1) NMDA receptor antagonist

NMDA受体拮抗剂
1.
objective The effect was investigated to induce NSC proliferation and differentiation in the adult rat SGZ、SVZ and cortex by NMDA receptor antagonist administration following focal ischemic insults produced by middle cerebral artery occlusion (MCAO).
结论 NMDA受体拮抗剂MK- 80 1在脑缺血后,能促进NSC的增殖、分化。
2.
Investigation of Internal Activating Neural Stem Cell by NMDA Receptor Antagonist Administration Following Focal Ischemic Insults;
结论:NMDA受体拮抗剂MK801在脑缺血后,能促进大鼠海马区NSCs的增殖、分化。
2) NMDA receptor antagonists

NMDA受体拮抗剂
1.
Objective To study the effect of NMDA receptor antagonists and GABA receptor antagonists on the dopamine content in the global cerebra of mice with Parkinson disease,providing theory basis for the pathogenesis of Parkinson disease.
方法采用MPTP腹腔注射建立C57BL小鼠PD模型,同时分别腹腔注射兴奋性氨基酸NMDA受体拮抗剂ketamine和GABA受体拮抗剂bicucullin,采用荧光分光光度计法测定各组小鼠全脑DA的含量。
2.
Objective To study the effect of NMDA receptor antagonists on the dopamine contents in the global cerebra of mice with Parkinson s disease,providing theory basis for the pathogenesis of Parkinson s disease.
方法采用MPTP腹腔注射建立C57BL小鼠帕金森氏病模型,同时用兴奋性氨基酸NMDA受体拮抗剂Ketamine和GABA受体拮抗剂,测定小鼠脑内多巴胺的含量。
3) Receptor antagonist

受体拮抗剂
1.
Advances on leukotrienes and leukotriene receptor antagonists in asthma;

白三烯受体拮抗剂研究新进展
2.
Eplerenone——a new aldosterone receptor antagonist with cardiovascular protective effect;

对心血管具有保护作用的醛固酮受体拮抗剂依普利酮
3.
Anti-asthmatic effects of interleukin-1 receptor antagonist in sensitized guinea pigs;

白介素-1受体拮抗剂对致敏豚鼠的抗喘作用(英文)
4) 5-HT3 receptor antagonist

5-HT3受体拮抗剂
1.
Ondansetron Hydrochloride is a high effective and high selective 5-HT3 receptor antagonist and is used on anti-emesis after chemotherapy and radiotherapy and postoperation.
盐酸昂丹司琼(Ondansetron Hydrochloride)是一种高效,高选择性的5-HT3受体拮抗剂[1,2],用于对抗癌症化学治疗和放射治疗引起的呕吐以及手术后的急性呕吐[3-5]。
5) AT1 receptor antagonist

AT1受体拮抗剂
1.
Objective To investigate the effects of AT1 receptor antagonist candesartan on acute pancreatitis(AP) of rats.
结论早期应用AT1受体拮抗剂坎地沙坦可以明显减轻大鼠胰腺的急性炎症病变及损伤。
6) H1-receptor antagonist

H1-受体拮抗剂
补充资料:NMDA
分子式:C5H9NO4
分子量:147.13
CAS号:6384-92-5
性质:熔点187-192°C。比旋光度-28° (c=1, HCl 6N)。水溶性slightly soluble。
分子量:147.13
CAS号:6384-92-5
性质:熔点187-192°C。比旋光度-28° (c=1, HCl 6N)。水溶性slightly soluble。
说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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