Lu Z Z, Zhang Y Y, Han Q D
Institute of Vascular Medicine, Third Hospital, Beijing Medical University.
Sheng Li Xue Bao. 1997 Aug;49(4):414-8.
The distribution of alpha 1-adrenoceptor and its subtypes in isolated aortae was compared between 12 month- and 10 week-old Wistar rats by determinating vasoconstrictor responses. In the 12 month-old rats, compared with the 10 week-old rats, (1) the maximal contraction induced by norepinephrine (NE) was reduced, without significant alteration of pD2 value; (2) the inhibitory effect of chlorethylclonidine (an irreversible antagonist for alpha 1B and alpha 1D subtype) on NE-induced contraction was weaker; (3) using NE as an agonist, the pA2 value for WB4101 (an alpha 1A- and alpha 1D-selective antagonist) was not changed, but the pA2 value for BMY7378 (an alpha 1D-selective antagonist) was decreased, while the pA2 value for sertindole (an alpha 1A-selective antagonist) was increased. Thus, differently from the 10 week-old rats in which only alpha 1D-adrenoceptors mediate NE-induced contraction in aortae, both alpha 1A- and alpha 1D-adrenoceptors (mainly alpha 1A) mediate the response in the 12 month-old rats.
通过测定血管收缩反应,比较了12月龄和10周龄Wistar大鼠离体主动脉中α1-肾上腺素能受体及其亚型的分布。在12月龄大鼠中,与10周龄大鼠相比,(1)去甲肾上腺素(NE)诱导的最大收缩降低,但pD2值无显著改变;(2)氯乙可乐定(一种α1B和α1D亚型的不可逆拮抗剂)对NE诱导收缩的抑制作用较弱;(3)以NE为激动剂,WB4101(一种α1A和α1D选择性拮抗剂)的pA2值未改变,但BMY7378(一种α1D选择性拮抗剂)的pA2值降低,而舍吲哚(一种α1A选择性拮抗剂)的pA2值升高。因此,与10周龄大鼠不同,在10周龄大鼠中只有α1D-肾上腺素能受体介导主动脉中NE诱导的收缩,而在12月龄大鼠中,α1A和α1D-肾上腺素能受体(主要是α1A)均介导该反应。