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Evidence-Based Complementary and Alternative Medicine
Volume 2019, Article ID 6495819, 17 pages
https://doi.org/10.1155/2019/6495819
Review Article

A Review of Oenanthe javanica (Blume) DC. as Traditional Medicinal Plant and Its Therapeutic Potential

1Bioengineering Laboratory, Guangdong Bioengineering Institute (Guangzhou Sugarcane Industry Research Institute), Guangdong Academy of Sciences, Guangzhou 510316, China
2Guangdong Key Lab of Sugarcane Improvement & Bio-Refinery, Guangzhou 510316, China
3Yunnan Agricultural University, Kunming 650000, China

Correspondence should be addressed to Chuan-li Lu; moc.361@7070-oaixiyul

Received 17 December 2018; Revised 25 February 2019; Accepted 5 March 2019; Published 1 April 2019

Academic Editor: José L. Rios

Copyright © 2019 Chuan-li Lu and Xiu-fen Li. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Oenanthe javanica, popularly known as water dropwort, has long been used in various ethnomedical systems in Asia, especially in China, Korean, and Japan, for treating various chronic and acute hepatitis, jaundice, alcohol hangovers, abdominal pain, and inflammatory conditions. The present review aims to provide a general report of the available literature on traditional uses, phytochemical, pharmacological, nutritional, and toxicological data related to the O. javanica as a potential source of new compounds with biological activities. Considering phytochemical studies, coumarins, flavonoids and flavonoid glycosides, organic acids, and polyphenols were the main classes of compounds identified in the whole plant which were correlated with their biological activities such as hepatoprotective, anti-inflammatory, immune enhancement, ethanol elimination, antioxidant, antiviral, neuroprotective, anti-cancer, anticoagulant, anti-fatigue, hypoglycemic, cardiovascular protection, analgesic, and insecticidal activities.

1. Introduction

Before modern drugs began to take shape in the medical care industry, people were highly dependent on conventional or traditional medicine, which have been recognized by the World Health Organization as reliable medicinal sources for therapeutic activities [1, 2]. Medicinal plants, the “backbone” of traditional medicine, are utilized today by more than 3.3 billion people in the less developed countries [3].

Oenanthe javanica (Blume) DC. (Apiaceae), which is a small perennial herb, has been cultivated in tropical and temperate regions of Asia for thousands of years and has long been used as a folk remedy for alleviating a wide spectrum of diseases. A variety of biological activities of O. javanica have been reported, including hepatoprotective [4, 5], anti-inflammatory [6, 7], immune enhancement [8], ethanol elimination [9], antioxidant [10], and antiviral [11]. Phytochemical assessments have revealed that O. javanica contains coumarins [12], flavonoids and flavonoid glycosides [13], and polyphenols [4]. In addition, toxicity studies have demonstrated that O. javanica does not exhibit acute or genetic toxicity [14, 15]. However, oral administration of dry O. javanica power could significantly increase the rate of mice sperm deformity and even induce reduction of weight and food consumption at a high dose [15]. Moreover, total phenolics acid extract from O. javanica at a high dose (equivalent to 20 times of recommended human clinical dose) showed a reversible subchronic toxicology [16].

Thus, this review is aimed at elucidating the biological and pharmacological activities, as well as toxicology of O. javanica.

2. Plant Description

Since O. javanica distributes and is cultivated in many areas of Asia and Australia, each group of local people have a specific name for this plant as listed in Table 1 [10, 1726]. In China, this plant is commonly known as Shui qin, Shui qin cai, Shui ying, and so on [17, 18], while it is known as Seri in Japan [1921]. The plant is called Minari [22], Selom [2326], and Phak-chilom [10] in Korea, Malaysia, and Thailand, respectively.

Table 1: Common names used for O. javanica in different countries.

This plant is a small perennial herb and grows up to 10-80 cm with fibrous roots that emerge from all nodes. The stems are light green, terete, glabrous, vertically veined, and hollow, which are more or less erect, but sometimes sprawl. Its basal petioles are 5-10 cm long. The leaves are aromatic and glabrous and have a sheath covering the stem. The blade is oblong-ovate with 1-2 pinnate, while ultimate segments are 5–50 mm long with 5–20 mm broad either ovate or rhombic-ovate shape, margins serrate. Cauline leaves gradually reduced upwards, smaller, becoming sessile on expanded sheaths. There are 5 white petals and 5 stamens for its flowers, with umbels 3–5 cm across, peduncles 2–16 cm, bracts absent or occasionally 1 bract, and rays 6–16(–30), 1–3 cm, subequal or unequal; bracteoles 2–8, linear, 2–4 cm, as long as pedicels; umbellules ca. 20-flowered; pedicels 1.5–4 mm. Calyx teeth ca. 0.5 mm. Its fruit is subglobose or ovoid, ca. 2.5 × 2 mm, while dorsal and intermediate ribs are slightly corky-thickened [27, 28].

3. Ethnomedicinal Uses of O. javanica

Generally, O. javanica is a valuable herbal plants consumed and used by East Asian countries for both food and various medicinal purposes (Table 2) [4, 5, 11, 13, 17, 23, 2941]. For example, the flower and stem (or the aerial parts) of this plant are commonly used in China for the treatment of various types of chronic and acute hepatitis [11, 17, 29, 30]. It is also used in China for jaundice [13, 23, 35, 36], fever [4, 35, 37], hypertension [13, 32, 3537], abdominal pain, and urinary difficulties [4, 35, 36, 39, 40], as well as for eliminating pathogenic wind [17, 29]. Similarly, treatments for fever and hypertension are also common medicinal uses in Korea and Malaysia [23, 3234]. In Korea, this plant is also used for treating alcohol hangovers and inflammatory conditions [11, 39, 41].

Table 2: Ethnomedicinal uses of O. javanica in different countries.

Besides medicinal applications, O. javanica has also been widely consumed as a dietary product. The whole plant or the aerial parts of O. javanica in Malaysia are a well-known vegetable and freshly consumed as the main ingredient in local famous food “ulam,” which constitutes an important part of the food intake among the local peoples especially the Malay and Indigenous communities [2326], while, in Korea, this plant is widely used in salad and soups [22]. In Japan, O. javanica named “seri” is one of the ingredients of the symbolic dish, Nanakusa-no-sekku, consumed in the Japanese spring-time festival [1921].

4. Phytochemistry of O. javanica/Chemical Components

4.1. Flavonoids and Flavonoid Glycosides

Flavonoids and flavonoid glycosides are abundant in O. javanica, and more than ten flavonols have been isolated and identified from O. javanica thus far, including apigenin [3], isorhamnetin-3-O-β-D-glucopyranoside [18], quercetin [37], isorhamnetin-3-O-galactoside [39], afzelin [41], persicarin, isorhamnetin, hyperoside [56], luteolin [57], kaempferol, rutin, nictoflorin, and quercetin-3-L-rhamnoside [58, 59] (their structures are depicted in Figure 1). In general, all of the flavonoids and flavonoid glycosides obtained from this plant have free phenolic hydroxyl groups in the 5, 7, and 4′-position. Most of them are substituted in the 3 and 3′-position. For all flavonoid glycosides obtained from this plant, aglycons are attached at 3-position.

Figure 1: Structures of flavonoids and flavonoid glycosides isolated from O. javanica.
4.2. Coumarins

Approximately nine coumarins have been identified from O. javanica, namely, xanthotoxin, bergapten, isopimpinellin [12], sioimperatorin, imperatorin, columbianadin, 5-hydroxy-8-methoxypsoralen, 6,7-dihydroxycoumarin, and scopoletin [18] (the structures are presented in Figure 2). Most of these components are the linear furanocoumarins, with the 5- and 8-positions being substituted by methoxyl and isoamylenoxyl groups.

