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Alpha-lipoic acid protects against pressure overload-induced heart failure via ALDH2-dependent Nrf1-FUNDC1 signaling.


ABSTRACT: Alpha-lipoic acid (?-LA), a well-known antioxidant, was proved to active ALDH2 in nitrate tolerance and diabetic animal model. However, the therapeutic advantage of ?-LA for heart failure and related signaling pathway have not been explored. This study was designed to examine the role of ?-LA-ALDH2 in heart failure injury and mitochondrial damage. ALDH2 knockout (ALDH2-/-) mice and primary neonatal rat cardiomyocytes (NRCMs) were subjected to assessment of myocardial function and mitochondrial autophagy. Our data demonstrated ?-LA significantly reduced the degree of TAC-induced LV hypertrophy and dysfunction in wild-type mice, not in ALDH2-/- mice. In molecular level, ?-LA significantly restored ALDH2 activity and expression as well as increased the expression of a novel mitophagy receptor protein FUNDC1 in wild-type TAC mice. Besides, we confirmed that ALDH2 which was activated by ?-LA governed the activation of Nrf1-FUNDC1 cascade. Our data suggest that ?-LA played a positive role in protecting the heart against adverse effects of chronic pressure overload.

SUBMITTER: Li W 

PROVIDER: S-EPMC7393127 | biostudies-literature | 2020 Jul

REPOSITORIES: biostudies-literature

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Alpha-lipoic acid protects against pressure overload-induced heart failure via ALDH2-dependent Nrf1-FUNDC1 signaling.

Li Wenjia W   Yin Lei L   Sun Xiaolei X   Wu Jian J   Dong Zhen Z   Hu Kai K   Sun Aijun A   Ge Junbo J  

Cell death & disease 20200730 7


Alpha-lipoic acid (α-LA), a well-known antioxidant, was proved to active ALDH2 in nitrate tolerance and diabetic animal model. However, the therapeutic advantage of α-LA for heart failure and related signaling pathway have not been explored. This study was designed to examine the role of α-LA-ALDH2 in heart failure injury and mitochondrial damage. ALDH2 knockout (ALDH2<sup>-/-</sup>) mice and primary neonatal rat cardiomyocytes (NRCMs) were subjected to assessment of myocardial function and mito  ...[more]

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