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双膦酸盐可抑制人成骨样细胞产生白细胞介素-6。

Bisphosphonates inhibit IL-6 production by human osteoblast-like cells.

作者信息

Giuliani N, Pedrazzoni M, Passeri G, Girasole G

机构信息

Istituto di Clinica Medica Generale, University of Parma, Italy.

出版信息

Scand J Rheumatol. 1998;27(1):38-41. doi: 10.1080/030097498441155.

Abstract

Since bisphosphonates prevent bone loss in osteoporosis and rheumatoid arthritis, diseases in which the osteoclastogenic and inflammatory cytokine interleukin-6 plays a pathophysiologic role, we studied whether these drugs regulate the production of this cytokine by osteoblasts. Spontaneous and IL-1 + TNF-alpha stimulated IL-6 release was measured in supernatants of cultures of human osteoblastic osteosarcoma cells MG-63, pretreated for 4 hours with different doses of etidronate, clodronate or alendronate using a specific bioassay. Etidronate [from 10(-4) to 10(-8) M] or alendronate [from 10(-6) to 10(-11) M] inhibited in a dose-dependent manner the cytokine-induced IL-6 secretion [60+/-9.5% at 10(-5) M and 65+/-12% at 10(-7) M, respectively; p < 0.01]. Though significant, the inhibitory effect of clodronate was less [35+/-7% at 10(-5) M, p < 0.05]. These in vitro observations might have in vivo relevance in explaining at least in part the mechanisms by which bisphosphonates inhibit systemic and periarticular bone resorption.

摘要

由于双膦酸盐可预防骨质疏松症和类风湿性关节炎中的骨质流失,而破骨细胞生成和炎性细胞因子白细胞介素-6在这些疾病中发挥病理生理作用,因此我们研究了这些药物是否调节成骨细胞产生这种细胞因子。使用特定生物测定法,在不同剂量依替膦酸、氯膦酸或阿仑膦酸预处理4小时的人成骨骨肉瘤细胞MG-63培养上清液中,测量自发和IL-1 + TNF-α刺激的IL-6释放。依替膦酸[10(-4)至10(-8) M]或阿仑膦酸[10(-6)至10(-11) M]以剂量依赖性方式抑制细胞因子诱导的IL-6分泌[在10(-5) M时分别为60±9.5%,在10(-7) M时为65±12%;p < 0.01]。虽然氯膦酸的抑制作用显著,但较小[在10(-5) M时为35±7%,p < 0.05]。这些体外观察结果可能在体内具有相关性,至少部分解释了双膦酸盐抑制全身和关节周围骨吸收的机制。

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