Mld. Weinberg et al., ARACHIDONIC-ACID PRODUCTS-MEDIATED CONTRACTION INDUCED BY BRADYKININ IN RELAXED MESENTERIC ARTERIAL RINGS FROM HOLTZMAN RATS, European journal of pharmacology, 320(2-3), 1997, pp. 145-150
This study describes the contractile action of bradykinin on rat isola
ted mesenteric arterial rings and a possible mechanism responsible for
this action. Bradykinin induced dose-dependent contraction of relaxed
mesenteric arterial rings from Holtzman rats, but not from Wistar rat
s. A second bradykinin challenge in the same ring induced a very small
effect or no effect at all. Destruction of the endothelium did not mo
dify the response to bradykinin. des-Arg(9)-[leu(8)]bradykinin failed
to antagonize bradykinin's action. HOE 140 (D-Arg[Hyp(3),Thi(5),D-TiC7
,Oic(8)]bradykinin) reduced bradykinin-induced contractions. Indometha
cin abolished the contractile response to bradykinin; prostaglandin F-
2 alpha induced a long-lasting contraction, dissimilar from that induc
ed by bradykinin; L-655,240 (4-chlorobenzyl)-5-fluoro-3-methyl-indol-2
-yl]-2,2 propanoic acid), an antagonist of the thromboxane receptor, i
nhibited bradykinin-induced contractions. These results suggest that b
radykinin-induced contraction in mesenteric arterial rings is indirect
, through activation of bradykinin B-2 receptors, resulting in liberat
ion of prostanoids from outside the endothelium. Thromboxane A(2) is p
robably an intermediate in this response but we cannot exclude the par
ticipation of other prostanoids.