The brain renin-angiotensin system: location and physiological roles

被引:400
作者
McKinley, MJ [1 ]
Albiston, AL [1 ]
Allen, AM [1 ]
Mathai, ML [1 ]
May, CN [1 ]
McAllen, RM [1 ]
Oldfield, BJ [1 ]
Mendelsohn, FAO [1 ]
Chai, SY [1 ]
机构
[1] Univ Melbourne, Howard Florey Inst Expt Physiol & Med, Melbourne, Vic 3010, Australia
基金
英国医学研究理事会;
关键词
cardiovascular regulation; fluid and electrolyte balance; AT(1) receptors; ventrolateral medulla; hypothalamus;
D O I
10.1016/S1357-2725(02)00306-0
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
Angiotensinogen, the precursor molecule for angiotensins I, II and III, and the enzymes renin, angiotensin-converting enzyme (ACE), and aminopeptidases A and N may all be synthesised within the brain. Angiotensin (Ang) AT(1), AT(2) and AT(4) receptors are also plentiful in the brain. AT(1) receptors are found in several brain regions, such as the hypothalamic paraventricular and supraoptic nuclei, the lamina terminalis, lateral parabrachial nucleus, ventrolateral medulla and nucleus of the solitary tract (NTS), which are known to have roles in the regulation of the cardiovascular system and/or body fluid and electrolyte balance. Immunohistochemical and neuropharmacological studies suggest that angiotensinergic neural pathways utilise Ang II and/or Ang III as a neurotransmitter or neuromodulator in the aforementioned brain regions. Angiotensinogen is synthesised predominantly in astrocytes, but the processes by which Ang II is generated or incorporated in neurons for utilisation as a neurotransmitter is unknown. Centrally administered AT(4) receptor antagonists or angiotensinogen antisense oligonucleotides inhibit sympathetic activity and reduce arterial blood pressure in certain physiological or pathophysiological conditions, as well as disrupting water drinking and sodium appetite, vasopressin secretion, sodium excretion, renin release and thermoregulation. The AT(4) receptor is identical to insulin-regulated aminopeptidase (IRAP) and plays a role in memory mechanisms. In conclusion, angiotensinergic neural pathways and angiotensin peptides are important in neural function and may have important homeostatic roles, particularly related to cardiovascular function, osmoregulation and thermorogulation. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:901 / 918
页数:18
相关论文
共 171 条
[61]   ANTISENSE INHIBITION OF AT(1) RECEPTOR MESSENGER-RNA AND ANGIOTENSINOGEN MESSENGER-RNA IN THE BRAIN OF SPONTANEOUSLY HYPERTENSIVE RATS REDUCES HYPERTENSION OF NEUROGENIC ORIGIN [J].
GYURKO, R ;
WIELBO, D ;
PHILLIPS, MI .
REGULATORY PEPTIDES, 1993, 49 (02) :167-174
[62]   REGIONAL EXPRESSION OF C-FOS ANTIGEN IN THE BASAL FOREBRAIN FOLLOWING INTRAVENTRICULAR INFUSIONS OF ANGIOTENSIN AND ITS MODULATION BY DRINKING EITHER WATER OR SALINE [J].
HERBERT, J ;
FORSLING, ML ;
HOWES, SR ;
STACEY, PM ;
SHIERS, HM .
NEUROSCIENCE, 1992, 51 (04) :867-882
[63]   Insulin stimulates cell surface aminopeptidase activity toward vasopressin in adipocytes [J].
Herbst, JJ ;
Ross, SA ;
Scott, HM ;
Bobin, SA ;
Morris, NJ ;
Lienhard, GE ;
Keller, SR .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1997, 272 (04) :E600-E606
[64]   ANGIOTENSINOGEN IN RAT CEREBROSPINAL-FLUID [J].
HILGENFELDT, U .
CLINICAL AND EXPERIMENTAL HYPERTENSION PART A-THEORY AND PRACTICE, 1984, 6 (10-1) :1815-1824
[65]   INVOLVEMENT OF ANGIOTENSIN RECEPTOR SUBTYPES IN OSMOTICALLY INDUCED RELEASE OF VASOPRESSIN [J].
HOGARTY, DC ;
TRAN, DN ;
PHILLIPS, MI .
BRAIN RESEARCH, 1994, 637 (1-2) :126-132
[66]   ANGIOTENSIN AT(1) RECEPTOR-MEDIATED VASOPRESSIN RELEASE AND DRINKING ARE POTENTIATED BY AN AT(2) RECEPTOR ANTAGONIST [J].
HOHLE, S ;
SPITZNAGEL, H ;
RASCHER, W ;
CULMAN, J ;
UNGER, T .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1995, 275 (03) :277-282
[67]   Sympathoexcitatory and pressor responses to increased brain sodium and ouabain are mediated via brain ANG II [J].
Huang, BS ;
Leenen, FHH .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1996, 270 (01) :H275-H280
[68]   ANGIOTENSINOGEN PRODUCTION BY RAT ASTROGLIAL CELLS-INVITRO AND INVIVO [J].
INTEBI, AD ;
FLAXMAN, MS ;
GANONG, WF ;
DESCHEPPER, CF .
NEUROSCIENCE, 1990, 34 (03) :545-554
[69]  
ITO AF, 1996, AM J PHYSIOL, V270, pR1317
[70]   ROLE OF PARAVENTRICULAR NUCLEUS IN CONTROL OF BLOOD-PRESSURE AND DRINKING IN RATS [J].
JENSEN, LL ;
HARDING, JW ;
WRIGHT, JW .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 262 (06) :F1068-F1075