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在饮食诱导肥胖的大鼠中,胰岛素吸收延迟与皮下储存库动力学改变相关。

Delayed insulin absorption correlates with alterations in subcutaneous depot kinetics in rats with diet-induced obesity.

作者信息

Gradel A K J, Porsgaard T, Brockhoff P B, Seested T, Lykkesfeldt J, Refsgaard H H F

机构信息

Department of Veterinary and Animal Sciences, Section of Experimental Animal Models, Faculty of Health and Medical Sciences University of Copenhagen Frederiksberg Denmark.

Global Drug Discovery, Novo Nordisk A/S Måløv Denmark.

出版信息

Obes Sci Pract. 2019 Mar 18;5(3):281-288. doi: 10.1002/osp4.326. eCollection 2019 Jun.

Abstract

OBJECTIVE

Obesity is associated with delayed insulin absorption upon subcutaneous (s.c.) dosing in humans. The aim of this study was to investigate whether alterations in depot structure and kinetics of the s.c. injection depot contribute to this delay.

METHODS

Rats fed a high-fat diet (HFD) and low-fat diet (LFD) were included in a series of insulin pharmacokinetic and imaging studies. Injection depots were visualized with micro X-ray computed tomography imaging upon s.c. administration of insulin aspart mixed with the contrast agent iomeprol, and insulin aspart exposure was measured by means of luminescent oxygen channelling immunoassay.

RESULTS

Body weight and fat mass were increased in rats fed an HFD vs. LFD ( < 0.05), whereas the lean mass was not. The HFD group exhibited delayed insulin absorption from the s.c. tissue ( < 0.001). This delay was associated with smaller injection depots upon s.c. dosing ( < 0.05) and correlated with a slower depot disappearance from the s.c. tissue ( < 0.05) compared with the LFD group. Depot disappearance from the s.c. tissue was inversely correlated with body fat mass ( < 0.05).

CONCLUSIONS

Alterations in s.c. injection depot structure and kinetics may play a role in the obesity-associated delay in insulin absorption.

摘要

目的

肥胖与人体皮下给药后胰岛素吸收延迟有关。本研究的目的是调查皮下注射 depot 的结构改变和动力学是否导致了这种延迟。

方法

喂食高脂饮食(HFD)和低脂饮食(LFD)的大鼠被纳入一系列胰岛素药代动力学和成像研究。皮下注射与造影剂碘海醇混合的门冬胰岛素后,用微型 X 射线计算机断层扫描成像观察注射 depot,并用发光氧通道免疫分析法测量门冬胰岛素的暴露量。

结果

与喂食 LFD 的大鼠相比,喂食 HFD 的大鼠体重和脂肪量增加(<0.05),而瘦体重未增加。HFD 组皮下组织胰岛素吸收延迟(<0.001)。与 LFD 组相比,这种延迟与皮下给药时较小的注射 depot 有关(<0.05),并与皮下组织中 depot 消失较慢相关(<0.05)。皮下组织中 depot 的消失与体脂量呈负相关(<0.05)。

结论

皮下注射 depot 的结构和动力学改变可能在肥胖相关的胰岛素吸收延迟中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5401/6587326/cf1ee17e541c/OSP4-5-281-g001.jpg

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