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Leptin resistance: underlying mechanisms and diagnosis
Leptin and its receptors have been identified as key regulators of body weight and energy homeostasis. A decrease in tissue sensitivity to leptin leads to the development of obesity and metabolic disorders, such as insulin resistance and dyslipidemia. Mechanisms underlying the development of leptin...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6354688/ https://www.ncbi.nlm.nih.gov/pubmed/30774404 http://dx.doi.org/10.2147/DMSO.S182406 |
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author | Gruzdeva, Olga Borodkina, Daria Uchasova, Evgenya Dyleva, Yulia Barbarash, Olga |
author_facet | Gruzdeva, Olga Borodkina, Daria Uchasova, Evgenya Dyleva, Yulia Barbarash, Olga |
author_sort | Gruzdeva, Olga |
collection | PubMed |
description | Leptin and its receptors have been identified as key regulators of body weight and energy homeostasis. A decrease in tissue sensitivity to leptin leads to the development of obesity and metabolic disorders, such as insulin resistance and dyslipidemia. Mechanisms underlying the development of leptin resistance include mutations in the genes encoding leptin and its receptors, as well as proteins involved in self-regulation of leptin synthesis and blood–brain barrier permeability. Leptin resistance encompasses a complex pathophysiological phenomenon with a number of potential research lines. In this review, we analyze the existing data on the methods used to diagnose leptin resistance. |
format | Online Article Text |
id | pubmed-6354688 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63546882019-02-15 Leptin resistance: underlying mechanisms and diagnosis Gruzdeva, Olga Borodkina, Daria Uchasova, Evgenya Dyleva, Yulia Barbarash, Olga Diabetes Metab Syndr Obes Review Leptin and its receptors have been identified as key regulators of body weight and energy homeostasis. A decrease in tissue sensitivity to leptin leads to the development of obesity and metabolic disorders, such as insulin resistance and dyslipidemia. Mechanisms underlying the development of leptin resistance include mutations in the genes encoding leptin and its receptors, as well as proteins involved in self-regulation of leptin synthesis and blood–brain barrier permeability. Leptin resistance encompasses a complex pathophysiological phenomenon with a number of potential research lines. In this review, we analyze the existing data on the methods used to diagnose leptin resistance. Dove Medical Press 2019-01-25 /pmc/articles/PMC6354688/ /pubmed/30774404 http://dx.doi.org/10.2147/DMSO.S182406 Text en © 2019 Gruzdeva et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Gruzdeva, Olga Borodkina, Daria Uchasova, Evgenya Dyleva, Yulia Barbarash, Olga Leptin resistance: underlying mechanisms and diagnosis |
title | Leptin resistance: underlying mechanisms and diagnosis |
title_full | Leptin resistance: underlying mechanisms and diagnosis |
title_fullStr | Leptin resistance: underlying mechanisms and diagnosis |
title_full_unstemmed | Leptin resistance: underlying mechanisms and diagnosis |
title_short | Leptin resistance: underlying mechanisms and diagnosis |
title_sort | leptin resistance: underlying mechanisms and diagnosis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6354688/ https://www.ncbi.nlm.nih.gov/pubmed/30774404 http://dx.doi.org/10.2147/DMSO.S182406 |
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