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氨氯地平对健康猫循环肾素-血管紧张素-醛固酮系统的影响。

Effect of amlodipine on the circulating renin-angiotensin-aldosterone system in healthy cats.

机构信息

Department of Veterinary Clinical Sciences, College of Veterinary Medicine, Iowa State University, Ames, Iowa, USA.

Ceva Santé Animale, Companion Animal Franchise, Libourne, France.

出版信息

J Vet Intern Med. 2024 Mar-Apr;38(2):913-921. doi: 10.1111/jvim.17006. Epub 2024 Feb 9.

Abstract

BACKGROUND

Systemic hypertension (SH) is a common cardiovascular disease in older cats that is treated primarily with the calcium channel blocker amlodipine besylate (AML). The systemic effect of AML on the classical and alterative arms of the renin-angiotensin-aldosterone system (RAAS) in cats is incompletely characterized.

HYPOTHESIS/OBJECTIVES: To determine the effect of AML compared to placebo on circulating RAAS biomarkers in healthy cats using RAAS fingerprinting.

ANIMALS

Twenty healthy client-owned cats.

METHODS

Cats were administered amlodipine besylate (0.625 mg in toto) or placebo by mouth once daily for 14 days in a crossover design with a 4-week washout period. Plasma AML concentrations and RAAS biomarker concentrations were measured at multiple timepoints after the final dose in each treatment period. Time-weighted averages for RAAS biomarkers over 24 hours after dosing were compared between treatment groups using Wilcoxon rank-sum testing.

RESULTS

Compared to placebo, AML treatment was associated with increases in markers of plasma renin concentration (median 44% increase; interquartile range [IQR] 19%-86%; P = .009), angiotensin I (59% increase; IQR 27-101%; P = .006), angiotensin II (56% increase; IQR 5-70%; P = .023), angiotensin IV (42% increase; -19% to 89%; P = .013); and angiotensin 1-7 (38% increase; IQR 9-118%; P = .015).

CONCLUSIONS AND CLINICAL IMPORTANCE

In healthy cats, administration of AML resulted in nonspecific activation of both classical and alternative RAAS pathways.

摘要

背景

全身性高血压(SH)是老年猫常见的心血管疾病,主要用钙通道阻滞剂苯磺酸氨氯地平(AML)治疗。AML 对猫的经典和替代肾素-血管紧张素-醛固酮系统(RAAS)臂的全身作用尚未完全描述。

假设/目的:使用 RAAS 指纹图谱确定 AML 与安慰剂相比对健康猫循环 RAAS 生物标志物的影响。

动物

20 只健康的宠物猫。

方法

猫以交叉设计口服给予苯磺酸氨氯地平(0.625mg 总量)或安慰剂,每天一次,每个治疗期有 4 周的洗脱期。在每个治疗期的最后一次给药后,多次测量血浆 AML 浓度和 RAAS 生物标志物浓度。使用 Wilcoxon 秩和检验比较两组之间 24 小时后给药的 RAAS 生物标志物的时间加权平均值。

结果

与安慰剂相比,AML 治疗与血浆肾素浓度标志物的增加相关(中位数增加 44%;四分位距 [IQR] 19%-86%;P=0.009)、血管紧张素 I(增加 59%;IQR 27-101%;P=0.006)、血管紧张素 II(增加 56%;IQR 5-70%;P=0.023)、血管紧张素 IV(增加 42%;-19%至 89%;P=0.013)和血管紧张素 1-7(增加 38%;IQR 9-118%;P=0.015)。

结论和临床意义

在健康的猫中,AML 的给药导致经典和替代 RAAS 途径的非特异性激活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3b3/10937479/3fa2b03db94a/JVIM-38-913-g002.jpg

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