Winsauer P J, Verrees J F, O'Halloran K P, Bixler M A, Mele P C
Behavioral Sciences Department, Armed Forces Radiobiology Research Institute, Bethesda, Maryland.
J Pharmacol Exp Ther. 1994 Jul;270(1):142-9.
Studies of radiation effects on performance are often complicated by concurrent radiation-induced decreases in feeding behavior (i.e., "anorexia"). To evaluate the pharmacological specificity of these decreases in food intake, the interactions of radiation with three prototypical drugs were studied. Single daily i.p. administration of a dose of chlordiazepoxide, ondansetron or 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT) was given to groups of rats for 5 days after either a single nonlethal 4.5-Gy dose of ionizing radiation (bremsstrahlung or gamma rays) or a sham exposure. The food intake for each group was measured 60 min and 24 hr after food presentation. Radiation alone significantly decreased food intake during the 60-min test on each treatment day and for the 5-day period when data were averaged. Chlordiazepoxide (1.8-18 mg/kg) and 8-OH-DPAT (0.1-1 mg/kg) produced significant dose-dependent increases in food intake during the 60-min test in both irradiated and sham-irradiated groups, whereas ondansetron (0.1-1 mg/kg) did not alter food intake at any dose tested. The dose effects at 60 min were significant on each treatment day for chlordiazepoxide, on 4 of 5 days for 8-OH-DPAT and for both drugs when data for all 5 days were combined. In no case, however, was a significant interaction obtained for radiation and any dose of the three drugs. After 24 hr, decreases in intake were obtained in a few subjects in 3 of 12 total radiation groups. These results suggest that radiation-induced decreases in food intake do not result from damage to the mechanisms by which chlordiazepoxide and 8-OH-DPAT increase food intake and that hyperphagic agents from these two different classes may have therapeutic value for attenuating radiation-induced anorexia.
辐射对行为影响的研究常常因辐射同时导致的摄食行为减少(即“厌食”)而变得复杂。为了评估这些食物摄入量减少的药理学特异性,研究了辐射与三种典型药物的相互作用。在给予大鼠单次非致死性4.5戈瑞剂量的电离辐射(轫致辐射或γ射线)或假照射后,连续5天每天给每组大鼠腹腔注射一剂氯氮卓、昂丹司琼或8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)。在提供食物后60分钟和24小时测量每组的食物摄入量。单独辐射在每个治疗日的60分钟测试期间以及在对数据进行平均的5天期间均显著降低了食物摄入量。在照射组和假照射组中,氯氮卓(1.8 - 18毫克/千克)和8-OH-DPAT(0.1 - 1毫克/千克)在60分钟测试期间均产生了显著的剂量依赖性食物摄入量增加,而昂丹司琼(0.1 - 1毫克/千克)在任何测试剂量下均未改变食物摄入量。氯氮卓在每个治疗日60分钟时的剂量效应均显著,8-OH-DPAT在5天中的4天显著,当将所有5天的数据合并时两种药物均显著。然而,在任何情况下,辐射与三种药物的任何剂量之间均未获得显著的相互作用。24小时后,在总共12个辐射组中的3组中,少数受试者的摄入量出现了下降。这些结果表明,辐射诱导的食物摄入量减少并非由氯氮卓和8-OH-DPAT增加食物摄入量的机制受损所致,并且来自这两个不同类别的促食欲剂可能对减轻辐射诱导的厌食具有治疗价值。