4.5 Article

Mitochondrial mechanism of neuroprotection by CART

Journal

EUROPEAN JOURNAL OF NEUROSCIENCE
Volume 26, Issue 3, Pages 624-632

Publisher

WILEY
DOI: 10.1111/j.1460-9568.2007.05691.x

Keywords

CART; mitochondria; neurodegeneration; neuroprotection; succinate dehydrogenase

Categories

Funding

  1. NINDS NIH HHS [R01 NS044313, R01 NS33668, R01 NS033668, P01 NS049210] Funding Source: Medline
  2. NINR NIH HHS [R01 NR003521, R01 NR003521-15] Funding Source: Medline

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We previously demonstrated that the neuropeptide cocaine- and amphetamine-regulated transcript (CART) is protective against focal cerebral ischemia in vivo and against neuronal cell death in culture induced by oxygen-glucose deprivation (OGD). The mechanism of neuroprotection by CART is unknown, in part due to lack of knowledge regarding its putative receptor. Using a yeast two-hybrid system with CART's carboxy-terminal to screen a mouse brain cDNA library, we uncovered a potential direct interaction between CART and subunit B of the mitochondrial enzyme succinate dehydrogenase (SDHB). We confirmed CART/SDHB binding using in vitro pull-down assay, and tested the effects of CART peptide on SDH activity, Complex II (CII) activity and ATP production in primary cultured cortical neurons under basal conditions and after OGD. At concentrations between 0.2 and 4 nM, CART significantly increased SDH function, CII activity and ATP generation in purified mitochondria and intact neurons under baseline conditions. Furthermore, pretreatment with CART enhanced mitochondrial mechanisms of neuronal survival and prevented the decline in SDH and CII activities and ATP production after OGD. The findings suggest that CART's neuroprotective mechanism of action may be linked to preservation of mitochondrial function and prevention of energy failure after ischemia-reperfusion injury.

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