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与乙烷-1-羟基-1,1-二膦酸盐(EHDP)相比,丙烷-2,2-二膦酸盐(PDP)对基质诱导的异位骨形成的影响。

Effects of propane-2, 2-diphosphonate (PDP) on matrix-induced ectopic bone formation in comparison to ethane-1-hydroxy-1, 1-diphosphonate (EHDP).

作者信息

Rüther W, Kindermann D, Gebhardt M, Münzenberg K J

机构信息

Department of Orthopedic, Friedrich-Wilhelms Universität, Bonn, Federal Republic of Germany.

出版信息

Clin Orthop Relat Res. 1990 Sep(258):122-34.

PMID:2118435
Abstract

The most prominent effect of propane-2, 2-diphosphonate (PDP) and ethane-1-hydroxy-1, 1-diphosphonate (EHDP) on matrix-induced ectopic bone in the rat was a dose-dependent inhibition of osteogenesis in the early phases of development. The delay was seen as a consequence of osteoprogenitor cell inhibition. Additionally, later phases of bone maturation were disturbed by interference with the mineralization and remodeling processes. However, direct effects on the calcium phosphates of bone are only of minor additional value, which remains of lesser importance in comparison to the cellular impairment. After withdrawal of diphosphonates, the effects were nearly completely remitted. Neither PDP nor EHDP, even given in high doses, resulted in a lasting reduction in ectopic mass. The remission may be referred to the recovery of cell activities, whereas the mineral impregnation of osteoidosis was, if at all, of little importance. For treatment of ectopic osteogenesis PDP proved inefficient.

摘要

丙烷-2,2-二膦酸盐(PDP)和乙烷-1-羟基-1,1-二膦酸盐(EHDP)对大鼠基质诱导的异位骨最显著的作用是在发育早期对成骨有剂量依赖性抑制。这种延迟被认为是骨祖细胞抑制的结果。此外,骨成熟的后期阶段因矿化和重塑过程受到干扰而受到影响。然而,对骨磷酸钙的直接作用只是次要的附加价值,与细胞损伤相比,其重要性仍然较低。停用二膦酸盐后,这些作用几乎完全消失。PDP和EHDP即使高剂量给药,也不会导致异位骨量持续减少。这种恢复可能归因于细胞活性的恢复,而类骨质矿化即使有作用也微不足道。对于异位骨形成的治疗,PDP被证明是无效的。

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