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. 2021 May 17;14(5):1185–1196. doi: 10.14202/vetworld.2021.1185-1196

Phytochemical composition and health properties of Sembung plant (Blumea balsamifera): A review

I Gede Widhiantara 1,2,, I Made Jawi 3
PMCID: PMC8243688  PMID: 34220120

Abstract

Indonesia’s mindset has been focusing on the use of natural medicines, food, and healing practices widely recognized by the nation’s culture. Traditional medicines and herbs used in traditional medicine can often lead to the discovery of drugs against certain diseases. The aim of this review was to study evidence-based data on the importance of Sembung plant, Blumea balsamifera, as a potential traditional medicine. The distribution, ethnopharmacology, secondary metabolites, and bioactivity against several diseases are focused in this review. Information and research related to Sembung plant were searched using the terms “B. balsamifera,” “phytochemicals,” and “pharmacological activity” on ResearchGate, Google Scholar, Science Direct, PubMed, and scientific information-based databases up to 2020. Several ethnomedical articles recommend B. balsamifera for the treatment of sinusitis, colic pain, cough, kidney stones, flu, or as a diuretic. This knowledge has already been applied in several countries in Southeast Asia. B. balsamifera has been reported to contain several phytochemicals both volatile (terpenoids, fatty acids, phenols, alcohol, aldehydes, ethers, ketones, pyridines, furans, and alkanes) and non-volatile (flavonoids, flavanones, and chalcones). Extracts and phytochemicals of B. balsamifera contain several biological capacities such as antioxidant, antimicrobial, antifungal, anti-inflammatory, hypolipidemic, anti-infertility, hepatoprotective activity, antidiabetic, gastroprotective, antitumor, anticancer, and immunomodulatory agent against Coronavirus disease-19 infection. This review provides essential data for the potential application of B. balsamifera as a nutraceutical or in future medicinal preparations.

Keywords: Asteraceae, Blumea balsamifera, future medicine, medicinal uses, phytochemical constituents

Introduction

Indonesia has enormous potential for the development of herbal medicines and traditional medicinal preparations that have been already traditionally used to treat various diseases [1]. Apart from Indonesia, the use of traditional medicines has also been developed in other countries of the Southeast Asian Association (ASEAN) in recent years [2]. The use of these traditional plants has been targeting several diseases, from a common cold to cancer [3]. Contemporary research has validated several parts of plants from roots, stems, and leaves in potential medicinal preparations by screening for active ingredients such as plant metabolites [4-6].

Blumea balsamifera (L) DC. (Asteraceae) or known as local Sembung (in Indonesia) has been widely used as a traditional medicinal preparation for thousands of years. Several countries in Southeast Asia, such as China, Malaysia, Thailand, Vietnam, and the Philippines, have also used the Sembung plant as a traditional medicine [7]. Species from the genus Blumea are distributed across tropical Asia, Africa, and Oceania [8], with the highest level of diversity in tropical Asia [9,10], including Indonesia. To date, as many as 49 species of Blumea are distributed worldwide, with 27 found in Southeast Asia [11]. In the last decade, researchers have focused their investigations on species from the genus Blumea that are used in Ayurvedic (Indian) medicinal ingredients and traditional drinks (Loloh) by Balinese people in Indonesia [12,13].

Therefore, this review provides evidence-based information on the potential biological activity of B. balsamifera, not only toward a central role as a nutraceutical in traditional medicine but also as an interesting plant to undergo further phytochemical and pharmacological studies.

Traditional Use in Several Countries

B. balsamifera is a wild terrestrial plant that can grow to an altitude of 2200-3500 m asl in humid to dry areas (Figure-1) [14]. B. balsamifera has many names in several countries such as Ainaxiang and Dafeng “ai” in China, and it is commonly used as an incense because of its high content in essential oil [15]. In Thailand, dried leaves of the Sembung (Naat) plant can be used as a cigarette to relieve sinusitis, colic pain, and cough and can be combined with other plants as a bath ingredient for women after giving birth [16]. In addition, Thai population also believes that Sembung “drives away spirits.” In the Philippines, people are more familiar with the name Sambong, used as a traditional medicine for patients with kidney stones, common cold or as a diuretic [17]. Other Asian countries such as Malaysia and India also use Sembung as an Ayurvedic medicine [18,19].

Figure-1.

Figure-1

Sembung plants (Blumea balsamifera). (a) Leaves and (b) Flowers.

The use of the Sembung plant in traditional medicine in Indonesia is also known to be very diverse. Within Indonesia, this plant is known by different local names: Sembung utan (Sundanese), Sembung gantung, kuwuk, mingsa, langu (Java), Kamadhin (Madura), Sembung (Bali), Capo (Sumatra), and Afoat, Ampampau, and Madikapu (Eastern Indonesia) [20]. The Sembung plant can be used as a traditional drink by Balinese people called “Loloh Sembung” [21]. Loloh Sembung is made by boiling and brewing fresh and dried leaves [13].

Progress on Phytochemical Studies Using B. balsamifera

Studies show that more than 100 phytochemical constituents of B. balsamifera can be both volatile and non-volatile. The volatile constituent compounds consist of terpenoids, fatty acids, phenols, alcohols, aldehydes, ether, ketones, pyridine, furans, and alkanes. Flavonoids, flavanones, and chalcones are non-volatile constituents [7]. The diversity of the constituents found in B. balsamifera has potential medicinal benefits, as shown in Table-1 [22-54].

Table-1.

The diversity of constituents, molecular formulas, and bioactivity.

Volatile constituents

Class Molecular formula* Bioactivity and medical benefit Reference
Terpenoids C5H8 Inhibition of NO production induced by LPS in RAW264.7 macrophages [24]
Fatty acid CH3(CH2) nCOOH (with n variation) Fatty acids, especially unsaturated fatty acids with n-3 and n-6 have good bioactive and nutritional compounds and play an important role in lipid homeostasis and cardiovascular disease prevention, prevention of chronic disease, anti-inflammatory [25-28]
Phenol C6H6O or C6H5OH Has antibacterial activity against S. aureus and high antioxidant activity, procoagulants [23,29]
Alcohol CH3CH2OH or C2H6O Has good antibacterial activity [30]
Aldehydes RCHO Anticancer and anti- inflammatory [31,32]
Ether C4H10O or (C2H5) 2O or CH3CH2OCH2CH3 As a natural anesthetic agent [33]
Ketones CH3COCH3 Anticancer, antimicrobial, and antioxidant activity [34-36]
Pyridine C5H5N Anticancer and phosphodiesterase-3 inhibitors, antibacterial activity, especially against methicillin-resistant S. aureus, antiepileptic, anticonvulsant agent [37-40]
Furan C4H4O Has anticancer potential in three human cancer cell lines, such as breast cancer cells (MCF-7), lung cancer cells (A549), and melanoma cancer cells (A-375). Has good antibacterial activity on Streptococcus pyogenes, Proteus vulgaris, and Escherichia coli. Has antidiabetic activity [41-43]
Alkanes CnH2n+2 (straight and branched chain alkanes) CnH2n (cyclic alkanes) Anticancer activity of pulmonary carcinoma cells (A549), and antibacterial and cytotoxic. [44,45]

Non-volatile constituents

Class Molecular formula* Bioactivity and medical benefit Reference

Flavones (Family of flavonoids) C15H10O2 Antioxidant activity and anti-tyrosinase activity [46]
Flavonols (Family of flavonoids) C15HO3R9 Wound healing and anti-inflammatory activity [22]
Flavonoid or bioflavonoid C6-C3-C6 Treat kidney disorders, hypertension, wounds, diarrhea, rheumatism, shortness of breath, colds and coughs, respiratory tract infections, stomach pain and treat urinary tract infections [47]
Two new flavonoids 1) C18H16O8 2) C20H20O8 Antiproliferative cancer cells, especially flavonoids compounds 1) 3, 3’, 4’ -Trihydroxy- 6, 7, 8 -trimethoxy flavone, versus compounds of 2) 3-Hydroxy-6,7,8,3’,4’- pentamethoxy flavone. [48]
Flavonoids C6-C3-C6 Inhibition of xanthine oxidase (XO) and enzymatically is able to produce anti-free radicals [49]
Chalcone C15H12O Anticancer, antibacterial, activity, cardiovascular infections, and antiparasitic. [50-54]
*

Source: pubchem.ncbi.nlm.nih.gov/compound. (National Library of Medicine). NO=Nitric oxide

Polyphenolic Compounds

The leaf extract of B. balsamifera was reported to contain 18 polyphenol compounds, including 17 flavonoids and one phenyl ethanone, after analysis using high-performance liquid chromatography (HPLC) [55]. In addition, the flavonoid contents of this plant demonstrated antityrosinase and anticancer activities [56,57].

