Shishido Toshihide, Sakai Saeko, Tosaka Tsuneo
Department of Urology, Kyorin University, School of Medicine, Mitaka-shi, Tokyo, Japan.
Neurourol Urodyn. 2009;28(5):447-54. doi: 10.1002/nau.20654.
The importance of the T- and L-type Ca(2+) channels on the alpha(1)-adrenoceptor-mediated contraction of guinea-pig vas deferens was investigated in relation to the SK and BK channels.
Isometric contractile response to electrical stimulation (ES) of 50 pulses at 40 Hz was recorded. ES responses were modulated via calcium and potassium channels in the presence of purinergic inhibitors.
The alpha(1)-adrenoceptor-mediated contraction of guinea-pig vas deferens consisted of early and late alpha(1)-components. The early alpha(1)-component was insensitive to nifedipine (10 microM) but was suppressed by T-type Ca(2+) channel antagonists mibefradil and amiloride with IC50 values (microM) of 7.2 +/- 1.8 (n = 5) and 27.2 +/- 10.4 (n = 6), respectively. The late alpha(1)-component was inhibited by nifedipine, nimodipine and nicardipine with IC50 values (microM) of 0.19 +/- 0.04 (n = 5), 1.9 +/- 0.8 (n = 5), and 4.2 +/- 2.5 (n = 5), respectively. Nicardipine also inhibited the early alpha(1)-component with an IC50 value of 20.3 +/- 2.5 microM (n = 5). An SK channel antagonist apamin (1-100 nM) increased both early and late alpha(1)-components. A BK channel antagonist iberiotoxin (100 nM) increased the late alpha(1)-component without affecting the early one.
The results may indicate that the alpha(1)-adrenoceptor-induced contraction was mediated by Ca(2+) influx through T- and L-type Ca(2+) channels for the early and late alpha(1)-components, respectively and that SK and BK channels contributed to protect the musculature of the guinea-pig vas deferens from excess tension development induced by sympathetic volley. Neurourol. Urodynam. 28:447-454, 2009. (c) 2009 Wiley-Liss, Inc.
研究T型和L型钙通道在α1肾上腺素能受体介导的豚鼠输精管收缩中与小电导钙激活钾通道(SK通道)和大电导钙激活钾通道(BK通道)的关系。
记录对40Hz频率下50个脉冲电刺激(ES)的等长收缩反应。在嘌呤能抑制剂存在的情况下,通过钙通道和钾通道调节ES反应。
α1肾上腺素能受体介导的豚鼠输精管收缩由早期和晚期α1成分组成。早期α1成分对硝苯地平(10μM)不敏感,但被T型钙通道拮抗剂米贝拉地尔和阿米洛利抑制,IC50值(μM)分别为7.2±1.8(n = 5)和27.2±10.4(n = 6)。晚期α1成分被硝苯地平、尼莫地平和尼卡地平抑制,IC50值(μM)分别为0.19±0.04(n = 5)、1.9±0.8(n = 5)和4.2±2.5(n = 5)。尼卡地平也抑制早期α1成分,IC50值为20.3±2.5μM(n = 5)。SK通道拮抗剂蜂毒明肽(1 - 100 nM)增加早期和晚期α1成分。BK通道拮抗剂iberiotoxin(100 nM)增加晚期α1成分,而不影响早期成分。
结果可能表明,α1肾上腺素能受体诱导的收缩分别由早期和晚期α1成分通过T型和L型钙通道的钙内流介导,并且SK通道和BK通道有助于保护豚鼠输精管的肌肉组织免受交感神经冲动引起的过度张力发展的影响。《神经泌尿学与尿动力学》28:447 - 454,2009年。(c)2009威利 - 利斯公司。