Impact of visceral adipose tissue on longevity and metabolic health: a comparative study of gene expression in perirenal and epididymal fat of Ames dwarf mice.

IF 5.3 2区 医学 Q1 GERIATRICS & GERONTOLOGY GeroScience Pub Date : 2024-12-01 Epub Date: 2024-03-22 DOI:10.1007/s11357-024-01131-1
Agnieszka Zaczek, Andrzej Lewiński, Małgorzata Karbownik-Lewińska, Andrea Lehoczki, Adam Gesing
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Abstract

Emerging research underscores the pivotal role of adipose tissue in regulating systemic aging processes, particularly when viewed through the lens of the endocrine hypotheses of aging. This study delves into the unique adipose characteristics in an important animal model of aging - the long-lived Ames dwarf (df/df) mice. Characterized by a Prop1df gene mutation, these mice exhibit a deficiency in growth hormone (GH), prolactin, and TSH, alongside extremely low circulating IGF-1 levels. Intriguingly, while surgical removal of visceral fat (VFR) enhances insulin sensitivity in normal mice, it paradoxically increases insulin resistance in Ames dwarfs. This suggests an altered profile of factors produced in visceral fat in the absence of GH, indicating a unique interplay between adipose tissue function and hormonal influences in these models. Our aim was to analyze the gene expression related to lipid and glucose metabolism, insulin pathways, inflammation, thermoregulation, mitochondrial biogenesis, and epigenetic regulation in the visceral (perirenal and epididymal) adipose tissue of Ames dwarf and normal mice. Our findings reveal an upregulation in the expression of key genes such as Lpl, Adrβ3, Rstn, Foxo1, Foxo3a, Irs1, Cfd, Aldh2, Il6, Tnfα, Pgc1α, Ucp2, and Ezh2 in perirenal and Akt1, Foxo3a, PI3k, Ir, Acly, Il6, Ring1a, and Ring 1b in epididymal fat in df/df mice. These results suggest that the longevity phenotype in Ames dwarfs, which is determined by peripubertal GH/IGF-1 levels, may also involve epigenetic reprogramming of adipose tissue influenced by hormonal changes. The increased expression of genes involved in metabolic regulation, tumor suppression, mitochondrial biogenesis, and insulin pathways in Ames dwarf mice highlights potentially beneficial aspects of this model, opening new avenues for understanding the molecular underpinnings of longevity and aging.

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内脏脂肪组织对寿命和代谢健康的影响:艾姆斯侏儒小鼠肾周脂肪和附睾脂肪基因表达的比较研究。
新近的研究强调了脂肪组织在调节全身衰老过程中的关键作用,尤其是通过内分泌衰老假说的视角来看。本研究深入探讨了一种重要的衰老动物模型--长寿艾姆斯侏儒(df/df)小鼠--的独特脂肪特征。由于 Prop1df 基因突变,这些小鼠表现出生长激素(GH)、催乳素和促甲状腺激素(TSH)缺乏,同时循环 IGF-1 水平极低。耐人寻味的是,手术切除内脏脂肪(VFR)会增强正常小鼠的胰岛素敏感性,但在艾姆斯侏儒身上却会增加胰岛素抵抗。这表明在缺乏 GH 的情况下,内脏脂肪中产生的因子谱发生了改变,表明在这些模型中脂肪组织功能和激素影响之间存在独特的相互作用。我们的目的是分析埃姆斯侏儒小鼠和正常小鼠内脏(肾周和附睾)脂肪组织中与脂质和葡萄糖代谢、胰岛素通路、炎症、体温调节、线粒体生物生成和表观遗传调控有关的基因表达。我们的研究结果表明,在侏儒/豚鼠肾周脂肪中,Lpl、Adrβ3、Rstn、Foxo1、Foxo3a、Irs1、Cfd、Aldh2、Il6、Tnfα、Pgc1α、Ucp2 和 Ezh2 等关键基因的表达上调;在附睾脂肪中,Akt1、Foxo3a、PI3k、Ir、Acly、Il6、Ring1a 和 Ring 1b 等关键基因的表达上调。这些结果表明,艾姆斯侏儒的长寿表型由围青春期 GH/IGF-1 水平决定,也可能涉及受激素变化影响的脂肪组织的表观遗传重编程。艾姆斯侏儒小鼠中涉及代谢调节、肿瘤抑制、线粒体生物生成和胰岛素通路的基因表达量增加,凸显了该模型的潜在益处,为了解长寿和衰老的分子基础开辟了新途径。
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来源期刊
GeroScience
GeroScience Medicine-Complementary and Alternative Medicine
CiteScore
10.50
自引率
5.40%
发文量
182
期刊介绍: GeroScience is a bi-monthly, international, peer-reviewed journal that publishes articles related to research in the biology of aging and research on biomedical applications that impact aging. The scope of articles to be considered include evolutionary biology, biophysics, genetics, genomics, proteomics, molecular biology, cell biology, biochemistry, endocrinology, immunology, physiology, pharmacology, neuroscience, and psychology.
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