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

B F Dorofeev, V B Chiger, A G Moiseenok
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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.

[含钙泛酸衍生物在链霉素中毒中的抗毒作用的可能机制]。
采用不同给药途径给药泛酸钙盐(CPN)、4'-磷酸泛酸钙盐(CPP)、s -硫泛酸钙盐(CSP)以及泛酸钙盐和泛醇钙盐,研究给药途径对链霉素(500 mg/kg,皮下)急性毒性的影响。结果表明,CPN、CPP和CSP皮下、肌肉、腹腔和静脉给药对链霉素的急性毒性较低。ED50值和抗毒作用范围(LD50/ED50)表明CPP静脉给药效果良好。在大鼠中,所有测试的化合物都使因暴露于亚毒性剂量(200 mg/kg)的链霉素而受损的肝脏排泄功能(溴磺胺试验)正常化。在链霉素与CPN、CPP或CSP联合治疗的动物中,磺胺基钠试验剂量的乙酰化水平最低,这可能是由于抗生素的排泄和乙酰化(解毒)增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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