Yamada M, Groshan K, Phung C T, Yamada M, Hisamitsu T, Richelson E
Department of Psychiatry, Mayo Foundation and Mayo Clinic Jacksonville, FL 32224, USA.
Brain Res Mol Brain Res. 1997 Feb;44(1):12-20. doi: 10.1016/s0169-328x(96)00139-8.
We molecularly cloned the kappa opioid receptor from a human substantia nigra cDNA library. When expressed in HEK293 cells, the cloned receptor had similar pharmacological characteristics to the rat kappa opioid receptor. Northern blot analysis showed the presence of a single transcript of about 6 kb in size for mRNA prepared from the substantia nigra. Using in situ hybridization histochemistry, we studied the expression of this receptor in postmortem human brains from control and Parkinson's disease subjects. Kappa opioid receptor mRNA was present in melanized (possibly dopaminergic) neurons of the substantia nigra and the nucleus paranigralis. On the other hand, Parkinson's disease brains had markedly fewer melanized neurons, as expected, and correspondingly very low or background levels of mRNA for the kappa opioid receptor. However, in some cases, remaining melanized neurons still expressed the receptor mRNA. From these results we suggest that dopaminergic neurons in the human substantia nigra and the nucleus paranigralis synthesize kappa opioid receptors and express them in their perikarya and their terminal regions. The kappa opioid receptor expressed in the melanized neurons may play a role in the normal function of dopaminergic systems and possibly in the etiology of Parkinson's disease.
我们从人黑质cDNA文库中对κ阿片受体进行了分子克隆。当在HEK293细胞中表达时,克隆的受体具有与大鼠κ阿片受体相似的药理学特性。Northern印迹分析显示,从黑质制备的mRNA存在一条约6 kb大小的单一转录本。利用原位杂交组织化学技术,我们研究了该受体在对照和帕金森病患者死后人类大脑中的表达情况。κ阿片受体mRNA存在于黑质和黑质旁核的黑素化(可能是多巴胺能)神经元中。另一方面,正如预期的那样,帕金森病患者的大脑中黑素化神经元明显减少,相应地,κ阿片受体的mRNA水平非常低或处于背景水平。然而,在某些情况下,剩余的黑素化神经元仍表达受体mRNA。根据这些结果,我们认为人黑质和黑质旁核中的多巴胺能神经元合成κ阿片受体,并在其胞体和终末区域表达它们。黑素化神经元中表达的κ阿片受体可能在多巴胺能系统的正常功能中发挥作用,并且可能与帕金森病的病因有关。