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吲哚美辛与双氯芬酸对实验性异位新骨形成抑制作用的比较。

A comparison of indomethacin and diclofenac in the inhibition of experimental heterotopic new bone formation.

作者信息

Nilsson O S, Bauer H C, Brosjö O, Törnkvist H

出版信息

Int Orthop. 1987;11(3):283-7. doi: 10.1007/BF00271462.

Abstract

The effect of the two nonsteroidal antiinflammatory drugs Diclofenac and Indomethacin on the formation of heterotropic and orthotopic bone in rats was compared. Experimental heterotopic bone formation was induced by implanting demineralized bone matrix into the abdominal wall of rats. Indomethacin (3 mg/kg), Diclofenac (3, 6 or 12 mg/kg), or saline were given as daily subcutaneous injections. 3H-proline and 45Ca were given 24 h before the animals were killed. The net amount of bone formed by induction after three weeks was decreased by 15% by Indomethacin and Diclofenac in a dose of 3 mg/kg. The higher dose of 6 mg/kg of Diclofenac caused a higher degree of inhibition (30%), while 12 mg/kg produced toxic effects. Orthotopic bone was not affected by treatment with Indomethacin or Diclofenac. Although both drugs inhibit prostaglandin synthesis to a different degree, they exert similar effects on induced heterotopic bone, suggesting that this action is caused by an inhibition of the inflammatory response to trauma.

摘要

比较了两种非甾体抗炎药双氯芬酸和吲哚美辛对大鼠异位骨和原位骨形成的影响。通过将脱矿骨基质植入大鼠腹壁诱导实验性异位骨形成。吲哚美辛(3mg/kg)、双氯芬酸(3、6或12mg/kg)或生理盐水每日皮下注射给药。在处死动物前24小时给予3H-脯氨酸和45Ca。三周后诱导形成的骨净量,吲哚美辛和3mg/kg剂量的双氯芬酸使其减少了15%。6mg/kg较高剂量的双氯芬酸引起更高程度的抑制(30%),而12mg/kg产生毒性作用。原位骨不受吲哚美辛或双氯芬酸治疗的影响。虽然两种药物对前列腺素合成的抑制程度不同,但它们对诱导的异位骨发挥相似的作用,这表明这种作用是由对创伤炎症反应的抑制引起的。

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