Noradrenergic alterations in Parkinson’s disease: a combined 11C-yohimbine PET/neuromelanin MRI study

蓝斑 神经黑素 神经科学 帕金森病 育亨宾 壳核 医学 心理学 脑岛 黑质 内科学 疾病 中枢神经系统 受体 敌手
作者
Chloé Laurencin,Sophie Lancelot,Sarah Brosse,Inès Mérida,Jérôme Redouté,Elise Greusard,Ludovic Lamberet,Véronique Liotier,Didier Le Bars,Nicolas Costes,Stéphane Thobois,Philippe Boulinguez,Bénédicte Ballanger
出处
期刊:Brain [Oxford University Press]
卷期号:147 (4): 1377-1388 被引量:18
标识
DOI:10.1093/brain/awad338
摘要

Abstract Degeneration of the noradrenergic system is now considered a pathological hallmark of Parkinson’s disease, but little is known about its consequences in terms of parkinsonian manifestations. Here, we evaluated two aspects of the noradrenergic system using multimodal in vivo imaging in patients with Parkinson’s disease and healthy controls: the pigmented cell bodies of the locus coeruleus with neuromelanin sensitive MRI; and the density of α2-adrenergic receptors (ARs) with PET using 11C-yohimbine. Thirty patients with Parkinson’s disease and 30 age- and sex-matched healthy control subjects were included. The characteristics of the patients’ symptoms were assessed using the Movement Disorder Society Unified Parkinson’s Disease Rating Scale (MDS-UPDRS). Patients showed reduced neuromelanin signal intensity in the locus coeruleus compared with controls and diminished 11C-yohimbine binding in widespread cortical regions, including the motor cortex, as well as in the insula, thalamus and putamen. Clinically, locus coeruleus neuronal loss was correlated with motor (bradykinesia, motor fluctuations, tremor) and non-motor (fatigue, apathy, constipation) symptoms. A reduction of α2-AR availability in the thalamus was associated with tremor, while a reduction in the putamen, the insula and the superior temporal gyrus was associated with anxiety. These results highlight a multifaceted alteration of the noradrenergic system in Parkinson’s disease since locus coeruleus and α2-AR degeneration were found to be partly uncoupled. These findings raise important issues about noradrenergic dysfunction that may encourage the search for new drugs targeting this system, including α2-ARs, for the treatment of Parkinson’s disease.
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