2012
DOI: 10.1016/j.fct.2012.01.031
|View full text |Cite
|
Sign up to set email alerts
|

Evaluation of hepatotoxicity and oxidative stress in rats treated with tert-butyl hydroperoxide

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

4
20
0

Year Published

2012
2012
2024
2024

Publication Types

Select...
8
1

Relationship

0
9

Authors

Journals

citations
Cited by 26 publications
(25 citation statements)
references
References 38 publications
4
20
0
Order By: Relevance
“…Results from this study confirmed t -BHP-induced hepatotoxic effects as shown by the significant increase in the activity of ALT, AST and LDH in the serum of t -BHP-treated rats. These observations are in accordance with those obtained by previous studies [66, 8789]. Alanine amino transferase, AST, and LDH are cytoplasmic, and the rise in their serum levels is attributed to damaged structural integrity of the liver and as a result these enzymes are released into the blood circulation after the rupture of the plasma membranes [66, 90].…”
Section: Discussionsupporting
confidence: 92%
See 1 more Smart Citation
“…Results from this study confirmed t -BHP-induced hepatotoxic effects as shown by the significant increase in the activity of ALT, AST and LDH in the serum of t -BHP-treated rats. These observations are in accordance with those obtained by previous studies [66, 8789]. Alanine amino transferase, AST, and LDH are cytoplasmic, and the rise in their serum levels is attributed to damaged structural integrity of the liver and as a result these enzymes are released into the blood circulation after the rupture of the plasma membranes [66, 90].…”
Section: Discussionsupporting
confidence: 92%
“…Present in the cells in both the reduced (GSH) and oxidized (GSSG) forms, but because of the action of the NADPH-dependent enzyme GR, the cellular content of glutathione is predominantly in favour of GSH under normal physiologic conditions [108]. In agreement with previous reports [6, 7, 88, 89], the current study revealed that t -BHP treatment resulted in a reduction in GSH levels both in the erythrocytes and liver, while GSSG level was only increased in the liver. The oxidation of GSH to GSSG is a sensitive marker of oxidative stress and under condition of increased stress, the GSH : GSSG ratio decreases either due to increased GSSG or decreased GSH levels [109].…”
Section: Discussionsupporting
confidence: 89%
“…Results from this study confirmed t-BHP-induced hepatotoxic effects as shown by the significant increase in the activity of ALT, AST and LDH in the serum of t-BHPtreated rats. These observations are in accordance with those obtained by previous studies [66,[87][88][89]. Alanine amino transferase, AST, and LDH are cytoplasmic, and the rise in their serum levels is attributed to damaged structural Evidence-Based Complementary and Alternative Medicine 13 integrity of the liver and as a result these enzymes are released into the blood circulation after the rupture of the plasma membranes [66,90].…”
Section: Discussionsupporting
confidence: 81%
“…In hepatocytes, t-BHP is metabolized by CYP450 into free radical intermediates such as t -butoxyl and t -methyl radicals [91], which induce lipid peroxidation and glutathione (GSH) depletion resulting in organelle damage and cell death [92]. Hence, t-BHP-induced hepatotoxicity model is widely used for evaluating merits of Nrf2-ARE signaling in hepatocytes.…”
Section: Role Of Nrf2 In Chemical-induced Liver Injurymentioning
confidence: 99%