Lees S, Eyre D R, Barnard S M
Bioengineering Department, Forsyth Dental Center, Boston, MA 02115.
Connect Tissue Res. 1990;24(2):95-105. doi: 10.3109/03008209009152426.
Crosslinking density in demineralized bone matrix collagen was found to depend on the beta-aminopropionitrile (BAPN) dose level for compact bone from rabbit femurs. The dependence was demonstrated for the hydroxypyridinium (HP) concentration, a mature crosslink. A more consistent dependence on BAPN dosage was observed for the fraction of the demineralized bone matrix insoluble in 0.5 M acetic acid (AIF) corresponding to the remaining crosslinked collagen. The average HP concentration in 21 week old controls was 0.24 moles HP/mole collagen which decreased to 0.13 +/- 0.04 for the same age rabbits dosed with 1 gm BAPN/kg/day for 13 wks. The comparable mean AIF values were 0.91 for controls and 0.75 for maximum dose level. Most of the effect of BAPN on crosslinking was observed at the lower dosages below 0.2 g/kg/day. On the other hand, overt osteolathyritic symptoms are seen only for BAPN dosages greater than 0.2 g/kg/day. The mean sonic plesio-velocity was previously found to decrease from 3.4 to 3.03 km/sec as the BAPN dosage was increased. A similar close relationship was discovered for the equatorial diffraction spacing in fully mineralized bone which increased from 1.235 for normal rabbit bone to 1.28 nm for maximum dose. Most of the effect on these physical properties is exhibited at the highest BAPN dosage after much of the decrease in mature crosslinking density has been observed and when the further decrease in mature crosslinking density proceeds very slowly with increased drug dosage. These observations suggest that osteolathyrism does not become manifest until practically all mature crosslinking that can be affected has been inhibited. The mineralization process apparently can be maintained in the newly laid collagen even in the presence of severe osteolathyritic conditions. Intermolecular crosslinking in bone collagen appears to play an important role in the development of bone properties whether by direct or indirect processes. Much of the effects on bone properties occur at the higher BAPN dosages where overt osteolathyrism is observed and where there seem to be only small changes in crosslinking density.
研究发现,脱矿骨基质胶原蛋白中的交联密度取决于兔股骨密质骨中β-氨基丙腈(BAPN)的剂量水平。对于成熟交联物羟基吡啶鎓(HP)浓度,这种依赖性得到了证实。对于脱矿骨基质中不溶于0.5M乙酸(AIF)的部分(对应于剩余的交联胶原蛋白),观察到对BAPN剂量更一致的依赖性。21周龄对照组的平均HP浓度为0.24摩尔HP/摩尔胶原蛋白,对于相同年龄、以1克BAPN/千克/天的剂量给药13周的兔子,该浓度降至0.13±0.04。对照组和最大剂量水平的可比平均AIF值分别为0.91和0.75。BAPN对交联的大部分影响在低于0.2克/千克/天的较低剂量下观察到。另一方面,仅在BAPN剂量大于0.2克/千克/天时才会出现明显的骨软化症状。先前发现,随着BAPN剂量增加,平均声近程速度从3.4千米/秒降至3.03千米/秒。对于完全矿化骨中的赤道衍射间距,也发现了类似的密切关系,其从正常兔骨的1.235纳米增加到最大剂量时的1.28纳米。对这些物理性质的大部分影响在成熟交联密度大幅下降后、且随着药物剂量增加成熟交联密度进一步下降非常缓慢时的最高BAPN剂量下表现出来。这些观察结果表明,直到几乎所有可能受到影响的成熟交联都被抑制,骨软化症才会显现出来。即使在存在严重骨软化症的情况下,新沉积的胶原蛋白中的矿化过程显然也可以维持。骨胶原蛋白中的分子间交联似乎在骨特性的发展中起着重要作用,无论是通过直接还是间接过程。对骨特性的大部分影响发生在较高的BAPN剂量下,此时会观察到明显的骨软化症,且交联密度似乎只有很小的变化。