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J Transl Med ; 15(1): 32, 2017 02 13.
Article in English | MEDLINE | ID: mdl-28193233

ABSTRACT

BACKGROUND: T2DM is a high-risk pregnancy with adverse fetal and maternal outcomes including repeated miscarriages and fetal malformations. Despite the established association between placental insufficiency and poor maternal Th1-adaptability to the development of pregnancy complications in T2DM, there have been no established data to assess benefits of pre-pregnancy immunosuppression relative to gestational outcomes in T2DM. We hypothesized that pre-pregnancy macrolide immune suppression can re-establish normal placental development and uterine vascular adaptation in a mouse model of obesity-associated T2DM. METHODS: Fetal live birth rate, postnatal variability, mid-gestational uterine and umbilical flow dynamics and certain morphological features of spiral artery modification were examined in the New Zealand Obese (NONcNZO10/Ltj) female mice (n = 56) weaned to ages of 32 weeks on a 60% calories/g high-fat diet (also referred to as HFD-dNONcNZO), and which received either tacrolimus (0.1 mg/kg s.c. q2d) , its vehicle (castor oil and ethanol) or metformin (in drinking water 200 mg/dL p.o. ad libitum). HFD-BALBc-Rag2/IL2-gc female mice (n = 24) were used as HFD-immunodeficient controls. RESULTS: Treatment of the HFD-dNONcNZO female mice with tacrolimus improved live birth rates and postnatal viability scores (p < 0.01), normalized OGTT (p < 0.001), inhibited fetal malformation rates, restored morphology of spiral arterial modification; and improved uterine arterial and umbilical blood flow (p < 0.01). Placental production of TNFαand IL16 in the tacrolimus-treated HFD-dNONcNZO dams were restored to non-diabetic levels and the treatment resulted in the inhibition of aberrant monocyte/macrophage activation during pregnancy in the HFD-dNONcNZO dams. CONCLUSIONS: Our present data suggest a casual association between chronic maternal overnutrition and aberrancy in the maternal Th1-immune maladaptation to pregnancy and defective spiral artery modification, placental insufficiency and adverse fetal outcomes in the T2DM subjects. Further safety studies into the use of tacrolimus in the pre-pregnancy glycemic control may be beneficial.


Subject(s)
Diabetes Mellitus, Experimental/complications , Fetal Diseases/etiology , Fetal Diseases/prevention & control , Pregnancy Outcome , Tacrolimus/therapeutic use , Animals , Bone and Bones/abnormalities , Bone and Bones/drug effects , Bone and Bones/embryology , Bone and Bones/pathology , Diabetes Mellitus, Experimental/drug therapy , Diet, High-Fat , Female , Fetal Diseases/drug therapy , Glucose Tolerance Test , Metformin/pharmacology , Metformin/therapeutic use , Mice, Inbred BALB C , Mice, Obese , Pregnancy , Spine/blood supply , Spine/drug effects , Spine/physiopathology , Tacrolimus/pharmacology , Umbilical Cord/blood supply , Uterine Artery/physiopathology , Vascular Remodeling/drug effects
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