Differential distribution of nitric oxide synthase isoforms in the rostral ventrolateral medulla of the rat

被引:44
作者
Chang, AYW
Chan, JYH
Chan, SHH [1 ]
机构
[1] Natl Sun Yat Sen Univ, Ctr Neurosci, Kaohsiung 80424, Taiwan
[2] Natl Sun Yat Sen Univ, Dept Sci Biol, Kaohsiung 80424, Taiwan
[3] Kaohsiung Vet Gen Hosp, Dept Med Educ & Res, Kaohsiung, Taiwan
关键词
nitric oxide synthase I; II; III; rostral ventrolateral medulla; cardiovascular regulation; sympathetic premotor neurons;
D O I
10.1159/000070093
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We evaluated the distribution of nitric oxide synthase (NOS) isoforms in the rostral ventrolateral medulla (RVLM), the medullary origin of sympathetic neurogenic vasomotor tone, and the contribution of NOS III to the cardiovascular actions of endogenous NO in the RVLM. Adult Sprague-Dawley rats were used. Reverse transcription-polymerase chain reaction or Western blot analysis revealed that NOS I, II or III was expressed in the ventrolateral medulla at the mRNA or protein level under basal conditions. However, laser scanning confocal microscopic analysis of double-immunofluorescence images showed that whereas NOS I or II immunoreactivity colocalized with cells within the confines of the RVLM that stained positively with the neuronal marker, NeuN, NOS III immunoreactivity was associated primarily with blood vessels. Furthermore, bilateral microinjection into the RVLM of the selective NOS III inhibitor, N-5-(1-iminoethyl)-L-ornithine, elicited minimal alterations in baseline systemic arterial pressure, heart rate or sympathetic vasomotor outflow in rats anesthetized with propofol. We conclude that whereas NOS I and II are present in neurons within the confines of the RVLM, NOS III is associated primarily with blood vessels. Our results further indicate that NOS III does not appear to contribute to the maintenance of basal sympathetic vasomotor outflows and arterial pressure by the endogenous NO at the RVLM. Copyright (C) 2003 National Science Council, ROC and S. Karger AG, Basel.
引用
收藏
页码:285 / 291
页数:7
相关论文
共 42 条
[21]   Role of nNOS in blood pressure regulation in eNOS null mutant mice [J].
Kurihara, N ;
Alfie, ME ;
Sigmon, DH ;
Rhaleb, NE ;
Shesely, EG ;
Carretero, OA .
HYPERTENSION, 1998, 32 (05) :856-861
[22]   Excitatory effects of nitric oxide within the rostral ventrolateral medulla of freely moving rats [J].
MartinsPinge, MC ;
BaraldiPassy, I ;
Lopes, OU .
HYPERTENSION, 1997, 30 (03) :704-707
[23]   5-hydroxytryptamine evokes endothelial nitric oxide synthase activation in bovine aortic endothelial cell cultures [J].
McDuffie, JE ;
Coaxum, SD ;
Maleque, MA .
PROCEEDINGS OF THE SOCIETY FOR EXPERIMENTAL BIOLOGY AND MEDICINE, 1999, 221 (04) :386-390
[24]  
MULLEN RJ, 1992, DEVELOPMENT, V116, P201
[25]   SYNTHESIS OF NITRIC-OXIDE IN CNS GLIAL-CELLS [J].
MURPHY, S ;
SIMMONS, ML ;
AGULLO, L ;
GARCIA, A ;
FEINSTEIN, DL ;
GALEA, E ;
REIS, DJ ;
MINCGOLOMB, D ;
SCHWARTZ, JP .
TRENDS IN NEUROSCIENCES, 1993, 16 (08) :323-328
[26]   Adenoviral vector demonstrates that angiotensin II-induced depression of the cardiac baroreflex is mediated by endothelial nitric oxide synthase in the nucleus tractus solitarii of the rat [J].
Paton, JFR ;
Deuchars, J ;
Ahmad, Z ;
Wong, LF ;
Murphy, D ;
Kasparov, S .
JOURNAL OF PHYSIOLOGY-LONDON, 2001, 531 (02) :445-458
[27]   Increased gene expression of neuronal nitric oxide synthase in brain of adult spontaneously hypertensive rats [J].
PlochockaZulinska, D ;
Krukoff, TL .
MOLECULAR BRAIN RESEARCH, 1997, 48 (02) :291-297
[28]   On the selectivity of 7-nitroindazole as an inhibitor of neuronal nitric oxide synthase [J].
Rainer, A ;
Zagvazdin, Y .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1998, 19 (09) :348-350
[29]   ROLE OF ENDOTHELIUM-DERIVED NITRIC-OXIDE IN THE REGULATION OF BLOOD-PRESSURE [J].
REES, DD ;
PALMER, RMJ ;
MONCADA, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (09) :3375-3378
[30]   CHARACTERIZATION OF 3 INHIBITORS OF ENDOTHELIAL NITRIC-OXIDE SYNTHASE INVITRO AND INVIVO [J].
REES, DD ;
PALMER, RMJ ;
SCHULZ, R ;
HODSON, HF ;
MONCADA, S .
BRITISH JOURNAL OF PHARMACOLOGY, 1990, 101 (03) :746-752