Differential effects of cobalt and mercury on lipid metabolism in the white adipose tissue of high-fat diet-induced obesity mice
Description
Metals and metalloid species are involved in homeostasis in energy systems such as glucose metabolism. Enlarged adipocytes are one of the most important causes of obesity-associated diseases. In this study, we studied the possibility that various metals, namely, CoCl2, HgCl2, NaAsO2 and MnCl2 pose risk to or have beneficial effects on white adipose tissue (WAT). Exposure to the four metals resulted in decreases in WAT weight and the size of enlarged adipocytes in mice fed a high-fat diet (HFD) without changes in liver weight, suggesting that the size and function of adipocytes are sensitive to metals. Repeated administration of CoCl2 significantly increased serum leptin, adiponectin and high-density lipoprotein (HDL) cholesterol levels and normalized glucose level and adipose cell size in mice fed HFD. In contrast, HgCl2 treatment significantly decreased serum leptin level with the down-regulation of leptin mRNA expression in WAT and a reduction in adipocyte size. Next, we tried to investigate possible factors that affect adipocyte size. Repeated exposure to HgCl2 significantly decreased the expression levels of factors upon the regulation of energy such as the PPARα and PPARγ mRNA expression levels in adipocytes, whereas CoCl2 had little effect on those genes expressions compared with that in the case of the mice fed HFD with a vehicle. In addition, repeated administration of CoCl2 enhanced AMPK activation in a dose-dependent manner in the liver, skeletal muscle and WAT; HgCl2 treatment also enhanced AMPK activation in the liver. Thus, both Co and Hg reduced WAT weight and the size of enlarged adipocytes, possibly mediated by AMKP activation in the mice fed HFD. However, inorganic cobalt may have a preventive role in obesity-related diseases through increased leptin, adiponectin and HDL-cholesterol levels, whereas inorganic mercury may accelerate the development of such diseases. These results may lead to the development of new approaches to establishing the role of metals in adipose tissue of obesity-related diseases. -- Highlights: ► The effects of metals on enlarged white adipose tissue (WAT) were studied. ► As, Hg, Mn and Co ions reduced the size of enlarged adipocytes. ► Co2+ increased serum leptin and adiponectin levels with AMPK activation in WAT. ► Hg2+ decreased serum leptin level and leptin mRNA expression in WAT. ► Metal exposure affects the adipocyte size and the function of WAT.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.taap.2011.10.004Additional details
Identifiers
- DOI
- 10.1016/j.taap.2011.10.004;
- PII
- S0041-008X(11)00396-6;
Publishing Information
- Journal Title
- Toxicology and Applied Pharmacology
- Journal Volume
- 258
- Journal Issue
- 1
- Journal Page Range
- p. 32-42
- ISSN
- 0041-008X
- CODEN
- TXAPA9
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 45036159
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- ADIPOSE TISSUE; ALANINES; CHOLESTEROL; COBALT; COBALT CHLORIDES; GLUCOSE; LEPTIN; LIPOPROTEINS; LIVER; MERCURY; MERCURY CHLORIDES; MESSENGER-RNA; METABOLIC DISEASES; MICE; PORPHYRINS; RECEPTORS; TRIGLYCERIDES
- Descriptors DEC
- ALDEHYDES; AMINO ACIDS; ANIMAL TISSUES; ANIMALS; BODY; CARBOHYDRATES; CARBOXYLIC ACIDS; CHLORIDES; CHLORINE COMPOUNDS; COBALT COMPOUNDS; COBALT HALIDES; CONNECTIVE TISSUE; DIGESTIVE SYSTEM; DISEASES; ELEMENTS; ESTERS; GLANDS; HALIDES; HALOGEN COMPOUNDS; HETEROCYCLIC ACIDS; HETEROCYCLIC COMPOUNDS; HEXOSES; HORMONES; HYDROXY COMPOUNDS; LIPIDS; MAMMALS; MEMBRANE PROTEINS; MERCURY COMPOUNDS; MERCURY HALIDES; METALS; MONOSACCHARIDES; NUCLEIC ACIDS; ORGANIC ACIDS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; ORGANS; PEPTIDE HORMONES; PEPTIDES; POLYPEPTIDES; PROTEINS; RNA; RODENTS; SACCHARIDES; STEROIDS; STEROLS; TRANSITION ELEMENT COMPOUNDS; TRANSITION ELEMENTS; VERTEBRATES
Optional Information
- Copyright
- Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.