Adriani Walter, Laviola Giovanni
Section of Behavioural Pathophysiology, Lab. Fisiopatologia O.S., Istituto Superiore di Sanitá, viale Regina Elena 299, Roma, Italy.
Neuropsychopharmacology. 2002 Aug;27(2):225-36. doi: 10.1016/S0893-133X(02)00300-7.
Individual differences in coping with novelty and in the response to psychoactive drugs have been related to early life events, such as the age of weaning. Outbred CD-1 mice underwent a precocious (postnatal day (pnd) 15, Wean-15 group), regular (pnd 21, Wean-21 group), or delayed (pnd 27, Wean-27 group) weaning, and were tested as adults (pnd > 60). In Experiment 1, animals underwent a treatment history with d-amphetamine (AMPH 0, 1, or 5 mg/kg once/day for three days) in a familiar environment. On testing day, mice were challenged with SAL or a standard 1 mg/kg AMPH dose (to evaluate acute drug effects and sensitization), and placed in the familiar environment. As expected, regular Wean-21 animals showed an AMPH-induced hyperactivity and a profile of conditioned locomotion, whereas the same dosage failed to induce any change in Wean-15 and Wean-27 groups. Levels of spontaneous novelty seeking were particularly elevated for Wean-27 mice, when compared with the other weaning groups. In Experiment 2, pairing of AMPH administration (0, 1, 2, 3.3, or 5 mg/kg once/day for three days) with a distinct environment produced a classical conditioned place preference. The magnitude of the preference profile was significantly more marked for Wean-15 mice, when compared with the other two weaning groups. Both experiments also provided evidence that the development of sensitization was particularly evident in Wean-27 mice. In summary, delayed weaning was associated in adult mice with both elevated levels of novelty seeking and increased sensitization to drug effects. Conversely, animals weaned precociously were much more responsive to AMPH-induced incentive conditioning. These results appear relevant to the issue of early experiences as possible risk factors for a number of psychiatric disorders in humans, including the abuse of drugs.
应对新事物和对精神活性药物反应的个体差异与早期生活事件有关,比如断奶年龄。远交群CD-1小鼠经历了早熟(出生后第15天,15日龄断奶组)、正常(出生后第21天,21日龄断奶组)或延迟(出生后第27天,27日龄断奶组)断奶,并在成年期(出生后第60天之后)接受测试。在实验1中,动物在熟悉的环境中接受了d-苯丙胺(0、1或5毫克/千克,每天一次,共三天)的治疗过程。在测试日,小鼠接受生理盐水或标准的1毫克/千克苯丙胺剂量挑战(以评估急性药物效应和致敏作用),并被置于熟悉的环境中。正如预期的那样,正常断奶的21日龄断奶组动物表现出苯丙胺诱导的多动和条件性运动模式,而相同剂量在15日龄断奶组和27日龄断奶组中未能诱导任何变化。与其他断奶组相比,27日龄断奶组小鼠的自发新奇寻求水平尤其升高。在实验2中,将苯丙胺给药(0、1、2、3.3或5毫克/千克,每天一次,共三天)与一个独特的环境配对产生了经典的条件性位置偏爱。与其他两个断奶组相比,15日龄断奶组小鼠的偏爱模式程度明显更显著。两个实验还提供了证据表明致敏作用的发展在27日龄断奶组小鼠中尤为明显。总之,延迟断奶在成年小鼠中与新奇寻求水平升高和对药物效应的致敏作用增加有关。相反,早熟断奶的动物对苯丙胺诱导的诱因条件作用反应更强。这些结果似乎与早期经历作为人类多种精神疾病(包括药物滥用)可能的风险因素这一问题相关。