Synaptic input organization of the melanocortin system predicts diet-induced hypothalamic reactive gliosis and obesity
Clicks: 156
ID: 270395
2010
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This
article has not been analysed, so there is no overall score —
reader engagement is measured and shown alongside.
Reader Engagement
Steady Performance
30.0
/100
156 views
38 readers
AI Quality Assessment
Not analyzed
Readership in this journal
SteadyRanked #26 of 50 articles by views in proceedings of the national academy of sciences
Most read
Least read
Bar heights use a square-root scale.
Mint this article as an NFT
Not yet mintedCreate a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.
5
SUSD
one-off · no wallet required
Abstract
The neuronal circuits involved in the regulation of feeding behavior and energy expenditure are soft-wired, reflecting the relative activity of the postsynaptic neuronal system, including the anorexigenic proopiomelanocortin (POMC)-expressing cells of the arcuate nucleus. We analyzed the synaptic input organization of the melanocortin system in lean rats that were vulnerable (DIO) or resistant (DR) to diet-induced obesity. We found a distinct difference in the quantitative and qualitative synaptology of POMC cells between DIO and DR animals, with a significantly greater number of inhibitory inputs in the POMC neurons in DIO rats compared with DR rats. When exposed to a high-fat diet (HFD), the POMC cells of DIO animals lost synapses, whereas those of DR rats recruited connections. In both DIO rats and mice, the HFD-triggered loss of synapses on POMC neurons was associated with increased glial ensheathment of the POMC perikarya. The altered synaptic organization of HFD-fed animals promoted increased POMC tone and a decrease in the stimulatory connections onto the neighboring neuropeptide Y (NPY) cells. Exposure to HFD was associated with reactive gliosis, and this affected the structure of the blood-brain barrier such that the POMC and NPY cell bodies and dendrites became less accessible to blood vessels. Taken together, these data suggest that consumption of an HFD has a major impact on the cytoarchitecture of the arcuate nucleus in vulnerable subjects, with changes that might be irreversible due to reactive gliosis.
| Reference Key |
horvath2010proceedingssynaptic
Use this key to autocite in the manuscript while using
SciMatic Manuscript Manager or Thesis Manager
|
|---|---|
| Authors | Tamas L. Horvath;Beatrix Sarman;Cristina García-Cáceres;Pablo J. Enriori;Peter Sotonyi;Marya Shanabrough;Erzsebet Borok;Jesus Argente;Julie A. Chowen;Diego Perez-Tilve;Paul T. Pfluger;Hella S. Brönneke;Barry E. Levin;Sabrina Diano;Michael A. Cowley;Matthias H. Tschöp;Tamas L. Horvath;Beatrix Sarman;Cristina García-Cáceres;Pablo J. Enriori;Peter Sotonyi;Marya Shanabrough;Erzsebet Borok;Jesus Argente;Julie A. Chowen;Diego Perez-Tilve;Paul T. Pfluger;Hella S. Brönneke;Barry E. Levin;Sabrina Diano;Michael A. Cowley;Matthias H. Tschöp; |
| Journal | proceedings of the national academy of sciences |
| Year | 2010 |
| DOI |
10.1073/pnas.1004282107
|
| URL | |
| Keywords |
|
Citations
No citations found. To add a citation, contact the admin at info@scimatic.org
Comments
No comments yet. Be the first to comment on this article.