Al-Damluji S, Grossman A, Turner P, Besser G M
Br J Clin Pharmacol. 1987 Jul;24(1):96-9. doi: 10.1111/j.1365-2125.1987.tb03142.x.
The purpose of this study was to investigate whether the alpha 1-adrenoceptor antagonist thymoxamine possesses antihistaminic activity in clinical doses in man, as has been reported on the guinea pig ileum in vitro. Five normal subjects were given on three separate occasions intravenous infusions of thymoxamine (0.15 mg kg-1 loading dose followed by 0.15 mg kg-1 h-1), chlorpheniramine (1.5 mg loading dose followed by 1.5 mg h-1) and normal saline (placebo). Intravenous bolus doses of histamine (1 and 2 micrograms kg-1) were given after pretreatment with propranolol 10 mg to block the beta-adrenoceptor agonist effects of the catecholamines released by the histamine injections. Histamine caused a dose-dependent reduction of FEV1 and FVC that was antagonised by chlorpheniramine but not by thymoxamine, suggesting that thymoxamine has no antihistaminic activity in the doses used in man. Thymoxamine caused a small enhancement of the bronchoconstrictor effect of the lower dose of histamine. The relatively selective action of thymoxamine makes it a suitable agent for the investigation of alpha 1-adrenoceptors.
本研究的目的是调查α1肾上腺素能受体拮抗剂百里胺在人体临床剂量下是否具有抗组胺活性,正如在豚鼠回肠体外实验中所报道的那样。五名正常受试者在三个不同的场合分别接受了静脉输注百里胺(负荷剂量0.15mg/kg,随后以0.15mg/kg·h-1持续输注)、氯苯那敏(负荷剂量1.5mg,随后以1.5mg/h持续输注)和生理盐水(安慰剂)。在用10mg普萘洛尔预处理以阻断组胺注射释放的儿茶酚胺的β肾上腺素能激动剂作用后,静脉推注组胺(1和2μg/kg)。组胺导致FEV1和FVC呈剂量依赖性降低,氯苯那敏可拮抗这种降低,但百里胺不能,这表明百里胺在人体所用剂量下没有抗组胺活性。百里胺使较低剂量组胺的支气管收缩作用略有增强。百里胺的相对选择性作用使其成为研究α1肾上腺素能受体的合适药物。