Carbamazepine increased pregnenolone synthesis blocked by peripheral type benzodiazepine receptor antagonist

Depression Pub Date : 1995-01-01 DOI:10.1002/depr.3050030602
Bai-Shen Pan M.D., Husseini K. Manji M.D., FRCPC, Mark E. Schmidt M.D., William Z. Potter M.D., Ph.D.
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引用次数: 1

Abstract

Despite the widespread use of carbamazepine (CBZ) in the treatment of a number of neuropsychiatric disorders, its mechanism(s) of action remain to be elucidated. In view of the postulated interaction of CBZ with peripheral type benzodiazepine (BDZ) receptors and the role of these receptors in regulating neuroactive steroid biosynthesis, we investigated the effects of CBZ on pregnenolone accumulation in cultured rat C6 glioma cells. We found that CBZ elevates pregnenolone accumulation over a period of 60 min, and that this effect was not due to inhibition of pregnenolone metabolism. Preincubation of C6 cells with the selective peripheral type benzodiazepine receptor antagonist PK11195 blocked the CBZ-induced elevation in pregnenolone-induced elevation in pregnenolone accumulation. The results suggest that CBZ stimulated pregnenolone biosynthesis in cultured C6 cells involves a direct or indirect interaction with peripheral type benzodiazepine receptors. These effects may provide additional insights into the mechanisms by which CBZ regulates neuronal excitability. Depression 3:267-y (1995/1996). © 1996 Wiley-Liss, Inc

卡马西平增加外周型苯二氮卓受体拮抗剂阻断的孕烯醇酮合成
尽管卡马西平(CBZ)广泛用于治疗许多神经精神疾病,但其作用机制仍有待阐明。考虑到CBZ与外周型苯二氮卓(BDZ)受体的相互作用以及这些受体在调节神经活性类固醇生物合成中的作用,我们研究了CBZ对培养大鼠C6胶质瘤细胞孕烯醇酮积累的影响。我们发现CBZ在60分钟内增加孕烯醇酮的积累,并且这种影响不是由于抑制孕烯醇酮的代谢。用选择性外周型苯二氮卓受体拮抗剂PK11195对C6细胞进行预孵育,可阻断cbz诱导的孕烯醇酮诱导的孕烯醇酮积累升高。结果表明,CBZ刺激C6细胞孕烯醇酮生物合成与外周型苯二氮卓受体直接或间接相互作用。这些影响可能为CBZ调节神经元兴奋性的机制提供额外的见解。萧条:267-y(1995/1996)。©1996 Wiley-Liss, Inc
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