摘要
实验应用Fos蛋白和酪氨酸羟化酶 (tyrosinehydroxylase ,TH)的双重免疫组化方法 ,观察肾脏动脉阻断(renalarteryocclusion ,RAO)是否激活脑干中核团的儿茶酚胺能神经元。所得结果如下 :(1)脑干中Fos样蛋白的基础性表达低 ;RAO可诱发孤束核 (nucleustractussolitarius ,NTS)、最后区 (areapostrema ,AP)、巨细胞旁外侧核 (paragi gantocellularislateralis ,PGL)和蓝斑 (locuscoeruleus ,LC)核团中许多神经元显示Fos样免疫反应 (Fos likeimmunoreactivi ty ,FLI)。 (2 )NTS、AP、PGL和LC核团中含有较多的儿茶酚胺能神经元 ;RAO能激活其中的部分儿茶酚胺能神经元。 (3)腺苷受体阻断剂 8 苯茶碱可明显减弱RAO所致的上述效应。以上结果表明 ,肾脏短暂缺血能激活脑干内的一些神经核团以及其中的部分儿茶酚胺能神经元。此效应可能是肾缺血时腺苷释放作用于肾内腺苷受体后引起肾传入神经活动增加的结果。
The present study was undertaken to define whether the renal artery occlusion (RAO) would activate the catecholaminergic neurons in the brainstem nuclei by double immunohistochemical method for detecting Fos and tyrosine hydroxylase. The results are as follows: (1) while the basal expression of Fos was relatively low in the brainstem, RAO was capable of inducing a robust Fos-like immunoreactive neurons in the nucleus tractus solitarius (NTS), area postrema (AP), nucleus paragigantocellularis lateralis (PGL) and locus coeruleus (LC); (2) numerous catecholaminergic neurons in NTS, AP, PGL and LC could be activated by RAO as shown by Fos expression; and (3) these responses to RAO were significantly attenuated by pretreatment with an adenosine receptor antagonist 8-phenyltheophylline. The results suggest that RAO can activate a large number of neurons including some catecholaminergic neurons in the brainstem nuclei. Such effects of renal ischemia may be attributed to RAO-induced adenosine release from the kidney which subsequently activates renal afferents.
出处
《生理学报》
CAS
CSCD
北大核心
2001年第6期445-450,共6页
Acta Physiologica Sinica
基金
ThisstudywassupportedbytheNationalNaturalScienceFoundationofChina (No 30 0 70 2 82 )