Figure 2: Structures of coumarins isolated from O. javanica.
4.3. Phenolic Constituents

Phenolics are also abundant in O. javanica, including neochlorogenic acid [4], chlorogenic acid [4, 5, 11, 60], caffeic acid [4, 5, 48, 57, 60], gallic acid [4, 57], α-tocopherol [10, 61], lunularin, p-hydroxyphenylethanol ferulate, 5-p-trans-coumaroylquinic acid [18], carvacrol, ferullic acid [57], and catechin [45] (the structures are presented in Figure 3). For phenolic acids and ester identified from O. javanica, most of them are caffeic acid derivatives. The content of total phenolic acids in O. javanica from Korean was 88.9 ± 0.46 mg GAE/g [45] and in O. javanica from Guizhou Province of China was 131.5-173.2 mg/g [62]. In addition, O. javanica extract contains α-tocopherol (146.8 mg/kg) [61], gallic acid (0.9 ± 0.23 mg/g), catechin (1.2 ± 0.19 mg/g), chlorogenic acid (227.1 ± 0.62 mg/g), and caffeic acid (4.0 ± 0.35 mg/g) [45].

Figure 3: Structures of phenolic constituents isolated from O. javanica.
4.4. Volatile Oils

The volatile constituents are extracted with steam distillation, vacuum simultaneous steam distillation and solvent extraction, and solid-phase microextraction, and 59 chemical constituents have been identified with gas chromatography-mass spectrometer and computer retrieval technique, including 28 hydrocarbons, 16 alcohols, 8 aldehydes, 4 esters, 2 ethers, and 1 ketone. Furthermore, by using the gas chromatography-olfactometry, p-cymene has been identified as a character-impact aroma-active compound of O. javanica, and α-terpinolene, α-terpinene, (E)-caryophyllene, and (Z,E)-α-farnesene also play significant roles in the aroma of O. javanica [42]. Lee et al. identified 15 compounds representing 100% of volatile oil, mainly including β-caryophyllene, δ-cadinene, β-bisabolene, α-terpinolene, γ-terpinene, and α-amorphene [44]. Zhang et al. reported 16 volatile constituents consisting of 96.46% of oil, and the principal constituents were eudesma-4(14),11-diene,2,3-dihydro-3-methyl-3-benzofuran-methanol, limonene, and allylphenoxyacetate [43]. The identified volatile constituents from O. javanica are presented in Table 3.

Table 3: Volatile compounds identified from O. javanica.
4.5. Other Ingredients

Other compounds, not list above, have been isolated from O. javanica including butanedioic acid [4], β-sitosterol [18], and falcarindiol [21]. Their structures are shown in Figure 4.

Figure 4: Structures of other ingredients isolated from O. javanica.

5. Nutrient Constituent of O. javanica

The fresh O. javanica plant has wide variety nutrients such as carbohydrates, proteins, vitamins, and fat, as well as mineral micronutrients, as shown in Table 4 [10, 4547]. O. javanica has high iron content, followed by kalium, calcium, natrium, and magnesium, which are useful for patients with mineral deficiencies problems. The plant has moisture content of up to 88% [10] and a total ashes value of 8.9% [45] suitable for body hydration.

Table 4: Nutritional composition of O. javanica.

6. Pharmacological Activities

6.1. Hepatoprotective Effect

Although O. javanica has been traditionally used as a Dai ethnic medicine for various liver diseases, the scientific evidence that justifies its usage has only recently been reported (summarized in Table 5). The significantly hepatoprotective effect of O. javanica extracts has been demonstrated on both cell lines and animal models.

Table 5: Summary of hepatoprotective activities of different parts, extracts, and active compounds of O. javanica.

Treatment with boiling water extract of O. javanica (at dose equivalent to 12 g fresh material/kg) showed a significantly suppression effect on the elevation of serum bilirubin level and the degeneration and necrosis of hepatic cells in α-naphthylisocyanate-stimulated Wistar rats, but no effect on serum alanine aminotransferase (ALT) level [49]. In addition, the hepatoprotective effects of total phenolics from O. javanica have been reported on different liver injury models, including -galactosamine- and carbon tetrachloride (CCl4)-induced acute liver injury in mice [4, 50, 51], CCl4-induced chronic hepatic fibrosis in rats [51], a-naphthylisothiocyanate-induced liver jaundice in rats [52], and high-sugar high fat-induced non-alcoholic fatty liver in rats [53].

Moreover, fermented O. javanica extracts, in which caffeic acid and chlorogenic acid were the major constituents, have been reported to dose-dependently inhibit tert-butylhydroperoxide-induced HepG2 cells death and lactate dehydrogenase leakage, as well as prevent the increase of hepatic enzyme markers ALT, aspartate aminotransferase (AST), and gene expressions of cytochrome P450 enzyme (CYP)2E1, CYP4A2 and PPARγ in CCl4-induced hepatic damage in rats [5], while other studies demonstrated that pretreatment by ethanol extract of O. javanica (500 μg/ml) or its active component (caffeic acid, 250 mM) could significantly reduce hydrogen peroxide (H2O2)-induced cellular toxicity in human liver hepatocellular carcinoma HepG2 cell line [48] and counteract the oxidative stresses through increasing the expressions of the endogenous enzymatic antioxidants such as superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx) in the liver cells of rat [32].

A recent study indicated that persicarin isolated from O. javanica could effectively prevent diabetes-induced liver damage by attenuating oxidative stress and inflammation response under hyperglycemic conditions [41]. Another study in a different experimental model of liver disease, nonalcoholic fatty liver disease (NAFLD), revealed that both boiling water extract and n-butanol extracts of O. javanica pretreatment effectively lowered plasma triglyceride and glucose levels [54]. In addition, the underlying mechanism of hepatoprotective effects of O. javanica was demonstrated to be attributed to the improvement of antioxidant capacity and the inhibition of hepatic stellate cell activation and hepatic malondialdehyde production, and consequent attenuation of inflammatory responses and chemical-induced liver injury [55].

The hepatoprotective activity of O. javanica extract was also caused by selective inhibition activity of cytochrome P450 and consequently affected various xenobiotic metabolism. Investigation in HepG2 also revealed that the root extract of O. javanica could significantly elevate the mRNA expressions (by 68% and 102%, respectively) and protein levels (by 112 and 157%, respectively) of CYP1A1 and CYP1A2 and these effects were much more pronounced than those of leaf and stem extracts [12]. Of note, this study provides additional evidence that the levels of major coumarin derivatives determined by GC–MS, including xanthotoxin, bergapten, and isopimpinellin, were significantly higher in root extract than in leaf or stem extracts, which might be responsible for those effects, suggesting dietary exposure to O. javanica may modulate phase I enzymes and thereby affect various xenobiotic metabolism [12]. Specifically, hyperoside (quercetin-3-O-galactoside), a flavonoid isolated from O. javanica, was reported to selectively inhibit the cytochrome P450 isoform and strongly decreased CYP2D6 activity at dose-, but not time-dependent manner in human liver microsomes (HLMs). In this case, hyperoside strongly inhibits CYP2D6-catalyzed dextromethorphan O-demethylation, with IC50 values of 1.2 and 0.81 μM after 0 and 15 min of preincubation and a Ki value of 2.01 μM in HLMs, respectively. Moreover, hyperoside decreased CYP2D6-catalyzed dextromethorphan O-demethylation activity of human recombinant cDNA-expressed CYP2D6, with an IC50 value of 3.87 μM using a cocktail probe assay. However, no inhibition of other CYPs by hyperoside was observed. These results suggest that hyperoside isolated from O. javanica might cause herb-drug interactions when coadministered with CYP2D6 substrates [22].

6.2. Anti-Inflammatory Effect

It has been reported that O. javanica extracts possessed significant anti-inflammatory activities, while isorhamnetin, hyperoside, and persicarin were revealed as its main active components for anti-inflammatory effect.

