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基质金属蛋白酶抑制作用可独立于瘦素损害小鼠脂肪组织发育。

Matrix metalloproteinase inhibition impairs murine adipose tissue development independently of leptin.

机构信息

Center for Molecular and Vascular Biology, KU Leuven, Leuven, Belgium.

出版信息

Endocr J. 2011;58(2):101-7. doi: 10.1507/endocrj.k10e-267. Epub 2011 Jan 13.

Abstract

Administration of Tolylsam, a MMP inhibitor with relative specificity for gelatinases, at a dose of 100 mg/kg/day to leptin-deficient (ob/ob) mice kept on high fat diet for 15 weeks, was associated with significantly reduced weight gain as compared to controls (p < 0.0005), resulting in lower body weight (p < 0.0005) at the end of the experiments. Food intake, physical activity and body temperature were not affected. Subcutaneous (SC) (2.9 ± 0.1g vs. 3.4 ± 0.2g in controls; p < 0.05) and gonadal (GON) (3.4 ± 0.1g vs. 3.7 ± 0.1g in controls; p = NS) fat mass were reduced by Tolylsam treatment. Reduced MMP-2 (gelatinase A) activity in adipose tissue extracts was confirmed by zymography. Mild adipocyte hypotrophy was observed in treated SC and GON adipose tissues. Blood vessel density was significantly reduced in Tolylsam treated SC (p < 0.05) and GON (p < 0.005) adipose tissues. Sirius red staining revealed comparable collagen content in both SC and GON fat of treated mice, whereas collagen disorganization (ratio thick/thin fibers) was also similar. Thus, gelatinase inhibition in mice with leptin deficiency resulted in lower body and fat pad weights, associated with mild adipocyte hypotrophy. This indicates that MMP inhibition may impair adipose tissue development independently of leptin.

摘要

给喂食高脂肪饮食 15 周的肥胖(ob/ob)瘦素缺乏症小鼠每天注射 100mg/kg 的 Tolylsam(一种对明胶酶具有相对特异性的 MMP 抑制剂),与对照组相比,体重增长明显减少(p<0.0005),导致实验结束时体重降低(p<0.0005)。食物摄入量、体力活动和体温不受影响。皮下(SC)(2.9±0.1g 比对照组 3.4±0.2g;p<0.05)和性腺(GON)(3.4±0.1g 比对照组 3.7±0.1g;p=NS)脂肪量减少。通过组织化学染色证实 Tolylsam 治疗可减少脂肪组织提取物中的 MMP-2(明胶酶 A)活性。在治疗的 SC 和 GON 脂肪组织中观察到脂肪细胞轻度萎缩。Tolylsam 处理的 SC(p<0.05)和 GON(p<0.005)脂肪组织中的血管密度显著降低。天狼星红染色显示治疗组小鼠的 SC 和 GON 脂肪中的胶原含量相当,而胶原排列紊乱(厚/细纤维比)也相似。因此,瘦素缺乏症小鼠的明胶酶抑制导致体重和脂肪垫重量降低,与脂肪细胞轻度萎缩有关。这表明 MMP 抑制可能独立于瘦素而损害脂肪组织发育。

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