Borea P A, Bertelli G M, Gilli G
Istituto di Farmacologia, Università di Ferrara, Italy.
Eur J Pharmacol. 1988 Feb 9;146(2-3):247-52. doi: 10.1016/0014-2999(88)90299-3.
Membrane preparations from guinea-pig brain were used to study the effects of temperature on the interaction of [3H][D-Ala2-MePhe-Gly-ol5] (DAGO), a selective mu agonist, [3H][D-Ala2,D-Leu5]enkephalin (DADLE), a nearly selective delta agonist and (+/-)[3H]ethylketazocine (EKC), a selective kappa agonist when binding was measured in the presence of an excess of DAGO and DADLE. Binding was endothermic (delta H0 = 10-17 kJ mol-1) and thus driven by the large increase in entropy (delta S0 = 200-230 J mol-1 K-1) for all ligands under examination. Van't Hoff plot for DAGO and DADLE showed a breakdown beyond 303 K which could have been due to lower in vitro stability of the proteins to conformational changes in the receptor proteins and/or to phase changes in the membranes. The present results do not agree with the hypothesis that agonist binding is associated with very small or negative delta S0 (in opposition to antagonists) in view of the information transfer involved (the biological effect).
利用豚鼠脑的膜制剂,在存在过量的[3H][D - Ala2 - MePhe - Gly - ol5](DAGO,一种选择性μ激动剂)、[3H][D - Ala2,D - Leu5]脑啡肽(DADLE,一种近乎选择性的δ激动剂)和(+/-)[3H]乙基酮唑辛(EKC,一种选择性κ激动剂)的情况下测量结合时,研究温度对这些物质相互作用的影响。结合是吸热的(ΔH0 = 10 - 17 kJ mol-1),因此对于所有被检测的配体而言,其结合是由熵的大幅增加(ΔS0 = 200 - 230 J mol-1 K-1)驱动的。DAGO和DADLE的范特霍夫图显示在303 K以上出现了异常,这可能是由于蛋白质对受体蛋白构象变化的体外稳定性较低和/或膜的相变所致。鉴于所涉及的信息传递(生物学效应),目前结果与激动剂结合与非常小或负的ΔS0(与拮抗剂相反)相关的假设不一致。