C-FOS EXPRESSION IN BRAIN IN RESPONSE TO HYPOTENSION AND HYPERTENSION IN CONSCIOUS RATS

被引:110
作者
GRAHAM, JC
HOFFMAN, GE
SVED, AF
机构
[1] UNIV PITTSBURGH,DEPT NEUROSCI,PITTSBURGH,PA 15260
[2] UNIV PITTSBURGH,DEPT NEUROBIOL,PITTSBURGH,PA 15260
来源
JOURNAL OF THE AUTONOMIC NERVOUS SYSTEM | 1995年 / 55卷 / 1-2期
关键词
BARORECEPTOR; NUCLEUS TRACTUS SOLITARIUS; PARAVENTRICULAR NUCLEUS; SUPRAOPTIC NUCLEUS; HYPOTHALAMUS; ISLANDS OF CALLEJA; CARDIOVASCULAR REGULATION;
D O I
10.1016/0165-1838(95)00032-S
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Hypotension- and hypertension-evoked expression of the protein product, Fos, of the immediate early gene c-fos was assessed throughout the rat brain as an approach for describing the neuronal populations that respond to alterations in arterial blood pressure. Conscious, chronically catheterized rats were treated with the vasoconstricting drug phenylephrine or the vasodilatating drug hydralazine to increase or decrease, respectively, arterial pressure by approx. 40 mmHg for 90 min. Rats were then anaesthetized, fixed by vascular perfusion, and sections representing the entire brain were processed for the immunocytochemical localization of Fos. In control rats treated with isotonic saline, few Fos-positive neurons were observed. In contrast, phenylephrine and hydralazine treatments resulted in different, yet reproducible, patterns of Fos expression in the brain, with hydralazine evoking Fos expression in more brain regions than phenylephrine. Brain regions containing Fos-positive neurons in rats treated with hydralazine included nucleus tract-us solitarius, area postrema, caudal ventrolateral medulla, rostral ventrolateral medulla, bed nucleus of the stria terminalis, amygdala, paraventricular nucleus, supraoptic nucleus, subfornical organ and the Islands of Calleja. The nucleus tractus solitarius, paraventricular nucleus and the amygdala also contained Fos-positive neurons in phenylephrine-treated rats, although the number of Fos-positive neurons was always less than that noted in the hydralazine-treated rats and the location of Fos-positive neurons within these regions tended to differ between treatments. These results generally fit within an emerging understanding of brain circuitry underlying cardiovascular regulation.
引用
收藏
页码:92 / 104
页数:13
相关论文
共 56 条
[1]   MONOSYNAPTIC CONNECTION FROM CAUDAL TO ROSTRAL VENTROLATERAL MEDULLA IN THE BARORECEPTOR REFLEX PATHWAY [J].
AGARWAL, SK ;
CALARESU, FR .
BRAIN RESEARCH, 1991, 555 (01) :70-74
[2]   LIGHT REGULATES EXPRESSION OF A FOS-RELATED PROTEIN IN RAT SUPRACHIASMATIC NUCLEI [J].
ARONIN, N ;
SAGAR, SM ;
SHARP, FR ;
SCHWARTZ, WJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (15) :5959-5962
[3]   HEMORRHAGE-INDUCED PRODUCTION OF FOS IN NEURONS OF THE LAMINA TERMINALIS - ROLE OF ENDOGENOUS ANGIOTENSIN-II [J].
BADOER, E ;
OLDFIELD, BJ ;
MCKINLEY, MJ .
NEUROSCIENCE LETTERS, 1993, 159 (1-2) :151-154
[4]   A COMPARISON OF HYPOTENSIVE AND NONHYPOTENSIVE HEMORRHAGE ON FOS EXPRESSION IN SPINALLY PROJECTING NEURONS OF THE PARAVENTRICULAR NUCLEUS AND ROSTRAL VENTROLATERAL MEDULLA [J].
BADOER, E ;
MCKINLEY, MJ ;
OLDFIELD, BJ ;
MCALLEN, RM .
BRAIN RESEARCH, 1993, 610 (02) :216-223
[5]   DISTRIBUTION OF HYPOTHALAMIC, MEDULLARY AND LAMINA TERMINALIS NEURONS EXPRESSING FOS AFTER HEMORRHAGE IN CONSCIOUS RATS [J].
BADOER, E ;
MCKINELY, MJ ;
OLDFIELD, BJ ;
MCALLEN, RM .
BRAIN RESEARCH, 1992, 582 (02) :323-328
[6]  
BLASCHKE TF, 1980, PHARMACOL BASIS THER, P739
[7]   CARDIOVASCULAR NEURONS OF BRAIN-STEM WITH PROJECTIONS TO SPINAL-CORD [J].
BROWN, DL ;
GUYENET, PG .
AMERICAN JOURNAL OF PHYSIOLOGY, 1984, 247 (06) :1009-1016
[8]  
BROWN DL, 1985, CIRC RES, V56, P359
[9]   CARDIOVASCULAR AND SINGLE-UNIT RESPONSES ELICITED BY STIMULATION OF THE ISLANDS OF CALLEJA AND BY CHANGES IN ARTERIAL-PRESSURE [J].
CALARESU, FR ;
ZHANG, J ;
CHITRAVANSHI, VC ;
MCKITRICK, DJ .
BRAIN RESEARCH, 1994, 655 (1-2) :45-50
[10]   UNITS IN THE AMYGDALA RESPONDING TO ACTIVATION OF CAROTID BARORECEPTORS AND CHEMORECEPTORS [J].
CECHETTO, DF ;
CALARESU, FR .
AMERICAN JOURNAL OF PHYSIOLOGY, 1984, 246 (05) :R832-R836