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Comparison of pharmacodynamics between insulin glargine 100 U/mL and insulin glargine 300 U/mL in healthy cats
Domestic Animal Endocrinology ( IF 2.1 ) Pub Date : 2020-11-17 , DOI: 10.1016/j.domaniend.2020.106595
N K Saini 1 , B Wasik 1 , J Pires 1 , D M Leale 1 , N Quach 1 , W T N Culp 2 , R J Samms 3 , A E Johnson 3 , J G Owens 3 , C Gilor 4
Affiliation  

Insulin glargine (IGla) is a synthetic human-recombinant insulin analog that is used routinely in people as a q24h basal insulin. The 300 U/mL (U300) formulation of IGla is associated with longer duration of action and less within-day variability, making it a better basal insulin compared with the 100 U/mL (U100) formulation. We hypothesized that in healthy cats, IGlaU300 has a flatter time-action profile and longer duration of action compared with IGlaU100. Seven healthy neutered male, purpose-bred cats were studied in a randomized, crossover design. Pharmacodynamics of IGlaU100 and IGlaU300 (0.8 U/kg, subcutaneous) were determined by the isoglycemic clamp method. The time-action profile of IGlaU300 was flatter compared with IGlaU100 as demonstrated by lower peak (5.6 ± 1.1 mg/kg/min vs 8.3 ± 1.9 mg/kg/min, respectively; P = 0.04) with no difference in total metabolic effect (ME; P = 0.7) or duration of action (16.8 h ± 4.7 h vs 13.4 h ± 2.6 h; P = 0.2). The greater fraction of ME in the 12- to 24-h period postinjection (35 ± 23% vs 7 ± 8% respectively; P = 0.048) and lower intraday GIR% variability (7.8 ± 3.7% vs 17.4 ± 8.2% respectively; P = 0.03) supports a flatter time-action profile of IGlaU300. There were no differences in onset and end of the action. In summary, although both formulations have a similar duration of action that is well below 24 h, the ME of IGlaU300 is more evenly distributed over a 24 h period in healthy cats, making it a better candidate for once-daily injection in diabetics compared with IGlaU100.



中文翻译:

甘精胰岛素 100 U/mL 和甘精胰岛素 300 U/mL 在健康猫中的药效学比较

甘精胰岛素 (IGla) 是一种合成的人重组胰岛素类似物,作为 q24h 基础胰岛素在人群中常规使用。与 100 U/mL (U100) 制剂相比,300 U/mL (U300) 的 IGla 制剂具有更长的作用持续时间和更少的日内变异性,使其成为更好的基础胰岛素。我们假设在健康猫中,与 IGlaU100 相比,IGlaU300 具有更平坦的时间-作用曲线和更长的作用持续时间。在随机交叉设计中研究了七只健康的绝育雄性猫。IGlaU100 和 IGlaU300(0.8 U/kg,皮下)的药效学通过等糖钳夹法测定。IGlaU300 的时间-作用曲线与 IGlaU100 相比更平坦,如较低的峰值所示(分别为 5.6 ± 1.1 mg/kg/min 和 8.3 ± 1.9 mg/kg/min;P = 0.04),总代谢效应(ME;P = 0.7)或作用持续时间(16.8 h ± 4.7 h vs 13.4 h ± 2.6 h;P = 0.2)没有差异。注射后 12 至 24 小时内 ME 的比例更大(分别为 35 ± 23% 和 7 ± 8%;P = 0.048)和更低的日内 GIR% 变异性(分别为 7.8 ± 3.7% 和 17.4 ± 8.2%;P = 0.03) 支持 IGlaU300 更平坦的时间-动作曲线。动作的开始和结束没有差异。总之,虽然两种制剂的作用持续时间相似,远低于 24 小时,但 IGlaU300 的 ME 在健康猫中的 24 小时内分布更均匀,使其成为糖尿病患者每日一次注射的更好候选者。 IGlaU100。

更新日期:2020-12-08
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