4.5 Article

In Vitro Fertilization Affects Growth and Glucose Metabolism in a Sex-Specific Manner in an Outbred Mouse Model

期刊

BIOLOGY OF REPRODUCTION
卷 90, 期 4, 页码 -

出版社

OXFORD UNIV PRESS INC
DOI: 10.1095/biolreprod.113.113134

关键词

ART; DOHaD; embryos

资金

  1. National Institute of Child Health and Human Development (NICHD) [RO1: HD 062803-01A1]
  2. American Diabetes Association

向作者/读者索取更多资源

The preimplantation period is a time of reprogramming that may be vulnerable to disruption. This question has wide clinical relevance since the number of children conceived by in vitro fertilization (IVF) is rising. To examine this question, outbred mice (CF1 Chi B6D2F1) conceived by IVF and cultured using Whitten medium and 20% O-2 (IVFWM group, less optimal) or K simplex optimized medium with amino acids and 5% O-2 (IVFKAA group, more optimal and similar to conditions used in human IVF) were studied postnatally. We found that flushed blastocysts transferred to recipient mice provided the best control group (FB group), as this accounted for the effects of superovulation, embryo transfer, and litter size. We observed that many physiological parameters were normal. Reassuringly, IVFKAA offspring did not differ significantly from FB offspring. However, male IVFWM mice (but not females) were larger during the first 19 wk of life and exhibited glucose intolerance. Male IVFWM mice also showed enlarged left heart despite normal blood pressure. Expression of candidate imprinted genes (H19, Igf2, and Slc38a4) in multiple adult tissues did not show differences among the groups; only Slc38a4 was down-regulated following IVF (in both culture conditions) in female adipose tissue. These studies demonstrate that adult metabolism is affected by the type of conditions encountered during the preimplantation stage. Further, the postnatal growth trajectory and glucose homeostasis following ex vivo manipulation may be sexual dimorphic. Future work on the long-term effects of IVF offspring should focus on glucose metabolism and the cardiovascular system.

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