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阿霉素对小鼠和大鼠心脏DNA合成的影响。

Effects of adriamycin on DNA synthesis in mouse and rat heart.

作者信息

Formelli F, Zedeck M S, Sternberg S S, Philips F S

出版信息

Cancer Res. 1978 Oct;38(10):3286-92.

PMID:688218
Abstract

Adriamycin induces an inhibition of DNA synthesis in mouse tissues within one hr after treatment. While the effects are short-lived in liver and small intestine, DNA synthesis in heart remains below control values for up to 7 days. After this period DNA synthesis in hearts of treated mice is elevated and remains above control values for as long as 4 weeks. Both 1-beta-D-arabinofuranosylcytosine and actinomycin D also induce inhibition of cardiac DNA synthesis soon after treatment; the effects of 1-beta-D-arabinofuranosylcytosine are over by the end of 24 hr while the effects of actinomycin D persist for at least 4 days. Actinomycin D treatment also induces an "over-shoot" of DNA synthesis in mouse heart. Adriamycin can induce a loss of prelabeled DNA from heart, although no pathological alterations are immediately obvious. The small intestine, however, shows extensive karyorrhexis. The initial effects on cardiac DNA synthesis occur in adrenalectomized animals, indicating that the effects are not mediated via the adrenal gland. We did find, however, that DNA synthesis in heart was sensitive to the effects of starvation. The results of this study indicate that inhibition of mouse heart DNA synthesis is not specific for Adriamycin and that the effects of Adriamycin in heart following a single treatment are long-lived.

摘要

阿霉素在治疗后1小时内可抑制小鼠组织中的DNA合成。虽然肝脏和小肠中的这种作用是短暂的,但心脏中的DNA合成在长达7天的时间内仍低于对照值。在此之后,经治疗小鼠心脏中的DNA合成升高,并在长达4周的时间内保持高于对照值。1-β-D-阿拉伯呋喃糖基胞嘧啶和放线菌素D在治疗后不久也会诱导心脏DNA合成受到抑制;1-β-D-阿拉伯呋喃糖基胞嘧啶的作用在24小时结束时消失,而放线菌素D的作用至少持续4天。放线菌素D处理也会诱导小鼠心脏中DNA合成的“过冲”现象。阿霉素可导致心脏中预先标记的DNA丢失,尽管没有立即出现明显的病理改变。然而,小肠显示出广泛的核碎裂。对心脏DNA合成的最初影响发生在肾上腺切除的动物中,这表明这些影响不是通过肾上腺介导的。不过,我们确实发现心脏中的DNA合成对饥饿的影响很敏感。这项研究的结果表明,小鼠心脏DNA合成的抑制并非阿霉素所特有的,单次治疗后阿霉素对心脏的影响是长期的。

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