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基于再生机制的淫羊藿黄酮在骨细胞微环境的药代动力学研究思路与方法

Authors :
程千
魏雅君
蒋俊
徐希明
Source :
Chinese Journal of Osteoporosis. Jun2017, Vol. 23 Issue 6, p824-830. 7p.
Publication Year :
2017

Abstract

With the aging of the world population and the improvement of people's living standards,more and more people are looking forward to and making efforts to let the body tissue regenerate,which made regenerative medicine a frontier and hot spot in medical research. As an important part of the human body,the skeleton plays a role in supporting,protecting,movement and so on. With aging,bone density decreases gradually,and may evolve into osteoporosis. People develop kyphosis and become not flexible. Bones break easily and are hard to restore,which seriously affects individuals’quality of life and safety. Using regenerative drugs to achieve bone regeneration is expected to overcome the problem of osteoporosis fundamentally. Studies had shown that epimedium flavonoids with different glycosylation number,type or location could exert anti-osteoporosis action,however their strength of activity were significant different. By studying Chinese and international literature and research,we hypothesize that the intensity of epimedium flavonoids’bone regenerate mechanism is closely related to its pharmacokinetics: the number of glycosylation and membrane permeability are negatively correlated; the number of glycosylation and solubility are positively correlated; glycosylation type and position determine membrane transport mode; the intracellular disposal changes glycosylation structure,and transforms them into more active flavonoids. In this review,from the perspective of pharmacokinetics,the influences of different glycosylation number,type or location on membrane transport and osteogenic differentiation in the bone cells microenvironment were discussed in depth. [ABSTRACT FROM AUTHOR]

Details

Language :
Chinese
ISSN :
10067108
Volume :
23
Issue :
6
Database :
Academic Search Index
Journal :
Chinese Journal of Osteoporosis
Publication Type :
Academic Journal
Accession number :
124714394
Full Text :
https://doi.org/10.3969/j.issn.1006-7108.2017.06.025