The extract of O. javanica showed a significant inhibitory effect on nitric oxide production (IC50 < 61 μg/ml) in interferon gamma/lipopolysaccharide stimulated RAW264.7 cells assay, without cytotoxicity [23], as well as an attenuate effect in phorbol 12-myristate 13-acetate-treated THP-1 or bone marrow derived macrophages cells on secretion of interleukin-1β and formation of Asc pyroptosome resulting from NOD-like receptor (NLR)P3, NLRC4 and absent in melanoma 2 (AIM2) inflammasome activation without interruption of cytokine transcription [6]. In addition, its main component, isorhamnetin, a 3′-O-methylated flavonoid, exhibited a selectively inhibitory effect on NLRP3 and AIM2 inflammasome activation and expression of proinflammatory cytokine, while hyperoside, another component of O. javanica, selectively interrupted NLRC4 and AIM2 inflammasome activation but did not alter cytokine expression. In addition, both of them showed an obvious suppression effect on caspase-1 secretion [6].

Furthermore, the anti-inflammatory effect of isorhamnetin in lipopolysaccharide-activated RAW264.7 cells was confirmed to be partly mediated by inhibiting the mitogen activated protein kinase (MAPK)-nuclear factor-kappa B (NF-κB) signaling pathway [7]. The in vivo anti-inflammatory activity of isorhamnetin was also confirmed in carrageenan-induced rats, which showed that oral administration of isorhamnetin (10 or 30 mg/kg) could markedly inhibit carrageenan-induced paw swelling, inflammatory cell infiltration, and proinflammatory gene expression in rats [7]. Moreover, the anti-inflammatory activities of isorhamnetin-3-O-galactoside and persicarin isolated from the aerial parts of O. javanica were demonstrated on high mobility group box 1 (HMGB1)-mediated inflammatory response, and the results showed that both of them could inhibit the releasing of HMGB1 and HMBG1-dependent inflammatory responses in human endothelial cells, as well as HMBG1-mediated hyperpermeability and leukocyte migration in mice [63, 64].

6.3. Enhancing Immunity

The effects of O. javanica extract on immune function/regulation were evaluated in normal and hydrocortisone-induced immunodepressed mice [8, 65].

Total flavone from O. javanica has been demonstrated to possess an upregulatory effect on cell immunity, humoral immunity, and nonspecific immunity in hydrocortisone-induced immunodepressed mice model, as it could obviously increase the carbon clearance index, the serum hemolysin content, and spleen and thymus index and enhance delayed-type hypersensitivity [8]. In line with these findings, the enhancement effect of total phenolics acid extract of O. javanica on immune function was also demonstrated on normal mice, by markedly increasing the content of serum hemolysin and interleukin-2, promoting proliferative response of splenic T-lymphocyte induced by concanavalin A, and improving the clearance rate of charcoal particles in peripheral blood in mice [65].

6.4. Ethanol Elimination/Alcohol Detoxication

Alcohol abuse, especially excess alcohol consumption or alcohol hangovers, is related to impaired liver function. According to surveys, prolonged use is related to increase the risk of liver disease, such as cirrhosis and liver failure.

A hot-water extract of O. javanica injection exhibited a rapidly reducing effect on the plasma ethanol level in ethanol-treated New Zealand white rabbit. In addition, oral administration of O. javanica extract and its n-butanol fraction could eliminate up to 44% and 70% of the plasma ethanol, respectively (compared to orally ethanol-treated mice). Specifically, the n-butanol fraction exhibited the strongest activity in eliminating plasma alcohol. These data indicated that O. javanica extract is effective in overcoming alcohol intoxication by accelerating ethanol metabolism [9]. Moreover, the methanol extract of O. javanica and persicarin isolated from the aerial parts of the plant possessed a dose-dependent stimulatory effect on alcohol-metabolizing enzymes, including alcohol dehydrogenase, aldehyde dehydrogenase, and the microsomal ethanol-oxidizing system in ethanol-treated rats [56].

6.5. Antioxidant Activity

The antioxidant activity of O. javanica have been evaluated using several types of assays, such as scavenging 2,2-diphenylpicrylhydrazyl (DPPH) radical, oxygen radical absorbance capacity (ORAC), ferric reducing antioxidant power (FRAP), and Xanthine oxidase assays. The antioxidant activity of O. javanica methanol extract was firstly revealed by Huda-Faujan et al. using FRAP tests [25]. In addition, the 95% ethanol extract of the dried leaves exhibited a radical scavenging for DPPH and inhibitory effect on SOD activity, with the inhibition rates of 56.87 ± 1.43% and 73.51 ± 0.54% at concentration of 10 mg/ml, respectively. However, there was no significant correlation between antioxidant activities and its phenolic contents [66]. Similarly, the antioxidant properties of methanol extract from O. javanica performed by using DPPH assay showed that IC50 value was 87.42 ± 0.64 μg/ml [23]. Recently, Kongkachuichai et al. showed that hydrophilic ORAC and FRAP activities of O. javanica were about 9000 and 2000 μmol Trolox equivalent /100 g fresh weight [10]. To date, studies dealing with the antioxidant activity of O. javanica related to phenolics are not conclusive.

6.6. Antiviral Effect

The anti-hepatitis B virus (HBV) effects of O. javanica were conducted in human hepatoma (HepG2.2.15 cells) culture system and HBV-infected duck models. Total phenolics, flavones, and ethyl acetate extracts from O. javanica have been revealed to possess significant anti-HBV activities. Flavones extract from O. javanica showed a significant inhibitory effect on HBsAg and HBeAg secretion in HepG2.2.15 cells within nontoxic concentrations, and on duck hepatitis B virus (DHBV)-DNA levels in HBV-infected duck model with concentrations of 0.50 and 1.00 g/kg. Results indicated that the half value of toxic concentration (TC50) and maximum nontoxic concentration (TC0) was 2.28 g/L and 1.00 g/L, respectively. The maximum inhibition peak of viremia was at dose of 1.00 g/kg and reached 54.3% on day 5 and 64.5% on day10, respectively [13].

Total phenolic acid from O. javanica (OJTP) also showed a strong inhibition effect on HBV-DNA (inhibition rate: 62.3%, 47.7%) and DNA (inhibition rate: 62.7%, 61.3%) expressions at 250 and 500 mg/L at day 8, respectively, in HepG2.2.15 cells. Besides, this inhibition rate remained high after 3 days of O. javanica treatment [67]. In addition, OJTP exhibited dose-dependent suppression activities against the production of the HBeAg and HBsAg in HepG2.2.15 cells line [11, 67], and DHBV-DNA replication in ducks [11]. The maximum inhibition peak of viremia was at dose of 0.20 g/kg and reached 64.10% on day 5 and 66.48% on day 10, respectively. Histopathological evaluation of the liver revealed significant improvement by OJTP. No matter whether 5-day or 10-day administration, or 3 days after 10-day administration, the groups treated with OJTP (500, 250, 125 mg/kg/d) had significantly inhibitory action on DHBV-DNA induced hepatitis model in Peking ducks. Histopathological evidences from the results showed that OJTP treated hepatic lobules were regular, and the denaturation, dropsy, and necrosis of cells were trivial. Meanwhile the hepatic cells are confused and disorderly, oxyphilous denaturation, and dropsy and necrosis is obviously surrounding hepatic lobules. These data indicated that OJTP has significantly inhibitory effects on DHBV-DNA and can protect duck livers from damage in virus hepatitis [68]. Similar results were reported by Huang et al. [69, 70]. In DHBV infected duck primary hepatocytes culture, water extract of O. javanica was shown to potentially inhibit DHBV-DNA levels with the inhibition rate of 64% at 2500 μg/ml and half value of effective concentration (EC50) was 1120.8 μg/ml, which was much less than its TC50 (10000 μg/ml), indicating O. javanica is a hopeful drug for controlling DHBV [69]. The mean inhibition rate of O. javanica on DHBV-NDA polymerase was 75.5% (at dose of 10000 μg/ml) in vitro and 73.3% (at dose of 8 g/kg) in vivo, indicating strong inhibition effect of O. javanica on DHBV-NDA polymerase. In addition, IC50 (407 μg/ml) was far less than TC50 (>10000 μg/ml) on liver cell [70].

