Suppr超能文献

未发作的遗传性癫痫易感大鼠中枢神经系统中的去甲肾上腺素能异常。

Noradrenergic abnormalities in the central nervous system of seizure-naive genetically epilepsy-prone rats.

作者信息

Dailey J W, Mishra P K, Ko K H, Penny J E, Jobe P C

机构信息

Department of Basic Sciences, University of Illinois College of Medicine, Peoria 61656.

出版信息

Epilepsia. 1991 Mar-Apr;32(2):168-73. doi: 10.1111/j.1528-1157.1991.tb05240.x.

Abstract

Norepinephrine (NE) concentrations were measured in 15 discrete areas of the central nervous system of two types of genetically epilepsy-prone rats (GEPRs) and in nonepileptic controls. Both moderate-seizure (GEPR-3) and severe-seizure (GEPR-9) animals had extensive abnormalities in brain NE concentration. Deficits of equal magnitude in GEPR-3s and GEPR-9s were found in the spinal cord, midbrain minus the inferior colliculus, inferior colliculus, hypothalamus, amygdala, hippocampus, occipital + parietal cortex, frontal cortex, and olfactory septum. Because both types of GEPRs share these deficits and share seizure susceptibility, we hypothesize that these areas are candidates for regulation of seizure susceptibility in GEPRs. In addition, because GEPR-9s have more severe seizures than GEPR-3s and because GEPR-9s had greater NE deficits in several brain areas (cerebellum, pons-medulla, thalamus, and possibly the temporal cortex and olfactory bulbs), we hypothesize that these areas may be important in regulation of seizure severity in GEPRs. All animals used in these experiments had been protected from seizure-provoking stimuli and were naive to seizures. Because the abnormalities in NE concentration were present in seizure-predisposed animals that were protected from seizures, we conclude that these abnormalities are important components of the seizure-predisposition characteristic of GEPRs and do not result from seizure experience.

摘要

在两种遗传性癫痫易感大鼠(GEPR)以及非癫痫对照大鼠的中枢神经系统的15个离散区域中测量了去甲肾上腺素(NE)浓度。中度癫痫发作(GEPR - 3)和重度癫痫发作(GEPR - 9)的动物在脑NE浓度方面均存在广泛异常。在脊髓、中脑(不包括下丘)、下丘、下丘脑、杏仁核、海马体、枕叶 + 顶叶皮质、额叶皮质和嗅隔中,发现GEPR - 3和GEPR - 9存在同等程度的缺乏。由于这两种类型的GEPR都存在这些缺乏且都具有癫痫易感性,我们推测这些区域是GEPR癫痫易感性调节的候选区域。此外,由于GEPR - 9比GEPR - 3有更严重的癫痫发作,并且GEPR - 9在几个脑区(小脑、脑桥 - 延髓、丘脑,可能还有颞叶皮质和嗅球)有更大的NE缺乏,我们推测这些区域可能在GEPR癫痫发作严重程度的调节中起重要作用。这些实验中使用的所有动物都免受诱发癫痫的刺激且未曾经历过癫痫发作。由于NE浓度异常存在于免受癫痫发作影响的癫痫易感动物中,我们得出结论,这些异常是GEPR癫痫易感性特征的重要组成部分,并非由癫痫发作经历所致。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验