Salinomycin, a polyether ionophoric antibiotic, inhibits adipogenesis

被引:11
作者
Szkudlarek-Mikho, Maria [1 ]
Saunders, Rudel A. [1 ]
Yap, Sook Fan [2 ]
Ngeow, Yun Fong [3 ]
Chin, Khew-Voon [1 ]
机构
[1] Univ Toledo, Coll Med, Dept Med Biochem & Canc Biol, Ctr Diabet & Endocrine Res, Toledo, OH 43614 USA
[2] Univ Tunku Abdul Rahman, Dept Preclin Sci, Fac Med & Hlth Sci, Petaling Jaya, Malaysia
[3] Univ Malaya, Fac Med, Dept Med Microbiol, Kuala Lumpur 50603, Malaysia
关键词
Adipogenesis; Salinomycin; Polyether antibiotic; Ionophoric antibiotic; Obesity; ACTIVATED-RECEPTOR-GAMMA; TOXICITY; MONENSIN; OBESITY; TISSUE; RHABDOMYOLYSIS; MECHANISM; APOPTOSIS; ASSAY; GENE;
D O I
10.1016/j.bbrc.2012.10.080
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The polyether ionophoric antibiotics including monensin, salinomycin, and narasin, are widely used in veterinary medicine and as food additives and growth promoters in animal husbandry including poultry farming. Their effects on human health, however, are not fully understood. Recent studies showed that salinomycin is a cancer stem cell inhibitor. Since poultry consumption has risen sharply in the last three decades, we asked whether the consumption of meat tainted with growth promoting antibiotics might have effects on adipose cells. We showed in this report that the ionophoric antibiotics inhibit the differentiation of preadipocytes into adipocytes. The block of differentiation is not due to the induction of apoptosis nor the inhibition of cell proliferation. In addition, salinomycin also suppresses the transcriptional activity of the CCAAT/enhancer binding proteins and the peroxisome proliferator-activated receptor gamma. These results suggest that the ionophoric antibiotics can be exploited as novel anti-obesity therapeutics and as pharmacological probes for the study of adipose biology. Further, the pharmacological effects of salinomycin could be a harbinger of its toxicity on the adipose tissue and other susceptible target cells in cancer therapy. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:487 / 493
页数:7
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