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炎症标志物表达对衰竭型实验模型胎肾后肾脏的影响。

Influence of the Expression of Inflammatory Markers on Kidney after Fetal Programming in an Experimental Model of Renal Failure.

机构信息

Discipline of General Pathology, Institute of Biological and Natural Sciences, Federal University of Triângulo Mineiro, Uberaba, MG, Brazil.

Department of Health Sciences, Lavras Federal University, Lavras, MG, Brazil.

出版信息

J Immunol Res. 2016;2016:9151607. doi: 10.1155/2016/9151607. Epub 2016 Nov 28.

Abstract

To evaluate the expression of inflammatory markers in experimental renal failure after fetal programming. The offspring aged two and five months were divided into four groups: CC (control dams, control offspring); DC (diabetic dams, control offspring); CFA (control dams, folic acid offspring, 250 mg/Kg); and DFA (diabetic dams, folic acid offspring). Gene expression of inflammatory markers MCP-1, IL-1, NOS3, TGF-, TNF-, and VEGF was evaluated by RT-PCR. MCP-1 was increased in the CFA and DFA groups at two and five months of age, as well as in DC5 when compared to CC5. There was a higher expression of IL-1 in the CFA2, DFA2, and DC2 groups. There was a decrease in NOS3 and an increase in TNF- in DFA5 in relation to CFA5. The gene expression of TGF- increased in cases that had received folic acid at two and five months, and VEGF decreased in the CFA5 and DFA5 groups. DC5 showed increased VEGF expression in comparison with CC5. Gestational diabetes mellitus and folic acid both change the expression of inflammatory markers, thus demonstrating that the exposure to harmful agents in adulthood has a more severe impact in cases which underwent fetal reprogramming.

摘要

为了评估胎儿编程后实验性肾衰竭中炎症标志物的表达。将 2 月龄和 5 月龄的后代分为 4 组:CC(对照母鼠,对照后代);DC(糖尿病母鼠,对照后代);CFA(对照母鼠,叶酸后代,250mg/Kg);和 DFA(糖尿病母鼠,叶酸后代)。通过 RT-PCR 评估炎症标志物 MCP-1、IL-1、NOS3、TGF-、TNF-和 VEGF 的基因表达。在 2 月龄和 5 月龄时,CFA 和 DFA 组以及 DC5 组的 MCP-1 表达增加,与 CC5 相比。在 CFA2、DFA2 和 DC2 组中,IL-1 的表达更高。与 CFA5 相比,DFA5 中 NOS3 减少,TNF-增加。在接受叶酸的情况下,TGF-的基因表达在 2 月龄和 5 月龄时增加,VEGF 在 CFA5 和 DFA5 组中减少。与 CC5 相比,DFA5 中 VEGF 的表达增加。妊娠糖尿病和叶酸都会改变炎症标志物的表达,因此表明在成年期暴露于有害剂具有更严重的影响在经历胎儿重编程的情况下。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7848/5149704/0add992665ae/JIR2016-9151607.001.jpg

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