| Literature DB >> 34015596 |
Mohammad Ghanbari1, Salar Momen Maragheh2, Aida Aghazadeh1, Seyed Reza Mehrjuyan3, Bashdar Mahmud Hussen4, Mahdi Abdoli Shadbad5, Narges Dastmalchi1, Reza Safaralizadeh6.
Abstract
Since adipose tissue (AT) can upregulate pro-inflammatory interleukins (ILs) via storing extra lipids in obesity, obesity is considered the leading cause of chronic low-grade inflammation. These ILs can pave the way for the infiltration of immune cells into the AT, ultimately resulting in low-grade inflammation and dysregulation of adipocytes. IL-1, which is divided into two subclasses, i.e., IL-1α and IL-1β, is a critical pro-inflammatory factor. In obesity, IL-1α and IL-1β can promote insulin resistance via impairing the function of adipocytes and promoting inflammation. The current study aims to review the detailed molecular mechanisms and the roles of IL-1α and IL-1β and their antagonist, interleukin-1 receptor antagonist(IL-1Ra), in developing obesity-related inflammatory complications, i.e., type II diabetes (T2D), non-alcoholic steatohepatitis (NASH), atherosclerosis, and cognitive disorders. Besides, the current study discusses the recent advances in natural drugs, synthetic agents, and gene therapy approaches to treat obesity-related inflammatory complications via suppressing IL-1.Entities:
Keywords: Gene therapy; Inflammatory Diseases; Interleukin 1; Low-Grade Inflammation; Molecular Mechanism; Obesity
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Year: 2021 PMID: 34015596 DOI: 10.1016/j.intimp.2021.107765
Source DB: PubMed Journal: Int Immunopharmacol ISSN: 1567-5769 Impact factor: 4.932