突触前受体的药理学研究进展
作者:师晨霞,任雷鸣
Author:
收稿日期: 年卷(期)页码:2005,(05):-423-426
期刊名称:华西药学杂志
Journal Name:WEST CHINA JOURNAL OF PHARMACEUTICAL SCIENCES
关键字:突触前受体;自调受体;旁调受体;突触前调节;钙通道;钾通道
Key words:
基金项目:
中文摘要
综述了突触前受体存在的证据、分类、调节和临床意义。突触前受体按不同的分类方法可分为突触前自调受体和旁调受体;抑制性和易化性突触前受体;G-蛋白偶联型和离子通道型突触前受体。突触前受体调节递质释放的机制,可能与钙通道、钾通道及囊泡释放复合物的调节有关。通过研制合适的突触前受体的激动剂或拮抗剂,适度调节神经末梢递质的释放,可达到控制或治疗多种疾病(如高血压、精神疾患、阿尔茨海默病、心肌缺血等)的目的。
参考文献
[1]Riker WK,Roberts JRJ,Standaert FG,et al.The motor nerve termi-nal as the primary focus for drug-induced facilitation of neuromuscu-lar transmission[J].J Pharmacol Exp Ther,1957,121:286
[2]Laduron PM.Presynaptic heteroreceptors in regulation of neuronaltransmission[J].Biochem Pharmacol,1985,34(4):467
[3]Wu LG,Saggau P.Presnaptic inhibition of elicited neurotransmitterrelease[J].Trends Neurosci,1997,20(5):204
[4]Langer SZ,Scatton B,Schoemaker H,et al.Presynaptic autorecep-tors and heteroreceptors are both alive and kicking[J].Trends Phar-macol Sci,1998,19(4):127
[5]MacDermott AB,Role LW,Siegelbaum SA.Presynaptic ionotropicreceptors and the control of transmitter release[J].Annu Rev Neu-rosci,1999,22:443
[6]Watson SP,Girglestone D.Receptor and ion channel nomenclaturesupplement[J].Trends Pharmcol Sci,1996,17(5):191
[7]McGehee DS,Role LW.Presynaptic ionotropic receptors[J].CurrOpin Neurobiol,1996,6(3):342
[8]Heidelberger R,Matthews G.Calcium influx and calcium current insingle synaptic terminals of goldfish retinal bipolar neurons[J].JPhysiol,1992,447(2):235
[9]DeWaard M,Lui H,Walker D,et al.Direct binding of G-proteinβ/γcomplex to voltage dependent calcium channels[J].Nature,1997,385(6615):446
[10]Reid CA,Clements JD,Bekkers JM.Non-uniform distribution ofCa channel subtypes on presynaptic terminals of excitatory synapses inhippocampal cultures[J].J Neurosci,1997,17(8):2738
[11]Krapivinsky G,Gordon EA,Wickman B,et al.The G protein gatedatrial K+channel,IKACh,is a heteromultimer of two inwardly rectify-ing K+channel proteins[J].Nature,1995,374(6518):135
[12]Scanziani M,Gahwiler BH,Thompson SM.Presynaptic inhibition ofexcitatory synaptic transmission by muscarinic and metabotropic gluta-mate receptor activation in the hippocampus:are Ca2+channels in-volved[J].Neuropharmacology,1995,349(11):1549
[13]Haeusler G,Lues I,Minck Ko,et al.Pharmacological basis for an-tihypertensive therapy with a novel dopamine agonist[J].Eur HeartJ,1992,13(Suppl D):129
[14]Tsuda K,Masuyama Y.Presynaptic regulation of neurotransmitter re-lease in hypertension[J].Clin Exp Pharmacol Physiol,1991,18(7):455
[15]梁敏,林赛娟,梁宁,等.乌拉地尔对高血压患者血浆4种神经肽含量的影响[J].中华麻醉学杂志,2000,20(1):24
[16]Moller HJ.Amisulpride:limbic specificity and the mechanism of an-tipsychotic atypicality[J].Prog Neuropsychopharmacol Biol Psychia-try,2003,27(7):1101
[17]李永生,黄流清,邵福源.中枢毒蕈碱受体亚型及其信号转导系统与认知功能障碍[J].中国老年学杂志,2004,24(10):982
[18]李明凯,罗晓星.组胺H3受体对心血管系统的调控作用[J].中国药理学通报,2002,18(6):608
[19]Levi R,Smith NC.Histamine H3-receptors:a new frontier in my-ocardial ischemia[J].J Pharmacol Exp Ther,2000,292(3):825
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