褪黑激素抑制电压门控钾 KV4.2 通道并负向调节大鼠松果体分泌褪黑激素。

IF 5 2区 生物学 Q2 CELL BIOLOGY
Hiroki Mishima, Shunsuke Ando, Hibiki Kuzuhara, Aya Yamamura, Rubii Kondo, Yoshiaki Suzuki, Yuji Imaizumi, Hisao Yamamura
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引用次数: 0

摘要

褪黑激素由松果体合成和分泌,并调节昼夜节律。尽管有报道称褪黑素可调节多种组织中离子通道的活性,但其对松果体离子通道的影响仍不清楚。本研究考察了褪黑激素对大鼠松果体细胞中电压门控 K+(KV)通道的影响,KV 通道在调节静息膜电位中发挥作用。褪黑激素的应用以浓度依赖性的方式降低了松果体 KV 电流(IC50=309 mM)。表达分析表明,KV4.2 通道在大鼠松果体中高度表达。用小干扰 RNA 敲除大鼠松果体细胞中的 KV4.2 通道后,褪黑激素敏感电流消失。在表达 KV4.2 通道的人胚肾 293(HEK293)细胞中,褪黑激素可降低外向电流(IC50=479 mM)。抑制作用是通过电压依赖性从稳态失活向超极化方向转变而产生的。即使在褪黑激素受体拮抗剂 100 nM 的吕吲哚存在的情况下,也能观察到这种抑制作用。褪黑激素还阻断了重组 HEK293 细胞中 KV4.3、KV1.1 和 KV1.5 通道的活性。施加 1 mM 褪黑激素会导致大鼠松果体细胞膜去极化。此外,用 5 mM 4-aminopyridine 抑制 KV4.2 通道可减轻 1 mM 去甲肾上腺素在大鼠松果体中诱导的褪黑激素分泌。这些结果有力地表明,褪黑激素直接抑制 KV4.2 通道,引起松果体细胞膜去极化,从而通过副交感神经信号通路导致褪黑激素分泌减少。这一机制可能是松果体分泌褪黑激素的负反馈机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Melatonin inhibits voltage-gated potassium KV4.2 channels and negatively regulates melatonin secretion in rat pineal glands.

Melatonin is synthesized in and secreted from the pineal glands and regulates circadian rhythms. Although melatonin has been reported to modulate the activity of ion channels in several tissues, its effects on pineal ion channels remain unclear. In the present study, the effects of melatonin on voltage-gated K+ (KV) channels, which play a role in regulating the resting membrane potential, were examined in rat pinealocytes. The application of melatonin reduced pineal KV currents in a concentration-dependent manner (IC50 = 309 µM). An expression analysis revealed that KV4.2 channels were highly expressed in rat pineal glands. Melatonin-sensitive currents were abolished by the small interfering RNA knockdown of KV4.2 channels in rat pinealocytes. In human embryonic kidney 293 (HEK293) cells expressing KV4.2 channels, melatonin decreased outward currents (IC50 = 479 µM). Inhibitory effects were mediated by a shift in the voltage dependence of steady-state inactivation in a hyperpolarizing direction. This inhibition was observed even in the presence of 100 nM luzindole, an antagonist of melatonin receptors. Melatonin also blocked the activity of KV4.3, KV1.1, and KV1.5 channels in reconstituted HEK293 cells. The application of 1 mM melatonin caused membrane depolarization in rat pinealocytes. Furthermore, KV4.2 channel inhibition by 5 mM 4-aminopyridine attenuated melatonin secretion induced by 1 µM noradrenaline in rat pineal glands. These results strongly suggest that melatonin directly inhibited KV4.2 channels and caused membrane depolarization in pinealocytes, resulting in a decrease in melatonin secretion through parasympathetic signaling pathway. This mechanism may function as a negative-feedback mechanism of melatonin secretion in pineal glands. NEW & NOTEWORTHY Melatonin is a hormone that is synthesized in and secreted from the pineal glands, which regulates circadian rhythms. However, the effects of melatonin on pineal ion channels remain unclear. The present study demonstrated that melatonin directly inhibited voltage-gated potassium KV4.2 channels, which are highly expressed in rat pinealocytes, and induced membrane depolarization, resulting in a decrease in melatonin secretion. This mechanism may function as a negative-feedback mechanism of melatonin secretion in pineal glands.

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来源期刊
CiteScore
9.10
自引率
1.80%
发文量
252
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Cell Physiology is dedicated to innovative approaches to the study of cell and molecular physiology. Contributions that use cellular and molecular approaches to shed light on mechanisms of physiological control at higher levels of organization also appear regularly. Manuscripts dealing with the structure and function of cell membranes, contractile systems, cellular organelles, and membrane channels, transporters, and pumps are encouraged. Studies dealing with integrated regulation of cellular function, including mechanisms of signal transduction, development, gene expression, cell-to-cell interactions, and the cell physiology of pathophysiological states, are also eagerly sought. Interdisciplinary studies that apply the approaches of biochemistry, biophysics, molecular biology, morphology, and immunology to the determination of new principles in cell physiology are especially welcome.
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