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实验性糖尿病中的骨质流失。与炎症介导的骨质减少模型的比较。

Bone loss in experimental diabetes. Comparison with the model of inflammation mediated osteopenia.

作者信息

Hadjidakis D, Lempert U G, Minne H W, Ziegler R

机构信息

Abteilung Innere Medizin I, Endokrinologie und Stoffwechsel, Ruprecht-Karls Universität, Heidelberg, Germany.

出版信息

Horm Metab Res. 1993 Feb;25(2):77-81. doi: 10.1055/s-2007-1002047.

Abstract

Osteopenia occurs in diabetes mellitus. Since bone status is altered in Inflammation Mediated Osteopenia (IMO), it was appropriate to study its course in diabetic animals in order to investigate the mechanism of diabetic osteopenia. To this end, we compared the bone loss in streptozotocin (STZ) diabetes with that of IMO. Female rats were studied in total of 8 groups: Control, IMO, Diabetes, IMO with Diabetes (IMO-DIA) on the 3rd and similar groups on the 6th week after induction of IMO with 8 s.c. injections of talcum suspension. Femoral mineral content as reflected by ash weight per femoral volume after 3 weeks was lower in IMO compared to control rats (p < 0.05) while after 6 weeks this difference was not significant. The femur ash weight per volume of diabetic rats was lower than the one of intact rats with and without IMO both after 3 and 6 weeks. Diabetic rats with and without IMO exhibited no difference in this respect. Spleen weight as a measure of the extent of inflammation per body weight was increased only in the IMO group. The diabetic rats with and without IMO did not differ significantly with regard to spleen weight. Similar changes were observed 6 weeks after the induction of IMO. However the difference between IMO and diabetes rats was of borderline significance and no difference existed between the IMO and IMO-diabetic group. The serum calcium levels of intact, IMO and diabetic rats showed no change during both experimental periods. Those of diabetic rats with IMO were higher than those of the diabetic and IMO animals after 6 weeks.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

骨质疏松症在糖尿病中较为常见。由于炎症介导的骨质疏松症(IMO)会改变骨骼状态,因此研究糖尿病动物中IMO的病程以探究糖尿病性骨质疏松症的机制是合适的。为此,我们比较了链脲佐菌素(STZ)诱导的糖尿病大鼠与IMO大鼠的骨质流失情况。总共对8组雌性大鼠进行了研究:对照组、IMO组、糖尿病组、IMO合并糖尿病组(IMO-DIA),分别在皮下注射8次滑石粉悬浮液诱导IMO后的第3周和第6周设置类似的分组。与对照大鼠相比,IMO组大鼠在诱导后3周时,每股骨体积的灰重所反映的股骨矿物质含量较低(p < 0.05),而在6周时这种差异不显著。在3周和6周时,糖尿病大鼠每体积的股骨灰重均低于有无IMO的正常大鼠。有无IMO的糖尿病大鼠在这方面无差异。作为体重炎症程度指标的脾脏重量仅在IMO组中增加。有无IMO的糖尿病大鼠在脾脏重量方面无显著差异。在诱导IMO 6周后观察到类似变化。然而,IMO组与糖尿病大鼠组之间的差异接近显著水平,IMO组与IMO-糖尿病组之间无差异。在两个实验期间,正常、IMO和糖尿病大鼠的血清钙水平均无变化。6周后,有IMO的糖尿病大鼠的血清钙水平高于糖尿病大鼠和IMO大鼠。(摘要截断于250字)

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