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组胺激活豚鼠气管肌细胞中的氯离子和钾离子电流:与毒蕈碱信号通路的汇聚

Histamine activates Cl- and K+ currents in guinea-pig tracheal myocytes: convergence with muscarinic signalling pathway.

作者信息

Janssen L J, Sims S M

机构信息

Department of Physiology, University of Western Ontario, London, Canada.

出版信息

J Physiol. 1993 Jun;465:661-77. doi: 10.1113/jphysiol.1993.sp019699.

Abstract
  1. We investigated the effects of histamine on membrane currents and contractile state of isolated guinea-pig tracheal myocytes using perforated patch and whole-cell recording techniques. The effects of histamine were compared to those of acetylcholine (ACh) and caffeine. 2. During voltage clamp (Vhold = -60 mV), histamine elicited contraction and an inward current (Ihist) which was often followed by current oscillations. Ihist had a reversal potential (Vrev) of -9 +/- 3 mV. 3. Ihist was dependent on the Cl- gradient and was antagonized by the Cl- channel blocker niflumic acid. Vrev was more positive (+2 +/- 1 mV) when K(+)-selective currents were blocked by Cs+ and TEA. When all external Na+ was replaced with N-methyl-D-glucamine, there was a small reduction in the amplitude of Ihist. 4. The histamine-induced current was similar to that elicited by ACh and by caffeine with respect to time course, amplitude, and current-voltage relationship. Responses to histamine and to ACh were non-additive, consistent with a convergence of histaminergic and cholinergic signalling pathways. Ihist was antagonized by the H1 histaminergic receptor antagonist astemizole, but not by atropine. 5. When recorded using the perforated patch configuration, Ihist could be elicited repeatedly for more than 30 min. When cells were studied in the whole-cell configuration using a pipette solution containing 0.025 mM EGTA, the amplitude of Ihist was initially the same as that obtained using perforated patch but then decreased; the time required for the responses to decrease to 50% (t1/2) was 8.2 +/- 1.0 min. When 1 mM EGTA was included in the pipette solution (whole-cell configuration), the initial response to histamine was significantly decreased in size and t1/2 was reduced to 3.3 +/- 0.7 min. 6. The characteristics of the signalling pathway were examined in cells studied using the whole-cell configuration with 0.025 mM EGTA in the recording pipette. Heparin significantly reduced t1/2 to 4.3 +/- 0.8 min. GTP gamma S elicited inward current and oscillations; both effects were enhanced by histamine. GTP gamma S also reduced t1/2 to 1.4 +/- 0.1 min. Pertussis toxin did not alter the amplitude or time course of Ihist. 7. We conclude that in guinea-pig tracheal myocytes, binding of histamine to H1 receptors leads to release of Ca2+ from intracellular stores and subsequent activation of Cl- and K+ conductances as well as contraction. Furthermore, we demonstrate that ACh elicits similar physiological responses due to a convergence of the histaminergic and muscarinic signalling pathways.
摘要
  1. 我们运用穿孔膜片钳和全细胞记录技术,研究了组胺对豚鼠离体气管肌细胞的膜电流和收缩状态的影响。将组胺的作用与乙酰胆碱(ACh)和咖啡因的作用进行了比较。2. 在电压钳制(Vhold = -60 mV)期间,组胺引发收缩和内向电流(Ihist),随后常伴有电流振荡。Ihist的反转电位(Vrev)为 -9 ± 3 mV。3. Ihist依赖于Cl-梯度,并被Cl-通道阻滞剂氟尼酸所拮抗。当K+选择性电流被Cs+和TEA阻断时,Vrev更正(+2 ± 1 mV)。当所有细胞外Na+被N-甲基-D-葡萄糖胺取代时,Ihist的幅度略有降低。4. 组胺诱导的电流在时间进程、幅度和电流-电压关系方面与ACh和咖啡因诱导的电流相似。对组胺和ACh的反应是非相加性的,这与组胺能和胆碱能信号通路的汇聚一致。Ihist被H1组胺能受体拮抗剂阿司咪唑所拮抗,但不被阿托品所拮抗。5. 当采用穿孔膜片钳配置进行记录时,Ihist可重复诱发超过30分钟。当使用含有0.025 mM EGTA的移液管溶液以全细胞配置研究细胞时,Ihist的幅度最初与采用穿孔膜片钳时相同,但随后降低;反应降低至50%所需的时间(t1/2)为8.2 ± 1.0分钟。当移液管溶液(全细胞配置)中包含1 mM EGTA时,对组胺的初始反应大小显著降低,t1/2降至3.3 ± 0.7分钟。6. 在记录移液管中含有0.025 mM EGTA的全细胞配置下研究的细胞中,检查了信号通路的特征。肝素显著将t1/2降低至4.3 ± 0.8分钟。GTPγS引发内向电流和振荡;这两种效应均被组胺增强。GTPγS也将t1/2降低至1.4 ± 0.1分钟。百日咳毒素未改变Ihist的幅度或时间进程。7. 我们得出结论,在豚鼠气管肌细胞中,组胺与H1受体结合导致细胞内储存的Ca2+释放,随后激活Cl-和K+电导以及收缩。此外,我们证明由于组胺能和毒蕈碱能信号通路的汇聚,ACh引发类似的生理反应。

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