Michelle Dawson posts

Post published on Twitter/X on 21 Jul 2020 12:44

Twitter/X DOI work crossref Extract quoted in the post External link integrated into the post Autism terms

Structured cited links

1 cited resource

DOI work Fetched Post crossref

Hafiz M. Mahmood, Hesham M. Aldhalaan, Tahani K. Alshammari, Mashael A. Alqasem, Musaad A. Alshammari, Norah A. Albekairi, Shakir D. AlSharari (2020). The Role of Nicotinic Receptors in the Attenuation of Autism‐Related Behaviors in a Murine BTBR T + tf/J Autistic Model. Autism Research, 13(8), 1311-1334. Wiley.

Publication date
21 Jul 2020
Identifier
10.1002/aur.2342
Authors
Hafiz M. Mahmood, Hesham M. Aldhalaan, Tahani K. Alshammari, Mashael A. Alqasem, Musaad A. Alshammari, Norah A. Albekairi, Shakir D. AlSharari
Source
Autism Research
Details
13(8), 1311-1334
Reference type
article
Publisher
Wiley
Metadata source
crossref

Abstract

Nicotinic receptors are distributed throughout the central and peripheral nervous system. Postmortem studies have reported that some nicotinic receptor subtypes are altered in the brains of autistic people. Recent studies have demonstrated the importance of nicotinic acetylcholine receptors (nAChRs) in the autistic behavior of BTBR T + tf/J mouse model of autism. This study was undertaken to examine the behavioral effects of targeted nAChRs using pharmacological ligands, including nicotine and mecamylamine in BTBR T + tf/J and C57BL/6J mice in a panel of behavioral tests relating to autism. These behavioral tests included the three‐chamber social interaction, self‐grooming, marble burying, locomotor activity, and rotarod test. We examined the effect of various oral doses of nicotine (50, 100, and 400 mcg/mL; po) over a period of 2 weeks in BTBR T + tf/J mouse model. The results indicated that the chronic administration of nicotine modulated sociability and repetitive behavior in BTBR T + tf/J mice while no effects observed in C57BL/6J mice. Furthermore, the nonselective nAChR antagonist, mecamylamine, reversed nicotine effects on sociability and increased repetitive behaviors in BTBR T + tf/J mice. Overall, the findings indicate that the pharmacological modulation of nicotinic receptors is involved in modulating core behavioral phenotypes in the BTBR T + tf/J mouse model. Lay Summary The involvement of brain nicotinic neurotransmission system plays a crucial role in regulating autism‐related behavioral features. In addition, the brain of the autistic‐like mouse model has a low acetylcholine level. Here, we report that nicotine, at certain doses, improved sociability and reduced repetitive behaviors in a mouse model of autism, implicating the potential therapeutic values of a pharmacological intervention targeting nicotinic receptors for autism therapy. Autism Res 2020, 13: 1311–1334. © 2020 International Society for Autism Research, Wiley Periodicals, Inc.

Study authors in this cited reference