Fatty Acids

Sembung leaves contain several fatty acids, as previously reported by Pang [7], including (11Z)-11-hexadecenoic acid, trans-2-undercenoic acid, 9-hexadecenoic acid, capric acid, and palmitic acid [58,59].

Terpenoid Compounds

The essential oil obtained from B. balsamifera leaves was reported to have the following terpenoids: 1,8-cineole (20.98%), borneol (11.99%), β-caryophyllene (10.38%), camphor (8.06%), 4-terpineol (6.49%), a-terpineol (5.91%), and caryophyllene oxide (5.35%). These compounds are widely used as fumigants or volatile agents to kill insect pests, nematodes, and other pests [60].

Flavonoids

Several studies reported that Sembung is rich in flavonoids such as 3,4,5-trihydroxy-3,7 dimethoxyflavonones, 3,4,5-trihydroxy-7-ethoxyflavanone, and the new biflavonoid, 3,-O-7-biluteolin, isolated using a Soxhlet extraction method [61]. A total of 27 compounds were identified using ultra-HPLC, including 16 flavonoid aglucagons, five flavonoid glycosides, five chlorogenic acid analogs, and one coumarin [22].

Progress on Pharmacological Studies of B. balsamifera

Various experimental studies both in vitro and in vivo have reported the pharmacological activities of B. balsamifera, such as antioxidant, cytotoxic, antimicrobial, antifungal, anti-inflammatory, and hypolipidemic. Table-2 [13,22,56,62-80] summarizes some studies on the pharmacological activity of B. balsamifera.

Table-2.

Pharmacological activities of Blumea balsamifera.

Pharmacological action Experimental model Extract Positive control Tested dose and Concentration Result Reference
Antioxidant The leaves of Sembung are boiled and brewed as an ingredient in the traditional Balinese Loloh drink. The dried leaves are extracted by brewing. Determination of antioxidant levels using the DPPH free radical scavenging assay method Fresh leaves and dry leaves - - Dried sembung leaves made by boiling method had high antioxidant content, namely, 5.55 ± 0.01 mg GAE/g sample [13]
Hydro ethanol extract of Sembung leaves induced in diabetic rats previously induced with STZ Hydro ethanol extract Diabetic rat (STZ) 300 and 600 mg/kg Increased levels of GSH and CAT as a marker of antioxidant activity [68]
Antimicrobial Sembung leaf extract was evaluated for its antibacterial activity using the disc diffusion test method and agar microdilution method Essential oil extract
Hexane
Dichloromethane
Penicillin
Chloramphenicol
Tetracycline
Gentamycin
Hexane (384 mg/disc) Dichloromethane (384 mg/disc) Essential oil (384 mg/disc) Essential oils had the strongest inhibitory power with MIC concentrations of 150 mg/mL against B. cereus and 1.2 mg/mL against S. aureus [62]
Sembung essential oil was evaluated in vitro for its effectiveness against Haemophilus parasuis by observing MIC and MBC Essential oil C-: Tween-80 C+: H. parasuis bacteria in TSB media 2 × MIC
1 × MIC
0.5 × MIC
0.25 × MIC
0.125 × MIC
MIC and MBC were 0.625 and 1.25 mg/mL, respectively. When the extract concentration increased, the bacterial inhibition curve was stronger and H. parasuis cells were damaged after 4 hours of administration of the extract [104]
Sembung leaf extract against acne-causing bacteria, Propionibacterium acnes Ethanol extract Clindamycin 125 ppm 5%; 10%; 15%; 20%; 25%; 50%; 75% (Concentration of Sembung leaf extract) The concentration of 75% showed the highest inhibitory power against P. acnes with a diameter of 2.26 cm
MIC was 5% concentration, which was 0.93 cm
[73]
Antifungal Sembung leaf extract was evaluated for its antifungal activity using the disc diffusion test method and agar microdilution method Essential oil extract
Hexane
Dichloromethane
Penicillin
Chloramphenicol
Tetracycline
Gentamycin
Hexane (384 mg/disc) Dichloromethane (384 mg/disc) Essential Oil (384 mg/disc) Essential oils had antifungal properties against C. albicans and had the potential to be developed as a treatment and prevention of infectious diseases [62]
Sembung leaf extract was tested for its ability against several pathogenic fungi. Ethyl acetate Clotrimazole 30 mg Had antifungal activity against A. niger, T. mentagrophytes, and C. albicans [63]
Sembung leaf extract was tested for its ability against Fluconazole resistant C. albicans Ethyl acetate Ketoconazole 15 mg 5%; 10%; 15%; 20% the concentration of Sembung leaf extract The ethyl acetate extract of Sembung leaves had no inhibitory activity against fluconazole resistant C. albicans [74]
Lozenges made from Sembung leaves as drops and mouthwash against C. albicans which causes aphthous stomatitis Ethanol extract - Pulvis Gummi Arabicum (PGA 5%: Mannitol 17.5%); F2(PGA 5%: 15%); F3(PGA 10%: mannitol 10%); F4(PGA 15%: Mannitol 5%); F5(PGA 17.5%: Mannitol 2.5%) The best tablet formulation was the F3 formula with mannitol and PGA levels with a tablet weight of 400 mg
Sembung extract had an activity against C. albicans with an inhibition zone of 10 mm and the lozenges meet the required standard of tablet properties
[107]
Anti-inflammatory activity Flavonoids isolated from the Sembung plant were used to improve wound healing in Sprague-Dawley rats - 30% glycerol High dose (2.52 g/kg)
Medium dose (1.26 g/kg)
Low dose (0.63 g/kg) total flavonoids from B. balsamifera
The CD68 level was used as an anti-inflammatory marker that was elevated in the total flavonoid group
Flavonoid glycosides had anti-inflammatory and wound healing activity
[22]
B. balsamifera oil (BBO) obtained from sembung was used as an ingredient for burns healing in rats as an animal model - - BBO was given to mice for 21 days and the rate of healing, decreased scabbing time, and re-epithelialization time were observed every 3 days for 21 days BBO was able to reduce tissue water content, accelerate scab reduction time, and accelerate healing
Growth factor expression occurred, but plasma inflammatory factor levels decreased
[76]
B. balsamifera essential oil (BBEOs) was applied to determine its anti-inflammatory properties - - BBEOs determined their chemical composition and anti-inflammatory activity using a model of skin injury in rat test animals induced by ultraviolet radiation (UV-B) The application of BBEOs could effectively inhibit skin injury due to UV-B exposure by reducing the expression of inflammatory factors such as TNF-α, IL-6, and IL-10 [77]
Nerve anti-inflammatory agent was isolated in B. balsamifera and tested on LPS-induced mic - - The anti-inflammatory potential of B. balsamifera nerves was tested on LPS-induced mice and its activity was examined by measuring the release of NO in microglial BV-2 cells of mice All isolates were able to show anti-inflammatory activity by inhibiting LPS-induced NO production in BV-2 cells mice
These results indicate the bioactive compounds isolated from B. balsamifera have the potential to be developed as neuro-inflammatory agents
[64]
Hypolipidemic activity Sembung leaf extract was used as a therapeutic agent for male reproductive problems due to high-fat diets in adult male rats Ethanol Sterile distilled water 2 mg/mL Sembung leaf extract Sembung leaf extract was able to improve the histological profile of the testes of rats and increase the diameter of the seminiferous tubules and the number of spermatogenic cells in mice that were induced by a high-fat diet
Sembung extract had hypolipidemic activity
[65]
Lansau or traditional ingredients of the Muna tribe, Southeast Sulawesi, Indonesia were used as hypolipidemic agents based on LDL parameters Traditional herb or Lansau consisted of various spices and traditional plants, one of which is B. balsamifera Simvastatin 250 mL and 500 mL for the Lansau dosage Elderly infusions containing traditional plants including B. balsamifera could be used as anti-hyperlipidemia based on decreased parameters of LDL levels in rat test animals [78]
Anti-Infertility activity Traditional Dayak plants including B. balsamifera were used as an anti-infertility ingredient in Swiss Webster (SW) mice - Sterile aquabidest 2.6 mg/kg bb B. balsamifera has the highest anti-infertility activity compared to other traditional plant extracts [66]
Hepatotoxicity and hepatoprotective activity Leaf extract of B. balsamifera was tested on male mice to determine hepatotoxicity Ethanol extract Na-CMC 1% The dose were 2; 2.5; 3.2; 4 g/kg body weight intraperitoneally (IP) The liver cells, cytoplasm, nucleus, and sinusoid in the liver of mice were damaged due to several changes in liver color and texture [79]
The leaf extract of B. balsamifera was tested for growth inhibition activity of human hepatocellular carcinoma cells (McA-RH777, and HepG2, respectively) in tested mice Methanol extract Induction of carcinoma cells without extracting - The anti-proliferation effect increased significantly and was able to reduce ligands related to tumor cell proliferation
These findings provide a report that Sembung has hepatoprotective potential
[67]
Anti-diabetic activity B. balsamifera (HEBB) leaf extract was evaluated for antidiabetic activity in STZ-induced rats Hydro-ethanol extract STZ and Glibenclamide (5 mg/kg/bw, po) HEBB 300 and 600 mg/kg Significant changes in serum lipid profiles and enzymes marker [68]
Gastro-protective activity Combination of hot water extract Glycyrrhiza glabra, Alyxia reinwardtii, B. balsamifera to determine gastro-ptotective activity in aspirin-induced mice Hot water extract Aspirin 450 mg/kg BW and Sucralfate 360 mg/kg BW G. glabra 273 mg/kg BW; Sembung leaf 457.5 mg/kg BW; and A. reinwardtii with various doses, namely 100 mg/kg BW (K1); 200 mg/kg (K2); 300 mg/kg BW (K3) The combination of herbal extracts was able to significantly provide a protective effect indicated by the small or small area of the peptic ulcer [69]
Antitumor activity B. balsamifera essential oil extract was tested for its antitumor activity Essential oil extract Trolox IC50 0.6342 mL/mL
LC50 65 mg/mL
Has antitumor activity tested on shrimp larvae [70]
Anticancer activity Fractionation of B. balsamifera leaf ethyl acetate extract to be tested for the anticancer ability of KB, MCF-7, and NCI-H187 Ethyl acetate extract fraction - - Compounds 2,4, and 9 were active against KB cells with IC50 values 17.09, 47.72, and 17.83 mg/mL
Compounds 2,3, and 5 showed moderate activity against NCI-H187 cells with IC50 values of 16.29, 29.97, and 20.59 mg/mL
Leteolin-7-methyl ether (9) had strong cytotoxicity against human lung cancer cells (NCI-H187) with an IC50 of 1.29 mg/mL and moderate toxicity to oral cancer cells (KB) with an IC50 of 17.83 mg/mL
[56]
Immunomodulator for SARS-CoV-2 Genes that can be involved in the regulation of biosynthesis of active compounds from B. balsamifera - - - The CCL and FPS genes had an immunostimulatory induction role, protect the hepatocytes from lipid peroxidation and catalytic activity [71,80]

