1α,25-dihydroxyvitamin D3 attenuates cyanide-induced neurotoxicity by inhibiting uncoupling protein-2 up-regulation

✍ Scribed by L. Li; K. Prabhakaran; X. Zhang; L. Zhang; H. Liu; J.L. Borowitz; G.E. Isom

• Publisher: John Wiley and Sons
• Year: 2008
• Tongue: English
• Weight: 496 KB
• Volume: 86
• Category: Article
• ISSN: 0360-4012
• DOI: 10.1002/jnr.21596

✦ Synopsis

1a,25-dihydroxyvitamin D 3 (VD 3 ) is a neuroprotectant that can reduce cytotoxicity produced by a variety of toxicants. The mechanism of the neuroprotection was studied in rat primary cortical cells in which Wy14,643, an agonist of peroxisome proliferator activated receptora (PPARa), enhances cyanide (KCN) neurotoxicity. In this cell model, Wy14,643 pretreatment enhanced cyanideinduced cell death, and the increased cell death was linked to up-regulation of uncoupling protein-2 (UCP-2). VD 3 reversed cyanide-induced mitochondrial dysfunction in cells pretreated with Wy14,643, as reflected by restoration of cellular ATP and mitochondrial membrane potential (DC m ). Analysis of cellular state 4 oxygen consumption showed increased mitochondrial uncoupling accompanied by up-regulation of UPC-2. The uncoupling was attenuated by prior treatment with VD 3 . The interaction of VD 3 with UCP-2 was attributed to increased expression of IjB, an inhibitor of NF-jB (transcription factor that regulates UCP-2 expression). The increased IjB levels lead to reduced nuclear translocation and DNA binding of nuclear factor-jB. The role of oxidative stress in the response was then evaluated. Cotreatment with Wy14,643 and cyanide markedly increased reactive oxygen species generation and decreased reduced glutathione levels. The oxidative stress was blocked by VD 3 pretreatment. It was concluded that VD 3 blocks Wy14,643 enhancement of cyanide neurotoxicity by suppressing the redox-mediated transcriptional up-regulation of UCP-2, resulting in reduced mitochondrial proton leak and stabilization of mitochondrial function. V