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Inactivation of the Constitutively Active Ghrelin Receptor Attenuates Limbic Seizure Activity in Rodents

机译:组成性活性Ghrelin受体的失活减弱了啮齿动物的肢体癫痫发作活动。

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摘要

Ghrelin is a pleiotropic neuropeptide that has been recently implicated in epilepsy. Animal studies performed to date indicate that ghrelin has anticonvulsant properties; however, its mechanism of anticonvulsant action is unknown. Here we show that the anticonvulsant effects of ghrelin are mediated via the growth hormone secretagogue receptor (GHSR). To our surprise, however, we found that the GHSR knockout mice had a higher seizure threshold than their wild-type littermates when treated with pilocarpine. Using both in vivo and in vitro models, we further discovered that inverse agonism and desensitization/internalization of the GHSR attenuate limbic seizures in rats and epileptiform activity in hippocampal slices. This constitutes a novel mechanism of anticonvulsant action, whereby an endogenous agonist reduces the activity of a constitutively active receptor.Electronic supplementary materialThe online version of this article (doi:10.1007/s13311-012-0125-x) contains supplementary material, which is available to authorized users.
机译:Ghrelin是一种多效性神经肽,最近与癫痫有关。迄今为止进行的动物研究表明,生长素释放肽具有抗惊厥作用。然而,其抗惊厥作用的机制尚不清楚。在这里,我们显示生长素释放肽的抗惊厥作用是通过生长激素促分泌素受体(GHSR)介导的。然而,令我们惊讶的是,我们发现,用毛果芸香碱处理后,GHSR基因敲除小鼠的癫痫发作阈值高于野生型同窝小鼠。使用体内和体外模型,我们进一步发现GHSR的反向激动作用和脱敏/内在化作用减弱了大鼠的边缘性癫痫发作和海马切片的癫痫样活动。这构成了一种抗惊厥作用的新机制,从而使内源性激动剂降低了组成型活性受体的活性。电子补充材料本文的在线版本(doi:10.1007 / s13311-012-0125-x)包含补充材料,可以通过购买获得给授权用户。

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