Sun J, Cairns N J, Perlmutter J S, Mach R H, Xu J
Department of Radiology, Washington University School of Medicine, 510 S. Kingshighway Boulevard, St. Louis, MO 63110, USA; Neurosurgery Department, The Second Affiliated Hospital of Medical College, Xi'an Jiaotong University, Xi'an, Shaanxi 710004, PR China.
Department of Neurology, Washington University School of Medicine, 510 S. Kingshighway Boulevard, St. Louis, MO 63110, USA; Department of Pathology & Immunology, Washington University School of Medicine, 510 S. Kingshighway Boulevard, St. Louis, MO 63110, USA.
Neuroscience. 2013 Sep 17;248:112-26. doi: 10.1016/j.neuroscience.2013.05.048. Epub 2013 Jun 1.
The regulation of D₃ receptor has not been well documented in diffuse Lewy body disease (DLBD). In this study, a novel D₃-preferring radioligand [(3)H]WC-10 and a D₂-preferring radioligand [(3)H]raclopride were used and the absolute densities of the dopamine D₃ and D₂ receptors were determined in the striatal regions and substantia nigra (SN) from postmortem brains from five cases of DLBD, which included dementia with Lewy bodies (DLB, n=4) and Parkinson disease dementia (PDD, n=1). The densities of the dopamine D₁ receptor, vesicular monoamine transporter 2 (VMAT2), and dopamine transporter (DAT) were also measured by quantitative autoradiography using [(3)H]SCH23390, [(3)H]dihydrotetrabenazine, and [(3)H]WIN35428, respectively. The densities of these dopaminergic markers were also measured in the same brain regions in 10 age-matched control cases. Dopamine D₃ receptor density was significantly increased in the striatal regions including caudate, putamen and nucleus accumbens (NAc). There were no significant changes in the dopamine D₁ and D₂ receptor densities in any brain regions measured. VMAT2 and DAT densities were reduced in all the brain regions measured in DLB/PDD, however, the significant reduction was found in the putamen for DAT and in the NAc and SN for VMAT2. The decrease of dopamine pre-synaptic markers implies neuronal loss in the substantia nigra pars compacta (SNpc) in these DLB/PDD cases, while the increase of D₃ receptors in striatal regions could be attributed to dopaminergic medication history and psychiatric states such as hallucinations. Whether it also reflects compensatory regulation upon dopaminergic denervation warrants further confirmations on larger populations.
在弥漫性路易体病(DLBD)中,D₃受体的调节尚未得到充分记载。在本研究中,使用了一种新型的对D₃有偏好的放射性配体[(3)H]WC - 10和一种对D₂有偏好的放射性配体[(3)H]雷氯必利,测定了5例DLBD患者尸检脑纹状体区域和黑质(SN)中多巴胺D₃和D₂受体的绝对密度,其中包括路易体痴呆(DLB,n = 4)和帕金森病痴呆(PDD,n = 1)。还分别使用[(3)H]SCH23390、[(3)H]二氢四苯嗪和[(3)H]WIN35428通过定量放射自显影法测量了多巴胺D₁受体、囊泡单胺转运体2(VMAT2)和多巴胺转运体(DAT)的密度。在10例年龄匹配的对照病例的相同脑区中也测量了这些多巴胺能标志物的密度。在包括尾状核、壳核和伏隔核(NAc)的纹状体区域,多巴胺D₃受体密度显著增加。在所测量的任何脑区中,多巴胺D₁和D₂受体密度均无显著变化。在DLB/PDD患者所测量的所有脑区中,VMAT2和DAT密度均降低,然而,DAT在壳核、VMAT2在NAc和SN有显著降低。多巴胺突触前标志物的减少意味着这些DLB/PDD病例中黑质致密部(SNpc)存在神经元丢失,而纹状体区域D₃受体的增加可能归因于多巴胺能用药史和幻觉等精神状态。它是否也反映了对多巴胺能去神经支配的代偿性调节,有待在更大规模人群中进一步证实。