The inhibition effect of ethyl acetate extract of O. javanica on HBsAg and HBeAg and its toxicity was demonstrated in the HBV transfected HepG2.2.15 cells. The results showed that the TC50 of the extract was 2284.73 ± 127.35 μg/ml, and the TC0 was 1000 μg/ml. After 6 and 9 days’ treatment, the extract significantly inhibited the secretion of HBsAg and HBeAg in HepG2.2.15 cell line at doses of 1000 and 500 μg/ml [71].

6.7. Neuroprotective Activity

The neuroprotective activities of O. javanica extracts have been uncovered by several studies, which showed that the extracts could improve cell proliferation and neuroblast differentiation, protect neurons from ischemic damage, and maintain antioxidants immunoreactivities [34, 38, 40, 72]. The ethanol extract of O. javanica showed an ameliorating effect on cell proliferation and neuroblast differentiation by increasing brain-derived neurotrophic factor immunoreactivity in the dentate gyrus of adolescent rat [40]. Park et al. revealed that treatment with O. javanica extract (at a dose of 200 mg/kg) exhibited a protective effect on the hippocampal cornus ammonis 1 pyramidal neurons against cresyl violet induced ischemic damage, and this protective effect is closely associated with increasing or maintaining intracellular antioxidant enzymes such as glutathione peroxidase [34]. The F-box-protein 7 (FBXO7) mutations were found in typical and young onset Parkinson’s disease, which plays an important role in the development of dopaminergic neurons. Increased stability and overexpression of FBXO7 may be beneficial to Parkinson’s disease. Chen et al. demonstrated that 95% ethanol extract of O. javanica could, through enhancing FBXO7 and decreasing tumor necrosis factor receptor-associated factor 2 expression, improve cell viability of both 1-methyl-4-phenylpyridinium ion (MPP+)-treated human embryonic kidney-293 (HEK-293) and SH-SY5Y cells, increase proteasome activity in MPP+-treated HEK-293 cells, and restore mitochondrial membrane potential in MPP+-treated SH-SY5Y cells. Thus, ethanol extract of O. javanica could be developed as a potential treatment of Parkinson’s disease [72]. In addition, Ma et al. documented that persicarin, isolated from n-butanol fraction of O. javanica, possessed an obvious neuroprotective activity in glutamate-injured rat cortical cells by reducing calcium influx, inhibiting the subsequent overproduction of nitric oxide and intracellular peroxide, restoring the reduced activities of glutathione reductase and glutathione peroxidase [38].

6.8. Anti-Cancer Activity

It was demonstrated that the total phenolics acid extract from O. javanica possessed an inhibitory effect on HepG2.2.15 cell proliferation, which could reduce cell growth at S phase [73]. In addition, an in vitro migration and invasion assay showed that isorhamnetin, a flavonoid isolated from O. javanica, possessed an anti-metastatic effect, which may correlate with its inhibition of reactive oxygen species-mediated hypoxia inducible factor-1α (HIF-1α) accumulation [74]. It could significantly inhibit cobalt chloride (CoCl2)- or hypoxia-induced HIF-1α accumulation in human cancer cells (HCT116 and HT29 cell lines), as well as suppress CoCl2-induced activity of hypoxia response element reporter gene and HIF-1α-dependent transcription of gene such as glucose transporter 1, lactate dehydrogenase A, carbonic anhydrase-IX, and pyruvate dehydrogenase kinase 1. And the inhibitory effect of isorhamnetin on H2O2-induced HIF-1α accumulation was also observed in HEK293 cells.

6.9. Anticoagulant/Antithrombotic Activities

Persicarin, isorhamnetin, hyperoside, and isorhamnetin-3-O-galactoside, which were isolated from O. javanica, were demonstrated to possess significantly antithrombotic activities [39, 75]. All of them could significantly prolong activated partial thromboplastin time and prothrombin time and inhibit both the activities and generations of thrombin and factor X in human umbilical vein endothelial cells (HUVECs). In accordance with these anticoagulant activities, these four compounds also exhibited inhibitory effect on tumor necrosis factor-alpha-induced plasminogen activator inhibitor type 1 (PAI-1) production. Moreover, persicarin and isorhamnetin showed a prolonged effect on bleeding time in vivo, while treatment with isorhamnetin-3-O-galactoside or persicarin resulted in a significant reduction effect on the ratio of PAI-1/tissue-type plasminogen activator. The anticoagulant and profibrinolytic effects showed that persicarin > isorhamnetin, hyperoside > isorhamnetin-3-O-galactoside, which suggest that the sulfonate group of persicarin or the methoxy group of isorhamnetin-3-O-galactoside positively regulates its anticoagulatory function.

6.10. Anti-Fatigue Effect

The anti-fatigue effect of O. javanica was studied in a wheel apparatus-induced fatigue mice model, and results indicated that oral administration of extract from O. javanica (125, 250 and 500 mg/kg per day) for 4 weeks could significantly prolong the exhausted running time, reduce serum levels of lactic acid, malondialdehyde, and urea nitrogen, increase the activities of serum lactate dehydrogenase and superoxide dismutase, and elevate glycogen reserves and hemoglobin concentration in whole blood [76]. And a further study demonstrated that treatment with extract from O. javanica for 10 days could obviously upregulate the decreases in locomotor activity, function of the axis of hypothalamic-pituitary-adrenal and gonadal axis, and situation of peripheral fatigue and downregulate the elevated levels of central neurotransmitters and radical toward normal values in forcing swimming-induced chronic fatigue syndrome mice model [77]. In addition, Su et al. further demonstrated that treatment with extract from O. javanica significantly improved hydrocortisone-induced decrease in locomotor activity, cyclic adenosine monophosphate (cAMP), ratio of cAMP/cGMP (cyclic guanosine monophosphate), total testosterone level, and increased of malondialdehyde (MDA) and SOD activity [78].

6.11. Hypoglycemic Effect

Oral administration of water extract of O. javanica (10 and 20 g/kg per day) for 2 days significantly lowered the blood glucose levels in normal mice and alloxan-induced hyperglycemic mice, but did not affect mice hyperglycemia induced by adrenaline [79]. In addition, a further study showed that pretreatment with water extract of O. javanica (50, 100, and 200 g/kg) could significantly suppress the blood glucose level and improve the decreased content of insulin in streptozotocin (STZ)-induced mice, and these effects may be due to its alleviation of the condition of the degeneration and necrosis of islet cells induced by STZ [80]. Furthermore, 95% ethanol extract of O. javanica (400 and 800 mg/kg) was also revealed to possess a moderate hypoglycemic activity in STZ-induced diabetic mice model, which could decrease the blood glucose level from 27.6 mM to 20.8 mM and 17.7 mM, respectively [62].

6.12. Cardiovascular Protection

The antiarrhythmic effect of O. javanica was demonstrated in aconitine-induced rats, which indicated that intravenous administration of O. javanica injection (1.5 g/kg) could significantly increase the threshold levels of ventricular premature, ventricular tachycardia, ventricular fibrillation, and cardiac arrest (respectively, 27%, 22%, 32%, and 19% higher than aconitine along-treated rats) and also make rats arrhythmia induced by barium chloride conversed to sinusrhythm within 6.29 min and keep sinusrhythm for another more 12.73 min, as well as decrease the rate of calcium chloride-induced rat ventricular fibrillation and death by 25% and 50%, respectively [81].

Moreover, persicarin and isorhamnetin-3-O-galactoside isolated from O. javanica were revealed to possess potential therapeutic for treatment of severe vascular inflammatory diseases, which could both, through reducing phorbol 12-myristate 13-acetate-stimulated phosphorylation of p38 MAPK, extracellular regulated kinases 1/2, and c-jun N-terminal kinase, suppress the expression of tumor necrosis factor-α and then inhibit the phorbol-12-myristate-13-acetate, cecal ligation, or puncture-induced endothelial protein C receptor [36].

