Literature DB >> 19666079

Cadmium reduces adipocyte size and expression levels of adiponectin and Peg1/Mest in adipose tissue.

Takashige Kawakami1, Hiroyuki Sugimoto, Rie Furuichi, Yoshito Kadota, Masahisa Inoue, Kojun Setsu, Shinya Suzuki, Masao Sato.   

Abstract

Adipose tissue dysfunction has been associated with diabetogenic effects. The effects of repeated Cd exposure on adipocytes remain largely unknown. We administered Cd at doses of 0, 5, 10, and 20 micromol/kgbw sc for 2 weeks (3.5 times/week) to mice and assessed the possible alteration of epididymal white adipose tissue (WAT), including histological difference, adipocyte differentiation and functional capacity. Whereas hepatic weight did not differ between the control and Cd-exposed groups, WAT weight, as well as adipose cell mass, significantly decreased in a dose-dependent manner in Cd-treated mice. The Cd concentration in WAT significantly increased in Cd-treated groups after 2 weeks of exposure. Next, we examined the effects of Cd on adipocyte differentiation and hypertrophy. Cd exposure significantly decreased the paternally expressed gene 1/Mesoderm-specific transcript mRNA expression levels. Both peroxisome proliferator-activated receptor gamma2 and CCAAT/enhancer-binding protein alpha mRNA expression levels in WAT tended to decrease in the Cd-treated groups. Next, we determined the effects of Cd exposure on the mRNA expression levels of adipose-derived hormones, such as adiponectin and resistin. The adiponectin mRNA expression level in WAT decreased after both 6h and 2 weeks of exposure to a high dose of Cd, and the reduction in resistin mRNA expression levels was observed after 2 weeks of exposure. These results suggest that Cd exposure causes abnormal adipocyte differentiation, expansion, and function, which might lead to development of insulin resistance, hypertension, and cardiovascular disease. 2009. Published by Elsevier Ireland Ltd.

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Year:  2009        PMID: 19666079     DOI: 10.1016/j.tox.2009.07.022

Source DB:  PubMed          Journal:  Toxicology        ISSN: 0300-483X            Impact factor:   4.221


  12 in total

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3.  Gestational Cd Exposure in the CD-1 Mouse Induces Sex-Specific Hepatic Insulin Insensitivity, Obesity, and Metabolic Syndrome in Adult Female Offspring.

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4.  Urinary cadmium concentrations and metabolic syndrome in U.S. adults: The National Health and Nutrition Examination Survey 2001-2014.

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Review 5.  The endocrine disruptor cadmium: a new player in the pathophysiology of metabolic diseases.

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6.  Identification of ARNT-regulated BIRC3 as the target factor in cadmium renal toxicity.

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Review 7.  Epigenetics, obesity and early-life cadmium or lead exposure.

Authors:  Sarah S Park; David A Skaar; Randy L Jirtle; Cathrine Hoyo
Journal:  Epigenomics       Date:  2016-12-16       Impact factor: 4.778

8.  Cadmium exposure increases the risk of juvenile obesity: a human and zebrafish comparative study.

Authors:  Adrian J Green; Cathrine Hoyo; Carolyn J Mattingly; Yiwen Luo; Jung-Ying Tzeng; Susan K Murphy; David B Buchwalter; Antonio Planchart
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9.  Effects of arsenic and heavy metals on metabolic pathways in cells of human origin: Similarities and differences.

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Review 10.  The hijacking of cellular signaling and the diabetes epidemic: mechanisms of environmental disruption of insulin action and glucose homeostasis.

Authors:  Robert M Sargis
Journal:  Diabetes Metab J       Date:  2014-02       Impact factor: 5.376

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