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. 2016 Jan 5;6(1):11. doi: 10.1007/s13205-015-0322-5

Emerging CAM Ziziphus nummularia with in vivo sedative-hypnotic, antipyretic and analgesic attributes

Abdur Rauf 1,✉, Jawad Ali 2, Haroon Khan 3, Mohammad S Mubarak 4, Seema Patel 5,✉
PMCID: PMC4701709  PMID: 28330081

Abstract

Ziziphus nummularia from Rhamnaceae family is traditionally used for sedative-hypnotic, antipyretic and analgesic purposes; however, scientific validations are lacking. This in vivo study was undertaken to verify the above ameliorative properties of Z. nummularia root methanolic extract. Various fractions of the extract were assayed on Balb/c mice by open field, Brewer’s yeast-induced hyperthermia and acetic acid-induced writhing experiments. The significance of the outcomes was analyzed with statistical tests. Various fractions of the extract exhibited marked dose-dependent (p < 0.05) sedative-hypnotic and antipyretic activities. The biological efficacies were most pronounced between 50 and 100 mg/kg. Further, the acetic acid-induced abdominal constrictions were significantly (p < 0.05) attenuated by the extract. Chloroform fraction of the extract was most dominant followed by ethyl acetate. The demonstrated therapeutic attributes of Z. nummularia extract can be exploited to isolate pharmaceutically relevant compounds.

Keywords: Ziziphus nummularia, Sedative, Hypnotic, Antipyretic, Antinociceptive, Anti-inflammation

Introduction

Since the dawn of human race, plants are being used as medicines (Petrovska 2012). World Health Organization (WHO) statistics reflects that 80 % of the world population, mostly from developing countries still rely on botanical for health care (Khan 2014). A vast majority of conventional drugs and most of the complementary and alternative medicines (CAM) are plant-derived (Mainardi et al. 2009). For their benign toxicity compared to chemotherapeutics, phytochemicals are widely used against a plethora of infectious, metabolic and degenerative diseases (Pandey and Rizvi 2009). The health restorative applications of plant products are exhaustive, yet the significant are antioxidant, anti-inflammatory, anticancer, anti-diabetic, analgesic, antimicrobial, antiulcer, etc. (Benzie and Wachtel-Galor 2011). The key phytochemicals have been characterized to be alkaloids, phenolic acids, flavonoids, terpenoids, sterols, saponins, tannins, etc., though each species has its distinct botanical repertoire. Most plants are geographically confined and the medicinal uses largely hinge on their local distribution and traditional knowledge on them (Saslis-Lagoudakis et al. 2014).

In this resource-depleted world, sustainability requires the search for food and medicine in the vicinity (Cordell 2011). Ziziphus is a genus in family Rhamnaceae with global distribution (Zhao et al. 2014). The common species of this genus are Z. jujube, Z. zizyphus, Z. mauritiana, Z. joazeiro, Z. lotus, Z. spina-christi, Z, spinosa, Z. oxyphylla, Z. oenoplia and Z. oxyphylla Edgew (Pawlowska et al. 2009). The ethnobotanical, phytochemical, economical, and pharmacological attributes of many species have been extensively studied. Some popular food and medicinal uses of this genus have been mentioned below. The drupes ‘jujube or Chinese dates’ are nutritious and popular fruits (Gao et al. 2013b). They are often processed into pulps, polysaccharides, antioxidants, pickles, jam, fermented (masau) (Adeli and Samavati 2014; Li et al. 2014; Elaloui et al. 2015). Usage of this genus as dietary supplements and herbal medicines in Tunisia (Elaloui et al. 2015), China (Plastina et al. 2012), Japan (Oshima et al. 2015), Korea (Kim et al. 2013), and other Asian countries (San et al. 2013) have been well-documented (Chen et al. 2014b). Many of the folkloric practices have been empirically validated now. The verified health benefits include antioxidant (Olajuyigbe and Afolayan 2011; Chen et al. 2014c), anti-inflammation (Yu et al. 2012), antibacterial and antifungal (Ghazghazi et al. 2014), antiulcerogenic (Wahida et al. 2007), immunomodulatory (Chen et al. 2014a), diabetes ameliorating (Goli-malekabadi et al. 2014), hepatoprotective (Kwape et al. 2013; Yue et al. 2014), hematopoietic (Chen et al. 2014b), antimutagenic (Boriollo et al. 2014), cytotoxic (Jafarian et al. 2014), and sedative-hypnotic (Gao et al. 2013a). The plant parts conferring the biological effects are diverse such as leaves (Nisar et al. 2007; Kwape et al. 2013; Goyal et al. 2013), fruits (Plastina et al. 2012; Chen et al. 2014a, b, c), seeds (Cao et al. 2010; San et al. 2013; Gao et al. 2013a), bark (Olajuyigbe and Afolayan 2011; Boriollo et al. 2014) and root (Rao et al. 2012).

