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内脏脂肪组织中胆红素还原酶-A 表达减少与人类肥胖症中脂肪细胞功能障碍和非酒精性脂肪性肝病有关。

Reduced Biliverdin Reductase-A Expression in Visceral Adipose Tissue is Associated with Adipocyte Dysfunction and NAFLD in Human Obesity.

机构信息

Department of Experimental Medicine, Sapienza University of Rome, 00161 Rome, Italy.

Department of Medical-Surgical Sciences and Bio-Technologies, Sapienza University of Rome, 04100 Latina, Italy.

出版信息

Int J Mol Sci. 2020 Nov 29;21(23):9091. doi: 10.3390/ijms21239091.

Abstract

Biliverdin reductase A (BVR-A) is an enzyme involved in the regulation of insulin signalling. Knockout (KO) mice for hepatic BVR-A, on a high-fat diet, develop more severe glucose impairment and hepato-steatosis than the wild type, whereas loss of adipocyte BVR-A is associated with increased visceral adipose tissue (VAT) inflammation and adipocyte size. However, BVR-A expression in human VAT has not been investigated. We evaluated BVR-A mRNA expression levels by real-time PCR in the intra-operative omental biopsy of 38 obese subjects and investigated the association with metabolic impairment, VAT dysfunction, and biopsy-proven non-alcoholic fatty liver disease (NAFLD). Individuals with lower VAT BVR-A mRNA levels had significantly greater VAT IL-8 and Caspase 3 expression than those with higher BVR-A. Lower VAT BVR-A mRNA levels were associated with an increased adipocytes' size. An association between lower VAT BVR-A expression and higher plasma gamma-glutamyl transpeptidase was also observed. Reduced VAT BVR-A was associated with NAFLD with an odds ratio of 1.38 (95% confidence interval: 1.02-1.9; χ test) and with AUROC = 0.89 ( = 0.002, 95% CI = 0.76-1.0). In conclusion, reduced BVR-A expression in omental adipose tissue is associated with VAT dysfunction and NAFLD, suggesting a possible involvement of BVR-A in the regulation of VAT homeostasis in presence of obesity.

摘要

胆红素还原酶 A(BVR-A)是参与胰岛素信号调节的一种酶。在高脂肪饮食条件下,肝 BVR-A 敲除(KO)小鼠比野生型小鼠发展出更严重的葡萄糖损伤和肝脂肪变性,而脂肪组织 BVR-A 的缺失与内脏脂肪组织(VAT)炎症和脂肪细胞增大有关。然而,尚未研究人 VAT 中的 BVR-A 表达。我们通过实时 PCR 评估了 38 名肥胖受试者术中网膜活检中的 BVR-A mRNA 表达水平,并研究了其与代谢损伤、VAT 功能障碍和活检证实的非酒精性脂肪性肝病(NAFLD)之间的关联。VAT 中 BVR-A mRNA 水平较低的个体的 VAT IL-8 和 Caspase 3 表达显著高于 BVR-A 水平较高的个体。较低的 VAT BVR-A mRNA 水平与脂肪细胞体积增大有关。还观察到较低的 VAT BVR-A 表达与较高的血浆 γ-谷氨酰转肽酶之间存在关联。VAT 中 BVR-A 的减少与 NAFLD 相关,比值比为 1.38(95%置信区间:1.02-1.9;卡方检验),AUROC 值为 0.89( = 0.002,95%CI = 0.76-1.0)。总之,网膜脂肪组织中 BVR-A 表达减少与 VAT 功能障碍和 NAFLD 相关,表明 BVR-A 可能参与肥胖时 VAT 稳态的调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2454/7730815/e14a277f8849/ijms-21-09091-g001.jpg

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