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牛海马体中5-羟色胺1A受体与叔胺类局部麻醉剂的相互作用。

Interaction of serotonin1A receptors from bovine hippocampus with tertiary amine local anesthetics.

作者信息

Kalipatnapu Shanti, Chattopadhyay Amitabha

机构信息

Centre for Cellular and Molecular Biology, Uppal Road, Hyderabad, India.

出版信息

Cell Mol Neurobiol. 2004 Jun;24(3):403-22. doi: 10.1023/b:cemn.0000022771.33702.85.

Abstract
  1. We have examined the interaction of tertiary amine local anesthetics with the bovine hippocampal serotonin1A (5-HT1A) receptor, an important member of the G-protein-coupled receptor superfamily. 2. The local anesthetics inhibit specific agonist and antagonist binding to the 5-HT1A receptor at a clinically relevant concentration range of the anesthetics. This is accompanied by a concomitant reduction in the binding affinity of the 5-HT1A receptor to the agonist. Interestingly, the extent of G-protein coupling of the receptor is reduced in the presence of the local anesthetics. 3. Fluorescence polarization measurements using depth-dependent fluorescent probes show that procaine and lidocaine do not show any significant change in membrane fluidity. On the other hand, tetracaine and dibucaine were found to alter fluidity of the membrane as indicated by a fluorescent probe which monitors the headgroup region of the membrane. 4. The local anesthetics showed inhibition of agonist binding to the 5-HT1A receptor in membranes depleted of cholesterol more or less to the same extent as that of control membranes in all cases. This suggests that the inhibition in ligand binding to the 5-HT1A receptor brought about by local anesthetics is independent of the membrane cholesterol content. 5. Our results on the effects of the local anesthetics on the ligand binding and G-protein coupling of the 5-HT1A receptor support the possibility that G-protein-coupled receptors could be involved in the action of local anesthetics.
摘要
  1. 我们研究了叔胺类局部麻醉药与牛海马5-羟色胺1A(5-HT1A)受体的相互作用,该受体是G蛋白偶联受体超家族的重要成员。2. 局部麻醉药在临床相关浓度范围内抑制特异性激动剂和拮抗剂与5-HT1A受体的结合。这伴随着5-HT1A受体对激动剂结合亲和力的相应降低。有趣的是,在局部麻醉药存在的情况下,受体的G蛋白偶联程度降低。3. 使用深度依赖性荧光探针的荧光偏振测量表明,普鲁卡因和利多卡因在膜流动性方面没有任何显著变化。另一方面,丁卡因和布比卡因被发现会改变膜的流动性,这由监测膜头基团区域的荧光探针所表明。4. 在所有情况下,局部麻醉药在去除胆固醇的膜中对激动剂与5-HT1A受体结合的抑制程度与对照膜或多或少相同。这表明局部麻醉药对5-HT1A受体配体结合的抑制与膜胆固醇含量无关。5. 我们关于局部麻醉药对5-HT1A受体配体结合和G蛋白偶联作用的结果支持了G蛋白偶联受体可能参与局部麻醉药作用的可能性。

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