5-HYDROXYTRYPTAMINE-INDUCED ENDOTHELIUM-DEPENDENT AND ENDOTHELIUM-INDEPENDENT RELAXATIONS IN ISOLATED DOG ANTERIOR SPINAL SMALL ARTERIES

Citation
Jx. Wang et al., 5-HYDROXYTRYPTAMINE-INDUCED ENDOTHELIUM-DEPENDENT AND ENDOTHELIUM-INDEPENDENT RELAXATIONS IN ISOLATED DOG ANTERIOR SPINAL SMALL ARTERIES, Canadian journal of physiology and pharmacology, 75(5), 1997, pp. 357-362
Citations number
27
Categorie Soggetti
Pharmacology & Pharmacy",Physiology
ISSN journal
00084212
Volume
75
Issue
5
Year of publication
1997
Pages
357 - 362
Database
ISI
SICI code
0008-4212(1997)75:5<357:5EAE>2.0.ZU;2-V
Abstract
The mode of action of 5-hydroxytryptamine (5HT) was investigated in is olated dog anterior spinal small arteries. Lower concentrations of 5HT (10(-9)-10(-7) M) caused a dose-dependent contraction and higher conc entrations (10(-6)-10(-3) M) produced a dose-dependent relaxation of t he arteries precontracted by 10(-7) M U 46619. The 5HT-induced relaxat ion was significantly antagonized by methiothepin (10(-9)-10(-6) M). K etanserin (10(-6) M) and ICS 205-930 (3 x.10(-6) M) did not affect the 5HT-induced relaxation of the arteries. The relaxant response to 5HT was reduced significantly by mechanical rubbing of the endothelial cel ls. The 5HT-induced endothelium-independent relaxation was also antago nized significantly by methiothepin (10(-6) M). Aspirin (5 x 10(-5) Ri f) or NW-nitro-L-arginine methyl ester (L-NAME) (10(-6) M) significant ly suppressed the 5HT-induced endothelium-dependent relaxation. L-Argi nine (10(-3) M) also significantly reversed the L-NAME-induced reducti on of the 5HT-induced endothelium-dependent relaxation. Treatment with L-NAME in the presence of aspirin also produced much greater reductio n of the 5HT-induced endothelium-dependent relaxation. Isocarbacyclin (10(-9)-10(-5) M) induced a concentration-dependent relaxation of the isolated spinal small arteries precontracted by 10(-7) M U 46619. Thes e results suggest that 5HT induces endothelium-dependent and -independ ent relaxations of the isolated anterior spinal small arteries mainly via activation of 5HT(1)-like receptor and that endogenous nitric oxid e and vasodilative prostaglandins may contribute to the 5HT-induced en dothelium-dependent relaxation of the arteries.