Ziziphus nummularia, is a species of the above genus, and native to the arid regions of India (Bachaya et al. 2009), Pakistan (Abbasi et al. 2013), Afghanistan, Iraq, Iran, Egypt, and Israel (Desai et al. 2008). The versatile uses of this species have been depicted in an insightful review (Pandey et al. 2010). Ethnobotanical survey for wild edible and medicinal plants have projected it as a major species in tribal communities of Lesser Himalayas-Pakistan (Abbasi et al. 2013). This plant is known for its palatable and vitamic C-rich drupes. Literature search reflects its usage as an astringent, treatment of scabies and other skin diseases (Khare 2003). Its use as antidiarrheal in Sariska region of India (Upadhyay et al. 2011) and anthelmintic in Pakistan (Bachaya et al. 2009) is prevalent. Also, the analgesic and anti-inflammatory efficacy of its cyclopeptide alkaloid-rich leaf extract has been reported (Goyal et al. 2013). However, there is no information of its beneficial role in insomnia, anxiety, pain, and fever. Though, some other species of Ziziphus genus have been proven effective in easing those ailments such as Z. jujube (Jiang et al. 2007; Cao et al. 2010; Yeung et al. 2012; Awad et al. 2014), Z. oxyphylla Edgew (Nisar et al. 2007; Kaleem et al. 2013), Z. mauritiana (San et al. 2013). So, this in vivo study was undertaken to evaluate the sedative-hypnotic, antipyretic and analgesic activities of Z. nummularia root extracts as a pharmacological justification of its traditional usage and premise for future drug discovery (Fig. 1).

Fig. 1.

Fig. 1

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The overview of Z. nummularia extract eliciting sedative, hypnotic, antipyretic, analgesics effect in balb/c mice

Materials and methods

Plant material

The roots of Z. nummularia were collected from Takht Bhai District Mardan, Khyber Pakhtunkhwa, Pakistan. The plant was identified and authenticated by Professor Dr. Abdur Rashid, a botanist at the Botany Department, University of Peshawar, Pakistan. A voucher specimen (BOT 200399) has been deposited in the herbarium of the department of Botany, University of Peshawar, Pakistan.

Experimental animals

Balb/c mice of both gender, each weighing about 24–26 g were kept under standard laboratory conditions at (25 ± 4 °C). The animals were fed with a laboratory diet and water ad libitum. All experiments were performed at the Pakistan Council of Scientific and Industrial Research (PCSIR), University of Peshawar, Pakistan and were approved by the local Ethical Committee of the Peshawar University, Pakistan.

Extraction and fractionation

The root fragments of Z. nummularia were shade-dried at room temperature followed by coarse grinding. The powdered material (300 g) was exhaustively extracted with 99 % methanol for 7 days. The extract was concentrated and dried in a rotary evaporator and which yielded 38 g of brownish mass. The solid mass was suspended in water and successively fractionated with various solvents of increasing polarity, and the corresponding fractions of n-hexane, chloroform, ethyl acetate, and ethanol were obtained.

Sedative activity (open field test)

The sedative effect of the crude extract was evaluated according to published procedures using the open field method (Walsh and Cummins 1976). This method has been proven effective in the assessment of locomotor activity and anxiety-linked behaviors (Lau et al. 2008). The apparatus used for the test consisted of a white wooden area (150 cm in diameter) enclosed in stainless steel walls and the area was divided by black lines, into four squares. The open field was placed inside a light and sound-attenuated room. The mice were adapted to red light (40 W) for 60 min prior to the start of experiment and fed ad libitum. The animals were administered with normal saline and Z. nummularia root extract at the doses of 50 and 100 mg/kg. After 30 min of the treatment, each mouse was placed in the center of the box and the numbers of lines crossed were counted.

