Wu S N, Li H F, Chiang H T
Department of Medical Education and Research, Veterans General Hospital, Kaohsiung, Taiwan, Republic of China.
Mol Pharmacol. 2000 May;57(5):865-74.
delta-Hexachlorocyclohexane (delta-HCH), a lipophilic neurodepressant agent, has been shown to inhibit neurotransmitter release and stimulate ryanodine-sensitive Ca(2+) channels. However, the effect of delta-HCH on neuronal activity remains unclear, although it may enhance the gamma-aminobutyric acid-induced current. Its effects on ionic currents were investigated in rat pituitary GH(3) cells and human neuroblastoma IMR-32 cells. In GH(3) cells, delta-HCH increased the amplitude of Ca(2+)-activated K(+) current (I(K(Ca))). delta-HCH (100 microM) slightly inhibited the amplitude of voltage-dependent K(+) current. delta-HCH (30 microM) suppressed voltage-dependent L-type Ca(2+) current (I(Ca, L)), whereas gamma-HCH (30 microM) had no effect on I(Ca, L). In the inside-out configuration, delta-HCH applied intracellularly did not change the single channel conductance of large conductance Ca(2+)-activated K(+) (BK(Ca)) channels; however, it did increase the channel activity. The delta-HCH-mediated increase in the channel activity is mainly mediated by its increase in the number of long-lived openings. delta-HCH reversibly increased the activity of BK(Ca) channels in a concentration-dependent manner with an EC(50) value of 20 microM. delta-HCH also caused a left shift in the midpoint for the voltage-dependent opening. In contrast, gamma-HCH (30 microM) suppressed the activity of BK(Ca) channels. Under the current-clamp mode, delta-HCH (30 microM) reduced the firing rate of spontaneous action potentials; however, gamma-HCH (30 microM) increased it. In neuroblastoma IMR-32 cells, delta-HCH also increased the amplitude of I(K(Ca)) and stimulated the activity of intermediate-conductance K(Ca) channels. This study provides evidence that delta-HCH is an opener of K(Ca) channels. The effects of delta-HCH on these channels may partially, if not entirely, be responsible for the underlying cellular mechanisms by which delta-HCH affects neuronal or neuroendocrine function.
δ-六氯环己烷(δ-HCH)是一种亲脂性神经抑制剂,已被证明可抑制神经递质释放并刺激对ryanodine敏感的Ca(2+)通道。然而,尽管δ-HCH可能增强γ-氨基丁酸诱导的电流,但其对神经元活动的影响仍不清楚。在大鼠垂体GH(3)细胞和人神经母细胞瘤IMR-32细胞中研究了其对离子电流的影响。在GH(3)细胞中,δ-HCH增加了Ca(2+)激活的K(+)电流(I(K(Ca)))的幅度。δ-HCH(100μM)轻微抑制了电压依赖性K(+)电流的幅度。δ-HCH(30μM)抑制了电压依赖性L型Ca(2+)电流(I(Ca, L)),而γ-HCH(30μM)对I(Ca, L)没有影响。在膜内向外模式下,细胞内施加的δ-HCH不会改变大电导Ca(2+)激活的K(+)(BK(Ca))通道的单通道电导;然而,它确实增加了通道活性。δ-HCH介导的通道活性增加主要由其增加的长寿命开放次数介导。δ-HCH以浓度依赖性方式可逆地增加BK(Ca)通道的活性,EC(50)值为20μM。δ-HCH还导致电压依赖性开放的中点向左移动。相比之下,γ-HCH(30μM)抑制了BK(Ca)通道的活性。在电流钳模式下,δ-HCH(30μM)降低了自发动作电位的发放频率;然而,γ-HCH(30μM)增加了发放频率。在神经母细胞瘤IMR-32细胞中也是如此,δ-HCH也增加了I(K(Ca))的幅度并刺激了中电导K(Ca)通道的活性。这项研究提供了证据表明δ-HCH是K(Ca)通道的开放剂。δ-HCH对这些通道的影响可能部分(如果不是全部)是其影响神经元或神经内分泌功能的潜在细胞机制的原因。