Dinu I R, Popa Simona Georgiana, Moţa Maria, Moţa E, Stănciulescu Camelia, Ioana M, Cruce M
Department of Diabetes, University of Medicine and Pharmacy of Craiova, Romania.
Rom J Morphol Embryol. 2011;52(3):791-5.
The endocannabinoid system (ECS) is an important physiological system that modulates appetite, food intake, energy homeostasis, substance addiction. It is comprised of the cannabinoid receptors (CB1 and CB2), the endogenous lipid ligands of these receptors and the enzymes that mediate the endogenous ligands' biosynthesis and degradation. CB1 receptor is expressed in the brain, adipose tissue, liver, skeletal muscle, gastrointestinal tract and pancreas. The CB1 receptor is encoded by CNR1 gene located at 6q14-q15 level. The aim of our study was to investigate the possible correlation between rs1049353 polymorphism of the CNR1 gene with levels of adiponectin in a group of subjects from Romania. The study included 305 subjects divided in two groups according to their fasting adiponectin levels. Fasting adiponectin levels were determined using ELISA technique. The genotyping of the rs1049353 polymorphism of the CNR1 gene was made using the Real-Time PCR technique. The statistical analysis was performed using De Finetti's program. The differences between the allelic frequencies indicated that the presence of G-wild allele seems to confer risk for expressing low levels of adiponectin (OR=1.917; 95%C.I.=1.353-2.715; p=0.00023) and A-mutant allele seems to be protective (OR=0.522; 95%C.I.=0.368-0.739; p=0.00023). At the test of allelic positivity, the presence of the G-allele conferred risk of hypoadiponectinemia (OR=2.113; 95%C.I.=1.324-3.373). In conclusion, this study indicates that the rs1049353 polymorphism of the CNR1 gene is associated with decreased levels of adiponectin. Further research is needed in order to elucidate the link between the polymorphisms of the CNR1 gene and adiponectin levels.
内源性大麻素系统(ECS)是一个重要的生理系统,可调节食欲、食物摄入、能量平衡和物质成瘾。它由大麻素受体(CB1和CB2)、这些受体的内源性脂质配体以及介导内源性配体生物合成和降解的酶组成。CB1受体在大脑、脂肪组织、肝脏、骨骼肌、胃肠道和胰腺中表达。CB1受体由位于6q14 - q15水平的CNR1基因编码。我们研究的目的是调查罗马尼亚一组受试者中CNR1基因的rs1049353多态性与脂联素水平之间可能存在的相关性。该研究纳入了305名受试者,根据其空腹脂联素水平分为两组。使用ELISA技术测定空腹脂联素水平。使用实时PCR技术对CNR1基因的rs1049353多态性进行基因分型。使用德菲内蒂程序进行统计分析。等位基因频率之间的差异表明,G野生型等位基因的存在似乎会增加脂联素低表达的风险(OR = 1.917;95%置信区间= 1.353 - 2.715;p = 0.00023),而A突变型等位基因似乎具有保护作用(OR = 0.522;95%置信区间= 0.368 - 0.739;p = 0.00023)。在等位基因阳性检测中,G等位基因的存在会增加低脂联素血症的风险(OR = 2. 113;95%置信区间= 1.324 - 3.373)。总之,本研究表明CNR1基因的rs1049353多态性与脂联素水平降低有关。需要进一步研究以阐明CNR1基因多态性与脂联素水平之间的联系。