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The remaining 9 rats in control group, 16 rats in treated grouop and 15 rats in model group were decollated and obtained brains to detect the relative mRNA expression of nuclear receptor-related factor 1 (Nurr1) and muscarinic acetylcholine receptor 5(M5) byusing RT-PCR, which was the consequence of those comparing with reference geneβ-actin mRNA expression.

将对照组、治疗组、模型组其余9、16、15只大鼠,断头取脑,采用RT-PCR方法检测大鼠脑组织孤儿核受体及乙酰胆碱毒蕈碱型受体5(M5)mRNA相对于内参基因β-actin mRNA的相对表达值。

Objective To investigate the expression of 5 muscarinic receptor subtypes in the scleral tissue of immature guinea pigs.

目的 探讨正常幼龄豚鼠眼巩膜组织毒蕈碱受体五种亚型的表达。

However, the effects of O-desmethyltramadol on muscarinic receptor functions have not been studiedin detail.

可是 O-去甲基曲马多对毒蕈碱受体功能的作用至今还没有详细研究。

Atropine is commonly administered to inhibit the effects of acetylcholine at muscarinic receptors, the authors note.

笔者提到,阿托品是最常用的抑制毒蕈碱受体中乙酰胆碱活性的药物。

Muscarinic receptors are involved in neuronal functions in thebrain and autonomic nervous system, and much attention has beenpaid to these receptors as targets for analgesic drugs in thecentral nervous system.

毒蕈碱受体参与脑和自主神经系统中的神经元功能,人们对这些受体作为镇痛药在中枢神经系统内的靶位给予了广泛关注。

The effect of muscarinic receptors agonist-carbachol on conjunctival fibroblasts'proliferation was studied by Cell Proliferation ELISA.

Brdu酶联免疫吸附试验检测毒蕈碱受体激动剂carbachol对结膜成纤维细胞增殖的影响。

Nicorandil inhibits muscarinic activation of the ERK signaling pathway by reducing the intracellular Ca(2+) concentration.

尼可地尔通过减少细胞内钙离子浓度能阻断毒蕈碱细胞外信号调节激酶信号路径的激活。

Methods and Results—We investigatedβ-adrenergic receptor and muscarinic receptor regulation of the cardiac NCX in control and heart failure conditions in atrially paced pigs.

方法和结果:研究者对房性起搏诱发的心衰组猪和对照组猪中β肾上腺素能受体和毒蕈碱样受体对心脏NCX的调节机制进行了研究。

After radial-arm maze training, the rats were tested after injection of antagonists to muscarinic and nicotinic acetylcholine receptors to determine their reliance on cholinergic mechanisms in solving the task.

经过径向臂迷宫训练,老鼠进行了测试后拮抗剂注射毒蕈碱和烟碱型乙酰胆碱受体,确定其对胆碱能机制的依赖解决的任务。

The effects of the IV anesthetics on tension ([Ca2+]i remains constant) in the absence or the presence of muscarinic receptor activation were assessed.

测量静脉麻醉药对缺乏或存在毒蕈碱受体活性的电压的影响。

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