Skärby T V, Larsson B
Department of Clinical Pharmacology, Lund University Hospital, Sweden.
J Auton Pharmacol. 1987 Sep;7(3):185-98. doi: 10.1111/j.1474-8673.1987.tb00148.x.
1 The influence on the shape of the Schild plot by a two-receptor system was studied in both functional and theoretical studies. In the functional studies, the alpha-adrenoreceptors in cat lingual arteries were studied since both alpha 1- and alpha 2-adrenoreceptors have been suggested to contribute to the noradrenaline-induced contractile response in this tissue. 2 The Schild plots constructed using noradrenaline (NA) as agonist and prazosin as antagonist gave a straight line with a slope close to unity. In contrast, the corresponding Schild plot constructed for rauwolscine appeared to be biphasic. 3 The results obtained in the functional study were discussed in view of Schild plots obtained from a theoretical model which was designed to take into consideration the presence of two distinct types of receptor, the percentile proportions of which could be altered. 4 The theoretical model indicates that the shape of the Schild plot can vary considerably depending on the relative contribution of each receptor subtype to the contractile response, the selectivity of the antagonist, and the range and number of antagonist concentrations used. 5 It is suggested that a response is predominantly mediated by alpha 1-adrenoreceptors and less by alpha 2-adrenoreceptors when the Schild plot for prazosin gives a slope close to unity and has a pA2-value representative for alpha 1-adrenoreceptors, and rauwolscine gives a slope less than unity and a significant shift of the NA concentration-response curve in concentrations around 10(-8) M. When the reverse is true (but with a significant shift caused by prazosin already at a concentration around 10(-9) M) the contraction elicited by NA is proposed to be predominantly mediated by alpha 2-adrenoreceptors and less by alpha 1-adrenoreceptors.
1 在功能和理论研究中均对双受体系统对希尔德图形状的影响进行了研究。在功能研究中,对猫舌动脉中的α - 肾上腺素能受体进行了研究,因为已有研究表明α1和α2肾上腺素能受体均参与该组织中去甲肾上腺素诱导的收缩反应。2 以去甲肾上腺素(NA)为激动剂、哌唑嗪为拮抗剂构建的希尔德图呈斜率接近1的直线。相比之下,为萝芙木碱构建的相应希尔德图似乎呈双相。3 鉴于从一个理论模型获得的希尔德图,对功能研究中获得的结果进行了讨论,该理论模型旨在考虑两种不同类型受体的存在,其百分比比例可以改变。4 理论模型表明,希尔德图的形状会根据每种受体亚型对收缩反应的相对贡献、拮抗剂的选择性以及所用拮抗剂浓度的范围和数量而有很大变化。5 有人提出,当哌唑嗪的希尔德图斜率接近1且具有代表α1肾上腺素能受体的pA2值,而萝芙木碱的斜率小于1且NA浓度 - 反应曲线在10^(-8) M左右的浓度下有明显偏移时,反应主要由α1肾上腺素能受体介导,α2肾上腺素能受体介导作用较小。当情况相反时(但哌唑嗪在约10^(-9) M浓度时就已引起明显偏移),则认为NA引起的收缩主要由α2肾上腺素能受体介导,α1肾上腺素能受体介导作用较小。