| Literature DB >> 27884797 |
Chun Jiang1, Ningren Cui2, Weiwei Zhong2, Christopher M Johnson2, Yang Wu2.
Abstract
A characteristic feature of Rett syndrome (RTT) is abnormal breathing accompanied by several other neurological and cognitive disorders. Since RTT rodent models became available, studies have begun shedding insight into the breathing abnormalities at behavioral, cellular and molecular levels. Defects are found in several groups of brainstem neurons involved in respiratory control, and potential neural mechanisms have been suggested. The findings in animal models are helpful in therapeutic strategies for people with RTT with respect to lowering sudden and unexpected death, preventing secondary developmental consequences, and improving the quality of lives.Entities:
Keywords: Animal models; Autonomic function; Brainstem; Breathing; CO(2) chemosensitivity; Mecp2; Rett syndrome
Mesh:
Year: 2016 PMID: 27884797 PMCID: PMC5438903 DOI: 10.1016/j.resp.2016.11.011
Source DB: PubMed Journal: Respir Physiol Neurobiol ISSN: 1569-9048 Impact factor: 1.931