Neuroprotective Effect of σ1-Receptors on the Cell Model of Huntington’s Disease


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详细

Huntington’s disease is a hereditary neurodegenerative disease that primarily affects striatal neurons. Recent studies demonstrated abnormalities in calcium regulation in striatal neurons in Huntington’s disease, which leads to elimination of synaptic connections between cortical and striatal neurons. In the present study, we focused on the neuroprotective properties of σ1-receptor, because one of its main functions is associated with modulation of calcium homeostasis in cells. The application of selective σ1-receptor agonists to the corticostriatal cell culture restores synaptic connections between the cortical and striatal neurons. Based on the obtained data, we assume that σ1-receptor is a promising target for the development of drugs for the therapy of Huntington’s disease.

作者简介

A. Bol’shakova

Laboratory of Molecular Neurodegeneration, Peter the Great St. Petersburg State Polytechnic University

Email: mnlabspb@gmail.com
俄罗斯联邦, St. Petersburg

N. Kraskovskaya

Laboratory of Molecular Neurodegeneration, Peter the Great St. Petersburg State Polytechnic University

编辑信件的主要联系方式.
Email: ninakraskovskaya@gmail.com
俄罗斯联邦, St. Petersburg

A. Gainullina

Laboratory of Molecular Neurodegeneration, Peter the Great St. Petersburg State Polytechnic University

Email: mnlabspb@gmail.com
俄罗斯联邦, St. Petersburg

E. Kukanova

Laboratory of Molecular Neurodegeneration, Peter the Great St. Petersburg State Polytechnic University

Email: mnlabspb@gmail.com
俄罗斯联邦, St. Petersburg

O. Vlasova

Laboratory of Molecular Neurodegeneration, Peter the Great St. Petersburg State Polytechnic University

Email: mnlabspb@gmail.com
俄罗斯联邦, St. Petersburg

I. Bezprozvanny

Laboratory of Molecular Neurodegeneration, Peter the Great St. Petersburg State Polytechnic University; Department of Physiology, UT Southwestern Medical Center at Dallas

编辑信件的主要联系方式.
Email: mnlabspb@gmail.com
俄罗斯联邦, St. Petersburg; Dallas


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