Title of article :
The effects of luteolin on osteoclast differentiation, function in vitro and ovariectomy-induced bone loss
Author/Authors :
Tae-Ho Kim، نويسنده , , Ji-Won Jung، نويسنده , , Byung Geun Ha، نويسنده , , Jung Min Hong، نويسنده , , Eui Kyun Park، نويسنده , , Hyun-Ju Kim، نويسنده , , Shin-Yoon Kim، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2011
Pages :
8
From page :
8
To page :
15
Abstract :
Flavonoids, a group of polyphenolic compounds abundant in plants, are known to prevent bone loss in ovariectomized (OVX) animal models. Inhibition of osteoclast differentiation and bone resorption is considered as an effective therapeutic approach in the treatment of postmenopausal bone loss. Luteolin, a plant flavonoid, has potent anti-inflammatory properties both in vivo and vitro. In this study, we found that luteolin markedly decreased the differentiation of both bone marrow mononuclear cells and Raw264.7 cells into osteoclasts. Luteolin also inhibited the bone resorptive activity of differentiated osteoclasts. We further investigated the effects of luteolin on ovariectomy-induced bone loss using micro-computed tomography, biomechanical tests and serum markers assay for bone remodeling. Oral administration of luteolin (5 and 20 mg/kg per day) to OVX mice caused significant increase in bone mineral density and bone mineral content of trabecular and cortical bones in the femur as compared to those of OVX controls, and prevented decreases of bone strength indexes induced by OVX surgery. Serum biochemical markers assays revealed that luteolin prevents OVX-induced increases in bone turnover. These data strongly suggest that luteolin has the potential for prevention of bone loss in postmenopausal osteoporosis by reducing both osteoclast differentiation and function.
Keywords :
Osteoclast , Ovariectomy , Bone loss , Flavonoid , Luteolin , Bone resorption
Journal title :
The Journal of Nutritional Biochemistry
Serial Year :
2011
Journal title :
The Journal of Nutritional Biochemistry
Record number :
1299740
Link To Document :
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