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Dendrobium nobile Lindl. alkaloids alleviate Mn-induced neurotoxicity via PINK1/Parkin-mediated mitophagy in PC12 cells.
Fu, Xiaolong; Chen, Shu; Wang, Xueting; Shen, Yanhua; Zeng, Ru; Wu, Qin; Lu, Yuanfu; Shi, Jingshan; Zhou, Shaoyu.
Afiliación
  • Fu X; Key Laboratory of Basic Pharmacology of Ministry of Education, Zunyi Medical University, Zunyi, Guizhou, China.
  • Chen S; Joint International Research Laboratory of Ethnomedicine, Zunyi Medical University, Zunyi, Guizhou, China.
  • Wang X; Key Laboratory of Basic Pharmacology of Guizhou Province, Zunyi Medical University, Zunyi, Guizhou, China.
  • Shen Y; Cell and Tissue Bank of Guizhou Province, Zunyi, Guizhou, China.
  • Zeng R; Key Laboratory of Basic Pharmacology of Ministry of Education, Zunyi Medical University, Zunyi, Guizhou, China.
  • Wu Q; Joint International Research Laboratory of Ethnomedicine, Zunyi Medical University, Zunyi, Guizhou, China.
  • Lu Y; Key Laboratory of Basic Pharmacology of Guizhou Province, Zunyi Medical University, Zunyi, Guizhou, China.
  • Shi J; Key Laboratory of Basic Pharmacology of Ministry of Education, Zunyi Medical University, Zunyi, Guizhou, China.
  • Zhou S; Joint International Research Laboratory of Ethnomedicine, Zunyi Medical University, Zunyi, Guizhou, China.
Biochem Biophys Rep ; 26: 100877, 2021 Jul.
Article en En | MEDLINE | ID: mdl-33889759
ABSTRACT
Modern pharmacological studies have demonstrated that Dendrobium nobile Lindl. Alkaloids (DNLA), the main active ingredients of Dendrobium nobile, is valuable as an anti-aging and neuroprotective herbal medicine. The present study was designed to determine whether DNLA confers protective function over neurotoxicant manganese (Mn)-induced cytotoxicity and the mechanism involved. Our results showed that pretreatment of PC12 cells with DNLA alleviated cell toxicity induced by Mn and improved mitochondrial respiratory capacity and oxidative status. Mn treatment increased apoptotic cell death along with a marked increase in the protein expression of Bax and a decrease in the expression of Bcl-2 protein, all of which were noticeably reversed by DNLA. Furthermore, DNLA significantly abolished the decrease in protein levels of both PINK1 and Parkin, and mitigated the increased expression of autophagy marker LC3-II and accumulation of p62 caused by Mn. These results demonstrate that DNLA inhibits Mn induced cytotoxicity, which may be mediated through modulating PINK1/Parkin-mediated autophagic flux and improving mitochondrial function.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Biochem Biophys Rep Año: 2021 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Biochem Biophys Rep Año: 2021 Tipo del documento: Article País de afiliación: China