Effects of positive allosteric modulation on electrophysiological properties of GABAAR signaling in Ts65Dn mice and induced pluripotent stem cell-derived neurons from persons with Down syndrome

• Grant number: 18/10131-9
• Support Opportunities: Scholarships abroad - Research Internship - Doctorate
• Effective date (Start): September 01, 2018
• Effective date (End): August 31, 2019
• Field of knowledge: Biological Sciences - Physiology - Physiology of Organs and Systems
• Principal Investigator: Carla Alessandra Scorza Bahi
• Grantee: Daniella Balduino Victorino
• Supervisor: Alberto C S Costa
• Host Institution: Escola Paulista de Medicina (EPM). Universidade Federal de São Paulo (UNIFESP). Campus São Paulo. São Paulo , SP, Brazil
• Research place: Case Western Reserve University, United States
• Associated to the scholarship: 16/17746-3 - Evaluation of the effects of benzodiazepines on the in vivo electrophysiological activity of the brain and in vitro neuronal viability in the Ts65Dn mouse model, BP.DR

Abstract

Down syndrome (DS) is the most frequent cause of genetically defined intellectual disability, which results from the presence of an extra copy of chromosome 21. A wide range of neurological phenotypes is typically observed in persons with DS, including an increased incidence of seizure disorders. Mouse models of DS, particularly Ts65Dn mice, and emerging translational approaches, such as trisomy 21 human induced pluripotent stem cells (T21-iPSCs), represent essential tools for studying and understanding the pathophysiology of DS co-morbidities. As recently reported, the hippocampus of Ts65Dn mice showed an intracellular accumulation of chloride as a result of increased hippocampal expression of the NKCC1 cotransporter, which led to the reversal of GABAAR responses from inhibitory to excitatory. In this context, positive allosteric modulators of GABAAR, such as benzodiazepines (BZDs), which act by enhancing GABA signaling, might produce paradoxical effects that may aggravate rather than ameliorate clinical conditions associated with increased neuronal excitability, such as seizure disorder. Therefore, the aim of the present study is to investigate the effects of BZDs on electrophysiological properties of GABAAR signaling in Ts65Dn mice and human neurons differentiated from T21-iPSCs. To determine GABAAR spiking activity, we will perform cell-attached patch-clamp recordings from neurons in culture and hippocampal slices before and after treatment with BZDs, while currents elicited by GABA will be recorded by whole-cell patch-clamp. In this study, we expect to provide a better understanding of molecular mechanisms underlying GABA-mediated neurotransmission and intellectual disability in DS. This study might also provide important clues toward a better clinical practice involving persons with this disorder.

Scientific publications

(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)

VICTORINO, DANIELLA B.; PINHEIRO, DANIEL J. L. L.; SCOTT-MCKEAN, JONAH J.; BARKER, SARAH; STASKO, MELISSA R.; FABER, JEAN; SCORZA, CARLA A.; COSTA, ALBERTO C. S.. Atypical electrophysiological and behavioral responses to diazepam in a leading mouse model of Down syndrome. SCIENTIFIC REPORTS, v. 11, n. 1, MAY 4 2021. (16/17746-3, 18/10131-9)

VICTORINO, DANIELLA B.; SCOTT-MCKEAN, JONAH J.; JOHNSON, MARK W.; COSTA, ALBERTO C. S.. Quantitative Analysis of Retinal Structure and Function in Two Chromosomally Altered Mouse Models of Down Syndrome. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, v. 61, n. 5, MAY 2020. (16/17746-3, 18/10131-9)