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大鼠三甲基锡神经毒性导致海马N-甲基-D-天冬氨酸受体结合的时空变化。

Spatiotemporal changes in hippocampal NMDA receptor binding as a consequence of trimethyltin neurotoxicity in the rat.

作者信息

Koczyk D, Jabłońska B

机构信息

Department of Neurophysiology, Nencki Institute of Experimental Biology, Warsaw, Poland.

出版信息

Neurosci Lett. 1998 Jul 17;251(1):29-32. doi: 10.1016/s0304-3940(98)00487-x.

DOI:10.1016/s0304-3940(98)00487-x
PMID:9714457
Abstract

In the present study we examined the presumable changes in the distribution of N-methyl-D-aspartate (NMDA) receptors in the hippocampus of rat exposed to a potent neurotoxic drug, trimethyltin (TMT). Using in vitro receptor binding autoradiography, [3H]MK801 labelling was determined at 7, 14, 21, 30 and 60 days after treatment with TMT (single dose of 8 mg/kg, i.p.) in various hippocampal areas thought to be affected by the neurotoxin. At 21-60 days after exposure, a decrease in receptor binding was observed in CA1 hippocampal subfield (10-20%, P< 0.05). A reduction in binding density also occurred in CA4/ CA3c, where labelling vanished completely at longer times. In the molecular layer (ML) of the dentate gyrus (DG), however, 16-37% (P<0.05) increase in receptor binding was found at 14-60 days postexposure. These results suggest that exposure to TMT leads to an altered topography of NMDA receptor density sites in the rat hippocampus. Dynamics of the reduction in receptor binding in CA4/CA3c and CA1 followed the development of the well-known degenerative effects induced by the neurotoxin. In contrast, the enhanced binding density in the ML of the DG may be a part of a mechanism of plastic response of granule cells to denervation/reinnervation.

摘要

在本研究中,我们检测了暴露于强效神经毒性药物三甲基锡(TMT)的大鼠海马中N-甲基-D-天冬氨酸(NMDA)受体分布的可能变化。使用体外受体结合放射自显影技术,在用TMT(腹腔注射单剂量8 mg/kg)处理后的7、14、21、30和60天,测定了[3H]MK801标记在被认为受神经毒素影响的各个海马区域中的情况。暴露后21至60天,在海马CA1亚区观察到受体结合减少(10 - 20%,P<0.05)。CA4/CA3c区域的结合密度也降低,在更长时间后标记完全消失。然而,在齿状回(DG)的分子层(ML)中,暴露后14至60天发现受体结合增加了16 - 37%(P<0.05)。这些结果表明,暴露于TMT会导致大鼠海马中NMDA受体密度位点的拓扑结构发生改变。CA4/CA3c和CA1中受体结合减少的动态变化与神经毒素诱导的众所周知的退行性效应的发展一致。相比之下,DG的ML中结合密度的增强可能是颗粒细胞对去神经/再神经支配的可塑性反应机制的一部分。

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