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高剂量非诺贝特刺激老年大鼠肾脏中的多种细胞应激途径。

High-Dose Fenofibrate Stimulates Multiple Cellular Stress Pathways in the Kidney of Old Rats.

作者信息

Wrońska Agata, Kieżun Jacek, Kmieć Zbigniew

机构信息

Department of Histology, Faculty of Medicine, Medical University of Gdańsk, 80-210 Gdańsk, Poland.

Department of Human Histology and Embryology, School of Medicine, University of Warmia and Mazury in Olsztyn, 10-082 Olsztyn, Poland.

出版信息

Int J Mol Sci. 2024 Mar 6;25(5):3038. doi: 10.3390/ijms25053038.

Abstract

We investigated the age-related effects of the lipid-lowering drug fenofibrate on renal stress-associated effectors. Young and old rats were fed standard chow with 0.1% or 0.5% fenofibrate. The kidney cortex tissue structure showed typical aging-related changes. In old rats, 0.1% fenofibrate reduced the thickening of basement membranes, but 0.5% fenofibrate exacerbated interstitial fibrosis. The PCR array for stress and toxicity-related targets showed that 0.1% fenofibrate mildly downregulated, whereas 0.5% upregulated multiple genes. In young rats, 0.1% fenofibrate increased some antioxidant genes' expression and decreased the immunoreactivity of oxidative stress marker 4-HNE. However, the activation of cellular antioxidant defenses was impaired in old rats. Fenofibrate modulated the expression of factors involved in hypoxia and osmotic stress signaling similarly in both age groups. Inflammatory response genes were variably modulated in the young rats, whereas old animals presented elevated expression of proinflammatory genes and TNFα immunoreactivity after 0.5% fenofibrate. In old rats, 0.1% fenofibrate more prominently than in young animals induced phospho-AMPK and PGC1α levels, and upregulated fatty acid oxidation genes. Our results show divergent effects of fenofibrate in young and old rat kidneys. The activation of multiple stress-associated effectors by high-dose fenofibrate in the aged kidney warrants caution when applying fenofibrate therapy to the elderly.

摘要

我们研究了降脂药物非诺贝特对肾脏应激相关效应器的年龄相关影响。将年轻和老年大鼠喂以含0.1%或0.5%非诺贝特的标准饲料。肾皮质组织结构显示出典型的衰老相关变化。在老年大鼠中,0.1%非诺贝特可减轻基底膜增厚,但0.5%非诺贝特会加剧间质纤维化。应激和毒性相关靶点的PCR阵列显示,0.1%非诺贝特轻度下调多个基因,而0.5%则上调多个基因。在年轻大鼠中,0.1%非诺贝特增加了一些抗氧化基因的表达,并降低了氧化应激标志物4-HNE的免疫反应性。然而,老年大鼠的细胞抗氧化防御激活受损。非诺贝特在两个年龄组中对缺氧和渗透压应激信号相关因子的表达调节相似。年轻大鼠中炎症反应基因受到不同程度的调节,而老年动物在给予0.5%非诺贝特后促炎基因表达升高且TNFα免疫反应性增强。在老年大鼠中,0.1%非诺贝特比年轻动物更显著地诱导磷酸化AMPK和PGC1α水平,并上调脂肪酸氧化基因。我们的结果表明非诺贝特在年轻和老年大鼠肾脏中的作用不同。在老年肾脏中高剂量非诺贝特激活多种应激相关效应器,这提示在对老年人应用非诺贝特治疗时需谨慎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ecc/10932055/50ada3ee129f/ijms-25-03038-g001.jpg

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