Faculty of Pharmaceutical Sciences, Josai University, 1-1 Keyakidai, Sakado, Saitama 350-0295, Japan.
Faculty of Pharmaceutical Sciences, Josai University, 1-1 Keyakidai, Sakado, Saitama 350-0295, Japan.
Phytomedicine. 2015 Nov 15;22(12):1120-4. doi: 10.1016/j.phymed.2015.08.013. Epub 2015 Sep 25.
Animal experiment studies have revealed a positive association between intake of citrus fruits and bone health. Nomilin, a limonoid present in citrus fruits, is reported to have many biological activities in mammalian systems, but the mechanism of nomilin on bone metabolism regulation is currently unclear.
To reveal the mechanism of nomilin on osteoclastic differentiation of mouse primary bone marrow-derived macrophages (BMMs) and the mouse RAW 264.7 macrophage cell line into osteoclasts.
Controlled laboratory study. Effects of nomilin on osteoclastic differentiation were studied in in vitro cell cultures.
Cell viability of RAW 264.7 cells and BMMs was measured with the Cell Counting Kit. TRAP-positive multinucleated cells were counted as osteoclast cell numbers. The number and area of resorption pits were measured as bone-resorbing activity. Osteoclast-specific genes expression was evaluated by quantitative real-time PCR; and proteins expression was evaluated by western blot.
Nomilin significantly decreased TRAP-positive multinucleated cell numbers compared with the control, and exhibited no cytotoxicity. Nomilin decreased bone resorption activity. Nomilin downregulated osteoclast-specific genes, NFATc1 and TRAP mRNA levels. Furthermore, nomilin suppressed MAPK signaling pathways.
This study demonstrates clearly that nomilin has inhibitory effects on osteoclastic differentiation in vitro. These findings indicate that nomilin-containing herbal preparations have potential utility for the prevention of bone metabolic diseases.
动物实验研究表明,摄入柑橘类水果与骨骼健康之间存在正相关关系。诺米林是柑橘类水果中存在的一种柠檬苦素,据报道,它在哺乳动物系统中具有许多生物活性,但诺米林对骨代谢调节的机制目前尚不清楚。
揭示诺米林对小鼠原代骨髓来源巨噬细胞(BMMs)和小鼠 RAW 264.7 巨噬细胞系向破骨细胞分化的作用机制。
体外细胞培养的对照实验室研究。
用细胞计数试剂盒测量 RAW 264.7 细胞和 BMMs 的细胞活力。TRAP 阳性多核细胞被计数为破骨细胞数量。作为骨吸收活性,测量破骨细胞的吸收陷窝的数量和面积。通过定量实时 PCR 评估破骨细胞特异性基因的表达;通过 Western blot 评估蛋白质表达。
与对照组相比,诺米林显著降低了 TRAP 阳性多核细胞的数量,且无细胞毒性。诺米林降低了骨吸收活性。诺米林下调了破骨细胞特异性基因 NFATc1 和 TRAP 的 mRNA 水平。此外,诺米林抑制了 MAPK 信号通路。
本研究清楚地表明,诺米林在体外对破骨细胞分化具有抑制作用。这些发现表明,含诺米林的草药制剂在预防骨代谢疾病方面具有潜在的应用价值。