Hobara Narumi, Gessei-Tsutsumi Noriko, Goda Mitsuhiro, Takayama Fusako, Akiyama Shinji, Kurosaki Yuji, Kawasaki Hiromu
Department of Clinical Pharmaceutical Science, Faculty of Pharmaceutical Sciences, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, Japan.
Hypertens Res. 2005 May;28(5):465-74. doi: 10.1291/hypres.28.465.
The aim of this study was to investigate age-related changes in the density of calcitonin gene-related peptide (CGRP)-containing nerve fibers in spontaneously hypertensive rats (SHR) and the effects of long-term inhibition of the renin-angiotensin system on these changes. The density of immunocytochemically stained nerve fibers in the mesenteric artery was quantified by computer-assisted image processing. An age-related decrease in the density of CGRP-like immunoreactive (LI)-containing nerve fivers but not neuropeptide Y (NPY)-LI-containing sympathetic nerve fibers was found in the mesenteric artery of SHR but not Wistar Kyoto rats (WKY). The density of NPY-LI-containing sympathetic nerve fibers was significantly greater in SHR than in WKY. SHR were treated for 7 weeks with angiotensin converting enzyme inhibitor (0.005% temocapril), angiotensin II type-1 (AT1) receptor antagonist (0.025% losartan) or vasodilator (0.01% hydralazine) in their drinking water. Each drug treatment significantly lowered the systolic blood pressure measured by tail-cuff method. Long-term treatment of SHR with temocapril and losartan significantly increased the density of CGRP-LI-containing nerve fibers in mesenteric arteries. However, the density after hydralazine treatment was similar to the level in non-treated SHR. The density of NPY-LI-containing nerve fibers was not increased by any of the drug treatments. These results suggest that long-term inhibition of the renin-angiotensin system in SHR prevents remodeling of CGRPergic nerve fibers and prevents the reduction of CGRPergic nerve function.
本研究旨在调查自发性高血压大鼠(SHR)中降钙素基因相关肽(CGRP)阳性神经纤维密度的年龄相关变化,以及长期抑制肾素-血管紧张素系统对这些变化的影响。通过计算机辅助图像处理对肠系膜动脉中免疫细胞化学染色的神经纤维密度进行定量分析。在SHR的肠系膜动脉中发现了含CGRP样免疫反应性(LI)神经纤维密度的年龄相关下降,但含神经肽Y(NPY)-LI的交感神经纤维密度未下降,而在Wistar Kyoto大鼠(WKY)中未发现这种情况。SHR中含NPY-LI的交感神经纤维密度显著高于WKY。给SHR在饮水中给予血管紧张素转换酶抑制剂(0.005%替莫卡普利)、血管紧张素II 1型(AT1)受体拮抗剂(0.025%氯沙坦)或血管扩张剂(0.01%肼屈嗪)治疗7周。每种药物治疗均显著降低了通过尾套法测量的收缩压。用替莫卡普利和氯沙坦对SHR进行长期治疗可显著增加肠系膜动脉中含CGRP-LI神经纤维的密度。然而,肼屈嗪治疗后的密度与未治疗的SHR水平相似。任何药物治疗均未增加含NPY-LI神经纤维的密度。这些结果表明,长期抑制SHR中的肾素-血管紧张素系统可防止CGRP能神经纤维的重塑,并防止CGRP能神经功能的降低。