6.13. Antinociceptive/Analgesic Effect

The antinociceptive active of O. javanica methanol extract (at 200 mg/kg) was tested in the acetic acid-induced abdominal writhing response in mice, which indicated that O. javanica extract could reduce about 30% of abdominal constriction, while positive control-aspirin could inhibit about 62% of writing inhibition. Furthermore, the underlying mechanism of antinociceptive effect of O. javanica extract was demonstrated to be mediated by the suppression of nitric oxide production and reducing the sensitization of the peritoneal nociceptor in mice [23].

6.14. Insecticidal Effect

Huo et al. pointed out that O. javanica extract possesses a marked effect to kill the tetranychina harti (Ewing), which supported its usage as a new plant candidate for acaricide [82].

7. Toxicological Studies and Adverse Reaction

O. javanica was documented to be a nontoxic level species by acute toxicity tests, because the maximum tolerated dose of it was higher than 15 g/kg for mice [14, 15, 83]. In an acute toxicity study, a single oral administration of fresh O. javanica (15 g/kg) did not cause young mice mortality or inductive changes in the ALT, blood glucose, total protein, albumin, urea, and creatinine levels, and no signs of abnormal behavioral changes or toxicity on organs including liver and kidney were observed after 14 days of treatment [14]. Furthermore, in Ames assay (8-5000 μg/vessel) and mouse bone marrow cell micronucleus test (2.50-10.00 g/kg), O. javanica showed no obvious genetic toxicity [15]. But an increasing effect on the rate of sperm deformity was observed in mice by oral administration of dry O. javanica power for 5 days (2.50, 5.00, and 10.00 g/kg, 1 g dry power equivalent to 13 g fresh material). Moreover, a subacute toxicity, including weight loss and reduction in food consumption, was also observed in mice by oral administration of dry O. javanica power for 30 days (5.00 g/kg/day) [15]. For subchronic toxicity assay, total phenolics acid extract from O. javanica at doses of 1500 and 750 mg/kg (26 weeks) showed no significant effect on rats body weight, food intake, behaviors, blood routine examination (counts of red blood cells, white blood cells, and platelets; percentages of neutrophils, lymphocytes, monocytes, and hemoglobin; and prothrombin time), serum biomarkers (AST, ALT, ALP, total bilirubin, urea nitrogen, Crea, total protein, albumin, total cholesterol, and blood glucose), or organs [heart, liver, spleen, lung, kidney, adrenal, testis (for male rat), ovary (for female rat), and brain]. However, at the dose of 3000 mg/kg, it showed a decreasing effect on weight gain and lymphocyte number, and an increasing effect on neutrophil, but no effect on other tested items. Furthermore, within a 4-week recovery period, the induced toxicity was basically recovered [16].

In addition, a rare case of irritant contact dermatitis owing to O. javanica was reported by Xia and Li [84], in which a 23-year-old male patient had edematous erythema and bullae appeared on his shoulder, back, and knees where fresh crush of O. javanica was applied. There was also burning-like epidermal exfoliation on the lesions. The patient felt strong burning pain but no itching and was cured by 7-day anti-inflammatory treatment.

8. Conclusions

The present review collectively discussed the ethnomedicinal uses of O. javanica and the available scientific reports on its phytochemistry, pharmacological activities, and toxicology. It is worth mentioning that although scientific studies of bioactivities of O. javanica might justify some of its ethnomedicinal claims, the data are insufficient and, to some extent, preliminary. In the future, further systemic studies in humans are necessary. Furthermore, a subchronic toxicology of O. javanica at high dose (equivalent to 20 times the recommended human clinical dose) was observed in rats, but the potential toxic component and its possible mechanism have not been revealed. It would also be beneficial for in vivo and clinical studies to evaluate the toxicity effects on the target organ.

Abbreviations

AIM2:Absent in melanoma 2
ALP:Alkaline phosphatase
ALT:Alanine aminotransferase
AST:Aspartate aminotransferase
cAMP:Cyclic adenosine monophosphate
cGMP:Cyclic guanosine monophosphate
CAT:Catalase
CC:Carbon tetrachloride
CoC:Cobalt chloride
CYPs:Cytochrome P450 enzymes
DHBV:Duck hepatitis B virus
DPPH:2,2-Diphenylpicrylhydrazyl radical
E:Half value of effective concentration
EEOJ:Ethanol extracts of O. javanica
FBXO7: F-box-protein 7
FRAP:Ferric reducing antioxidant power
GPx:Glutathione peroxidase
:Hydrogen peroxide
HBeAg:Hepatitis B e antigen
HBsAg:Hepatitis B surface antigen
HBV:Hepatitis B virus
HIF-1α:Hypoxia-induced hypoxia inducible factor-1α
HLMs:Human liver microsomes
HMGB1:High mobility group box 1
HUVECs:Human umbilical vein endothelial cells
I:Half maximal inhibitory concentration
MAPK:Mitogen activated protein kinase
NF-κB:Nuclear factor-kappa B
MDA:Malondialdehyde
MP:1-Methyl-4-phenylpyridinium ion
HEK-293:Human embryonic kidney-293 cell (ATCC No. CRL-1573)
NALFD:Nonalcoholic fatty liver disease
NLR:NOD-like receptors
OJTP:Total phenolic acid from O. javanica
ORAC:Oxygen radical absorbance capacity
PAI-1:Plasminogen activator inhibitor type 1
SOD:Superoxide dismutase
STZ:Streptozotocin
T:Half value of toxic concentration.

Conflicts of Interest

The authors confirm that this article’s content has no conflicts of interest.

Acknowledgments

This work was financed by the National Natural Science Foundation of China (No. 81602991), GDAS’ Project of Science and Technology Development (No. 2019GDASYL-0103039), and “Light of West China” Program of Chinese Academy of Sciences.

