Came P E, O'Connor J R, Dobson R A, Wagner R B, Fabian R J
Antimicrob Agents Chemother. 1979 Dec;16(6):813-22. doi: 10.1128/AAC.16.6.813.
Win 42122-2 is a new aminoglycoside antibiotic obtained from a mutant strain of Micromonospora purpurea. In vitro and in vivo comparisons of Win 42122-2 with gentamicin and amikacin revealed that Win 42122-2 generally was less active than gentamicin against Pseudomonas and many Enterobacteriacae, especially Klebsiella and indole-negative Proteus. Against most gentamicin-susceptible isolates, Win 42122-2 was more active than amikacin. Gentamicin-resistant clinical isolates were usually resistant to Win 42122-2, although it was active against certain gentamicin-resistant organisms, depending upon the aminoglycoside-modifying enzymes harbored by the organism. However, Win 42122-2 was markedly less toxic than gentamicin in subacute nephrotoxicity studies in rats, ototoxicity experiments in guinea pigs, and ataxia determinations in cats. This series of antibacterial determinations and toxicity evaluations indicated that the reduced toxicity of the antibiotic may be sufficient to provide an improved therapeutic ratio over gentamicin and other aminoglycosides, even though Win 42122-2 is less potent than gentamicin against some bacteria.
温42122 - 2是从紫色小单孢菌的一个突变菌株中获得的一种新型氨基糖苷类抗生素。对温42122 - 2与庆大霉素和阿米卡星进行的体外和体内比较显示,在针对假单胞菌和许多肠杆菌科细菌(尤其是克雷伯菌属和吲哚阴性变形杆菌)方面,温42122 - 2的活性通常低于庆大霉素。在针对大多数对庆大霉素敏感的分离株时,温42122 - 2比阿米卡星更具活性。耐庆大霉素的临床分离株通常对温42122 - 2也耐药,不过它对某些耐庆大霉素的微生物有活性,这取决于该微生物所携带的氨基糖苷修饰酶。然而,在大鼠的亚急性肾毒性研究、豚鼠的耳毒性实验以及猫的共济失调测定中,温42122 - 2的毒性明显低于庆大霉素。这一系列的抗菌测定和毒性评估表明,尽管温42122 - 2对某些细菌的效力低于庆大霉素,但其较低的毒性可能足以提供比庆大霉素和其他氨基糖苷类药物更高的治疗指数。