Targeting the PHD2/HIF-1α/HO-1 pathway: A key role of trimetazidine in hypertensive nephropathy.

IF 3.5 4区 医学 Q3 PERIPHERAL VASCULAR DISEASE
Daqian Gu, Meixian Chen, Yuhui Yang, Chen Lu, Chao Li, Yi Lin
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引用次数: 0

Abstract

Objective: This study seeks to unravel the effects of trimetazidine (TMZ) on hypertensive nephropathy (HN) in mice and its underlying mechanisms.

Methods: Sixty male 129 mice (8-10 weeks old) were randomly categorized into six groups (n = 10 per group): control, model, TMZ, TMZ + small interfering RNA targeting prolyl hydroxylase domain protein 2 (si-PHD2), TMZ + zinc protoporphyrin [ZnPP, a heme oxygenase-1 (HO-1) inhibitor], and TMZ + KC7F2 [a hypoxia-inducible factor-1 alpha (HIF-1α) inhibitor]. All groups except the control group received angiotensin II to induce HN models. TMZ was administered by gavage for 28 days, while the other TMZ-based groups received additional si-PHD2, ZnPP, or KC7F2. Blood pressure, renal function, proinflammatory cytokines, and kidney pathology were measured. Protein/mRNA levels of PHD2, HO-1, HIF-1α, and Collagen I were analyzed via reverse transcription quantitative polymerase chain reaction/Western blot.

Results: The model group showed increased blood pressure, renal injury, fibrosis, and elevated levels of PHD2, HIF-1α, HO-1, Collagen I, and inflammatory markers compared to the control group (P < 0.05). TMZ treatment alleviated renal damage and downregulated PHD2, while upregulating HIF-1α and HO-1. These effects were further enhanced by PHD2 knockdown (TMZ + si-PHD2), but reversed by the inhibition of HO-1 or HIF-1α (TMZ + ZnPP, TMZ + KC7F2).

Conclusion: TMZ improves HN in mice by modulating the PHD2/HIF-1α/HO-1 pathway.

靶向PHD2/HIF-1α/HO-1通路:曲美他嗪在高血压肾病中的关键作用
目的:探讨曲美他嗪(TMZ)对小鼠高血压肾病(HN)的治疗作用及其机制。方法:选取8 ~ 10周龄雄性129只小鼠60只,随机分为对照组、模型组、TMZ组、TMZ +脯氨酰羟化酶结构域蛋白2 (si-PHD2)小干扰RNA组、TMZ +原卟啉锌[血红素加氧酶-1 (HO-1)抑制剂ZnPP]组和TMZ + KC7F2[缺氧诱导因子-1α (HIF-1α)抑制剂]组6组(每组10只)。除对照组外,其余各组均给予血管紧张素ⅱ诱导HN模型。TMZ组灌胃28 d,其他TMZ组加用si-PHD2、ZnPP或KC7F2。测量血压、肾功能、促炎细胞因子和肾脏病理。通过逆转录定量聚合酶链反应/Western blot分析PHD2、HO-1、HIF-1α和Collagen I蛋白/mRNA水平。结果:与对照组相比,模型组出现血压升高、肾损伤、纤维化、PHD2、HIF-1α、HO-1、I型胶原蛋白和炎症标志物水平升高(P结论:TMZ通过调节PHD2/HIF-1α/HO-1通路改善小鼠HN。
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来源期刊
CiteScore
3.90
自引率
0.80%
发文量
66
审稿时长
6-12 weeks
期刊介绍: Clinical and Experimental Hypertension is a reputable journal that has converted to a full Open Access format starting from Volume 45 in 2023. While previous volumes are still accessible through a Pay to Read model, the journal now provides free and open access to its content. It serves as an international platform for the exchange of up-to-date scientific and clinical information concerning both human and animal hypertension. The journal publishes a wide range of articles, including full research papers, solicited and unsolicited reviews, and commentaries. Through these publications, the journal aims to enhance current understanding and support the timely detection, management, control, and prevention of hypertension-related conditions. One notable aspect of Clinical and Experimental Hypertension is its coverage of special issues that focus on the proceedings of symposia dedicated to hypertension research. This feature allows researchers and clinicians to delve deeper into the latest advancements in this field. The journal is abstracted and indexed in several renowned databases, including Pharmacoeconomics and Outcomes News (Online), Reactions Weekly (Online), CABI, EBSCOhost, Elsevier BV, International Atomic Energy Agency, and the National Library of Medicine, among others. These affiliations ensure that the journal's content receives broad visibility and facilitates its discoverability by professionals and researchers in related disciplines.
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