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Wnt/LRP5/β-连环蛋白信号通路对绝经后骨质疏松症发病机制的影响

[Effect of the Wnt/LRP5/β-catenin signaling pathway on the pathogenesis of postmenopausal osteoporosis].

作者信息

Wang Yan, Liu Yan, Ma Jian-xia, Li Bao-xin, Li Yu-kun

机构信息

Department of Endocrinology, Third Hospital of Hebei Medical University, Shijiazhuang 050051, China.

出版信息

Zhonghua Fu Chan Ke Za Zhi. 2011 Oct;46(10):769-72.

Abstract

OBJECTIVE

To investigate the role of the Wnt/LRP5/β-catenin signaling pathway in the pathogenesis of postmenopausal osteoporosis.

METHODS

Fifty female Wistar rats aged 6-month-old, were randomly divided into control group (NS, n = 24) and ovariectomized group (NOVX, n = 26), NOVX underwent bilateral ovariectomy. At 0, 4 and 8 weeks, all of rats were measured blood estrogen (E(2)) and bone mineral density (BMD), 4 and 8 weeks, low density lipoprotein receptor-related protein 5 (LRP5), β-catenin and Runx2 mRNA in bone were measured respectively by reverse transcription (RT)-PCR.

RESULTS

In 4 and 8 weeks, compared with NS which had (117 ± 29) and (114 ± 15) pmol/L in E(2) level, (0.098 ± 0.016) and (0.095 ± 0.028) g/cm(2) in BMD, NOVX had significantly decreased to (92 ± 15) and (95 ± 22) pmol/L in E(2) level (P < 0.05), (0.076 ± 0.016) and (0.052 ± 0.013) g/cm(2) in BMD values (P < 0.01). And bone tissue LRP5, β-catenin and Runx2 mRNA expression was 1.02 ± 0.06, 1.04 ± 0.05, 1.07 ± 0.21 in NS, NOVX was significantly reduced to 0.97 ± 0.04, 0.58 ± 0.05, 0.86 ± 0.03 (P < 0.05).

CONCLUSION

Wnt/LRP5/β-catenin signaling pathway may be important in the pathogenesis of postmenopausal osteoporosis.

摘要

目的

探讨Wnt/LRP5/β-连环蛋白信号通路在绝经后骨质疏松症发病机制中的作用。

方法

将50只6月龄雌性Wistar大鼠随机分为对照组(NS,n = 24)和去卵巢组(NOVX,n = 26),对NOVX组进行双侧卵巢切除术。在0、4和8周时,检测所有大鼠的血雌激素(E₂)和骨密度(BMD),在4和8周时,分别通过逆转录(RT)-PCR检测骨组织中低密度脂蛋白受体相关蛋白5(LRP5)、β-连环蛋白和Runx2 mRNA的表达。

结果

在4周和8周时,与E₂水平分别为(117±29)和(114±15)pmol/L、BMD分别为(0.098±0.016)和(0.095±0.028)g/cm²的NS组相比,NOVX组的E₂水平显著降低至(92±15)和(95±22)pmol/L(P<0.05),BMD值分别为(0.076±0.016)和(0.052±0.013)g/cm²(P<0.01)。并且骨组织中LRP5、β-连环蛋白和Runx2 mRNA的表达在NS组分别为1.02±0.06、1.04±0.05、1.07±0.21,在NOVX组显著降低至0.97±0.04、0.58±0.05、0.86±0.03(P<0.05)。

结论

Wnt/LRP5/β-连环蛋白信号通路可能在绝经后骨质疏松症的发病机制中起重要作用。

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