[Effect of pepstatin A on Candida albicans infection in the mouse].

Dermatologische Monatschrift Pub Date : 1990-01-01
C Zotter, U F Haustein, C Schönborn, H D Grimmecke, H Wand
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Abstract

The intravenous injection of 10(6) to 10(7) Candida albicans cells revealed to be a reliable model in mice produce infections of the kidney. Higher germ contents could be yielded in the kidney after the application of protease positive Candida-strains as compared to protease negative ones. Additionally, after the infection with protease positive strains a proteolytic activity could be found in the kidney homogenates in vitro on casein plates. The modulation of this Candida infection by pepstatin A, an inhibitor of extracellular yeast proteases in vitro, has also been studied in the same mice model in vivo. The growth rate of Candida albicans has been measured in the left kidney by counting the germ content as described by Haenel. Infections could be reduced after single doses of 120 micrograms pepstatin A contrary to 60 micrograms pepstatin A. The same was with three doses of 180 micrograms at 24 h intervals. This protease inhibitory effect could also be found in kidney homogenates in vitro on casein plates and lasted until 48 h post injection. On the basis of this positive effects on the Candida infection in mice pepstatin A should be considered as an adjuvans in the therapy of severe yeast infections.

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[胃抑素A对小鼠白色念珠菌感染的影响]。
静脉注射10(6)~ 10(7)个白色念珠菌细胞是小鼠肾脏感染的可靠模型。与蛋白酶阴性念珠菌菌株相比,应用蛋白酶阳性念珠菌菌株可在肾脏中产生更高的细菌含量。另外,蛋白酶阳性菌株感染后,肾脏匀浆在酪蛋白板上具有蛋白水解活性。体外细胞外酵母菌蛋白酶抑制剂pepstatin A对这种念珠菌感染的调节也在同一小鼠体内模型中进行了研究。白色念珠菌的生长速度已在左肾通过计数细菌含量的描述Haenel测量。与60微克胃抑素A相比,单次给药120微克胃抑素A可以减少感染。每隔24小时给药3次,每次给药180微克,同样可以减少感染。这种蛋白酶抑制作用在离体肾匀浆酪蛋白板上也能发现,并持续到注射后48 h。在此基础上,胃抑素A对小鼠念珠菌感染的积极作用,应考虑作为一种佐剂治疗严重酵母菌感染。
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