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Author (up) Gatford, K.L.; Kennaway, D.J.; Liu, H.; Schultz, C.G.; Wooldridge, A.L.; Kuchel, T.R.; Varcoe, T.J. url  doi
  Title Simulated shift work during pregnancy does not impair progeny metabolic outcomes in sheep Type Journal Article
  Year 2020 Publication The Journal of Physiology Abbreviated Journal J Physiol  
  Volume in press Issue Pages in press  
  Keywords Animals; developmental programming; maternal; metabolism; progeny; sheep; shift work  
  Abstract KEY POINTS: Maternal shift work increases the risk of pregnancy complications, although its effects on progeny health after birth were not clear. We evaluated the impact of a simulated shift work protocol for one third, two thirds, or all of pregnancy on metabolic health of sheep progeny. Simulated shift work had no effect on growth, body size, body composition or glucose tolerance in pre-pubertal or young adult progeny. Glucose stimulated insulin secretion was reduced in adult female progeny and insulin sensitivity was increased in adult female singleton progeny. The results of this study does not support the hypothesis that maternal shift work exposure impairs metabolic health of progeny in altricial species ABSTRACT: Disrupted maternal circadian rhythms, such as those experienced during shift work, are associated with impaired progeny metabolism in rodents. The effects of disrupted maternal circadian rhythms on progeny metabolism have not been assessed in altricial, non-litter bearing species. We therefore assessed postnatal growth from birth to adulthood, and body composition, glucose tolerance, insulin secretion and insulin sensitivity in pre-pubertal and young adult progeny of sheep exposed to control conditions (CON: 10 males, 10 females) or to a simulated shift work (SSW) protocol for the first 1/3 (SSW0-7: 11 males, 9 females), the first 2/3 (SSW0-14: 8 males, 11 females), or all (SSW0-21: 8 males, 13 females) of pregnancy. Progeny growth did not differ between maternal treatments. In pre-pubertal progeny (12-14 weeks of age), adiposity, glucose tolerance and insulin secretion during an intravenous glucose tolerance test and insulin sensitivity did not differ between maternal treatments. Similarly, in young adult progeny (12-14 months of age), food intake, adiposity and glucose tolerance did not differ between maternal treatments. At this age, however, insulin secretion in response to a glucose bolus was 30% lower in female progeny in the combined SSW groups compared to control females (P = 0.031), and insulin sensitivity of SSW0-21 singleton females was 236% that of CON singleton female progeny (P = 0.025). At least in this model, maternal SSW does not impair progeny metabolic health, with some evidence of greater insulin action in female young adult progeny. This article is protected by copyright. All rights reserved.  
  Address Basil Hetzel Research Institute for Translational Health Research, Adelaide, South Australia, 5011, Australia  
  Corporate Author Thesis  
  Publisher Place of Publication Editor  
  Language English Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 0022-3751 ISBN Medium  
  Area Expedition Conference  
  Notes PMID:32918750 Approved no  
  Call Number GFZ @ kyba @ Serial 3135  
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