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Effects of Bromocriptine on Responses to Stress in Spontaneously Hypertensive Rats

 

作者: JAMES SOWERS,  

 

期刊: Hypertension  (OVID Available online 1981)
卷期: Volume 3, issue 5  

页码: 544-550

 

ISSN:0194-911X

 

年代: 1981

 

出版商: OVID

 

关键词: bromocriptine;immobilization stress;spontaneously hypertensive rats

 

数据来源: OVID

 

摘要:

SUMMARY Treatment of 2-montb-old spontaneously hypertensive rats (SHR) and age-matched Wlstar- Kyoto (WKY) normotensive controls with the dopamine agonist, bromocriptine, for 7 days significantly affected hormonal responses to immobilization stress in both groups. However, basal blood pressures and pressor responses to immobilization stress were significantly reduced only in SHR. Basal levels of catecholamines were similar in the two groups of rats, but catecbolamlne responses to immobilization stress following saline (vehicle) treatment were markedly greater in SHR; following bromocriptine treatment for 7 days, catecholamine responses were similar in the two groups. Basal serum prolactin levels and prolactin responses to immobilization were greater in SHR after saline treatment; after bromocriptine, they were similar in the two groups. Basal plasma renin activity (PRA) and PRA responses to immobilization were significantly less in SHR following saline treatment; after bromocriptine treatment, these responses were paradoxically greater in SHR without being significantly changed in WKY. Basal levels of plasma aldosterone and corticosterone following saline were significantly greater, but responses to immobilization less, in SHR. Bromocriptine treatment decreased aldosterone and corticosterone responses to stress in WKY but paradoxically increased these responses in SHR. These results suggest that increased pressor responses to stress are dependent on heightened sympathetic nerve activity, perhaps secondary to decreased central dopaminergic activity. Increased basal prolactin levels and stress-mediated prolactin responses may be related to decreased central dopaminergic activity. Paradoxical PRA, plasma aldosterone, and corticosterone responses to stress following bromocriptine suggest altered dopaminergic modulation of these hormones in the SHR.

 

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