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The long term goal of our research is to investigate the biochemical mechanisms of redox imbalance stress and its role in adult-onset metabolic syndrome. In particular, we are studying how mitochondrial redox sensitive proteins respond to redox imbalance stress and explore such responses as potential therapeutic targets for fighting aging-related metabolic diseases. Our current projects are focused on two NADH/NAD-dependent mitochondrial proteins: dihydrolipoamide dehydrogenase (DLDH) and complex I (NADH-ubiquinone oxidoreductase), both of which can be simultaneously analyzed by blue native gel electrophoresis and also show adaptive responses to NADH/NAD redox imbalance stress under pathophysiological conditions.
The DLDH project studies its adaptive response as a viable druggable target for induction of stroke- or hypoxia tolerance and the mechanisms of this protein’s oxidative modifications in redox signaling and neuroprotection.
The complex I project on studies the mechanisms of complex I adaptive hyperactivity observed in diabetic pancreas and other tissues with the goal of exploring strategies that down-regulating complex I hyperactivity by restoring NADH/NAD redox balance may serve as a therapeutic approach for treating diabetes mellitus.
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论文共 134 篇作者统计合作学者相似作者
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Antioxidants & redox signalingno. 10-12 (2023): 794-806
Haoxin Liu,Liang-Jun Yan
Endocrinesno. 19 (2023): 236-249
Zhao Liu,Mengjie Liu,Gongwei Jia,Jiani Li,Lingchuan Niu, Huiji Zhang,Yunwen Qi,Houchao Sun,Liang-Jun Yan,Jingxi Ma
Frontiers in Endocrinology (2023): 1345489-1345489
Nutrientsno. 7 (2023): 1732-1732
Biomoleculesno. 1078 (2022): 1078
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