Nagai T, Egashira T, Yamanaka Y, Kohno M
Department of Pharmacology, Medical College of Oita, Japan.
Arch Environ Contam Toxicol. 1991 Apr;20(3):432-6. doi: 10.1007/BF01064416.
Effects of glycyrrhizin (GR) on an injury of the liver caused by ischemia-reperfusion in rats were determined. In the liver ischemia-reperfusion model, levels of serum AST, ALT and LDH, lipid peroxides in the liver tissue, and blood superoxide dismutase activity were significantly increased. On the contrary, total glutathione content in the liver tissue was decreased. When rats were given GR 100 mg/kg for 10 days, GR suppressed the elevation of the lipid peroxide level, serum AST, ALT, LDH level, and the decrease in glutathione content during the period of reperfusion. The suppressive effect of GR was similar with that of alpha-tocopherol (VE). GR showed neither 1,1-diphenyl-2-picrylhydrazyl (DPPH) nor 5,5-dimethyl-1-pyrroline-N-oxide(DMPO)-OOH radical-trapping ability, but exhibited DMPO-OH radical-trapping action, while, VE exhibited both DPPH and DMPO-OOH radical-trapping ability. These results indicate that the hydroxyl radical trapping action of GR is the likely mechanism suppressing liver injury caused by ischemia-reperfusion.
研究了甘草酸(GR)对大鼠肝脏缺血再灌注损伤的影响。在肝脏缺血再灌注模型中,血清AST、ALT和LDH水平、肝组织脂质过氧化物以及血液超氧化物歧化酶活性显著升高。相反,肝组织中总谷胱甘肽含量降低。当给大鼠连续10天给予100 mg/kg GR时,GR可抑制再灌注期间脂质过氧化物水平、血清AST、ALT、LDH水平的升高以及谷胱甘肽含量的降低。GR的抑制作用与α-生育酚(VE)相似。GR既不具有1,1-二苯基-2-苦基肼(DPPH)也不具有5,5-二甲基-1-吡咯啉-N-氧化物(DMPO)-OOH自由基捕获能力,但具有DMPO-OH自由基捕获作用,而VE同时具有DPPH和DMPO-OOH自由基捕获能力。这些结果表明,GR的羟基自由基捕获作用可能是抑制缺血再灌注所致肝损伤的机制。