References

  1. World Health Organization, WHO Traditional Medicine Strategy: 2014-2023, WHO Press, Switzerland, 2013.
  2. N. S. Zahidin, S. Saidin, R. M. Zulkifli, I. I. Muhamad, H. Ya'akob, and H. Nur, “A review of acalypha indica L. (Euphorbiaceae) as traditional medicinal plant and its therapeutic potential,” Journal of Ethnopharmacology, vol. 207, pp. 146–173, 2017. View at Publisher · View at Google Scholar · View at Scopus
  3. R. Singh, “Medicinal plants: a review,” Journal of Plant Sciences, vol. 3, no. 1, pp. 50–55, 2015. View at Google Scholar
  4. G. Ai, Z.-M. Huang, Q.-C. Liu, Y.-Q. Han, and X. Chen, “The protective effect of total phenolics from oenanthe javanica on acute liver failure induced by D-galactosamine,” Journal of Ethnopharmacology, vol. 186, pp. 53–60, 2016. View at Publisher · View at Google Scholar · View at Scopus
  5. S.-A. Yang, Y.-S. Jung, S.-J. Lee et al., “Hepatoprotective effects of fermented field water-dropwort (Oenanthe javanica) extract and its major constituents,” Food and Chemical Toxicology, vol. 67, pp. 154–160, 2014. View at Publisher · View at Google Scholar · View at Scopus
  6. H. Ahn and G.-S. Lee, “Isorhamnetin and hyperoside derived from water dropwort inhibits inflammasome activation,” Phytomedicine, vol. 24, pp. 77–86, 2017. View at Publisher · View at Google Scholar · View at Scopus
  7. J. H. Yang, S. C. Kim, B. Y. Shin et al., “O-methylated flavonol isorhamnetin prevents acute inflammation through blocking of NF-κB activation,” Food and Chemical Toxicology, vol. 59, pp. 362–372, 2013. View at Publisher · View at Google Scholar · View at Scopus
  8. Z. H. Liu and L. Zhang, “Effects of total flavone extract from shuiqin (Oenanthe javanica) on immune function of immunosuppression mice,” Chinese Journal of Traditional Medical Science and Technology, vol. 23, no. 4, pp. 423–425, 2016. View at Google Scholar
  9. J. Y. Kim, K.-H. Kim, Y. J. Lee, S. H. Lee, J. C. Park, and D. H. Nam, “Oenanthe javanica extract accelerates ethanol metabolism in ethanol-treated animals,” BMB Reports, vol. 42, no. 8, pp. 482–485, 2009. View at Publisher · View at Google Scholar · View at Scopus
  10. R. Kongkachuichai, R. Charoensiri, K. Yakoh, A. Kringkasemsee, and P. Insung, “Nutrients value and antioxidant content of indigenous vegetables from Southern Thailand,” Food Chemistry, vol. 173, pp. 836–846, 2015. View at Publisher · View at Google Scholar · View at Scopus
  11. Y.-Q. Han, Z.-M. Huang, X.-B. Yang, H.-Z. Liu, and G.-X. Wu, “In vivo and in vitro anti-hepatitis B virus activity of total phenolics from oenanthe javanica,” Journal of Ethnopharmacology, vol. 118, no. 1, pp. 148–153, 2008. View at Publisher · View at Google Scholar · View at Scopus
  12. J. K. Kim, E.-C. Shin, G. G. Park, Y.-J. Kim, and D.-H. Shin, “Root extract of water dropwort, Oenanthe javanica (Blume) DC, induces protein and gene expression of phase I carcinogen-metabolizing enzymes in HepG2 cells,” Springer Plus, vol. 5, no. 1, pp. 413–418, 2016. View at Google Scholar · View at Scopus
  13. W.-N. Wang, X.-B. Yang, H.-Z. Liu, Z.-M. Huang, and G.-X. Wu, “Effect of Oenanthe javanica flavone on human and duck hepatitis B virus infection,” Acta Pharmacologica Sinica, vol. 26, no. 5, pp. 587–592, 2005. View at Publisher · View at Google Scholar · View at Scopus
  14. Z. X. Yu, L. H. Wei, Y. Gao, and X. Q. Guo, “Study on acute toxicity of Oenanthe javanica,” Journal of Anhui Agricultural Sciences, vol. 45, no. 2, pp. 106-107, 2017. View at Google Scholar
  15. Y. Wang, K. F. Wu, H. Yu, M. Gao, J. Liu, and R. H. Zhang, “Toxicological security evaluation of Oenanthe Javanica,” Food Research and Development, vol. 37, no. 22, pp. 196–201, 2016. View at Google Scholar
  16. B. Q. Xu, Z. M. Huang, R. S. Li, and H. T. Zhang, “Long-term toxicity study the capsule of total phenolics acid extracted from oenanthe javanica in wistar rats,” Pharmacology and Clinics of Chinese Materia Medica, vol. 30, no. 2, pp. 82–86, 2014. View at Google Scholar
  17. Z. M. Huang, X. B. Yang, and W. B. Cao, “Textual study on Oenanthe javanica documented in ancient Chinese medicinal literatures,” Chinese Traditional and Herbal Drugs, vol. 32, no. 1, pp. 59–62, 2001. View at Google Scholar
  18. J. Zhang, S.-H. Li, and R.-H. Gu, “Chemical constituents in oenanthe javanica,” Chinese Traditional and Herbal Drugs, vol. 43, no. 7, pp. 1289–1292, 2012. View at Google Scholar · View at Scopus
  19. T. Fujita, Y. Kadoya, H. Aota, and M. Nakayama, “A new phenylpropanoid glucoside and other constituents of oenanthe javanica,” Bioscience, Biotechnology, and Biochemistry, vol. 59, no. 3, pp. 526–528, 1995. View at Publisher · View at Google Scholar · View at Scopus
  20. A. Hayashi, T. Nakayama, Y. Aoyagi, and K. Kimoto, “Purification of nicotianamine from Hayatouri (Sechium edule) and estimation of quantitative determination method,” Journal of the Japanese Society for Food Science and Technology, vol. 52, no. 4, pp. 154–159, 2005. View at Publisher · View at Google Scholar · View at Scopus
  21. J. Yoshida, H. Seino, Y. Ito et al., “Inhibition of glycogen synthase kinase-3β by falcarindiol isolated from Japanese parsley (Oenanthe javanica),” Journal of Agricultural and Food Chemistry, vol. 61, no. 31, pp. 7515–7521, 2013. View at Publisher · View at Google Scholar · View at Scopus
  22. M. Song, M. Hong, M. Y. Lee et al., “Selective inhibition of the cytochrome P450 isoform by hyperoside and its potent inhibition of CYP2D6,” Food and Chemical Toxicology, vol. 59, pp. 549–553, 2013. View at Publisher · View at Google Scholar · View at Scopus
  23. K. H. Lee, A. M. Padzil, A. Syahida et al., “Evaluation of anti-inflammatory, antioxidant and antinociceptive activities of six Malaysian medicinal plants,” Journal of Medicinal Plant Research, vol. 5, no. 23, pp. 5555–5563, 2011. View at Google Scholar · View at Scopus
  24. M. Z. Nur Ain Izzati and W. I. Wan Hasmida, “Isolation of microfungi from Malay traditional vegetables and secondary metabolites produced by Fusarium species,” Sains Malaysiana, vol. 40, no. 5, pp. 437–444, 2011. View at Google Scholar · View at Scopus
  25. N. Huda-Faujan, A. Noriham, A. S. Norrakiah, and A. S. Babji, “Antioxidant activity of plants methanolic extracts containing phenolic compounds,” African Journal of Biotechnology, vol. 8, no. 3, pp. 484–489, 2009. View at Google Scholar · View at Scopus
  26. A. S. Babji, N. H. Ismail, K. Rammaya, and N. M. Nadzri, “Quality improvement of chicken ball by adding selom leaves (Oenanthe javanica), mengkudu (Morinda citrifolia) extracts and red palm fat (Carotino®),” Sains Malaysiana, vol. 43, no. 10, pp. 1509–1514, 2014. View at Google Scholar · View at Scopus
  27. F. D. Pu and F. W. Mark, “Oenanthe Linnaeus,” in Editorial Committee of Flora of China, pp. 130–132, Flora of China, Science Press, Beijing, China, 2005. View at Google Scholar
  28. R. F. Polomski, D. G. Bielenberg, T. Whitwell, M. D. Taylor, W. C. Bridges, and S. J. Klaine, “Differential nitrogen and phosphorus recovery by five aquatic garden species in laboratory-scale subsurface-constructed wetlands,” HortScience, vol. 43, no. 3, pp. 868–874, 2008. View at Publisher · View at Google Scholar · View at Scopus
