–1281. [DOI] [PubMed] [Google Scholar]
  • 111. Ghayur MN, Gilani AH. Inhibitory activity of ginger rhizome on airway and uterine smooth muscle preparations. Eur Food Res Technol. 2007;224:477–481. [Google Scholar]
  • 112. Buddhakala N, Talubmook C, Sriyotha P, et al. Inhibitory effects of ginger oil on spontaneous and PGF2alpha-induced contraction of rat myometrium. Planta Med. 2008;74:385–391. [DOI] [PubMed] [Google Scholar]
  • 113. Khaki A, Farnam A, Badie AD, et al. Treatment effects of onion (Allium cepa) and ginger (Zingiber officinale) on sexual behavior of rat after inducing an antiepileptic drug (lamotrigine). Balkan Med J. 2012;29:236–242. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 114. Shalaby M, Hamowieh A. Safety and efficacy of Zingiber officinale roots on fertility of male diabetic rats. Food Chem Toxicol. 2010;48:2920–2924. [DOI] [PubMed] [Google Scholar]
  • 115. Rezk R, Ibrahim M, Darwish M. Efficacy of ginger in alleviating the severe radiation-induced biochemical, histological and embryological impactions pregnant female albino rats. Isotope Radiat Res. 2005;37:625–645. [Google Scholar]
  • 116. Wilkinson JM. Effect of ginger tea on the fetal development of Sprague-Dawley rats. Reprod Toxicol. 2000;14:507–512. [DOI] [PubMed] [Google Scholar]
  • 117. Shanoon A. Effects of Zingiber officinale powder on semen characteristic and blood serum sex hormones concentration in broilers breeder male. Int J Poult Sci. 2011;10:863–866. [Google Scholar]
  • 118. Gardiner P. Lemon balm (Melissa officinalis): The Longwood Herbal Task Force; 2000. [updated June 24, 2003; cited 2017]. 1–18. Available from: http://www.mcp.edu/herbal/default.htm.
  • 119. Weidner MS, Sigwart K. Investigation of the teratogenic potential of a Zingiber officinale extract in the rat. Reprod Toxicol. 2000;15:75–80. [DOI] [PubMed] [Google Scholar]
  • 120. Hemati A, Azarnia M, Nabiuni M, et al. Effect of the hydroalcoholic extract of Heracleum persicum (Golpar) on folliculogenesis in female Wistar Rats. Cell J (Yakhteh). 2012;14(1):47. [PMC free article] [PubMed] [Google Scholar]
  • 121. Firouzabadi FB, Mirhosseini M. Effect of Persian hogweed (Heracleum persicum) on the morphological changes in mice testes and the level of hormone testosterone. Razi J Med Sci. 2012;19(99):18–24. [Google Scholar]
  • 122. Hughes BG, Lawson LD. Antimicrobial effects of Allium sativum L. (garlic), Allium ampeloprasum L. (elephant garlic), and Allium cepa L. (onion), garlic compounds and commercial garlic supplement products. Phytother Res. 1991;5:154–158. [Google Scholar]
  • 123. Sadeghi M, Zolfaghari B, Senatore M, et al. Antifungal cinnamic acid derivatives from Persian leek (Allium ampeloprasum subsp. persicum). Phytochem Lett. 2013;6:360–363. [Google Scholar]
  • 124. Najafipour F, Rahimi AO, Mobaseri M, et al. Therapeutic effects of stinging nettle (Urtica dioica) in women with hyperandrogenism. Int J Curr Res Acad Rev. 2014;2(7):153–160. [Google Scholar]
  • 125. Sourtiji A. Comparison of the effect of mefenamic acid and the hydroalcoholic extract of Urtica dioica on the volume of heavy menstrual bleeding in students at Azad University of Babol (2011-2012). AMUJ. 2013;16(4):27–36. [Google Scholar]
  • 126. Sahin M, Yilmaz H, Gursoy A, Demirel AN, Tutuncu NB, Guvener ND. Gynaecomastia in a man and hyperoestrogenism in a woman due to ingestion of nettle (Urtica dioica). N Z Med J. 2007;120(1265):U2803. [PubMed] [Google Scholar]
  • 127. Fattahi S, Ardekani AM, Zabihi E, et al. Antioxidant and apoptotic effects of an aqueous extract of Urtica dioica on the MCF-7 human breast cancer cell line. Asian Pac J Cancer Prev. 2013;14:5317–5323. [DOI] [PubMed] [Google Scholar]
