2016
DOI: 10.22159/ajpcr.2016.v9i6.14271
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In-Vitro Antioxidant and in-Vivo Hepato Protective Activity of Ethanol Extracts From the Bark of Shorea Robusta (Dipterocarpaceae) Against Carbon Tetra Chloride Induced Liver Toxicity in Rats

Abstract: Objective: The study is designed for the evaluation of in vivo hepatoprotective and in vitro antioxidant activity of ethanol extracts from the bark of Shorea robusta (EESR) (Dipterocarpaceae) by carbon tetra chloride (CCl 4 ) induced hepatotoxicity in rats.Methods: EESR was evaluated for hepatoprotective activity in rats by inducing liver damage by CCl 4 . The antioxidant activity of EESR was assayed by various in vitro antioxidant methods and activities were compared to standard ascorbic acid. Results:Ethanol… Show more

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Cited by 3 publications
(2 citation statements)
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“…This elevation was attributed to the leakage of enzymes from cells into the circulatory system due to altered permeability and loss of functional integrity of liver membrane as a result of severe hepatic injury [42,43]. The results obtained in this work are similar to findings of Biswas et al [44]. CCl 4 undergoes reductive metabolism by the hepatic cytochrome P450 into a highly reactive + CCl 3 , which is converted into peroxyl radical ( + OOCCl 3 ) in the presence of oxygen [45].…”
Section: Discussionsupporting
confidence: 86%
“…This elevation was attributed to the leakage of enzymes from cells into the circulatory system due to altered permeability and loss of functional integrity of liver membrane as a result of severe hepatic injury [42,43]. The results obtained in this work are similar to findings of Biswas et al [44]. CCl 4 undergoes reductive metabolism by the hepatic cytochrome P450 into a highly reactive + CCl 3 , which is converted into peroxyl radical ( + OOCCl 3 ) in the presence of oxygen [45].…”
Section: Discussionsupporting
confidence: 86%
“…Briefly, 3 mL of extract with different concentration (50 mg/mL, 100 mg/mL, 150 mg/mL, 250 mg/mL, and 500 mg/mL) was mixed with 1 mL of DPPH (0.1 mM) solution in ethanol. The mixture was shaken vigorously and left to stand for 30 min in the dark at room temperature, and the absorbance was then measured with a quartz glass cuvette (Hellma; Mullheim, Germany) at 517 nm against a blank using an ultraviolet (UV)-visible spectrophotometer (Pharma Spec UV-1700; Shimadzu; Kyoto, Japan) [25]. A low absorbance of the reaction mixture indicated a high free radical scavenging activity.…”
Section: Dpph Radical Scavenging Activitymentioning
confidence: 99%