MIC=Minimum inhibition concentration, B. cereus=Bacillus cereus, S. aureus=Staphylococcus aureus, DPPH: 2,2-diphenylpicrylhydrazyl, A. niger=Aspergillus niger, T. mentagrophytes=Trichophyton mentagrophytes, C. albicans=Candida albicans, NO=Nitric oxide, LPS=Lipopolysaccharide, STZ=Streptozotocin, GSH=Glutathione, CAT=Catalase

Antioxidant Activity

B. balsamifera extract has demonstrated high antioxidant activity. Fresh and dry leaf extracts from B. balsamifera have been used as a traditional drink by Balinese people in Indonesia called Loloh. It was reported that dried leaves of B. balsamifera, obtained by brewing, had a tannin content of 13.15±0.11 mg GAE/g, while boiled dried leaves showed a high antioxidant capacity of 5.55±0.01 mg GAE/g [13]. Apart from B. balsamifera, other species such as Blumea lanceolaria were also reported to have good health benefits. The antioxidant activity of the methanol extract of B. lanceolaria leaves was assessed through three different methods 2,2-diphenylpicrylhydrazyl, ferric reducing antioxidant power test, and total phenolic content test, showing an antioxidant activity of 302.37±59.78 mg/100 g, 4.60±0.17 mg/100 g, and 1298.93 mg/100 g [81], respectively.

Essential oils obtained from B. balsamifera have been widely used in various countries, especially in tropical Asia. Parts of the B. balsamifera plant were also reported to contain different essential oils. The highest yield of essential oil, 0.65 mL/100 g, was obtained from young leaves. In addition, shoots and young leaves also showed the strongest antioxidant activity. Dimethoxydurene, β-caryophyllene, and a-caryophyllene, which played an important role in the plant’s antioxidant activity, have the potential to be developed as ingredients in the cosmetic and medicinal industries [58].

Antimicrobial Activity

B. balsamifera leaves have been used in the treatment of bacterial infections. The essential oil, and n-hexane, dichloromethane, and methanol extracts of B. balsamifera have been evaluated for their antibacterial activity using agar diffusion and microdilution methods. The essential oil gave the best results with a minimum inhibition concentration (MIC) value of 150 mg/mL against Bacillus cereus and a MIC of 1.2 mg/mL against Staphylococcus aureus. Besides, the n-hexane extract also showed good bactericidal activity [62]. Compounds with high antioxidant activity, such as d-elements, a-cubenene, caryophyllene, caryophyllene epoxide, g-eudesmol, xanthoxylin, and a-eudesmol, were identified from the essential oil of B. balsamifera [82].

The ethanol extract of the stems, roots, and leaves of B. lanceolaria also showed good antimicrobial activity against S. aureus, namely, 10-12 mm, when compared with standard antibiotics, 2-10 mm [23]. Blumea lacera leaf extract, for example, was reported to have antimicrobial activity [83].

Antifungal Activity

Antifungal activity had also been reported in B. balsamifera extract. Antifungal activity tests have been carried out on Aspergillus niger, Trichophyton mentagrophytes, and Candida albicans. Compounds with antifungal activity in Sembung leaves include icthyothereol acetate and cryptomeridiol [63]. The antifungal role of B. lacera was studied against Aspergillus flavus, A. niger, Alternaria sp., Penicillium sp., and Fusarium sp. Almost all extracts from both methanol, acetone, and water extracts were reported to have antifungal activity, when compared to standard carbendazim [84].

Anti-inflammatory Activity

Scientific evidence has demonstrated B. balsamifera anti-inflammatory activity. When the wound healing process occurs, it will go through several stages such as inflammatory response, migration, proliferation, and regeneration of new tissue [85]. Total flavonoids isolated from B. balsamifera were used as a skin wound healing agent in Sprague-Dawley rats. The healing activity was determined by measuring CD68 levels, vascular endothelial growth factor, transformation growth factor-β1, and hydroxyproline. The results of that study indicated that flavonoids were key in the successful wound healing process, increasing the expression of growth factors [22].

The study of the anti-inflammatory process was also carried out using Blumea aurita. B. aurita had the highest percentage of inhibition of edema (EI% = 53%) after 4 h of oral administration of the extract at a dose of 400 mg/kg, followed by 6 h (EI% = 67%) at a dose of 800 mg/kg, with albino Wistar mice [86]. The aqueous extract of Blumea mollis was also used in an acute and chronic anti-inflammatory therapy on carrageenan-induced rat leg edema [87].

In addition, B. balsamifera extract was also reported to have anti-inflammatory neuroprotective activity by reducing nitric oxide in lipopolysaccharide-induced rat microglial BV-2 cells. This inhibition may have occurred due to the interaction of the bioactive compounds of B. balsamifera extract with iNOS protein [64].

Hypolipidemic Activity

Hypolipidemic drug agents lower lipoprotein concentrations, transporting excess cholesterol, and triglycerides in the blood [88]. The antihyperlipidemic nature or potential in plants is important in reducing atherosclerosis [89]. The Sembung plant has been used as an antihyperlipidemic agent in vitro in 3-4 months old adult male Wistar rats (Rattus norvegicus) with induced high-fat feed. The Sembung extract had anti-hyperlipidemic activity by increasing spermatocytes [65]. A traditional drink from Southeast Sulawesi, Indonesia, “Lansau,” made from 44 traditional ingredients (including Sembung) showed that Lansau’s ethanol extract was antihyperlipidemic, reducing fat degeneration and being able to repair cell damage at a dose of 27,628 mg/kg [90].

Anti-infertility Activity

Infertility can be defined as a medical condition that can cause psychological and physical harm. Several factors such as age, tubal factors in women, obesity, significant reduction in semen parameters, cigarette consumption, and excessive alcohol consumption in men could trigger infertility [91]. Ethnopharmacological surveys on uses of traditional medicines against infertility have been widely completed around the world [92].

