Hippocampus-dependent fear conditioning is not sensitized by muscarinic receptor activation following systemic injection of pilocarpine

Q3 Medicine
A.A. Hoeller , G. Lach , A.P.R. Costa , R. Walz , Z.A. Bortolotto , T.C.M. De Lima
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Abstract

The regulation of muscarinic acetylcholine receptors (mAChR) critically influences emotional outcomes. Previous researches indicate that a single systemic injection of pilocarpine – a mAChR agonist – displays long-term defensive behaviors in rats evaluated in distinct unconditioned tests up to 3 months following treatment. However, it is not clear whether these effects share underlying behavioral phenotypes involved in conditioned responses. With this in mind, we examined whether mAChR activation modulates contextual fear conditioning (CFC) and/or hippocampal synaptic plasticity. Adult male Wistar rats were injected with pilocarpine (150 mg/kg) and behaviorally evaluated in the CFC test or followed by synaptic plasticity (LTP/LTD) investigation in CA1 stratum radiatum of hippocampal slices. There was no difference between groups in the quantification of freezing behavior during the test period (24 h after treatment) besides a decrease of freezing 1 month later. Similarly, no changes were observed in rats conditioned 24 h later and tested 1 month after. Synaptic plasticity investigation following short- or long-term treatment revealed no differences between control and treated subjects. In summary, our results show that hippocampus-dependent fear behavior and memory consolidation mediated by hippocampal cholinergic inputs are not sensitive to activation of mAChR by a systemic nonconvulsant dose of pilocarpine. Therefore, we suggest that the long-term defensive behaviors and anxiogenic-like features displayed by pilocarpine observed in rats are mediated by different underlying mechanisms and or set of synapses.

全身注射匹罗卡品后,毒蕈碱受体激活不会使海马体依赖性恐惧条件反射增敏
毒蕈碱乙酰胆碱受体(mAChR)的调节对情绪结果有重要影响。先前的研究表明,单次全身注射匹罗卡品(一种mAChR激动剂)在治疗后3个月的不同无条件测试中显示出大鼠的长期防御行为。然而,尚不清楚这些影响是否与条件反应相关的潜在行为表型相同。考虑到这一点,我们研究了mAChR激活是否调节情境恐惧条件反射(CFC)和/或海马突触可塑性。给成年雄性Wistar大鼠注射匹罗卡品(150 mg/kg),进行CFC试验和海马CA1 辐射层突触可塑性(LTP/LTD)研究。在试验期间(处理后24 h),除1个月后冻结行为减少外,各组间冻结行为量化无差异。同样,在24 h后和1个月后进行测试的大鼠也没有观察到变化。短期或长期治疗后的突触可塑性调查显示对照组和治疗组之间没有差异。总之,我们的研究结果表明,由海马胆碱能输入介导的海马体依赖性恐惧行为和记忆巩固对全身非惊厥剂量的匹罗卡平激活mAChR不敏感。因此,我们认为在大鼠中观察到的毛罗卡品所表现出的长期防御行为和焦虑样特征是由不同的潜在机制和一组突触介导的。
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期刊介绍: Neurology, Psychiatry & Brain Research publishes original papers and reviews in biological psychiatry, brain research, neurology, neuropsychiatry, neuropsychoimmunology, psychopathology, psychotherapy. The journal has a focus on international and interdisciplinary basic research with clinical relevance. Translational research is particularly appreciated. Authors are allowed to submit their manuscript in their native language as supplemental data to the English version. Neurology, Psychiatry & Brain Research is related to the oldest German speaking journal in this field, the Centralblatt fur Nervenheilkunde, Psychiatrie und gerichtliche Psychopathologie, founded in 1878. The tradition and idea of previous famous editors (Alois Alzheimer and Kurt Schneider among others) was continued in modernized form with Neurology, Psychiatry & Brain Research. Centralblatt was a journal of broad scope and relevance, now Neurology, Psychiatry & Brain Research represents a journal with translational and interdisciplinary perspective, focusing on clinically oriented research in psychiatry, neurology and neighboring fields of neurosciences and psychology/psychotherapy with a preference for biologically oriented research including basic research. Preference is given for papers from newly emerging fields, like clinical psychoimmunology/neuroimmunology, and ideas.
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