Activity of Eurycoma longifolia root extract against Plasmodium falciparum in vitro

2009 ◽  
Vol 121 (S3) ◽  
Author(s):  
Walther H. Wernsdorfer ◽  
Sabariah Ismail ◽  
Kit Lam Chan ◽  
Kanungnit Congpuong ◽  
Gunther Wernsdorfer
Keyword(s):  
Plasmodium Falciparum ◽  
Root Extract ◽  
Eurycoma Longifolia

scholarly journals First Report ofEurycoma longifoliaJack Root Extract Causing Relaxation of Aortic Rings in Rats

2016 ◽  
Vol 2016 ◽  
pp. 1-9 ◽  
Author(s):  
Bae Huey Tee ◽  
See Ziau Hoe ◽  
Swee Hung Cheah ◽  
Sau Kuen Lam
Keyword(s):  
Erectile Function ◽  
Receptor Activation ◽  
Root Extract ◽  
Ang Ii ◽  
Angiotensin I ◽  
Eurycoma Longifolia ◽  
Vasodilatory Effect

AlthoughEurycoma longifoliahas been studied for erectile function, the blood pressure- (BP-) lowering effect has yet to be verified. Hence, this study aims at investigating the BP-lowering properties of the plant with a view to develop an antihypertensive agent that could also preserve erectile function. Ethanolic root extract was partitioned by hexane, dichloromethane (DCM), ethyl acetate, butanol, and water. The DCM fraction, found to be potent in relaxing phenylephrine- (PE-) precontracted rat aortic rings, was further purified by column chromatography. Subfraction DCM-II, being the most active in relaxing aortae, was studied for effects on the renin-angiotensin and kallikrein-kinin systems in aortic rings. The effect of DCM-II on angiotensin-converting enzyme (ACE) activity was also evaluatedin vitro. Results showed that DCM-II reduced (p<0.05) the contractions evoked by angiotensin I and angiotensin II (Ang II). In PE-precontracted rings treated with DCM-II, the Ang II-induced contraction was attenuated (p<0.05) while bradykinin- (BK-) induced relaxation enhanced (p<0.001).In vitro, DCM-II inhibited (p<0.001) the activity of ACE. These data demonstrate that the vasodilatory effect of DCM-II appears to be mediatedviainhibition of Ang II type 1 receptor and ACE as well as enhancement of Ang II type 2 receptor activation and BK activity.

scholarly journals In Vitro Antibacterial Activity of Eurycoma Longifolia Jack (Tongkat Ali) Root Extract

2020 ◽  
Vol 14 (1) ◽  
Author(s):  
Faisal GG ◽  
Zakaria SM ◽  
Najmuldeen GF
Keyword(s):  
Antibacterial Activity ◽  
Ethanolic Extract ◽  
Inhibition Zone ◽  
Root Extract ◽  
Bacterial Strains ◽  
Gram Positive ◽  
Eurycoma Longifolia ◽  
Herbal Plants ◽  
Eurycoma Longifolia Jack

Introduction: Currently, researchers are aiming to explore herbal plants to replace synthetic drugs because herbal plants contain high active compounds and fewer side effects. Our study was done to determine the antibacterial activity of Eurycoma longifolia Jack (E. longifolia) root using ethanol based extract. Methods: Five types of pathogenic bacterial strains were used; Gram-positive (Staphylococcus aureus and Bacillus cereus) and Gram-negative (Escherichia coli, Salmonella typhi and Pseudomonas aeruginosa). Disc diffusion assay and Minimum Inhibitory Concentration (MIC) tests were used to determine the inhibition zone and turbidity of suspension which reflects the antibacterial activity of the extract. Results: The ethanolic extract of E. longifolia Jack root extract showed positive results against Gram-positive bacteria (S. aureus and B. cereus) and Gramnegative (S. typhi). B.cereus and S.typhi showed inhibition zone values of 11.76mm and 14.33mm at the extract concentration of 150mg/ml that were higher than the positive control values (9.00, 12.67mm) respectively. However, E. coli and P. aeruginosa did not show any inhibition by the ethanol-based extract. Conclusion: From the results we can conclude that E.Longifolia root extract possesses antibacterial activity that can be further explored to produce new medicinal products.

scholarly journals In vitro Anti-Toxoplasma gondii Activity of Root Extract/Fractions of Eurycoma longifolia Jack

2012 ◽  
Vol 12 (1) ◽  
Author(s):  
Nowroji Kavitha ◽  
Rahmah Noordin ◽  
Kit-Lam Chan ◽  
Sreenivasan Sasidharan
Keyword(s):  
Toxoplasma Gondii ◽  
Root Extract ◽  
Eurycoma Longifolia ◽  
Eurycoma Longifolia Jack

In vitro metabolism of selected bioactive compounds of Eurycoma longifolia root extract to identify suitable markers in doping control

