Sulaiman Siti A, De Blasio Miles J, Harland M Lyn, Gatford Kathryn L, Owens Julie A
Robinson Research Institute and Adelaide Medical School, University of Adelaide, South Australia, Australia.
Robinson Research Institute and Adelaide Medical School, University of Adelaide, South Australia, Australia
Am J Physiol Endocrinol Metab. 2017 Oct 1;313(4):E381-E390. doi: 10.1152/ajpendo.00033.2017. Epub 2017 Jul 5.
Restricted growth before birth (IUGR) increases adult risk of Type 2 diabetes by impairing insulin sensitivity and secretion. Altered fetal one-carbon metabolism is implicated in developmental programming of adult health and disease by IUGR. Therefore, we evaluated effects of maternal dietary supplementation with methyl donors and cofactors (MMDS), designed to increase fetal supply, on insulin action in the spontaneously IUGR twin lamb. In vivo glucose-stimulated insulin secretion and insulin sensitivity were measured at in singleton controls (CON, = 7 lambs from 7 ewes), twins (IUGR, = 8 lambs from 8 ewes), and twins from ewes that received MMDS (2 g rumen-protected methionine, 300 mg folic acid, 1.2 g sulfur, 0.7 mg cobalt) daily from 120 days after mating (~0.8 of term) until delivery (IUGR+MMDS, = 8 lambs from 4 ewes). Body composition and pancreas morphometry were assessed in lambs at IUGR reduced size at birth and increased neonatal fractional growth rate. MMDS normalized long bone lengths but not other body dimensions of IUGR lambs at birth. IUGR did not impair glucose control or insulin action at , compared with controls. MMDS increased metabolic clearance rate of insulin and increased β-cell numerical density and tended to improve insulin sensitivity, compared with untreated IUGR lambs. This demonstrates that effects of late-pregnancy methyl donor supplementation persist until at least the third week of life. Whether these effects of MMDS persist beyond early postnatal life and improve metabolic outcomes after IUGR in adults and the underlying mechanisms remain to be determined.
出生前生长受限(IUGR)会损害胰岛素敏感性和分泌,从而增加成年人患2型糖尿病的风险。胎儿一碳代谢的改变与IUGR对成人健康和疾病的发育编程有关。因此,我们评估了旨在增加胎儿供应的母体膳食补充甲基供体和辅助因子(MMDS)对自然发生IUGR的双胎羔羊胰岛素作用的影响。在单胎对照(CON,来自7只母羊的7只羔羊)、双胎(IUGR,来自8只母羊的8只羔羊)以及从交配后120天(约孕期的0.8)至分娩期间每天接受MMDS(2克瘤胃保护蛋氨酸、300毫克叶酸、1.2克硫、0.7毫克钴)的母羊所产双胎(IUGR + MMDS,来自4只母羊的8只羔羊)中,在出生时测量体内葡萄糖刺激的胰岛素分泌和胰岛素敏感性。评估了出生时羔羊的身体组成和胰腺形态学。IUGR导致出生时体型减小,新生儿生长分数率增加。MMDS使IUGR羔羊出生时的长骨长度恢复正常,但未使其他身体尺寸恢复正常。与对照组相比,IUGR在出生时并未损害血糖控制或胰岛素作用。与未治疗的IUGR羔羊相比,MMDS提高了胰岛素的代谢清除率,增加了β细胞数量密度,并倾向于改善胰岛素敏感性。这表明妊娠晚期补充甲基供体的作用至少持续到生命的第三周。MMDS的这些作用是否会在出生后早期生命之外持续存在,并改善IUGR成年后的代谢结局以及潜在机制仍有待确定。