Resstel L B M, Joca S R L, Guimarães F G, Corrêa F M A
Department of Pharmacology, School of Medicine of Ribeirão Preto, University of São Paulo, 14049-900, Ribeirão Preto, São Paulo, Brazil.
Neuroscience. 2006 Dec 1;143(2):377-85. doi: 10.1016/j.neuroscience.2006.08.002. Epub 2006 Sep 14.
To explore the ventral medial prefrontal cortex (vMPFC) involvement in behavioral and autonomic fear-conditioned responses to context, vMPFC synaptic transmission was temporarily inhibited by bilateral microinjections of 200 nL of the nonselective synapse blocker CoCl(2) (1 mM). Behavioral activity (freezing, motor activity and rearing) as well as evoked cardiovascular responses (arterial pressure and heart rate) was analyzed. Rats were pre-exposed to the footshock chamber (context) and shock stimulus was used unconditioned stimulus. During re-exposure to context, conditioned rats spent 80% of the session in freezing while non-conditioned rats (no shock group) spent less than 15% of the session time in freezing. Conditioned rats had significantly lower activity scores than non-conditioned animals. Exposure to context increased mean arterial pressure (MAP) and heart rate (HR) of both groups. MAP and HR of the conditioned animals were markedly increased and remained at a high and stable level, whereas MAP and HR increases in non-conditioned animals were less pronounced and declined during the session. CoCl(2) microinjected in the vMPFC significantly reduced freezing and attenuated MAP and HR increase of the conditioned group. Cobalt-induced vMPFC inhibition also significantly reduced MAP and HR increase observed in non-conditioned animals, without any behavioral changes. The effect of vMPFC acute ablation on MAP and HR did not seem to be specific to the fear response because they were also evident in non-conditioned animals. The results indicate that vMPFC integrity is crucial for expression of fear-conditioned responses to context, such as freezing and cardiovascular changes, suggesting that fear-conditioned responses to context involve cortical processing prior to amygdalar output. They also indicate a cardiovascular response observed during re-exposure of non-conditioned rats to the context is completely dependent on vMPFC integrity.
为了探究腹内侧前额叶皮质(vMPFC)在对环境的行为和自主恐惧条件反应中的作用,通过双侧微量注射200 nL非选择性突触阻断剂CoCl₂(1 mM)暂时抑制vMPFC的突触传递。分析行为活动(僵住、运动活动和竖毛)以及诱发的心血管反应(动脉压和心率)。将大鼠预先暴露于足底电击箱(环境),并使用电击刺激作为非条件刺激。在再次暴露于该环境期间,条件性大鼠在80%的测试时段内处于僵住状态,而非条件性大鼠(无电击组)在僵住状态下的测试时段时间不到15%。条件性大鼠的活动得分显著低于非条件性动物。暴露于该环境会使两组动物的平均动脉压(MAP)和心率(HR)升高。条件性动物的MAP和HR显著升高并维持在较高且稳定的水平,而非条件性动物的MAP和HR升高不太明显且在测试时段内下降。向vMPFC微量注射CoCl₂可显著降低条件性大鼠的僵住程度,并减弱其MAP和HR的升高。钴诱导的vMPFC抑制还显著降低了非条件性动物中观察到的MAP和HR升高,但未引起任何行为变化。vMPFC急性损毁对MAP和HR的影响似乎并非特定于恐惧反应,因为在非条件性动物中也很明显。结果表明,vMPFC的完整性对于对环境的恐惧条件反应的表达至关重要,如僵住和心血管变化,这表明对环境的恐惧条件反应在杏仁核输出之前涉及皮质处理。它们还表明,非条件性大鼠再次暴露于该环境期间观察到的心血管反应完全依赖于vMPFC的完整性。