北极永久日光环境对人类胆固醇合成周期性的影响。

Arctic medical research Pub Date : 1995-07-01
S Biali, P J Jones, R A Pederson, I Iqbal, P Suedfeld
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摘要

为了确定与人类胆固醇合成控制相关的因素,在没有时间线索的永久日光北极环境中,在18 d的开始和结束时,对5名健康个体的胆固醇生成、激素水平和食物消费行为进行了周期性检查。在第2天(第1期)和第16天(第2期),通过氘掺入血浆游离胆固醇,在30小时内每隔6小时测定胆固醇分数合成率。同时测定各时间点血浆总胆固醇、胰岛素和葡萄糖依赖性胰岛素多肽水平。在每个阶段之前和期间记录食物摄入和睡眠模式。胆固醇分数合成率(FSR)在各阶段均表现出周期性,但在第一阶段(FSR率= 0.038 +/- 0.038 pools.d-1)和第二阶段(FSR率= 0.037 +/- 0.072 pools.d-1)之间无显著差异。II期FSR周期长度与第一餐和最后一餐之间的持续时间(r2 = 0.81, p = 0.037)和总清醒时间(r2 = 0.99, p = 0.001)相关。胰岛素和葡萄糖依赖的促胰岛素多肽水平与FSR周期性无关。这些结果表明,在控制全身胆固醇合成节律方面,进餐时间和睡眠/觉醒周期比胰岛素和葡萄糖依赖的促胰岛素多肽更重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Influence of a perpetual-daylight Arctic environment on periodicity in human cholesterol synthesis.

To identify factors associated with control of human cholesterol synthesis, periodicity in cholesterogenesis, hormonal levels and food consumption behavior were examined in 5 healthy individuals at the beginning and end of 18 d in a perpetual daylight Arctic environment devoid of time cues. At d 2 (phase I) and d 16 (phase II), cholesterol fractional synthesis rate was determined at 6 h intervals over 30 h as deuterium incorporation into plasma free cholesterol. Total plasma cholesterol, insulin and glucose-dependent insulinotropic polypeptide were also measured at each timepoint. Food intake and sleeping patterns were recorded prior to and during each phase. Cholesterol fractional synthesis rate (FSR) exhibited periodicity in all subjects on each phase, but did not differ between phase I (FSR rate = 0.038 +/- 0.038 pools.d-1) and phase II (FSR rate = 0.037 +/- 0.072 pools.d-1) phases. Phase II FSR period length was associated with both the duration between first and last meals (r2 = 0.81, p = 0.037) and total hours spent awake (r2 = 0.99, p = 0.001). Insulin and glucose-dependent insulinotropic polypeptide levels were not associated with FSR periodicity. These results suggest that meal timing and sleep/wake cycles are more important factors than insulin and glucose-dependent insulinotropic polypeptide in controlling the rhythms of whole body cholesterol synthesis.

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