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未成熟大鼠海马切片中N-甲基-D-天冬氨酸受体介导的[3H]花生四烯酸释放的调节

Modulation of NMDA receptor-mediated release of [3H]arachidonate in hippocampal slices of immature rats.

作者信息

Salińska E, Lazarewicz J W

机构信息

Department of Neurochemistry, Polish Academy of Sciences, Warsaw.

出版信息

Acta Neurobiol Exp (Wars). 1995;55(1):11-21. doi: 10.55782/ane-1995-1057.

Abstract

Using superfusion with albumin-containing medium of hippocampal and striatal slices of adult and developing rats at postnatal days (PND) 7-10, prelabelled with [3H]arachidonic acid ([3H]AA), we detected N-methyl-D-aspartate (NMDA) evoked release to the superfusion medium of radiolabelled material, 70% of which was associated with arachidonic acid (AA) and its metabolites. [3H]AA release was much more pronounced in PND 7-10 rats than in adults, and the response to NMDA in the hippocampal slices exceeded the reactions in the striatal slices. The subsequent experiments, employing only hippocampal slices of PND 7-10 rats, demonstrated that NMDA-stimulated [3H]AA release was dose-dependent in the micromolar range, was sensitive to NMDA receptor antagonists, and was inhibited in calcium-free medium and in the presence of quinacrine. [3H]AA release induced by 100 microM NMDA was not significantly inhibited by magnesium but was completely blocked by 7 Cl-kynurenic acid and ifenprodil (both antagonists 100 microM). The sulfhydryl reducing reagent dithiothreitol induced [3H]AA release; this response was sensitive to NMDA receptor antagonists. These data indicate that the NMDA induced, calcium triggered, and phospholipase A2 dependent AA release is highly pronounced in the developing rat hippocampus. NMDA receptors mediating AA release in the hippocampus of PND 7-10 rats are subject to glycine, polyamine and redox modulation, but they show low sensitivity to Mg2+ inhibition.

摘要

对出生后第7 - 10天的成年和发育中大鼠的海马体和纹状体切片,用含白蛋白的培养基进行灌流,这些切片预先用[3H]花生四烯酸([3H]AA)标记,我们检测到N - 甲基 - D - 天冬氨酸(NMDA)诱发放射性标记物质释放到灌流培养基中,其中70%与花生四烯酸(AA)及其代谢产物相关。[3H]AA的释放在出生后第7 - 10天的大鼠中比成年大鼠明显得多,并且海马体切片中对NMDA的反应超过纹状体切片中的反应。随后仅使用出生后第7 - 10天大鼠海马体切片进行的实验表明,NMDA刺激的[3H]AA释放在微摩尔范围内呈剂量依赖性,对NMDA受体拮抗剂敏感,并且在无钙培养基和奎纳克林存在下受到抑制。100微摩尔NMDA诱导的[3H]AA释放未被镁显著抑制,但被7 - 氯犬尿喹啉酸和艾芬地尔(两者均为100微摩尔拮抗剂)完全阻断。巯基还原剂二硫苏糖醇诱导[3H]AA释放;这种反应对NMDA受体拮抗剂敏感。这些数据表明,在发育中的大鼠海马体中,NMDA诱导的、钙触发的和磷脂酶A2依赖性的AA释放非常明显。介导出生后第7 - 10天大鼠海马体中AA释放的NMDA受体受到甘氨酸、多胺和氧化还原调节,但它们对Mg2 +抑制的敏感性较低。

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