Results 11 to 20 of about 6,404 (164)

Caspase-6 Controls Lipid and Energy Metabolism in Diet-Induced Obesity. [PDF]

open access: yesAdv Sci (Weinh)
This study reveals an unknown metabolic role of caspase‐6 beyond cell death. Caspase‐6 deficiency protects against HFD‐induced obesity by increasing energy expenditure, reducing inflammation, and improving glucose metabolism. Mechanistically, caspase‐6 cleaves PPARγ and SP1 to suppress ATGL expression.
Gupta A   +7 more
europepmc   +2 more sources

The Furan Fatty Acids 11M5 and 11D5 Can Act as Activators of Human Peroxisome Proliferator-Activated Receptor Gamma. [PDF]

open access: yesMol Nutr Food Res
Furan fatty acids are abundant in food such as fatty fish. Here we show that some of these can bind to and act as activators of the nuclear receptors, peroxisome proliferator‐activated receptor gamma (PPAR‐gamma) and retinoid X receptor (RXR), in human cells.
Pospiech J   +5 more
europepmc   +2 more sources

Molecular Dynamics Simulation and Essential Dynamics of Deleterious Proline 12 Alanine Single-Nucleotide Polymorphism in PPARγ2 Associated with Type 2 Diabetes, Cardiovascular Disease, and Nonalcoholic Fatty Liver Disease

open access: yesPPAR Research, 2022
Background. Peroxisome proliferator-activated receptor-γ (PPARγ) gene is located at 3p25 position. PPARγ functions as the master regulator of glucose homeostasis and lipoprotein metabolism, and recent studies have reported that it is involved in various ...
Somayye Taghvaei, Leila Saremi
doaj   +1 more source

Cytosolic and nuclear distribution of PPARγ2 in differentiating 3T3-L1 preadipocytes

open access: yesJournal of Lipid Research, 1998
In light of the pivotal role that PPARγ2 plays in the expression of fat specific genes (e.g., A-FABP), we have examined the hypothesis that a rise in PPARγ2 protein is required for the expression of A-FABP, and that the acceleration of fat cell ...
Philippe Thuillier   +3 more
doaj   +1 more source

Genetics and Clinical Characteristics of PPARγ Variant-Induced Diabetes in a Chinese Han Population

open access: yesFrontiers in Endocrinology, 2021
ObjectivesPPARγ variants cause lipodystrophy, insulin resistance, and diabetes. This study aimed to determine the relationship between PPARγ genotypes and phenotypes and to explore the pathogenesis of diabetes beyond this relationship.MethodsPPARγ2 exons
Siqian Gong   +17 more
doaj   +1 more source

Safflower yellow improves insulin sensitivity in high‐fat diet‐induced obese mice by promoting peroxisome proliferator‐activated receptor‐γ2 expression in subcutaneous adipose tissue

open access: yesJournal of Diabetes Investigation, 2020
Aims/Introduction Safflower yellow (SY) and its main component, hydroxysafflor yellow A, have been demonstrated to show anti‐obesity effects. Peroxisome proliferator‐activated receptor‐γ2 (PPARγ2) is a critical transcription factor in adipose tissue ...
Kemin Yan   +9 more
doaj   +1 more source

The PPARγ2 P12A polymorphism is not associated with all-cause mortality in patients with type 2 diabetes mellitus [PDF]

open access: yes, 2016
The high mortality risk of patients with type 2 diabetes mellitus may well be explained by the several comorbidities and/or complications. Also the intrinsic genetic component predisposing to diabetes might have a role in shaping the risk of diabetes ...
Alberico, Federica   +13 more
core   +1 more source

The PPARγ2 Pro12Ala variant is protective against progression of nephropathy in people with type 2 diabetes [PDF]

open access: yes, 2015
Cross-sectional studies suggest the association between diabetic nephropathy and the PPARγ2 Pro12Ala polymorphism of the peroxisome proliferator-activated receptor γ2 (PPARγ2).
BRUZZESE, DARIO   +7 more
core   +1 more source

Comparison of three aerobic exercise methods with different intensities on PPARγ2 gene expression in subcutaneous adipose tissue of male Wistar rats [PDF]

open access: yesفصلنامه ابن سینا, 2021
Background and aims: PPARγ is one of the proteins that plays a very important role in regulating adipose tissue metabolism under physiological and metabolic conditions.
Ali Barzegari   +2 more
doaj  

Inhibition of Ubiquitin Ligase F-box and WD Repeat Domain-containing 7α (Fbw7α) Causes Hepatosteatosis through Krüppel-like Factor 5 (KLF5)/Peroxisome Proliferator-activated Receptor γ2 (PPARγ2) Pathway but Not SREBP-1c Protein in Mice [PDF]

open access: yes, 2011
F-box and WD repeat domain-containing 7α (Fbw7α) is the substrate recognition component of a ubiquitin ligase that controls the degradation of factors involved in cellular growth, including c-Myc, cyclin E, and c-Jun.
Ema Masatsugu   +31 more
core   +1 more source

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