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Impact of adrenomedullin blockage on lipid metabolism in female mice exposed to high-fat diet

机译:肾上腺髓质素堵塞对高脂饮食暴露女鼠脂代谢的影响

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Purpose Adrenomedullin (ADM) levels are elevated in gestational and type 2 diabetic patients. ADM also stimulates lipolysis in vitro. Disturbed lipid metabolism has been implicated in the pathogenesis of diabetes. Here, we explore whether blockade of ADM is beneficial for metabolic homeostasis in a diabetic mouse model.Methods C57BL/6J female mice were placed on either a control or a high fat high sucrose (HFHS) diet for 8 weeks. At week 4, osmotic mini-pumps were implanted for constant infusion of either saline or ADM antagonist, ADM22_52- Glucose tolerance tests were performed prior to infusion and 4 weeks after infusion began. Animals were then sacrificed and visceral adipose tissue collected for further analysis.Results Mice fed HFHS displayed glucose intolerance, increased mRNA expressions in VAT for Adm and its receptor components, Crlr. HFHS fed mice also had increased basal and isoprenaline-induced glycerol release by VAT explants. ADM22-52 did not significantly affect glucose intolerance. ADM22-52 did suppress basal and isoprenaline-induced glycerol release by VAT explants. This alteration was associated with enhanced mRNA expression of insulin signaling factors Insr and Glut4, and adipogenic factor Pck1.Conclusions HFHS diet induces glucose intolerance and enhances ADM and its receptor expressions in VAT in female mice. ADM22_52 treatment did not affect glucose intolerance in HFHS mice, but reduced both basal and isoprenaline-induced lipolysis, which is associated with enhanced expression of genes involved in adipogenesis. These results warrant further research on the effects of ADM blockade in improving lipid homeostasis in diabetic patients.
机译:目的在妊娠期和2型糖尿病患者中升高肾上腺尿素(ADM)水平。 ADM还刺激体外脂解。令人不安的脂质代谢已涉及糖尿病的发病机制。在这里,我们探讨了患有糖尿病小鼠模型中的代谢稳定性的障碍物是否有益于糖尿病小鼠模型中的代谢稳态。将C57BL / 6J雌性小鼠置于对照或高脂肪的高蔗糖(HFHS)饮食中8周。在第4周,植入渗透迷你泵用于持续输注盐水或ADM拮抗剂,在输注之前进行ADM22_52-葡萄糖耐量试验,输注后4周开始。然后处死动物并收集用于进一步分析的内脏脂肪组织。喂养HFH的小鼠展示葡萄糖不耐受,增加了ADM及其受体组分的增值税中的mRNA表达,CRL。喂养小鼠的HFHS也增加了基础和异丙酚诱导的甘油释放的甘油释放。 ADM22-52没有显着影响葡萄糖不耐受。 ADM22-52确实抑制了基础和异丙酚诱导的甘油释放的甘油释放。这种改变与胰岛素信号传导因子INSR和GLUT4的增强mRNA表达相关,脂肪因子PCK1。结论HFHS饮食诱导血糖不耐受,并增强雌性小鼠的增值税中的ADM及其受体表达。 ADM22_52治疗不影响HFHS小鼠中的葡萄糖不耐受,而是减少了基础和异丙酚诱导的脂肪解,这与增强脂肪发生的基因的表达有关。这些结果有权进一步研究ADM阻滞在改善糖尿病患者脂质稳态的影响。

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