Ghahramanian Golzar Mina, Babri Shirin, Ataie Zohre, Ebrahimi Hadi, Mirzaie Fariba, Mohaddes Gisou
Neuroscience Research Centre (NSRC), Tabriz University of Medical Sciences, Tabriz, Iran.
Adv Pharm Bull. 2013;3(2):265-71. doi: 10.5681/apb.2013.043. Epub 2013 Aug 20.
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.
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.
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).
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.
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。
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)。
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。
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。