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对声音源性癫痫敏感小鼠中的γ-氨基丁酸和苯二氮䓬结合位点

gamma-Aminobutyric acid and benzodiazepine binding sites in audiogenic seizure-susceptible mice.

作者信息

Horton R W, Prestwich S A, Meldrum B S

出版信息

J Neurochem. 1982 Sep;39(3):864-70. doi: 10.1111/j.1471-4159.1982.tb07972.x.

Abstract

The properties of gamma-aminobutyric acid recognition sites, benzodiazepine binding sites and the effect of exogeneous gamma-aminobutyric acid on benzodiazepine binding were determined in crude membrane fractions prepared from the brains of DBA/2 mice at ages before (8-9 and 17-18 days), during (22-23 and 28-29 days) and after (40-43 days) the age of high susceptibility to audiogenic seizures. These have been compared with data from age-matched mice of a strain (TO) with lower audiogenic seizure susceptibility. The number of high-affinity [3H]gamma-aminobutyric acid binding sites was lower at all ages in DBA/2 mice compared with TO mice, but the affinity was higher in DBA/2 mice. The number of low-affinity [3H]gamma-aminobutyric acid binding sites was lower at 8-9 days and 40-43 days in DBA/2 mice, but was not significantly different from TO mice at other ages. For [3H]flunitrazepam binding, the only difference found was a slight reduction in the number of binding sites at 28-29 days of age in DBA/2 mice. gamma-Aminobutyric acid stimulation of [3H]flunitrazepam binding was not significantly different up to 22-23 days of age, but was higher in DBA/2 mice at 28-29 days and lower at 40-43 days. Impairment of gamma-aminobutyric acid function is a possible permissive factor in the age-dependent audiogenic seizure susceptibility in DBA/2 mice.

摘要

在从DBA/2小鼠大脑制备的粗制膜组分中,测定了γ-氨基丁酸识别位点、苯二氮䓬结合位点的特性,以及外源性γ-氨基丁酸对苯二氮䓬结合的影响。这些小鼠处于对听源性惊厥高易感性年龄之前(8 - 9天和17 - 18天)、期间(22 - 23天和28 - 29天)和之后(40 - 43天)。已将这些结果与来自低听源性惊厥易感性品系(TO)的年龄匹配小鼠的数据进行了比较。与TO小鼠相比,DBA/2小鼠在所有年龄段的高亲和力[³H]γ-氨基丁酸结合位点数量均较低,但DBA/2小鼠的亲和力较高。DBA/2小鼠在8 - 9天和40 - 43天时低亲和力[³H]γ-氨基丁酸结合位点数量较低,但在其他年龄段与TO小鼠无显著差异。对于[³H]氟硝西泮结合,唯一发现的差异是DBA/2小鼠在28 - 29天龄时结合位点数量略有减少。在22 - 23天龄之前,γ-氨基丁酸对[³H]氟硝西泮结合的刺激作用无显著差异,但DBA/2小鼠在28 - 29天时较高,在40 - 43天时较低。γ-氨基丁酸功能受损可能是DBA/2小鼠年龄依赖性听源性惊厥易感性的一个允许因素。

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