Local plant extracts from the Dayak tribe, Kalimantan, Indonesia, such as B. balsamifera¸ Croton tiglium, Metroxylon sagu, and Fagraea racemosa Jack, have been used as anti-infertility substances in vitro. All extracts were able to inhibit the estrous and metestrus cycles. A decrease in the corpus luteum and fetus was attributed to the anti-infertility effect of the extract against the inhibition of folliculogenesis. Researchers also reported that B. balsamifera extract had promising anti-infertility activity compared to other plant extracts used in this study [66].

Hepatoprotective Activity

The incidence of liver diseases affects millions of people worldwide. The prevalence of liver cirrhosis from autopsy studies ranges globally from 4.5% to 9.5% of the global population [93,94], with more than 50 million people worldwide (adult population) potentially affected by chronic liver disease [95].

A phytotherapy approach in the development of modern medicines is still very much needed [96]. The benefits of the phytochemical compounds in B. balsamifera have been widely used to improve physiological disorders and other degenerative diseases. Researchers also mentioned that the methanol extract of B. balsamifera (BME) induced growth and developmental inhibition of human hepatocellular carcinoma cells (McA-RH7777 and HepG2, respectively) in mice. These results were confirmed by the antiproliferative effect of BME, which increased slightly but significantly reduced the level of proliferation-related ligand (APRIL) stimulating tumor cells [67].

The hepatoprotective effect was also reported for the ethanol extract of B. lacera, which showed minimal damage to liver structures, decreased aspartate aminotransferase, Alkaline phosphatase, and bilirubin in ethanol-induced rats [97].

Antidiabetic Activity

The use of B. balsamifera as an antidiabetic in traditional medicine has been widely used, especially in Ayurvedic medicine in India. The administration of a hydro-ethanolic extract from B. balsamifera (HEBB) at doses of 300 and 600 mg/kg, in streptozotocin (STZ)-induced diabetic rats, showed a decrease in blood glucose, lipid profile, serum marker enzymes, and levels of glutathione and catalase, when compared with the diabetes control group [68].

Other species such as B. lacera D.C (Asteraceae) was also reported to have antidiabetes benefits. Methanol extract B. lanceolaria (MEBL) and water extract B. lanceolaria were tested on hyperglycemic rats induced by STZ. Treatment with MEBL at doses of 200 and 400 mg/kg BW was able to lower blood glucose levels, increasing glycated hemoglobin, restoring lipid levels, rejuvenating pancreatic beta cells, and increasing the level of insulin secretion in the blood [98].

Gastroprotective Activity

Digestive disorders such as peptic ulcers are caused by an imbalance of aggressive factors (gastric acid and pepsin) and defense factors (mucosal secretion, bicarbonate secretion, and to mucosal epithelial regeneration) [69]. Some traditional plants, such as Sembung can be used as a medicinal ingredient for gastrointestinal disorders. Experimentally, the gastroprotective effect of herbal ingredients was applied to mice in a model of aspirin-induced gastric ulcers. This study confirmed that the herbal extract formulation using Sembung was able to provide a gastroprotective effect, with the lowest eosinophil and mast cells count [69,99].

Antitumor Activity

The essential oil extract of B. balsamifera was reported to have 42 types of chemical components, which were tested for their antitumor activity using the method of shrimp-larvae mortality determination, which is a simple, convenient, and inexpensive method of determining internal biological activity initiated by Jiang et al. [70]. This method has been widely used in determining the toxic components and contaminants in food, as well as the determination of biological activity [100]. The method was carried out using 25-30 larvae in each group. Treatment was given when shrimp eggs hatched (1% DMSO was added to dissolve the sample). The survival rate was observed for 24 h at room temperature. The treatment at 65 mg mL showed strong cytotoxicity to shrimp larvae. In conclusion, this extract was set as potential for further studies on antitumor activity [70].

Anticancer Activity

Cancer is a potentially life-threatening disease with more than 100 different types already occurring due to molecular changes in cells [101]. Cancer is also reported to be the third leading cause of death worldwide after cardiovascular and infectious diseases [102]. Medicinal plants have been reported as potential cancer treatment agents, as about 50% of compounds derived from medicinal plants demonstrate anticancer activity [103].

A study reported the anticancer activity of the BME on mice induced by human hepatocellular carcinoma cells (McA-RH7777 and HepG2, respectively). BME was able to reduce the level of APRIL, which is able to stimulate tumor cells. APRIL is a new member of the tumor necrosis factor, which is reported to stimulate tumor cell growth, modulate tumor cell apoptosis, and regulate humoral immunity [104,105].

The anticancer potential of other species such as Blumea eriantha was also tested in vitro using the microtetrazolium assay (MTT) test on cervical cancer cell (HeLa) and B16F10 cell gallus. The expressions of the p53 and Bcl-2 genes associated with apoptosis were also determined. The results showed that the methanol extract of B. eriantha induced strong antioxidant and anticancer properties. In addition, this extract was also to prevent cancer cell metastasis [106].

Immunomodulator Activity for Severe Acute Respiratory Syndrome-Coronavirus (SARS-CoV-2) in CoV Disease (COVID)-19

Novel COVID-2019, related with SARS, has been declared as a global pandemic causing deaths in 216 countries worldwide [107]. Until now, no vaccine or special treatment for SARS-CoV-2 has been available despite the extraordinary recent research efforts [108]. The use of drugs such as remdesivir, lopinavir/ritonavir, and hydroxychloroquine has been widely claimed to reduce the symptoms of COVID-19. To date, 200 clinical trials have been registered on the clinicaltrials.gov site. However, the expediency of drugs being studied is still unclear [109].

Therefore, the use of traditional medicinal plants is recommended by some for management or increasing the immune status of patients with COVID-19. A report showed that 90% of traditional medicines resulted in 90% recovery in 214 patients treated for COVID-19 [110]. The use of traditional medicine also claimed to be able to prevent COVID-19 infection in healthy people and to increase the immunity of patients with mild or severe COVID-19 symptoms [110]. In Indonesia, the use of “Empon-empon” (In Java) or Loloh (Balinese) made from traditional medicinal plants is also believed to have a role in modulating the immune system in COVID-19 patients [71].

Therapeutic agents against COVID-19 can be divided into several categories based on specific pathways: (1) Preventing the synthesis and replication of viral RNA, (2) blocking the virus in order not to bind to human cell receptors or by inhibiting the assembly process of viral genetic material, (3) restoring the innate immunity of the host, and (4) acting on specific receptors or enzymes so that the virus does not enter the host cell. Until now, there is still no specific scientific data mentioning B. balsamifera as an antiviral agent for COVID-19. Therefore, we suggest that the antiviral potential of its phytocomponents could be tested through computational studies (in silico studies), in vitro, and in vivo. Figure-2 summarizes the potency of B. balsamifera as a medicinal agent and possible anti-SARS-CoV-2.

Figure-2.

Figure-2

Summary of the potential of natural products from the Sembung plant (Blumea balsamifera).

Future Prospective

More exploration and research have been carried out to verify the benefits of B. balsamifera, which is widely used against various diseases by people in several countries. The diversity of its constituents, molecular structure, bioactivity, and pharmacological studies has been extensively described in this review. Researchers have also demonstrated the efficacy of this plant in treating diseases (Table-2). However, further and more detailed studies should be carried out to assess the use of this plant in a number of other experimental animals such as Ferret (Mustela putorius) [111], or Zebrafish (Danio rerio) as well as on human subjects (can be considered) [112]. It has been reported that the leaves of B. balsamifera are the most widely used part in extracts (water, methanol, and ethanol) in studies against cancer, diabetes, hyperlipidemia, infertility, and infectious diseases. Its biological activity is still not fully proven, so other clinical studies would be needed [3].

Some other species of this family have been the focus of some research. B. lacera was reported to be antidiabetic, antifungal, and hepatoprotective; B. eriantha was able to demonstrate its anticancer activity. Therefore, research should focus in the identification and isolation of bioactive compounds according to the known pharmacological activity of B. balsamifera. Especially during the COVID-19 pandemic, authentic Indonesian herbal ingredients are needed to assess their benefits in modulating the immune system.

Conclusion

The Sembung plant (B. balsamifera) has proven to possess important biological activities with additional potential to be developed as a candidate for future essay-based isolation and identification of its bioactive.

Authors’ Contributions

IGW designed and prepared the manuscript. IMJ made a critical comment in this manuscript. Both authors read and approved the final manuscript.

