Liddell N E, Maren T H
J Pharmacol Exp Ther. 1975 Oct;195(1):1-7.
Two carbonic anhydrase inhibitors, acetazolamide and benzolamide, are capable of increasing the toxicity of sodium salicylate in mice. Beginning at about 2 mg/kg, each of the inhibitors, in combination with a fixed (400 mg/kg) dose of salicylate, generates a dose-mortality curve that reaches a plateau at about 60% deaths at 6 to 8 mg/kg. This effect can be duplicated by 8 to 10% inspired CO2. It appears that the respiratory acidosis secondary to the inhibition of red cell carbonic anhydrase is responsible for the increased toxicity; earlier work by others shows that acidosis increases the concentration of salicylate in the brain. In the treatment of salicylate poisoning by carbonic anhydrase inhibitors, the goal is to alkalinize the urine and increase the excretion of salicylate. With the newer inhibitor, benzolamide, it is possible to dissociate the respiratory acidosis from the renal effect. Maximal alkalinization of the urine is possible with a dose (about 1 mg/kg) below that which generates a respiratory acidosis. With this dose, there is no increase in the early toxicity of salicylate.
两种碳酸酐酶抑制剂,乙酰唑胺和苯唑酰胺,能够增加小鼠体内水杨酸钠的毒性。从约2毫克/千克开始,每种抑制剂与固定剂量(400毫克/千克)的水杨酸盐联合使用时,会产生一条剂量-死亡率曲线,在6至8毫克/千克时死亡率达到约60%的平台期。吸入8%至10%的二氧化碳可产生相同效果。似乎红细胞碳酸酐酶受抑制继发的呼吸性酸中毒是毒性增加的原因;其他人早期的研究表明,酸中毒会增加水杨酸盐在大脑中的浓度。在使用碳酸酐酶抑制剂治疗水杨酸盐中毒时,目标是使尿液碱化并增加水杨酸盐的排泄。使用较新的抑制剂苯唑酰胺时,有可能将呼吸性酸中毒与肾脏效应分离。在产生呼吸性酸中毒的剂量(约1毫克/千克)以下,有可能实现尿液的最大程度碱化。使用此剂量时,水杨酸盐的早期毒性不会增加。