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γ-亚麻酸和抗坏血酸盐可改善糖尿病大鼠后代的骨骼骨化。

Gamma-linoleic acid and ascorbate improves skeletal ossification in offspring of diabetic rats.

作者信息

Braddock Rattana, Simán C Martin, Hamilton Katherine, Garland Hugh O, Sibley Colin P

机构信息

School of Biological Sciences, University of Manchester, Manchester M13 9PT, United Kingdom.

出版信息

Pediatr Res. 2002 May;51(5):647-52. doi: 10.1203/00006450-200205000-00017.

Abstract

Maternal diabetes causes a range of complications in offspring, including reduced skeletal ossification. This study examined whether feeding gamma-linoleic acid (GLA) and ascorbate, alone or in combination, to diabetic pregnant rats improves skeletal development in their offspring. In addition, Ca(2+) concentration was monitored in maternal plasma and fetal tissue, as well as placental mRNA expression of calbindin-D(9k). Female rats rendered diabetic with streptozotocin were fed GLA (500 mg/kg/d), ascorbate (290 mg/kg/d), ascorbyl-GLA (790 mg/kg/d), or GLA and ascorbate (500 and 290 mg/kg/d, respectively) throughout pregnancy. Fetal skeletons were studied after alizarin red staining. Fewer ossification centers were observed in offspring of diabetic rats compared with offspring of control rats (68 +/- 4% of control, p = 0.01). An almost complete restoration of ossification occurred with all the treatments (92-95 +/- 3% of control). The effects of treatment on fetal ossification could not be explained by altered maternal plasma Ca(2+) concentrations or by mRNA expression of the placental Ca(2+)-transporting protein calbindin-D(9K). We conclude that GLA and/or ascorbate treatment was effective against diabetes-induced fetal ossification defects by a mechanism not related to placental Ca(2+) supply.

摘要

母体糖尿病会导致后代出现一系列并发症,包括骨骼骨化减少。本研究探讨了给糖尿病妊娠大鼠单独或联合喂食γ-亚麻酸(GLA)和抗坏血酸是否能改善其后代的骨骼发育。此外,还监测了母体血浆和胎儿组织中的Ca(2+)浓度,以及胎盘钙结合蛋白-D(9k)的mRNA表达。用链脲佐菌素使雌性大鼠患糖尿病,在整个孕期给它们喂食GLA(500毫克/千克/天)、抗坏血酸(290毫克/千克/天)、抗坏血酸-GLA(790毫克/千克/天)或GLA和抗坏血酸(分别为500和290毫克/千克/天)。茜素红染色后研究胎儿骨骼。与对照大鼠的后代相比,糖尿病大鼠的后代中观察到的骨化中心较少(为对照的68±4%,p = 0.01)。所有治疗均使骨化几乎完全恢复(为对照的92-95±3%)。治疗对胎儿骨化的影响无法用母体血浆Ca(2+)浓度的改变或胎盘Ca(2+)转运蛋白钙结合蛋白-D(9K)的mRNA表达来解释。我们得出结论,GLA和/或抗坏血酸治疗通过一种与胎盘Ca(2+)供应无关的机制有效对抗糖尿病诱导的胎儿骨化缺陷。

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