The protective effects of Salusin-α against oxidative stress and inflammatory response in mice with gestational diabetes mellitus (GDM).

IF 2.5 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Yujie Zhang, Yi Ye, Xiaorui Jia, Pu Wang, Zheng Xiong, Hui Zhu
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引用次数: 0

Abstract

Gestational diabetes mellitus (GDM) is one of the most prevalent metabolic diseases in pregnant women. In this study, we investigated the effects of Salusin-α in rodent models of GDM. We observed decreased levels of Salusin-α in the placental tissue of GDM mice. Salusin-α alleviated GDM symptoms by reducing blood glucose and increasing serum insulin levels. Further analysis revealed that Salusin-α improved lipid profiles and foetal outcomes in GDM mice. Additionally, Salusin-α mitigated oxidative and nitrosative stress in the placental tissue of GDM mice by enhancing the levels of Vitamin E, Vitamin C, and reduced GSH, while decreasing levels of TBARS and nitric oxide metabolites (nitrite + nitrate = NOx). Salusin-α also reduced the levels of MCP-1 and IL-8. Mechanically, Salusin-α inhibited the activation of p38/NF-κB by reducing phosphorylated p38 and phosphorylated NF-κB p65. In conclusion, our findings support the potential clinical application of Salusin-α as a novel peptide for molecular intervention in GDM.

Salusin-α对妊娠期糖尿病小鼠氧化应激和炎症反应的保护作用。
妊娠期糖尿病(GDM)是孕妇最常见的代谢性疾病之一。本研究探讨了Salusin-α对GDM小鼠模型的影响。我们观察到GDM小鼠胎盘组织中Salusin-α水平降低。Salusin-α通过降低血糖和提高血清胰岛素水平来缓解GDM症状。进一步分析表明,Salusin-α改善了GDM小鼠的脂质谱和胎儿结局。此外,Salusin-α通过提高维生素E、维生素C水平和降低GSH,同时降低TBARS和一氧化氮代谢物(亚硝酸盐+硝酸盐= NOx)水平,减轻了GDM小鼠胎盘组织的氧化应激和亚硝化应激。Salusin-α也能降低MCP-1和IL-8的水平。机械上,Salusin-α通过降低磷酸化的p38和磷酸化的NF-κB p65来抑制p38/NF-κB的活化。总之,我们的研究结果支持Salusin-α作为分子干预GDM的新型肽的潜在临床应用。
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来源期刊
Archives of Physiology and Biochemistry
Archives of Physiology and Biochemistry ENDOCRINOLOGY & METABOLISM-PHYSIOLOGY
CiteScore
6.90
自引率
3.30%
发文量
21
期刊介绍: Archives of Physiology and Biochemistry: The Journal of Metabolic Diseases is an international peer-reviewed journal which has been relaunched to meet the increasing demand for integrated publication on molecular, biochemical and cellular aspects of metabolic diseases, as well as clinical and therapeutic strategies for their treatment. It publishes full-length original articles, rapid papers, reviews and mini-reviews on selected topics. It is the overall goal of the journal to disseminate novel approaches to an improved understanding of major metabolic disorders. The scope encompasses all topics related to the molecular and cellular pathophysiology of metabolic diseases like obesity, type 2 diabetes and the metabolic syndrome, and their associated complications. Clinical studies are considered as an integral part of the Journal and should be related to one of the following topics: -Dysregulation of hormone receptors and signal transduction -Contribution of gene variants and gene regulatory processes -Impairment of intermediary metabolism at the cellular level -Secretion and metabolism of peptides and other factors that mediate cellular crosstalk -Therapeutic strategies for managing metabolic diseases Special issues dedicated to topics in the field will be published regularly.
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