Zhang Qing-Yu, Fan Xiao-Na, Cao Yi
Key Laboratory of Animal Models and Human Disease Mechanisms of the Chinese Academy of Sciences & Yunnan Province, Kunming Institute of Zoology, Kunming Yunnan 650223, China.
Dongwuxue Yanjiu. 2011 Feb;32(1):31-9. doi: 10.3724/SP.J.1141.2011.01031.
To make Macaca mulatta and Tupaia belangeri as experimental animals for studying functions of opioid and cannabinoid receptors in drug addiction, we examined expression of the opioid and cannabinoid receptors in nervous and immune system of the two animals. We dissected normal adult M. mulatta and T. belangeri, collected tissues of cortex, cerebellum, brain stem, hippocampus, spinal cord, and spleen, and then applied the semi-quantitative PCR and real-time quantitative PCR methods to investigate the mRNA expression levels of the opioid and cannabinoid receptors in these tissues. In M. mulatta, the cannabinoid receptor 1 (CNR1) mRNA was expressed in the all tissues; in contrast, the cannabinoid receptor 2 (CNR2) mRNA was only present in the spleen. The mu opioid receptor (MOPR) was detected in all tissues, and the kappa opioid receptor (KOPR) was found in the cortex, cerebellum, brain stem, and spinal cord, but not in hippocampus and spleen. However, the delta opioid receptor (DOPR) was restrictively expressed in the hippocampus. In T. belangeri, CNR1 and CNR2 were expressed in the five regions of the brain. CNR2, but no CNR1, was also detected in the spleen. MOPR was expressed in all examined tissues, and its expression levels in the brain were higher than that in the spleen. DOPR and KOPR were not found in all tissues. Taken together, the expression profiles of cannabinoid receptors in human being, M. mulatta, T. belangeri, and rat were similar, and the expression patterns of the opioid receptors in M. mulatta were more close to human beings. The opioid and cannabinoid receptors were expressed in the tissues of nervous and immune systems of M. mulatta and T. belangeri, and both animals could be used for studying drug addiction. Macaca mulatta is still the best experimental animal for drug addiction research because it shows very similar expression profiles of these receptors to human beings.
为了将猕猴和树鼩作为研究阿片类和大麻素受体在药物成瘾中功能的实验动物,我们检测了这两种动物神经和免疫系统中阿片类和大麻素受体的表达。我们解剖了成年正常猕猴和树鼩,收集了皮质、小脑、脑干、海马、脊髓和脾脏组织,然后应用半定量PCR和实时定量PCR方法研究这些组织中阿片类和大麻素受体的mRNA表达水平。在猕猴中,大麻素受体1(CNR1)mRNA在所有组织中均有表达;相比之下,大麻素受体2(CNR2)mRNA仅存在于脾脏中。μ阿片受体(MOPR)在所有组织中均被检测到,κ阿片受体(KOPR)在皮质、小脑、脑干和脊髓中被发现,但在海马和脾脏中未被发现。然而,δ阿片受体(DOPR)在海马中限制性表达。在树鼩中,CNR1和CNR2在脑的五个区域中表达。脾脏中也检测到了CNR2,但未检测到CNR1。MOPR在所有检测组织中均有表达,其在脑中的表达水平高于脾脏。在所有组织中均未发现DOPR和KOPR。综上所述,人类、猕猴、树鼩和大鼠中大麻素受体的表达谱相似,猕猴中阿片受体的表达模式与人类更接近。阿片类和大麻素受体在猕猴和树鼩的神经和免疫系统组织中均有表达,这两种动物均可用于研究药物成瘾。猕猴仍然是药物成瘾研究的最佳实验动物,因为它显示出这些受体的表达谱与人类非常相似。