Overexpression of eNOS in NTS causes hypotension and bradycardia in vivo

被引:89
作者
Sakai, K [1 ]
Hirooka, Y [1 ]
Matsuo, I [1 ]
Eshima, K [1 ]
Shigematsu, H [1 ]
Shimokawa, H [1 ]
Takeshita, A [1 ]
机构
[1] Kyushu Univ, Grad Sch Med Sci, Dept Cardiovasc Med, Higashi Ku, Fukuoka 8128582, Japan
关键词
genes; nitric oxide; brain; sympathetic nervous system;
D O I
10.1161/01.HYP.36.6.1023
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
The role of nitric oxide (NO) in the brain in the control of blood pressure and the sympathetic nervous system is debated. This study examined the effect of overexpression of endothelial NO synthase (eNOS) in the nucleus tractus solitarii (NTS) on blood pressure in conscious rats. Adenovirus vectors encoding either eNOS (AdeNOS) or beta -galactosidase were transfected into the NTS in vivo. In the AdeNOS-treated rats, the local expression of eNOS in the NTS was confirmed by immunohistochemical staining and Western blot analysis for the eNOS protein and by increased production of nitrite/nitrate in the NTS measured by in vivo microdialysis. Blood pressure and heart rate, monitored by the use of a radiotelemetry system in a conscious state, were significantly decreased in the AdeNOS-treated group at day 5 to day 10 after the gene transfer. Urinary norepinephrine excretion also was decreased at day 7 after the gene transfer in the AdeNOS-treated group. Our results indicate that overexpression of eNOS in the NTS decreases blood pressure, heart rate, and sympathetic nerve activity in conscious rats.
引用
收藏
页码:1023 / 1028
页数:6
相关论文
共 27 条
[11]  
JONES NM, 1995, J NEUROCHEM, V64, P2057
[12]   Chemically defined neuron groups and their subpopulations in the glomerular layer of the rat main olfactory bulb .2. Prominent differences in the intraglomerular dendritic arborization and their relationship to olfactory nerve terminals [J].
Kosaka, K ;
Toida, K ;
Margolis, FL ;
Kosaka, T .
NEUROSCIENCE, 1997, 76 (03) :775-786
[13]   Retrograde transfer of replication deficient recombinant adenovirus vector in the central nervous system for tracing studies [J].
Kuo, H ;
Ingram, DK ;
Crystal, RG ;
Mastrangeli, A .
BRAIN RESEARCH, 1995, 705 (1-2) :31-38
[14]   Adenoviral gene transfer to spinal cord neurons: intrathecal vs. intraparenchymal administration [J].
Mannes, AJ ;
Caudle, RM ;
O'Connell, BC ;
Iadarola, MJ .
BRAIN RESEARCH, 1998, 793 (1-2) :1-6
[15]   Role of nitric oxide in the nucleus of the solitary tract of rats [J].
Matsumura, K ;
Tsuchihashi, T ;
Kagiyama, S ;
Abe, I ;
Fujishima, M .
BRAIN RESEARCH, 1998, 798 (1-2) :232-238
[16]  
Matsuo I, 1998, CIRCULATION, V98, P541
[17]   Altered vascular function after adenovirus-mediated overexpression of endothelial nitric oxide synthase [J].
Ooboshi, H ;
Chu, Y ;
Rios, CD ;
Faraci, FM ;
Davidson, BL ;
Heistad, DD .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1997, 273 (01) :H265-H270
[18]  
Paxinos G, 1998, RAT BRAIN IN STEREOTAXIC COORDINATES, FOURTH ED., pix
[19]  
SPYER KM, 1990, CENTRAL REGULATION A, V98, P168
[20]   Inhibition of NO synthesis induces inflammatory changes and monocyte chemoattractant protein-1 expression in rat hearts and vessels [J].
Tomita, H ;
Egashira, K ;
Kubo-Inoue, M ;
Usui, M ;
Koyanagi, M ;
Shimokawa, H ;
Takeya, M ;
Yoshimura, T ;
Takeshita, A .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1998, 18 (09) :1456-1464