Novel 1, 2, 3-triazole derivatives useful as modulators of nicotinic acetylcholine receptors.
用作烟碱型乙酰胆碱受体的调节剂的新颖的1,2,3 -三唑衍生物。
Objective Changes in the contents and function of nicotine acetylcholine receptors in skeletal muscle of rats during aging.
目的探讨大鼠老化过程中骨骼肌乙酰胆碱受体的含量及功能变化。
Objective to investigate the changes of M-acetylcholine receptors in atrial and ventricular myocardium of rats at different ages.
目的观察成年大鼠心房肌和心室肌m受体密度的增龄性变化。
The compounds of the invention are found to be cholinergic ligands at the nicotinic acetylcholine receptors and modulators of the monoamine receptors and transporters.
发现本发明化合物是烟碱样乙酰胆碱受体的胆碱能配体和单胺受体和转运蛋白的调节剂。
This study shows that there is some pharmacological difference between Imidacloprid and Dimehypo during their interactions with the postsynaptic acetylcholine receptors.
这些结果说明，吡虫啉、杀虫双和乙酰胆碱受体发生相互作用过程存在差异。
Objective to investigate the influence of fluorosis on nicotinic acetylcholine receptors (nAChRs) in protein and gene levels in SH-SY5Y cells and the mechanism of the receptor modification.
目的观察氟中毒对神经细胞中尼古丁受体亚单位蛋白和基因表达水平的影响及氟中毒引起尼古丁受体功能改变的发生机制。
Neuronal nicotinic acetylcholine receptors (nAChRs) are widely distributed in the central nervous system, and they participate in complex neuronal signal transduction and regulation in the brain.
神经元烟碱受体广泛地分布于中枢神经系统并参与脑内信号传导系统的调节过程。
Symptoms associated with Parkinson's can be helped by reducing acetylcholine-mediated neurotransmission in the brain, but little work has focused on brainstem muscarine receptors in this disease.
帕金森病的这些症状可以通过减少脑内乙酰胆碱介导的神经传递而缓解，但很少有人注意到脑干细胞毒蕈碱受体的作用。
NA contains a great variety of neurotransmitters including acetylcholine, biogenic amines, neuropeptides and amino acids, and their receptors.
疑核内含有大量的神经递质，如乙酰胆碱，生物胺，神经肽，氨基酸等及其受体。
Included here are drugs that directly stimulate muscarinic receptors and drugs that potentiate cholinergic activity, usually by slowing the breakdown of acetylcholine (CHOLINESTERASE INHIBITORS).
包括直接兴奋毒蕈碱受体的药物和(胆碱酯酶抑制剂)。
Included here are drugs that directly stimulate muscarinic receptors and drugs that potentiate cholinergic activity, usually by slowing the breakdown of acetylcholine (CHOLINESTERASE INHIBITORS).
包括直接兴奋毒蕈碱受体的药物和(胆碱酯酶抑制剂)。
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