Department of Neuroscience, University of Siena, Via Moro, 4, 53100 Siena, Italy.
Pharmacol Biochem Behav. 2011 Oct;99(4):749-58. doi: 10.1016/j.pbb.2011.06.031. Epub 2011 Jul 1.
Repeated unavoidable stress induces in rats decreased reactivity to avoidable stressors and an anhedonia-like condition that are reverted by long-term antidepressant treatments and regarded as models of core symptoms of depression. Morphine-sensitized rats present resilience to stress-induced behavioral deficits and, if hyporeactivity to stress models a depressive symptom, stress resistance can be regarded as a manic symptom. This hypothesis is supported by the observation that long-term lithium administration reinstates sensitivity to stress in sensitized rats. The first aim of the study was to examine the effects of carbamazepine, a standard antimanic treatment, on the stress resilience of sensitized rats, to further characterize morphine sensitization as a model of manic symptom. Carbamazepine administration abolished stress resilience but did not interfere with the expression of sensitization. The second aim of the study was to assess whether repeated carbamazepine treatment affected the dopaminergic and behavioral responses to a natural reward, a palatable food (vanilla sugar, VS), in non food-deprived sensitized and control rats and compare these possible effects with those of repeated lithium administration. Control and sensitized rats showed increased extraneuronal dopamine levels in the nucleus accumbens shell after VS consumption and competence to acquire an instrumental VS-sustained appetitive behavior (VAB). Repeated carbamazepine treatment abolished the dopaminergic response to VS consumption and disrupted the competence to acquire VAB in control rats. Lithium-treated rats showed a dopaminergic response to VS and easily acquired the appetitive behavior. In sensitized rats, neither carbamazepine nor lithium administration interfered with the dopaminergic response to VS and the acquisition of VAB. In summary, the effect of carbamazepine on the stress resilience of sensitized rats further supported the hypothesis that morphine sensitization might model some symptoms of mania. Moreover, in control rats carbamazepine treatment elicited an anhedonia-like condition that clearly distinguished the effects of this drug from those of lithium.
反复不可避免的应激会导致大鼠对可避免的应激源的反应性降低,并产生快感缺失样状态,这两种状态可通过长期抗抑郁治疗得到逆转,并被认为是抑郁核心症状的模型。吗啡敏化大鼠对应激引起的行为缺陷具有弹性,如果对压力的低反应性模拟抑郁症状,那么对压力的抵抗力可以被视为躁狂症状。这一假设得到了以下观察结果的支持:长期给予锂可恢复敏化大鼠对压力的敏感性。研究的第一个目的是研究卡马西平(一种标准的抗躁狂药物)对敏化大鼠应激弹性的影响,以进一步将吗啡敏化作为躁狂症状的模型。卡马西平给药消除了应激弹性,但不干扰敏化的表达。研究的第二个目的是评估重复卡马西平治疗是否会影响多巴胺能和行为对自然奖赏(美味糖,VS)的反应,在非食物剥夺的敏化和对照大鼠中,并将这些可能的影响与重复锂治疗进行比较。对照和敏化大鼠在消耗 VS 后,伏隔核壳内的细胞外多巴胺水平增加,并且具有获得仪器性 VS 维持的食欲行为(VAB)的能力。重复卡马西平治疗消除了 VS 消耗后的多巴胺反应,并破坏了对照大鼠获得 VAB 的能力。锂处理的大鼠对 VS 表现出多巴胺反应,并且容易获得食欲行为。在敏化大鼠中,卡马西平和锂治疗均不干扰 VS 的多巴胺反应和 VAB 的获得。总之,卡马西平对敏化大鼠应激弹性的影响进一步支持了吗啡敏化可能模拟某些躁狂症状的假设。此外,在对照大鼠中,卡马西平治疗引起快感缺失样状态,这清楚地区分了该药物与锂的作用。