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骨碎补对人骨细胞增殖及免疫调节活性的影响。

Effects of Drynariae rhizoma on the proliferation of human bone cells and the immunomodulatory activity.

作者信息

Jeong Ji-Cheon, Lee Boo-Tae, Yoon Cheol-Ho, Kim Hyung-Min, Kim Cheorl-Ho

机构信息

Department of Internal Medicine, Biochemistry and Molecular Biology, College of Oriental Medicine, Dongguk University and National Research Laboratory for Glycobiology, Sukjang-Dong 707, Kyungju, Kyungbuk 780-714, Republic of Korea.

出版信息

Pharmacol Res. 2005 Feb;51(2):125-36. doi: 10.1016/j.phrs.2004.06.005.

Abstract

Drynariae Rhizoma (DR), a traditional Korea medicine, which is known for its effect to strengthen myoskeletal systems, frequently appears as the main ingredient in prescriptions for bone injuries. However, it is unclear how it pharmacologically contributes to the reformation of bone. In this study, the effect of DR on bone cells was investigated in vitro for the first time. The human osteoprecursor cells (OPC-1) were incubated in the medium with different concentrations of DR and the cell proliferation was studied. When the concentration of DR was < or = 120 microg ml(-1), the proliferation of OPC-1 was enhanced. However, the proliferation of OPC-1 was inhibited by DR with the concentrations of > 250 microg ml(-1). Under most treatments, the cells presented very pale expression for cyclooxygenase-2 (Cox-2) protein; slightly intensified band showed at the highest DR concentration, 120 microg ml(-1) during the course of culture. On the other hand, we investigated the immunomodulatory activity of DR on cellular and humoral immunity. When different doses of ethanolic and water extracts of DR was administered to mice, it was dose-dependently potentiated the delayed-type hypersensitivity reaction induced by both sheep red blood cells (SRBC) and oxazolone. It significantly enhanced the production of circulating antibody titre in mice in response to SRBC. But, DR did not any effect on macrophage phagocytosis. Prolonged administration of DR significantly ameliorated the total white blood cell count and also restored the immunosuppressive effects induced by cyclophosphamide. The present investigation reveals that DR possesses immunomodulatory activity. From the results, it was concluded that DR directly stimulated the proliferation, alkaline phosphatase activity, protein secretion and particularly type I collagen synthesis of OPC-1 at dose-dependent manner, and stimulated both the cellular and the humoral immunity.

摘要

骨碎补是一种传统的韩国药物,以其增强肌肉骨骼系统的功效而闻名,经常作为骨伤处方的主要成分出现。然而,其在药理上如何促进骨重塑尚不清楚。在本研究中,首次在体外研究了骨碎补对骨细胞的影响。将人骨前体细胞(OPC-1)在含有不同浓度骨碎补的培养基中培养,并研究细胞增殖情况。当骨碎补浓度≤120μg/ml时,OPC-1的增殖增强。然而,当骨碎补浓度>250μg/ml时,OPC-1的增殖受到抑制。在大多数处理下,细胞中环氧合酶-2(Cox-2)蛋白的表达非常微弱;在培养过程中,在最高骨碎补浓度120μg/ml时,条带略有增强。另一方面,我们研究了骨碎补对细胞免疫和体液免疫的免疫调节活性。当向小鼠给予不同剂量的骨碎补乙醇提取物和水提取物时,其剂量依赖性地增强了由绵羊红细胞(SRBC)和恶唑酮诱导的迟发型超敏反应。它显著增强了小鼠对SRBC的循环抗体滴度的产生。但是,骨碎补对巨噬细胞吞噬作用没有任何影响。长期给予骨碎补显著改善了白细胞总数,并恢复了环磷酰胺诱导的免疫抑制作用。本研究表明骨碎补具有免疫调节活性。从结果得出结论,骨碎补以剂量依赖性方式直接刺激OPC-1的增殖、碱性磷酸酶活性、蛋白质分泌,特别是I型胶原合成,并刺激细胞免疫和体液免疫。

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