ReferenceID 6488

Vitamin E rescues valproic acid-induced testicular injury in rats: Role of autophagy

Life Sci

Aims: Valproic acid (VPA), a commonly used antiepileptic drug, can induce testicular oxidative stress and injury. Altered autophagic response usually follows testicular injury. The study aims to evaluate the role of auto

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Reference Id
6488
Evidence Id
23078
Core Evidence Id
23078
Source Reference Id
6280
Herb2 Reference Id
HBREF007077
Subject Paper Key
HBIN048145_35227771
Pubmed Id
35227771
Doi
10.1016/j.lfs.2022.120434
Paper Title
Vitamin E rescues valproic acid-induced testicular injury in rats: Role of autophagy
Paper Abstract
Aims: Valproic acid (VPA), a commonly used antiepileptic drug, can induce testicular oxidative stress and injury. Altered autophagic response usually follows testicular injury. The study aims to evaluate the role of autophagy in the protective effect of the antioxidant vitamin E (Vit E) against VPA-induced testicular injury. Materials and methods: VPA (100, 300, and 500 mg/kg/day) was administered for 8 days. The protective group received both Vit E (50 mg/kg) and VPA (500 mg/kg). The testicular weight, sperm analysis, and serum testosterone concentration, as well as testicular histopathology, steroidogenic gene expression, and oxidative stress markers were evaluated. The mRNA or protein expression of autophagy-related proteins [adenosine monophosphate-activated protein kinase (AMPK), mammalian target of rapamycin (mTOR), microtubule-associated protein light chain 3 (LC3), Beclin1, and p62] were measured using RT-PCR or immunohistochemistry. Key findings: VPA resulted in lower testes weight and sperm quality with aberrant morphology. VPA dose-dependently induced testicular oxidative stress, which was associated with decreased steroidogenic gene expression and serum testosterone levels, as well as deteriorated histopathology. These biochemical and histological changes were also associated with autophagy induction (higher LC3 and Beclin1, and lower p62) that was lost with the highest toxic dose (500 mg/kg). The attenuated autophagy with the highest dose was accompanied by AMPK downregulation and mTOR upregulation. Vit E protected against VPA-mediated oxidative stress and toxicity while also restoring autophagic response and AMPK/mTOR levels. Significance: The study highlights vitamin E as a valuable protective asset against VPA-induced testicular injury, possibly through AMPK-mTOR-dependent autophagy induction.
Journal
Life Sci
Publish Year
2022
Experiment Subject
Experiment Type
Animal Experiment
Phenotype Related
Testicular Injury
Paper Title Cn
Paper Title En
Vitamin E rescues valproic acid-induced testicular injury in rats: Role of autophagy
Bilingual Status
semi_complete