Evaluation of anti-inflammatory effect of traditional medicinal plants, Gynura segetum
Evaluation of anti-inflammatory effect of traditional medicinal plants, Gynura segetum
CellMed. 2014. Feb, 4(1): 4-4
Copyright © 2014, Association of Humanitas Medicine
This is an open access article under the CC BY-NC license. (
  • Received : December 18, 2013
  • Accepted : February 07, 2014
  • Published : February 28, 2014
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About the Authors
Lay-Jing, Seow
Hooi-Kheng, Beh
Amirin, Sadikun
Mohd Zaini, Asmawi

Gynura segetum , family Asteraceae is a cultivated species and can be found growing in the tropical regions of Indonesia and Malaysia. The plant is known for its use for the treatment of cancer, inflammation, diabetes, hypertension and skin afflictions. In the current study, anti-inflammatory effect of Gynura segetum leaf has been investigated. The present study investigated the in vivo anti-inflammatory effect of Gynura segetum leaf by using hen’s egg test-chorioallantoic membrane (HET-CAM) assay. Different solvent extract of Gynura segetum leaf were tested, the most active methanol extract was further fractionated and tested. Among the extracts tested, the methanol extract showed a significant good anti-inflammatory effect (76.8% inhibition at 50 μ) on the HET-CAM assay as compared with the anti-inflammatory drug indomethacin (82.1% inhibition). However, the fractionated sample exhibited a significantly lower activity in comparison to crude methanol extract. The results demonstrated that Gynura segetum leaf displayed remarkable anti-inflammatory effects, which support the folkloric uses of this plant for treatment of inflammation.
Herbal Herbal medicines are the therapeutic experiences of generations of practicing physicians of traditional medicine over hundreds of years and they are known to be oldest health care products that have been used by mankind all over the world to treat various types of ailments ( Torey et al., 2010 ). Currently, attention is being focused on the investigation of the efficacy of traditionally used plants as they are affordable and have fewer adverse effects ( Masresha et al, 2012 ).
Gynura segetum, family Compositae (Asteraceae) is a cultivated species and can be found growing in the tropical regions of Indonesia and Malaysia. Gynura segetum has drawn a lot of attention due to its uses in traditional medicine. The plant is known for its use for the treatment of cancer, inflammation, diabetes, hypertension and skin afflictions. A variety of chemical compounds has been identified from this genus such as flavonoids, pyrolizidine alkaloids, triterpenes, sterides and sesquiterpenoids ( Zhu et al., 2013 ).
In previous study, the leaf extracts of Gynura segetum showed potential anti-angiogenic effects in chick embryo chorioallantoic membrane (CAM) model ( Seow et al., 2011 ). Anti-angiogenic activity of Gynura segetum’s leaf extracts provided a pharmacological basis on its folkloric use for the treatment of inflammatory diseases and cancer.
Anti-angiogenic strategies are emerging as an important tool for the treatment of cancer and inflammatory diseases. Therefore, researchers are growing interests in using natural anti-angiogenic agents, especially extracted from plants ( Peng et al., 2009 ). Most of the research on anti-angiogenic agents has been directed towards inflammation treatment ( Ahn et al., 2007 ; Jung et al., 2009 ; Kim et al., 2004 ; Krenn and Paper, 2009 ). Collectively, this suggested that many herbs and their phytochemicals may exert both anti-angiogenic effects and anti-inflammatory activity. Thus, there is an interest to discover local medicinal plant for anti-angiogenic and anti-inflammatory effects.
Although the plant is traditionally used in inflammatory disorders, but to the best of our knowledge, there is lack of research on the use of leaf extract of Gynura segetum in inflammation. Therefore, investigation of anti-inflammatory effects of Gynura segetum would be desirable. In the present study, the anti-inflammatory activity of Gynura segetum’s leaf was evaluated in a modified version of the chicken chorioallantoic membrane assay (HET-CAM assay), as this model is an in vivo model chronic inflammation, which in this study induced by Sodium dodecyl sulfate (SDS).
