Kalkman H O, Engel G, Hoyer D
Eur J Pharmacol. 1986 Sep 23;129(1-2):139-45. doi: 10.1016/0014-2999(86)90345-6.
5-Hydroxytryptamine (5-HT), 5-carboxamidotryptamine (5-CT), 8-OH-DPAT and RU 24969 relax the guinea-pig ileum precontracted with histamine. This relaxation was characterized using 5-CT as agonist with a series of 8 competitive antagonists. [125I]LSD binding was measured in a membrane preparation of the longitudinal muscle of the guinea-pig ileum in the presence of 3 X 10(-7) M cinanserin in order to suppress binding to 5-HT2 receptors. There was a significant correlation (P less than 0.01) between the antagonism of 5-CT-induced relaxation (pA2 values) and the affinity values of the antagonists for [125I]LSD binding (pKD values). It was also shown that 5-CT relaxed histamine-precontracted longitudinal muscle strips of the guinea-pig ileum. The results suggest that the 5-HT receptor-mediating relaxation in the guinea-pig ileum can be labelled with [125I]LSD and that this receptor does not belong to the 5-HT2, 5-HT1A, 5-HT1B or 5-HT1C receptor subtypes.
5-羟色胺(5-HT)、5-羧酰胺色胺(5-CT)、8-羟基二丙胺基四氢萘(8-OH-DPAT)和RU 24969可使预先用组胺收缩的豚鼠回肠松弛。以5-CT作为激动剂,与一系列8种竞争性拮抗剂一起使用,对这种松弛作用进行了表征。在存在3×10⁻⁷ M西萘胺的情况下,在豚鼠回肠纵肌的膜制剂中测量[¹²⁵I]麦角酸二乙胺(LSD)结合,以抑制与5-HT₂受体的结合。5-CT诱导的松弛作用的拮抗作用(pA₂值)与拮抗剂对[¹²⁵I]LSD结合的亲和力值(pKD值)之间存在显著相关性(P<0.01)。还表明5-CT可使组胺预先收缩的豚鼠回肠纵肌条松弛。结果表明,豚鼠回肠中介导松弛作用的5-HT受体可用[¹²⁵I]LSD标记,且该受体不属于5-HT₂、5-HT₁A、5-HT₁B或5-HT₁C受体亚型。