Circadian misalignment induces fatty acid metabolism gene profiles and compromises insulin sensitivity in human skeletal muscle.
Circadian misalignment induces fatty acid metabolism gene profiles and compromises insulin sensitivity in human skeletal muscle.
复制标题
昼夜节律失调诱导人骨骼肌脂肪酸代谢基因谱和胰岛素敏感性。
DOI:
10.1073/pnas.1722295115
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发表时间:
2018-07-24
影响因子:
11.1
通讯作者:
Schrauwen P
中科院分区:
文献类型:
--
作者:
Wefers J;van Moorsel D;Hansen J;Connell NJ;Havekes B;Hoeks J;van Marken Lichtenbelt WD;Duez H;Phielix E;Kalsbeek A;Boekschoten MV;Hooiveld GJ;Hesselink MKC;Kersten S;Staels B;Scheer FAJL;Schrauwen P
Shift workers are affected by circadian misalignment and have an increased risk to develop metabolic diseases such as type 2 diabetes. Here, we show that during simulated short-term night shift work insulin sensitivity at the level of skeletal muscle is decreased in male volunteers, which could contribute to the development of type 2 diabetes in the long term. We also find that the muscle molecular clock does not align rapidly to the new behavioral cycle. Importantly, on the level of the transcriptome, circadian misalignment induced upregulation of fatty acid metabolism pathways, potentially resulting in substrate competition on the cellular level. These findings help to better understand the negative consequences during night shift work. Circadian misalignment, such as in shift work, has been associated with obesity and type 2 diabetes. However, direct effects of circadian misalignment on skeletal muscle insulin sensitivity and the muscle molecular circadian clock have never been studied in humans. Here, we investigated insulin sensitivity and muscle metabolism in 14 healthy young lean men [age 22.4 ± 2.8 years; body mass index (BMI) 22.3 ± 2.1 kg/m2 (mean ± SD)] after a 3-d control protocol and a 3.5-d misalignment protocol induced by a 12-h rapid shift of the behavioral cycle. We show that short-term circadian misalignment results in a significant decrease in muscle insulin sensitivity due to a reduced skeletal muscle nonoxidative glucose disposal (rate of disappearance: 23.7 ± 2.4 vs. 18.4 ± 1.4 mg/kg per minute; control vs. misalignment; P = 0.024). Fasting glucose and free fatty acid levels as well as sleeping metabolic rate were higher during circadian misalignment. Molecular analysis of skeletal muscle biopsies revealed that the molecular circadian clock was not aligned to the inverted behavioral cycle, and transcriptome analysis revealed the human PPAR pathway as a key player in the disturbed energy metabolism upon circadian misalignment. Our findings may provide a mechanism underlying the increased risk of type 2 diabetes among shift workers.
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影响因子:
15.8
作者:
Civitarese AE;Carling S;Heilbronn LK;Hulver MH;Ukropcova B;Deutsch WA;Smith SR;Ravussin E;CALERIE Pennington Team
通讯作者:
CALERIE Pennington Team
影响因子:
8.1
作者:
Dyar KA;Ciciliot S;Wright LE;Biensø RS;Tagliazucchi GM;Patel VR;Forcato M;Paz MI;Gudiksen A;Solagna F;Albiero M;Moretti I;Eckel-Mahan KL;Baldi P;Sassone-Corsi P;Rizzuto R;Bicciato S;Pilegaard H;Blaauw B;Schiaffino S
通讯作者:
Schiaffino S
影响因子:
8.2
作者:
Sharma A;Laurenti MC;Dalla Man C;Varghese RT;Cobelli C;Rizza RA;Matveyenko A;Vella A
通讯作者:
Vella A
DOI:
10.1126/science.1243417
发表时间:
2013-11-01
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Peek CB;Affinati AH;Ramsey KM;Kuo HY;Yu W;Sena LA;Ilkayeva O;Marcheva B;Kobayashi Y;Omura C;Levine DC;Bacsik DJ;Gius D;Newgard CB;Goetzman E;Chandel NS;Denu JM;Mrksich M;Bass J
通讯作者:
Bass J
DOI:
10.1016/j.tem.2016.03.005
发表时间:
2016-05
期刊:
Trends in endocrinology and metabolism: TEM
影响因子:
--
作者:
Qian J;Scheer FAJL
通讯作者:
Scheer FAJL