Possible involvement of nitric oxide in the central salt-loading-induced cardiovascular responses in conscious rats

被引:6
作者
Jin, QH
Kunitake, T
Chu, CP
Qiu, DL
Kato, K
Ishizuka, Y
Kannan, H
机构
[1] Miyazaki Med Coll, Dept Physiol, Miyazaki 8891692, Japan
[2] Yabian Univ, Coll Med, Dept Physiol, Yanji 133000, Jilin, Peoples R China
[3] Miyazaki Med Coll, Dept Psychiat, Miyazaki 8891692, Japan
关键词
paraventricular nucleus; blood pressured heart rate; nitric oxide;
D O I
10.1016/S0006-8993(02)03982-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The objective of this study was to elucidate the possible involvement of nitric oxide (NO) in the cardiovascular responses induced by central salt loading. Direct perfusion of the hypothalamic paraventricular nucleus (PVN) region with hypertonic saline (0.3 or 0.45 M) was performed in conscious rats by using an in vivo brain microdialysis technique. The extracellular concentration of NO metabolites in the PVN region was measured, as were the blood pressure (BP) and heart rate (HR). Perfusion of 0.45 M saline increased the BP HR, and NO metabolite levels in the PVN region; however, perfusion of 0.3 M saline enhanced only the level of NO metabolites but did not induce changes in the BP and HR. Next, we determined whether the NO was involved in the cardiovascular responses induced by hypertonic saline. Pretreatment with N-G-methyl-L-arginine (L-NMMA), an inhibitor of NO synthase, attenuated the increases in the BP and HR induced by direct perfusion of 0.45 M saline, while direct infusion of 3-morpholmosyndnonimine (SIN-1, a NO donor) in the PVN region induced increases in the BP and HR. These results suggest that local perfusion of the PVN region with hypertonic saline elicits a local release of NO, which may be carried out by activating nitric oxide synthase to produce cardiovascular responses. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:224 / 231
页数:8
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