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热诱导惊厥改变未成熟大鼠脑中γ-氨基丁酸A型(GABAA)和苯二氮䓬受体结合。

Hyperthermia-induced seizures modify the GABAA and benzodiazepine receptor binding in immature rat brain.

作者信息

González-Ramírez M, Orozco S, Salgado H, Feria A, Rocha L

机构信息

Unidad de Investigación Médica en Enfermedades Neurológicas, H. Especialidades, CMN S XXI, Av. Cuauhtémoc 330, Col. Doctores México, D.F., C.P. 06720.

出版信息

Cell Mol Neurobiol. 2005 Sep;25(6):955-71. doi: 10.1007/s10571-005-8467-0.

Abstract

Effects of hyperthermia-induced seizures (HS) on GABAA and benzodiazepine (BDZ) receptor binding in immature rat brain were evaluated using in vitro autoradiography. HS were induced in 10-day-old rats by a regulated stream of moderately heated air directed 50 cm above the animals. Rats were killed 30 min, 24 h, or 20 days after HS and their brains were used for in vitro autoradiography experiments to determine GABAA and BDZ receptor binding. GABAA binding was significantly enhanced in all brain areas evaluated 30 min after HS, an effect that endures 24 h and 20 days after seizures. Concerning BDZ receptor binding, a significant increase was detected in entorhinal and perirhinal cortices and decreased in basolateral amygdala 30 min following HS. One day after HS, animals demonstrated enhanced BDZ binding in the cingulate, frontal, posterior parietal, entorhinal, temporal, and perirhinal cortices; striatum, accumbens, substantia nigra pars compacta, and amygdala nuclei. Twenty days after HS enhanced BDZ binding was restricted in the cingulated, frontal, anterior and posterior parietal cortices, as well as in substantia nigra pars reticulata, whereas decreased values were found in accumbens nucleus and substantia nigra pars compacta. Our data indicate differential effects of HS in GABAA and BDZ binding in immature brain. HS-induced GABAA and BDZ changes are different from those previously described in experimental models of temporal lobe epilepsy in adult animals.

摘要

采用体外放射自显影法评估热诱导惊厥(HS)对未成熟大鼠脑内γ-氨基丁酸A型(GABAA)和苯二氮䓬(BDZ)受体结合的影响。通过将适度加热的空气以规则气流导向10日龄大鼠上方50厘米处来诱导HS。在HS发作后30分钟、24小时或20天处死大鼠,取其脑用于体外放射自显影实验,以测定GABAA和BDZ受体结合情况。HS发作后30分钟,所有评估脑区的GABAA结合均显著增强,这种效应在惊厥后24小时和20天持续存在。关于BDZ受体结合,HS发作后30分钟,在内嗅皮质和梨状周皮质检测到显著增加,而在基底外侧杏仁核则减少。HS发作后一天,动物在扣带回、额叶、顶叶后部、内嗅、颞叶和梨状周皮质;纹状体、伏隔核、黑质致密部和杏仁核核团表现出BDZ结合增强。HS发作后20天,增强的BDZ结合局限于扣带回、额叶、顶叶前后皮质以及黑质网状部,而在伏隔核和黑质致密部则发现结合值降低。我们的数据表明HS对未成熟脑内GABAA和BDZ结合有不同影响。HS诱导的GABAA和BDZ变化与成年动物颞叶癫痫实验模型中先前描述的不同。

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