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树叶的乙醇提取物通过抑制骨质疏松症中的破骨细胞生成来改善骨质流失。

The Ethanol Extracts of Leaves Ameliorate the Bone Loss via the Inhibition of Osteoclastogenesis in Osteoporosis.

作者信息

Seo Yo-Seob, Lim HyangI, Seo Jeong-Yeon, Kang Kyeong-Rok, Kim Do Kyung, Lee Hyun-Hwa, Oh Deuk-Sil, Kim Jae-Sung

机构信息

Institute of Dental Science, Chosun University, Gwangju 61452, Republic of Korea.

Department of Oral and Maxillofacial Radiology, School of Dentistry, Chosun University, Gwangju 61452, Republic of Korea.

出版信息

Plants (Basel). 2023 Jan 5;12(2):253. doi: 10.3390/plants12020253.

Abstract

The aim of this study was to evaluate the anti-osteoporosis effects of leaf ethanol extract (OFLEE) in bone marrow-derived macrophages (BMM) and animals with osteoporosis. OFLEE not only suppressed tartrate-resistant acid phosphatase (TRAP)-positive cells with multiple nuclei but also decreased TRAP activity in BMM treated with macrophage colony stimulating factor (M-CSF) and receptor activator of nuclear factor-κB (NF-κB) ligand (RANKL). The formation of F-actin rings and the expression and activation of matrix metalloproteinases were decreased by OFLEE in BMM treated with M-CSF and RANKL. OFLEE suppressed M-CSF- and RANKL-induced osteoclastogenesis by inhibiting NF-κB phosphorylation, tumor necrosis factor receptor-associated factor 6, c-fos, the nuclear factor of activated T-cells, cytoplasmic 1, and cathepsin K in BMM. OFLEE downregulated reactive oxygen species, cyclooxygenase-2, inducible nitric oxide synthase, prostaglandin E, tumor necrosis factor α, interleukin (IL)-1β, IL-6, IL-17, and RANKL in BMM treated with M-CSF and RANKL. Oral administration of OFLEE suppressed osteoporotic bone loss without hepatotoxicity in ovariectomy-induced osteoporosis animals. Our findings suggest that OFLEE, with anti-inflammatory effects, prevents osteoporotic bone loss through the suppression of osteoclastic differentiation in BMM and animals with osteoporosis.

摘要

本研究旨在评估叶乙醇提取物(OFLEE)对骨髓来源巨噬细胞(BMM)和骨质疏松动物的抗骨质疏松作用。OFLEE不仅抑制了具有多个细胞核的抗酒石酸酸性磷酸酶(TRAP)阳性细胞,还降低了用巨噬细胞集落刺激因子(M-CSF)和核因子κB(NF-κB)配体受体激活剂(RANKL)处理的BMM中的TRAP活性。OFLEE降低了用M-CSF和RANKL处理的BMM中F-肌动蛋白环的形成以及基质金属蛋白酶的表达和激活。OFLEE通过抑制BMM中的NF-κB磷酸化、肿瘤坏死因子受体相关因子6、c-fos、活化T细胞核因子、细胞质1和组织蛋白酶K来抑制M-CSF和RANKL诱导的破骨细胞生成。OFLEE下调了用M-CSF和RANKL处理的BMM中的活性氧、环氧化酶-2、诱导型一氧化氮合酶、前列腺素E、肿瘤坏死因子α、白细胞介素(IL)-1β、IL-6、IL-17和RANKL。在卵巢切除诱导的骨质疏松动物中,口服OFLEE可抑制骨质疏松性骨丢失且无肝毒性。我们的研究结果表明,具有抗炎作用的OFLEE通过抑制BMM和骨质疏松动物中的破骨细胞分化来预防骨质疏松性骨丢失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d67/9866894/a186591848f5/plants-12-00253-g001.jpg

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