Nitric oxide and homeostatic control: an intercellular signalling molecule contributing to autonomic and neuroendocrine integration?

被引:88
作者
Stern, JE [1 ]
机构
[1] Wright State Univ, Dept Pharmacol & Toxicol, Dayton, OH 45435 USA
关键词
autonomic; neuroendocrine; hypothalamus; synaptic; GABA;
D O I
10.1016/j.pbiomolbio.2003.11.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Accumulated evidence indicates that nitric oxide (NO) plays a pivotal role in the central control of bodily homeostasis, including cardiovascular and fluid balance regulation. Two major neuronal substrates mediating NO actions in the control of homeostasis are the paraventricular nucleus (PVN) of the hypothalamus, considered a key center for the integration of neuroendocrine and autonomic functions, and the supraoptic nucleus (SON). In this work, a comprehensive review of NO modulatory actions within the SON/PVN, including NO actions on neuroendocrine and autonomic outputs, as well as the cellular mechanisms underlying these effects is provided. Furthermore, this review comprises recent progress from our laboratory that adds to our current understanding of the cellular sources, targets and mechanisms underlying NO actions within neuroendocrine and autonomic hypothalamic neuronal circuits. By combining in vitro patch clamp recordings, tract-tracing neuroanatomy, immunohistochemistry and live imaging techniques, we started to shed light into the cellular sources and signals driving NO production within the SON and PVN, as well as NO actions and mechanisms targeting discrete neuronal populations within these circuits. Based on this new information, we have expanded one of the current working models in the field, highlighting a key role for NO as a signaling molecule that facilitates crosstalk among various cell types and systems. We propose that this dynamic NO signaling mechanisms may constitute a neuroanatomical and functional substrate underlying the ability of the SON and PVN to coordinate complex neuroendocrine and autonomic output patterns. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:197 / 215
页数:19
相关论文
共 49 条
[1]   Fluorescent imaging of nitric oxide production in neuronal varicosities associated with intraparenchymal arterioles in rat hippocampal slices [J].
Brown, LA ;
Key, BJ ;
Lovick, TA .
NEUROSCIENCE LETTERS, 2000, 294 (01) :9-12
[2]   Endothelial and neuronal nitric oxide synthases are present in the suprachiasmatic nuclei of Syrian hamsters and rats [J].
Caillol, M ;
Devinoy, E ;
Lacroix, MC ;
Schirar, A .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2000, 12 (02) :649-661
[3]   RELATIONSHIP OF VASOPRESSIN WITH NADPH-DIAPHORASE IN THE HYPOTHALAMONEUROHYPOPHYSEAL SYSTEM [J].
CALKA, J ;
BLOCK, CH .
BRAIN RESEARCH BULLETIN, 1993, 32 (03) :207-210
[4]   GABA - A DOMINANT NEUROTRANSMITTER IN THE HYPOTHALAMUS [J].
DECAVEL, C ;
VANDENPOL, AN .
JOURNAL OF COMPARATIVE NEUROLOGY, 1990, 302 (04) :1019-1037
[5]   ENDOTHELIAL NITRIC-OXIDE SYNTHASE LOCALIZED TO HIPPOCAMPAL PYRAMIDAL CELLS - IMPLICATIONS FOR SYNAPTIC PLASTICITY [J].
DINERMAN, JL ;
DAWSON, TM ;
SCHELL, MJ ;
SNOWMAN, A ;
SNYDER, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (10) :4214-4218
[6]  
FORSTERMANN U, 1994, METHOD ENZYMOL, V233, P258
[7]   NITRIC-OXIDE SIGNALING IN THE CENTRAL-NERVOUS-SYSTEM [J].
GARTHWAITE, J ;
BOULTON, CL .
ANNUAL REVIEW OF PHYSIOLOGY, 1995, 57 :683-706
[8]   Distinct distribution and time-course changes in neuronal nitric oxide synthase and inducible NOS in the paraventricular nucleus following lipopolysaccharide injection [J].
Harada, S ;
Imaki, T ;
Chikada, N ;
Naruse, M ;
Demura, H .
BRAIN RESEARCH, 1999, 821 (02) :322-332
[9]   Central nitric oxide donors attenuate cardiovascular and central norepinephrine responses to stress [J].
Hashiguchi, H ;
Ye, SH ;
RossCisneros, F ;
Alexander, N .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1997, 272 (05) :R1447-R1453
[10]   Local circuit regulation of paraventricular nucleus stress integration - Glutamate-GABA connections [J].
Herman, JP ;
Tasker, JG ;
Ziegler, DR ;
Cullinan, WE .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2002, 71 (03) :457-468