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静脉注射精氨酸血红素后小鼠的巴比妥酸盐和乙醇睡眠时间以及普萘洛尔的药代动力学

Barbiturate and ethanol sleeping times and pharmacokinetics of propranolol in mice after intravenous administration of haem arginate.

作者信息

Tokola O

出版信息

Pharmacol Toxicol. 1987 Jan;60(1):51-3. doi: 10.1111/j.1600-0773.1987.tb01718.x.

Abstract

Haem arginate is a new haem compound recently introduced for treatment of porphyrias. Previously haematin has been reported to increase certain hydroxylase activities in extrahepatic tissues, but even in therapeutic doses it impairs the microsomal foreign substance metabolism in the liver. Haem arginate at a dose equivalent to haem 10 mg/kg (threefold therapeutic dose) did not prolong the hexobarbital sleeping time of mice, 20 mg/kg did prolong the hexobarbital and possibly also the ethanol sleeping time. Haem arginate administered in high doses prior to oral propranolol did not alter the bioavailability of the latter. With regard to drug interactions haem arginate may be safer than haematin.

摘要

精氨酸血红素是一种最近用于治疗卟啉症的新型血红素化合物。以前有报道称,高铁血红素可增加肝外组织中某些羟化酶的活性,但即使在治疗剂量下,它也会损害肝脏中的微粒体异物代谢。剂量相当于10mg/kg血红素(三倍治疗剂量)的精氨酸血红素不会延长小鼠的己巴比妥睡眠时间,20mg/kg则会延长己巴比妥睡眠时间,可能还会延长乙醇睡眠时间。在口服普萘洛尔之前高剂量给予精氨酸血红素不会改变后者的生物利用度。关于药物相互作用,精氨酸血红素可能比高铁血红素更安全。

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