Takeda Hiroshi, Tominari Tsukasa, Hirata Michiko, Watanabe Kenta, Matsumoto Chiho, Grundler Florian M W, Inada Masaki, Miyaura Chisato
Cooperative Major of Advanced Health Science, Tokyo University of Agriculture and Technology.
Department of Biotechnology and Life Science, Tokyo University of Agriculture and Technology.
Biol Pharm Bull. 2017;40(5):716-721. doi: 10.1248/bpb.b16-00897.
Lutein is a member of the xanthophyll family of carotenoids, which are known to prevent hypoxia-induced cell damage in the eye by removing free radicals. However, its role in other tissues is controversial, and the effects of lutein on bone tissues are unknown. To identify a possible role of lutein in bone tissues, we examined the effects of lutein on bone formation and bone resorption and on femoral bone mass in mice. Lutein enhanced the formation of mineralized bone nodules in cultures of osteoblasts. On the other hand, lutein clearly suppressed 1α, 25-dihydroxyvitamin D-induced bone resorption as measured by pit formation in organ culture of mouse calvaria. In co-cultures of bone marrow cells and osteoblasts, lutein suppressed 1α, 25-dihydroxyvitamin D-induced osteoclast formation. In cultures of bone marrow macrophages, lutein suppressed soluble RANKL, the receptor activator of nuclear factor-kappaB (NF-κB) ligand, induced osteoclast formation. When five-week-old male mice were orally administered lutein for 4 weeks, the femoral bone mass was clearly enhanced in cortical bone, as measured by bone mineral density in dual X-ray absorptiometry and micro computed tomography (µCT) analyses. The present study indicates that lutein enhances bone mass in growing mice by suppressing bone resorption and stimulating bone formation. Lutein may be a natural agent that promotes bone turnover and may be beneficial for bone health in humans.
叶黄素是类胡萝卜素中叶黄素家族的一员,已知其可通过清除自由基来预防缺氧诱导的眼部细胞损伤。然而,它在其他组织中的作用存在争议,叶黄素对骨组织的影响尚不清楚。为了确定叶黄素在骨组织中的可能作用,我们研究了叶黄素对小鼠骨形成、骨吸收以及股骨骨量的影响。叶黄素增强了成骨细胞培养物中矿化骨结节的形成。另一方面,通过小鼠颅骨器官培养中的凹坑形成测量,叶黄素明显抑制了1α,25 - 二羟基维生素D诱导的骨吸收。在骨髓细胞与成骨细胞的共培养中,叶黄素抑制了1α,25 - 二羟基维生素D诱导的破骨细胞形成。在骨髓巨噬细胞培养中,叶黄素抑制了可溶性核因子κB受体活化因子配体(RANKL)诱导的破骨细胞形成。当对五周龄雄性小鼠口服叶黄素4周时,通过双能X线吸收法和显微计算机断层扫描(µCT)分析中的骨矿物质密度测量,皮质骨中的股骨骨量明显增加。本研究表明,叶黄素通过抑制骨吸收和刺激骨形成来增加生长中小鼠的骨量。叶黄素可能是一种促进骨转换且对人类骨骼健康有益的天然物质。