Korean J Physiol Pharmacol.
1997 Oct;1(5):547-553.
Role of tyrosine kinases in vascular contraction in deoxycorticosterone
acetate-salt hypertensive rats
- Affiliations
-
- 1Department of Physiology, College of Medicine, Chosun University, Kwanaiu 501-759, South Korea.
Abstract
-
It has been known that activation of tyrosine kinases is involved in
signal transduction. Role of the tyrosine kinase in vascular smooth
muscle contraction was examined in deoxycorticosterone acetate
(DOCA)-salt hypertensive rats. Male Sprague-Dawley rats underwent
uninephrectomy, one week after which they were subcutaneously implanted
with DOCA (200 mg/kg) and supplied with 1% NaCl and 0.2% KCl drinking
water for 4-6 weeks. Control rats were treated the same except for that
no DOCA was implanted. Helical strips of carotid arteries were mounted
in organ baths for measurement of isometric force development.
Genistein was used as a tyrosine kinase inhibitor.
Concentration-response curves to 5-hydroxytryptamine (5-HT) shifted to
the right by genistein in both DOCA-salt hypertensive and control rats.
Although the sensitivity to genistein was similar between the two
groups, the maximum force generation by 5-HT was less inhibited by
genistein in arteries from DOCA-salt hypertensive rats than in those
from controls. Genistein-induced relaxations were attenuated in
arteries from DOCA-salt rats. Genistein affected the contraction to
phorbol 12, 13-dibutyrate (PDBu) neither in DOCA-salt nor in control
arteries. These observations suggest that tyrosine kinase is involved
in 5-HT-induced vascular contraction, of which role is reduced in
DOCA-salt hypertension.