Intravenous angiotensin induces brain c-fos expression and vasopressin release in the near-term ovine fetus

被引:14
作者
Shi, LJ
Hu, F
Morrissey, P
Yao, JM
Xu, Z
机构
[1] Harbor UCLA Med Ctr, Dept Obstet & Gynecol, Torrance, CA 90502 USA
[2] Res & Educ Inst, Torrance, CA 90502 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2003年 / 285卷 / 06期
关键词
angiotensin II; fetal brain development; arginine vasopressin;
D O I
10.1152/ajpendo.00289.2003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The effect of intravenous angiotensin II (ANG II) on fetal brain c-fos expression and arginine vasopressin (AVP) release was studied in the near-term ovine fetus. Fetuses with chronically implanted catheters received an intravenous infusion of ANG II or saline. Fetal plasma AVP concentrations were significantly increased after the peripheral administration of ANG II, with peak levels (3-fold) at 30 min after the intravenous infusion. There was no change in fetal plasma osmolality, sodium, and hematocrit levels between the control and experimental groups or between the periods before and after the infusion of ANG II. Intravenous ANG II administration induced Fos immunoreactivity (Fos-IR) in the circumventricular organs and the median preoptic nucleus of the fetal brain. Fos-IR was also demonstrated in the fetal supraoptic nuclei (SON). Double labeling demonstrated that the AVP-containing neurons in the SON were expressing c-fos in response to intravenous ANG II. These results indicate that the peripheral ANG II in the fetus may play a significant role in stimulating the central hypothalamic-neurohypophysial system during late gestation. It supports the hypothesis that circulating ANG II may act at the fetal AVP neurons in the hypothalamus in body fluid balance via the circumventricular organs, which are situated outside the blood-brain barrier, and the central neural pathway between these two brain structures has been relatively established in utero, at least at near-term.
引用
收藏
页码:E1216 / E1222
页数:7
相关论文
共 34 条
  • [1] Hypothalamic paraventricular nucleus and cardiovascular regulation
    Badoer, E
    [J]. CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2001, 28 (1-2): : 95 - 99
  • [2] BARGMANN WOLFGANG, 1951, AMER SCI, V39, P255
  • [3] 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
  • [4] Osmoreceptors in the central nervous system
    Bourque, CW
    Oliet, SHR
    [J]. ANNUAL REVIEW OF PHYSIOLOGY, 1997, 59 : 601 - 619
  • [5] Angiotensin II indirectly vasoconstricts the ovine uterine circulation
    Cox, BE
    Williams, CE
    Rosenfeld, CR
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2000, 278 (02) : R337 - R344
  • [6] EPSTEIN AN, 1978, FRONTIERS ENDOCRINOL, P101
  • [7] EPSTEIN AN, 1982, PHYSL MECH MOTIVATIO, P165
  • [8] Angiotensin, thirst, and sodium appetite
    Fitzsimons, JT
    [J]. PHYSIOLOGICAL REVIEWS, 1998, 78 (03) : 583 - 686
  • [9] EFFECT OF INTRACEREBROVENTRICULAR DEUTERIUM-OXIDE ON WATER-INTAKE AND AVP RELEASE INDUCED BY INTRAVENOUS-INFUSION OF ANGIOTENSIN-II IN SHEEP
    HJELMQVIST, H
    RUNDGREN, M
    [J]. ACTA PHYSIOLOGICA SCANDINAVICA, 1990, 138 (02): : 155 - 160
  • [10] ISMAY MJA, 1979, J PHYSIOL-LONDON, V288, P467