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1-甲基-3-酮-4-苯基喹核溴化物(MA540)和胍乙啶对大鼠和犬的急性及靶器官毒性

The acute and target organ toxicity of 1-methyl-3-keto-4-phenylquinuclidinium bromide (MA540) and guanethidine in the rat and dog.

作者信息

Hartnagel R E, Phillips B M, Fonseca E H, Kowalski R L

出版信息

Arzneimittelforschung. 1976;26(9):1671-2.

PMID:1036698
Abstract

The effects of acute and repeated increasing oral doses of 1-methyl-3-keto-4-phenylquinuclidinium bromide (MA540) and guanethidine in the rat and dog have been described. On repeated oral administration guanethidine produced histopathological changes in cervical ganglia of rats and dogs which were clearly dose-dependent and reproduced lesions reported in the literature. Repeated oral administration of MA540 resulted in no histopathological changes in either species. The maximum tolerated oral dose for guanethidine was estimated to be 515 mg/kg in the rat and 26 mg/kg in the dog compared with an estimated maximum tolerated oral dose for MA540 of 1750 mg/kg in the rat and 460 mg/kg in the dog. On the basis of these findings it is suggested that subchronic studies with MA540 in the rat and dog should provide evidence which would justify the use of MA540 in man at daily oral doses as high as 9 mg/kg.

摘要

已描述了急性和重复递增口服剂量的1-甲基-3-酮-4-苯基喹核溴化物(MA540)和胍乙啶对大鼠和犬的影响。重复口服胍乙啶会在大鼠和犬的颈神经节产生组织病理学变化,这些变化明显呈剂量依赖性,并且重现了文献中报道的病变。重复口服MA540在两种动物中均未导致组织病理学变化。胍乙啶在大鼠中的最大耐受口服剂量估计为515 mg/kg,在犬中为26 mg/kg,而MA540在大鼠中的估计最大耐受口服剂量为1750 mg/kg,在犬中为460 mg/kg。基于这些发现,建议在大鼠和犬中进行MA540的亚慢性研究应能提供证据,证明MA540以高达9 mg/kg的每日口服剂量用于人体是合理的。

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