Hypnotic properties in phenobarbitone-induced sleeping time

The test mice were divided into groups of six each. Mice of the control group (negative control) were orally treated with normal saline (10 ml/kg) whereas those of the positive control group were given the standard drug bromazepam (5 mg/kg). This drug, from the class benzodiazepines (BZD) imparts short-term relief from anxiety by modulating the neurotransmitters in brain (Mandrioli et al. 2010). The remaining mice were treated with the Z. nummularia root extract at 50 and 100 mg/kg doses. After 30 min of treatment, all animals were injected with the barbiturate drug phenobarbitone sodium at a dose of 35 mg/kg and observed for onset and duration of sleep. The hypnotic effect of the extract was evaluated.

Brewer’s-yeast-induced hyperthermia

The antipyretic activities of Z. nummularia root extract were assessed in Brewer’s yeast (Saccharomyces cerevisiae)-induced hyperthermia (Tomazetti et al. 2005). Pyrexia was induced in mice by injection of 10 ml/kg of 15 % suspension of yeast. The normal body temperature of the animals was recorded with a digital clinical thermometer (Hartmann, Germany) using rectum, while the tail was fastened with an adhesive tape. The rectal temperature of each mouse was measured again after 19 h of yeast injection as described above. Mice that developed a minimum increase of 0.5 °C or more temperature were selected for the experiment. These rodents were categorized in group of size 6. A group of mice was fed with saline (10 ml/kg) and used as negative control, whereas other groups was treated either with paracetmol (100 mg/kg through intraperitoneal injection) as standard drug or Z. nummularia root extract at the doses of 50 and 100 mg/kg. After the respective treatment, the rectal temperature of each animal was again recorded at 1 h intervals for following 5 h. The obtained data were used for the calculation of percentage reduction in rectal temperature. Antipyretic activity was defined as the efficacy of test drug to abate the induced-pyrexia (Muhammad et al. 2013).

Reduction in temperature%=B-CB-A×100

where A is the normal body temperature, B is the temperature after pyrexia induction, C is the temperature after 1, 3 and 5 h.

Acetic acid-induced writhing test

Intraperitoneal injection of acetic acid triggers writhing, most likely due to the release of TNF-α, interleukin 1β and interleukin 8 by macrophages and mast cells (Ribeiro et al. 2000). The mice were divided into groups of 6 for evaluation of the analgesic effect of Z. nummularia roots extract. One group was injected with normal saline (10 ml/kg) and used as negative control. Another group was injected with diclofenac (5 and 10 mg/kg). The last group was treated with Z. nummularia root extract at 50 and 100 mg/kg. The mice were injected with acetic acid (1 % intraperitoneal) and the subsequent abdominal constriction (writhing) was counted for 10 min after 5 min of acetic acid injection.

Statistical analyses

The results are expressed as the mean ± standard error of the mean (SEM). One-way analysis of variance (ANOVA) was used for analysis of data followed by Dunnett’s test for multiple comparisons (Hoffman et al. 2008). Differences were considered significant at p ≤ 0.05.

Results and discussion

Effect of extract/fractions in open field test

The efficacy of intraperitoneally administered Z. nummularia root extract (50 and 100 mg/kg) and bromazepam in mice have been illustrated in Fig. 2. The extract showed marked sedative effect with decreased locomotion in dose-dependent manner. The chloroform fraction was the most dominant followed by ethyl acetate with (p < 0.05 and p < 0.01) at 50 and 100 mg/kg.

Fig. 2.

Fig. 2

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Data shows the number of lines crossed by animals in a box, 30 min after treatment with normal saline (10 ml/kg, control), extract/fractions of Z. nummularia roots (50 and 100 mg/kg) or bromazepam (5 mg/kg). Values are given as mean ± S.E.M, (n = 6). *p < 0.05 or **p < 0.01, p < 0.001, all compared with control

Effect of extract in open field test

The effect of Z. nummularia roots extract at 50 and 100 mg/kg, in phenobarbitone-sleep in mice is shown in Table 1. The extract significantly (p < 0.05) reduced the sleep latency time (time taken for the onset of sleep) and increased the sleep in dose-dependent manner. Chloroform followed by ethyl acetate extract was the most potent fraction in inducing sleep and increasing its duration. The soporific effect elicited by the extract in bromazepam treated group was highly significant (p < 0.001).

