Dubrovsky B O, Liquornik M S, Noble P, Gijsbers K
Department of Psychiatry, McGill University, Montreal, Canada.
Brain Res Bull. 1987 Dec;19(6):635-8. doi: 10.1016/0361-9230(87)90049-9.
The effect of a Ring A-reduced metabolite of corticosterone, 5 alpha-dihydrocorticosterone (DHB) on long-term potentiation (LTP) in the dentate gyrus (DG) of the rat were studied in barbiturate-anaesthetised animals. It was observed that DHB significantly impairs the development of LTP, more particularly the population spike (PS) component of the evoked potential (EP) to perforant path (PP) stimulation. Nutralipid, an inert control solvent of the steroid, did not affect LTP development. We argue that both, membrane and intracellular effects of DHB, are involved in the mechanisms responsible for DHB blocking of LTP.
在巴比妥类麻醉的动物中,研究了皮质酮的A环还原代谢产物5α-二氢皮质酮(DHB)对大鼠齿状回(DG)长时程增强(LTP)的影响。观察到DHB显著损害LTP的发展,更特别的是对穿通通路(PP)刺激的诱发电位(EP)的群体峰电位(PS)成分。Nutralipid,一种类固醇的惰性对照溶剂,不影响LTP的发展。我们认为,DHB的膜效应和细胞内效应均参与了DHB阻断LTP的机制。