Department of Psychology and Neuroscience Graduate Program, University of Guelph, Guelph, Ontario, Canada.
Physiol Behav. 2013 Aug 15;120:228-32. doi: 10.1016/j.physbeh.2013.08.015. Epub 2013 Aug 16.
The role of the endocannabinoid system in vomiting has been previously studied using several animal species. These investigations have clearly demonstrated an anti-emetic role for the eCB, anandamide, in these animal models; however, research concerning the role of 2-arhachidonoylglycerol (2AG) has been less clear. The aim of the present study was to assess the effects of exogenous 2AG administration in the house musk shrew, Suncus murinus. In Experiment 1, shrews were injected with vehicle or 2AG (1, 2, 5, 10 mg/kg) 15 min prior to behavioral testing in which the frequency of vomiting episodes was observed. In Experiment 2, shrews were pre-treated with 2AG (2, 5 mg/kg) prior to being administered the emetic drug, lithium chloride (LiCl). It was found that 2AG alone did not induce emesis, but interfered with vomiting in response to LiCl administration. The anti-emetic effects of 2AG in Suncus murinus do not appear to be mediated by CB1 receptors, as concomitant pretreatment with the CB1 receptor antagonist, SR141716, did not reverse the suppressive effects of 2AG. These results confirm that manipulations that increase levels of 2AG exert anti-emetic effects in the house musk shrew.
内源性大麻素系统在呕吐中的作用以前曾在几种动物物种中进行过研究。这些研究清楚地表明,在这些动物模型中,大麻素内酰胺(anandamide)具有止吐作用;然而,关于 2-花生四烯酸甘油(2AG)作用的研究则不太明确。本研究的目的是评估外源性 2AG 给药在麝鼩中的作用。在实验 1 中,在行为测试前 15 分钟,将动物注射载体或 2AG(1、2、5、10mg/kg),观察呕吐发作的频率。在实验 2 中,先给麝鼩预先用 2AG(2、5mg/kg)处理,然后再给予催吐药物氯化锂(LiCl)。结果发现,2AG 本身不会引起呕吐,但会干扰对 LiCl 给药的呕吐反应。2AG 在 Suncus murinus 中的止吐作用似乎不是由 CB1 受体介导的,因为同时预先用 CB1 受体拮抗剂 SR141716 处理并不能逆转 2AG 的抑制作用。这些结果证实,增加 2AG 水平的操作在麝鼩中具有止吐作用。