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EFFECT OF BLUMEA LACERA ON TISSUE GSH, LIPID PEROX IDATION AND HEPATIC CELLS IN ETHANOL INDUCED HEPATOTOXICITY IN RATS

By: Contributor(s): Publication details: M P Innovare Academic Sciences Pvt Ltd 2019Edition: Vol.11(12)Description: 46-50pSubject(s): Online resources: In: International journal of pharmacy and pharmaceutical scienceSummary: Objective: To evaluate hepatoprotecti ve effects of ethanol extract of aerial part of Blumea lacera (BLEE) against ethanol - induced hepatotoxicity in rats. Method s: The in vivo antioxidant activity of BLEE was assessed by determining the tissue g lutathione (GSH) and lipid peroxidation (LPO) lev els. The BLEE at the doses of 200 and 400 mg/kg and silymarin 100 mg /kg administered to the ethanol challenged rats. The effect s of BLEE and silymarin on Physical and Biochemical Parameters were measured. Similarly , histopathological changes of the liver w ere studied. Result s : The BLEE showed in vivo antioxidant activity. A significant (P<0.001) decrease in SGOT, SGPT, ALP, total and direct bilirubin was observed in BLEE treated group at doses i.e. 200 mg/kg and 400 mg/kg as compared to intoxicated group. Liver damage in animal pretreated with BLEE was minimal with distinct preservation of structures and the architectural frame of the hepatic cells.
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Objective:
To evaluate hepatoprotecti
ve effects of ethanol extract of aerial part of
Blumea lacera
(BLEE) against ethanol
-
induced hepatotoxicity in rats.
Method
s:
The
in vivo
antioxidant activity of BLEE was assessed by determining the tissue g
lutathione (GSH) and lipid peroxidation
(LPO) lev
els. The
BLEE at the doses of 200 and 400
mg/kg and silymarin 100 mg
/kg
administered to the ethanol challenged rats. The effect
s of BLEE and silymarin on
Physical and Biochemical Parameters were measured. Similarly
, histopathological changes of
the liver w
ere studied.
Result
s
:
The BLEE
showed
in vivo
antioxidant activity.
A significant (P<0.001) decrease
in SGOT, SGPT, ALP, total and direct bilirubin
was observed
in BLEE
treated group at doses i.e.
200 mg/kg and 400 mg/kg as compared to intoxicated group.
Liver
damage in animal pretreated with BLEE was
minimal with distinct preservation of structures and the
architectural frame of the hepatic cells.

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