Document Detail

Accumulation of SNAP25 in mouse gustatory and somatosensory cortices in response to food and chemical stimulation.
MedLine Citation:
PMID:  22641083     Owner:  NLM     Status:  Publisher    
Food intake stimuli, including taste, somatosensory, and tactile stimuli, are received by receptors in the oral cavity, and this information is then transferred to the cerebral cortex. Signals from recently ingested food during the weaning period can affect synaptic transmission, resulting in biochemical changes in the cerebral cortex that modify gustatory and somatosensory nervous system plasticity. In this study, we investigated the expression patterns of molecular markers in mouse gustatory and somatosensory cortices during the weaning period. The expression of SNAP25, a component of the soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) complex, was increased in the insular and somatosensory cortices at postnatal week 3 compared to postnatal week 2. Additionally, SNAP25 protein in the cerebral cortex accumulated in weaning mice fed solid food but not in mice fed only mother's milk at the weaning stage. Chemical stimulation by saccharin or capsaicin at the weaning stage also increased SNAP25 immunoreactivity in the insular or somatosensory cortical area, respectively. These results suggest that recently ingested chemical signals in the oral cavity during weaning increase the accumulation of SNAP25 in the gustatory and somatosensory cortices and promote neural plasticity during the development of the gustatory and somatosensory nervous systems.
Shinpei Kawakami; Makoto Ohmoto; Shunsuke Itoh; Reiko Yuasa; Hiroyuki Inagaki; Eisaku Nishimura; Tatsuhiko Ito; Takumi Misaka
Related Documents :
16633723 - Vitamin a deficiency modifies the mferg: a case study of rod influence on the mferg.
21765003 - Evaluation and comparison of food records, recalls, and frequencies for energy and prot...
18716353 - Leptin gene and leptin receptor gene polymorphisms are associated with sweet preference...
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2012-5-25
Journal Detail:
Title:  Neuroscience     Volume:  -     ISSN:  1873-7544     ISO Abbreviation:  -     Publication Date:  2012 May 
Date Detail:
Created Date:  2012-5-29     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  7605074     Medline TA:  Neuroscience     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Copyright Information:
Copyright © 2012. Published by Elsevier Ltd.
Health Care Division, MORINAGA & CO., LTD, 2-1-1 Shimosueyoshi, Tsurumi-ku, Yokohama 230-8504, Japan; Department of Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Ex Vivo-Expanded Bone Marrow Mesenchymal Stem Cells Facilitate Recovery from Chemically Induced Acut...
Next Document:  H(2)S Functions as a Nociceptive Messenger Through Transient Receptor Potential Ankyrin 1 (Trpa1) Ac...