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兰伯特-伊顿综合征抗体可抑制电鳐神经末梢中乙酰胆碱的释放及P/Q型钙离子通道。

Lambert-Eaton syndrome antibodies inhibit acetylcholine release and P/Q-type Ca2+ channels in electric ray nerve endings.

作者信息

Satoh Y, Hirashima N, Tokumaru H, Takahashi M P, Kang J, Viglione M P, Kim Y I, Kirino Y

机构信息

School of Pharmaceutical Sciences, The University of Tokyo, Bunkyo-ku, Tokyo 113, Japan.

出版信息

J Physiol. 1998 Apr 15;508 ( Pt 2)(Pt 2):427-38. doi: 10.1111/j.1469-7793.1998.427bq.x.

Abstract
  1. The types of voltage-dependent calcium channels (VDCCs) present in the cholinergic terminals isolated from the electric organ of the ray, Narke japonica, were characterized on the basis of their pharmacological sensitivity to specific antagonists. Inhibition of these channel types by autoantibodies from patients with the Lambert-Eaton syndrome (LES) was then studied to determine the specificity of the pathogenic IgG. 2. In normal untreated synaptosomal preparations, maximal doses of N- and P and/or Q-type Ca2+ channel antagonists, omega-conotoxin GVIA and omega-agatoxin IVA, inhibited depolarization-evoked ACh release by 47 % and 43 %, respectively. Calciseptine, an L-type VDCC antagonist, caused a 20 % reduction in the release. This indicates that the exocytotic release process is predominantly mediated by N- and P/Q-type VDCCs. 3. LES IgG or sera caused an inhibition of ACh release by 39-45 % in comparison with the control antibody-treated preparations. The ionomycin-induced ACh release, however, was not altered by the antibodies. Additionally, the same LES antibodies inhibited whole-cell calcium currents (ICa) in bovine adrenal chromaffin cells. Thus, the pathogenic antibodies exert their action on VDCCs present in the synaptosomes. 4. The efficacy of three Ca2+ channel antagonists in blocking ACh release was determined in preparations pretreated with LES IgG. omega-Agatoxin IVA produced only an additional 3-5 % reduction in release beyond that obtained with LES antibodies. Despite the pretreatment with LES IgG, omega-conotoxin GVIA and calciseptine inhibited the release to nearly their control levels. 5. These results indicate that LES antibodies mainly downregulate P/Q-type Ca2+ channels which contribute to presynaptic transmitter release from the cholinergic nerve terminals of electric organ. 6. The present findings are consistent with the hypothesis that P/Q-type VDCCs at the neuromuscular junction are the target of LES antibodies and that their inhibition by the antibodies produces the characteristic neuromuscular defect in this disease.
摘要
  1. 根据从日本电鳐(Narke japonica)电器官分离出的胆碱能终末中存在的电压依赖性钙通道(VDCCs)对特定拮抗剂的药理敏感性,对其类型进行了表征。然后研究了来自兰伯特 - 伊顿综合征(LES)患者的自身抗体对这些通道类型的抑制作用,以确定致病性IgG的特异性。2. 在正常未处理的突触体制剂中,N型和P型及/或Q型Ca2 +通道拮抗剂、ω-芋螺毒素GVIA和ω-阿加毒素IVA的最大剂量分别使去极化诱发的ACh释放抑制了47%和43%。L型VDCC拮抗剂钙西菌素使释放减少了20%。这表明胞吐释放过程主要由N型和P/Q型VDCC介导。3. 与对照抗体处理的制剂相比,LES IgG或血清使ACh释放抑制了39 - 45%。然而,离子霉素诱导的ACh释放未被抗体改变。此外,相同的LES抗体抑制了牛肾上腺嗜铬细胞中的全细胞钙电流(ICa)。因此,致病性抗体对突触体中存在的VDCC发挥作用。4. 在经LES IgG预处理的制剂中测定了三种Ca2 +通道拮抗剂阻断ACh释放的效力。ω-阿加毒素IVA除了与LES抗体获得的抑制作用外,仅使释放额外减少了3 - 5%。尽管用LES IgG进行了预处理,ω-芋螺毒素GVIA和钙西菌素仍将释放抑制至接近其对照水平。5. 这些结果表明,LES抗体主要下调P/Q型Ca2 +通道,这些通道有助于从电器官的胆碱能神经终末进行突触前递质释放。6. 目前的研究结果与以下假设一致:神经肌肉接头处的P/Q型VDCC是LES抗体的靶点,并且抗体对它们的抑制在该疾病中产生了特征性的神经肌肉缺陷。

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1
An autoimmune animal model of the Lambert-Eaton syndrome.兰伯特-伊顿综合征的自身免疫动物模型。
Ann N Y Acad Sci. 1998 May 13;841:670-6. doi: 10.1111/j.1749-6632.1998.tb11000.x.

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