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[泛酸钙衍生物在链霉素中毒时抗毒作用的可能机制]

[Possible mechanisms of the antitoxic action of calcium-containing derivatives of pantothenic acid in streptomycin poisoning].

作者信息

Dorofeev B F, Chiger V B, Moiseenok A G

出版信息

Antibiot Med Biotekhnol. 1987 Dec;32(12):906-10.

PMID:3439795
Abstract

Calcium salts of pantothenate (CPN), 4'-phosphopantothenate (CPP), S-sulfopantetheine (CSP), as well as pantetheine and panthenol were administered to mice by various routes and the influence of the administration route on acute toxicity of streptomycin (500 mg/kg, subcutaneously) was studied. It was shown that with subcutaneous, intramuscular, intraperitoneal and intravenous administration of CPN, CPP and CSP the acute toxicity of streptomycin was lower. The value of ED50 and the ranges of the antitoxic action (LD50/ED50) were indicative of high efficacy of CPP on its intravenous administration. In rats all the tested compounds normalized the liver excreting function (bromsulphalein test) impaired by exposure to streptomycin in subtoxic doses (200 mg/kg). The lowest levels of acetylation of the sulfacyl sodium test dose were observed in the animals treated with streptomycin in combination with CPN, CPP or CSP which could be explained by increased excretion and acetylation (detoxication) of the antibiotic.

摘要

泛酸盐(CPN)、4'-磷酸泛酸盐(CPP)、S-磺基泛酰巯基乙胺(CSP)的钙盐以及泛酰巯基乙胺和泛醇通过不同途径给予小鼠,并研究给药途径对链霉素(500mg/kg,皮下注射)急性毒性的影响。结果表明,通过皮下、肌肉、腹腔和静脉注射CPN、CPP和CSP,链霉素的急性毒性较低。ED50值和抗毒作用范围(LD50/ED50)表明CPP静脉给药时具有高效性。在大鼠中,所有受试化合物均使因亚毒性剂量(200mg/kg)链霉素暴露而受损的肝脏排泄功能(溴磺酚酞试验)恢复正常。在用链霉素与CPN、CPP或CSP联合治疗的动物中,观察到磺胺酰钠试验剂量的乙酰化水平最低,这可能是由于抗生素排泄和乙酰化(解毒)增加所致。

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