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用孢子霉素处理的小鼠的组织药代动力学及DNA合成抑制

Tissue pharmacokinetics and inhibition of DNA synthesis in mice treated with sporamycin.

作者信息

Komiyama K, Umezawa I

出版信息

J Antibiot (Tokyo). 1978 May;31(5):473-6. doi: 10.7164/antibiotics.31.473.

Abstract

Examination of blood and organ concentrations of sporamycin in normal mice showed a rapid decrease of sporamycin from peripheral blood and a high level of sporamycin in urine 10 minutes after intravenous injection of the antibiotic. At the same time, the highest level was found in the kidneys and low levels were found in the lungs and spleen. When sporamycin was added to mouse organ homogenate at 37 degrees C, remarkable inactivation of sporamycin by the homogenate of the liver, kidney, testis, etc., was noted but this inactivation was slight by tumor homogenate. Sporamycin inhibited the tritiated thymidine incorporation into DNA of normal tissues, but a different pattern of inhibition and recovery on the incorporation of 3H-TdR into DNA was observed among mouse organs. It was noted that the antibiotic may damage normal tissues in spite of a rapid excretion and inactivation of sporamycin in mice, but this damage was recovered rapidly within 1 approximately 2 days after the treatment.

摘要

对正常小鼠体内sporamycin的血液和器官浓度进行检测发现,静脉注射该抗生素10分钟后,外周血中的sporamycin迅速减少,尿液中的sporamycin水平较高。与此同时,在肾脏中发现sporamycin水平最高,而在肺和脾脏中发现水平较低。当在37摄氏度下将sporamycin添加到小鼠器官匀浆中时,发现肝脏、肾脏、睾丸等的匀浆对sporamycin有显著的灭活作用,但肿瘤匀浆的这种灭活作用较弱。Sporamycin抑制氚标记胸腺嘧啶核苷掺入正常组织的DNA,但在小鼠器官中观察到3H-TdR掺入DNA的抑制和恢复模式不同。值得注意的是,尽管sporamycin在小鼠体内排泄和灭活迅速,但该抗生素仍可能损害正常组织,但这种损害在治疗后1至2天内迅速恢复。

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