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豚鼠心房细胞中P2嘌呤受体刺激增强延迟整流钾电流

Enhancement of delayed rectifier K+ current by P2-purinoceptor stimulation in guinea-pig atrial cells.

作者信息

Matsuura H, Tsuruhara Y, Sakaguchi M, Ehara T

机构信息

Department of Physiology, Saga Medical School, Japan.

出版信息

J Physiol. 1996 Feb 1;490 ( Pt 3)(Pt 3):647-58. doi: 10.1113/jphysiol.1996.sp021174.

Abstract
  1. We studied the effects of P2-purinoceptor stimulation on the delayed rectifier K+ current (IK) in guinea-pig atrial myocytes using a whole-cell voltage-clamp technique. 2. External application of ATP increased IK, evoked by a 500 ms depolarizing pulse from a holding potential of -40 mV, under conditions in which the L-type Ca2+ channel was blocked; the effect was dose dependent with a half-maximal concentration (K1/2) of 0.95 microM. ATP (50 microM) produced a maximal increase of IK of about a factor of 2. 3. External ADP also enhanced IK in a dose-dependent manner with a K1/2 of 3.65 microM, whereas adenosine (100 microM) failed to evoke this response. Theophylline (500 microM), a blocker of the Pi-purinoceptor, did not antagonize the stimulating action of ATP on IK. These results indicate that IK was enhanced via P2-purinoceptors. 4. External ATP or ADP did not produce a significant change in the current kinetics of IK. 5. Pre-incubation of the atrial myocytes with pertussis toxin (PTX, 5 micrograms ml-1) did not affect the stimulating action of ATP on IK, indicating that PTX-sensitive G proteins did not mediate the ATP action. 6. The enhancement of IK by ATP developed slowly; the effects usually reached a maximum approximately 30-60 s after the application of ATP. This suggests the involvement of a diffusible cytosolic second messenger(s) in the response. ATP could further increase IK after maximal enhancement by isoprenaline (0.5-1.0 microM), suggesting that the intermediate steps were independent of cyclic AMP-dependent protein kinase (protein kinase A). 7. Potentiation of IK by ATP was not attenuated by either (i) pretreatment of the cells with 5 microM 1-(5-isoquinolinylsulphonyl)-2-methylpiperazine dihydrochloride (H-7) or (ii) intracellular perfusion of 20 mM 1,2-bis(O-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid (BAPTA), suggesting that protein kinase C and intracellular Ca2+ did not mediate the response. 8. It is concluded that the activation of P2-purinoceptors increases IK through intracellular mechanisms independent of protein kinase A, protein kinase C or intracellular free Ca2+ in guinea-pig atrial myocytes.
摘要
  1. 我们采用全细胞膜片钳技术研究了P2嘌呤受体刺激对豚鼠心房肌细胞延迟整流钾电流(IK)的影响。2. 在L型钙通道被阻断的条件下,从-40 mV的 holding 电位施加500 ms去极化脉冲诱发IK,胞外施加ATP可增加IK;该效应呈剂量依赖性,半数最大浓度(K1/2)为0.95 μM。ATP(50 μM)使IK最大增加约2倍。3. 胞外ADP也以剂量依赖性方式增强IK,K1/2为3.65 μM,而腺苷(100 μM)未能诱发此反应。磷酸嘌呤受体阻断剂茶碱(500 μM)不拮抗ATP对IK的刺激作用。这些结果表明IK通过P2嘌呤受体增强。4. 胞外ATP或ADP对IK的电流动力学未产生显著变化。5. 用百日咳毒素(PTX,5 μg/ml)预孵育心房肌细胞不影响ATP对IK的刺激作用,表明PTX敏感的G蛋白不介导ATP的作用。6. ATP对IK的增强作用发展缓慢;效应通常在施加ATP后约30 - 60 s达到最大值。这表明反应涉及一种可扩散的胞质第二信使。在异丙肾上腺素(0.5 - 1.0 μM)最大增强后,ATP可进一步增加IK,表明中间步骤独立于环磷酸腺苷依赖性蛋白激酶(蛋白激酶A)。7. ATP对IK的增强作用未被以下两种情况减弱:(i)用5 μM 1 -(5 - 异喹啉磺酰基)- 2 - 甲基哌嗪二盐酸盐(H - 7)预处理细胞;(ii)细胞内灌注20 mM 1,2 - 双(O - 氨基苯氧基)乙烷 - N,N,N',N' - 四乙酸(BAPTA),表明蛋白激酶C和细胞内Ca2+不介导该反应。8. 结论是,在豚鼠心房肌细胞中,P2嘌呤受体的激活通过独立于蛋白激酶A、蛋白激酶C或细胞内游离Ca2+的细胞内机制增加IK。

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