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首页> 外文期刊>Osteoarthritis and cartilage >Effect of hyaluronic acid (MW 500-730 kDa) on proteoglycan and nitric oxide production in human osteoarthritic chondrocyte cultures exposed to hydrostatic pressure.
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Effect of hyaluronic acid (MW 500-730 kDa) on proteoglycan and nitric oxide production in human osteoarthritic chondrocyte cultures exposed to hydrostatic pressure.

机译:透明质酸(MW 500-730 kDa)对暴露于静水压力的人骨关节炎软骨细胞培养物中蛋白聚糖和一氧化氮产生的影响。

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OBJECTIVE: This study investigated the in vitro effects of hyaluronic acid (HA) of molecular weight (MW) 500-730 kDa on human articular chondrocytes cultivated for 48 h in the presence of interleukin-1beta (IL-1beta) with and without hydrostatic cyclical pressure. DESIGN: The effects of 10 and 100 microg/ml HA with and without IL-1beta were assessed in the culture medium of cells exposed to pressurization cycles in the form of sinusoidal waves (minimum pressure 1MPa, maximum pressure 5MPa) at a frequency of 0.25Hz for 3h, by the immunoenzymatic method on microplates for the quantitative measurement of human proteoglycans (PG) and by the Griess method for nitrites (NO). Morphological analyses were performed by transmission electron microscopy (TEM) and scanning electron microscopy (SEM). RESULTS: The presence of IL-1beta determines a significant decrease in PG and a significant increase in NO concentrations measured in the culture medium. When the cells are cultured in the presence of IL-1beta and HA atthe two concentrations, a statistically significant restoration of PG and a decrease in NO levels are observed. Under pressurization conditions, we observed that the PG concentration in the medium of cells presented a very significant increase in all the conditions used in the study, except for IL-1beta alone. NO production decreased very significantly in the presence of IL-1beta+HA 10 and IL-1beta+HA 100. The results of metabolic evaluation are confirmed by morphological findings obtained by TEM and SEM. CONCLUSIONS: These in vitro studies confirm both the protective role of HA (MW 500-730 kDa), which counteracts the IL-1beta-induced effects, and the importance of pressure on chondrocyte metabolism and morphology.
机译:目的:研究在有白细胞介素-1β(IL-1β)存在和不存在静水循环的条件下,分子量(MW)500-730 kDa的透明质酸(HA)对人关节软骨细胞培养48 h的体外作用。压力。设计:在暴露于加压周期的正弦波形式(最小压力1MPa,最大压力5MPa)的频率为0.25的暴露于加压循环的细胞培养基中,评估了有和无IL-1beta的10和100 microg / ml HA的作用通过微量酶标板上的免疫酶法定量检测人蛋白聚糖(PG)的频率为3 h,通过亚硝酸盐(NO)的Griess方法检测3 h。形态分析通过透射电子显微镜(TEM)和扫描电子显微镜(SEM)进行。结果:IL-1β的存在决定了培养基中PG的显着降低和NO浓度的显着提高。当在两种浓度的IL-1β和HA存在下培养细胞时,观察到PG的统计学显着恢复和NO水平的降低。在加压条件下,我们观察到细胞培养基中的PG浓度在研究中使用的所有条件下均呈现非常显着的增加,仅IL-1beta除外。在IL-1beta + HA 10和IL-1beta + HA 100的存在下,NO的产生非常显着降低。通过TEM和SEM获得的形态学结果证实了代谢评估的结果。结论:这些体外研究证实了HA(MW 500-730 kDa)的保护作用,抵消了IL-1β诱导的作用,以及压力对软骨细胞代谢和形态的重要性。

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