Department of Pharmacology, Shiga University of Medical Sciences, Otsu, Shiga, Japan.
J Pharmacol Sci. 2010;112(3):378-81. doi: 10.1254/jphs.09316sc. Epub 2010 Feb 18.
We compared mechanical responses to uridine-5'triphosphate (UTP) and 2-(methylthio)adenosine-5'diphosphate (2MeSADP) of cerebral arteries isolated from dogs and monkeys. In the dog, UTP induced endothelium-independent contraction, whereas 2MeSADP induced endothelium-dependent relaxation that was abolished by N(G)-nitro-L-arginine (L-NA). In the monkey, both UTP and 2MeSADP induced endothelium-dependent relaxation. L-NA largely inhibited the UTP-induced relaxation whereas it partially inhibited the 2MeSADP-induced relaxation, and both remaining relaxations were abolished by charybdotoxin plus apamin. In conclusion, dog and monkey cerebral arteries respond differentially to UTP and similarly to 2MeSADP; however, involvement of endothelium-derived relaxing factor in the endothelium-dependent relaxation by 2MeSADP is quite different between the two species.
我们比较了从狗和猴子分离的脑动脉对尿苷 5'-三磷酸(UTP)和 2-(甲硫基)腺苷 5'-二磷酸(2MeSADP)的机械反应。在狗中,UTP 诱导内皮非依赖性收缩,而 2MeSADP 诱导内皮依赖性松弛,该松弛被 N(G)-硝基-L-精氨酸(L-NA)消除。在猴子中,UTP 和 2MeSADP 均诱导内皮依赖性松弛。L-NA 很大程度上抑制 UTP 诱导的松弛,而部分抑制 2MeSADP 诱导的松弛,并且两种剩余的松弛均被 Chrybdotoxin 和 Apamin 消除。总之,狗和猴脑动脉对 UTP 的反应不同,而对 2MeSADP 的反应相似;然而,在两种物种中,2MeSADP 诱导的内皮依赖性松弛中内皮衍生的舒张因子的参与完全不同。