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二氮嗪、甲苯磺丁脲和ATP4-对胰岛素分泌细胞系中核苷酸依赖性钾通道的相互作用。

Interaction of diazoxide, tolbutamide and ATP4- on nucleotide-dependent K+ channels in an insulin-secreting cell line.

作者信息

Dunne M J, Illot M C, Peterson O H

机构信息

Department of Physiology, University of Liverpool, England.

出版信息

J Membr Biol. 1987;99(3):215-24. doi: 10.1007/BF01995702.

Abstract

The single-channel current recording technique has been used to study the effects of diazoxide, tolbutamide and ATP, separately and combined, on the gating of nucleotide-regulated K+ channels in the insulin-secreting cell line RINm5F. The effects of diazoxide, tolbutamide and ATP4- were studied at the intracellular membrane surface, using the open-cell membrane patch configuration. Alone diazoxide was found only inconsistently to evoke channel stimulation, 57% of all applications of the drug (72 times in 48 separate patches) having no effect at concentrations between 0.02 and 0.4 mM. In the presence of ATP, however, diazoxide consistently evoked channel activation (seen 87 times in 49 patches, 95% of all applications). The interactions of diazoxide and ATP seemed competitive. Stimulation of channels by diazoxide in the presence of 1 mM ATP was suppressed if the concentration of ATP was elevated to 2 or 5 mM. In solutions in which Mg2+ had been chelated with EDTA, diazoxide failed to activate channels closed by 1 mM ATP; however, this was not due to a direct effect on the channels caused by the absence of Mg2+, but could be explained by the enhanced ATP4- concentration after Mg2+ removal. When the total ATP concentration was lowered to give the same [ATP4-] in the absence of Mg2+ to that present in the control experiments, diazoxide was able to evoke full activation. Channel inhibition evoked by tolbutamide, 0.01 to 1.0 mM, did not require the presence of either ATP or Mg2+. In the presence of ATP tolbutamide further reduced the number of channel openings. Diazoxide was able to compete with tolbutamide for control of channel activity, an effect that was augmented by the presence of ATP. In the presence of 0.1 mM tolbutamide, diazoxide was unable to stimulate channel openings; however, if the dose of tolbutamide was lowered or ATP made available to the inside of the membrane, channel stimulation occurred.

摘要

单通道电流记录技术已被用于分别及联合研究二氮嗪、甲苯磺丁脲和ATP对胰岛素分泌细胞系RINm5F中核苷酸调节的钾通道门控的影响。使用去细胞膜片钳配置,在细胞内膜表面研究了二氮嗪、甲苯磺丁脲和ATP4-的作用。单独使用时,发现二氮嗪仅偶尔能引起通道刺激,在0.02至0.4 mM浓度下,该药物的所有应用中有57%(48个独立膜片中共72次)无作用。然而,在ATP存在的情况下,二氮嗪始终能引起通道激活(在49个膜片中出现87次,占所有应用的95%)。二氮嗪与ATP的相互作用似乎具有竞争性。如果将ATP浓度提高到2或5 mM,在1 mM ATP存在的情况下,二氮嗪对通道的刺激作用会受到抑制。在Mg2+已被EDTA螯合的溶液中,二氮嗪无法激活被1 mM ATP关闭的通道;然而,这并非由于Mg2+缺失对通道产生的直接影响,而是可以通过Mg2+去除后ATP4-浓度的升高来解释。当总ATP浓度降低,以使在无Mg2+时的[ATP4-]与对照实验中的相同,二氮嗪能够引起完全激活。0.01至1.0 mM甲苯磺丁脲引起的通道抑制不需要ATP或Mg2+的存在。在ATP存在的情况下,甲苯磺丁脲进一步减少了通道开放的数量。二氮嗪能够与甲苯磺丁脲竞争对通道活性的控制,ATP的存在会增强这种作用。在0.1 mM甲苯磺丁脲存在的情况下,二氮嗪无法刺激通道开放;然而,如果降低甲苯磺丁脲的剂量或使ATP进入膜内,则会发生通道刺激。

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