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Gelatinases impart susceptibility to high-fat diet induced obesity in mice

机译:明胶酶赋予高脂肪饮食诱导小鼠肥胖的敏感性

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摘要

Gelatinases play a role in adipose and muscle hypertrophy, and could be involved in tissue remodeling in response to high-fat diet (HFD) intake. This study tested potential roles of gelatinases (matrix metalloproteinses-2 and -9, MMP-2 and -9) in relationship to an antigrowth factor (myostatin, MSTN) known to be dysregulated in relation to HFD induced obesity (HFDIO) propensity. In vitro and ex vivo analyses demonstrated that MMP-9 increased mature MSTN levels, indicating a potential role of gelatinases in MSTN activation in vivo. HFD intake resulted in increased body weight and circulating blood glucose values in C57BL/6J and MMP-9 null mice, with no changes observed in SWR/J mice. HFD intake attenuated MMP-9 and MMP-2 mRNA levels in SWR/J mice while elevating MMP-2 levels in skeletal musclein C57BL/6J mice. In MMP-9 null mice, the effects of HFD intake were muted. Consistent with changes in mRNA levels, HFD intake increased MMP-9 activity in muscle tissue of C57BL/6J mice, demonstrating a strong relationship between HFDIO susceptibility and local MMP regulation. Overall, resistance to HFDIO appears to correspond to low MMP-9 and MSTN levels, suggesting a role of MMP-9 in MSTN activation in local tissue responses to HFD intake.
机译:明胶酶在脂肪和肌肉肥大中起作用,并可能响应高脂饮食(HFD)的摄入而参与组织重塑。这项研究测试了明胶酶(基质金属蛋白酶2和-9,MMP-2和-9)与已知因HFD诱发肥胖(HFDIO)倾向失调的抗生长因子(肌生长抑制素,MSTN)的潜在作用。体外和离体分析表明MMP-9增加了成熟的MSTN水平,表明明胶酶在体内MSTN激活中具有潜在作用。 HFD摄入导致C57BL / 6J和MMP-9无效小鼠的体重增加和循环血糖值升高,而SWR / J小鼠未观察到变化。 HFD摄入降低了SWR / J小鼠的MMP-9和MMP-2 mRNA水平,同时提高了C57BL / 6J小鼠骨骼肌的MMP-2水平。在MMP-9无效的小鼠中,HFD摄入量的影响被静音。与mRNA水平的变化一致,HFD摄入增加了C57BL / 6J小鼠肌肉组织中MMP-9的活性,这表明HFDIO敏感性与局部MMP调节之间存在很强的关系。总体而言,对HFDIO的耐药性似乎与低MMP-9和MSTN水平相对应,表明MMP-9在MSTN激活中对HFD摄入的局部组织反应中具有作用。

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