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Milk-Derived Tripeptides IPP (Ile-Pro-Pro) and VPP (Val-Pro-Pro) Promote Adipocyte Differentiation and Inhibit Inflammation in 3T3-F442A Cells

机译:牛奶衍生的三肽IPP(Ile-Pro-Pro)和VPP(Val-Pro-Pro)促进3T3-F442A细胞的脂肪细胞分化并抑制炎症

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摘要

Milk derived tripeptides IPP (Ile-Pro-Pro) and VPP (Val-Pro-Pro) have shown promise as anti-hypertensive agents due to their inhibitory effects on angiotensin converting enzyme (ACE). Due to the key inter-related roles of hypertension, chronic inflammation and insulin resistance in the pathogenesis of metabolic syndrome, there is growing interest in investigating established anti-hypertensive agents for their effects on insulin sensitivity and inflammation. In this study, we examined the effects of IPP and VPP on 3T3-F442A murine pre-adipocytes, a widely used model for studying metabolic diseases. We found that both IPP and VPP induced beneficial adipogenic differentiation as manifested by intracellular lipid accumulation, upregulation of peroxisome proliferator-activated receptor gamma (PPARγ) and secretion of the protective lipid hormone adiponectin by these cells. The observed effects were similar to those induced by insulin, suggesting potential benefits in the presence of insulin resistance. IPP and VPP also inhibited cytokine induced pro-inflammatory changes such as reduction in adipokine levels and activation of the nuclear factor kappa B (NF-κB) pathway. Taken together, our findings suggest that IPP and VPP exert insulin-mimetic adipogenic effects and prevent inflammatory changes in adipocytes, which may offer protection against metabolic disease.
机译:牛奶衍生的三肽IPP(Ile-Pro-Pro)和VPP(Val-Pro-Pro)由于其对血管紧张素转化酶(ACE)的抑制作用,显示出有望作为抗高血压药。由于高血压,慢性炎症和胰岛素抵抗在代谢综合征的发病机理中起着关键的相互关联的作用,人们越来越有兴趣研究已建立的抗高血压药对胰岛素敏感性和炎症的影响。在这项研究中,我们检查了IPP和VPP对3T3-F442A小鼠前脂肪细胞(一种广泛用于研究代谢性疾病的模型)的影响。我们发现IPP和VPP均诱导了有益的成脂分化,表现为细胞内脂质蓄积,过氧化物酶体增殖物激活受体γ(PPARγ)的上调和这些细胞分泌保护性脂质激素脂联素。观察到的效果类似于胰岛素诱导的效果,表明在存在胰岛素抵抗的情况下具有潜在的益处。 IPP和VPP还抑制细胞因子诱导的促炎性变化,例如降低脂肪因子水平和激活核因子κB(NF-κB)通路。两者合计,我们的研究结果表明IPP和VPP发挥模仿胰岛素的脂肪形成作用,并防止脂肪细胞发生炎症性变化,这可能为抵抗代谢性疾病提供保护。

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  • 总页数 15
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