5-hydroxytryptamine-induced relaxation of neonatal porcine vena cava in vitro.

Abstract:

:5-hydroxytryptamine (5-HT) caused concentration-dependent relaxation of isolated rings from porcine vena cava contracted with alpha-methyl 5-HT or prostaglandin F2 alpha. Relaxation was not blocked by propranolol (1 micron), atropine (1 micron), indomethacin (3 microns), mepyramine (1 micron), cimetidine (1 micron), or cocaine (10 microns). Further receptor analysis could not be performed by antagonism of the relaxant response but was possible using 5-HT induced increases in cyclic AMP. Methysergide (1 micron) but not cyproheptadine (0.1 micron), specifically antagonised the 5-HT induced increase in cyclic AMP with an estimated pA2 of 7.19. The alpha-methyl analogue of 5-HT, a potent agonist at M and D receptors, did not cause relaxation or elevate cyclic AMP. These results suggest that the 5-HT receptor described here is not of the classical M or D type and unlike that described thus far in the vasculature. This receptor shares some similarities with brain 5-HT1 receptors since both may be linked with adenylate cyclase.

journal_name

Life Sci

journal_title

Life sciences

authors

Trevethick MA,Feniuk W,Humphrey PP

doi

10.1016/0024-3205(84)90240-6

subject

Has Abstract

pub_date

1984-07-30 00:00:00

pages

477-86

issue

5

eissn

0024-3205

issn

1879-0631

pii

0024-3205(84)90240-6

journal_volume

35

pub_type

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