Ⅱ型碳酸酐酶阻断剂对体外破骨细胞的抑制作用
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作者Author单位AddressE-Mail
王文军 WANG Wenjun 吉林大学中日联谊医院骨科,吉林长春130031 The Japan-China Union Hospital of Jilin University,Jilin Changchun 130031  
李建军 LI Jianjun 吉林大学第一医院骨科  
李小春 LI Xiaochun 长春中医学院  
冷向阳 LENG Xiangyang 长春中医学院  
期刊信息:《中国骨伤》2003年,第16卷,第7期,第409-411页
DOI:doi:10.3969/j.issn.1003-0034.yyyy.nn.zzz
基金项目:
中文摘要:

目的:研究Ⅱ型碳酸酐酶阻断剂对体外破骨细胞骨吸收过程的影响。

方法:由一日龄SD大鼠四肢长骨分离破骨细胞并接种于象牙骨片上共同培养,在培养液中分别加入不同浓度的Ⅱ型碳酸酐酶阻断剂乙酰唑胺,观察3天和9天时破骨细胞骨吸收能力的变化,从而证实Ⅱ型碳酸酐酶对破骨细胞性骨吸收的影响。

结果 10-6M乙酰唑胺使骨吸收陷窝数和吸收面积均显著减少,浓度为10-8M时只对骨吸收面积有显著抑制作用。

结论:Ⅱ型碳酸酐酶阻断剂通过调整破骨细胞内pH值影响破骨细胞分化、成熟及活化进而影响骨吸收。可以对老年性骨质疏松症疾病的治疗发挥早期、连续、持久作用。
【关键词】骨质疏松  组织学  碳酸脱水酶  细胞培养
 
Inhibition of osetoclasts in vitro by carbonic anhydrase Ⅱ inhibitor
ABSTRACT  

Objective:To study effects of carbonic anhydrase Ⅱ inhibitor on bone resorption process of osteoclasts in vitro

Methods:The osteoclasts from long bones of SD rats aged one-day were isolated and seeded in ivory bones for culture. Carbonic anhydrase Ⅱ inhibitor-acetazolamide with different concentrations was added to culture media.Changes of the bone resorption ability of the osteoclasts were observed in 3rd and 9th days.The effects of carbonic anhydrase Ⅱ on osteoclast bone resorption were comfirmed.

Results:Both the pit numbers and the pit areas were significantly reduced after using acetazolamide at the concentration of 10-6 M,while only the pit areas were reduced at the concentration of 10-8 M.

Conclusion:Carbonic anhydrase Ⅱ inhibitor played a major role in osteoclast differentiation,maturity and activation by effecting the steady state of pH.Thus,it affected the bone resorption and could play an earlier,successive,continual role in treatment of senile osteoporosis.
KEY WORDS  Osteoporosis  Histology  Carbonate dehydratase  Cell culture
 
引用本文,请按以下格式著录参考文献:
中文格式:王文军,李建军,李小春,冷向阳.Ⅱ型碳酸酐酶阻断剂对体外破骨细胞的抑制作用[J].中国骨伤,2003,16(7):409~411
英文格式:WANG Wenjun,LI Jianjun,LI Xiaochun,LENG Xiangyang.Inhibition of osetoclasts in vitro by carbonic anhydrase Ⅱ inhibitor[J].zhongguo gu shang / China J Orthop Trauma ,2003,16(7):409~411
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