  • 128. Pourahmadi M, Bagheri M, Karimi Jashni H, et al. The effect of hydroalchoholic extract Urtica dioica on concentrations of sex hormones in adult male rats. PARS J Med Sci. 2013;10(4):29–34. [Google Scholar]
  • 129. Morovvati H, Najafzadehvarzi H, Rashidi K. Effect of Urtica dioica extract on histological and histometrical changes of testis of hamster after testosterone administration. Zahedan J Res Med Sci. 2013;15(11):4–8. [Google Scholar]
  • 130. Ghafari S, Balajadeh BK, Golalipour M. Effect of Urtica dioica L. (Urticaceae) on testicular tissue in STZ-induced diabetic rats. Pak J Biol Sci. 2011;14:798–804. [DOI] [PubMed] [Google Scholar]
  • 131. Jalili C, Salahshoor MR, Naseri A. Protective effect of Urtica dioica L against nicotine-induced damage on sperm parameters, testosterone and testis tissue in mice. Iran J Reprod Med. 2014;12:401–408. [PMC free article] [PubMed] [Google Scholar]
  • 132. Mehrotra S, Hoque M, Agarwal S. Follicular development and induction of estrus in anestrus goats by medicinal plants. Indian Vet J. 2009;86:527–528. [Google Scholar]
  • 133. Taavoni S, Ekbatani N, Kashaniyan M, et al. Effect of valerian on sleep quality in postmenopausal women: a randomized placebo-controlled clinical trial. Menopause. 2011;18:951–955. [DOI] [PubMed] [Google Scholar]
  • 134. Mirabi P, Dolatian M, Mojab F, et al. Effects of valerian on the severity and systemic manifestations of dysmenorrhea. Int J Gynecol Obstet. 2011;115:285–288. [DOI] [PubMed] [Google Scholar]
  • 135. Gholamzade N, Kargar H, Ghassemi F. Hydro-alcoholic extract of Valeriana officinalis on histologic change of ovary in rats. Int J Biol Pharm Allied Sci. 2013;2:308–313. [Google Scholar]
  • 136. Mahmoudian A, Rajaei Z, Haghir H, et al. Effects of valerian consumption during pregnancy on cortical volume and the levels of zinc and copper in the brain tissue of mouse fetus. J Chin Integr Med. 2012;10:424–429. [DOI] [PubMed] [Google Scholar]
  • 137. Mokhtari M, Ebrahimpoor MR, Harfsheno S. The effects of alcoholic extract of Marrubum vulgare on hormonal parameters in female rat model of polycystic ovarian syndrome. Med Sci J Islamic Azad Univ Tehran Medical Branch. 2014;24(2):74–80. [Google Scholar]
  • 138. Ulbricht C, Basch E, Weissner W, et al. An evidence-based systematic review of herb and supplement interactions by the Natural Standard Research Collaboration. Expert Opinion on Drug Safety. 2006;5(5):719–728. [DOI] [PubMed] [Google Scholar]
  • 139. Boswell-Ruys CL, Ritchie HE, Brown-Woodman PD. Preliminary screening study of reproductive outcomes after exposure to yarrow in the pregnant rat. Birth Defects Res B Dev Reprod Toxicol. 2003;68:416–420. [DOI] [PubMed] [Google Scholar]
  • 140. Dalsenter PR, Cavalcanti AM, Andrade AJ, et al. Reproductive evaluation of aqueous crude extract of Achillea millefolium L.(Asteraceae) in Wistar rats. Reprod Toxicol. 2004;18:819–823. [DOI] [PubMed] [Google Scholar]
  • 141. Innocenti G, Vegeto E, Dall’Acqua S, et al. In vitro estrogenic activity of Achillea millefolium L. Phytomedicine. 2007;14:147–152. [DOI] [PubMed] [Google Scholar]
  • 142. Mazandarani M, Osia N, Ghafourian M. Antioxidant activity and ethno pharmacological survey of Achillea biebersteinii Afan in the treatment of dysmenorrhoea in traditional medicine of Golestan province, Iran. Int J Womens Health Reprod Sci. 2015;3:107–110. [Google Scholar]

Articles from Journal of Evidence-based Complementary & Alternative Medicine are provided here courtesy of SAGE Publications

RESOURCES