Key result
Novokinin induces vasorelaxation in the mesenteric artery of spontaneously hypertensive rats via an AT2- and IP-receptor-dependent mechanism mediated by prostaglandin I2.
Why the study?
Does novokinin induce vasorelaxation in the mesenteric artery of spontaneously hypertensive rats?
Does novokinin induce vasorelaxation in the mesenteric artery of spontaneously hypertensive rats?
Answers are grounded in this paper and cite their sources.
Novokinin induces vasorelaxation via an AT2- and IP-receptor-dependent, nitric oxide-independent mechanism involving prostaglandin I2.
In this study, we found that novokinin (Arg-Pro-Leu-Lys-Pro-Trp), a potent hypotensive peptide acting through the AT(2) receptor, has vasorelaxing activity in the mesenteric artery isolated from spontaneously hypertensive rats. The vasorelaxing activity was significantly blocked by PD123319, indomethacin, and CAY10441, which are an AT(2) receptor antagonist, a cyclooxygenase inhibitor, and an IP receptor antagonist, respectively. N(G)-nitro-L-arginine methyl ester, an inhibitor of nitric oxide synthase, did not block the vasorelaxing activity. These results suggest that the vasorelaxing activity of novokinin, which contributes to the hypotensive effect, is mainly mediated by prostaglandin I(2) (prostacyclin) and the IP receptor downstream of the AT(2) receptor.
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Yamada et al. (2008) studied Spontaneously hypertensive rats (SHRs). Novokinin was evaluated on Vasorelaxing activity. Novokinin induces vasorelaxation in the mesenteric artery of spontaneously hypertensive rats via an AT2- and IP-receptor-dependent mechanism mediated by prostaglandin I2.
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