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1
Does ghrelin level change after epileptic seizure in rats?大鼠癫痫发作后生长激素释放肽水平是否变化?
Seizure. 2011 May;20(4):347-9. doi: 10.1016/j.seizure.2011.01.001. Epub 2011 Feb 3.
2
Ghrelin, des-acyl ghrelin, and obestatin: regulatory roles on the gastrointestinal motility.胃饥饿素、去酰基胃饥饿素和肥胖抑制素:对胃肠动力的调节作用
Int J Pept. 2010;2010. doi: 10.1155/2010/305192. Epub 2010 Mar 15.
3
Ghrelin attenuates kainic acid-induced neuronal cell death in the mouse hippocampus.生长激素释放肽减轻小鼠海马区海人酸诱导的神经元细胞死亡。
J Endocrinol. 2010 Jun;205(3):263-70. doi: 10.1677/JOE-10-0040. Epub 2010 Mar 29.
4
Ghrelin in central neurons.Ghrelin 在中枢神经元中的作用。
Curr Neuropharmacol. 2009 Mar;7(1):37-49. doi: 10.2174/157015909787602779.
5
The role of nitric oxide in the inhibitory effect of ghrelin against penicillin-induced epileptiform activity in rat.一氧化氮在胃饥饿素对大鼠青霉素诱导的癫痫样活动的抑制作用中的作用。
Neuropeptides. 2009 Aug;43(4):295-302. doi: 10.1016/j.npep.2009.05.005. Epub 2009 Jun 23.
6
Altered GABAergic neurotransmission is associated with increased kainate-induced seizure in prostaglandin-endoperoxide synthase-2 deficient mice.γ-氨基丁酸能神经传递的改变与前列腺素内过氧化物合酶-2缺陷小鼠中增加的红藻氨酸诱导的癫痫发作有关。
Brain Res Bull. 2008 Mar 28;75(5):598-609. doi: 10.1016/j.brainresbull.2007.10.004. Epub 2007 Nov 9.
7
Progress in neuroprotective strategies for preventing epilepsy.预防癫痫的神经保护策略进展
Prog Neurobiol. 2008 Apr;84(4):363-404. doi: 10.1016/j.pneurobio.2007.10.010. Epub 2007 Dec 8.
8
Seizure activity and changes in hippocampal extracellular glutamate, GABA, dopamine and serotonin.癫痫发作活动以及海马细胞外谷氨酸、γ-氨基丁酸、多巴胺和5-羟色胺的变化。
Epilepsy Res. 2008 Jan;78(1):50-9. doi: 10.1016/j.eplepsyres.2007.10.007. Epub 2007 Dec 3.
9
Ghrelin in neuroendocrine organs and tumours.神经内分泌器官及肿瘤中的胃饥饿素
Pituitary. 2007;10(3):213-25. doi: 10.1007/s11102-007-0023-0.
10
Antiepileptic effects of ghrelin on pentylenetetrazole-induced seizures in rats.胃饥饿素对戊四氮诱导的大鼠癫痫发作的抗癫痫作用。
Peptides. 2007 Jun;28(6):1214-9. doi: 10.1016/j.peptides.2007.04.003. Epub 2007 Apr 19.

神经肽Y受体阻断可防止胃饥饿素在大鼠海马体中的抗惊厥作用。

NPY Receptors Blockade Prevents Anticonvulsant Action of Ghrelin in the Hippocampus of Rat.

作者信息

Ghahramanian Golzar Mina, Babri Shirin, Ataie Zohre, Ebrahimi Hadi, Mirzaie Fariba, Mohaddes Gisou

机构信息

Neuroscience Research Centre (NSRC), Tabriz University of Medical Sciences, Tabriz, Iran.

出版信息

Adv Pharm Bull. 2013;3(2):265-71. doi: 10.5681/apb.2013.043. Epub 2013 Aug 20.

DOI:10.5681/apb.2013.043
PMID:24312846
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3848244/
Abstract

PURPOSE

Ghrelin has been shown to have antiepileptic function. However, the underlying mechanisms by which, ghrelin exerts its antiepileptic effects are still unclear. In the present study, we investigated whether neuropeptide Y (NPY) mediates ghrelin anticonvulsant effect in the brain through its Y1, Y2 or Y5 receptors.

METHODS

Male Wistar rats were bilaterally microinjected with ghrelin 0.3 nmol/μl/side and NPY antagonists; GR231118 (Y1 receptor antagonist), BIIE0246 (Y2 receptor antagonist), CGP71683 (Y5 receptor antagonist) or solvents (Saline, DMSO) into the dorsal hippocampus 20 minutes before ghrelin administration. Thirty minutes after ghrelin microinjection, a single convulsive dose of pentylenetetrazole (PTZ) (50 mg/kg) was injected intraperitoneally (ip). Afterwards, duration of seizure and total seizure score (TSS) were assessed for 30 minutes in all animals.

RESULTS

Intrahippocampal injection of 0.3 nmol/μl/side ghrelin decreased duration of seizure and TSS induced by PTZ. The suppression of both duration (p<0.001) and TSS (p<0.001) induced by ghrelin in hippocampus were significantly blocked by GR231118 (10 μg/μl/side), BIIE0246 (400 pmol/μl/side) and CGP 71683A (5 nmol/μl/side).

CONCLUSION

Our findings suggest that NPY Y1, Y2 and Y5 receptors in the hippocampus may somehow mediate the anticonvulsive action of ghrelin. Therefore, it is possible to speculate that ghrelin acts in the hippocampus to modulate seizures via NPY.

摘要

目的

已证实胃饥饿素具有抗癫痫功能。然而,胃饥饿素发挥其抗癫痫作用的潜在机制仍不清楚。在本研究中,我们调查了神经肽Y(NPY)是否通过其Y1、Y2或Y5受体介导胃饥饿素在脑中的抗惊厥作用。

方法

在给雄性Wistar大鼠注射胃饥饿素前20分钟,将胃饥饿素0.3 nmol/μl/侧和NPY拮抗剂;GR231118(Y1受体拮抗剂)、BIIE0246(Y2受体拮抗剂)、CGP71683(Y5受体拮抗剂)或溶剂(生理盐水、二甲基亚砜)双侧微量注射到背侧海马体中。在微量注射胃饥饿素30分钟后,腹腔注射(ip)单剂量惊厥剂量的戊四氮(PTZ)(50 mg/kg)。之后,对所有动物评估30分钟的癫痫发作持续时间和总癫痫发作评分(TSS)。

结果

海马体内注射0.3 nmol/μl/侧胃饥饿素可缩短PTZ诱导的癫痫发作持续时间和TSS。GR231118(10 μg/μl/侧)、BIIE0246(400 pmol/μl/侧)和CGP 71683A(5 nmol/μl/侧)可显著阻断胃饥饿素在海马体中对癫痫发作持续时间(p<0.001)和TSS(p<0.001)的抑制作用。

结论

我们的研究结果表明,海马体中的NPY Y1、Y2和Y5受体可能以某种方式介导胃饥饿素的抗惊厥作用。因此,可以推测胃饥饿素在海马体中通过NPY调节癫痫发作。