[1]唐崇曦 戴燚△ 唐光平 徐平.青娥方对膝骨关节炎伴骨质疏松模型大鼠早期软骨下骨整合素及抑癌基因表达的影响[J].中国中医骨伤科杂志,2022,30(05):1-5.
 TANG Chongxi DAI Yi TANG Guangping XU Ping.Efficacy of Qing’e Decoction on the Expression of αvβ3 Integrin and P53 Gene in SubchondralBone of Knee Osteoarthritis with Osteoporosis Model Rats[J].Chinese Journal of Traditional Medical Traumatology & Orthopedics,2022,30(05):1-5.
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青娥方对膝骨关节炎伴骨质疏松模型大鼠早期软骨下骨整合素及抑癌基因表达的影响()
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《中国中医骨伤科杂志》[ISSN:1005-0205/CN:42-1340/R]

卷:
第30卷
期数:
2022年05期
页码:
1-5
栏目:
实验研究
出版日期:
2022-05-15

文章信息/Info

Title:
Efficacy of Qing’e Decoction on the Expression of αvβ3 Integrin and P53 Gene in SubchondralBone of Knee Osteoarthritis with Osteoporosis Model Rats
文章编号:
1005-0205(2022)05-0001-05
作者:
唐崇曦1 戴燚12△ 唐光平2 徐平2
1湖北中医药大学(武汉,430065)
2武汉市中医医院骨伤科
Author(s):
TANG Chongxi1 DAI Yi12△ TANG Guangping2 XU Ping2
1Hubei University of Chinese Medicine,Wuhan 430065, China; 2Wuhan Hospital of Traditional Chinese Medicine,Wuhan 430050, China.
关键词:
青娥方骨质疏松骨关节炎整合素抑癌基因
Keywords:
Qing’e decoction osteoporosis osteoarthritis integrin tumor suppressor gene
分类号:
R-33
文献标志码:
A
摘要:
目的:观察青娥方药液对膝骨关节炎伴骨质疏松模型大鼠软骨下骨中整合素αvβ3及P53基因表达的影响。方法:将30只SD大鼠编号后,随机分为正常组(A组)、青娥方组(B组)、骨质疏松组(C组)、骨关节炎伴骨质疏松组(D组)和骨关节炎组(E组),每组6只。将 B组、C组和D组大鼠腹腔注射麻醉后,行骨质疏松造模。1个月后,再将B组、D组、E组三组大鼠麻醉后行骨关节炎造模,术后行相同处理。经二次造模1 d后,B组大鼠持续4周每天灌服1次药液。其余各组大鼠以相同剂量每天灌服1次生理盐水。结果:正常组整合素αvβ3基因在第2,4周均呈弱上调表达,表达水平维持相对稳定; B组整合素αvβ3基因表达随着时间的推移先呈现出较A组增高的水平,但逐渐出现下降趋势; B组整合素αvβ3及P53基因水平表达相对稳定,趋近A组; 相较于D组,B组大鼠经青娥方治疗后,其胫骨髁软骨下骨组织中的整合素αvβ3基因表达水平在第2,4周的差异有统计学意义(P<0.05)。C组、D组、E组三个时间点P53基因均呈弱上调表达,随着时间的推移,P53表达水平小幅度上升; B组P53基因表达水平与A组差异无统计学意义(P>0.05),且低于同时期其他三组。结论:青娥方能够抑制整合素αvβ3在软骨下骨组织中的表达,从而降低破骨细胞活性,减少骨吸收,有利于促进骨吸收、骨形成平衡的恢复,而对P53基因表达的抑制作用尚不明显。
Abstract:
To observe the efficacy of Qing’e prescription on αvβ3 integrin and P53 gene expression levels in subchondral bone tissue of osteoporotic knee osteoarthritis(KOA)rats, and to explore the mechanism of Qing’e policy on subchondral bone tissue in further discussion, so as to provide theoretical reference for the clinical treatment of osteoporotic KOA. Methods:30 SD rats were randomly divided into normal group(group A), Qing’e prescription group(group B), osteoporosis model group(group C), osteoporosis osteoarthritis model group(group D)and osteoarthritis model(group E), with 6 rats in each group. Their osteoporosis models were established after group B, group C and group D rats being anesthetized by intraperitoneal injection. The osteoarthritis model of rats in groups B, D and E was established after anesthesia, and the same treatment was performed after operation one month after modeling. Then group B was perfused with Qing’e prescription solution on the second day after operation, and the other groups were perfused with the same amount of normal saline, once a day for 4 weeks. Results:The expression of αvβ3 integrin was weakly up-regulated at 2 and 4 weeks in group A, and the expression level remained relatively. With the passage of time, the αvβ3 integrin expression in group B first increased compared with group A, but gradually decree sed stable. Compared with group D, the difference of the αvβ3 integrin expression level in the subchondral bone tissue of tibial condyle in group B after treatment with Qing’e prescription in the second and fourth weeks was statistically significant. The expression of P53 gene was weakly up-regulated in group C, group D and group E. With the passage of time, the expression level of P53 increased slightly, there was no significant difference in P53 gene expression between group B and group A, and it was lower than that of the other three groups at the same time. Conclusion:Qing’e prescription can inhibit the expression of αvβ3 integrin in subchondral bone tissue, and reduce the bone resorption of subchondral bone in osteoporotic osteoarthritis, and inhibit the imbalance of bone resorption in the process of bone reconstruction, but the inhibitory efficacy on P53 gene expression is not obvious.

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备注/Memo

备注/Memo:
基金项目:全国中医药创新骨干人才培训项目(国中医人教函2019-128号)
湖北省自然科学基金项目(2017CFB485)
武汉市卫健委重大项目(WZ21M02)
通信作者 E-mail:daiyiwh@163.com
更新日期/Last Update: 1900-01-01