The course of CCl4 induced hepatotoxicity is altered in mGSTA4-4 null (-/-) mice

Seema Dwivedi, Rajendra Sharma, Abha Sharma, Piotr Zimniak, Jeffrey D. Ceci, Yogesh C. Awasthi, Paul J. Boor

Research output: Contribution to journalArticle

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Abstract

Glutathione S-transferases (GSTs) play a key role in cellular detoxification of environmental toxicants through their conjugation to glutathione (GSH). Recent studies have shown that the α-class GSTs also provide protection against oxidative stress and lipid peroxidation (LPO). GSTA4-4 is a member of a sub group of the α-class GSTs. It has been shown to metabolize 4-hydroxynonenal (4-HNE) with high catalytic efficiency through its conjugation to glutathione (GSH) and has been suggested to be a major component of cellular defense against toxic electrophiles such as 4-HNE generated during LPO. Since the hepatotoxicity of carbon tetrachloride (CCl 4) has been suggested to be due to the generation of free radicals leading to membrane LPO, the present studies were designed to compare hepatotoxicity of CCl4 in GSTA4-4 null (-/-) and wild type (+/+) mice. The results show that administration of a single dose of CCl4 (1 ml/kg i.p.) resulted in time dependent hepatotoxicity in both -/- and +/+ mice; the extent of cellular damage by serum enzymes suggests that progression was more rapid in -/- mice, although injury was similar by 24 h. Histopathologic examination showed similar degrees of centrilobular necrosis by 24 h but much greater surrounding degenerative change, including cellular swelling, disarray, and vacuolization, in the liver of -/- mice. As expected -/- mice did not show any expression of mGSTA4-4; after CCl4 a compensatory increase in the activities of total GST activity was noted at 24 h. Major alterations in other antioxidant enzymes was not observed. 4-HNE levels in the liver of -/- mice were about four-fold higher than in +/+ mice, suggesting a positive correlation between 4-HNE levels and the altered course of CCl4 hepatotoxicity. These studies suggest that GSTA4-4 is an important component during the early stages (1-6 h) of cellular defense against oxidative stress and LPO although, it is not effective in protecting against the ultimate degree of overall cell injury.

Original languageEnglish (US)
Pages (from-to)58-66
Number of pages9
JournalToxicology
Volume218
Issue number1
DOIs
StatePublished - Jan 20 2006

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Glutathione Transferase
Oxidative stress
Lipid Peroxidation
Lipids
Liver
Glutathione
Detoxification
Carbon Tetrachloride
Poisons
Enzymes
Membrane Lipids
Oxidative Stress
Free Radicals
Swelling
Antioxidants
Wounds and Injuries
mGSTA4-4
4-hydroxy-2-nonenal
Necrosis
Serum

Keywords

  • Carbon tetrachloride
  • Glutathione-S- transferase
  • Hepatotoxicity
  • Lipid peroxidation

ASJC Scopus subject areas

  • Toxicology

Cite this

Dwivedi, S., Sharma, R., Sharma, A., Zimniak, P., Ceci, J. D., Awasthi, Y. C., & Boor, P. J. (2006). The course of CCl4 induced hepatotoxicity is altered in mGSTA4-4 null (-/-) mice. Toxicology, 218(1), 58-66. https://doi.org/10.1016/j.tox.2005.10.012

The course of CCl4 induced hepatotoxicity is altered in mGSTA4-4 null (-/-) mice. / Dwivedi, Seema; Sharma, Rajendra; Sharma, Abha; Zimniak, Piotr; Ceci, Jeffrey D.; Awasthi, Yogesh C.; Boor, Paul J.

In: Toxicology, Vol. 218, No. 1, 20.01.2006, p. 58-66.

Research output: Contribution to journalArticle

Dwivedi, S, Sharma, R, Sharma, A, Zimniak, P, Ceci, JD, Awasthi, YC & Boor, PJ 2006, 'The course of CCl4 induced hepatotoxicity is altered in mGSTA4-4 null (-/-) mice', Toxicology, vol. 218, no. 1, pp. 58-66. https://doi.org/10.1016/j.tox.2005.10.012
Dwivedi S, Sharma R, Sharma A, Zimniak P, Ceci JD, Awasthi YC et al. The course of CCl4 induced hepatotoxicity is altered in mGSTA4-4 null (-/-) mice. Toxicology. 2006 Jan 20;218(1):58-66. https://doi.org/10.1016/j.tox.2005.10.012
Dwivedi, Seema ; Sharma, Rajendra ; Sharma, Abha ; Zimniak, Piotr ; Ceci, Jeffrey D. ; Awasthi, Yogesh C. ; Boor, Paul J. / The course of CCl4 induced hepatotoxicity is altered in mGSTA4-4 null (-/-) mice. In: Toxicology. 2006 ; Vol. 218, No. 1. pp. 58-66.
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