Acknowledgments

The author would like to thank the Ministry of Research, Technology and Higher Education of the Republic of Indonesia (KEMENRISTEKDIKTI) for supporting the study with the Domestic Postgraduate Education Scholarship (BPPDN) with Decision Letter Number: B/276/D3.2/KD.02.00/2019 and Dhyana Pura University, Bali. Thanks to Putu Angga Wiradana, who helped in editing, preparing, and revision of the manuscript.

Competing Interests

The authors declare that they have no competing interests.

Publisher’s Note

Veterinary World remains neutral with regard to jurisdictional claims in published institutional affiliation.

References

  • 1.Ansori A.N.M, Fadholly A, Hayaza S, Susilo R.J.K, Inayatillah B, Winarni D, Husen S.A. A Review on medicinal properties of mangosteen (Garcinia mangostana L.) Res. J. Pharm. Technol. 2020;13(2):974. [Google Scholar]
  • 2.Peltzer K, Pengpid S. Utilization and practice of traditional/complementary/alternative medicine (T/CAM) in Southeast Asian Nations (ASEAN) member states. Stud. Ethnomed. 2015;9(2):209–218. [Google Scholar]
  • 3.Wannes W.A, Tounsi M.S. Phytochemical composition and health properties of Lycium europaeum L.:A review. Acta Ecol. Sin. 2020;2(10):1–12. [Google Scholar]
  • 4.Wannes W.A, Tounsi M.S, Marzouk B. A review of Tunisian medicinal plants with anticancer activity. J. Complement. Integr. Med. 2018;15(1):52. doi: 10.1515/jcim-2017-0052. [DOI] [PubMed] [Google Scholar]
  • 5.Wink M. Evolutionary advantage and molecular modes of action of multi-component mixtures used in phytomedicine. Curr. Drug Metab. 2008;9(10):996–1009. doi: 10.2174/138920008786927794. [DOI] [PubMed] [Google Scholar]
  • 6.Wink M. Modes of action of herbal medicines and plant secondary metabolites. Medicines. 2015;2(3):251–286. doi: 10.3390/medicines2030251. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Pang Y, Wang D, Fan Z, Chen X, Yu F, Hu X, Wang K, Yuan L. Blumea balsamifera a phytochemical and pharmacological review. Molecules. 2014;19(7):9453–9477. doi: 10.3390/molecules19079453. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Peng Y, Yang C, Luo Y. Blumea htamanthii (Asteraceae), a new species from Myanmar. PhytoKeys. 2020;138:225–232. doi: 10.3897/phytokeys.138.38815. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Pornpongrungrueng P, Borchsenius F, Englund M, Anderberg A.A, Gustafsson M.H.G. Phylogenetic relationships in Blumea (Asteraceae:Inuleae) as evidenced by molecular and morphological data. Plant Syst. Evol. 2007;269(3-4):223–243. [Google Scholar]
  • 10.Pornpongrungrueng P, Borchsenius F, Gustafsson M.H.G. Relationships within Blumea (Inuleae, Asteraceae) and the utility of the 5SNTS in specieslevel phylogeny reconstruction. Taxon. 2009;58(4):1181–1193. [Google Scholar]
  • 11.Pornpongrungrueng P, Gustafsson M.H.G, Borchsenius F, Koyama H, Chantaranothai P. Blumea (Compositae:Inuleae) in continental Southeast Asia. Kew Bull. 2016;71(1):1. [Google Scholar]
  • 12.Kim J.S, Kang S.S. Chemical constituents of plants from the genus Patrinia. Nat. Prod. Sci. 2013;19(2):77–119. [Google Scholar]
  • 13.Kusumawati I, Yogeswara I. Antioxidant and antibacterial capacity of Loloh Sembung (Blumea balsamifera) based on extraction method. Maj. Obat Tradis. 2016;21(3):143–148. [Google Scholar]
  • 14.Rahardjo S.S. Review tanaman sembung [Blumea balsamifera (L.)] Proc. Mulawarman Pharm. Conf. 2016;3(1):18–28. [Google Scholar]
  • 15.Chen M. Studies on the Active Constituents of Blumea balsamifera. Shanghai, China: Shanghai Jiao Tong University; 2019. [Google Scholar]
  • 16.Ruangrungsi N, Tantivatana P, Tappayuthpijarn P, Borris R.P, Cordell G.C. Traditional medicinal plants of Thailand VI. isolation of cryptomeridiol from Blumea balsamifera. ScienceAsia. 1985;11(1):047. [Google Scholar]
  • 17.Montealegre C.M, De Leon R.L. Blumea balsamifera (Sambong) tea as a therapeutic drink for calcium oxalate stones. MATEC Web Conf. 2016;62(02002):4. [Google Scholar]
  • 18.Tomar A, Tomar C.A. Folk medicinal use of Blumea lacera (BURM. F.) DC. To cure threadworms. J. Med. Plants Stud. 2017;5(2):336–337. [Google Scholar]
  • 19.Zaki P.H, Gandaseca S, Rashidi N.M, Ismail M.H. Traditional usage of medicinal plants by Temiar tribes in the State of Kelantan, Peninsular Malaysia. For. Soc. 2019;3(2):227–234. [Google Scholar]
  • 20.Nursamsu N, Firmansyah F. Utilization of Sembung (Blumea balsamifera) leaves as traditional medicine in the Javanese village of the youth vocational sub-district of Aceh Tamiang district in 2015. 2017 [Google Scholar]
  • 21.Sõukand R, Quave C.L, Pieroni A, Pardo-de-Santayana M, Tardío J, Kalle R, Łuczaj L, Svanberg I, Kolosova V, Aceituno-Mata L, Menendez-Baceta G, Kołodziejska-Degórska I, Pirożnikow E, Petkevičius R, Hajdari A, Mustafa B. Plants used for making recreational tea in Europe:A review based on specific research sites. J. Ethnobiol. Ethnomed. 2013;9(1):58. doi: 10.1186/1746-4269-9-58. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Pang Y, Zhang Y, Huang L, Xu L, Wang K, Wang D, Guan L, Zhang Y, Yu F, Chen Z, Xie X. Effects and mechanisms of total flavonoids from Blumea balsamifera (L.) DC. on skin wound in rats. Int. J. Mol. Sci. 2017;18(12):2766. doi: 10.3390/ijms18122766. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Vineet K.M, Ajit K.P, Vanlalhmangaihi K, Nachimuthu S.K, Bhim P.S. Antimicrobial and antioxidant activities of Blumea lanceolaria (Roxb.) J. Med. Plants Res. 2015;9(4):84–90. [Google Scholar]
  • 24.Chen M, Qin J.J, Fu J.J, Hu X.J, Liu X.H, Zhang W.D, Jin H.Z. Blumeaenes A-J, sesquiterpenoid esters from Blumea balsamifera with NO inhibitory activity. Planta Med. 2010;76(9):897–902. doi: 10.1055/s-0029-1240800. [DOI] [PubMed] [Google Scholar]
  • 25.Rajaram S. Health benefits of plant-derived a-linolenic acid. Am. J. Clin. Nutr. 2014;100(Suppl 1):443S–448S. doi: 10.3945/ajcn.113.071514. [DOI] [PubMed] [Google Scholar]
  • 26.Vangaveti V.N, Jansen H, Kennedy R.L, Malabu U.H. Hydroxyoctadecadienoic acids:Oxidised derivatives of linoleic acid and their role in inflammation associated with metabolic syndrome and cancer. Eur. J. Pharmacol. 2016;15(785):70–76. doi: 10.1016/j.ejphar.2015.03.096. [DOI] [PubMed] [Google Scholar]
  • 27.López-Vicario C, Rius B, Alcaraz-Quiles J, García-Alonso V, Lopategi A, Titos E, Clària J. Pro-resolving mediators produced from EPA and DHA:Overview of the pathways involved and their mechanisms in metabolic syndrome and related liver diseases. Eur. J. Pharmacol. 2016;15(785):133–143. doi: 10.1016/j.ejphar.2015.03.092. [DOI] [PubMed] [Google Scholar]
  • 28.Calder P.C. Marine omega-3 fatty acids and inflammatory processes:Effects, mechanisms and clinical relevance. Biochim. Biophys. Acta. 2015;1851(4):469–484. doi: 10.1016/j.bbalip.2014.08.010. [DOI] [PubMed] [Google Scholar]
  • 29.Li H, Cuiwu L, Aiyuan L, Baoyao W, Jianwen T, Lue L. Pro-coagulant activity of phenolic acids isolated from Blumea riparia. Nat. Prod. Commun. 2010;5(8):1263–1266. [PubMed] [Google Scholar]
