Hofflin J M, Remington J S
Antimicrob Agents Chemother. 1987 Apr;31(4):492-6. doi: 10.1128/AAC.31.4.492.
We investigated the efficacy of clindamycin in a murine model of toxoplasmic encephalitis using direct intracerebral inoculation. Clindamycin reduced mortality from 40% in normal mice and 100% in cortisone-treated mice to 0% in both groups. Although we were unable to document appreciable levels of clindamycin in the brains of infected mice, the histological features of cerebral infection were markedly altered. The formation of large numbers of cysts and the intense inflammatory response seen in the brains of normal mice and the unchecked infection and tissue necrosis in the brains of cortisone-treated mice were absent in the brains of clindamycin-treated mice. Enumeration of cysts in the brains of mice 10 weeks after infection revealed a significantly lower number in the clindamycin-treated mice. Spread of infection to other organs was also decreased during clindamycin administration. These observations suggest that clindamycin may have a role in the therapy of toxoplasmic encephalitis.
我们通过直接脑内接种,在鼠类弓形虫性脑炎模型中研究了克林霉素的疗效。克林霉素使正常小鼠的死亡率从40%以及经可的松治疗小鼠的死亡率从100%均降至两组的0%。尽管我们未能证明感染小鼠脑内有可观水平的克林霉素,但脑内感染的组织学特征有显著改变。在克林霉素治疗的小鼠脑内,未出现正常小鼠脑内大量囊肿的形成及强烈炎症反应,也未出现经可的松治疗小鼠脑内未受控制的感染及组织坏死。感染10周后对小鼠脑内囊肿计数显示,克林霉素治疗组小鼠的囊肿数量显著减少。在给予克林霉素期间,感染向其他器官的扩散也有所减少。这些观察结果表明,克林霉素可能在弓形虫性脑炎的治疗中发挥作用。