- Plant material
The leaves of Gynura segetum were collected from Jabatan Pertanian Relau, Penang. A voucher specimen (No.11013) has been deposited at the herbarium of School of Biological Sciences, Universiti Sains Malaysia.
- Plant extraction and fractionation
The extraction of Gynura segetum ’s leaves was performed similarly as described in previous study ( Seow et al., 2011 ). Further fractionation of the most active methanol extract was carried out by resin column chromatography. The Amberlite XAD resins (100 g) were swollen in water overnight and packed into a sintered glass column measuring 25 cm long and 5.5 cm in diameter. The resins were subsequently flushed with 2 L of methanol and 2 L of water to remove impurities in the resins ( Cho et al., 2009 ). Crude methanol extract (10 g) was dissolved in 1mL of methanol and then added in water. The sample was loaded into this reverse phase column and first eluted with water, followed by water-methanol mixture (1:1) and finally with acetone. Five fractions were collected and the solvent was removed using a rotary evaporator to afford 7.69 g, 7.67 g, 5.22 g, 4.81 g, and 2.18 g for fractions R1, R2, R3, R4, and R5 respectively. Dried sample from each fraction (10 mg) were reconstituted in 2 mL of DMSO (0.05%) and subjected to HET-CAM analysis.
- Preparation of test samples
The test substances and control were dissolved in DMSO (0.05%) to reach final concentration of 5 mg/ml. For the preparation of the discs, 10μl of these solutions were applied dropwise on sterile filter paper of 3mm diameter, dried under a laminar flow hood to give concentration of 50 μg per disc. Indomethacin was applied as positive control and CAMs treated with 10 μl of DMSO (0.05%) as blank control.
- Hen’s egg test-chorioallantoic membrane (HET-CAM) assay
The HET-CAM assay was performed according to the method of Burgermeister et al. (2002) with some modifications. Discs of every test substances as well as positive control were placed on 10 - 15 eggs, each. The effects were compared to those of DMSO (0.05%) discs and disc with 50 μg/disc SDS. All tests run in triplicate and the evaluation was performed using a score system followed by the conversion of the score index in the proportional inhibition of inflammation: Inhibition < 40%, no anti-inflammatory effect; Inhibition 40 - 55%, uncertain antiinflammatory effect; Inhibition 55 - 70%, weak antiinflammatory effect; Inhibition 70 - 85%, good antiinflammatory effect; Inhibition > 85%, strong antiinflammatory effect.
- Statistical analysis
The data was expressed as means ± SEM. Statistical comparison between groups was analyzed by one way analysis of variance and post hoc Tukey’s test (SPSS, Inc., version 20). p values less than 0.05 was considered to be significant.
Anti-inflammatory activity of Gynura segetum ’s leaves were examined by the in vivo HET-CAM assay and the results are summarized in Table 1 . The membrane irritation induced by SDS is shown in Fig. 1A . The granuloma is strongly vascularized and a star-like capillaries network is formed surrounding the disc containing SDS. However, a complete normalized of capillaries network can be observed if anti-inflammatory test substances applied together with SDS. Indomethacin as positive control exhibited strong anti-inflammatory effect with inhibition 82.1% (50 μg/disc). As shown in Fig. 1B , the network of blood vessels is normal and no granuloma can be observed.
Anti-inflammatory effect (HET-CAM assay) ofGynura segetum’s leaf extracts, fractions and positive control
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All tested samples shown significant result (p < 0.001) compared with control, except MeOH. aPE: Petroleum ether extract; CHCl3: Chloroform extract; MeOH: Methanol extract; CHCl3 part: Chloroform fraction; EA part: ethyl acetate fraction; BU part: Butanol fraction; bThe result was expressed as means ± SEM (n = 6).
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HET-CAM assay. (A) Membrane irritation induced by SDS; (B) CAM treated with Indomethacin (82.1% of inhibition); (C) The best anti-inflammatory effects of treatment with Methanol extract (76.8% of inhibition).
