PMID- 32332768 OWN - NLM STAT- MEDLINE DCOM- 20201130 LR - 20210424 IS - 2045-2322 (Electronic) IS - 2045-2322 (Linking) VI - 10 IP - 1 DP - 2020 Apr 24 TI - Late-pregnancy uterine artery ligation increases susceptibility to postnatal Western diet-induced fat accumulation in adult female offspring. PG - 6926 LID - 10.1038/s41598-020-63392-y [doi] LID - 6926 AB - Stressors during the fetal and postnatal period affect the growth and developmental trajectories of offspring, causing lasting effects on physiologic regulatory systems. Here, we tested whether reduced uterine artery blood flow in late pregnancy would alter body composition in the offspring, and whether feeding offspring a western diet (WD) would aggravate these programming effects. Pregnant rats underwent bilateral uterine artery ligation (BUAL) or sham surgery on gestational day (GD)18 (term = GD22). At weaning, offspring from each group received either a normal diet (ND) or a WD. BUAL surgery increased fetal loss and caused offspring growth restriction, albeit body weights were no longer different at weaning, suggesting postnatal catch-up growth. BUAL did not affect body weight gain, fat accumulation, or plasma lipid profile in adult male offspring. In contrast, while ND-fed females from BUAL group were smaller and leaner than their sham-littermates, WD consumption resulted in excess weight gain, fat accumulation, and visceral adiposity. Moreover, WD increased plasma triglycerides and cholesterol in the BUAL-treated female offspring without any effect on sham littermates. These results demonstrate that reduced uterine artery blood flow during late pregnancy in rodents can impact body composition in the offspring in a sex-dependent manner, and these effects may be exacerbated by postnatal chronic WD consumption. FAU - Jahandideh, Forough AU - Jahandideh F AUID- ORCID: 0000-0001-9731-0854 AD - Department of Anesthesiology & Pain Medicine, University of Alberta, Edmonton, Alberta, Canada. AD - Women and Children's Health Research Institute, University of Alberta, Edmonton, Alberta, Canada. FAU - Bourque, Stephane L AU - Bourque SL AD - Department of Anesthesiology & Pain Medicine, University of Alberta, Edmonton, Alberta, Canada. AD - Women and Children's Health Research Institute, University of Alberta, Edmonton, Alberta, Canada. AD - Department of Pediatrics, University of Alberta, Edmonton, Alberta, Canada. FAU - Armstrong, Edward A AU - Armstrong EA AD - Department of Pediatrics, University of Alberta, Edmonton, Alberta, Canada. FAU - Cherak, Stephana J AU - Cherak SJ AD - Department of Anesthesiology & Pain Medicine, University of Alberta, Edmonton, Alberta, Canada. FAU - Panahi, Sareh AU - Panahi S AD - Department of Anesthesiology & Pain Medicine, University of Alberta, Edmonton, Alberta, Canada. FAU - Macala, Kimberly F AU - Macala KF AD - Women and Children's Health Research Institute, University of Alberta, Edmonton, Alberta, Canada. AD - Department of Surgery, University of Alberta, Edmonton, Alberta, Canada. FAU - Davidge, Sandra T AU - Davidge ST AD - Women and Children's Health Research Institute, University of Alberta, Edmonton, Alberta, Canada. AD - Department of Obstetrics and Gynecology, University of Alberta, Edmonton, Alberta, Canada. FAU - Yager, Jerome Y AU - Yager JY AD - Women and Children's Health Research Institute, University of Alberta, Edmonton, Alberta, Canada. jyager@ualberta.ca. AD - Department of Pediatrics, University of Alberta, Edmonton, Alberta, Canada. jyager@ualberta.ca. LA - eng GR - CIHR/Canada PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20200424 PL - England TA - Sci Rep JT - Scientific reports JID - 101563288 RN - 0 (Lipids) SB - IM MH - Adipocytes/pathology MH - Animals MH - Animals, Newborn MH - Body Composition MH - Body Weight MH - Cell Size MH - *Diet, Western MH - Female MH - Glucose Tolerance Test MH - Ligation MH - *Lipid Metabolism MH - Lipids/blood MH - Male MH - Obesity, Abdominal/blood/pathology MH - Organ Size MH - Pregnancy MH - Rats, Long-Evans MH - Uterine Artery/*pathology PMC - PMC7181802 COIS- The authors declare no competing interests. EDAT- 2020/04/26 06:00 MHDA- 2020/12/01 06:00 PMCR- 2020/04/24 CRDT- 2020/04/26 06:00 PHST- 2019/08/20 00:00 [received] PHST- 2020/02/28 00:00 [accepted] PHST- 2020/04/26 06:00 [entrez] PHST- 2020/04/26 06:00 [pubmed] PHST- 2020/12/01 06:00 [medline] PHST- 2020/04/24 00:00 [pmc-release] AID - 10.1038/s41598-020-63392-y [pii] AID - 63392 [pii] AID - 10.1038/s41598-020-63392-y [doi] PST - epublish SO - Sci Rep. 2020 Apr 24;10(1):6926. doi: 10.1038/s41598-020-63392-y.