Häggblad J, Heilbronn E
Br J Pharmacol. 1983 Nov;80(3):471-6. doi: 10.1111/j.1476-5381.1983.tb10717.x.
The effect of some drugs on the release of endogenous acetylcholine from the phrenic nerve-hemidiaphragm preparation of the rat was measured. Muscarinic ligands had no effect. 8-Br-cyclic GMP, a penetrating analogue of cyclic guanosine 3',5'-monophosphate (cyclic GMP) was also without effect. 8-Br-cyclic AMP somewhat enhanced the basal release while the potassium-induced release remained unaltered. In supersensitivity experiments, no specific binding of ligand [3H]-quinuclidinylbenzilate [( 3H]-QNB) was found in homogenates of the diaphragm, either before or after atropine treatment, while concomitant binding studies in the CNS demonstrated the expected increase in muscarinic binding sites after atropine. Our conclusion is that muscarinic acetylcholine receptors are probably absent from the presynaptic motor endplate area of the rat. Certain preliminary results suggest that a presynaptic nicotinic mechanism might be involved in the release of acetylcholine.
测定了某些药物对大鼠膈神经 - 半膈制备物中内源性乙酰胆碱释放的影响。毒蕈碱配体无作用。8 - 溴环鸟苷酸(8 - Br - cyclic GMP),一种环鸟苷3',5'-单磷酸(环鸟苷酸,cyclic GMP)的可渗透类似物,也无作用。8 - 溴环腺苷酸(8 - Br - cyclic AMP)在一定程度上增强了基础释放,而钾诱导的释放保持不变。在超敏实验中,无论是在阿托品处理之前还是之后,在膈膜匀浆中均未发现配体[³H] - 奎宁环基苯甲酸酯([³H] - QNB)的特异性结合,而在中枢神经系统进行的同步结合研究表明,阿托品处理后毒蕈碱结合位点有预期的增加。我们的结论是,大鼠突触前运动终板区域可能不存在毒蕈碱型乙酰胆碱受体。某些初步结果表明,突触前烟碱机制可能参与乙酰胆碱的释放。