伊拉克新诊断糖尿病患者诱导型一氧化氮合酶Sirtuin1

Mahmood Abdulhameed Hazim, P. Saifullah, Beydaa Ahmed Abd
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引用次数: 0

摘要

在哺乳动物中,Sirtuins (SIRTs)是沉默信息调控2家族的成员,Sirtuin1调节多种细胞功能。对细胞损伤具有抗氧化、抗炎、抗凋亡作用。SIRT1通过线粒体生物发生组织、细胞能量和氧化还原状态来保存细胞。血管组织也受到SIRT1的保护。糖尿病患者胰岛素生成细胞中SIRT1 (L107P)外显子1突变导致一氧化氮合酶(iNOS)、TNF-α过量产生。新诊断伊拉克糖尿病患者SIRT1蛋白水平与家族史、年龄、性别、病程的关系及其与同组生化指标的相关性iNOS, TNF-α的测定。这项研究共涉及40名志愿者。将20名志愿者分为新诊断(DMT1)病程小于1年,第1组分为男性10名,女性10名(有家族史10名,无家族史10名),第2组为健康志愿者。组1所有DMT1患者均接受胰岛素治疗。健康志愿者(20名)作为对照组。没有健康的志愿者是酒精,吸烟,或有(CVD)心血管疾病史,甲状腺疾病,激素异常问题被排除在本研究之外。本研究采用酶联免疫吸附试验(ELISA)检测SIRT1、tnf - α、iNOS。采用分光光度计技术测定患者组和健康志愿者组的空腹血糖、体重指数(BMI)、尿素、肌酐、血脂等生化指标。采用统计分析系统SAS(2012)程序对研究参数中不同因素的影响进行分析。采用最小显著性差异-LSD检验(ANOVA)进行均值间的显著性比较。估计本研究中不同参数之间的相关系数。结果显示,新诊断DMT1的健康志愿者组除HDL降低外,FBG、尿素、肌酐和血脂水平均显著升高,BMI降低。在新诊断为DMT1的健康志愿者组中,SIRT1蛋白显著降低,tnf - α和iNOS显著增加。SIRT1与fg、TG呈高度负相关。VLDL、TG/HDL、A.I.与持续时间、尿素、肌酐、T.CH呈显著负相关。低密度脂蛋白。与年龄、BMI、HDL、CH/HDL、LDL/HDL无显著相关。性别对SIRT1的影响不显著。家族史对患者的影响。有家族史组与无家族史组SIRT1均不显著。有家族病史的DMT1患者血清中SIRT1水平可降低,SIRT1水平的降低反映了SIRT1基因的突变,SIRT1水平的降低增加了DMT1并发症的发生率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sirtuin1, Inducible Nitric Oxide Synthase in Newly Diagnosed Iraqi Diabetic Patients
In Mammals Sirtuins (SIRTs) are members of the silent information regulator two family Sirtuin1 regulate a variety of cellular functions. It shows anti-oxidative, anti-inflammatory, and anti-apoptotic effects against cellular damage.SIRT1 conserves the cells by the mitochondrial biogenesis organizing, cellular energy and oxido reduction state. Vascular tissues are protected by SIRT1 too. In diabetic patients mutation in exon1 of SIRT1 (L107P) in insulin-generating cells conducted in over production of nitric oxide synthase (iNOS), TNF-α.Assessment of SIRT1 protein levels in newly diagnosed Iraqi diabetic in regards to family history Age, gender, and duration of disease, and its correlation with biochemical parameter in the same group. Measurement of iNOS, TNF-α.This study involved totally 40 volunteers. This group were subdivided (20) volunteers as newly diagnosis (DMT1) duration disease ˂1 year, group1 was subdivided to 10 male and 10 female: (10 with family history and 10 without family history) and group two healthy volunteers. Group1 All DMT1 were under insulin treatment. Healthy Volunteers (20) included in this study as control groups. None Healthy Volunteers were alcoholic, smoke, or having a history of (CVD) cardiovascular disease, thyroid disease, and hormonal abnormalities problems were exempted from this study.In the present study SIRT1, TNF-alpha, iNOS were measured by enzyme linked immune absorbent assay (ELISA). Biochemical parameters fasting glucose, body mass index (BMI), urea, creatinine and lipid profile that were measured by spectrophotometer technique in patients and healthy volunteers groups.The Statistical Analysis System- SAS (2012) program was used to effect of difference factors in study parameters. Least significant difference –LSD test (ANOVA) was used to significant compare between means. Estimate of correlation coefficient between difference parameters in this study.The results showed that a highly significant increase in levels of FBG, Urea, creatinine and lipid profile except HDL was decrease levels, BMI was decrease in newly diagnosis DMT1 with healthy volunteers groups. A significant decrease in SIRT1 protein, and a highly significant increase in TNF-alpha and iNOS in newly diagnosis DMT1 with healthy volunteers groups. A highly negative significantly correlation coefficient between SIRT1 and F.G., TG., VLDL,TG/HDL, A.I. and negative significantly correlation duration, urea, creatinine,T.CH., LDL. And non-significant correlation with age, BMI, HDL, CH/HDL and LDL/HDL.. Effect of gender were insignificant of SIRT1. Effect of family history in patients. SIRT1 were all insignificant in patients with family history as with non-family history group. SIRT1 could decreases in the sera of DMT1 patients with family history, the decreased SIRT1 level reflect a mutation in SIRT1 gene, the decreases in SIRT1 on increases the incident of DMT1 complication.
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