骨保护素
去卵巢大鼠
骨质疏松症
内分泌学
兰克尔
内科学
骨钙素
骨重建
破骨细胞
激活剂(遗传学)
骨髓
皮质骨
化学
受体
骨愈合
医学
骨吸收
骨病
骨细胞
药理学
受体拮抗剂
敌手
选择性雌激素受体调节剂
骨密度
中枢神经系统
骨矿物
口服
骨组织
作者
Seyedeh Mahnaz Karimi,Mohammad Bayat,Atarodsadat Mostafavinia,Javad Malakootikhah,Mohammad Reza Shams-Ardekani,Ardalan Yazdani,Saman Akbarzadeh,Roja Rahimi
标识
DOI:10.2174/0122150838388381251119054527
摘要
Background: Pistacia atlantica Desf. is a widely used medicinal plant in traditional medicine and has long been used by native populations for various therapeutic purposes, including the treatment of osteoporosis and fractures. This study investigated the therapeutic effects of P. atlantica oleo-gum-resin on the gene expression and histological parameters in a postmenopausal osteoporosis model. Methods: Osteoporosis was induced in rats via ovariectomy. Rats received oral administration of P. atlantica oleo-gum-resin and its nanocapsulated form (50, 100, 200 mg/kg) for eight weeks. Stereological analysis was performed by evaluating total bone density, cortical bone thickness, trabeculated bone number, and total bone marrow density. Additionally, the number of osteocytes, osteoblasts, and osteoclasts was calculated. The expression of osteocalcin, Osteoprotegerin (OPG), Receptor Activator of Nuclear factor Kappa-B (RANK), and Receptor Activator of Nuclear factor Kappa-B ligand (RANKL) was detected by real-time polymerase chain reaction (Real-time PCR). Results: P. atlantica oleo-gum-resin and its encapsulated form, with a dose of 100 and 200 mg/kg, significantly increased the volumes of total bone, bone marrow, trabecular bone, cortical bone, and the numbers of osteocytes and osteoblasts of callus compared to the control rats. Additionally, mRNA expression of osteocalcin and OPG increased significantly, whereas RANK and RANKL decreased in the tibial callus compared with the control group. Conclusion: P. atlantica protected against bone loss in OVX-induced osteoporotic rats and could be considered as an anti-osteoporotic candidate for human osteoporotic disorders. However, further clinical studies are necessary to validate its effectiveness and safety in the treatment of postmenopausal osteoporosis.
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