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妊娠糖尿病。妊娠早期胰岛素间歇性停用后糖尿病大鼠后代的骨骼畸形。

Diabetes in pregnancy. Skeletal malformations in the offspring of diabetic rats after intermittent withdrawal of insulin in early gestation.

作者信息

Eriksson U J, Dahlström E, Hellerström C

出版信息

Diabetes. 1983 Dec;32(12):1141-5. doi: 10.2337/diab.32.12.1141.

Abstract

Precise timing of the teratogenic period in diabetic pregnancy is of clinical importance since correction of the glucose intolerance during this period may protect the offspring from malformations. An experimental approach to elucidate this problem with regard to skeletal development was made in groups of pregnant streptozotocin-diabetic rats (MDI), which were treated with daily insulin injections except for a 2-day period in the first half of pregnancy. The degree of metabolic derangement was estimated by measurements of serum glucose concentrations. During the insulin-free period, the rats showed severe hyperglycemia (greater than 20 mM) while during ongoing insulin treatment, only brief periods of hyper- or hypoglycemia were observed. Insulin treatment was withdrawn successively between gestational days 3 and 12. Control groups consisted of normal pregnant rats (N) or pregnant rats with manifest diabetes (MD) without insulin treatment. The serum glucose levels of the N animals were below 6 mM while those of the MD animals were above 25 mM throughout pregnancy. Skeletal malformations in the viable offspring were recorded on gestational day 20 after Alizarin staining of calcified ossification centers, which also allowed an estimate of skeletal development as a whole. Untreated diabetes in the MD rats induced a high rate of fetal resorptions, a decrease in fetal weight and viability, as well as retardation of skeletal development. Intermittent insulin treatment in the MDI rats ameliorated, but did not abolish, these changes. In the MD group 9 of 48 viable fetuses showed severe malformations of either the lower jaw (micrognathia) or of the lumbosacral region (caudal dysgenesis).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

糖尿病妊娠致畸期的精确时间具有临床重要性,因为在此期间纠正葡萄糖不耐受可能保护后代免受畸形影响。我们采用实验方法,对妊娠的链脲佐菌素诱导糖尿病大鼠(MDI)分组,除了在妊娠前半期有2天未接受治疗外,其余时间每天注射胰岛素,以阐明骨骼发育方面的这一问题。通过测量血清葡萄糖浓度来评估代谢紊乱程度。在无胰岛素治疗期间,大鼠出现严重高血糖(大于20 mM),而在持续胰岛素治疗期间,仅观察到短暂的高血糖或低血糖期。在妊娠第3天至12天期间逐渐停止胰岛素治疗。对照组由正常妊娠大鼠(N)或未接受胰岛素治疗的显性糖尿病妊娠大鼠(MD)组成。N组动物的血清葡萄糖水平在整个妊娠期低于6 mM,而MD组动物的血清葡萄糖水平在整个妊娠期高于25 mM。在妊娠第20天,对存活后代进行茜素染色,记录钙化骨化中心的骨骼畸形情况,这也有助于整体评估骨骼发育。MD大鼠未经治疗的糖尿病导致高比例的胎儿吸收、胎儿体重和活力下降以及骨骼发育迟缓。MDI大鼠的间歇性胰岛素治疗改善了这些变化,但并未消除。在MD组的48只存活胎儿中,有9只出现了严重畸形,如下颌(小颌畸形)或腰骶部(尾椎发育不全)。

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