Literature DB >> 17671736

Change in lipid components in the adipose and liver tissues of regucalcin transgenic rats with increasing age: suppression of leptin and adiponectin gene expression.

Masayoshi Yamaguchi1, Taeko Nakagawa.   

Abstract

Regucalcin plays a multifunctional role as a regulatory protein in intracellular signaling pathway in many cell types. Regucalcin transgenic (TG) rats have been shown to experience hyperlipidemia with increasing age. This study was undertaken to determine whether lipid components in the adipose and liver tissues are changed in regucalcin TG rats in vivo. Female regucalcin TG rats were used at 7 or 50 weeks of age. Serum triglyceride or HDL-cholesterol concentrations were significantly increased in 7-week-old regucalcin TG rats as compared with those in 7-week-old normal rats. Serum triglyceride, total cholesterol, HDL-cholesterol, or free fatty acid concentrations were significantly increased in 50-week-old regucalcin TG rats. Meanwhile, triglyceride content in the adipose tissues was significantly increased in 50-week-old regucalcin TG rats,while the free fatty acid content was not significantly changed. Triglyceride, total cholesterol, or free fatty acid content in the liver tissues was significantly decreased in 50-week-old regucalcin TG rats. Liver glycogen content was significantly decreased in 7- or 50-week-old regucalcin TG rats. In addition, regucalcin mRNA and its protein levels were seen in the adipose tissues of normal rats. Those levels were not significantly changed in regucalcin TG rats at 50 weeks of age. Leptin mRNA expression in the adipose or liver tissues was significantly decreased in 50-week-old regucalcin TG rats. Adiponectin mRNA levels were not significantly changed in the adipose tissues of 50-week-old regucalcin TG rats, while the levels were significantly decreased in the liver tissues. This study demonstrates that the disorder of lipid metabolism in the adipose and liver tissues is induced in regucalcin TG rats with aging, and that the gene expression of leptin or adiponectin is suppressed in TG rats.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17671736

Source DB:  PubMed          Journal:  Int J Mol Med        ISSN: 1107-3756            Impact factor:   4.101


  6 in total

1.  Conjugated linoleic acid isomers modulate protein expression profile in rat hepatocytes.

Authors:  E Rossi; L Della Casa; S Piana; A Iannone
Journal:  Genes Nutr       Date:  2012-05-05       Impact factor: 5.523

Review 2.  Regucalcin and metabolic disorders: osteoporosis and hyperlipidemia are induced in regucalcin transgenic rats.

Authors:  Masayoshi Yamaguchi
Journal:  Mol Cell Biochem       Date:  2010-03-28       Impact factor: 3.396

3.  Aging induces tissue-specific changes in cholesterol metabolism in rat brain and liver.

Authors:  Kosara Smiljanic; Tim Vanmierlo; Aleksandra Mladenovic Djordjevic; Milka Perovic; Natasa Loncarevic-Vasiljkovic; Vesna Tesic; Ljubisav Rakic; Sabera Ruzdijic; Dieter Lutjohann; Selma Kanazir
Journal:  Lipids       Date:  2013-09-22       Impact factor: 1.880

4.  Suppressed glycolytic metabolism in the prostate of transgenic rats overexpressing calcium-binding protein regucalcin underpins reduced cell proliferation.

Authors:  Cátia V Vaz; Ricardo Marques; Henrique J Cardoso; Cláudio J Maia; Sílvia Socorro
Journal:  Transgenic Res       Date:  2015-11-09       Impact factor: 2.788

5.  Development of hepatocellular adenomas and carcinomas in mice with liver-specific G6Pase-α deficiency.

Authors:  Roberta Resaz; Cristina Vanni; Daniela Segalerba; Angela R Sementa; Luca Mastracci; Federica Grillo; Daniele Murgia; Maria Carla Bosco; Janice Y Chou; Ottavia Barbieri; Luigi Varesio; Alessandra Eva
Journal:  Dis Model Mech       Date:  2014-09       Impact factor: 5.758

6.  Genome-wide association study of meat quality traits in a White Duroc×Erhualian F2 intercross and Chinese Sutai pigs.

Authors:  Junwu Ma; Jie Yang; Lisheng Zhou; Zhiyan Zhang; Huanban Ma; Xianhua Xie; Feng Zhang; Xinwei Xiong; Leilei Cui; Hui Yang; Xianxian Liu; Yanyu Duan; Shijun Xiao; Huashui Ai; Jun Ren; Lusheng Huang
Journal:  PLoS One       Date:  2013-05-28       Impact factor: 3.240

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.