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缺血诱导的神经元细胞丢失与沙鼠海马结构中非典型1型血管紧张素受体表达的丧失有关。

Ischemia-induced neuronal cell loss is associated with loss of atypical angiotensin type-1 receptor expression in the gerbil hippocampal formation.

作者信息

Häuser W, Jöhren O, de Oliveira A M, Shibata S, Saavedra J M

机构信息

Section on Pharmacology, National Institute of Mental Health, 10 Center Drive MSC 1514, Bldg. 10, Room 2D-57, Bethesda, MD 20892-1514, USA.

出版信息

Brain Res. 1999 Jan 30;817(1-2):34-44. doi: 10.1016/s0006-8993(98)01193-7.

Abstract

The hippocampal formation of Mongolian gerbils expresses high amounts of atypical angiotensin II type-1 receptors. We studied the expression of these receptors by in situ hybridization using specific [35S]-labeled riboprobes and by receptor autoradiography using [125I]Sarcosine1-angiotensin II. Angiotensin II receptor mRNA was found in the pyramidal cell layer of the CA1, CA2 and CA3 subfields, with the highest expression in the CA2 subfield, and in the granular cell layer of the dentate gyrus. Angiotensin II binding was detected in the stratum oriens and stratum radiatum of the CA1 and CA2 subfields, in the stratum oriens of the CA3 subfield, and in the molecular layer of the dentate gyrus. We then studied the effect of ischemia on hippocampal angiotensin II receptor expression, 1, 4 and 15 days after bilateral occlusion of the common carotid arteries for 5 min. No changes in angiotensin II receptor mRNA or binding were detected 1 day after ischemia. Delayed, progressive loss of angiotensin II mRNA and binding occurred 4 and 15 days after ischemia, in the CA1, CA2 and CA3 subfields. The decline was faster in the CA1 subfield, and paralleled the loss of neurons after ischemia. In the dentate gyrus, angiotensin II receptor mRNA and angiotensin II binding were not changed when compared to sham operated controls. The decrease of angiotensin II receptor expression may reflect the loss of angiotensin II receptor-producing neurons rather than a down-regulation of receptor expression.

摘要

蒙古沙鼠的海马结构表达大量非典型1型血管紧张素II受体。我们使用特异性[35S]标记的核糖探针通过原位杂交以及使用[125I]肌氨酸1 - 血管紧张素II通过受体放射自显影术研究了这些受体的表达。在CA1、CA2和CA3亚区的锥体细胞层中发现了血管紧张素II受体mRNA,其中CA2亚区表达最高,在齿状回的颗粒细胞层中也有表达。在CA1和CA2亚区的原层和放射层、CA3亚区的原层以及齿状回的分子层中检测到血管紧张素II结合。然后我们研究了双侧颈总动脉闭塞5分钟后1、4和15天缺血对海马血管紧张素II受体表达的影响。缺血1天后未检测到血管紧张素II受体mRNA或结合的变化。缺血4天和15天后,CA1、CA2和CA3亚区出现血管紧张素II mRNA和结合的延迟性、进行性丧失。CA1亚区的下降更快,与缺血后神经元的丧失平行。在齿状回中,与假手术对照组相比,血管紧张素II受体mRNA和血管紧张素II结合没有变化。血管紧张素II受体表达的降低可能反映了产生血管紧张素II受体的神经元的丧失,而不是受体表达的下调。

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