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植物中毒导致袋鼠的α-突触核蛋白病和神经黑色素病。

Plant poisoning leads to alpha-synucleinopathy and neuromelanopathy in kangaroos.

机构信息

School of Medicine, Western Sydney University, Campbelltown, NSW, Australia.

Florey Institute of Neuroscience and Mental Health, Parkville, Victoria, Australia.

出版信息

Sci Rep. 2019 Nov 13;9(1):16546. doi: 10.1038/s41598-019-53396-8.

Abstract

The pathogenesis of synucleinopathies, common neuropathological lesions normally associated with some human neurodegenerative disorders such as Parkinson's disease, dementia with Lewy bodies and multiple system atrophy, remains poorly understood. In animals, ingestion of the tryptamine-alkaloid-rich phalaris pastures plants causes a disorder called Phalaris staggers, a neurological syndrome reported in kangaroos. The aim of the study was to characterise the clinical and neuropathological changes associated with spontaneous cases of Phalaris staggers in kangaroos. Gross, histological, ultrastructural and Immunohistochemical studies were performed to demonstrate neuronal accumulation of neuromelanin and aggregated α-synuclein. ELISA and mass spectrometry were used to detect serum-borne α-synuclein and tryptamine alkaloids respectively. We report that neurons in the central and enteric nervous systems of affected kangaroos display extensive accumulation of neuromelanin in the perikaryon without affecting neuronal morphology. Ultrastructural studies confirmed the typical structure of neuromelanin. While we demonstrated strong staining of α-synuclein, restricted to neurons, intracytoplasmic Lewy bodies inclusions were not observed. α-synuclein aggregates levels were shown to be lower in sera of the affected kangaroos compared to unaffected herd mate kangaroos. Finally, mass spectrometry failed to detect the alkaloid toxins in the sera derived from the affected kangaroos. Our preliminary findings warrant further investigation of Phalaris staggers in kangaroos, potentially a valuable large animal model for environmentally-acquired toxic synucleinopathy.

摘要

α-突触核蛋白病的发病机制尚不清楚,α-突触核蛋白病是一种常见的神经病理学病变,通常与一些人类神经退行性疾病有关,如帕金森病、路易体痴呆和多系统萎缩。在动物中,摄入富含色胺生物碱的雀麦草料植物会导致一种称为雀麦蹒跚病的疾病,这是一种在袋鼠中报道的神经综合征。本研究的目的是描述与袋鼠自发发生的雀麦蹒跚病相关的临床和神经病理学变化。进行了大体、组织学、超微结构和免疫组织化学研究,以证明神经元中存在神经黑色素和聚集的α-突触核蛋白的积累。使用 ELISA 和质谱分别检测血清中携带的α-突触核蛋白和色胺生物碱。我们报告说,受影响的袋鼠中枢和肠神经系统的神经元在胞质中广泛积累神经黑色素,而不影响神经元形态。超微结构研究证实了神经黑色素的典型结构。虽然我们证明了α-突触核蛋白的强烈染色,仅限于神经元,但未观察到细胞内路易体包涵体。与未受影响的同群袋鼠相比,受影响的袋鼠血清中的α-突触核蛋白聚集水平较低。最后,质谱未能从受影响的袋鼠血清中检测到生物碱毒素。我们的初步发现证明了在袋鼠中进一步研究雀麦蹒跚病的必要性,这可能是一种有价值的环境获得性毒性突触核蛋白病的大动物模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/000f/6853926/4df8fd59840a/41598_2019_53396_Fig1_HTML.jpg

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