کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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2574125 | 1561249 | 2015 | 11 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Participation of the TRP channel in the cardiovascular effects induced by carvacrol in normotensive rat Participation of the TRP channel in the cardiovascular effects induced by carvacrol in normotensive rat](/preview/png/2574125.png)
Carvacrol has been described as an agonist/antagonist of different transient receptor potential (TRP) channels and voltage-dependent calcium channels (Cavs). The aim of this study was to evaluate the role of Cav and TRP channels following carvacrol stimulation. Initially, in mesenteric artery rings carvacrol relaxed phenylephrine-induced contractions. Furthermore, carvacrol inhibited contraction elicited by CaCl2 in depolarizing nominally without Ca2 + medium and antagonized the contractions induced by S(−)-Bay K 8644 and inhibited Ca2 + currents indicating the inhibition of Ca2 + influx through L-type Cav. Additionally, carvacrol antagonized the contractions induced by CaCl2 in the presence of nifedipine/Cyclopiazonic acid/phenylephrine or nifedipine/Cyclopiazonic acid/KCl 60, suggesting a possible inhibition of calcium influx by store operated channels (SOCs), receptor operated channels (ROCs) and/or TRP channels. Interestingly, among the TRP channel blockers used, the effect induced by carvacrol was attenuated by Mg2 + and potentiated by La3 + and Gd3 +, suggesting that TRP channels are involved in relaxation induced by carvacrol. Monoterpene also induced hypotension and bradycardia in non-anesthetized normotensive rats and negative inotropic and chronotropic effects. In conclusion, these results suggest that the hypotensive effect of carvacrol is probably due to bradycardia and a peripheral vasodilatation that involves, at least, the inhibition of the Ca2 + influx through Cav and TRP channels.
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Journal: Vascular Pharmacology - Volumes 67–69, April–June 2015, Pages 48–58