Okamoto T, Kanda T
Research Laboratories, Nippon Chemiphar Co., Ltd., Misato, Saitama 341-0005, Japan.
Int J Mol Med. 1999 Aug;4(2):149-52. doi: 10.3892/ijmm.4.2.149.
The administration of concanavalin A (Con A) to mice induces cytokine-dependent hepatitis. In the present study, the effect of glycyrrhizin on Con A-induced hepatitis was examined. Treatment of mice with Con A (0.2 mg/mouse, i.v.) induced elevation of the plasma transaminase activities at 24 h. Mice were treated with glycyrrhizin (100, 200 and 400 mg/kg, i.p.), and glycyrrhizin at the doses of 200 and 400 mg/kg inhibited the Con A-induced elevation of the plasma transaminase activities. At 1 h after Con A treatment, interferon-gamma, tumor necrosis factor-alpha, interleukin-2 and interleukin-6 proteins were released into the plasma. Although treatment with glycyrrhizin at 200 mg/kg inhibited Con A-induced hepatitis, it did not affect the release of any of these Con A-induced cytokines into the plasma. The present results clearly show that glycyrrhizin inhibited Con A-induced hepatitis without affecting cytokine expression.
给小鼠注射伴刀豆球蛋白A(Con A)可诱发细胞因子依赖性肝炎。在本研究中,检测了甘草酸对Con A诱导的肝炎的影响。用Con A(0.2 mg/小鼠,静脉注射)处理小鼠在24小时时可导致血浆转氨酶活性升高。用甘草酸(100、200和400 mg/kg,腹腔注射)处理小鼠,200和400 mg/kg剂量的甘草酸可抑制Con A诱导的血浆转氨酶活性升高。在Con A处理后1小时,干扰素-γ、肿瘤坏死因子-α、白细胞介素-2和白细胞介素-6蛋白释放到血浆中。尽管200 mg/kg的甘草酸处理可抑制Con A诱导的肝炎,但它并不影响这些Con A诱导的细胞因子中的任何一种释放到血浆中。目前的结果清楚地表明,甘草酸可抑制Con A诱导的肝炎而不影响细胞因子表达。