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他克莫司和环孢素A对培养的人肝细胞中炎性细胞因子诱导的白蛋白分泌抑制作用的影响。

Effect of tacrolimus and cyclosporine A on suppression of albumin secretion induced by inflammatory cytokines in cultured human hepatocytes.

作者信息

Li Y, Liu F-Y, Liu Z-H, Huang Y-F, Li L-S, Zhang X, Peng Y-M

机构信息

Division of Nephrology, The Second Xiangya Hospital, Central South University, 410011, Changsha, China.

出版信息

Inflamm Res. 2006 May;55(5):216-20. doi: 10.1007/s00011-006-0074-0.

Abstract

OBJECTIVE AND DESIGN

To investigate the effect of tacrolimus (FK506) and cyclosporine A (CSA) on albumin secretion and on the IL-6 -induced suppression of albumin synthesis in cultured human hepatocytes.

METHODS

HepG2 cells were cultured separately with IL-6, IL-10 (0-10 ng/ml) and FK506, CSA (0-100 ng/ml) for 48 h. In another experiment, HepG2 cells were incubated with different amounts of FK506 and CSA (0-10 ng/ml) in the presence of IL-6 (5 ng/ml). The albumin levels in these groups of hepatic cultures were measured by radioimmunoassay. The concentration of LDH secreted by cells stimulated with FK506 and CSA was detected by spectrophotometry.

RESULTS

IL-6 decreased the levels of albumin in a dose-dependent manner (P < 0.01), maximal inhibition was observed at 5 ng/ml. Neither IL-10 nor FK506 modulated albumin production. However, FK506 decreased LDH levels in the supernatant of cells (P < 0.05) and prevented the IL-6-induced suppression of albumin synthesis (P < 0.01) in a dose dependent manner. In contrast, CSA caused only a slight decrease in albumin levels (P < 0.05). In addition, CSA slightly increased the amount of LDH in HepG2 cells and did not interfere with the IL-6-induced decrease in albumin synthesis.

CONCLUSIONS

These findings suggest that IL-6, but not IL- 10, may play an important role in the suppression of hepatic albumin secretion. FK506 but not CSA protects against the suppression of hepatic albumin synthesis caused by IL-6.

摘要

目的与设计

研究他克莫司(FK506)和环孢素A(CSA)对培养的人肝细胞中白蛋白分泌以及白细胞介素-6(IL-6)诱导的白蛋白合成抑制作用的影响。

方法

将HepG2细胞分别与IL-6、IL-10(0 - 10 ng/ml)以及FK506、CSA(0 - 100 ng/ml)共同培养48小时。在另一项实验中,将HepG2细胞在存在IL-6(5 ng/ml)的情况下与不同量的FK506和CSA(0 - 10 ng/ml)一起孵育。通过放射免疫测定法测量这些肝培养组中的白蛋白水平。用分光光度法检测经FK506和CSA刺激的细胞分泌的乳酸脱氢酶(LDH)浓度。

结果

IL-6以剂量依赖性方式降低白蛋白水平(P < 0.01),在5 ng/ml时观察到最大抑制作用。IL-10和FK506均未调节白蛋白的产生。然而,FK506以剂量依赖性方式降低细胞上清液中的LDH水平(P < 0.05)并防止IL-6诱导的白蛋白合成抑制(P < 0.01)。相比之下,CSA仅使白蛋白水平略有下降(P < 0.05)。此外,CSA使HepG2细胞中的LDH量略有增加,并且不干扰IL-6诱导的白蛋白合成减少。

结论

这些发现表明,IL-6而非IL-10可能在抑制肝脏白蛋白分泌中起重要作用。FK506而非CSA可防止IL-6引起的肝脏白蛋白合成抑制。

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