  29. S. Z. Li, Compendium of Materia Medica, People’s Medical Publishing House, Beijing, China, 1978.
  30. W. P. Wei, Shen Nong’s Herbal, People’s Medical Publishing House, Beijing, China, 1963.
  31. J. C. Park, H. S. Young, Y. B. Yu, and J. H. Lee, “Isorhamnetin sulphate from the leaves and stems of Oenanthe javanica in Korea,” Planta Medica, vol. 61, no. 4, pp. 377-378, 1995. View at Publisher · View at Google Scholar · View at Scopus
  32. C. H. Lee, J. H. Park, J. H. Cho et al., “Effect of oenanthe javanica extract on antioxidant enzyme in the rat liver,” Chinese Medical Journal, vol. 128, no. 12, pp. 1649–1654, 2015. View at Google Scholar
  33. I.-W. Choi, H.-Y. Kim, J.-H. Quan, J.-G. Ryu, R. Sun, and Y.-H. Lee, “Monitoring of Fasciola species contamination in water dropwort by COX1 mitochondrial and ITS-2 rDNA sequencing analysis,” The Korean Journal of Parasitology, vol. 53, no. 3, pp. 641–645, 2015. View at Publisher · View at Google Scholar · View at Scopus
  34. J. H. Park, J. H. Cho, I. H. Kim et al., “Oenanthe javanica extract protects against experimentally induced ischemic neuronal damage via its antioxidant effects,” Chinese Medical Journal, vol. 128, no. 21, pp. 2932–2937, 2015. View at Google Scholar
  35. Q. Jiang, F. Wang, M.-Y. Li, J. Ma, G.-F. Tan, and A.-S. Xiong, “Selection of suitable reference genes for qPCR normalization under abiotic stresses in Oenanthe javanica (BI.) DC,” PLoS ONE, vol. 9, no. 3, Article ID e92262, 2014. View at Google Scholar · View at Scopus
  36. S.-K. Ku, M.-S. Han, and J.-S. Bae, “Down-regulation of endothelial protein C receptor shedding by persicarin and isorhamnetin-3-O-galactoside,” Thrombosis Research, vol. 132, no. 1, pp. e58–e63, 2013. View at Publisher · View at Google Scholar · View at Scopus
  37. X. B. Yang, Z. M. Huang, W. B. Cao et al., “Antidiabetic effect of Oenanthe javanica flavone,” Acta Pharmacologica Sinica, vol. 21, no. 3, pp. 239–242, 2000. View at Google Scholar · View at Scopus
  38. C. J. Ma, K. Y. Lee, E. J. Jeong et al., “Persicarin from water dropwort (Oenanthe javanica) protects primary cultured rat cortical cells from glutamate-induced neurotoxicity,” Phytotherapy Research, vol. 24, no. 6, pp. 913–918, 2010. View at Publisher · View at Google Scholar · View at Scopus
  39. S.-K. Ku, T. H. Kim, S. Lee, S. M. Kim, and J.-S. Bae, “Antithrombotic and profibrinolytic activities of isorhamnetin-3-O-galactoside and hyperoside,” Food and Chemical Toxicology, vol. 53, pp. 197–204, 2013. View at Publisher · View at Google Scholar · View at Scopus
  40. B. H. Chen, J. H. Park, J. H. Cho et al., “Ethanol extract of Oenanthe javanica increases cell proliferation and neuroblast differentiation in the adolescent rat dentate gyrus,” Neural Regeneration Research, vol. 10, no. 2, pp. 271–276, 2015. View at Google Scholar
  41. J. Y. Lee, M. Y. Kim, S. H. Shin et al., “Persicarin isolated from Oenanthe javanica protects against diabetes-induced oxidative stress and inflammation in the liver of streptozotocin-induced type 1 diabetic mice,” Experimental and Therapeutic Medicine, vol. 13, no. 4, pp. 1194–1202, 2017. View at Publisher · View at Google Scholar · View at Scopus
  42. W. H. Seo and H. H. Baek, “Identification of characteristic aroma-active compounds from water dropwort (Oenanthe javanica DC.),” Journal of Agricultural and Food Chemistry, vol. 53, no. 17, pp. 6766–6770, 2005. View at Publisher · View at Google Scholar · View at Scopus
  43. S. L. Zhang, G. P. Dong, and G. M. Liu, “Study on the chemical constituents of essential oil in Oenanthe javanica (BL.) DC,” Lishizhen Medicine and Materia Medica Research, vol. 20, no. 2, pp. 350-351, 2009. View at Google Scholar
  44. E. K. Lee, M. C. Shin, and S. H. Jung, “Volatile compound analysis and anti-oxidant and anti-inflammatory effects of Oenanthe Javanica, Perilla frutescens, and Zanthoxylum piperitum essential oils,” Asian Journal of Beauty & Cosmetology, vol. 15, no. 3, pp. 355–366, 2017. View at Publisher · View at Google Scholar
  45. S.-J. Hwang, S.-J. Park, and J.-D. Kim, “Component analysis and antioxidant activity of oenanthe javanica extracts,” Korean Journal of Food Science and Technology, vol. 45, no. 2, pp. 227–234, 2013. View at Publisher · View at Google Scholar · View at Scopus
  46. L. Jian, “Analysis of the major nutritional components in Oenanthe javanica and Apium graveolens celery,” Northern Horticulture, vol. 30, pp. 33-34, 2008. View at Google Scholar
  47. S. L. Wu, F. Liu, Y. Y. Li, M. Tang, and S. H. Li, “Detection of the main nutrient contents on several kinds of edible wild herbs from Mountain Emei,” Northern Horticulture, vol. 34, no. 20, pp. 26–28, 2012. View at Google Scholar
  48. H. Choi, Y. You, K. Hwang et al., “Isolation and identification of compound from dropwort (Oenanthe javanica) with protective potential against oxidative stress in HepG2 cells,” Food Science and Biotechnology, vol. 20, no. 6, pp. 1743–1746, 2011. View at Publisher · View at Google Scholar · View at Scopus
  49. Z. M. Huang, X. B. Yang, W. B. Cao et al., “Experimental study on subsidence of jaundice and Gptase by the decoction of Shui Qin (Oenanthe javanica),” Chinese Pharmaceutical Journal, vol. 24, no. 2, pp. 84–85, 128, 1989. View at Google Scholar
  50. H. G. Chen, G. X. Nian, X. B. Yang, and Z. M. Huang, “Protective effect of total phenolics acid of Oenanthe javanica on hepatic injury mice induced by D-galn,” Pharmaceutical Journal of Chinese People’s Liberation Army, vol. 25, no. 6, pp. 492–495, 2009. View at Google Scholar
  51. G. X. Nian, Z. M. Huang, X. B. Yang, and J. G. Song, “Protective effect of total phenolics acid of Oenanthe javanica on Mice models of CCl4 hepatic injury,” Pharmaceutical Journal of Chinese peoples Liberation Army, vol. 24, no. 6, pp. 501–504, 2008. View at Google Scholar
  52. G. X. Nian, Z. M. Huang, X. B. Yang, and J. G. Song, “Experimental study of OJTPA on jaundice-reliveing effects,” Pharmaceutical Journal of Chinese People’s Liberation Army, vol. 25, no. 2, pp. 124–127, 2009. View at Google Scholar
  53. K. Z. Hu, G. X. Nian, K. Yang, and Z. M. Huang, ““The study of therapeutical effect of total phenolic acid extracted from Oenanthe jananica (Bl) DC on non-alcoholic fatty liver in rats,” Pharmaceutical Journal of Chinese People’s Liberation Army, vol. 25, no. 1, pp. 29–33, 2009. View at Google Scholar
  54. Y. Jeong, Y. J. Lee, K. M. Lee, and J. Y. Kim, “The effects of Oenanthe javanica extracts on hepatic fat accumulation and plasma biochemical profiles in a nonalcoholic fatty liver disease model,” Journal of the Korean Society for Applied Biological Chemistry, vol. 52, no. 6, pp. 632–637, 2009. View at Publisher · View at Google Scholar
  55. G. X. Nian, Z. M. Huang, X. B. Yang, R. S. Li, and J. G. Song, “Effect of total phenolics acid of Oenanthe javanica on hepatic fibrosis in rats,” Pharmaceutical Journal of Chinese People’s Liberation Army, vol. 26, no. 1, pp. 22–26, 2010 (Chinese). View at Google Scholar
  56. J. C. Park and J. W. Choi, “Effects of methanol extract of Oenanthe javanica on the hepatic alcohol-metabolizing enzyme system and its bioactive component,” Phytotherapy Research, vol. 11, no. 3, pp. 260–262, 1997. View at Publisher · View at Google Scholar · View at Scopus
