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- Pirenzenpine is a relatively selective M1 subtype muscarinic receptor antagonist and used to treat digestive system ulcer. 哌仑西平是一种M1受体选择性的抗胆碱药,临床上用于治疗消化性溃疡。
- Nilvebrant L, Hallen B, Larsson G.Tolterodine, a new bladder selective muscarinic receptor antagonist: Preclinical pharmacological and clinical data[J].Life Sci,1997,60:1129. 吴士良;杨勇;薛兆英;等.;新型抗胆碱能药物托特罗定治疗膀胱过度活动症的临床研究[J]
- Keywords tolterodine;muscarinic receptor antagonist;incontinence;synthesis;resolution; 托特罗定;毒蕈碱受体拮抗剂;尿失禁;合成;拆分;
- muscarinic receptor antagonist 毒蕈碱受体拮抗剂
- Human Interleukin 1 receptor antagonist， IL... 人白介素1受体拮抗剂（IL1Ra）试剂盒；
- Experimental study of selective muscarinic receptor antagonists on attenuation of morphine tolerance and dependence in rats 选择性毒蕈碱受体拮抗剂减轻吗啡耐受和依赖的实验研究
- Amiodarone also acts as a thyroid hormone receptor antagonist. 胺碘酮也可作为甲状腺激素受体拮抗剂。
- Objective:To synthesize a new H1 receptor antagonist olopatadine. 目的:合成新型H1受体阻滞剂奥洛他定。
- Spectroscopic Analysis on 5-HT3 Receptor Antagonist Dolasetron Mesylate[J]. 引用该论文 陈晓红;张倩芝;张卫红;陈建.
- The modulatory effect of Ach on the IATP may be achieved by activating muscarinic receptor (M receptor). 乙酰胆碱对I(下标ATP)的调制作用是通过毒蕈碱样乙酰胆碱受体（M受体）激活实现的。
- M5 muscarinic receptor may be a useful pharmacological target for the treatment of heroin addiction. M5毒蕈碱受体可作为改变海洛因行为学效应的有效药理学靶点之一.
- At the end of observation, the activity of AChE and ATPase and the gene expression of muscarinic receptor, M1 and M2 in cardiac muscle were measured. 同时测定心脏AChE活力、ATPase活力和M1、M2受体基因表达水平。
- The effects of the receptor antagonist of glutamic acid on the brain tissue of severely scalded rats. 谷氨酸受体拮抗剂在严重烧伤大鼠脑组织中的作用。
- The classical DA receptor antagonist haloperi-dol at 5 mg/kg(i.p.) produced a 45.1% decrease. 腹腔注射典型的多巴胺受体阻滞剂氟哌啶醇5mg/kg下降45.;1%25。
- Thymus tissues were cultured with or without retinoic acid and/or retinoic acid receptor antagonist. 方法:采用体外胸腺组织培养体系,在培养体系中加入视黄酸或视黄酸受体拮抗剂。
- The endothelin receptor antagonist bosentan is one of the effective drugs for pulmonary arterial hypertension. 内皮素受体拮抗剂波生坦是治疗肺动脉高压的有效药物之一。
- CONCLUSION The research indicated that cetirizine is an anti-allergic H1 receptor antagonist with high efficacy. 结论 盐酸西替利嗪是一个具有抗过敏、高效、速效的H1受体阻断药。
- In contrast, microinjection of M5 muscarinic receptor sense oligonucleotide (S-ONs) into the VTA did not block the expression of behavioral sensitization or the expression of FosB in the NAc or DG in the heroin sensitized rats. 但VTA中注射有义寡核苷酸(M5S-ONs)不能明显抑制大鼠行为敏化的表达,也不能抑制海洛因敏化大鼠NAc和DG中FosB蛋白的表达。
- The enhancement of FosB-positive neurons in the NAc or DG could be inhibited by microinjection of M5 muscarinic receptor AS-ONs into the VTA before the heroin-induced locomotor sensitization was performed. 海洛因诱导的行为敏化大鼠中NAc及DG中的FosB免疫反应阳性神经元的表达增加,而在VTA内注射M5AS-ONs能明显抑制NAc及DG中FosB阳性神经元表达的增加;
