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对乙酰氨基酚降低咖啡因毒性。

Reduction in caffeine toxicity by acetaminophen.

作者信息

Deng J F, Spyker D A, Rall T W, Steward O

出版信息

J Toxicol Clin Toxicol. 1982 Dec;19(10):1031-43. doi: 10.3109/15563658208992538.

DOI:10.3109/15563658208992538
PMID:6308277
Abstract

A patient who allegedly consumed 100 tablets of an over-the-counter analgesic containing sodium acetylsalicylate, caffeine, and acetaminophen displayed no significant CNS stimulation despite the presence of 175 micrograms of caffeine per mL of serum. Because salicylates have been reported to augment the stimulatory effects of caffeine on the CNS, attention was focused on the possibility that the presence of acetaminophen (52 micrograms/mL) reduced the CNS toxicity of caffeine. Studies in DBA/2J mice showed that: 1) pretreatment with acetaminophen (100 mg/kg) increased the interval between the administration of caffeine (300 to 450 mg/kg IP) and the onset of fatal convulsions by a factor of about two; and 2) pretreatment with acetaminophen (75 mg/kg) reduced the incidence of audiogenic seizures produced in the presence of caffeine (12.5 to 75 mg/kg IP). The frequency of sound-induced seizures after 12.5 or 25 mg/kg caffeine was reduced from 50 to 5% by acetaminophen. In the absence of caffeine, acetaminophen (up to 300 mg/kg) did not modify the seizures induced by maximal electroshock and did not alter the convulsant dose of pentylenetetrezol in mice (tests performed by the Anticonvulsant Screening Project of NINCDS). Acetaminophen (up to 150 micrograms/mL) did not retard the incorporation of radioactive adenosine into ATP in slices of rat cerebral cortex. Thus the mechanism by which acetaminophen antagonizes the actions of caffeine in the CNS remains unknown.

摘要

一名据称服用了100片含乙酰水杨酸、咖啡因和对乙酰氨基酚的非处方镇痛药的患者,尽管血清中每毫升含有175微克咖啡因,但未表现出明显的中枢神经系统刺激症状。由于已有报道称水杨酸盐会增强咖啡因对中枢神经系统的刺激作用,因此注意力集中在对乙酰氨基酚(52微克/毫升)的存在是否降低了咖啡因的中枢神经系统毒性这一可能性上。对DBA/2J小鼠的研究表明:1)用对乙酰氨基酚(100毫克/千克)预处理可使给予咖啡因(腹腔注射300至450毫克/千克)至致命惊厥发作的间隔时间延长约两倍;2)用对乙酰氨基酚(75毫克/千克)预处理可降低在咖啡因(腹腔注射12.5至75毫克/千克)存在下产生的听源性惊厥的发生率。对乙酰氨基酚可使12.5或25毫克/千克咖啡因诱导的声音诱发惊厥频率从50%降至5%。在没有咖啡因的情况下,对乙酰氨基酚(高达300毫克/千克)不会改变最大电休克诱发的惊厥,也不会改变小鼠戊四氮的惊厥剂量(由国家神经疾病和中风研究所抗惊厥筛选项目进行测试)。对乙酰氨基酚(高达150微克/毫升)不会延缓放射性腺苷掺入大鼠大脑皮层切片中的三磷酸腺苷。因此,对乙酰氨基酚拮抗咖啡因在中枢神经系统中作用的机制仍然未知。

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