Mechanisms of brain renin angiotensin system-induced drinking and blood pressure: importance of the subfornical organ

被引:75
作者
Coble, Jeffrey P. [1 ]
Grobe, Justin L. [1 ,3 ]
Johnson, Alan Kim [1 ,2 ]
Sigmund, Curt D. [1 ,3 ]
机构
[1] Univ Iowa, Dept Pharmacol, Roy J & Lucille Carver Coll Med, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Psychol, Roy J & Lucille Carver Coll Med, Iowa City, IA 52242 USA
[3] Univ Iowa, Hypertens Res Ctr, Roy J & Lucille Carver Coll Med, Iowa City, IA 52242 USA
基金
美国国家卫生研究院;
关键词
angiotensin; blood pressure; barin; fluid; renin; PROTEIN-KINASE-C; HYPOTHALAMIC PARAVENTRICULAR NUCLEUS; CENTRAL-NERVOUS-SYSTEM; FOREBRAIN CIRCUMVENTRICULAR ORGANS; FIBRILLARY ACIDIC PROTEIN; FOS-LIKE IMMUNOREACTIVITY; GLIAL-SPECIFIC ABLATION; SODIUM APPETITE; RAT-BRAIN; ANG-II;
D O I
10.1152/ajpregu.00486.2014
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
It is critical for cells to maintain a homeostatic balance of water and electrolytes because disturbances can disrupt cellular function, which can lead to profound effects on the physiology of an organism. Dehydration can be classified as either intra-or extracellular, and different mechanisms have developed to restore homeostasis in response to each. Whereas the renin-angiotensin system (RAS) is important for restoring homeostasis after dehydration, the pathways mediating the responses to intra-and extracellular dehydration may differ. Thirst responses mediated through the angiotensin type 1 receptor (AT(1)R) and angiotensin type 2 receptors (AT(2)R) respond to extracellular dehydration and intracellular dehydration, respectively. Intracellular signaling factors, such as protein kinase C (PKC), reactive oxygen species (ROS), and the mitogen-activated protein (MAP) kinase pathway, mediate the effects of central angiotensin II (ANG II). Experimental evidence also demonstrates the importance of the subfornical organ (SFO) in mediating some of the fluid intake effects of central ANG II. The purpose of this review is to highlight the importance of the SFO in mediating fluid intake responses to dehydration and ANG II.
引用
收藏
页码:R238 / R249
页数:12
相关论文
共 156 条
  • [1] Distribution of cells expressing human renin-promoter activity in the brain of a transgenic mouse
    Allen, A. M.
    O'Callaghan, E. L.
    Hazelwood, L.
    Germain, S.
    Castrop, H.
    Schnermann, J.
    Bassi, J. K.
    [J]. BRAIN RESEARCH, 2008, 1243 : 78 - 85
  • [2] Localization and function of angiotensin AT1 receptors
    Allen, AM
    Zhuo, JL
    Mendelsohn, FAO
    [J]. AMERICAN JOURNAL OF HYPERTENSION, 2000, 13 (01) : 31S - 38S
  • [3] Role of protein kinase Cβ in phorbol ester-induced c-fos gene expression in neurons of normotensive and spontaneously hypertensive rat brains
    Amemiya, T
    Kambe, T
    Fukumori, R
    Kubo, T
    [J]. BRAIN RESEARCH, 2005, 1040 (1-2) : 129 - 136
  • [4] Differential regulation of angiotensinogen and AT1A receptor mRNA within the rat subfornical organ during dehydration
    Barth, SW
    Gerstberger, R
    [J]. MOLECULAR BRAIN RESEARCH, 1999, 64 (02): : 151 - 164
  • [5] BICKERTON R, 1961, P SOC EXP BIOL MED, V106, P834
  • [6] THIRST INDUCED BY INCREASING BRAIN SODIUM CONCENTRATION IS MEDIATED BY BRAIN ANGIOTENSIN
    BLAIRWEST, JR
    BURNS, P
    DENTON, DA
    FERRARO, T
    MCBURNIE, MI
    TARJAN, E
    WEISINGER, RS
    [J]. BRAIN RESEARCH, 1994, 637 (1-2) : 335 - 338
  • [7] BOOTH DA, 1968, J PHARMACOL EXP THER, V160, P336
  • [8] Brody M.J., 1980, Frontiers in Neuroendocrinology, V6, P249
  • [9] ANTEROVENTRAL 3RD VENTRICLE PERIVENTRICULAR ABLATION - TEMPORARY ADIPSIA AND PERSISTING THIRST DEFICITS
    BUGGY, J
    JOHNSON, AK
    [J]. NEUROSCIENCE LETTERS, 1977, 5 (3-4) : 177 - 182
  • [10] PREOPTIC-HYPOTHALAMIC PERIVENTRICULAR LESIONS - THIRST DEFICITS AND HYPERNATREMIA
    BUGGY, J
    JOHNSON, AK
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1977, 233 (01): : R44 - R52