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“黑麦草蹒跚病”(一种钾离子通道的神经紊乱疾病)的分子机制。

The molecular mechanism of "ryegrass staggers," a neurological disorder of K+ channels.

作者信息

Imlach Wendy L, Finch Sarah C, Dunlop James, Meredith Andrea L, Aldrich Richard W, Dalziel Julie E

机构信息

AgResearch, Grasslands Research Centre, Palmerston North, New Zealand.

出版信息

J Pharmacol Exp Ther. 2008 Dec;327(3):657-64. doi: 10.1124/jpet.108.143933. Epub 2008 Sep 18.

DOI:10.1124/jpet.108.143933
PMID:18801945
Abstract

"Ryegrass staggers" is a neurological condition of unknown mechanism that impairs motor function in livestock. It is caused by infection of perennial ryegrass pastures by an endophytic fungus that produces neurotoxins, predominantly the indole-diterpenoid compound lolitrem B. Animals grazing on such pastures develop uncontrollable tremors and become uncoordinated in their movement. Lolitrem B and the structurally related tremor inducer paxilline both act as potent large conductance calcium-activated potassium (BK) channel inhibitors. Using patch clamping, we show that their different apparent affinities correlate with their toxicity in vivo. To investigate whether the motor function deficits produced by lolitrem B and paxilline are due to inhibition of BK ion channels, their ability to induce tremor and ataxia in mice deficient in this ion channel (Kcnma1(-/-)) was examined. Our results show that mice lacking Kcnma1 are unaffected by these neurotoxins. Furthermore, doses of these substances known to be lethal to wild-type mice had no effect on Kcnma1(-/-) mice. These studies reveal the BK channel as the molecular target for the major components of the motor impairments induced by ryegrass neurotoxins. Unexpectedly, when the response to lolitrem B was examined in mice lacking the beta4 BK channel accessory subunit (Kcnmb4(-/-)), only low-level ataxia was observed. Our study therefore reveals a new role for the accessory BK beta4 subunit in motor control. The beta4 subunit could be considered as a potential target for treatment of ataxic conditions in animals and in humans.

摘要

“黑麦草蹒跚病”是一种发病机制不明的神经疾病,会损害家畜的运动功能。它是由一种内生真菌感染多年生黑麦草牧场所致,这种真菌会产生神经毒素,主要是吲哚二萜类化合物洛替米B。在这类牧场上放牧的动物会出现无法控制的颤抖,行动变得不协调。洛替米B和结构相关的震颤诱导剂柄曲霉素均作为有效的大电导钙激活钾(BK)通道抑制剂。通过膜片钳技术,我们发现它们不同的表观亲和力与它们在体内的毒性相关。为了研究洛替米B和柄曲霉素导致的运动功能缺陷是否是由于BK离子通道受到抑制,我们检测了它们在缺乏该离子通道(Kcnma1(-/-))的小鼠中诱发震颤和共济失调的能力。我们的结果表明,缺乏Kcnma1的小鼠不受这些神经毒素的影响。此外,已知对野生型小鼠致命的这些物质剂量对Kcnma1(-/-)小鼠没有影响。这些研究揭示了BK通道是黑麦草神经毒素诱导的主要运动障碍成分的分子靶点。出乎意料的是,在缺乏BK通道β4辅助亚基(Kcnmb4(-/-))的小鼠中检测对洛替米B的反应时,仅观察到低水平的共济失调。因此,我们的研究揭示了BKβ4辅助亚基在运动控制中的新作用。β4亚基可被视为治疗动物和人类共济失调病症的潜在靶点。

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