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小鼠脑室内注射N-甲基-D-天冬氨酸、海藻酸和喹啉酸诱发癫痫发作的比较分析。

Comparative analysis of seizures induced by intracerebroventricular administration of NMDA, kainate and quisqualate in mice.

作者信息

Mathis C, Ungerer A

机构信息

Laboratoire de Psychophysiologie, Université Louis Pasteur, URA 1295 CNRS, Strasbourg, France.

出版信息

Exp Brain Res. 1992;88(2):277-82. doi: 10.1007/BF02259102.

Abstract

The dose-related time course and occurrence of different seizure subtypes was examined in mice after i.c.v. administration of N-methyl-D-aspartate (NMDA), kainate (KA) or quisqualate (QA). At doses of 0.2 to 1 nmol, NMDA dose-dependently induced a single clonic-tonic seizure. Low doses (0.1 to 0.3 nmol) of KA induced only mild myoclonus and whole body clonus, which were dose-dependently replaced by short-delay clonic-tonic seizures at higher doses (0.4 to 1.2 nmol). In contrast, mice treated with 13 to 32 nmol of QA exhibited either mild myoclonus or whole body clonus as well as clonic-tonic seizures. Clonic-tonic seizures induced by NMDA or KA appeared at shorter latencies than those induced by QA, whereas whole body clonus induced by KA or QA appeared with long onset latencies. These results clearly show that i.c.v. administration of NMDA, KA and QA produces different patterns of seizures in mice. This study confirms that NMDA, KA and QA induce convulsions through different underlying mechanisms and suggests that different anatomical pathways are involved in these models.

摘要

在小鼠脑室内注射N-甲基-D-天冬氨酸(NMDA)、海藻酸(KA)或喹啉酸(QA)后,研究了不同癫痫发作亚型的剂量相关时间进程和发生率。在0.2至1纳摩尔的剂量下,NMDA剂量依赖性地诱发单次阵挛-强直发作。低剂量(0.1至0.3纳摩尔)的KA仅诱发轻度肌阵挛和全身阵挛,在较高剂量(0.4至1.2纳摩尔)时,这些症状剂量依赖性地被短延迟阵挛-强直发作所取代。相比之下,用13至32纳摩尔QA处理的小鼠表现出轻度肌阵挛或全身阵挛以及阵挛-强直发作。NMDA或KA诱发的阵挛-强直发作比QA诱发的发作潜伏期短,而KA或QA诱发的全身阵挛发作潜伏期长。这些结果清楚地表明,脑室内注射NMDA、KA和QA在小鼠中产生不同的癫痫发作模式。本研究证实,NMDA、KA和QA通过不同的潜在机制诱发惊厥,并表明这些模型涉及不同的解剖学途径。

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