Lower susceptibility of female mice to acetaminophen hepatotoxicity: Role of mitochondrial glutathione, oxidant stress and c-jun N-terminal kinase

K Du, CD Williams, MR McGill, H Jaeschke - Toxicology and applied …, 2014 - Elsevier
K Du, CD Williams, MR McGill, H Jaeschke
Toxicology and applied pharmacology, 2014Elsevier
Acetaminophen (APAP) overdose causes severe hepatotoxicity in animals and humans.
However, the mechanisms underlying the gender differences in susceptibility to APAP
overdose in mice have not been clarified. In our study, APAP (300 mg/kg) caused severe
liver injury in male mice but 69–77% lower injury in females. No gender difference in
metabolic activation of APAP was found. Hepatic glutathione (GSH) was rapidly depleted in
both genders, while GSH recovery in female mice was 2.6 fold higher in the mitochondria at …
Abstract
Acetaminophen (APAP) overdose causes severe hepatotoxicity in animals and humans. However, the mechanisms underlying the gender differences in susceptibility to APAP overdose in mice have not been clarified. In our study, APAP (300 mg/kg) caused severe liver injury in male mice but 69–77% lower injury in females. No gender difference in metabolic activation of APAP was found. Hepatic glutathione (GSH) was rapidly depleted in both genders, while GSH recovery in female mice was 2.6 fold higher in the mitochondria at 4 h, and 2.5 and 3.3 fold higher in the total liver at 4 h and 6 h, respectively. This faster recovery of GSH, which correlated with greater induction of glutamate-cysteine ligase, attenuated mitochondrial oxidative stress in female mice, as suggested by a lower GSSG/GSH ratio at 6 h (3.8% in males vs. 1.4% in females) and minimal centrilobular nitrotyrosine staining. While c-jun N-terminal kinase (JNK) activation was similar at 2 and 4 h post-APAP, it was 3.1 fold lower at 6 h in female mice. However, female mice were still protected by the JNK inhibitor SP600125. 17β-Estradiol pretreatment moderately decreased liver injury and oxidative stress in male mice without affecting GSH recovery. Conclusion: The lower susceptibility of female mice is achieved by the improved detoxification of reactive oxygen due to accelerated recovery of mitochondrial GSH levels, which attenuates late JNK activation and liver injury. However, even the reduced injury in female mice was still dependent on JNK. While 17β-estradiol partially protects male mice, it does not affect hepatic GSH recovery.
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