4.7 Article

Puerarin Attenuates Cadmium-Induced Neuronal Injury via Stimulating Cadmium Excretion, Inhibiting Oxidative Stress and Apoptosis

Journal

BIOMOLECULES
Volume 11, Issue 7, Pages -

Publisher

MDPI
DOI: 10.3390/biom11070978

Keywords

puerarin; cadmium; cadmium excretion; oxidative stress; apoptosis

Funding

  1. National Natural Science Foundation of China [31772808, 31872533, 31802260, 31702305]
  2. National Key Research and Development Program of China [2016YFD0501208]
  3. National Science Grant of Jiangsu Province [BK20180917]
  4. National Science Research Projects in Colleges and Universities of Jiangsu Province [18KJB230009]
  5. Excellent Young Teachers Program of Yangzhou University
  6. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)

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This study evaluated the neuroprotective potential of Puerarin against cadmium-induced neuronal injury for the first time, showing that Puerarin ameliorated neuronal injury and oxidative stress induced by cadmium. Additionally, Puerarin stimulated cadmium excretion, thereby reducing apoptosis in cerebral cortical neurons.
Cadmium (Cd) is a potential pathogenic factor in the nervous system associated with various neurodegenerative disorders. Puerarin (Pur) is an isoflavone purified from the Chinese medical herb, kudzu root, and exhibits antioxidant and antiapoptotic properties in the brain. In this study, the detailed mechanisms underlying the neuroprotective potential of Pur against Cd-induced neuronal injury was evaluated for the first time in vivo in a rat model and in vitro using primary rat cerebral cortical neurons. The results of the in vivo experiments showed that Pur ameliorated Cd-induced neuronal injury, reduced Cd levels in the cerebral cortices, and stimulated Cd excretion in Cd-treated rats. We also observed that the administration of Pur rescued Cd-induced oxidative stress, and attenuated Cd-induced apoptosis by concomitantly suppressing both the Fas/FasL and mitochondrial pathways in the cerebral cortical neurons of rats both in vivo and in vitro. Our results demonstrate that Pur exerted its neuroprotective effects by stimulating Cd excretion, ameliorating Cd-induced oxidative stress and apoptosis in rat cerebral cortical neurons.

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