Literature DB >> 19129679

Peroxisome proliferator-activated receptor gamma and cardiovascular diseases.

Hiroyuki Takano1, Issei Komuro.   

Abstract

Peroxisome proliferator-activated receptors (PPARs) are members of the nuclear receptor superfamily and form heterodimers with retinoid X receptor. Three PPAR isoforms have been isolated and termed alpha, beta (or delta) and gamma. Although PPARgamma is expressed predominantly in adipose tissue and associated with adipocyte differentiation and glucose homeostasis, PPARgamma is also present in a variety of cell types. Synthetic antidiabetic thiazolidinediones (TZDs) are well known as ligands and activators for PPARgamma. After it was reported that activation of PPARgamma suppressed production of pro-inflammatory cytokines in activated macrophages, medical interest in PPARgamma has grown and there has been a huge research effort. PPARgamma is currently known to be implicated in various human chronic diseases such as diabetes mellitus, atherosclerosis, rheumatoid arthritis, inflammatory bowel disease, and Alzheimer's disease. Many studies suggest that TZDs not only ameliorate insulin sensitivity, but also have pleiotropic effects on many tissues and cell types. Although activation of PPARgamma seems to have beneficial effects on cardiovascular diseases, the mechanisms by which PPARgamma ligands prevent their development are not fully understood. Recent data about the actions and its mechanisms of PPARgamma-dependent pathway in cardiovascular diseases are discussed here.

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Year:  2009        PMID: 19129679     DOI: 10.1253/circj.cj-08-1071

Source DB:  PubMed          Journal:  Circ J        ISSN: 1346-9843            Impact factor:   2.993


  18 in total

1.  Transforming growth factor-β inhibits myocardial PPARγ expression in pressure overload-induced cardiac fibrosis and remodeling in mice.

Authors:  Kaizheng Gong; Yiu-Fai Chen; Peng Li; Jason A Lucas; Fadi G Hage; Qinglin Yang; Susan E Nozell; Suzanne Oparil; Dongqi Xing
Journal:  J Hypertens       Date:  2011-09       Impact factor: 4.844

2.  Peroxisome-proliferator-activated receptors regulate redox signaling in the cardiovascular system.

Authors:  Teayoun Kim; Qinglin Yang
Journal:  World J Cardiol       Date:  2013-06-26

3.  Signaling events in pathogen-induced macrophage foam cell formation.

Authors:  Yazdani B Shaik-Dasthagirisaheb; Samrawit Mekasha; Xianbao He; Frank C Gibson; Robin R Ingalls
Journal:  Pathog Dis       Date:  2016-07-31       Impact factor: 3.166

4.  Adipose-specific disruption of autotaxin enhances nutritional fattening and reduces plasma lysophosphatidic acid.

Authors:  Rodolphe Dusaulcy; Chloé Rancoule; Sandra Grès; Estelle Wanecq; André Colom; Charlotte Guigné; Laurens A van Meeteren; Wouter H Moolenaar; Philippe Valet; Jean Sébastien Saulnier-Blache
Journal:  J Lipid Res       Date:  2011-03-18       Impact factor: 5.922

Review 5.  PPARs: regulators of metabolism and as therapeutic targets in cardiovascular disease. Part II: PPAR-β/δ and PPAR-γ.

Authors:  Lu Han; Wen-Jun Shen; Stefanie Bittner; Fredric B Kraemer; Salman Azhar
Journal:  Future Cardiol       Date:  2017-06-05

Review 6.  PPARs: regulators of metabolism and as therapeutic targets in cardiovascular disease. Part I: PPAR-α.

Authors:  Lu Han; Wen-Jun Shen; Stefanie Bittner; Fredric B Kraemer; Salman Azhar
Journal:  Future Cardiol       Date:  2017-06-05

7.  Elevated myocardial Na+/H+ exchanger isoform 1 activity elicits gene expression that leads to cardiac hypertrophy.

Authors:  Jin Xue; Fatima Mraiche; Dan Zhou; Morris Karmazyn; Tatsujiro Oka; Larry Fliegel; Gabriel G Haddad
Journal:  Physiol Genomics       Date:  2010-05-11       Impact factor: 3.107

Review 8.  Pulmonary hypertension and metabolic syndrome: Possible connection, PPARγ and Caveolin-1.

Authors:  Rajamma Mathew
Journal:  World J Cardiol       Date:  2014-08-26

9.  Heat stress promotes lipid accumulation by inhibiting the AMPK-PGC-1α signaling pathway in 3T3-L1 preadipocytes.

Authors:  Yanna Huang; Hongyue Xie; Peng Pan; Qiuhong Qu; Qin Xia; Xiaotong Gao; Sanbao Zhang; Qinyang Jiang
Journal:  Cell Stress Chaperones       Date:  2021-03-20       Impact factor: 3.667

10.  Advanced glycation end products induce peroxisome proliferator-activated receptor γ down-regulation-related inflammatory signals in human chondrocytes via Toll-like receptor-4 and receptor for advanced glycation end products.

Authors:  Ying Ju Chen; Meei Ling Sheu; Keh Sung Tsai; Rong Sen Yang; Shing Hwa Liu
Journal:  PLoS One       Date:  2013-06-12       Impact factor: 3.240

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