自主神经突触病患者尿中去甲肾上腺素和多巴胺排泄减少。

IF 3.9 3区 医学 Q1 CLINICAL NEUROLOGY
David S Goldstein, Patti Sullivan, Courtney Holmes
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引用次数: 0

摘要

背景:自主突触核蛋白病以自主功能衰竭和细胞内α -突触核蛋白沉积为特征。这三种情况分别是路易体病(lbd)、帕金森病(PD)和纯自主神经衰竭(PAF)以及非lbd突触核蛋白病多系统萎缩(MSA)。这些疾病都涉及大脑、交感神经支配器官或两者的儿茶酚胺能异常;然而,关于肾脏儿茶酚胺能在自主神经突触核蛋白病中的功能知之甚少。我们测量了PD、PAF和MSA组和对照组中交感神经递质去甲肾上腺素、激素肾上腺素、自分泌-旁分泌物质多巴胺、儿茶酚胺前体3,4-二羟基苯丙氨酸(DOPA)、3,4-二羟基苯二醇(DHPG,去甲肾上腺素的主要神经元代谢物)和3,4-二羟基苯乙酸(DOPAC,多巴胺的主要代谢物)的尿排泄率。方法:回顾1995年至2024年在美国国立卫生研究院(NIH)临床中心收集尿液(通常为3.5小时)的所有研究参与者的数据。对照组既没有自主神经衰竭,也没有运动障碍。结果:PD患者去甲肾上腺素排泄率较对照组降低(p = 0.0001), PAF患者去甲肾上腺素排泄率较对照组降低(p = 0.0001)。结论:自主神经突触核蛋白病与尿中去甲肾上腺素和多巴胺排泄率降低有关。由于人体中几乎所有的尿多巴胺都来源于循环多巴,所以尿中去甲肾上腺素和多巴胺的低排泄率可能反映了肾交感去甲肾上腺素能系统、多巴-多巴自分泌-旁分泌系统或两者的功能障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Decreased urinary excretion of norepinephrine and dopamine in autonomic synucleinopathies.

Background: Autonomic synucleinopathies feature autonomic failure and intracellular deposition of the protein alpha-synuclein. Three such conditions are the Lewy body diseases (LBDs) Parkinson's disease (PD) and pure autonomic failure (PAF) and the non-LBD synucleinopathy multiple system atrophy (MSA). These diseases all entail catecholaminergic abnormalities in the brain, sympathetically innervated organs, or both; however, little is known about renal catecholaminergic functions in autonomic synucleinopathies. We measured urinary excretion rates of the sympathetic neurotransmitter norepinephrine, the hormone epinephrine, the autocrine-paracrine substance dopamine, the catecholamine precursor 3,4-dihydroxyphenylalanine (DOPA), 3,4-dihydroxyphenylglycol (DHPG, the main neuronal metabolite of norepinephrine), and 3,4-dihydroxyphenylacetic acid (DOPAC, a major dopamine metabolite), in PD, PAF, and MSA groups and controls.

Methods: Data were reviewed from all research participants who had urine collections (usually 3.5 h) at the National Institutes of Health (NIH) Clinical Center from 1995 to 2024. The control cohort had neither autonomic failure nor a movement disorder.

Results: Norepinephrine excretion rates were decreased compared with controls in PD (p = 0.0001), PAF (p < 0.0001), and MSA (p < 0.0001). Dopamine excretion was also decreased in the three groups (PD: p = 0.0136, PAF: p = 0.0027, MSA: p = 0.0344). DHPG excretion was decreased in PD (p = 0.0004) and PAF (p = 0.0004) but not in MSA. DOPA and epinephrine excretion did not differ among the study groups.

Conclusions: Autonomic synucleinopathies involve decreased urinary excretion rates of norepinephrine and dopamine. Since virtually all of urinary dopamine in humans is derived from circulating DOPA, the low rates of urinary norepinephrine and dopamine excretion may reflect dysfunctions in the renal sympathetic noradrenergic system, the DOPA-dopamine autocrine-paracrine system, or both systems.

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来源期刊
Clinical Autonomic Research
Clinical Autonomic Research 医学-临床神经学
CiteScore
7.40
自引率
6.90%
发文量
65
审稿时长
>12 weeks
期刊介绍: Clinical Autonomic Research aims to draw together and disseminate research work from various disciplines and specialties dealing with clinical problems resulting from autonomic dysfunction. Areas to be covered include: cardiovascular system, neurology, diabetes, endocrinology, urology, pain disorders, ophthalmology, gastroenterology, toxicology and clinical pharmacology, skin infectious diseases, renal disease. This journal is an essential source of new information for everyone working in areas involving the autonomic nervous system. A major feature of Clinical Autonomic Research is its speed of publication coupled with the highest refereeing standards.
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