Changes of PPAR γ, UCP1 and β3-AR mRNA expression of HFD-induced mice with EPO injection

MIAO Ying-ying, LU Ming, ZHAO Jun-qiang

Chinese Journal of Clinical Anatomy ›› 2017, Vol. 35 ›› Issue (6) : 645-649.

Chinese Journal of Clinical Anatomy ›› 2017, Vol. 35 ›› Issue (6) : 645-649. DOI: 10.13418/j.issn.1001-165x.2017.06.011

Changes of PPAR γ, UCP1 and β3-AR mRNA expression of HFD-induced mice with EPO injection

  • MIAO Ying-ying1, LU Ming1, ZHAO Jun-qiang2
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Abstract

Objective Erythropoietin (EPO) has been reported to have a beneficial effect on obesity. The aim of the study is to investigate the changes of body weight and fat content of EPO in high fat diet (HFD) mice, the expression of PPAR γ, UCP1, β3-AR mRNA in white adipose tissue (WAT) and brown adipose tissue (BAT).    Methods    20 HFD-fed C57BL/6J male mice were randomly divided into control group (HFD-Con) and EPO group (HFD-EPO). The expression of PPAR γ, UCP1 and β3-AR mRNA in subcutaneous fat, epididymal fat and brown fat were detected by real-time quantitative RT-PCR.   Results  Compared with the control group, the body weight of the EPO mice was (24.53±2.03) g and the control group was (31.78±1.68) g. The weight of subcutaneous fat and epididymal fat in HFD-EPO group were significantly decreased. HE staining showed that the size of adipocytes of HFD-EPO group was decreased compared with HFD-Con group. Quantitative real-time PCR results showed that the expression of PPAR γ, UCP1 and β3-AR mRNA in subcutaneous adipose tissue and epididymal adipose tissue did not change significantly, while the expression of PPAR γ, UCP1 and β3-AR in brown fat were significantly increased.   Conclusion The expression of PPAR γ, UCP1 and β3-AR in brown fat may be related to the weight loss caused by EPO injection after high fat diet.

Key words

High fat diet /  Erythropoietin /  Peroxisome proliferator-activated receptors &gamma /  Uncoupling protein 1 /  &beta / 3-adrenergic receptor

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MIAO Ying-ying, LU Ming, ZHAO Jun-qiang. Changes of PPAR γ, UCP1 and β3-AR mRNA expression of HFD-induced mice with EPO injection[J]. Chinese Journal of Clinical Anatomy. 2017, 35(6): 645-649 https://doi.org/10.13418/j.issn.1001-165x.2017.06.011

References

[1] van Marken Lichtenbelt WD, Vanhommerig JW, Smulders NM, et al. Cold-activated brown adipose tissue in healthy men [J]. N Engl J Med, 2009, 360 (15):1500-1508.
[2] Virtanen KA, Lidell ME, Orava J, et al. Functional brown adipose tissue in healthy adults [J]. N Engl J Med, 2009, 360(15):1518-1525.
[3] Cypess AM, Lehman S, Williams G, et al. Identification and importance of brown adipose tissue in adult humans [J]. N Engl J Med, 2009, 360(15):1509-1517.
[4] Cazzola M. How and when to use erythropoietin [J]. Curr Opin Hematol, 1998, 5(2):103-108.
[5] Katz O, Stuible M, Golishevski N, et al. Erythropoietin treatment leads to reduced blood glucose levels and body mass: insights from murine models [J]. J Endocrinol, 2010, 205(1):87-95.
[6] Teng R, Gavrilova O, Suzuki N, et al. Disrupted erythropoietin signalling promotes obesity and alters hypothalamus proopiomelanocortin production [J]. Nat Commun, 2011, 2:520.
[7] Kotanko P, Thijssen S, Levin NW. Association between erythropoietin responsiveness and body com- position in dialysis patients [J]. Blood Purif, 2008, 26(1):82-89.
[8] Townsend KL, Tseng YH. Of mice and men: novel insights regarding constitutive and recruitable brown adipocytes [J]. Int J Obes Suppl, 2015, 5(Suppl 1):S15-20.
[9] Lee YH, Jung YS, Choi D. Recent advance in brown adipose physiology and its therapeutic potential [J]. Exp Mol Med, 2014, 46:e78.
[10] Saito M. Human brown adipose tissue: regulation and anti-obesity potential [J]. Endocr J, 2014, 61(5):409-416.
[11] Liu Y, Luo B, Shi R, et al. Nonerythropoietic erythropoietin-derived peptide sup-presses adipogenesis, inflammation, obesity and insulin resistance [J]. Sci Rep, 2015, 5:15134.
[12] Alnaeeli M, Raaka BM, Gavrilova O, et al. Erythropoietin signaling: a novel regulator of white adipose tissue inflammation during diet-induced obesity [J]. Diabetes, 2014, 63(7):2415-2531.
[13] Christensen B, Nellemann B, Jorgensen JO, et al. Erythropoietin does not activate erythropoietin receptor signaling or lipolytic pathways in human subcutaneous white adipose tissue in vivo [J]. Lipids Health Dis, 2016, 15(1):160.
[14] Hu E, Kim JB, Sarraf P, et al. Inhibition of adipogenesis through MAP kinase-mediated phosphorylation of PPARgamma [J]. Science, 1996, 274(5295):2100-2103.
[15] Sugimoto S, Nakajima H, Kodo K, et al. Miglitol increases energy expenditure by upregulating uncoupling protein 1 of brown adipose tissue and reduces obesity in dietary-induced obese mice [J]. Nutr Metab (Lond), 2014 , 11(1):14.
[16] Sell H, Deshaies Y, Richard D. The brown adipocyte: update on its metabolic role [J]. Int J Biochem Cell Biol, 2004, 36(11):2098-2104.

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