Mitophagy impairment and oxidative stress are cardinal pathological hallmarks in Parkinson's disease (PD), a common age-related neurodegenerative condition. The specific interactions between mitophagy and reactive oxygen species (ROS) have attracted considerable attention even though their exact interplay in PD has not been fully elucidated. We highlight the interactions between ROS and mitophagy, with a focus on the signalling pathways downstream to ROS that triggers mitophagy and draw attention to potential therapeutic compounds that target these pathways in both experimental and clinical models. Identifying a combination of ROS inhibitors and mitophagy activators to provide a physiologic balance in this complex signalling pathways may lead to a more optimal outcome. Deciphering the exact temporal relationship between mitophagy and oxidative stress and their triggers early in the course of neurodegeneration can unravel mechanistic clues that potentially lead to the development of compounds for clinical drug trials focusing on prodromic PD or at-risk individuals.
机构:
Inst for Basic Sci Korea, Ctr Nanoparticle Res, Seoul 08826, South Korea
Seoul Natl Univ, Sch Chem & Biol Engn, Seoul 08826, South Korea
Seoul Natl Univ, Inst Chem Proc, Seoul 08826, South KoreaInst for Basic Sci Korea, Ctr Nanoparticle Res, Seoul 08826, South Korea
Kwon, Hyek Jin
Kim, Dokyoon
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Inst for Basic Sci Korea, Ctr Nanoparticle Res, Seoul 08826, South KoreaInst for Basic Sci Korea, Ctr Nanoparticle Res, Seoul 08826, South Korea
Kim, Dokyoon
Seo, Kyungho
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Inst for Basic Sci Korea, Ctr Nanoparticle Res, Seoul 08826, South KoreaInst for Basic Sci Korea, Ctr Nanoparticle Res, Seoul 08826, South Korea
Seo, Kyungho
Kim, Young Geon
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Inst for Basic Sci Korea, Ctr Nanoparticle Res, Seoul 08826, South Korea
Seoul Natl Univ, Sch Chem & Biol Engn, Seoul 08826, South Korea
Seoul Natl Univ, Inst Chem Proc, Seoul 08826, South KoreaInst for Basic Sci Korea, Ctr Nanoparticle Res, Seoul 08826, South Korea
Kim, Young Geon
Han, Sang Ihn
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Inst for Basic Sci Korea, Ctr Nanoparticle Res, Seoul 08826, South Korea
Seoul Natl Univ, Sch Chem & Biol Engn, Seoul 08826, South Korea
Seoul Natl Univ, Inst Chem Proc, Seoul 08826, South KoreaInst for Basic Sci Korea, Ctr Nanoparticle Res, Seoul 08826, South Korea
Han, Sang Ihn
Kang, Taegyu
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Inst for Basic Sci Korea, Ctr Nanoparticle Res, Seoul 08826, South Korea
Seoul Natl Univ, Sch Chem & Biol Engn, Seoul 08826, South Korea
Seoul Natl Univ, Inst Chem Proc, Seoul 08826, South KoreaInst for Basic Sci Korea, Ctr Nanoparticle Res, Seoul 08826, South Korea
Kang, Taegyu
Soh, Min
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Inst for Basic Sci Korea, Ctr Nanoparticle Res, Seoul 08826, South Korea
Seoul Natl Univ, Sch Chem & Biol Engn, Seoul 08826, South Korea
Seoul Natl Univ, Inst Chem Proc, Seoul 08826, South KoreaInst for Basic Sci Korea, Ctr Nanoparticle Res, Seoul 08826, South Korea
Soh, Min
Hyeon, Taeghwan
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Inst for Basic Sci Korea, Ctr Nanoparticle Res, Seoul 08826, South Korea
Seoul Natl Univ, Sch Chem & Biol Engn, Seoul 08826, South Korea
Seoul Natl Univ, Inst Chem Proc, Seoul 08826, South KoreaInst for Basic Sci Korea, Ctr Nanoparticle Res, Seoul 08826, South Korea
机构:
Konkuk Univ, Dept Biotechnol, Res Inst Inflammatory Dis, Chungju 380701, South KoreaKonkuk Univ, Dept Biotechnol, Res Inst Inflammatory Dis, Chungju 380701, South Korea
Kumar, Hemant
Kim, In Su
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Konkuk Univ, Dept Biotechnol, Res Inst Inflammatory Dis, Chungju 380701, South KoreaKonkuk Univ, Dept Biotechnol, Res Inst Inflammatory Dis, Chungju 380701, South Korea
Kim, In Su
Choi, Dong-Kug
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Konkuk Univ, Dept Biotechnol, Res Inst Inflammatory Dis, Chungju 380701, South KoreaKonkuk Univ, Dept Biotechnol, Res Inst Inflammatory Dis, Chungju 380701, South Korea