Marquardt D L, Motulsky H J, Wasserman S I
J Appl Physiol Respir Environ Exerc Physiol. 1982 Sep;53(3):731-6. doi: 10.1152/jappl.1982.53.3.731.
Muscarinic cholinergic receptors have been implicated in the regulation of bronchomotor tone, bronchial mucus secretion, and lung mast-cell mediator release. Rat lung membranes prepared by homogenization, sonication, and sedimentation of 37,000 g in sucrose have been demonstrated to possess muscarinic cholinergic receptors as assessed by radioligand binding employing l-quinuclidinyl[phenyl-4-3H]benzilate ([3H]QNB). QNB binding was saturable, stereoselective, and reversible in the presence of 1 microM atropine. The rat lung muscarinic receptor demonstrated a Kd of 0.268 +/- 0.126 (+/- SD) nM and a density of 35.4 +/- 4.6 fmol/mg protein by Scatchard analysis. The Hill coefficient was 1.015 +/- 0.085, indicating noncooperative binding. Muscarinic cholinergic receptors in the rat lung were equal in number to alpha 1-adrenergic receptors, but beta-adrenergic receptors are 14 times more prevalent as defined by [3H]prazosin and l-[propyl-2, 3-3H]dihydroalprenolol ([3H]DNA) binding. Dexamethasone (140 micrograms) administration in vivo caused an increase in all three receptor types by 24-48 h, suggesting steroids regulate not only the number of beta-receptors but also that of alpha- and cholinergic receptors. These data suggest new avenues by which steroids may regulate lung function.
毒蕈碱型胆碱能受体与支气管运动张力、支气管黏液分泌及肺肥大细胞介质释放的调节有关。通过匀浆、超声处理及在蔗糖中37,000g离心沉淀制备的大鼠肺膜,经使用l-喹核醇基[苯基-4-³H]苯甲酸酯([³H]QNB)的放射性配体结合评估,已证明其具有毒蕈碱型胆碱能受体。在1μM阿托品存在下,QNB结合是可饱和的、立体选择性的且可逆的。通过Scatchard分析,大鼠肺毒蕈碱受体的解离常数(Kd)为0.268±0.126(±标准差)nM,蛋白质密度为35.4±4.6fmol/mg。希尔系数为1.015±0.085,表明为非协同结合。大鼠肺中的毒蕈碱型胆碱能受体数量与α1-肾上腺素能受体相等,但根据[³H]哌唑嗪和l-[丙基-2,3-³H]二氢阿普洛尔([³H]DNA)结合确定,β-肾上腺素能受体的数量多14倍。体内给予地塞米松(140μg)在24 - 48小时内使所有三种受体类型的数量增加,提示类固醇不仅调节β-受体的数量,还调节α-和胆碱能受体的数量。这些数据提示了类固醇调节肺功能的新途径。