  • 30.Ongsakul M, Jindarat A, Rojanaworarit C. Antibacterial effect of crude alcoholic and aqueous extracts of six medicinal plants against Staphylococcus aureus and E. coli. Health (San Francisco) 2009;23(3):153–156. [Google Scholar]
  • 31.Bębenek E, Chrobak E, Marciniec K, Kadela-Tomanek M, Trynda J, Wietrzyk J, Boryczka S. Biological activity and in silico study of 3-modified derivatives of betulin and betulinic aldehyde. Int. J. Mol. Sci. 2019;20(6):1372. doi: 10.3390/ijms20061372. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Joshi H, Singh B.K, Saxena G, Singh V, Singh R.P, Arya E. Novel halogens substituted coumarin-aldehyde as an anti-inflammatory agent. World J. Pharm. Pharm. Sci. 2014;2(3):1–15. [Google Scholar]
  • 33.Chang C.Y, Goldstein E, Agarwal N, Swan K.G. Ether in the developing world:Rethinking an abandoned agent. BMC Anesthesiol. 2015;15(1):149. doi: 10.1186/s12871-015-0128-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Poff A.M, Ari C, Arnold P, Seyfried T.N, D'Agostino D.P. Ketone supplementation decreases tumor cell viability and prolongs survival of mice with metastatic cancer. Int. J. Cancer. 2014;135(7):1711–1720. doi: 10.1002/ijc.28809. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Kawase M, Motohashi N, Sakagami H, Kanamoto T, Nakashima H, Ferenczy L, Wolfard K, Miskolci C, Molnár J. Antimicrobial activity of trifluoromethyl ketones and their synergism with promethazine. Int. J. Antimicrob. Agents. 2001;18(2):161–165. doi: 10.1016/s0924-8579(01)00340-5. [DOI] [PubMed] [Google Scholar]
  • 36.Greco T, Glenn T.C, Hovda D.A, Prins M.L. Ketogenic diet decreases oxidative stress and improves mitochondrial respiratory complex activity. J. Cereb. Blood Flow Metab. 2016;36(9):1603–1613. doi: 10.1177/0271678X15610584. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Davari A.S, Abnous K, Mehri S, Ghandadi M, Hadizadeh F. Synthesis and biological evaluation of novel pyridine derivatives as potential anticancer agents and phosphodiesterase-3 inhibitors. Bioorg. Chem. 2014;57(10):83–89. doi: 10.1016/j.bioorg.2014.09.003. [DOI] [PubMed] [Google Scholar]
  • 38.Reen G.K, Kumar A, Sharma P. In vitro and in silico evaluation of 2-(substituted phenyl) oxazolo[4,5-b]pyridine derivatives as potential antibacterial agents. Med. Chem. Res. 2017;26(12):3336–3344. [Google Scholar]
  • 39.Ulloora S, Adhikari A.V, Shabaraya R. Synthesis and antiepileptic studies of new imidazo[1,2-a]pyridine derivatives. Chin. Chem. Lett. 2013;24(9):853–856. doi: 10.1016/j.bmcl.2013.03.086. [DOI] [PubMed] [Google Scholar]
  • 40.Bhandari S, Tripathi A.C, Saraf S.K. Novel 2-pyrazoline derivatives as potential anticonvulsant agents. Med. Chem. Res. 2013;22(11):5290–5296. [Google Scholar]
  • 41.Rao G.P.C, Ramesh V, Ramachandran D, Chakravarthy A.K. Design, synthesis and anticancer evaluation of novel furan sulphonamide derivatives. Russ. J. Gen. Chem. 2019;89(3):486–491. [Google Scholar]
  • 42.Malladi S, Nadh R.V, Babu K.S, Babu P.S. Synthesis and antibacterial activity studies of 2,4-di substituted furan derivatives. Beni Suef Univ. J. Basic Appl. Sci. 2017;6(4):345–353. [Google Scholar]
  • 43.Babu S.P, Babu K.S. Synthesis and antidiabetic activity of 2, 4- disubstituted furan derivatives. Pharm. Chem. 2012;4(6):2178–2186. [Google Scholar]
  • 44.Liang Q, Linxia X, Rui L. Convenient synthesis and biological evaluation of Bis (indolyl) methane alkaloid and Bis (aryl) alkanes derivatives with anticancer properties keywords. Beilstein Arch. 2020;2020(1):202060. [Google Scholar]
  • 45.de Martins C.M, do Nascimento E.A, de Morais S.A.L, de Oliveira A, Chang R, Cunha L.C.S, Martins M.M, Martins C.H.G, da Moraes T.S, Rodrigues P.V, da Silva C.V, de Aquino F.J.T. Chemical constituents and evaluation of antimicrobial and cytotoxic activities of Kielmeyera coriacea Mart. and Zucc. essential oils. Evid. Based Complement. Altern. Med. 2015;2015:842047. doi: 10.1155/2015/842047. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Dao V.Q, Thi T, Giang L, Cang D.T, Nguyen L, Linh T, Thi Ben T, Ai Uyen N.P, Suong N.K. Antioxidant and antityrosinase activities of flavonoid from Blumea balsamifera (L.) DC. leaves. Eur. J. Res. Med. Sci. 2017;5(1):1–6. [Google Scholar]
  • 47.Boy H.I.A, Rutilla A.J.H, Santos K.A, Ty A.M.T, Yu A.I, Mahboob T, Tangpong J, Nissapatorn V. Recommended medicinal plants as source of natural products:A review. Digit. Chin. Med. 2018;1(2):131–142. [Google Scholar]
  • 48.Tambewagh U.U, Javir G.R, Joshi K.S, Rojatkar S.R. Two new polyoxygenated flavonoids from Blumea eriantha DC, methanol extract and their antiproliferative activity. Nat. Prod. Res. 2019;3(10):1–8. doi: 10.1080/14786419.2019.1672063. [DOI] [PubMed] [Google Scholar]
  • 49.Nessa F, Ismail Z, Mohamed N. Xanthine oxidase inhibitory activities of extracts and flavonoids of the leaves of Blumea balsamifera. Pharm. Biol. 2010;48(12):1405–1412. doi: 10.3109/13880209.2010.487281. [DOI] [PubMed] [Google Scholar]
  • 50.Madhavi S, Sreenivasulu R, Yazala J.P, Raju R.R. Synthesis of chalcone incorporated quinazoline derivatives as anticancer agents. Saudi Pharm. J. 2017;25(2):275–279. doi: 10.1016/j.jsps.2016.06.005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Choudhary A.L, Juyal V. Synthesis of chalcone and their derivatives as antimicrobial agents. Int. J. Pharm. Pharm. Sci. 2011;3(3):125–128. [Google Scholar]
  • 52.Hsieh C.T, Hsieh T.J, El-Shazly M, Chuang D.W, Tsai Y.H, Yen C.T, Wu S.F, Wu Y.C, Chang F.R. Synthesis of chalcone derivatives as potential antidiabetic agents. Bioorg. Med. Chem. Lett. 2012;22(12):3912–3915. doi: 10.1016/j.bmcl.2012.04.108. [DOI] [PubMed] [Google Scholar]
  • 53.Nurkenov O.A, Ibraev M.K, Schepetkin I.A, Khlebnikov A.I, Seilkhanov T.M, Arinova A.E, Isabaeva M.B. Synthesis, structure, and anti-inflammatory activity of functionally substituted chalcones and their derivatives. Russ. J. Gen. Chem. 2019;89(7):1360–1367. [Google Scholar]
  • 54.Aljamali N.M, Daylee S.H, Kadhium A.J. Review on chemical-biological fields of chalcone compounds. Forefront J. Eng. Technol. 2020;2(1):33–44. [Google Scholar]
  • 55.Tan D, Yang Z, Zhang Q, Ling H, Du Y, Lu Y, Xie T, Zhou X, Qin L, He Y. Simultaneous quantitative determination of polyphenolic compounds in Blumea balsamifera (Ai-Na-Xiang, Sembung) by high-performance liquid chromatography with photodiode array detector. Int. J. Anal. Chem. 2020;2020:9731327. doi: 10.1155/2020/9731327. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.Saewan N, Koysomboon S, Chantrapromma K. Anti-tyrosinase and anticancer activities of flavonoids from Blumea balsamifera DC. J. Med. Plants Res. 2011;5(6):1018–1025. [Google Scholar]
  • 57.Fazilatun N, Nornisah M, Zhari I. Superoxide radical scavenging properties of extracts and flavonoids isolated from the leaves of Blumea balsamifera. Pharm. Biol. 2005;43(1):15–20. [Google Scholar]
