Tune B M, Browning M C, Hsu C Y, Fravert D
J Infect Dis. 1982 Feb;145(2):174-80. doi: 10.1093/infdis/145.2.174.
Prevention of cephalosporin nephrotoxicity in animal models by probenecid or p-aminohippurate requires treatment regimen that produce sustained inhibition of cortical accumulation of the toxic antibiotic. In contrast, cephaloridine nephrotoxicity in the rabbit can be prevented by a limited single dose of cephalothin. In the present report further studies were done in which it was demonstrated that cephaloridine nephrotoxicity can be prevented by doses of other cephalosporins or penicillins that produce little or no reduction of the cortical concentrations of toxic cephalosporin. More limited studies revealed similar protection by benzylpenicillin against cephaloglycin, also without reduction of cortical concentration. Finally, similar limited-dose administration of penicillin eliminated tha additive toxicity of cefazolin and neomycin. This selective protection against the toxic cephalosporins by the less toxic or nontoxic cephalosporins and by the penicillins, without inhibition of overall cortical accumulation of the toxic antibiotic, may provide a subcellular probe for the study of the molecular basis of cephalosporin nephrotoxicity.
在动物模型中,丙磺舒或对氨基马尿酸预防头孢菌素肾毒性需要采用能持续抑制有毒抗生素在皮质蓄积的治疗方案。相比之下,兔中的头孢利定肾毒性可通过单次有限剂量的头孢噻吩来预防。在本报告中进行了进一步研究,结果表明,其他头孢菌素或青霉素的剂量可预防头孢利定肾毒性,而这些剂量对有毒头孢菌素的皮质浓度几乎没有降低或没有降低作用。更有限的研究表明,苄青霉素对头孢甘氨酸也有类似的保护作用,同样不会降低皮质浓度。最后,类似的有限剂量青霉素给药消除了头孢唑林和新霉素的相加毒性。毒性较低或无毒的头孢菌素以及青霉素对有毒头孢菌素的这种选择性保护,而不抑制有毒抗生素在皮质的总体蓄积,可能为研究头孢菌素肾毒性的分子基础提供一种亚细胞探针。