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DOI 10.1016/j.heliyon.2023.e23114

Медицинская библиотека · Heliyon · 2023

Adipose tissue inflammation linked to obesity: A review of current understanding, therapies and relevance of phyto-therapeutics.

Aruwa Christiana Eleojo, Sabiu Saheed

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Аннотация

Obesity is a current global challenge affecting all ages and is characterized by the up-regulated secretion of bioactive factors/pathways which result in adipose tissue inflammation (ATI). Current obesity therapies are mainly focused on lifestyle (diet/nutrition) changes. This is because many chemosynthetic anti-obesogenic medications cause adverse effects like diarrhoea, dyspepsia, and faecal incontinence, among others. As such, it is necessary to appraise the efficacies and mechanisms of action of safer, natural alternatives like plant-sourced compounds, extracts [extractable phenol (EP) and macromolecular antioxidant (MA) extracts], and anti-inflammatory peptides, among others, with a view to providing a unique approach to obesity care. These natural alternatives may constitute potent therapies for ATI linked to obesity. The potential of MA compounds (analysed for the first time in this review) and extracts in ATI and obesity management is elucidated upon, while also highlighting research gaps and future prospects. Furthermore, immune cells, signalling pathways, genes, and adipocyte cytokines play key roles in ATI responses and are targeted in certain therapies. As a result, this review gives an in-depth appraisal of ATI linked to obesity, its causes, mechanisms, and effects of past, present, and future therapies for reversal and alleviation of ATI. Achieving a significant decrease in morbidity and mortality rates attributed to ATI linked to obesity and related comorbidities is possible as research improves our understanding over time.

Для цитирования: Aruwa Christiana Eleojo, Sabiu Saheed. Adipose tissue inflammation linked to obesity: A review of current understanding, therapies and relevance of phyto-therapeutics.. Heliyon. 2023. DOI: 10.1016/j.heliyon.2023.e23114.
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