  • 58.Yuan Y, Huang M, Pang Y.X, Yu F.L, Chen C, Liu L.W, Chen Z.X, Zhang Y.B, Chen X.L, Hu X. Variations in essential oil yield, composition, and antioxidant activity of different plant organs from Blumea balsamifera (L.) DC. at different growth times. Molecules. 2016;21(8):1024. doi: 10.3390/molecules21081024. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59.Aboaba S, Choudhary I. Chemical Composition and Biological Activities of the Volatile Oils of Palisota hirsute(Thunb) K. Schum and Trema orientalis(L) Blume. Intern. J. Chem. 2015;7(2):21. [Google Scholar]
  • 60.Chu S.S, Du S.S, Liu Z.L. Fumigant compounds from the essential oil of Chinese Blumea balsamifera leaves against the Maize Weevil (Sitophilus zeamais) J. Chem. 2013;2013:289874. [Google Scholar]
  • 61.Kusumawati I.G.A, Reyunika I.N, Yogeswara I.B.A, Mustika I.G, Adi Putra I.M.W, Santoso U, Marsono Y. Effect of loloh sembung (Blumea balsamifera) maturity stage on antioxidant activity. Indones. J. Nutr. Diet. 2019;6(1):1–6. [Google Scholar]
  • 62.Sakee U, Maneerat S, Cushnie T.P.T, De-eknamkul W. Antimicrobial activity of Blumea balsamifera (Lin.) DC. extracts and essential oil. Nat. Prod. Res. 2011;25(19):1849–1856. doi: 10.1080/14786419.2010.485573. [DOI] [PubMed] [Google Scholar]
  • 63.Ragasa C.Y, Kristin C, Co A.L, Rideout J.A. Antifungal metabolites from Blumea balsamifera. Nat. Prod. Res. 2005;19(3):231–237. doi: 10.1080/14786410410001709773. [DOI] [PubMed] [Google Scholar]
  • 64.Ma J, Ren Q, Dong B, Shi Z, Zhang J, Jin D.Q, Xu J, Ohizumi Y, Lee D, Guo Y. NO inhibitory constituents as potential anti-neuroinflammatory agents for AD from Blumea balsamifera. Bioorg. Chem. 2018;76(2):449–457. doi: 10.1016/j.bioorg.2017.12.008. [DOI] [PubMed] [Google Scholar]
  • 65.Widhiantara I.G, Permatasari A.A.A, Siswanto F.M, Dewi N.P.E. Leaf extract of sembung (Blumea balsamifera) improves testicular histology of Wistar rats induced high-fat feed. J. Bioteknol. Biosains. Indones. 2018;5(2):111. [Google Scholar]
  • 66.Haryono A, Gunawan Y.E, Suatma S, Sumitro S, Rahmadu M. Anti-fertility effect of various plants at dayak tribe to swiss webster mice. J. Trop. Life Sci. 2013;3(2):108–112. [Google Scholar]
  • 67.Norikura T, Kojima-Yuasa A, Shimizu M, Huang X, Xu S, Kametani S, Rho S.N, Kennedy D.P, Matsui-Yuasa I. Anticancer activities and mechanisms of Blumea balsamifera extract in hepatocellular carcinoma cells. Am. J. Chin. Med. 2008;36(2):411–424. doi: 10.1142/S0192415X08005862. [DOI] [PubMed] [Google Scholar]
  • 68.Roy K, Saha S, Biswas S, Ahmed W, Mariappan G. In vivo assessment of antidiabetic and antioxidant activities of Blumea balsamifera in streptozotocin-diabetic rats. Res. J. Med. Plant. 2013;7(1):48–57. [Google Scholar]
  • 69.Nugroho A.E, Wijayanti A, Mutmainah M, Susilowati R, Rahmawati N. Gastroprotective effect of combination of hot water extracts of licorice (Glycyrrhiza glabra), pulasari stem bark (Alyxia reinwardtii), and sembung leaf (Blumea balsamifera) against aspirin-induced gastric ulcer model rats. J. Evid. Based Complement. Altern. Med. 2016;21(4):NP77–84. doi: 10.1177/2156587216637469. [DOI] [PubMed] [Google Scholar]
  • 70.Jiang Z, Zhou Y, Ge W, Yuan K. Phytochemical compositions of volatile oil from Blumea balsamifera and their biological activities. Pharmacogn. Mag. 2014;10(39):346. doi: 10.4103/0973-1296.137377. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 71.Hartanti D, Dhiani B.A, Charisma S.L, Wahyuningrum R. The potential roles of jamu for COVID-19:A learn from the traditional Chinese medicine. Pharm. Sci. Res. 2020;7(4):12–22. [Google Scholar]
  • 72.He C, Yang P, Wang L, Jiang X, Zhang W, Liang X, Yin L, Yin Z, Geng Y, Zhong Z, Song X, Zou Y, Li L, Lv C. Antibacterial effect of Blumea balsamifera DC. essential oil against Haemophilus parasuis. Arch. Microbiol. 2020;202(9):2499–2508. doi: 10.1007/s00203-020-01946-4. [DOI] [PubMed] [Google Scholar]
  • 73.Alana A.T, Yuniarni U, Hazar S. Test the antibacterial activity of the ethanol extract of sembung (Blumea balsamifera L) against acne-causing bacteria Propionibacterium acnes. Pros Farm. 2016;2:39–44. [Google Scholar]
  • 74.Jumariswan J, Sari I, Suwarno R. Uji antijamur ekstrak etil asetat daun sembung (Blumea balsamifera (L) DC) terhadap pertumbuhan jamur Candida albicans resisten flukonazol. Semin. Nas. Biot. 2017;4(1):392–396. [Google Scholar]
  • 75.Yaminulloh S, Suprapto . Formulasi Tablet Hisap Ekstrak Etanol Daun Sembung (Blumea balsamifera L.) Dengan Variasi Konsentrasi Pulvis Gummi Arabicum dan Manitol Serta uji Antijamur Terhadap Candida albicans. Indonesia: Universitas Muhammadiyah Surakarta; 2017. [Google Scholar]
  • 76.Fan Z.W, Pang Y.X, Wang K, Yu F.L, Wang D, Yang Q, Ma Q.S, Li X.T, Zou J, Zhang W.Q, Wu L.F. Blumea balsamifera oil for the acceleration of healing of burn injuries. Molecules. 2015;20(9):17166–17179. doi: 10.3390/molecules200917166. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77.Zhang B, Tang M, Zhang W, Zhangb C, Ai Y, Liang X, Shi Y, Chen Y, Zhang L, He T. Chemical composition of Blumea balsamifera and Magnolia sieboldii essential oils and prevention of UV-B radiation-induced skin photoaging. Nat. Prod. Res. 2020 doi: 10.1080/14786419.2020.1809401. [DOI] [PubMed] [Google Scholar]
  • 78.Ihsan S, Sonaru F, Satriani H, Wahyuni I. Efek antihiperlidemia obat tradisonal khas suku muna “lansau”berdasarkan parameter kadar LDL. Sainstech Farm. 2018;11(1):7–11. [Google Scholar]
  • 79.Arifin H, Widianingsih I, Marusin N, Andalas J.F.F. The effect of acute administration of ethanol extract of Capo leaves (Blumea balsamifera DC) on the morphological and histological features of the liver of male white mice. J. Sains Tek. Far. 2007;12:82–88. [Google Scholar]
  • 80.Pang Y.X, Guan L.L, Wu L.F, Chen Z.X, Wang K, Xie X.L, Yu F.L, Chen X.L, Zhang Y.B, Jiang Q. Cloning and sequence analysis of the Blumea balsamifera DC farnesyl diphosphate synthase gene. Genet. Mol. Res. 2014;13(4):9874–9882. doi: 10.4238/2014.November.27.15. [DOI] [PubMed] [Google Scholar]
  • 81.Lalmuanthanga C, Roy D.C, Roy R.K, Sarma Y, Borah P, Tamuli S, Hmarthansanga L, Shantabi L, Devi I. Antioxidant activity of methanolic extract of Blumea lanceolaria. Int. J. Chem. Stud. 2019;7(3):3546–3548. [Google Scholar]
  • 82.Wang Y.H, Zhang Y.R. Variations in compositions and antioxidant activities of essential oils from leaves of Luodian Blumea balsamifera from different harvest times in China. PLoS One. 2020;15(6):e0234661. doi: 10.1371/journal.pone.0234661. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 83.Kimbonguila A, Matos L, Petit J, Scher J, Nzikou J.M. Effect of physical treatment on the physicochemical, rheological and functional properties of yam meal of the cultivar “Ngumvu”from Dioscorea alata L. of Congo. Int. J. Recent Sci. Res. 2019;8:22213–22217. [Google Scholar]
