Literature DB >> 1787451

Effect of diabetes mellitus on mouse pre-implantation embryo development.

K H Moley1, W K Vaughn, A H DeCherney, M P Diamond.   

Abstract

Fifteen spontaneously diabetic, non-obese mice (NOD strain), 17 non-diabetic NOD mice (in which diabetes had not yet developed) and 9 diabetic NOD mice were treated with insulin. All animals were superovulated with 5 iu of pregnant mares' serum gonadotrophin followed 48 h later by 5 iu human chorionic gonadotrophin (hCG) and mated overnight with NOD males of proven fertility. To assess in-vitro and early in-vivo development, 23 NOD mice were killed 72 h after hCG treatment. Embryos were recovered from oviduct flushings and cultured in Ham's F-10 medium with 0.1% bovine serum albumin at 37 degrees C in an atmosphere of 5% O2, 5% CO2, and 90% N2. Development was assessed at intervals of 24 h for 72 h. Compared with embryos from non-diabetic NOD mice (n = 81), embryos from diabetic NOD mice (n = 68) demonstrated marked impairment in growth assessed by distribution of developmental stages at each observation period (24, 48, 72 h, all P less than 0.001) and by overall rates of progression of developmental stages (P less than 0.01). In diabetic NOD mice treated with insulin, embryo development (n = 7) was not significantly different from that of embryos from non-diabetic NOD mice (n = 81), but was significantly faster than in embryos from diabetic NOD mice not treated with insulin (n = 68) (P less than 0.001, for all periods, overall rate P less than 0.01). To assess late in-vivo growth, 18 NOD mice were killed 120 h after hCG.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1991        PMID: 1787451     DOI: 10.1530/jrf.0.0930325

Source DB:  PubMed          Journal:  J Reprod Fertil        ISSN: 0022-4251


  29 in total

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3.  Sirt3-dependent deacetylation of SOD2 plays a protective role against oxidative stress in oocytes from diabetic mice.

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Review 4.  On the emerging role of rabbit as human disease model and the instrumental role of novel transgenic tools.

Authors:  V Duranthon; N Beaujean; M Brunner; K E Odening; A Navarrete Santos; I Kacskovics; L Hiripi; E J Weinstein; Z Bosze
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5.  Interferon gamma contributes to preimplantation embryonic development and to implantation site structure in NOD mice.

Authors:  A V C Seaward; S D Burke; B A Croy
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Review 6.  Uterine Glands: Developmental Biology and Functional Roles in Pregnancy.

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7.  In vitro study of the carry-over effect associated with early diabetic embryopathy in the rat.

Authors:  S Pampfer; Y D Wuu; I Vanderheyden; R De Hertogh
Journal:  Diabetologia       Date:  1994-09       Impact factor: 10.122

8.  Male mice that do not express group VIA phospholipase A2 produce spermatozoa with impaired motility and have greatly reduced fertility.

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Journal:  J Biol Chem       Date:  2004-07-12       Impact factor: 5.157

9.  Decreased oocyte-granulosa cell gap junction communication and connexin expression in a type 1 diabetic mouse model.

Authors:  Ann M Ratchford; Cybill R Esguerra; Kelle H Moley
Journal:  Mol Endocrinol       Date:  2008-10-01

10.  Maternal diabetes causes mitochondrial dysfunction and meiotic defects in murine oocytes.

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