  57. S. C. Hou, Bioactivity studies on the phenolics from Oenanthe javanica and preparation of its microcapsule [MSc., thesis], Yangzhou University, 2017.
  58. K. Chen, P. T. E. Ni Ya Zi, H. Zhang, D. Liu, X. Ye, and J. Chen, “Optimization of flavonoids extration from Oenanthe javanica by response surface methodology and the study on chemical compositions,” Journal of Chinese Institute of Food Science and Technology, vol. 14, no. 11, pp. 83–89, 2014. View at Google Scholar · View at Scopus
  59. K. K. Chen, Chemical and bioactive studies on the flavonoids of Oenanthe javanica, [MSc., thesis], Zhejiang University, 2014.
  60. C. C. Li, Y. M. Zuo, X. M. Jiang, Q. Wu, X. Q. Guo, and W. Pan, “Simultaneous determination of six constituents from Oenanthe javanica and establishment of the fingerprints,” Chinese Traditional Patent Medicine, vol. 38, no. 12, pp. 2621–2625, 2016. View at Google Scholar
  61. L. S. Ching and S. Mohamed, “Alpha-tocopgerol content in ble tropical plants,” Journal of Agricultural and Food Chemistry, vol. 49, no. 6, pp. 3101–3105, 2001. View at Google Scholar
  62. X. Q. Guo, L. H. Wei, T. T. Dai, and Q. Wu, “The detection of the chemical compounds in Oenanthe javanica and its hypoglycemic activity,” Food & Machinery, vol. 33, no. 1, pp. 155–157, 173, 2017. View at Google Scholar
  63. T. H. Kim, S.-K. Ku, and J.-S. Bae, “Anti-inflammatory activities of isorhamnetin-3-O-galactoside against HMGB1-induced inflammatory responses in both HUVECs and CLP-induced septic mice,” Journal of Cellular Biochemistry, vol. 114, no. 2, pp. 336–345, 2013. View at Publisher · View at Google Scholar · View at Scopus
  64. T. H. Kim, S. K. Ku, and J. S. Bae, “Persicarin is anti-inflammatory mediator against HMGB1-induced inflammatory responses in HUVECs and in CLP-induced sepsis mice,” Journal of Cellular Physiology, vol. 228, no. 4, pp. 696–703, 2013. View at Publisher · View at Google Scholar · View at Scopus
  65. W. Zhang, Z. M. Huang, and X. N. Chen, “Effect of total phenolics acid extracted from Oenanthe javanica on immune function in normal mice,” Pharmaceutical Journal of Chinese People’s Liberation Army, vol. 29, no. 1, pp. 17–19, 2013. View at Google Scholar
  66. A. Rafat, K. Philip, and S. Muniandy, “Antioxidant potential and phenolic content of ethanol extract of selected Malaysian plants,” Research Journal of BioTechnology, vol. 5, no. 1, pp. 16–20, 2010. View at Google Scholar · View at Scopus
  67. X.-J. Wang, Z.-M. Huang, X.-B. Yang, and J.-G. Song, “Inhibition of total phenolics acid extracted from Oenanthe Javanica on HBV-DNA, cccDNA in cultured cell line 2. 2. 15,” Chinese Pharmacological Bulletin, vol. 25, no. 8, pp. 1099–1102, 2009. View at Google Scholar · View at Scopus
  68. X. J. Wang, Z. M. Huang, X. B. Yang, R. S. Li, and J. G. Song, “Effect of total phenolics acid of Oenanthe javanica on the duck Hepatitis B,” Pharmaceutical Journal of Chinese People’s Liberation Army, vol. 25, no. 6, pp. 501–505, 2009. View at Google Scholar
  69. Z. M. Huang, X. B. Yang, W. B. Cao et al., “Inhibition of shuiqin on DHBV in vitro,” Chinese Pharmaceutical Journal, vol. 32, no. 11, pp. 720–723, 1997. View at Google Scholar · View at Scopus
  70. Z. M. Huang, X. B. Yang, W. B. Cao, X. W. Shao, and H. S. Chen, “Mechanism studies on anti-duck hepatitis B virus of water extract of Oenanthe javanica,” Chinese Science Bulletin, vol. 42, no. 17, pp. 1863–1867, 1997. View at Google Scholar
  71. X. B. Yang, Z. M. Huang, W. B. Cao et al., “Inhibition of ethyl acetate extract of Oenanthe javanica on secreti of HBsAg and HBeAg in cultured cell line 2215 (Hep G2),” Pharmaceutical Journal of Chinese People’s Liberation Army, vol. 16, no. 1, pp. 4–8, 2000. View at Google Scholar
  72. C.-M. Chen, I.-C. Chen, Y.-L. Chen et al., “Medicinal herbs Oenanthe javanica (Blume) DC., Casuarina equisetifolia L. and Sorghum bicolor (L.) Moench protect human cells from MPP+ damage via inducing FBXO7 expression,” Phytomedicine, vol. 23, no. 12, pp. 1422–1433, 2016. View at Publisher · View at Google Scholar · View at Scopus
  73. W. Zhang, X. N. Chen, and Z. M. Huang, “Effect of total phenolics acid extracted from Oenanthe javanica on cell cycle in human Hepatoma 2.2.15 cell,” Pharmaceutical Journal of Chinese People's Liberation Army, vol. 29, no. 4, pp. 369–371, 2013. View at Google Scholar
  74. S. Seo, K. Seo, S. H. Ki, and S. M. Shin, “Isorhamnetin inhibits reactive oxygen species-dependent hypoxia inducible factor (HIF)-1α accumulation,” Biological & Pharmaceutical Bulletin, vol. 39, no. 11, pp. 1830–1838, 2016. View at Publisher · View at Google Scholar · View at Scopus
  75. S.-K. Ku, T. H. Kim, and J.-S. Bae, “Anticoagulant activities of persicarin and isorhamnetin,” Vascular Pharmacology, vol. 58, no. 4, pp. 272–279, 2013. View at Publisher · View at Google Scholar · View at Scopus
  76. C. H. Su, X. N. Chen, X. B. Yang, and Z. M. Huang, “Study on the anti-fatigue effect of the extract of Oenanthe javanica and its probable mechanism in mice,” Pharmaceutical Journal of Chinese People's Liberation army, vol. 27, no. 2, pp. 103–106, 2011. View at Google Scholar
  77. C. H. Su, X. N. Chen, X. B. Yang, Z. M. Huang, W. B. Cao, and H. Y. Chen, “Therapeutic effect of extract of Oenanthe javanica against syndrome in mice,” China Journal of Traditional Chinese Medicine and Pharmacy, vol. 27, no. 12, pp. 3100–3103, 2012. View at Google Scholar
  78. C. H. Su, X. B. Yang, Z. M. Huang et al., “Effect of extract of Oenanthe javanica against kidney Yang deficiency in mice caused by hydrocortisone,” Chinese Journal of Information on Traditional Chinese Medicine, vol. 18, no. 12, pp. 39–42, 2011. View at Google Scholar
  79. Z. M. Huang, X. B. Yang, W. B. Cao, H. Y. Chen, M. Zheng, and Z. Z. Zhang, “Effects of Oenanthe javanica (SQ) on blood glucose in normal and diabetes mice,” Pharmacology and Clinics of Chinese Materia Medica, vol. 12, no. 5, pp. 35-36, 1996. View at Google Scholar
  80. X. B. Yang, Z. M. Huang, H. Y. Chen, J. H. Wang, and W. B. Cao, “Study on the protective effect of water extract of O. javanica on STZ-induced islet injury,” Journal of Practical traditional Chinese Medicine, vol. 22, no. 7, pp. 395-396, 2006. View at Google Scholar
  81. G. J. Ji, X. L. Yao, Z. M. Zhang, and Z. M. Huang, “Antiarrhythmic effect of Oenanthe javanica (Bl.) DC. Injection,” China Journal of Chinese Materia Medica, vol. 15, no. 7, pp. 45–47, 1990. View at Google Scholar
  82. Y. B. Huo, J. He, Z. Q. Ma, and X. Zhang, “Acaricidal activities of acetone extracts from 107 plant species for Tetranychina harti,” Acta Agrestia Sinica, vol. 21, no. 6, pp. 1200–1207, 2013. View at Google Scholar
  83. Y. Wang, K. F. Wu, H. Yu, Y. J. Liu, and J. Liu, “Acute and genetic toxicity studies on wild Oenanthe javanica,” Guizhou Medical Journal, vol. 40, no. 4, pp. 375–377, 2016. View at Google Scholar
  84. Q. Xia and L. Li, “Contact dermatitis owing to Oenanthe javanica Blume DC: a case report,” Journal of Clinical Dermatology, vol. 29, no. 4, pp. 233–233, 2000. View at Google Scholar