  • 84.Khan P.A, Ekka A. Antifungal activity of Blumea lacera. Int. J. Adv. Sci. Eng. Technol. 2018;6(4):6–8. [Google Scholar]
  • 85.Li Y, Jalili R.B, Ghahary A. Accelerating skin wound healing by M-CSF through generating SSEA-1 and -3 stem cells in the injured sites. Sci. Rep. 2016;6(1):28979. doi: 10.1038/srep28979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 86.Lutfi M.F. Evaluation of the anti-inflammatory effects of Blumea aurita. Glob. J. Med. Res. 2014;13(4):23–29. [Google Scholar]
  • 87.Devi G.B.B, Amutha K. Anti-inflammatory and anti-pyretic activities of Blumea mollis (D. Don) MERR. Res. J. Pharmacogn. Phytochem. 2011;3(1):14–16. [Google Scholar]
  • 88.Sullivan P.J, Agardy F.J, Clark J.J.J. The Environmental Science of Drinking Water. Amsterdam, Netherlands: Elsevier; 2005. Living with the risk of polluted water; pp. 143–96. [Google Scholar]
  • 89.Koriem K.M.M. Antihyperlipidemic activity of the medicinal plants among Kadazan and Dusun communities in Sabah, Malaysia:A review. Asian Pac. J. Trop. Biomed. 2014;4(10):768–779. [Google Scholar]
  • 90.Rustam R, Rauf A, Maryana N, Pudjianto P, Dadang D. Leafminer parasitoid community in upland vegetable plantations. J. Nat. Indones. 2012;11(1):40. [Google Scholar]
  • 91.Deshpande P, Gupta A. Causes and prevalence of factors causing infertility in a public health facility. J. Hum. Reprod. Sci. 2019;12(4):287. doi: 10.4103/jhrs.JHRS_140_18. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 92.Atanasov A.G, Waltenberger B, Pferschy-Wenzig E.M, Linder T, Wawrosch C, Uhrin P, Temml V, Wang L, Schwaiger S, Heiss E.H, Rollinger J.M, Schuster D, Breuss J.M, Bochkov V, Mihovilovic M.D, Kopp B, Bauer R, Dirsch V.M, Stuppner H. Discovery and resupply of pharmacologically active plant-derived natural products:A review. Biotechnol. Adv. 2015;33(8):1582–1614. doi: 10.1016/j.biotechadv.2015.08.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 93.Graudal N, Leth P, Mårbjerg L, Galløe A.M. Characteristics of cirrhosis undiagnosed during life:A comparative analysis of 73 undiagnosed cases and 149 diagnosed cases of cirrhosis, detected in 4929 consecutive autopsies. J. Intern. Med. 1991;230(2):165–171. doi: 10.1111/j.1365-2796.1991.tb00425.x. [DOI] [PubMed] [Google Scholar]
  • 94.Lim Y.S, Kim W.R. The global impact of hepatic fibrosis and end-stage liver disease. Clin. Liver Dis. 2008;12(4):733–746. doi: 10.1016/j.cld.2008.07.007. [DOI] [PubMed] [Google Scholar]
  • 95.Murray C.J, Lopez A.D. Alternative projections of mortality and disability by cause 1990-2020:Global burden of disease study. Lancet. 1997;349(9064):1498–1504. doi: 10.1016/S0140-6736(96)07492-2. [DOI] [PubMed] [Google Scholar]
  • 96.Ali S.A, Sharief N.H, Mohamed Y.S. Hepatoprotective activity of some medicinal plants in Sudan. Evid. Based Complement. Altern. Med. 2019;2019:2196315. doi: 10.1155/2019/2196315. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 97.Shirode D.S, Kulkarni A.V, Jain B.B. Effect of Blumea lacera on tissue, GSH, lipid peroxidation and hepatic cells in ethanol imduced hepatotoxicity in rats. Int. J. Pharm. Pharm. Sci. 2019;11(12):46–50. [Google Scholar]
  • 98.Rath D, Panigrahy S.R, Panigrahi S.K, Kar D.M, Maharana L. Antidiabetic effect of extracts of Blumea lacera DC. in streptozotocin-induced hyperglycemic rats. Int. J. Pharm. Pharm. Sci. 2017;9(10):218. [Google Scholar]
  • 99.Mutmainah Susilowati R, Rahmawati N, Nugroho A.E. Gastroprotective effects of combination of hot water extracts of turmeric (Curcuma domestica L.), cardamom pods (Ammomum compactum S.) and sembung leaf (Blumea balsamifera DC.) against aspirin-induced gastric ulcer model in rats. Asian Pac. J. Trop. Biomed. 2014;4(Suppl 1):S500–4. doi: 10.12980/APJTB.4.2014C972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 100.Harwig J, Scott P.M. Brine shrimp (Artemia salina L.) larvae as a screening system for fungal toxins. Appl. Microbiol. 1971;21(6):1011–1016. doi: 10.1128/am.21.6.1011-1016.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 101.Shaikh R, Pund M, Dawane A, Iliyas S. Evaluation of anticancer, antioxidant, and possible anti-inflammatory properties of selected medicinal plants used in Indian traditional medication. J. Tradit. Complement. Med. 2014;4(4):253–257. doi: 10.4103/2225-4110.128904. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 102.Kelloff G.J. Perspectives on cancer chemoprevention research and drug development. Adv. Cancer Res. 1999;78:199–334. doi: 10.1016/s0065-230x(08)61026-x. [DOI] [PubMed] [Google Scholar]
  • 103.Greenwell M, Rahman P.K.S. Medicinal plants:Their use in anticancer treatment. Int. J. Pharm. Sci. Res. 2015;6(10):4103–4112. doi: 10.13040/IJPSR.0975-8232.6(10).4103-12. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 104.Hahne M, Kataoka T, Schröter M, Hofmann K, Irmler M, Bodmer J.L, Schneider P, Bornand T, Holler N, French L.E, Sordat B, Rimoldi D, Tschopp J. APRIL, a new ligand of the tumor necrosis factor family, stimulates tumor cell growth. J. Exp. Med. 1998;188(6):1185–1190. doi: 10.1084/jem.188.6.1185. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 105.Roth W, Wagenknecht B, Klumpp A, Naumann U, Hahne M, Tschopp J, Weller M. APRIL, a new member of the tumor necrosis factor family, modulates death ligand-induced apoptosis. Cell Death Differ. 2001;8(4):403–410. doi: 10.1038/sj.cdd.4400827. [DOI] [PubMed] [Google Scholar]
  • 106.Gore M, Desai N.S. Characterization of phytochemicals and evaluation of anticancer potential of Blumea eriantha DC. Physiol. Mol. Biol. Plants. 2014;20(4):475–486. doi: 10.1007/s12298-014-0246-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 107.Benarba B, Pandiella A. Medicinal plants as sources of active molecules against COVID-19. Front. Pharmacol. 2020;11:1189. doi: 10.3389/fphar.2020.01189. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 108.Amanat F, Krammer F. SARS-CoV-2 vaccines:Status report. Immunity. 2020;52(4):583–589. doi: 10.1016/j.immuni.2020.03.007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 109.Li H, Wang Y.M, Xu J.Y, Cao B. Potential antiviral therapeutics for 2019 novel coronavirus. Zhonghua Jie He He Hu Xi Za Zhi. 2020;43(3):170–172. doi: 10.3760/cma.j.issn.1001-0939.2020.03.004. [DOI] [PubMed] [Google Scholar]
  • 110.Du H.Z, Hou X.Y, Miao Y.H, Huang B.S, Liu D.H. Traditional Chinese medicine:An effective treatment for 2019 novel coronavirus pneumonia (NCP) Chin. J. Nat. Med. 2020;18(3):206–210. doi: 10.1016/S1875-5364(20)30022-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 111.Oh D.Y, Hurt A.C. Using the ferret as an animal model for investigating influenza antiviral effectiveness. Front. Microbiol. 2016;7:80. doi: 10.3389/fmicb.2016.00080. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 112.Friedman L.M, Furberg C.D, DeMets D.L. Introduction to clinical trials. In:Fundamentals of Clinical Trials. New York: Springer; 2010. pp. 1–18. [Google Scholar]

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