Table 1.

The effect of Z. nummularia root fractions in phenobarbitone-induced sleep in mice

Drug Intraperitoneal dose Onset of sleep (min) Duration of sleep (min)
Normal saline 10 ml/kg + phenobarbitone 23.27 ± 1.09 7.56 ± 2.45
Crude extract 50 mg/kg + phenobarbitone 18.10 ± 2.70 15.40 ± 1.75
100 mg/kg + phenobarbitone 14.33 ± 1.08* 23.88 ± 2.75*
Hexane 50 mg/kg + phenobarbitone 19.66 ± 1.12 9.45 ± 0.67
100 mg/kg + phenobarbitone 19.00 ± 1.05 9.60 ± 1.06
Chloroform 50 mg/kg + phenobarbitone 15.33 ± 1.21* 22.33 ± 1.12*
100 mg/kg + phenobarbitone 10.56 ± 0.99** 27.05 ± 1.35**
Ethyl acetate 50 mg/kg + phenobarbitone 18.44 ± 1.12* 20.12 ± 1.45*
100 mg/kg + phenobarbitone 12.57 ± 1.49* 23.67 ± 1.56*
Aqueous 50 mg/kg + phenobarbitone 17.44 ± 1.06 17.04 ± 0.99*
100 mg/kg + phenobarbitone 13.03 ± 0.89* 23.55 ± 1.77*
Bromazepam 5 mg/kg + phenobarbitone 3.25 ± 1.10*** 61.45 ± 1.10***
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* Data shows the onset and duration of sleep (in min) in mice pretreated with normal saline (10 ml/kg), extract/fractions (50 and 100 mg/kg) or bromazepam (5 mg/kg) and then all groups were treated with phenobarbitone (35 mg/kg). Data presented as mean ± S.E.M, (n = 6). * p < 0.05, ** p < 0.01, *** p < 0.001, all with respect to control

Effect of extract in yeast induced hyperthermia

The antipyretic effect of Z. nummularia root extract in yeast-induced hyperthermia has been presented in Fig. 3. The extract produced profound antipyretic effect in a dose-dependent manner during various assessment times (1–5 h). Additionally, the post chloroform treatment caused pronounced reduction in induced pyrexia with 45.77 and 67.44 % effect at 50 and 100 mg/kg, respectively after 1 h of injection.

Fig. 3.

Fig. 3

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The percent antipyretic effect of extract/fractions of Z. nummularia roots in acetic acid-induced writhing. Data presented as mean ± S.E.M, (n = 6). *p < 0.05, **p < 0.01, all with respect to control

Effect of extract in acetic acid induced-writhing

The antinociceptive activity of the Z. nummularia root extract has been shown in Fig. 4. As per the result, the extract significantly reduced pain sensation in acetic acid-induced writhing test. For all fractions of the extract, dose-dependent effects have been observed at 50 and 100 mg/kg, and the analgesic effect of chloroform fraction was most pronounced with 57.86 and 74.28 % at 50 and 100 mg/kg, respectively.

Fig. 4.

Fig. 4

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The percent antinociceptive effect of extract/fractions of Z. nummularia roots in acetic acid-induced writhing. Data presented as mean ± S.E.M, (n = 6). *p < 0.05, **p < 0.01, ***p < 0.001, all with respect to control

Discussion

The findings from this investigation suggest that the roots extract of Z. nummularia displays significant in vivo sedative-hypnotic, antipyretic, and analgesic effects. The open field test is one of the commonly used behavioral test protocol for screening of sedative and anxiolytic activity of substances in laboratory animals (de la Peña et al. 2013), whereas the phenobarbitone-induced sleeping time test (Inganakal et al. 2012) is employed for the assessment of hypnotic properties. The roots extract significantly reduced the movement of mice in the open field test apparatus implying the tranquilizing nature of its components. While the precise mechanistic of therapeutic role is not known, several probable causes were formulated. The allosteric modulation of γ-aminobutyric acid (GABA) receptors in mice brain might be the underlying mechanism (Shrestha et al. 2012). The prolongation of the sleeping duration suggested the hypnotic properties of the extract. The effect could have been mediated by the induction of central nervous system (CNS) depressant activity by the bioactive components of the extract (Ya’u et al. 2011). In this investigation, the crude extracts showed remarkable sedative-hypnotic effect which varied upon fractionation. The chloroform fraction was most potent followed by ethyl acetate whereas the hexane fraction did not produce significant results. From the results, it could be assumed that the sedative-hypnotic constituents of Z. nummularia roots are mostly concentrated in chloroform and ethyl acetate fractions. Results revealed that Z. nummularia root extract elicits antipyretic effects in yeast-induced hyperthermia in the murine models. Chloroform fractions proved to be the most active fraction followed by ethyl acetate, suggesting the presence of pharmacologically important components in them.

