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沙鼠正常和癫痫海马中的生长抑素受体:亚型特异性定位及其改变。

The somatostatin receptors in the normal and epileptic hippocampus of the gerbil: subtype-specific localization and its alteration.

作者信息

Kang Tae-Cheon, An Sung-Jin, Park Seung-Kook, Hwang In Koo, Seo Myung-Oak, Kim Hyun Sook, Kang Jung Hoon, Kwon Oh-Shin, Won Moo Ho

机构信息

Department of Anatomy, College of Medicine, Hallym University, Chunchon, Kangwon-Do 200-702, South Korea.

出版信息

Brain Res. 2003 Oct 3;986(1-2):91-102. doi: 10.1016/s0006-8993(03)03192-5.

Abstract

We investigated the distribution of somatostatin receptors (SSTs) in the hippocampi of SR (seizure-resistant) and SS (seizure-sensitive) gerbils in order to characterize the alterations in SST expressions induced by seizure activity. SST2A immunodensity in the hippocampus of SS gerbils was lower than that of SR gerbils, though its localization in the hippocampus was similar in both SR and SS gerbils. SST3 immunodensity in the hippocampus of SS gerbils was lower than in SR gerbils. In SR gerbils, strong SST4 immunoreactivity was detected in the dentate gyrus and in the CA3 region, in contrast little immunoreactivity was detected in these regions in SS gerbils. In SR and SS gerbils, the strong SST5 immunoreactivity in the hippocampus was also detected in the stratum oriens of the CA2-3 regions and the septal area of CA1 region. However, SST5 immunodensity in the stratum radiatum in SS gerbils was lower than in SR gerbils. These results are the first comprehensive description of the distribution of SSTs in the normal and epileptic hippocampus of gerbils, and suggest that these alterations in the hippocampus of the SS gerbil may be related with a regulatory mechanism for seizure activity in these seizure prone animals.

摘要

我们研究了抗癫痫(SR)和癫痫敏感(SS)沙鼠海马中生长抑素受体(SSTs)的分布,以表征癫痫活动诱导的SST表达变化。SS沙鼠海马中的SST2A免疫密度低于SR沙鼠,尽管其在海马中的定位在SR和SS沙鼠中相似。SS沙鼠海马中的SST3免疫密度低于SR沙鼠。在SR沙鼠中,在齿状回和CA3区域检测到强SST4免疫反应性,相比之下,在SS沙鼠的这些区域中检测到的免疫反应性较弱。在SR和SS沙鼠中,在CA2-3区域的海马原层和CA1区域的隔区也检测到强SST5免疫反应性。然而,SS沙鼠辐射层中的SST5免疫密度低于SR沙鼠。这些结果首次全面描述了沙鼠正常和癫痫海马中SSTs的分布,并表明SS沙鼠海马中的这些变化可能与这些癫痫易感动物的癫痫活动调节机制有关。

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