کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1178053 962660 2016 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Mechanistic study of the inhibitory activity of Geum urbanum extract against α-Synuclein fibrillation
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
پیش نمایش صفحه اول مقاله
Mechanistic study of the inhibitory activity of Geum urbanum extract against α-Synuclein fibrillation
چکیده انگلیسی


• Geum urbanum inhibits α-Synuclein fibrillation.
• Geum urbanum partly disintegrates preformed α-Synuclein fibrils.
• The fibrillation ability of the aggregation prone intermediate(s) may be reduced.
• Geum urbanum may direct aggregation towards a non-fibrillar state.

The presence of Lewy bodies and Lewy neurites is a major pathological hallmark of Parkinson's disease and is hypothesized to be linked to disease development, although this is not yet conclusive. Lewy bodies and Lewy neurites primarily consist of fibrillated α-Synuclein; yet, there is no treatment available targeting stabilization of α-Synuclein in its native state. The aim of the present study was to investigate the inhibitory activity of an ethanolic extract of Geum urbanum against α-Synuclein fibrillation and examine the structural changes of α-Synuclein in the presence of the extract. The anti-fibrillation and anti-aggregation activities of the plant extract were monitored by thioflavin T fibrillation assays and size exclusion chromatography, while structural changes were followed by circular dichroism, Fourier transform infrared spectroscopy, intrinsic fluorescence, small angle X-ray scattering and electron microscopy. Since the extract is a complex mixture, structure-function relationships could not be determined. Under the experimental conditions investigated, Geum urbanum was found to inhibit α-Synuclein fibrillation in a concentration dependent way, and to partly disintegrate preformed α-Synuclein fibrils. Based on the structural changes of α-Synuclein in the presence of extract, we propose that Geum urbanum delays α-Synuclein fibrillation either by reducing the fibrillation ability of one or more of the aggregation prone intermediates or by directing α-Synuclein aggregation towards a non-fibrillar state. However, whether these alterations of the fibrillation pathway lead to less pathogenic species is yet to be determined.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics - Volume 1864, Issue 9, September 2016, Pages 1160–1169
نویسندگان
, , , , , , , ,