TY - JOUR
T1 - Influence of combination of docosahexaenoic acid supplement and a polyherbal formulation (Liv. 52) on carbon tetrachlorideinduced hepatic injury
T2 - A preclinical study
AU - Satyam, Shakta Mani
AU - Bairy, Laxminarayana Kurady
AU - Ern, Ong Tze
AU - Yen, Yong Gin
AU - Kanasin, Aishuryia
AU - Muthaiah, Thivyashini
AU - Ratnam, Umashangari Sangga
AU - Yadav, Kameshwor
N1 - Publisher Copyright:
© 2020 Journal of Datta Meghe Institute of Medical Sciences University | Published by Wolters Kluwer - Medknow.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020/1/1
Y1 - 2020/1/1
N2 - Background: Docosahexaenoic acid (DHA) has diverse functions in normal metabolism and health and are widely used as a nutritional supplement. Liv. 52 is a polyherbal formulation used in hepatic dysfunction. The present study was undertaken to investigate the influence of oral supplementation of Liv. 52 and DHA alone and their combination against carbon tetrachloride (CCl4) induced hepatic injury in Wistar rats. Materials and Methods: Hepatotoxicity was induced by administering 1:1 mixture of CCl4 and olive oil; 1 ml/kg/72 h i.p. A total of 54 adult female Wistar (150-200 g) rats were divided into nine groups of six rats each as followsGroup 1Normal healthy control (1 ml/kg/day of 2% gum acacia), Group 2: Negative control (CCl4 + 1 ml/kg/day of 2% gum acacia), Group 3: Positive control (CCl4 + Silymarin 50 mg/kg/day), Group 49: CCl4 + Liv. 52-225 mg/kg/day, 450 mg/kg/day, DHA300 mg/kg/day, 600 mg/kg/day alone and their combination. The treatment duration was 7 days. Hepatoprotective potential was studied by the estimation of serum alanine transaminase (ALT), aspartate transaminase (AST), and alkaline phosphatase (ALP) in experimental rats. Results: Serum ALT, AST, and ALP were significantly increased (P 0.05) in hepatotoxic control rats compared to normal healthy control rats. There was statistically significant change (P 0.05) in serum levels of ALT, AST, and ALP among Silymarin, Liv. 52 and DHA treated rats in comparison to hepatotoxic control rats. Conclusions: The present study revealed that Liv. 52 and DHA alone and in combination ameliorates the hepatic injury induced by CCl4 in Wistar rats..
AB - Background: Docosahexaenoic acid (DHA) has diverse functions in normal metabolism and health and are widely used as a nutritional supplement. Liv. 52 is a polyherbal formulation used in hepatic dysfunction. The present study was undertaken to investigate the influence of oral supplementation of Liv. 52 and DHA alone and their combination against carbon tetrachloride (CCl4) induced hepatic injury in Wistar rats. Materials and Methods: Hepatotoxicity was induced by administering 1:1 mixture of CCl4 and olive oil; 1 ml/kg/72 h i.p. A total of 54 adult female Wistar (150-200 g) rats were divided into nine groups of six rats each as followsGroup 1Normal healthy control (1 ml/kg/day of 2% gum acacia), Group 2: Negative control (CCl4 + 1 ml/kg/day of 2% gum acacia), Group 3: Positive control (CCl4 + Silymarin 50 mg/kg/day), Group 49: CCl4 + Liv. 52-225 mg/kg/day, 450 mg/kg/day, DHA300 mg/kg/day, 600 mg/kg/day alone and their combination. The treatment duration was 7 days. Hepatoprotective potential was studied by the estimation of serum alanine transaminase (ALT), aspartate transaminase (AST), and alkaline phosphatase (ALP) in experimental rats. Results: Serum ALT, AST, and ALP were significantly increased (P 0.05) in hepatotoxic control rats compared to normal healthy control rats. There was statistically significant change (P 0.05) in serum levels of ALT, AST, and ALP among Silymarin, Liv. 52 and DHA treated rats in comparison to hepatotoxic control rats. Conclusions: The present study revealed that Liv. 52 and DHA alone and in combination ameliorates the hepatic injury induced by CCl4 in Wistar rats..
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U2 - 10.4103/jdmimsu.jdmimsu_219_19
DO - 10.4103/jdmimsu.jdmimsu_219_19
M3 - Article
AN - SCOPUS:85094571922
SN - 0974-3901
VL - 15
SP - 114
EP - 117
JO - Journal of Datta Meghe Institute of Medical Sciences University
JF - Journal of Datta Meghe Institute of Medical Sciences University
IS - 1
ER -