Abstract
Estrogen deficiency in postmenopausal women causes homeostatic imbalance of bone, resulting in bone loss and osteoporosis. Agastache rugosa, a plant belonging to the Lamiaceae family, is an aromatic herb, and the leaves of this herb are widely used as food ingredients. Extracts of A. rugosa have various bioactivities including anti-HIV integration, anti-inflammatory, and anti-atherogenic properties. However, the beneficial effect of A. rugosa on bone has not been studied. Therefore, we investigated the effects of water extract of A. rugosa (WEAR) on osteoclast differentiation and estrogen deficiency-induced bone loss in ovariectomized (OVX) mice as an animal model for postmenopausal osteoporosis. The oral administration of WEAR remarkably improved OVX-induced trabecular bone loss and fat accumulation in the bone marrow. WEAR suppressed receptor activator of nuclear factor-κB ligand (RANKL)-induced osteoclast differentiation in osteoclast precursor cells, subsequently inhibiting resorption activity on a bone mimetic surface. WEAR inhibited the expression of cellular oncogene fos (c-Fos) and nuclear factor of activated T-cells cytoplasmic 1 (NFATc1), key osteoclastogenic transcription factors, by decreasing RANKL-induced activation of mitogen-activated protein kinases (MAPKs), and nuclear factor-κB (NF-κB) pathways. We also identified seventeen phytochemicals present in WEAR, including five phenols and twelve flavonoids, and found eleven bioactive constituents that have anti-osteoclastogenic effects. Collectively, these results suggest that WEAR could be used to treat and prevent postmenopausal osteoporosis by suppressing osteoclastogenesis.
Highlights
Osteoporosis is a metabolic disease characterized by low bone mass and microarchitectural deterioration of bone tissue: it can lead to impaired bone strength and an increased risk of fracture [1].Bone remodeling is the continuous process through osteoclastic bone resorption and osteoblastic bone formation
OVX-induced estrogen deficiency leads to a reduction in BMD with bone metabolic changes similar to those occurring in human postmenopausal osteoporosis [17]
Because water extract of A. rugosa (WEAR) suppressed RANKL-induced osteoclast differentiation, we investigated the effect of WEAR on the expression of cellular oncogene fos (c-Fos) and nuclear factor of activated T-cells cytoplasmic 1 (NFATc1)
Summary
Bone remodeling is the continuous process through osteoclastic bone resorption and osteoblastic bone formation. This process is necessary to maintain mineral homeostasis and to repair damaged bone. Excessive bone resorption by osteoclasts bone formation by osteoblasts can cause pathological bone diseases, such as osteoporosis and rheumatoid arthritis [1,2]. Osteoclasts are multinucleated giant bone-resorbing cells formed by the proliferation, differentiation, and fusion of monocyte/macrophage lineage precursor cells. A receptor activator of nuclear factor-κB ligand (RANKL) is an essential cytokine that stimulates osteoclast differentiation, which includes proliferation, fusion, maturation, and resorption stages [3]. RANKL is produced by various bone cell types including mature osteoblasts, hypertrophic chondrocytes, and osteocytes
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