Na-Cl Cotransporter (SLC12A3) Inhibition Exacerbates Age-Related Macular Degeneration Via the Nrf2/HO-1 Ferroptosis Pathway.

IF 4.7 2区 医学 Q1 OPHTHALMOLOGY
Chengming Chen, Tingke Xie, Huan Zhang, Lifu Chang, Yanyan Lan, Chao Fan, Dongyu Wei, Xiaolan Wang, Sida Liu, Yixuan Chen, Yuhao Chen, Xuejiao Wang, Xiaolong Yan, Lei Shang, Liyuan Tao, Jing Han
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Abstract

Purpose: To explore the causal links between antihypertension drugs usage and age-related macular degeneration (AMD).

Methods: Multiple genetic analyses, including summary data-based Mendelian randomization (SMR), traditional MR, and colocalization analysis, were used to explore the causal associations between antihypertension drugs and AMD. Clinical data from the UK Biobank and the National Health and Nutrition Examination Survey (NHANES) was applied to refined risk assessment of specific antihypertensive medications in the context of AMD development. In vitro and in vivo oxidative stress models, mediated by NaIO3, were utilized to study the impact of specific antihypertensive drugs and target genes on AMD pathogenesis.

Results: Genetic analyses substantiated the causal relationship between increased SLC12A3 expression and a lowered AMD risk. Colocalization analysis supported the shared causal attributes between SLC12A3 expression and AMD. Cross-sectional analysis results based on UK Biobank indicated that AMD risk was significantly lower in participants taking thiazide diuretics with other antihypertensives or not on antihypertensives compared to those on thiazides alone. The results based on NHANES support the above results. In vivo and in vitro experiments showed that thiazide diuretics worsened retinal damage in AMD mouse models, and SLC12A3 knockdown disrupted the balance of oxidative stress in retinal pigment epithelium (RPE) cells. Further molecular mechanism experiments showed that SLC12A3 knockdown promoted retinal degeneration by regulating RPE ferroptosis through activation of the Nrf2/HO-1 pathway.

Conclusions: Our study underscores a notable causal association between thiazide diuretic use and AMD risk and reveals a potential mechanism by which inhibition or downregulation of SLC12A3 (sodium-chloride cotransporter [NCC]) contributes to AMD progression. However, deeper exploration is needed to enhance the accuracy and validity of our findings.

Na-Cl共转运体(SLC12A3)抑制通过Nrf2/HO-1铁下沉途径加剧年龄相关性黄斑变性
目的:探讨抗高血压药物使用与年龄相关性黄斑变性(AMD)之间的因果关系。方法:采用多种遗传分析,包括基于汇总数据的孟德尔随机化(SMR)、传统MR和共定位分析,探讨抗高血压药物与AMD之间的因果关系。来自英国生物银行和国家健康与营养调查(NHANES)的临床数据被应用于AMD发展背景下特定抗高血压药物的精细风险评估。利用NaIO3介导的体内外氧化应激模型,研究特异性降压药物和靶基因对AMD发病机制的影响。结果:遗传分析证实了SLC12A3表达增加与AMD风险降低之间的因果关系。共定位分析支持SLC12A3表达与AMD之间存在共同的因果属性。基于UK Biobank的横断面分析结果表明,与单独使用噻嗪类利尿剂的受试者相比,服用噻嗪类利尿剂与其他抗高血压药物或不服用抗高血压药物的受试者AMD风险显著降低。基于NHANES的结果支持上述结果。体内和体外实验表明噻嗪类利尿剂加重AMD小鼠模型视网膜损伤,SLC12A3敲低破坏视网膜色素上皮(RPE)细胞氧化应激平衡。进一步的分子机制实验表明,SLC12A3敲低通过激活Nrf2/HO-1通路调节RPE铁下垂,从而促进视网膜变性。结论:本研究强调噻嗪类利尿剂与AMD风险之间存在显著的因果关系,并揭示了抑制或下调SLC12A3(氯化钠共转运体[NCC])促进AMD进展的潜在机制。然而,为了提高我们研究结果的准确性和有效性,还需要进行更深入的探索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.90
自引率
4.50%
发文量
339
审稿时长
1 months
期刊介绍: Investigative Ophthalmology & Visual Science (IOVS), published as ready online, is a peer-reviewed academic journal of the Association for Research in Vision and Ophthalmology (ARVO). IOVS features original research, mostly pertaining to clinical and laboratory ophthalmology and vision research in general.
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