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Isocitrate Dehydrogenase Alpha-1 Modulates Lifespan and Oxidative Stress Tolerance in Caenorhabditis elegans .

Zhi-Han LinShun-Ya ChangWen-Chi ShenYen-Hung LinChiu-Lun ShenSin-Bo LiaoYu-Chun LiuChang-Shi ChenTsui-Ting ChingHorng-Dar Wang
Published in: International journal of molecular sciences (2022)
Altered metabolism is a hallmark of aging. The tricarboxylic acid cycle (TCA cycle) is an essential metabolic pathway and plays an important role in lifespan regulation. Supplementation of α-ketoglutarate, a metabolite converted by isocitrate dehydrogenase alpha-1 ( idha-1 ) in the TCA cycle, increases lifespan in C. elegans . However, whether idha-1 can regulate lifespan in C. elegans remains unknown. Here, we reported that the expression of idha-1 modulates lifespan and oxidative stress tolerance in C. elegans . Transgenic overexpression of idha-1 extends lifespan, increases the levels of NADPH/NADP + ratio, and elevates the tolerance to oxidative stress. Conversely, RNAi knockdown of idha-1 exhibits the opposite effects. In addition, the longevity of eat-2 (ad1116) mutant via dietary restriction (DR) was reduced by idha-1 knockdown, indicating that idha-1 may play a role in DR-mediated longevity. Furthermore, idha-1 mediated lifespan may depend on the target of rapamycin (TOR) signaling. Moreover, the phosphorylation levels of S6 kinase (p-S6K) inversely correlate with idha-1 expression, supporting that the idha-1 -mediated lifespan regulation may involve the TOR signaling pathway. Together, our data provide new insights into the understanding of idha-1 new function in lifespan regulation probably via DR and TOR signaling and in oxidative stress tolerance in C. elegans .
Keyphrases
  • oxidative stress
  • dna damage
  • signaling pathway
  • poor prognosis
  • induced apoptosis
  • ischemia reperfusion injury
  • diabetic rats
  • endoplasmic reticulum stress
  • wild type
  • artificial intelligence