Simonnet G, Giorguieff-Chesselet M F, Carayon A, Bioulac B, Cesselin F, Glowinski J, Vincent J D
J Physiol (Paris). 1981 Apr;77(1):71-9.
The central renin-angiotensin system is implicated most importantly in the control of water balance, blood pressure and endocrine function (AVP and ACTH). Several central structures are sensitive to angiotensin II (A II), principally: the subfornical organ, the vascular organ of the lamina terminalis, the area postrema and the preoptic area. Furthermore, binding studies with radio-active ligands and also immunohistofluorescence have shown respectively the presence of A II receptors and immunoreactive material bound by A II antibodies in other central structures, and in particular parts of the motor system. In the present study, a double approach, both electrophysiological and biochemical, was used to investigate the possible role of the peptide A II in the neostriatum of the rat. 1 Microiontophoretic application of A II was shown to modify the spontaneous activity of some neurones (15/68) in the neostriatum. Generally, the action of A II was inhibitory and the inhibition was blocked by Sar1-Ileu8-A II, a specific A II antagonist. 2 Angiotensin II 10(-6) M; 10(-5) M; 5.10(-5) M) stimulated the spontaneous release of 3H-dopamine continuously synthetized from 3H-tyrosine in striatal slices of the rat. The A II-evoked release of 3H-dopamine was prevented when slices were superfused with a calcium-free medium containing EGTA. It was also suppressed in the presence of the specific antagonist Sar1-Ileu8-A II. 3 Kainic acid lesion of the intrastriatal cell bodies produced a moderate decrease of A II in the striatum (38%) whilst the activity of the converting enzyme decreased dramatically (-68%). These results suggest that there are angiotensin-containing nerve endings in the neostriatum, and that the cell bodies of such nerves are located outside this structure. Their functional role is discussed.
中枢肾素-血管紧张素系统在水盐平衡、血压和内分泌功能(抗利尿激素和促肾上腺皮质激素)的调控中起着最为重要的作用。几个中枢结构对血管紧张素II(A II)敏感,主要包括:穹窿下器官、终板血管器、最后区和视前区。此外,放射性配体结合研究以及免疫荧光研究分别显示,在其他中枢结构,尤其是运动系统的某些部位,存在A II受体以及与A II抗体结合的免疫反应性物质。在本研究中,采用电生理和生化双重方法,研究了肽A II在大鼠新纹状体中的可能作用。1 微离子电泳施加A II可改变新纹状体中部分神经元(15/68)的自发活动。一般来说,A II的作用是抑制性的,且这种抑制作用可被特异性A II拮抗剂Sar1-Ileu8-A II阻断。2 血管紧张素II(10(-6) M、10(-5) M、5×10(-5) M)可刺激从3H-酪氨酸持续合成的3H-多巴胺在大鼠纹状体切片中的自发释放。当切片在含有乙二醇双四乙酸(EGTA)的无钙培养基中灌流时,A II诱发的3H-多巴胺释放受到抑制。在特异性拮抗剂Sar1-Ileu8-A II存在的情况下,其释放也受到抑制。3 纹状体内细胞体的海人酸损伤使纹状体中A II适度减少(38%),而转化酶的活性则显著下降(-68%)。这些结果表明,新纹状体中存在含血管紧张素的神经末梢,且此类神经的细胞体位于该结构之外。文中对它们的功能作用进行了讨论。