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有证据表明,血清素能机制参与了氟西汀对遗传性癫痫易感性大鼠的抗惊厥作用。

Evidence that a serotonergic mechanism is involved in the anticonvulsant effect of fluoxetine in genetically epilepsy-prone rats.

作者信息

Yan Q S, Jobe P C, Dailey J W

机构信息

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

出版信息

Eur J Pharmacol. 1994 Jan 24;252(1):105-12. doi: 10.1016/0014-2999(94)90581-9.

Abstract

Fluoxetine (15 mg/kg i.p.) decreased the audiogenic seizure intensity in 33% of severe seizure genetically epilepsy-prone rats (GEPR-9s). 5-Hydroxytryptophan (5-HTP, 12.5 mg/kg i.p.) produced no anticonvulsant effect in GEPR-9s. When GEPR-9s were treated with a combination of these two drugs, the combination treatment decreased the audiogenic seizure intensity in 83% of the animals tested. Brain microdialysis studies showed that the same combination of 5-HTP and fluoxetine also produced a marked potentiation of the increase in the extracellular serotonin concentration in the thalamus of freely-moving GEPR-9s when compared with administration of either drug alone. A negative correlation between audiogenic seizure intensity and extracellular serotonin concentration existed after either fluoxetine alone or the combination treatment. No significant changes in extracellular norepinephrine concentrations were observed after the combination treatment. These results coupled with our earlier reports strongly suggest that a serotonergic mechanism is involved in the anticonvulsant effects of fluoxetine in GEPRs.

摘要

氟西汀(腹腔注射15毫克/千克)使33%的严重癫痫发作型遗传性癫痫易感大鼠(GEPR - 9s)的听源性惊厥强度降低。5-羟色氨酸(5-HTP,腹腔注射12.5毫克/千克)对GEPR - 9s没有抗惊厥作用。当用这两种药物联合治疗GEPR - 9s时,联合治疗使83%的受试动物的听源性惊厥强度降低。脑微透析研究表明,与单独给予任何一种药物相比,5-HTP和氟西汀的相同组合还显著增强了自由活动的GEPR - 9s丘脑细胞外5-羟色胺浓度的升高。单独使用氟西汀或联合治疗后,听源性惊厥强度与细胞外5-羟色胺浓度之间存在负相关。联合治疗后细胞外去甲肾上腺素浓度没有显著变化。这些结果与我们早期的报告相结合,强烈表明5-羟色胺能机制参与了氟西汀对GEPRs的抗惊厥作用。

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