نتایج جستجو برای: pparα genotypes

تعداد نتایج: 57885  

2010
Michung Yoon

Peroxisome proliferator-activated receptor α (PPARα) is a member of the steroid hormone receptor superfamily and is well known to act as the molecular target for lipid-lowering drugs of the fibrate family. At the molecular level, PPARα regulates the transcription of a number of genes critical for lipid and lipoprotein metabolism. PPARα activators are further shown to reduce body weight gain and...

2012
Neerupma Silswal Nikhil K. Parelkar Michael J. Wacker Mostafa Badr Jon Andresen

We sought to determine direct vascular effects of peroxisome proliferator-activated receptor alpha (PPARα) agonists using isolated mouse aortas and middle cerebral arteries (MCAs). The PPARα agonists GW7647, WY14643, and gemfibrozil acutely relaxed aortas held under isometric tension and dilated pressurized MCAs with the following order of potency: GW7647≫WY14643>gemfibrozil. Responses were end...

2013
Emma S. Garratt Mark H. Vickers Peter D. Gluckman Mark A. Hanson Graham C. Burdge Karen A. Lillycrop

The genes encoding nuclear receptors comprise multiple 5'untranslated exons, which give rise to several transcripts encoding the same protein, allowing tissue-specific regulation of expression. Both human and mouse peroxisome proliferator activated receptor (PPAR) α genes have multiple promoters, although their function is unknown. Here we have characterised the rat PPARα promoter region and ha...

Journal: :Journal of molecular endocrinology 2011
Nora Martínez Melisa Kurtz Evangelina Capobianco Romina Higa Verónica White Alicia Jawerbaum

Maternal diabetes impairs fetoplacental metabolism and growth. Peroxisome proliferator-activated receptor α (PPARα) is a nuclear receptor capable of regulating lipid metabolism and inflammatory pathways. In this study, we analyzed whether placental and fetal PPARα activation regulates lipid metabolism and nitric oxide (NO) production in term placentas from diabetic rats. Diabetes was induced by...

Journal: :Hepatology 2012
Andrew D Patterson Yatrik M Shah Tsutomu Matsubara Kristopher W Krausz Frank J Gonzalez

Acetaminophen (APAP) overdose causes acute liver failure in humans and rodents due in part to the destruction of mitochondria as a result of increased oxidative stress followed by hepatocellular necrosis. Activation of the peroxisome proliferator-activated receptor alpha (PPARα), a member of the nuclear receptor superfamily that controls the expression of genes encoding peroxisomal and mitochon...

2014
Dong-Gyu Kim Jae Cheal Yoo Eunju Kim Young-Sun Lee Oleg V. Yarishkin Da Yong Lee Kun Ho Lee Seong-Geun Hong Eun Mi Hwang Jae-Yong Park

BACKGROUND Mitochondrial trans-2-enoyl-CoA reductase (MECR) is involved in mitochondrial synthesis of fatty acids and is highly expressed in mitochondria. MECR is also known as nuclear receptor binding factor-1, which was originally reported with yeast two-hybrid screening as a binding protein of the nuclear hormone receptor peroxisome proliferator-activated receptor α (PPARα). However, MECR an...

Journal: :Nigerian journal of physiological sciences : official publication of the Physiological Society of Nigeria 2013
Igbe Ighodaro Omogbai Kelly Eric Oyekan Adebayo

Diminished insulin sensitivity is a characteristic feature of various pathological conditions such as hypertension and activation of peroxisome proliferator activated receptor α (PPARα) has been shown to enhance insulin resistance and reduce capacity for glucose uptake in muscles. The present study was designed to evaluate the interactions of PPARα and GLUT4 in a model of hypertensive renal inj...

2012
Juan Suárez Yanina Romero-Zerbo Lucia Márquez Patricia Rivera Mar Iglesias Francisco J. Bermúdez-Silva Montserrat Andreu Fernando Rodríguez de Fonseca

Studies in animal models and humans suggest anti-inflammatory roles on the N-acylethanolamide (NAE)-peroxisome proliferators activated receptor alpha (PPARα) system in inflammatory bowel diseases. However, the presence and function of NAE-PPARα signaling system in the ulcerative colitis (UC) of humans remain unknown as well as its response to active anti-inflammatory therapies such as 5-aminosa...

2017
Kenta Takei Song‐iee Han Yuki Murayama Aoi Satoh Fusaka Oikawa Hiroshi Ohno Yoshinori Osaki Takashi Matsuzaka Motohiro Sekiya Hitoshi Iwasaki Shigeru Yatoh Naoya Yahagi Hiroaki Suzuki Nobuhiro Yamada Yoshimi Nakagawa Hitoshi Shimano

AIMS/INTRODUCTION Peroxisome proliferator-activated receptor-α (PPARα) is a therapeutic target for hyperlipidemia. K-877 is a new selective PPARα modulator (SPPARMα) that activates PPARα transcriptional activity. The aim of the present study was to assess the effects of K-877 on lipid metabolism in vitro and in vivo compared with those of classical PPARα agonists. MATERIALS AND METHODS To com...

Journal: :Drug discoveries & therapeutics 2011
M Terada M Araki B Ashibe K Motojima

The peroxisome proliferator-activated receptor (PPAR) subtype specificity of GW501516, a well-known PPARδ-specific agonist, was studied by examining its effects on the expression of endogenous genes in primary hepatocytes and the liver of wild-type and PPARα-null mice. GW501516, like the PPARα-specific agonist Wy14,643, induced the expression of several PPAR target genes in a dose-dependent man...

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