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乙醇依赖大鼠在向下丘、黑质或内侧隔微量注射γ-氨基丁酸(GABA)激动剂后对听源性惊厥易感性的特征分析。

Characterization of susceptibility to audiogenic seizures in ethanol-dependent rats after microinjection of gamma-aminobutyric acid (GABA) agonists into the inferior colliculus, substantia nigra or medial septum.

作者信息

Frye G D, McCown T J, Breese G R

出版信息

J Pharmacol Exp Ther. 1983 Dec;227(3):663-70.

Abstract

The relative anticonvulsant potential of the gamma-aminobutyric acid (GABA) agonist, muscimol, was compared after microinjection into either the inferior colliculus, substantia nigra or medial septum of ethanol-dependent rats. Bilateral microinjection of muscimol (10-30 ng) into the inferior colliculus 15 to 60 min before testing suppressed all sound-induced seizure components (wild running, clonus and tonus) in rats withdrawn from ethanol for 6.5 to 8.5 hr. However, forelimb tremors were not altered. Audiogenic seizures were suppressed for at least 3 hr after muscimol (30 ng). In the medial septum and substantia nigra, microinjection of muscimol (30-100 ng) only partially reduced the tonic component of audiogenic seizures and exerted no effect on the frequency of wild running or clonus. GABA (10 micrograms) and two other GABA agonists [4,5,6,7-tetrahydroisoxazolo[5, 40c]pyridin-3-ol (THIP), 300 ng and chlordiazepoxide, 10-30 micrograms], microinjected into the inferior colliculus, also reduced audiogenic seizure susceptibility. However, 1, 3-butanediol, which suppresses ethanol withdrawal seizures after peripheral administration in rats, was inactive. The relative proconvulsant potential of the GABA antagonist, bicuculline methiodide, also was compared after microinjection into either the inferior colliculus, substantia nigra or medial septum of ethanol naive rats. In each animal, audiogenic seizure-like wild running, clonus and tonus were evoked by microinjecting bicuculline methiodide into the inferior colliculus at the rate of 6.0 ng/6 min. However, these reactions did not occur when bicuculline methiodide was applied at a slower rate (1.8 ng/6 min).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

将γ-氨基丁酸(GABA)激动剂蝇蕈醇微量注射到乙醇依赖大鼠的下丘、黑质或内侧隔后,比较了其相对抗惊厥潜力。在测试前15至60分钟,将蝇蕈醇(10 - 30纳克)双侧微量注射到下丘,可抑制撤乙醇6.5至8.5小时大鼠的所有声音诱发的癫痫发作成分(狂奔、阵挛和强直)。然而,前肢震颤未改变。蝇蕈醇(30纳克)注射后,声源性癫痫发作被抑制至少3小时。在内侧隔和黑质,微量注射蝇蕈醇(30 - 100纳克)仅部分降低了声源性癫痫发作的强直成分,对狂奔或阵挛的频率没有影响。将GABA(10微克)和另外两种GABA激动剂[4,5,6,7 - 四氢异恶唑并[5,4 - c]吡啶 - 3 - 醇(THIP),300纳克和氯氮卓,10 - 30微克]微量注射到下丘,也降低了声源性癫痫发作易感性。然而,在大鼠外周给药后可抑制乙醇戒断性癫痫发作的1,3 - 丁二醇没有活性。还比较了将GABA拮抗剂甲磺酸荷包牡丹碱微量注射到未接触乙醇大鼠的下丘、黑质或内侧隔后的相对促惊厥潜力。在每只动物中,以6.0纳克/6分钟的速率将甲磺酸荷包牡丹碱微量注射到下丘,可诱发声源性癫痫样的狂奔、阵挛和强直。然而,当以较慢速率(1.8纳克/6分钟)应用甲磺酸荷包牡丹碱时,这些反应未发生。(摘要截断于250字)

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