2018 ◽  
Vol 11 (1) ◽  
pp. 86-94 ◽  
Author(s):  
Pia Bräuer ◽  
Patricia Anielski ◽  
Stefan Schwaiger ◽  
Hermann Stuppner ◽  
Thi Van Anh Tran ◽  
...  
Keyword(s):  
Bioactive Compounds ◽  
Doping Control ◽  
In Vitro Metabolism ◽  
Root Extract ◽  
Eurycoma Longifolia ◽  
In Doping

scholarly journals In Vitro Antimalarial Activity and Cytotoxity of 20 Ethanolic Crude Extracts from Thai Herbs Against Plasmodium Falciparum TM267

2017 ◽  
Vol 35 (2) ◽  
pp. 109
Author(s):  
Natharinee Horata ◽  
Sarawut Suttirat ◽  
Taweebhorn Panpanich ◽  
Anuthida Siriphor ◽  
Budsaraporn Navaprayoonvach ◽  
...  
Keyword(s):  
Plasmodium Falciparum ◽  
Molecular Docking ◽  
Antimalarial Activity ◽  
Vero Cells ◽  
Ocimum Sanctum ◽  
Root Extract ◽  
Active Compounds ◽  
Crude Extracts ◽  
Plumbago Indica

Objective: To determine the antimalarial activity of ethanol crude extracts from 20 Thai herbs against Plasmodiumfalciparum (P. falciparum) chloroquine-resistant strain TM267. Molecular docking of the active compounds from the selected Thaiherbs were analyzed with Plasmodium falciparum dihydrofolate reductase (PfDHFR).Material and Method: An in vitro study of antimalarial activity against P. falciparum TM267 was done using a parasitelactate dehydrogenese assay, and the cytotoxic effects of extracts were tested against Vero cells using a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. The 50% inhibitory concentration (IC50) and 50%cytotoxicity concentration were calculated from the dose-response curves. Molecular docking and post-dockingwere analyzed with the x-ray crystal structure of PfDHFR-thymidylate synthase complexed with pyrimethamine,nicotinamide adenine dinucleotide phosphate and deoxyuridylate.Results: Of these, the Plumbago indica L. root extract showed high antimalarial activity, with an IC50 value of 3.7μg/ml and less cytotoxicity when tested against Vero cells, followed by the Citrus hystrix DC. fruit extract, Vitex trifoliaLinn. root extract, Ocimum sanctum L. leave extract, of Allium sativum L. bulb extract and Salacia chinensis L. stem extract,respectively. All 7 active compounds reported from these herbal extracts had high docking scores against PfDHFR.The Citrusoside C from Citrus hystrix DC. had the highest docking score.Conclusion: It could be purposed that there were active compounds in Plumbago indica L., Vitex trifolia Linn. and Citrus hystrix DC. which are potential inhibitors against malaria that could bind to the active site of PfDHFR. However, the active Citrusosides from Citrus hystrix DC. should be further investigated for their effectiveness against malaria. 

Ultrastructural observations on the in vitro cytoadherence of Plasmodium falciparum infected red blood cells

1990 ◽  
Vol 48 (3) ◽  
pp. 914-915
Author(s):  
D.J.P. Ferguson ◽  
A.R. Berendt ◽  
J. Tansey ◽  
K. Marsh ◽  
C.I. Newbold
Keyword(s):  
Plasmodium Falciparum ◽  
Red Blood Cells ◽  
Blood Cells ◽  
Umbilical Vein ◽  
Cell Types ◽  
Amelanotic Melanoma ◽  
Cytoplasmic Process ◽  
Umbilical Vein Endothelial Cells

In human malaria, the most serious clinical manifestation is cerebral malaria (CM) due to infection with Plasmodium falciparum. The pathology of CM is thought to relate to the fact that red blood cells containing mature forms of the parasite (PRBC) cytoadhere or sequester to post capillary venules of various tissues including the brain. This in vivo phenomenon has been studied in vitro by examining the cytoadherence of PRBCs to various cell types and purified proteins. To date, three Ijiost receptor molecules have been identified; CD36, ICAM-1 and thrombospondin. The specific changes in the PRBC membrane which mediate cytoadherence are less well understood, but they include the sub-membranous deposition of electron-dense material resulting in surface deformations called knobs. Knobs were thought to be essential for cytoadherence, lput recent work has shown that certain knob-negative (K-) lines can cytoadhere. In the present study, we have used electron microscopy to re-examine the interactions between K+ PRBCs and both C32 amelanotic melanoma cells and human umbilical vein endothelial cells (HUVEC).We confirm previous data demonstrating that C32 cells possess numerous microvilli which adhere to the PRBC, mainly via the knobs (Fig. 1). In contrast, the HUVEC were relatively smooth and the PRBCs appeared partially flattened onto the cell surface (Fig. 2). Furthermore, many of the PRBCs exhibited an invagination of the limiting membrane in the attachment zone, often containing a cytoplasmic process from the endothelial cell (Fig. 2).

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