Spinal Surgeon Department, Southern Medical University, Guangzhou, Guangdong Province, China.
Osteoporos Int. 2010 Jan;21(1):129-35. doi: 10.1007/s00198-009-0928-8. Epub 2009 Apr 15.
We explored the relationship between extracts of oxyntic mucosa (EOM) and the biological activity of osteoblasts in rats. We found that EOM could enhance the activity of bone formation in osteoblast. Our results suggest that EOM likely play a role in the cases of osteopenia induced by gastrectomy.
Surgical removal of the stomach (gastrectomy) leads to osteopenia in animals and in humans. It was demonstrated that EOM could induce transient hypocalcaemia and stimulate an uptake of Ca(2+) into bone in rats. The main aim of this study has been to clarify whether this procedure was performed through osteoblast, which is responsible for bone formation.
Osteoblasts were isolated, cultured, and identified in vitro. Preparing the rats' EOM and diluting into low, middle, and high concentrations, respectively. After osteoblasts were treated by different concentration EOMs or saline (for control), the intracytoplasm [Ca(2+)]i was measured by laser scanning confocal microscopy; the proliferation of osteoblast cells were detected with cell counting kit 8 (CCK-8); and the expressions of collagen type I and osteocalcin were assayed by reverse transcriptase polymerase chain reaction and Western blot.
EOMs were found to induce a dose-related rapid increase of intracytoplasm [Ca(2+)]i in osteoblasts and could stimulate osteoblasts to enhance proliferation and upregulate the expressions of collagen type I and osteocalcin significantly (p < 0.05) compared with the control group.
It was confirmed that EOM could stimulate osteoblasts to elevate the cytoplasm [Ca(2+)]i and promote the multiplication and the activity of bone formation in osteoblasts.
探讨胃黏膜泌酸细胞(EOM)提取物与大鼠成骨细胞生物活性的关系。我们发现 EOM 可增强成骨细胞的骨形成活性。我们的结果表明,EOM 可能在胃切除术后引起的骨质疏松症中发挥作用。
体外分离、培养和鉴定成骨细胞。制备大鼠 EOM 并分别稀释为低、中、高浓度。用不同浓度的 EOM 或生理盐水(对照)处理成骨细胞后,用激光扫描共聚焦显微镜测量细胞内 [Ca 2+] i;用细胞计数试剂盒 8(CCK-8)检测成骨细胞的增殖;用逆转录聚合酶链反应和 Western blot 检测Ⅰ型胶原和骨钙素的表达。
EOM 诱导成骨细胞内 [Ca 2+] i 呈剂量依赖性快速增加,并能刺激成骨细胞显著增强增殖,上调Ⅰ型胶原和骨钙素的表达(p<0.05),与对照组相比。
证实 EOM 可刺激成骨细胞升高细胞质 [Ca 2+] i ,促进成骨细胞的增殖和骨形成活性。