期刊文献+

氨茶碱对三磷酸腺苷诱发兔窦房结电生理反应的抑制作用

Inhibitory effects of aminophylline on the electrophysiological responses to adenosine triphosphate in the rabbit sinoatrial node pacemaker cells
下载PDF
导出
摘要 目的 分析氨茶碱对三磷酸腺苷 (ATP)诱发兔窦房结电生理反应的抑制作用。方法 细胞内微电极技术记录兔离体窦房结细胞动作电位。结果 ATP( 0 3~ 3 0mmol/L)单次槽内注入给药 ,浓度依赖性减慢窦房结自发搏动速率 2 2 %~ 4 3% ,降低舒张期除极速率 4 2 9%~ 6 6 7% ,增大动作电位幅值 7 1%~ 9 2 % ,加快最大除极速率 32 0 %~ 75 5 % ,使动作电位复极 5 0 %和 90 %的时程 (APD50 和APD90 )缩短 7 1%~ 11 8%和7 3%~ 9 3%。P1受体阻断剂氨茶碱 ( 0 1mmol/L)显著拮抗ATP的作用 ,P2受体阻断剂反应蓝 2( 0 0 5mmol/L)则不影响ATP的作用。 Objective To study the inhibitory effect of aminophylline on the electrophysiological responses to adenosine triphosphate (ATP) in the rabbit sinoatrial node pacemaker cells.Methods Intracellular microelectrode method was used to record the parameters of action potential in the rabbit sinoatrial nodes. Results ATP (0 3~3 mmol/L) decreased the rate of pacemaker firing by 22%~43% and velocity of diastolic depolarization by 42 9%~66 7%, increased the amplitude of action potential(AP) by 7 1%~9 2% and maximal rate of depolarization by 32 0%~75 5%,shortened action poteutial duration (APD 50 ) by 7 1%~11 8% and APD 90 by 7 3%~9 3%,all being concentration dependent.The electrophysiological effects of ATP on pacemaker cells were significantly inhibited by P1 receptor antagonist aminophylline at 0 1 mmol/L,and the effects of ATP were not significantly affected by P2 receptor antagonist reactive blue 2 at 0 05 mmol/L.Conclusion The electrophysiological effects of ATP in the rabbit sinoatria lnode pacemaker cells might be mediated via P1 receptors.
出处 《中国药物与临床》 CAS 2003年第5期396-398,共3页 Chinese Remedies & Clinics
基金 河北省自然科学基金资助项目 (3 982 94 3 0 2 481)
关键词 氨茶碱 三磷酸腺苷 窦房结 电生理反应 抑制作用 抗心律失常药物 Adenosine triphosphate Aminophylline Sinoatrial node Rabbits Microelectrodes
  • 相关文献

参考文献10

  • 1[1]Ren LM.P receptors and their pharmacologic role in cardiovascular system.In:Su DF,ed.Cardiovascular Pharmacology.Beijing:Science Press,2001.130-149.
  • 2[2]Pelleg A,Belhassen B,Ilia R,et al.Comparative electrophysiologic effects of adenosine in the canine heart:influence of atropine,propranolol, vagotomy,dipyridamole and aminophylline.Am J Cardiol,1985,55(5):571-576.
  • 3[3]Mantelli L,Amerin S,Filippi S,et al.Blockade of adenosine receptors unmasks a stimulatory effect of ATP on cardiac contractility.Br J Pharmacol,1993,109(4):1268-1271.
  • 4[4]Belhassen B,Pelleg A.Electrophysiologic effects of adenosine triphosphate and adenosine on the mammalian heart:clinical and experimental aspects.J Am Coll Cardiol,1984,4(2):414-424.
  • 5[5]Fredholm BB,Abbracchio MP,Burnstock G,et al.Nomenclature and classification of purinoceptors.Pharmacol Rev,1994,46(2):143-156.
  • 6[6]Communi D,Raspe E,Pirotton S,et al.Cloning and functional expression of a human uridine nucleotide receptor.J Biol Chem,1996,270(52):30849-30852.
  • 7[7]Parr CE,Sullivan DM,Paradiso AM,et al.Cloning and expression of a human P2u-nucleotide receptor,a target for cystic fibrosis pharmacology.Proc Natl Acad Sci USA,1995,91(26):3275-3279.
  • 8[8]Pearson JD.Ectonucleotidases of vascular endothelial cells:characterisation and possible physiological roles.In:Kreutzberg GW,Reddington M,Zimmermann H,eds.Cellular Biology of Ectoenzymes.Berlin/Heidelberg:Springer-Verlag,1986.17-25.
  • 9[9]Pelleg A,Mitsuoka T,Erix L,et al.Adenosine mediates the negative chronotropic action of adenosine 5′-triphosphate in the canine sinus node.J Pharmacol Exp Ther,1987,242(3):791-795.
  • 10[10]Qin K,Ren LM,Zhao D.Uridine triphosphate prolongs action potential duration of guinea-pig papillary muscles via P2Y2 purinoceptors.Acta Pharmacol Sin,2001,22(1):21-25.

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部