Among the extract tested, the methanol extract showed good anti-inflammatory activity with inhibition 76.8% (50 μg/disc). The methanol extract neutralized the formation of blood vessels around the granuloma and the capillaries network appeared normal ( Fig. 1C ). The anti-inflammatory effect of methanol extract was almost comparable to the antiinflammatory drug indomethacin at the same concentration. Methanol extract did not show any statistically significant difference as compared with indomethacin ( p > 0.05).
Further fractionation on the most active methanol extract was carried out and five fractions obtained were tested at the same dosage (50 μg/disc). All these fractions (R1 to R5) exhibited lower activity than the crude methanol extract. There was no significant difference ( p > 0.05) between the fractions.
To the best of our knowledge, this is the first report of the anti-inflammatory activity of Gynura segetum ’s leaves by using chick embryo chorioallantoic membrane (CAM) assay. The major advantage of a chick embryo chorioallantoic membrane is simple to use and low cost. The CAM system allows several compounds to be tested simultaneously in the same embryo, fast and suitable for large scale screening. The vascular system of CAM is directly accessible to observation and experimentation, and there are no metabolic or hormonal influences ( Mathur et al., 2006 ). It allows to directly studying the in vivo effect of the test compound ( Min et al., 2004 ).
The modified of the chicken chorioallantoic membrane assay (HET-CAM assay) is an in vivo model chronic inflammation. Chronic inflammation involves proliferation, migration and recruitment of tissue and inflammatory cells, which damaged the normal tissue. Inflammatory tissue is hypoxic and induces angiogenesis through upregulation of factors such as vascular endothelial growth factor (VEGF). The angiogenic factor stimulates the proliferation and migration of endothelial cells in existing blood vessel to generate the new blood vessels. New blood vessels maintain the chronic inflammatory by transporting inflammatory cells to the inflammation site and supplying the nutrients and oxygen to the proliferating inflamed tissue ( Griffioen and Molema, 2000 ; Jackson et al., 1997 ; Walsh and Pearson, 2001 ).
According to Jackson et al. (1997) , angiogenesis and inflammation are codependent processes. An inflammatory state can promote angiogenesis, and angiogenesis can facilitate chronic inflammation. Earlier study had demonstrated that the leaf extracts of Gynura segetum reduced the growth of blood vessels and exhibited the potent anti-angiogenic effect in chick embryo chorioallantoic membrane (CAM) model ( Seow et al., 2011 ). Preliminary phytochemical screening revealed the presence of alkaloids, terpenes, flavonoids, tannins and saponins in leaves of Gynura segetum ( Seow et al., 2013 ). The presence of phenolic compounds in the plants indicates that this plant may have potential used in hyperglycemia, antioxidant, anticancer and anti-inflammatory etc ( Doss and Phil, 2009 ; Rathore et al., 2012 ). The anti-inflammatory activity of Gynura segetum ’s leaves seems to be closely linked with its anti-angiogenic activity and the chemical constituents.
In the present study, the methanol extract of Gynura segetum ’s leaves neutralized the capillaries network and shown no granuloma tissue on CAM. These results suggested that Gynura segetum ’s leaves as an angiogenesis inhibitor can reduce the inflammation and help to restore the appropriate tissue and function.
In conclusions, this study demonstrated that the methanol extract of Gynura segetum ’s leaves performed potent antiinflammatory by in vivo HET-CAM assay. This finding provided a pharmacological background on the traditional use of Gynura segetum for treatment of inflammatory disease.
The authors acknowledge the financial support given by the Universiti Sains Malaysia (USM). The authors also thank the School of Pharmaceutical Sciences, USM for providing the required facilities and excellent technical assistance. The first author was supported by MyBrain 15 (MyPhD) scholarship sponsored by the Ministry of Higher Education (MOHE) Malaysia.CONFLICT OF INTERESTThe authors have no conflicts of interest to declare.
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