Bacchi C J, Nathan H C, Hutner S H, McCann P P, Sjoerdsma A
Science. 1980 Oct 17;210(4467):332-4. doi: 10.1126/science.6775372.
alpha-Difluoromethylornithine (RMI 71,782), a specific irreversible inhibitor of the first step in polyamine biosynthesis, that is, the formation of putrescine from ornithine by ornithine decarboxylase, cures mice infected with a virulent, rodent-passaged strain of Trypanosoma brucei brucei. This parasite is closely related to the trypanosomes that cause human sleeping sickness. The drug, which is remarkably nontoxic, was effective when administered in drinking water or by intubation. The ability of the compound to inhibit ornithine decarboxylase in vitro was demonstrated by the reduced amounts of putrescine synthesized from tritiated ornithine in Trypanosoma brucei suspensions. These observations direct attention to polyamine metabolism as a target for chemotherapy of parasitic diseases.
α-二氟甲基鸟氨酸(RMI 71,782)是多胺生物合成第一步(即鸟氨酸通过鸟氨酸脱羧酶形成腐胺)的特异性不可逆抑制剂,可治愈感染了强毒性、经啮齿动物传代的布氏布氏锥虫菌株的小鼠。这种寄生虫与导致人类昏睡病的锥虫密切相关。该药物毒性极低,通过饮水或插管给药时均有效。在布氏锥虫悬浮液中,由氚标记的鸟氨酸合成的腐胺量减少,证明了该化合物在体外抑制鸟氨酸脱羧酶的能力。这些观察结果将注意力引向多胺代谢,使其成为寄生虫病化疗的一个靶点。