Abstract

Studies conducted in the recent years by biologists strongly suggest that physiological and reparative osteogenesis, as well as of the functional, adaptive, and post-traumatic reconstruction of bone tissues are based on common and stereotypical molecular and cellular mechanisms. Our experimental studies have shown that all stages of the bone microstructure morphogenesis are synchronously and continuously associated with focal and stereotypical angiogenesis (capillarogenesis). A powerful factor in the implementation of reparative osteogenesis is the osteoinductive interaction of the ends of the damaged bone segments, which positively shows itself even in cases of large diastasis between the fragments (provided that the fragments are steadily fixed). After any kind of stable osteosynthesis, by ensuring the stability of the bone fragments for the entire period of consolidation, an endosteal cortical bone regeneration by direct osteogenesis (i.e. without fibro-cartilaginous tissue) is observed in the minimum amount at the shortest time period. Periosteal bone formation in this case is actually a reserve source of bone formation, which becomes effective during insufficiently stable conditions. The instability of the bone damage area particularly that of the metal implants results in the most severe destructive consequences.

Highlights

  • Фундаментальные исследования последних лет, выполненные биологами на молекулярно-клеточном уровне, позволяют по-новому представить процессы физиологического и репаративного остеогенеза

  • Osteogenic differentiation of human mesenchymal stem cells is regulated by bone morphogenetic protein-6

  • Vascular endothelial growth factor (VEGF) directly enhances osteoclastic bone resorption and survival of mature osteoclasts

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Summary

Introduction

Фундаментальные исследования последних лет, выполненные биологами на молекулярно-клеточном уровне, позволяют по-новому представить процессы физиологического и репаративного остеогенеза. При обеспечении стабильности зоны костного повреждения на весь период консолидации после любого вида стабильного остеосинтеза формируется эндостально-кортикальный костный регенерат за счет прямого остеогенеза (то есть без фиброзно-хрящевой ткани) минимального объема и в кратчайшие сроки. 4. Перестройка микрососудов в зоне костного интермедиарного регенерата кортикальной пластинки на месте сросшегося перелома через 8 недель после накостного стабильного остеосинтеза.

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Conclusion

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