首页> 外文期刊>The Journal of Experimental Biology >K+ transport in Malpighian tubules of Tenebrio molitor L.: is a K-ATP channel involved?
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K+ transport in Malpighian tubules of Tenebrio molitor L.: is a K-ATP channel involved?

机译:黄粉虫的马尔必氏小管中的K +转运:是否涉及K-ATP通道?

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摘要

The presence of ATP-regulated K+ (K-ATP) channels in Tenebrio molitor Malpighian tubules was investigated by examining the effect of glibenclamide on both fluid secretion and basolateral membrane potentials (V-bl). Glibenclamide, a KATP channel blocker, slowed fluid secretion of Tenebrio tubules. In low bath K+ concentration (5 mmol 1(-1)), glibenclamide either hyperpolarized or depolarized V-bl, resembling the effect seen with Ba2+. Subsequent addition of 6 mmol 1(-1) Ba2+ caused a further hyper- or depolarization of V-bl. In control Ringer (50 mmol 1(-1) KCl, 90 mmol 1(-1) NaCl), glibenclamide had no visible effect on V-bl. The effect of ouabain was investigated in low bath [K+] in the presence of Ba2+. V-bl responded by a small but significant hyperpolarization from -51 +/- 4 mV to -56 +/- 4 mV (n=16, P<0.001) in response to 1 mmol 1(-1) ouabain. Repeating the experiments in the presence of both glibenclamide and Ba2+ resulted in a depolarization of V-bl when ouabain was added. In low bath [K+] (high Na+), the Na+/K+-ATPase is expected to function at a high rate. In the presence of Ba2+, replacing Na+ by K+ rapidly depolarized V-bl, but this was followed by a repolarization. Repeating the experiments in the presence of glibenclamide markedly reduced the depolarizing effect and abolished the repolarization, with a gradual decrease in the sensitivity of V-bl to the surrounding [K+]. These results suggest the presence of K-ATP channels in the basolateral membrane. Glibenclamide had no visible effect on V-bl in high K+ or in the absence of Ba2+, indicating that other highly conductive K+ channels may mask the effect on K-ATP channels. This is the first demonstration of the presence of K-ATP channels in an insect epithelium. [References: 34]
机译:通过检查格列本脲对体液分泌和基底外侧膜电位(V-b1)的影响,研究了黄粉虫Malpighian小管中ATP调节的K +(K-ATP)通道的存在。格列本脲,一种KATP通道阻滞剂,减缓了黄粉虫小管的液体分泌。在低浴液K +浓度(5 mmol 1(-1))中,格列本脲V-bl超极化或去极化,类似于Ba2 +所见的效果。随后添加6 mmol 1(-1)Ba2 +导致V-bl进一步超极化或去极化。在对照林格(50 mmol 1(-1)KCl,90 mmol 1(-1)NaCl)中,格列本脲对V-b1没有可见作用。在Ba2 +存在下于低浴液[K +]中研究了哇巴因的作用。 V-b1对1 mmol 1(-1)哇巴因有一个小的但显着的超极化响应,从-51 +/- 4 mV到-56 +/- 4 mV(n = 16,P <0.001)。当加入哇巴因时,在格列本脲和Ba 2+的存在下重复实验会导致V-b1的去极化。在低水浴[K +](高Na +)中,预计Na + / K + -ATPase的功能较高。在存在Ba2 +的情况下,用K +代替Na +会使V-bl快速去极化,但是随后进行了重新极化。在格列本脲存在下重复实验可显着降低去极化作用,并消除了复极化,同时V-b1对周围[K +]的敏感性逐渐降低。这些结果表明在基底外侧膜中存在K-ATP通道。在高K +或不存在Ba2 +的情况下,格列本脲对V-bl没有明显影响,表明其他高导电性K +通道可能掩盖了对K-ATP通道的影响。这是昆虫上皮细胞中存在K-ATP通道的首次证明。 [参考:34]

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