Koo Myoung-Seo, Ozawa Tomoko, Santos Raquel A, Lamborn Kathleen R, Bollen Andrew W, Deen Dennis F, Kahl Stephen B
Department of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, California 94143, USA.
J Med Chem. 2007 Feb 22;50(4):820-7. doi: 10.1021/jm060895b. Epub 2007 Jan 25.
Three structurally similar tetraphenylporphyrins bearing polyhedral borane anions have been synthesized and their toxicological profiles obtained in rats. These conjugates were found to have quite different acute toxicities as manifested at the maximum tolerated dose (MTD). When given at the MTD and observed over 28 days, the most acutely toxic porphyrin was found to be devoid of toxicity, as measured by blood chemistry panels. The remaining two less acutely toxic compounds both elicited significant changes, characterized by moderate to severe thrombocytopenia, failure to gain weight normally and changes in liver enzymes indicative of mild hepatotoxicity. All toxic effects were transient, with platelets rebounding to above normal levels at day 28. We conclude that thrombocytopenia is the dose limiting toxicity for boronated porphyrins in mammals and suggest that these effects may be due to the porphyrin, not the borane or carborane.
已合成了三种带有多面体硼烷阴离子的结构相似的四苯基卟啉,并在大鼠身上获得了它们的毒理学特征。这些共轭物在最大耐受剂量(MTD)时表现出截然不同的急性毒性。当以MTD给药并观察28天时,通过血液化学指标测定发现,毒性最强的卟啉并无毒性。其余两种毒性稍弱的化合物均引发了显著变化,表现为中度至重度血小板减少、体重未能正常增加以及肝酶变化,提示存在轻度肝毒性。所有毒性作用都是短暂的,血小板在第28天反弹至正常水平以上。我们得出结论,血小板减少是硼化卟啉在哺乳动物中的剂量限制性毒性,并表明这些作用可能归因于卟啉,而非硼烷或碳硼烷。