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卡莫瑞林对健康犬血糖控制的影响。

The effect of capromorelin on glycemic control in healthy dogs.

作者信息

Pascutti K M, O'Kell A L, Hill R C, Castro R A, Salute M E, Gilor C

机构信息

Department of Small Animal Clinical Sciences, University of Florida, College of Veterinary Medicine, 2015 SW 16th Ave, Gainesville, FL 32610, USA.

Department of Small Animal Clinical Sciences, University of Florida, College of Veterinary Medicine, 2015 SW 16th Ave, Gainesville, FL 32610, USA.

出版信息

Domest Anim Endocrinol. 2022 Oct;81:106732. doi: 10.1016/j.domaniend.2022.106732. Epub 2022 May 8.

Abstract

Capromorelin is a ghrelin-receptor agonist widely used as an appetite stimulant in dogs. Capromorelin disrupts glucose homeostasis in cats but information regarding its effects on canine glucose homeostasis is lacking. The study objective was to evaluate the effect of capromorelin on glucose homeostatic mechanisms in healthy dogs. Eight clinically healthy client-owned adult dogs were enrolled in this prospective, cross-over, placebo-controlled study. Dogs were randomized to receive capromorelin (Entyce, 3 mg/kg) or placebo, q24h for 3 d. A wk later, treatments were crossed over. Interstitial glucose (IG) concentrations were measured using a flash glucose monitoring system throughout. On d 1 of each treatment, blood glucose (BG), insulin, glucagon, glucose-dependent insulinotropic peptide (GIP), and glucagon-like peptide-1 (GLP-1) concentrations were measured before drug administration, then before and 30-120 min after feeding a glucose-rich diet (Ensure Plus, 21 kcal/kg). Data were analyzed as a 2-period crossover design using generalized least squares estimation. Capromorelin administration increased mean 48 h IG by10% and mean BG by 20% at 90 and 120 min post-prandially (P < 0.0001). Post-prandially, there was a time-by-treatment effect for insulin (P = 0.03) and GIP (P = 0.0002) because capromorelin doubled geometric mean insulin concentrations at 120 min and increased geometric mean GIP concentrations more rapidly than after placebo. There were no differences in glucagon or GLP-1 concentrations between treatment groups. The increase in post-prandial blood glucose was not the result of overt suppression of incretin hormone secretion. There was also no suppressive effect of capromorelin on insulin.

摘要

卡莫瑞林是一种胃饥饿素受体激动剂,在犬类中广泛用作食欲刺激剂。卡莫瑞林会破坏猫的葡萄糖稳态,但缺乏关于其对犬类葡萄糖稳态影响的信息。本研究的目的是评估卡莫瑞林对健康犬类葡萄糖稳态机制的影响。八只临床健康的成年宠物犬被纳入这项前瞻性、交叉、安慰剂对照研究。犬只被随机分为接受卡莫瑞林(Entyce,3 mg/kg)或安慰剂治疗,每24小时给药一次,持续3天。一周后,进行治疗交叉。全程使用动态葡萄糖监测系统测量组织间葡萄糖(IG)浓度。在每种治疗的第1天,在给药前、喂食富含葡萄糖的饮食(安素益力佳,21 kcal/kg)前以及喂食后30 - 120分钟测量血糖(BG)、胰岛素、胰高血糖素、葡萄糖依赖性促胰岛素多肽(GIP)和胰高血糖素样肽 - 1(GLP - 1)浓度。使用广义最小二乘法估计将数据作为两阶段交叉设计进行分析。给予卡莫瑞林后,餐后90分钟和120分钟时平均48小时IG增加了10%,平均BG增加了20%(P < 0.0001)。餐后,胰岛素(P = 0.03)和GIP(P = 0.0002)存在时间 - 治疗交互效应,因为卡莫瑞林使120分钟时的几何平均胰岛素浓度增加了一倍,且使几何平均GIP浓度升高的速度比安慰剂组更快。治疗组之间胰高血糖素或GLP - 1浓度没有差异。餐后血糖升高不是肠促胰岛素激素分泌明显受抑制的结果。卡莫瑞林对胰岛素也没有抑制作用。

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