患有肾病和草酸钙尿石的猫的代谢组学变化。

Dennis E Jewell, Selena K Tavener, Regina L Hollar, Kiran S Panickar
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引用次数: 1

摘要

导读:在家养猫中,肾脏疾病(RD)和草酸钙(CaOx)肾尿石的发生率很高。通过了解潜在的代谢组学变化,有助于控制这些疾病的食物可能会得到加强。目的:评估代谢组学特征,以确定代谢组学靶点,从而有助于肾脏疾病和CaOx尿石的治疗。方法:对42只猫进行回顾性调查,其中19只为健康猫,11只为RD猫,12只为CaOx肾结石猫。对成年猫(2 - 7岁)和临终猫的血浆代谢组学、身体成分和肾功能障碍标志物进行评估。肾切片在生命结束时用Pizzolato染色法检测CaOx晶体。在生命结束时,还通过分析从肾脏取出的结石来评估CaOx结石的存在。结果:共鉴定出791种代谢物,其中91种具有显著性(p)。结论:代谢组学变化显示出特异性代谢物,对两种肾脏疾病都有普遍反应,而代谢组学特征仍然可以区分RD猫和CaOx猫尿石。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Metabolomic changes in cats with renal disease and calcium oxalate uroliths.

Metabolomic changes in cats with renal disease and calcium oxalate uroliths.

Metabolomic changes in cats with renal disease and calcium oxalate uroliths.

Introduction: There is a significant incidence of cats with renal disease (RD) and calcium oxalate (CaOx) kidney uroliths in domesticated cats. Foods which aid in the management of these diseases may be enhanced through understanding the underlying metabolomic changes.

Objective: Assess the metabolomic profile with a view to identifying metabolomic targets which could aid in the management of renal disease and CaOx uroliths.

Method: This is a retrospective investigation of 42 cats: 19 healthy kidney controls, 11 with RD, and 12 that formed CaOx nephroliths. Cats were evaluated as adults (2 through 7 years) and at the end of life for plasma metabolomics, body composition, and markers of renal dysfunction. Kidney sections were assessed by Pizzolato stain at the end of life for detection of CaOx crystals. CaOx stone presence was also assessed by analysis of stones removed from the kidney at the end of life.

Results: There were 791 metabolites identified with 91 having significant (p < 0.05, q < 0.1) changes between groups. Many changes in metabolite concentrations could be explained by the loss of renal function being most acute in the cats with RD while the cats with CaOx stones were intermediate between control and RD (e.g., urea, creatinine, pseudouridine, dimethylarginines). However, the concentrations of some metabolites differentiated RD from CaOx stone forming cats. These were either increased in the RD cats (e.g., cystathionine, dodecanedioate, 3-(3-amino-3-carboxypropyl) uridine, 5-methyl-2'-deoxycytidine) or comparatively increased in the CaOx stone forming cats (phenylpyruvate, 4-hydroxyphenylpyruvate, alpha-ketobutyrate, retinal).

Conclusions: The metabolomic changes show specific metabolites which respond generally to both renal diseases while the metabolomic profile still differentiates cats with RD and cats with CaOx uroliths.

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