Anevska K, Wark J D, Wlodek M E, Romano T
1Department of Physiology, Anatomy and Microbiology,La Trobe University,Bundoora,Australia.
3Department of Medicine,The University of Melbourne and Bone and Mineral Medicine,Royal Melbourne Hospital,Parkville,Australia.
J Dev Orig Health Dis. 2019 Apr;10(2):144-153. doi: 10.1017/S204017441800020X. Epub 2018 Apr 10.
Low birth weight programs diseases in adulthood, including adverse bone health. These diseases can have intergenerational and transgenerational origins, whereby transmission to subsequent generations occurs via both parental lines. Uteroplacental insufficiency surgery (Restricted) or sham surgery (Control) was performed on gestational day 18, in F0 Wistar-Kyoto rats. F1 Restricted males and females mated with breeders in order to generate F2 offspring of maternal and paternal lineages. F2 males and females were randomly selected for breeding to generate F3 offspring. F2 and F3 offspring did not have differences in birth weight irrespective of F1 low birth weight and parental line. Maternal line females had minor alterations to trabecular content and density at 6 months, these differences were not sustained at 12 months. Maternal line males had changes to trabecular content at 6 and 12 months; however, differences were no longer present at 16 months. Despite altered bone geometry at 12 and 16 months, bending strength remained unaffected at both ages. Bone health of paternal line females was not affected at 6 and 12 months. Paternal line males at 6 months had changes to trabecular and cortical content; cortical thickness, periosteal circumference and bending strength; however, these differences were no longer sustained at 12 and 16 months. Our data demonstrate that there is no transgenerational transmission of adverse bone health in F2 and F3 offspring, derived from low F1 birth weight females and males. Our results are novel, as bone health across generations and both parental lines has not been investigated in a model of low birth weight due to uteroplacental insufficiency.
低出生体重会引发成年期疾病,包括骨骼健康问题。这些疾病可能具有代际和跨代起源,即通过父母双方遗传给后代。在妊娠第18天,对F0代Wistar-Kyoto大鼠进行子宫胎盘功能不全手术(限制组)或假手术(对照组)。F1代限制组的雄性和雌性与繁殖者交配,以产生母系和父系的F2代后代。随机选择F2代的雄性和雌性进行繁殖,以产生F3代后代。无论F1代出生体重低以及亲代系如何,F2代和F3代后代的出生体重均无差异。母系雌性在6个月时小梁含量和密度有轻微改变,但这些差异在12个月时未持续存在。母系雄性在6个月和12个月时小梁含量有变化;然而,在16个月时差异不再存在。尽管在12个月和16个月时骨几何形状发生改变,但两个年龄段的弯曲强度均未受影响。父系雌性在6个月和12个月时骨骼健康未受影响。父系雄性在6个月时小梁和皮质含量、皮质厚度、骨膜周长和弯曲强度有变化;然而,这些差异在12个月和16个月时不再持续。我们的数据表明,来自低出生体重的F1代雌性和雄性的F2代和F3代后代中不存在骨骼健康问题的跨代遗传。我们的结果是新颖的,因为在子宫胎盘功能不全导致低出生体重的模型中,尚未对跨代以及父母双方系的骨骼健康进行研究。