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Bone Protective Effects and Intervention Mechanism of α-Zearalanol in Ovariectomized Rat

机译:卵巢切除大鼠α-唑烷醇的骨保护作用及干预机制

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Objective: To assess bone protective effects and intervention mechanism of α-Zearalanol in ovariectomized rat. Methods: 60 female SD rats were randomly separated into 6 groupsxontrol group (n=10); ovariectomized group (OVX) (n=10); the OVX + E_2 group(OVX + E_2) (n=10); the high-dose OVX + α-ZAL group (OVX + HZ) (n=10); the moderate-dose OVX + α-ZAL group (OVX + MZ) (n=10); the low dose OVX + α-ZAL group (OVX + LZ) (n=10). α-ZAL was administered intragastrically to the rats. After 35 days, the total body Bone mineral density (BMD) was assessed in the rats. All sections were processed for hematoxylin-eosin staining (H.E.), and Basic fibroblast growth factor (bFGF), Tartrate-resistant acid phosphatase (TRAP), Bone morphogenetic proteins (BMP), and Bone Gla protein (BGP) immunoreactivity was assessed. Serum tumor necrosis factor-α (TNF-α) and bone specific alkaline phosphatase (BALP) levels were assessed using commercially available ELISA kits. Results: The expression of BMP and bFGF were significantly increased in OVX + MZ and OVX + LZ. The expression of TRAP, TNF-α, BGP and BALP were significantly decreased in OVX + MZ and OVX + LZ. BMD was significantly increased in OVX + MZ and OVX + LZ (vs. OVX, P<0.05). Conclusion: The results of this experiment demonstrate that α-ZAL can increase the expression of bFGF and BMP while reducing the expression of TRAP, BGP, TNF-α and BALP. The administration of α-ZAL to ovariectomized rats reverses bone loss and prevents osteoporosis.
机译:目的:评价卵巢切除大鼠α-唑烷醇的骨保护作用及干预机制。方法:将60只雌性SD大鼠随机分离成6组Xontrol基团(n = 10);卵巢切除术组(OVX)(n = 10); OVX + E_2组(OVX + E_2)(n = 10);高剂量OVX +α-Zal基团(OVX + Hz)(n = 10);中等剂量OVX +α-Zal组(OVX + MZ)(n = 10);低剂量OVX +α-ZAL(OVX + LZ)(n = 10)。 α-Zal对大鼠胃内给药。 35天后,在大鼠中评估全身骨密度(BMD)。针对苏木精 - 曙红染色(H.)处理的所有部分,并评估碱性成纤维细胞生长因子(BFGF),酒石酸耐酸性磷酸酶(捕获),骨形态发生蛋白(BMP)和骨GLA蛋白(BGP)免疫反应性。使用市售的ELISA试剂盒评估血清肿瘤坏死因子-α(TNF-α)和骨特异性碱性磷酸酶(BALP)水平。结果:OVX + MZ和OVX + LZ中BMP和BFGF的表达显着增加。 OVX + MZ和OVX + LZ,捕集器,TNF-α,BGP和BALP的表达显着降低。 OVX + MZ和OVX + LZ(VS. OVX,P <0.05)显着增加BMD。结论:该实验的结果表明,α-Zal可以增加BFGF和BMP的表达,同时降低陷阱,BGP,TNF-α和BALP的表达。 α-Zal给卵巢切除大鼠的给药逆转骨质损失并防止骨质疏松症。

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