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代谢紊乱实验模型动态变化中的代谢特征及其调控

Features of Metabolism and Its Regulation in the Dynamics of Experimental Models of Metabolic Disorders.

作者信息

Shestopalov A V, Krolenko E V, Nedorubov A A, Borisenko O V, Popruga K E, Makarov V V, Yudin S M, Gaponov A M, Rumyantsev S A

机构信息

Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Ministry of Health of the Russian Federation, Moscow, Russia.

Pirogov Russian National Research Medical University, Ministry of Health of the Russian Federation, Moscow, Russia.

出版信息

Bull Exp Biol Med. 2024 Dec;178(2):280-286. doi: 10.1007/s10517-025-06321-1. Epub 2025 Jan 6.

DOI:10.1007/s10517-025-06321-1
PMID:39760942
Abstract

Changes in the lipid and carbohydrate metabolism, adipokines, and growth factors during the development of metabolic disorders were studied in three mouse models: C57BL/6 (alimentary obesity), db/db (leptin-resistant obesity), and NOD (diabetes mellitus) lines. In the group of alimentary obesity, moderate fatty infiltration of the liver and hypertrophy of the adipose tissue, hyperglycemia, and increased concentrations of adiponectin, transforming growth factor β1 (TGF-β1), leptin, and cholesterol were detected. In the group of leptin-resistant obesity, multiple pathological changes in tissues, severe hyperglycemia and hyperleptinemia, hyperinsulinemia, and reduced concentrations of triglycerides, adiponectin, myostatin, and TGF-β1 were detected. In NOD mice, reduced number of insulin-positive β cells, hyperinsulinemia, and a decrease in adiponectin, TGF-β1, leptin, and myostatin concentrations were detected.

摘要

在三种小鼠模型中研究了代谢紊乱发展过程中脂质和碳水化合物代谢、脂肪因子及生长因子的变化,这三种小鼠模型分别是:C57BL/6(饮食性肥胖)、db/db(瘦素抵抗性肥胖)和NOD(糖尿病)品系。在饮食性肥胖组中,检测到肝脏有中度脂肪浸润、脂肪组织肥大、高血糖,以及脂联素、转化生长因子β1(TGF-β1)、瘦素和胆固醇浓度升高。在瘦素抵抗性肥胖组中,检测到组织出现多种病理变化、严重高血糖和高瘦素血症、高胰岛素血症,以及甘油三酯、脂联素、肌肉生长抑制素和TGF-β1浓度降低。在NOD小鼠中,检测到胰岛素阳性β细胞数量减少、高胰岛素血症,以及脂联素、TGF-β1、瘦素和肌肉生长抑制素浓度降低。

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本文引用的文献

1
Characterization of Risk Factors for Modeling of Type 2 Diabetes Mellitus Induced by a High-Fat Diet in C57BL/6 Mice.高脂饮食诱导 C57BL/6 小鼠 2 型糖尿病建模的危险因素特征分析。
Bull Exp Biol Med. 2024 Feb;176(4):461-465. doi: 10.1007/s10517-024-06047-6. Epub 2024 Mar 15.
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Changes of the Concentration of Short-Chain Fatty Acids in the Intestines of Mice with Different Types of Obesity.不同类型肥胖症小鼠肠道内短链脂肪酸浓度的变化。
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Novel insights into the genetically obese (ob/ob) and diabetic (db/db) mice: two sides of the same coin.
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Microbiome. 2021 Jun 28;9(1):147. doi: 10.1186/s40168-021-01097-8.
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Central signalling cross-talk between insulin and leptin in glucose and energy homeostasis.胰岛素和瘦素在葡萄糖和能量稳态中的中枢信号转导交叉对话。
J Neuroendocrinol. 2021 Apr;33(4):e12944. doi: 10.1111/jne.12944. Epub 2021 Feb 21.
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Tissue-Specific Effects of Leptin on Glucose and Lipid Metabolism.瘦素对葡萄糖和脂代谢的组织特异性作用。
Endocr Rev. 2021 Jan 28;42(1):1-28. doi: 10.1210/endrev/bnaa027.
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TGF-β1 - A truly transforming growth factor in fibrosis and immunity.TGF-β1 - 在纤维化和免疫中真正具有转化生长作用的因子。
Semin Cell Dev Biol. 2020 May;101:123-139. doi: 10.1016/j.semcdb.2019.12.010. Epub 2019 Dec 24.
7
Insulin as a hormone regulator of the synthesis and release of leptin by white adipose tissue.胰岛素作为一种激素,调节白色脂肪组织合成和分泌瘦素。
Peptides. 2018 Aug;106:49-58. doi: 10.1016/j.peptides.2018.06.007. Epub 2018 Jun 25.
8
Loss of intra-islet heparan sulfate is a highly sensitive marker of type 1 diabetes progression in humans.胰岛内硫酸乙酰肝素的丧失是人类1型糖尿病进展的高度敏感标志物。
PLoS One. 2018 Feb 7;13(2):e0191360. doi: 10.1371/journal.pone.0191360. eCollection 2018.
9
Of Mice, Dirty Mice, and Men: Using Mice To Understand Human Immunology.小鼠、脏小鼠与人类:利用小鼠理解人类免疫学
J Immunol. 2017 Jul 15;199(2):383-388. doi: 10.4049/jimmunol.1700453.
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Metabolite profiling in plasma and tissues of ob/ob and db/db mice identifies novel markers of obesity and type 2 diabetes.肥胖症和 2 型糖尿病的新型标志物可通过对 ob/ob 和 db/db 小鼠的血浆和组织进行代谢组学分析鉴定。
Diabetologia. 2015 Sep;58(9):2133-43. doi: 10.1007/s00125-015-3656-y. Epub 2015 Jun 10.