The acetic acid-induced writhing test is considered very effective in detecting antinociceptive effects of various extracts. Its sensitivity is much higher than other methods (hot plate, tail flick, carrageenan-induced paw edema, formalin-induced paw licking, etc.) used for this purpose (Ramirez et al. 2010). The abdominal constrictions and the resultant painful sensations provoked by the acid has been attributed to the perturbation and interplay of bradykinin, prostaglandins, interleukin-1β (IL-1β), interleukin-8 (IL-8), and tumor necrosis factor-α (TNF-α) (Ribeiro et al. 2000). The Z. nummularia root extract at the doses of 50–100 mg/kg, moderated the abdominal constrictions in a dose-dependent manner. One possible mechanism of this action could be the diminished production of prostaglandin E2 (PGE2) (Ying et al. 2014). The extract could be interfering with both central (opioid and cholinergic pathways) and peripheral (COX-2) pathways in eliciting the anti-inflammatory effects (Sawada et al. 2014). The chloroform fraction was the most effective followed by the ethyl acetate fraction in reducing pain and sensitivity. It indicates the accumulation of the antinociceptive constituents in these fractions.

Anxiety and sleep interruptions have become the norm of current stressful living (Han et al. 2012). Also, the instances of depression, suicidal attempts are soaring (Cash and Bridge 2009). Reliance on the prescription drugs is not free of side effects. The frequent intake aggregates the metabolic system in long term, becomes ineffective and overdose proves fatal. Opioid analgesics (buprenorphine, fentanyl, codeine, ativan, dextropropoxyphene, methadone, oxycodone, carisoprodol, etc.) overdose-caused death cases are rising dramatically (Paulozzi et al. 2012). The deadly combination opioid, benzodiazepines, and/or alcohol use poses huge risk of morbidity (Gudin et al. 2013). On the other hand, CAM are naturally sourced, thus pose lower genotoxicity compared to chemicals. In this regard, Z. nummularia root extract merits further investigation. Isolation of the functional constituents and their structural elucidation warrants impetus. In a preliminary screening study, the phytochemicals alkaloids (ziziphines), carbohydrates, saponins, flavonoids, anthocyanins, and tannins were found in the ethanolic extract of Z. oenoplia (Suksamrarn et al. 2005; Rao et al. 2012). These components might be instrumental in inducing the tested biological responses. The hypnotic efficacy of Z. jujuba Mill. jujubosides has been correlated to the impact on circadian rhythm and the serotonergic system (Cao et al. 2010). Further studies on the therapeutic importance of this plant might provide affordable medication to large section population in the developing countries. However, possible health risks must be verified for broader remedial applications.

Conclusion

The cumulative findings from this study suggest that the root extract of Z. nummularia exhibits remarkable sedative-hypnotic, antipyretic and analgesic effects in mice. These findings explain the rationale of traditional medicinal use of Z. nummularia for alleviating pain, fever, insomnia, seizures, muscle spasms, anxiety etc. However, more in-depth studies are required to establish the safety, efficacy, and active constituents of this plant. This study is expected to inspire further investigation into this underutilized medicinal plant.

Acknowledgments

The author Abdur Rauf is grateful for the financial support provided by the Higher Education Commission (HEC) of Pakistan and the Institute of Chemical Sciences, University of Peshawar, Pakistan under grant number 112-26510-2PS1-258.

Compliance with ethical standards

Conflict of interest

The authors have declared that there is no conflict of interest.

Contributor Information

Abdur Rauf, Email: mashaljcs@yahoo.com.

Seema Patel, Email: seemabiotech83@gmail.com.

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