维甲酸衍生物和 TXNRD1 蛋白通过年龄-愤怒信号通路对链脲佐菌素诱导的妊娠糖尿病的保护作用

IF 1.4 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Wensheng Wang, Lin Wang
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引用次数: 0

摘要

背景:研究维甲酸衍生物在小鼠体内模型妊娠期糖尿病(GDM)发病机制中的作用。材料与方法:通过腹腔注射链脲佐菌素(STZ),剂量为65 mg/kg体重,连续5天诱导小鼠糖尿病。STZ注射后,小鼠按0.12、0.25 mg/kg剂量,经生理盐水交替灌胃1周。结果:维甲酸衍生物能显著改善糖尿病小鼠的FBG和FINS水平(P<0.05)。给予维甲酸衍生物可显著提高糖尿病小鼠血液中HDL水平(P<0.05),降低TC和TG水平(P<0.05)。维甲酸衍生物可显著降低糖尿病小鼠胰腺组织中CRP、il -6和TNF-α的产生(P<0.05)。维甲酸衍生物给药可显著提高糖尿病小鼠胰腺组织SOD活性和CAT水平(P<0.05),降低MDA水平(P<0.05)。以0.25 mg/kg剂量给予维甲酸衍生物后,糖尿病小鼠TXNRD1表达与正常小鼠相当。结果表明,维a酸衍生物与TXNRD1蛋白的结合亲和力在-10 ~ 9.4 kcal/ mol之间。结论:维a酸衍生物可有效调节链脲霉素诱导的糖尿病小鼠体内空腹血糖、胰岛素水平、高密度脂质水平和甘油三酯水平的变化。糖尿病小鼠给予维甲酸衍生物后,链脲佐菌素诱导的c反应蛋白和炎性细胞因子的过量产生也被下调。因此,维甲酸衍生物可作为治疗妊娠期糖尿病的药物进行进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protective effect of tretinoin derivative and TXNRD1 protein on streptozotocin induced gestational diabetes via an age-rage signaling-pathway
Background: In the present study effect of tretinoin derivative was investigated on the pathogenesis of gestational diabetes mellitus (GDM) in mice model in vivo. Materials and Methods: Diabetes was induced in mice by injecting Streptozotocin (STZ) for 5consecutive days at a dose of 65 mg/kg body weight through the intraperitoneal route. Tretinoin derivative was given to the mice at 0.12 and 0.25 mg/kg doses through gavage in normal saline alternately for one week after STZ injection.Results: The results demonstrated that tretinoin derivative administration to the diabetic mice significantly (P<0.05) alleviated the blood FBG and FINS levels. Administration of tretinoin derivative to the diabetic mice significantly (P<0.05) promoted the blood HDL level and alleviated TC and TG levels. The administration of tretinoin derivative to the diabetic mice significantly (P<0.05) alleviated the CRP, IL-6and TNF-α production in pancreatic tissues. Tretinoin derivative administration to the diabetic mice significantly (P<0.05) elevated the SOD activity, and CAT level and lowered the MDA level in pancreatic tissues. The TXNRD1 expression in diabetic mice was comparable to that in the normal group after administration of tretinoin derivativeat the dose of 0.25 mg/kg dose. In silico data demonstrated that tretinoin derivativeinteracts with TXNRD1 protein with the binding affinity ranging from –10 to 9.4 kcal/ mol. Conclusion: In conclusion, tretinoin derivative administration effectively regulated streptozotocin-induced changes in fasting blood glucose, insulin level, high-density lipid level and triglyceride level in diabetic mice in vivo. The streptozotocin-induced excessive production of C-reactive protein and inflammatory cytokines was also down-regulated in diabetic mice on administration of tretinoin derivative. Therefore, tretinoin derivative can be investigated further as a therapeutic agent for the treatment of gestational diabetes mellitus.
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来源期刊
Acta biochimica Polonica
Acta biochimica Polonica 生物-生化与分子生物学
CiteScore
2.40
自引率
0.00%
发文量
99
审稿时长
4-8 weeks
期刊介绍: Acta Biochimica Polonica is a journal covering enzymology and metabolism, membranes and bioenergetics, gene structure and expression, protein, nucleic acid and carbohydrate structure and metabolism.
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