Astrocyte Responses Influence Local Effects of Whole‐Brain Magnetic Stimulation in Parkinsonian Rats

Author:

Natale Giuseppina1,Colella Micol2,De Carluccio Maria13,Lelli Daniele2,Paffi Alessandra2,Carducci Filippo4,Apollonio Francesca2,Palacios Daniela56,Viscomi Maria Teresa56,Liberti Micaela2,Ghiglieri Veronica67ORCID

Affiliation:

1. Department of Neuroscience Università Cattolica del Sacro Cuore Rome Italy

2. Department of Information Engineering, Electronics and Telecommunications Sapienza University of Rome Rome Italy

3. Department of Neurosciences and Neurorehabilitation IRCCS San Raffaele Pisana Rome Italy

4. Neuroimaging Laboratory, Department of Physiology and Pharmacology "Vitorio Erspamer" Sapienza University of Rome Rome Italy

5. Department of Life Sciences and Public Health, Section of Histology and Embryology Università Cattolica del Sacro Cuore Rome Italy

6. Fondazione Policlinico Universitario Agostino Gemelli IRCCS Rome Italy

7. Department of Human Sciences and Quality of Life Promotion San Raffaele University Rome Italy

Abstract

AbstractBackgroundExcessive glutamatergic transmission in the striatum is implicated in Parkinson's disease (PD) progression. Astrocytes maintain glutamate homeostasis, protecting from excitotoxicity through the glutamate–aspartate transporter (GLAST), whose alterations have been reported in PD. Noninvasive brain stimulation using intermittent theta‐burst stimulation (iTBS) acts on striatal neurons and glia, inducing neuromodulatory effects and functional recovery in experimental parkinsonism.ObjectiveBecause PD is associated with altered astrocyte function, we hypothesized that acute iTBS, known to rescue striatal glutamatergic transmission, exerts regional‐ and cell‐specific effects through modulation of glial functions.Methods6‐Hydroxydopamine‐lesioned rats were exposed to acute iTBS, and the areas predicted to be more responsive by a biophysical, hyper‐realistic computational model that faithfully reconstructs the experimental setting were analyzed. The effects of iTBS on glial cells and motor behavior were evaluated by molecular and morphological analyses, and CatWalk and Stepping test, respectively.ResultsAs predicted by the model, the hippocampus, cerebellum, and striatum displayed a marked c‐FOS activation after iTBS, with the striatum showing specific morphological and molecular changes in the astrocytes, decreased phospho‐CREB levels, and recovery of GLAST. Striatal‐dependent motor performances were also significantly improved.ConclusionThese data uncover an unknown iTBS effect on astrocytes, advancing the understanding of the complex mechanisms involved in TMS‐mediated functional recovery. Data on numerical dosimetry, obtained with a degree of anatomical details never before considered and validated by the biological findings, provide a framework to predict the electric‐field induced in different specific brain areas and associate it with functional and molecular changes. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Funder

Università Cattolica del Sacro Cuore

Publisher

Wiley

Subject

Neurology (clinical),Neurology

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3