Levi F, Halberg F, Haus E, Sanchez de la Peña S, Sothern R B, Halberg E, Hrushesky W, Brown H, Scheving L E, Kennedy B J
Chronobiologia. 1980 Apr-Jun;7(2):227-44.
An attempt to pre-set the circadian rhythm in murine chronotolerance for adriamycin (ADR) given i.p. or i.v. with ACTH was performed in three studies. In CDF1 mice standardized in LD12:12, it was demonstrated that 1) the circadian rhythm in murine chronotolerance for ADR exhibits a different timing depending upon whether the intravenous or intraperitoneal route is used for the administration of this anticancer agent; 2) ACTH or saline pretreatment does not enhance optimal circadian-stage-qualified ADR tolerance, whatever its route of injection, with any of the circadian stages and schedules explored; 3) near-optimal tolerance can be achieved by a fixed 'best' interval (among those investigated) between ACTH and ADR, irrespective of circadian stage. Tolerance equivalent to optimal circadian-stage-qualified ADR tolerance results from the administration of ACTH 1-17 (HOE433 = Synchrodyn) 24 hours before ADR injection; 4) and acrophase advance of over 6 hours of the tolerance rhythm results from ACTH 1-17 administration at 6 HALO. The acrophase changes do not directly account for an optimal ADR tolerance at a fixed interval of 24 hours after ACTH 1-17. Thus, ACTH may be considered a potential relative chronizer of murine chronotolerance for ADR.
在三项研究中尝试预先设定小鼠对腹腔注射或静脉注射阿霉素(ADR)与促肾上腺皮质激素(ACTH)联合使用时的昼夜耐受性节律。在光暗周期为12:12的标准化CDF1小鼠中,结果表明:1)小鼠对ADR的昼夜耐受性节律的时间因使用静脉注射还是腹腔注射这种抗癌药物而有所不同;2)无论注射途径如何,在探索的任何昼夜阶段和给药方案下,ACTH或生理盐水预处理均不能增强最佳昼夜阶段合格的ADR耐受性;3)无论昼夜阶段如何,通过ACTH和ADR之间固定的“最佳”间隔(在所研究的间隔中)可实现接近最佳的耐受性。在ADR注射前24小时给予促肾上腺皮质激素1-17(HOE433 = Synchrodyn)可产生与最佳昼夜阶段合格的ADR耐受性相当的耐受性;4)在6个时相提前量(HALO)时给予促肾上腺皮质激素1-17会导致耐受性节律的峰相位提前超过6小时。峰相位变化并不能直接解释在促肾上腺皮质激素1-17后24小时固定间隔时的最佳ADR耐受性。因此,ACTH可被视为小鼠对ADR昼夜耐受性的潜在相对时间调节剂。