Fatty Acid, Obesity and Metabolic Syndrome

A special issue of Nutrients (ISSN 2072-6643). This special issue belongs to the section "Lipids".

Deadline for manuscript submissions: 5 September 2024 | Viewed by 2449

Special Issue Editor


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Guest Editor
Endocrinology and Metabolism Laboratory, West Division, Faculty of Medicine, University of Chile, Santiago 8320000, Chile
Interests: metabolism; fatty acid; obesity

Special Issue Information

Dear Colleagues,

Fatty acids (FA) are central in various physiological processes and are acquired from dietary sources or generated by de novo lipogenesis in the hepatic and adipose cells and stored as triglycerides that act as fuel reservoirs. Among the FA classes, the long-chain polyunsaturated FA (LCPUFA) are especially relevant because they are an integral part of cell membranes and participate in synthesizing bioactive molecules that regulate multiple signaling pathways. Therefore, the importance of FA in conditions of health or diseases is indisputable. Metabolic syndrome (MS) is a conjunction of several disorders, including abdominal obesity, hyperglycemia, hypertriglyceridemia, and hypertension. It is well documented that abnormal FA metabolism, such as excessive intake of saturated and trans-fatty acid, leads to a pro-inflammatory state that finally originates the components of MS. On the other hand, n-3 PUFA and short-chain fatty acids generated through colonic fermentation of dietary fibers have anti-inflammatory properties with beneficial effects on MS. Albeit to the increase of knowledge, there are still important issues that must be addressed together with the special attention to discoveries about properties of FA and its derivatives.

The importance of fatty acids (FA) in multiple biological processes is widely recognized; however, alterations in its metabolism and the excessive consumption of saturated and trans-FA are involved in the origin of obesity and its related disorders, resulting in metabolic syndrome (MS). On the other hand, n-3 long-chain polyunsaturated FA (LCPUFA) and short-chain fatty acids have demonstrated beneficial effects in the control of components of MS; however, important issues must be addressed to understand the molecular basis behind the healthy or unhealthy effects of different types of FA. Moreover, more research must be done to elucidate the achievements of dietary strategies involving FA supplementation. The role of FA in the early stages of development, and maternal–fetal FA transfer, is of particular interest because of its implications in the development of MS in the offspring. Similarly, the increase in pediatric obesity requires deepening into the mechanism pathophysiology that conditions the development of MS, among them the role of FA. We are pleased to invite you to submit articles in relation to these topics and others that contribute to increase the knowledge about the of fatty acids on obesity and MS. We are certain that this Special Issue will be a great contribution to basic and clinical researchers interested in avoiding and treating the deleterious consequences of MS.

Dr. Manuel A. Maliqueo
Guest Editor

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Keywords

  • fatty acid
  • polyunsaturated fatty acid (PUFA)
  • obesity
  • dyslipidemia
  • hypertension
  • diabetes
  • non-alcoholic fatty liver disease (NALFD)
  • maternal obesity
  • fetal development
  • pediatric obesity
  • n-3 PUFA supplementation
  • n-6 PUFA
  • short-chain fatty acids
  • microbiome

Published Papers (2 papers)

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Research

15 pages, 11898 KiB  
Article
BMP8B Activates Both SMAD2/3 and NF-κB Signals to Inhibit the Differentiation of 3T3-L1 Preadipocytes into Mature Adipocytes
by Shenjie Zhong, Xueqing Du, Jing Gao, Guangdong Ji and Zhenhui Liu
Nutrients 2024, 16(1), 64; https://doi.org/10.3390/nu16010064 - 25 Dec 2023
Viewed by 907
Abstract
Bone morphogenetic protein 8B (BMP8B) has been found to regulate the thermogenesis of brown adipose tissue (BAT) and the browning process of white adipose tissue (WAT). However, there is no available information regarding the role of BMP8B in the process of adipocyte differentiation. [...] Read more.
Bone morphogenetic protein 8B (BMP8B) has been found to regulate the thermogenesis of brown adipose tissue (BAT) and the browning process of white adipose tissue (WAT). However, there is no available information regarding the role of BMP8B in the process of adipocyte differentiation. Here, we showed that BMP8B down-regulates transcriptional regulators PPARγ and C/EBPα, thereby impeding the differentiation of 3T3-L1 preadipocytes into fully mature adipocytes. BMP8B increased the phosphorylation levels of SMAD2/3, and TP0427736 HCl (SMAD2/3 inhibitor) significantly reduced the ability of BMP8B to inhibit adipocyte differentiation, suggesting that BMP8B repressed adipocyte differentiation through the SMAD2/3 pathway. Moreover, the knockdown of BMP I receptor ALK4 significantly reduced the inhibitory effect of BMP8B on adipogenesis, indicating that BMP8B triggers SMAD2/3 signaling to suppress adipogenesis via ALK4. In addition, BMP8B activated the NF-κB signal, which has been demonstrated to impede PPARγ expression. Collectively, our data demonstrated that BMP8B activates both SMAD2/3 and NF-κB signals to inhibit adipocyte differentiation. We provide previously unidentified insight into BMP8B-mediated adipogenesis. Full article
(This article belongs to the Special Issue Fatty Acid, Obesity and Metabolic Syndrome)
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15 pages, 2163 KiB  
Article
Effects of a High-Fat Diet and Docosahexaenoic Acid during Pregnancy on Fatty Acid Composition in the Fetal Livers of Mice
by Daniela Álvarez, Macarena Ortiz, Gabriel Valdebenito, Nicolás Crisosto, Bárbara Echiburú, Rodrigo Valenzuela, Alejandra Espinosa and Manuel Maliqueo
Nutrients 2023, 15(21), 4696; https://doi.org/10.3390/nu15214696 - 6 Nov 2023
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Abstract
A high-fat diet (HFD) during pregnancy promotes fat accumulation and reduces docosahexaenoic acid (DHA) levels in the liver of the offspring at postnatal ages, which can depend on fetal sex. However, the prenatal mechanisms behind these associations are still unclear. Thus, we analyzed [...] Read more.
A high-fat diet (HFD) during pregnancy promotes fat accumulation and reduces docosahexaenoic acid (DHA) levels in the liver of the offspring at postnatal ages, which can depend on fetal sex. However, the prenatal mechanisms behind these associations are still unclear. Thus, we analyzed if an HFD alters DHA content and the expression of molecules related to fatty acid (FA) metabolism in the fetal liver. Female C57BL/6 mice were fed a control diet or HFD for 4–6 weeks before pregnancy until the gestational day (GD) 17.5. A subgroup of each diet received DHA (100 mg/Kg) orally from GD 6.5 until 16.5. On GD 17.5, maternal livers, placentas, and livers from male and female fetuses were collected for FA profiling with gas-chromatography and gene expression of molecules related to FA metabolism using qPCR. PPAR-α protein expression was evaluated using Western blot. The gene expression of placental FA transporters was also assessed. An HFD increased eicosapentaenoic acid (EPA) and decreased DHA levels and protein expression of PPAR-α in the fetal livers of both sexes. DHA increased the gene expression of Ppara, Cpt1, and Acsl1 in the livers of female fetuses. Therefore, an HFD reduces DHA levels and PPAR-α, a master regulator of gene expression, in the fetal liver. In turn, the livers of female fetuses seem to be more sensitive to DHA action. Full article
(This article belongs to the Special Issue Fatty Acid, Obesity and Metabolic Syndrome)
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