Obesity-associated insulin resistance is correlated to adipose tissue vascular endothelial growth factors and metalloproteinase levels.

Q1 Biochemistry, Genetics and Molecular Biology BMC Physiology Pub Date : 2012-04-02 DOI:10.1186/1472-6793-12-4
Francisco José Tinahones, Leticia Coín-Aragüez, Maria Dolores Mayas, Eduardo Garcia-Fuentes, Carmen Hurtado-Del-Pozo, Joan Vendrell, Fernando Cardona, Rosa-Maria Calvo, Maria-Jesus Obregon, Rajaa El Bekay
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引用次数: 79

Abstract

Background: The expansion of adipose tissue is linked to the development of its vasculature, which appears to have the potential to regulate the onset of obesity. However, at present, there are no studies highlighting the relationship between human adipose tissue angiogenesis and obesity-associated insulin resistance (IR).

Results: Our aim was to analyze and compare angiogenic factor expression levels in both subcutaneous (SC) and omentum (OM) adipose tissues from morbidly obese patients (n = 26) with low (OB/L-IR) (healthy obese) and high (OB/H-IR) degrees of IR, and lean controls (n = 17). Another objective was to examine angiogenic factor correlations with obesity and IR.Here we found that VEGF-A was the isoform with higher expression in both OM and SC adipose tissues, and was up-regulated 3-fold, together with MMP9 in OB/L-IR as compared to leans. This up-regulation decreased by 23% in OB/-H-IR compared to OB/L-IR. On the contrary, VEGF-B, VEGF-C and VEGF-D, together with MMP15 was down-regulated in both OB/H-IR and OB/L-IR compared to lean patients. Moreover, MMP9 correlated positively and VEGF-C, VEGF-D and MMP15 correlated negatively with HOMA-IR, in both SC and OM.

Conclusion: We hereby propose that the alteration in MMP15, VEGF-B, VEGF-C and VEGF-D gene expression may be caused by one of the relevant adipose tissue processes related to the development of IR, and the up-regulation of VEGF-A in adipose tissue could have a relationship with the prevention of this pathology.

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肥胖相关的胰岛素抵抗与脂肪组织血管内皮生长因子和金属蛋白酶水平相关。
背景:脂肪组织的扩张与其脉管系统的发育有关,这似乎有可能调节肥胖的发生。然而,目前还没有研究强调人类脂肪组织血管生成与肥胖相关的胰岛素抵抗(IR)之间的关系。结果:我们的目的是分析和比较低(OB/L-IR)(健康肥胖)和高(OB/H-IR) IR程度的病态肥胖患者(n = 26)和瘦对照组(n = 17)皮下(SC)和网膜(OM)脂肪组织中的血管生成因子表达水平。另一个目的是检查血管生成因子与肥胖和IR的相关性。在这里,我们发现VEGF-A是OM和SC脂肪组织中表达较高的异构体,与OB/L-IR中的MMP9相比,其表达上调了3倍。与OB/L-IR相比,OB/-H-IR的上调率下降了23%。相反,与瘦患者相比,OB/H-IR和OB/L-IR中VEGF-B、VEGF-C和VEGF-D以及MMP15均下调。此外,在SC和OM中,MMP9与HOMA-IR呈正相关,VEGF-C、VEGF-D和MMP15与HOMA-IR呈负相关。结论:我们提出MMP15、VEGF-B、VEGF-C和VEGF-D基因表达的改变可能是由与IR发生相关的脂肪组织过程之一引起的,而脂肪组织中VEGF-A的上调可能与该病理的预防有关。
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来源期刊
BMC Physiology
BMC Physiology Biochemistry, Genetics and Molecular Biology-Physiology
CiteScore
9.60
自引率
0.00%
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0
期刊介绍: BMC Physiology is an open access journal publishing original peer-reviewed research articles in cellular, tissue-level, organismal, functional, and developmental aspects of physiological processes. BMC Physiology (ISSN 1472-6793) is indexed/tracked/covered by PubMed, MEDLINE, BIOSIS, CAS, EMBASE, Scopus, Zoological Record and Google Scholar.
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