Mancini L, Becherini L, Benvenuti S, Brandi M L
Department of Clinical Physiopathology, University of Florence, Italy.
Int J Clin Pharmacol Res. 1997;17(2-3):93-6.
Nitric oxide is a short-lived free radical produced by different isoforms of the enzyme nitric oxide synthase. It regulates a whole range of functions in the body, but little is known about its effects on bone. Rat osteoclasts and a human preosteoclast cell line (FLG 29.1) have been shown to produce nitric oxide and to express nitric oxide synthases. In the present study we investigated the role of a nitric oxide donor, 3-morpholinosydnonimine hydrochloride, on the FLG 29.1 cells. 3-Morpholinosydnonimine hydrochloride has been shown to significantly increase IL6 production and tartrate resistant acid phosphatase activity in FLG 29.1 cells, indicating a positive modulation of osteoclast differentiation. However FLG 29.1 cell adhesion on osteoblast-like cells was significantly inhibited, suggesting an inhibition of osteoclast motility. All these results confirm the bidirectional effect of nitric oxide whose basal production is necessary in promoting osteoclast differentiation, while at high levels it is effective in inhibiting osteoclast activity.
一氧化氮是一种由一氧化氮合酶的不同同工型产生的短寿命自由基。它调节身体的一系列功能,但对其对骨骼的影响知之甚少。已证明大鼠破骨细胞和人破骨前体细胞系(FLG 29.1)可产生一氧化氮并表达一氧化氮合酶。在本研究中,我们研究了一氧化氮供体盐酸3-吗啉代西多非明对FLG 29.1细胞的作用。盐酸3-吗啉代西多非明已被证明可显著增加FLG 29.1细胞中IL6的产生和抗酒石酸酸性磷酸酶活性,表明对破骨细胞分化有正向调节作用。然而,FLG 29.1细胞在成骨样细胞上的黏附受到显著抑制,提示破骨细胞运动受到抑制。所有这些结果证实了一氧化氮的双向作用,其基础产生对于促进破骨细胞分化是必要的,而在高水平时它可有效抑制破骨细胞活性。