Griffin Ann E, Macdonald Ruth, Wagenmakers Anton J M, Marshall Janice M, Poucher Simon M
School of Clinical and Experimental Medicine, The Medical School, University of Birmingham, Birmingham B15 2TT, United Kingdom.
Cardiovascular and Gastro-intestinal Research Department, AstraZeneca Pharmaceuticals, Mereside, Alderley Park, Macclesfield, Cheshire, SK10 4TG, United Kingdom.
J Pharmacol Toxicol Methods. 2017 Jul;86:67-75. doi: 10.1016/j.vascn.2017.04.001. Epub 2017 Apr 6.
Accurate assessment of muscle insulin sensitivity requires measurement of insulin concentration in interstitial fluid (ISF), but has proved difficult. We aimed to optimise measurement of ISF insulin concentrations in rat muscles in vivo using microdialysis.
Factorial experimental design experiments were performed in vitro to determine optimal conditions for insulin recovery with microdialysis probes. These conditions were tested in vivo, adjusted appropriately and used in lean and obese Zucker rats to compare ISF insulin concentrations basally and during hyperinsulinaemic-euglycaemic (HE) clamp.
Optimal conditions in vivo were: a 100kDa microdialysis probe inserted in muscle, perfused with 1% BSA, 1.5mM glucose in 0.9% sodium chloride at 1μl/min. Samples were collected into siliconised glass microvials. As a reference for insulin, we established a protocol of inulin infusion, beginning at -80min and reaching equilibrium within 60min. HE clamp, beginning at 0min, increased ISF insulin concentration from 122±56 basally to 429±180pmol/l (P<0.05) in lean rats and from 643±165 to 1087±243pmol/l (P=0.07) in obese rats; ISF insulin concentrations were significantly higher throughout in obese rats. The difference between ISF and plasma insulin concentration (ISF:plasma ratio) was substantially higher in obese rats, but fell to similar values in obese and lean rats during HE clamp.
Optimising insulin recovery with microdialysis allowed accurate measurement of basal ISF insulin in muscle of lean and obese Zucker rats and indicates insulin transport across capillaries is impaired in obese rats, basally and during hyperinsulinaemia.
准确评估肌肉胰岛素敏感性需要测量间质液(ISF)中的胰岛素浓度,但事实证明这很困难。我们旨在利用微透析技术优化大鼠肌肉中ISF胰岛素浓度的体内测量方法。
进行析因实验设计实验以确定微透析探针回收胰岛素的最佳条件。这些条件在体内进行测试,适当调整后用于瘦型和肥胖型 Zucker 大鼠,以比较基础状态和高胰岛素-正常血糖(HE)钳夹期间的 ISF 胰岛素浓度。
体内的最佳条件为:将 100kDa 的微透析探针插入肌肉,用含 1%牛血清白蛋白、1.5mM 葡萄糖的 0.9%氯化钠溶液以 1μl/分钟的速度灌注。样品收集到硅化玻璃微量瓶中。作为胰岛素的参考,我们建立了菊粉输注方案,从-80 分钟开始,60 分钟内达到平衡。HE 钳夹从 0 分钟开始,使瘦型大鼠的 ISF 胰岛素浓度从基础状态下的 122±56 升高至 429±180pmol/l(P<0.05),肥胖型大鼠从 643±165 升高至 1087±243pmol/l(P=0.07);肥胖型大鼠在整个过程中的 ISF 胰岛素浓度显著更高。肥胖型大鼠中 ISF 与血浆胰岛素浓度的差异(ISF:血浆比值)明显更高,但在 HE 钳夹期间肥胖型和瘦型大鼠的该比值降至相似值。
通过微透析优化胰岛素回收可准确测量瘦型和肥胖型 Zucker 大鼠肌肉中的基础 ISF 胰岛素,并表明肥胖型大鼠在基础状态和高胰岛素血症期间跨毛细血管的胰岛素转运受损。