2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) inhibition of fat cell differentiation

被引:19
作者
Brodie, AE
Azarenko, VA
Hu, CY
机构
[1] Department of Animal Sciences, Oregon State University, Corvallis
关键词
2,3,7,8-TCDD; adipocytes; differentiation;
D O I
10.1016/0378-4274(95)03537-0
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Fat and liver are the major sites for the deposition of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) given in vivo to rats. Although a great deal of information is available on the effects of TCDD in liver, very little is known of the effects in fat. The epididymal fat pads were removed and the stromal-vascular cells, released by collagenase digestion, were put into primary culture, 2, 4, 6 and 8 days after intubating 175 mu g/kg TCDD into male Sprague-Dawley rats. Following 7 days in culture, the cells were examined morphologically and assayed for an early (lipoprotein lipase, LPL) and late marker of fat cell differentiation (glycerol-3-phosphate dehydrogenase, GPDH). With rats sacrificed 6 or 8 days after TCDD intubation, the harvested cells from pair-fed rats contained significantly more fat and had a significantly higher level of GPDH enzyme activity, indicating more differentiation. The mRNA for LPL and GPDH genes was also higher for cells from pair-fed rats. In addition, for the rats that were sacrificed 4-8 days after TCDD intubation, despite similar food intake, the pair-fed control rats gained more total body weight than the treated rats. Although there was a body weight difference, there was no significant difference between the weights of the epididymal fat pads. This is the first report to demonstrate that TCDD inhibits the differentiation of fat cells.
引用
收藏
页码:55 / 59
页数:5
相关论文
共 19 条
[1]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[2]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[3]   DEVELOPMENT OF A CHEMICALLY DEFINED SERUM-FREE MEDIUM FOR DIFFERENTIATION OF RAT ADIPOSE PRECURSOR CELLS [J].
DESLEX, S ;
NEGREL, R ;
AILHAUD, G .
EXPERIMENTAL CELL RESEARCH, 1987, 168 (01) :15-30
[4]  
ENAN E, 1992, J BIOL CHEM, V267, P19785
[5]   EVIDENCE FOR A 2ND PATHWAY IN THE ACTION MECHANISM OF 2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN (TCDD) - SIGNIFICANCE OF AH-RECEPTOR MEDIATED ACTIVATION OF PROTEIN-KINASE UNDER CELL-FREE CONDITIONS [J].
ENAN, E ;
MATSUMURA, F .
BIOCHEMICAL PHARMACOLOGY, 1995, 49 (02) :249-261
[6]   SIGNIFICANCE OF TCDD-INDUCED CHANGES IN PROTEIN-PHOSPHORYLATION IN THE ADIPOCYTE OF MALE GUINEA-PIGS [J].
ENAN, E ;
MATSUMURA, F .
JOURNAL OF BIOCHEMICAL TOXICOLOGY, 1994, 9 (03) :159-170
[7]   2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN INDUCED ALTERATIONS IN PROTEIN-PHOSPHORYLATION IN GUINEA-PIG ADIPOSE-TISSUE [J].
ENAN, E ;
MATSUMURA, F .
JOURNAL OF BIOCHEMICAL TOXICOLOGY, 1993, 8 (02) :89-99
[8]   GROWTH INHIBITORY AND ANTIMITOGENIC ACTIVITY OF 2,3,7,8-TETRACHLORODIBENZO-PARA-DIOXIN (TCDD) IN T47D HUMAN BREAST-CANCER CELLS [J].
FERNANDEZ, P ;
SAFE, S .
TOXICOLOGY LETTERS, 1992, 61 (2-3) :185-197
[9]   DOSE-RESPONSE AND TIME COURSE OF HYPOTHYROXINEMIA AND HYPOINSULINEMIA AND CHARACTERIZATION OF INSULIN HYPERSENSITIVITY IN 2,3,7,8-TETRACHLORODIBENZO-PARA-DIOXIN (TCDD) TREATED RATS [J].
GORSKI, JR ;
ROZMAN, K .
TOXICOLOGY, 1987, 44 (03) :297-307
[10]   ELEVATED PLASMA-CORTICOSTERONE LEVELS AND HISTOPATHOLOGY OF THE ADRENALS AND THYMUSES IN 2,3,7,8-TETRACHLORODIBENZO-PARA-DIOXIN-TREATED RATS [J].
GORSKI, JR ;
MUZI, G ;
WEBER, LW ;
PEREIRA, DW ;
IATROPOULOS, MJ ;
ROZMAN, K .
TOXICOLOGY, 1988, 53 (01) :19-32