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Cannabinoids and Their Interactions with Diazepam on Modulation of Serum Corticosterone Concentration in Male Mice

机译:大麻素及其与地西p的相互作用对雄性小鼠血清皮质酮浓度的调节

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Experimental results indicate a mutual interaction between cannabinoidergic and GABAergic systems; however, the interaction between these systems on corticosterone release has not been fully investigated. In this study, we treated male mice with either cannabinoid compounds alone or in combination with diazepam. Blood samples were collected at 60 min post-injection. The serum corticosterone (CORT) level was measured using ELISA technique. Acute treatment of mice by cannabinoid receptor agonist WIN55212-2 (2.5 mg/kg; i.p.) resulted in a significant reduction of CORT, while treatment with either endocannabinoid reuptake inhibitor AM404 or endocannabinoid degradation enzyme inhibitor URB597 increased CORT compared to control group. Co-administration of AM404 or URB597 with cannabinoid CB1 receptor antagonist AM251 blocked the effect of these compounds on CORT. Treatment of mice with different doses of diazepam alone did not alter CORT compared to control group. However, co-administration of diazepam and either AM404 or WIN55212-2 significantly reduced CORT compared to the respective group treated with cannabinoid compound alone. Co-administration of ineffective dose of URB597 and ineffective dose of diazepam increased CORT level compared to groups treated with each compound alone. In conclusion, our findings suggest that the endogenous cannabinoid system is active as a modulator of CORT in mice and diazepam can alter the effect of cannabinoid system in the modulation of neuroendocrine functions. Keywords Corticosterone - Cannabinoid - Diazepam - ELISA
机译:实验结果表明,大麻素能系统和GABA能系统之间存在相互作用。然而,尚未完全研究这些系统之间在皮质酮释放上的相互作用。在这项研究中,我们用大麻素化合物单独或与地西epa组合治疗了雄性小鼠。注射后60分钟收集血样。使用ELISA技术测量血清皮质酮(CORT)水平。大麻素受体激动剂WIN55212-2(2.5 mg / kg; i.p.)对小鼠的急性治疗导致CORT显着降低,而与对照组相比,使用内源性大麻素再摄取抑制剂AM404或内源性大麻素降解酶抑制剂URB597可以提高CORT。 AM404或URB597与大麻素CB1受体拮抗剂AM251共同给药可阻断这些化合物对CORT的作用。与对照组相比,单独使用不同剂量地西epa的小鼠治疗不会改变CORT。但是,与单独使用大麻素类化合物治疗的组相比,地西epa和AM404或WIN55212-2的共同给药显着降低了CORT。与单独使用每种化合物治疗的组相比,无效剂量的URB597和无效剂量的地西epa的共同给药增加了CORT水平。总之,我们的发现表明,内源性大麻素系统在小鼠中可作为CORT的调节剂,而地西epa可改变大麻素系统在调节神经内分泌功能中的作用。皮质酮-大麻素-地西p-ELISA

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