Boutin B K, Peeler J T, Twedt R M
Food and Drug Administration, Division of Microbiology, Cincinnati, Ohio.
J Toxicol Environ Health. 1989;26(1):75-81. doi: 10.1080/15287398909531234.
Purified Alternaria alternata altertoxins I, II, and III were evaluated for comparative cytotoxicity and ability to inhibit gap junction communication in the Chinese hamster lung metabolic cooperation assay. The noncytotoxic test range for each altertoxin was determined for the metabolic communication assays: altertoxin I, 1, 2, 3, 4, 5 micrograms/ml; altertoxin II, 0.02, 0.008, 0.006, 0.004, 0.002, 0.0008 micrograms/ml; and altertoxin III, 0.2, 0.1, 0.08, 0.06, 0.04 micrograms/ml. Altertoxin II was the most cytoxic in the V79 system, followed by altertoxins III and I. The last cytotoxic of the three, altertoxin I, weakly disrupted metabolic communication at two concentrations (4 and 5 micrograms/ml). Altertoxins III and II did not significantly inhibit gap junction communication more than the weak tumor promoter 4-O-methyl ether tetradecanoylphorbol 13-acetate.
对纯化的链格孢菌互隔交链孢毒素I、II和III进行了评估,以比较它们在中华仓鼠肺代谢合作试验中的细胞毒性和抑制间隙连接通讯的能力。确定了每种互隔交链孢毒素在代谢通讯试验中的无细胞毒性测试范围:互隔交链孢毒素I为1、2、3、4、5微克/毫升;互隔交链孢毒素II为0.02、0.008、0.006、0.004、0.002、0.0008微克/毫升;互隔交链孢毒素III为0.2、0.1、0.08、0.06、0.04微克/毫升。在V79系统中,互隔交链孢毒素II的细胞毒性最强,其次是互隔交链孢毒素III和I。这三种毒素中细胞毒性最小的互隔交链孢毒素I,在两个浓度(4和5微克/毫升)下对代谢通讯的干扰较弱。互隔交链孢毒素III和II对间隙连接通讯的抑制作用并不比弱肿瘤启动子4-O-甲基醚十四烷酰佛波醇13-乙酸酯更显著。