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辛伐他汀凝胶对小鼠颅骨的影响。

Effects of simvastatin gels on murine calvarial bone.

作者信息

Thylin Michael R, McConnell Jay C, Schmid Marian J, Reckling Ryon R, Ojha Junu, Bhattacharyya Indraneel, Marx David B, Reinhardt Richard A

机构信息

Department of Surgical Specialties, University of Nebraska Medical Center, College of Dentistry, Lincoln 68583-0757, USA.

出版信息

J Periodontol. 2002 Oct;73(10):1141-8. doi: 10.1902/jop.2002.73.10.1141.

Abstract

BACKGROUND

The cholesterol-lowering drug simvastatin has been shown to stimulate murine calvarial bone growth after multiple injections. The purpose of this study was to test if similar bone stimulation could be induced by 2 single-dose drug delivery systems appropriate to periodontal therapy.

METHODS

ICR Swiss mice were treated with the following protocols: 1) injection of methylcellulose gel alone, subcutaneously over the calvarium (INJ-GEL; n = 8); 2) injection of gel with simvastatin (INJ-SIM; 2.2 mg, n = 16); 3) polylactide membrane (PLA) containing gel alone implanted over calvarium (MEM-GEL; n = 10); 4) implanted PLA membrane containing gel and simvastatin (MEM-SIM; n = 10); and 5) untreated mice (n = 12). Animals were sacrificed after 22 or 44 days, calvaria decalcified and stained with hematoxylin and eosin, and images digitized and measured for bone thickness and area. Data were compared using analysis of variance.

RESULTS

INJ-SIM stimulated a 53% (P = 0.02) increase at the thickest point of calvarial bone, while MEM-SIM caused a highly significant (P < or = 0.0005) increase in bone thickness (159% to 172%) and bone area (144% to 180%) compared to gel controls. Simvastatin gels caused soft tissue inflammation, which appeared to be related to bone increases. If INJ-SIM animals showing leakage of gel and/or no inflammation were excluded from analysis, INJ-SIM resulted in more bone (58% to 83%) than gel controls. An insignificant amount of SIM-stimulated bone was lost over the long term (44 days).

CONCLUSIONS

A single, high dose of simvastatin gel can stimulate murine cranial bone apposition, particularly when delivered under an occlusive membrane. Both approaches should be investigated further for possible development for periodontal therapy.

摘要

背景

降胆固醇药物辛伐他汀经多次注射后已被证明可刺激小鼠颅骨生长。本研究的目的是测试两种适用于牙周治疗的单剂量药物递送系统是否能诱导类似的骨刺激。

方法

对ICR瑞士小鼠采用以下方案进行治疗:1)单独皮下注射甲基纤维素凝胶于颅骨上(注射凝胶组;n = 8);2)注射含辛伐他汀的凝胶(注射辛伐他汀组;2.2 mg,n = 16);3)将仅含凝胶的聚乳酸膜(PLA)植入颅骨上(膜凝胶组;n = 10);4)植入含凝胶和辛伐他汀的PLA膜(膜辛伐他汀组;n = 10);5)未治疗的小鼠(n = 12)。在22天或44天后处死动物,颅骨脱钙并用苏木精和伊红染色,图像数字化并测量骨厚度和面积。使用方差分析比较数据。

结果

注射辛伐他汀组在颅骨最厚点刺激骨厚度增加53%(P = 0.02),而与凝胶对照组相比,膜辛伐他汀组导致骨厚度(159%至172%)和骨面积(144%至180%)高度显著增加(P≤0.0005)。辛伐他汀凝胶引起软组织炎症,这似乎与骨增加有关。如果将显示凝胶渗漏和/或无炎症的注射辛伐他汀组动物排除在分析之外,注射辛伐他汀组比凝胶对照组产生更多的骨(58%至83%)。长期(44天)来看,辛伐他汀刺激产生的骨量减少不明显。

结论

单次高剂量的辛伐他汀凝胶可刺激小鼠颅骨骨沉积,特别是在封闭膜下给药时。这两种方法都应进一步研究,以探讨其在牙周治疗中的潜在应用。

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