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肥胖相关和糖尿病肾病的哥廷根小型猪模型中的肾功能和形态学变化。

Functional and morphological renal changes in a Göttingen Minipig model of obesity-related and diabetic nephropathy.

机构信息

Novo Nordisk A/S, Måløv, Denmark.

Department of Veterinary and Animal Sciences, University of Copenhagen, Frederiksberg, Denmark.

出版信息

Sci Rep. 2023 Apr 12;13(1):6017. doi: 10.1038/s41598-023-32674-6.

Abstract

Obesity-related glomerulopathy and diabetic nephropathy (DN) are serious complications to metabolic syndrome and diabetes. The purpose was to study effects of a fat, fructose and cholesterol-rich (FFC) diet with and without salt in order to induce hypertension on kidney function and morphology in Göttingen Minipigs with and without diabetes. Male Göttingen Minipigs were divided into 4 groups: SD (standard diet, n = 8), FFC (FFC diet, n = 16), FFC-DIA (FFC diet + diabetes, n = 14), FFC-DIA + S (FFC diet with extra salt + diabetes, n = 14). Blood and urine biomarkers, glomerular filtration rate (GFR), blood pressure (BP) and resistive index (RI) were evaluated after 6-7 months (T1) and 12-13 months (T2). Histology, electron microscopy and gene expression (excluding FFC-DIA + S) were evaluated at T2. All groups fed FFC-diet displayed obesity, increased GFR and RI, glomerulomegaly, mesangial expansion (ME) and glomerular basement membrane (GBM) thickening. Diabetes on top of FFC diet led to increased plasma glucose and urea and proteinuria and tended to exacerbate the glomerulomegaly, ME and GBM thickening. Four genes (CDKN1A, NPHS2, ACE, SLC2A1) were significantly deregulated in FFC and/or FFC-DIA compared to SD. No effects on BP were observed. Göttingen Minipigs fed FFC diet displayed some of the renal early changes seen in human obesity. Presence of diabetes on top of FFC diet exacerbated the findings and lead to changes resembling the early phases of human DN.

摘要

肥胖相关性肾小球病和糖尿病肾病(DN)是代谢综合征和糖尿病的严重并发症。本研究旨在研究高脂肪、果糖和胆固醇丰富(FFC)饮食加或不加盐诱导高血压对伴或不伴糖尿病的哥廷根小型猪肾功能和形态的影响。雄性哥廷根小型猪分为 4 组:SD(标准饮食,n = 8)、FFC(FFC 饮食,n = 16)、FFC-DIA(FFC 饮食+糖尿病,n = 14)、FFC-DIA+S(FFC 饮食加额外盐+糖尿病,n = 14)。在 6-7 个月(T1)和 12-13 个月(T2)时评估血和尿生物标志物、肾小球滤过率(GFR)、血压(BP)和阻力指数(RI)。在 T2 时评估组织学、电子显微镜和基因表达(不包括 FFC-DIA+S)。所有 FFC 饮食组均表现出肥胖、GFR 和 RI 增加、肾小球肿大、系膜扩张(ME)和肾小球基底膜(GBM)增厚。糖尿病加上 FFC 饮食导致血浆葡萄糖、尿素和蛋白尿增加,并倾向于加重肾小球肿大、ME 和 GBM 增厚。与 SD 相比,FFC 和/或 FFC-DIA 中 4 个基因(CDKN1A、NPHS2、ACE、SLC2A1)的表达明显下调。BP 无变化。喂食 FFC 饮食的哥廷根小型猪显示出人类肥胖早期肾脏变化的一些特征。糖尿病的存在使 FFC 饮食的发现更加恶化,并导致类似于人类 DN 早期阶段的变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e69/10097698/7d31dbd3fbb3/41598_2023_32674_Fig1_HTML.jpg

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