Pharmacology & Therapeutics, Journal Year: 2024, Volume and Issue: unknown, P. 108753 - 108753
Published: Nov. 1, 2024
Language: Английский
Pharmacology & Therapeutics, Journal Year: 2024, Volume and Issue: unknown, P. 108753 - 108753
Published: Nov. 1, 2024
Language: Английский
Nature Metabolism, Journal Year: 2023, Volume and Issue: 5(5), P. 735 - 759
Published: May 4, 2023
Language: Английский
Citations
114Journal of Hepatology, Journal Year: 2023, Volume and Issue: 78(5), P. 1048 - 1062
Published: Feb. 3, 2023
Alongside the liver, white adipose tissue (WAT) is critical in regulating systemic energy homeostasis. Although each organ has its specialised functions, they must work coordinately to regulate whole-body metabolism. Adipose tissues and liver are relatively resilient can adapt an surplus by facilitating triglyceride (TG) storage up a certain threshold level without significant metabolic disturbances. However, lipid WAT beyond "personalised" adiposity becomes dysfunctional, leading inflexibility, progressive inflammation, aberrant adipokine secretion. Moreover, failure of store mobilise lipids results knock-on overload, particularly liver. Factors contributing hepatic overload include released from WAT, dietary fat intake, enhanced de novo lipogenesis. In contrast, extrahepatic mechanisms counteracting toxic entail coordinated compensation through oxidation fatty acids brown as TGs WAT. Failure these integrated homeostatic leads quantitative increases qualitative alterations lipidome Initially, hepatocytes preferentially accumulate TG species "benign" non-alcoholic with time, inflammatory responses ensue, progressing into more severe conditions such steatohepatitis, cirrhosis, hepatocellular carcinoma, some individuals (often early prognostic clue). Herein, we highlight pathogenic importance obesity-induced "adipose failure", resulting decreased functionality (i.e. capacity flexibility), development progression NAFL/NASH.
Language: Английский
Citations
105Endocrine Reviews, Journal Year: 2023, Volume and Issue: 45(2), P. 227 - 252
Published: Aug. 25, 2023
Chronic complications of diabetes are due to myriad disorders numerous metabolic pathways that responsible for most the morbidity and mortality associated with disease. Traditionally, divided into those microvascular macrovascular origin. We suggest revising this antiquated classification vascular, parenchymal, hybrid (both vascular parenchymal) tissue origin, since profile ranges from involving only tissues mostly parenchymal organs. A major paradigm shift has occurred in recent years regarding pathogenesis complications, which focus shifted studies on risks interplay between risk protective factors. While factors clearly important development chronic diabetes, have established equally significant modulating severity complications. These responses may help explain differential even lack pathologies, some tissues. Nevertheless, despite growing number field, comprehensive reviews their mechanisms action not available. This review thus focused clinical, biochemical, molecular support idea endogenous factors, roles initiation progression diabetes. In addition, also aimed identify main needs field future studies.
Language: Английский
Citations
64Nature Reviews Endocrinology, Journal Year: 2023, Volume and Issue: 20(3), P. 136 - 148
Published: Dec. 21, 2023
Language: Английский
Citations
59Nature Reviews Endocrinology, Journal Year: 2024, Volume and Issue: unknown
Published: Oct. 24, 2024
Language: Английский
Citations
23Advances in Nutrition, Journal Year: 2023, Volume and Issue: 14(4), P. 612 - 628
Published: April 7, 2023
Various health-related effects of long-chain (LC) ω-3 PUFAs, EPA, and DHA have been suggested. LC PUFAs reduce TG concentrations anti-inflammatory, immunomodulatory, antiplatelet, vascular protective effects. Controversially, they might help in restoring glucose homeostasis via the gut microbiota. However, previous studies not shown clear benefits for CVDs. REDUCE-IT STRENGTH-representative randomized controlled trials (RCTs) that examined whether would prevent major adverse cardiovascular (CV) events (MACE)-showed conflicting results with differences types, doses, or comparators study populations. Therefore, we performed a meta-analysis using RCTs to address this inconsistency assess clinical biological PUFAs. We included involved ≥500 participants ≥1 y follow-up. Of 17 involving 143,410 people, PUFA supplementation showed beneficial on CV death (RR: 0.94; 95% CI: 0.88, 0.99; P = 0.029) fatal nonfatal MI 0.83; 0.72, 0.95; 0.010). EPA alone better 3-point MACE, death, MI. were found stroke, all-cause mortality, hospitalization heart failure. note, both EPA/DHA combination significant increase risk new-onset atrial fibrillation. Thus, well-designed are needed investigate underlying mechanisms distinct compared cardiometabolic diseases. This review discusses potential safety from perspective focusing recent updates controversies.
Language: Английский
Citations
39Prostaglandins & Other Lipid Mediators, Journal Year: 2023, Volume and Issue: 166, P. 106718 - 106718
Published: Feb. 21, 2023
Language: Английский
Citations
27Nutrients, Journal Year: 2023, Volume and Issue: 15(15), P. 3317 - 3317
Published: July 26, 2023
Docosahexaenoic acid (C22:6n-3, DHA) is the precursor of specialized pro-resolving lipid mediators (SPMs), such as resolvin, protectin, and maresin families which have been considered therapeutic bioactive compounds for human health. Growing evidence indicates that DHA SPMs are beneficial strategies in amelioration, regulation, duration inflammatory processes through different biological actions. The present review discusses reported benefits on various diseases their potential clinical applications.
Language: Английский
Citations
25Journal of Cellular Physiology, Journal Year: 2024, Volume and Issue: 239(4)
Published: Jan. 29, 2024
Obesity and metabolic diseases, such as insulin resistance, type 2 diabetes, nonalcoholic fatty liver disease, cardiovascular ailments, represent formidable global health challenges, bearing considerable implications for both morbidity mortality rates. It has become increasingly evident that chronic, low-grade inflammation plays a pivotal role in the genesis advancement of these conditions. The involvement C-C chemokine ligand (CCL2) its corresponding receptor, receptor (CCR2), been extensively documented numerous inflammatory maladies. Recent evidence indicates CCL2/CCR2 pathway extends beyond immune cell recruitment inflammation, exerting notable influence on progression syndrome. present review seeks to furnish comprehensive exposition CCL2-CCR2 signaling axis within context obesity disorders, elucidating molecular mechanisms, functional roles, therapeutic implications.
Language: Английский
Citations
11Nature Metabolism, Journal Year: 2022, Volume and Issue: 4(11), P. 1459 - 1473
Published: Nov. 7, 2022
Abstract Noradrenaline (NA) regulates cold-stimulated adipocyte thermogenesis 1 . Aside from cAMP signalling downstream of β-adrenergic receptor activation, how NA promotes thermogenic output is still not fully understood. Here, we show that coordinated α -adrenergic (AR) and β 3 -AR induces the expression genes futile creatine cycle 2,3 , early B cell factors, oestrogen-related receptors PGC1α are required for this response in vivo. triggers physical functional coupling between subtype (ADRA1A) Gα q to promote a manner dependent on effector proteins cycle, kinase tissue-non-specific alkaline phosphatase. Combined s selectively adipocytes continual rise whole-body energy expenditure, effect. Thus, ADRA1A–Gα –futile axis key regulator facultative adaptive thermogenesis.
Language: Английский
Citations
30