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研究蛋白结合型尿毒症毒素清除的动物模型:系统评价。

Animal Models for Studying Protein-Bound Uremic Toxin Removal-A Systematic Review.

机构信息

Division of Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Universiteitsweg 99, 3584 CG Utrecht, The Netherlands.

Department of Nephrology and Hypertension, University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands.

出版信息

Int J Mol Sci. 2023 Aug 25;24(17):13197. doi: 10.3390/ijms241713197.

Abstract

Protein-bound uremic toxins (PBUTs) are associated with the progression of chronic kidney disease (CKD) and its associated morbidity and mortality. The conventional dialysis techniques are unable to efficiently remove PBUTs due to their plasma protein binding. Therefore, novel approaches are being developed, but these require validation in animals before clinical trials can begin. We conducted a systematic review to document PBUT concentrations in various models and species. The search strategy returned 1163 results for which abstracts were screened, resulting in 65 full-text papers for data extraction (rats ( = 41), mice ( = 17), dogs ( = 3), cats ( = 4), goats ( = 1), and pigs ( = 1)). We performed descriptive and comparative analyses on indoxyl sulfate (IS) concentrations in rats and mice. The data on large animals and on other PBUTs were too heterogeneous for pooled analysis. Most rodent studies reported mean uremic concentrations of plasma IS close to or within the range of those during kidney failure in humans, with the highest in tubular injury models in rats. Compared to nephron loss models in rats, a greater rise in plasma IS compared to creatinine was found in tubular injury models, suggesting tubular secretion was more affected than glomerular filtration. In summary, tubular injury rat models may be most relevant for the in vivo validation of novel PBUT-lowering strategies for kidney failure in humans.

摘要

蛋白结合尿毒症毒素 (PBUTs) 与慢性肾脏病 (CKD) 的进展及其相关发病率和死亡率有关。由于其与血浆蛋白结合,传统的透析技术无法有效地清除 PBUTs。因此,正在开发新的方法,但在临床试验开始之前,这些方法需要在动物中进行验证。我们进行了一项系统评价,以记录各种模型和物种中的 PBUT 浓度。搜索策略返回了 1163 个结果,对摘要进行了筛选,最终有 65 篇全文论文用于数据提取(大鼠 (=41)、小鼠 (=17)、狗 (=3)、猫 (=4)、山羊 (=1)和猪 (=1))。我们对大鼠和小鼠中硫酸吲哚酚 (IS) 浓度进行了描述性和比较性分析。关于大型动物和其他 PBUT 的数据过于异质,无法进行汇总分析。大多数啮齿动物研究报告的血浆 IS 尿毒症浓度接近或在人类肾衰竭范围内,在大鼠的肾小管损伤模型中最高。与大鼠的肾单位丢失模型相比,在肾小管损伤模型中,IS 与肌酐的比值升高幅度更大,这表明肾小管分泌受到的影响比肾小球滤过更大。总之,大鼠的肾小管损伤模型可能与体内验证针对人类肾衰竭的新型 PBUT 降低策略最相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a7d/10487432/db625d884cce/ijms-24-13197-g001.jpg

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