muscarinic receptor
毒蕈碱受体
muscarinic agonist
毒蕈碱激动剂
muscarinic antagonist
毒蕈碱拮抗剂
muscarinic blockade
毒蕈碱阻断
muscarinic activity
毒蕈碱活性
muscarinic effects
毒蕈碱效应
muscarinic stimulation
毒蕈碱刺激
muscarinic agent
毒蕈碱制剂
muscarinic drug
毒蕈碱类药物
muscarinic nerves
毒蕈碱能神经
muscarinic receptors play a vital role in the parasympathetic nervous system.
毒蕈碱受体在副交感神经系统中起着至关重要的作用。
acetylcholine acts as the primary agonist for both nicotinic and muscarinic receptors.
乙酰胆碱是烟碱型和毒蕈碱型受体的主要激动剂。
atropine is a well-known competitive antagonist of muscarinic acetylcholine receptors.
阿托品是毒蕈碱型乙酰胆碱受体的著名竞争性拮抗剂。
scientists classify muscarinic receptors into five distinct subtypes, labeled m1 through m5.
科学家将毒蕈碱受体分为五种不同的亚型，标记为m1至m5。
activation of muscarinic receptors typically leads to a decrease in heart rate.
毒蕈碱受体的激活通常会导致心率下降。
scopolamine effectively blocks muscarinic signaling in the central nervous system.
东莨菪碱有效地阻断中枢神经系统中的毒蕈碱信号传导。
the m2 muscarinic receptor subtype is predominantly found in the heart muscle.
m2毒蕈碱受体亚型主要存在于心肌中。
selective muscarinic agonists are being investigated as potential treatments for cognitive disorders.
选择性毒蕈碱激动剂正在被研究作为认知障碍的潜在治疗方法。
side effects of these drugs are often caused by non-selective muscarinic binding.
这些药物的副作用通常是由非选择性毒蕈碱结合引起的。
the signal transduction mechanism involves g-proteins coupled to the muscarinic receptor.
信号转导机制涉及与毒蕈碱受体偶联的g蛋白。
bladder contraction is regulated by the m3 muscarinic receptor subtype.
膀胱收缩受m3毒蕈碱受体亚型的调节。
pilocarpine is a medication used to stimulate muscarinic receptors in the eye.
毛果芸香碱是一种用于刺激眼部毒蕈碱受体的药物。
muscarinic receptor
毒蕈碱受体
muscarinic agonist
毒蕈碱激动剂
muscarinic antagonist
毒蕈碱拮抗剂
muscarinic blockade
毒蕈碱阻断
muscarinic activity
毒蕈碱活性
muscarinic effects
毒蕈碱效应
muscarinic stimulation
毒蕈碱刺激
muscarinic agent
毒蕈碱制剂
muscarinic drug
毒蕈碱类药物
muscarinic nerves
毒蕈碱能神经
muscarinic receptors play a vital role in the parasympathetic nervous system.
毒蕈碱受体在副交感神经系统中起着至关重要的作用。
acetylcholine acts as the primary agonist for both nicotinic and muscarinic receptors.
乙酰胆碱是烟碱型和毒蕈碱型受体的主要激动剂。
atropine is a well-known competitive antagonist of muscarinic acetylcholine receptors.
阿托品是毒蕈碱型乙酰胆碱受体的著名竞争性拮抗剂。
scientists classify muscarinic receptors into five distinct subtypes, labeled m1 through m5.
科学家将毒蕈碱受体分为五种不同的亚型，标记为m1至m5。
activation of muscarinic receptors typically leads to a decrease in heart rate.
毒蕈碱受体的激活通常会导致心率下降。
scopolamine effectively blocks muscarinic signaling in the central nervous system.
东莨菪碱有效地阻断中枢神经系统中的毒蕈碱信号传导。
the m2 muscarinic receptor subtype is predominantly found in the heart muscle.
m2毒蕈碱受体亚型主要存在于心肌中。
selective muscarinic agonists are being investigated as potential treatments for cognitive disorders.
选择性毒蕈碱激动剂正在被研究作为认知障碍的潜在治疗方法。
side effects of these drugs are often caused by non-selective muscarinic binding.
这些药物的副作用通常是由非选择性毒蕈碱结合引起的。
the signal transduction mechanism involves g-proteins coupled to the muscarinic receptor.
信号转导机制涉及与毒蕈碱受体偶联的g蛋白。
bladder contraction is regulated by the m3 muscarinic receptor subtype.
膀胱收缩受m3毒蕈碱受体亚型的调节。
pilocarpine is a medication used to stimulate muscarinic receptors in the eye.
毛果芸香碱是一种用于刺激眼部毒蕈碱受体的药物。
探索常用高频词汇