Prefrontal cortex-nucleus reuniens-hippocampus network exhibits sex-differentiated responses to stress and antidepressant treatment in rats.

IF 3.5 3区 医学 Q2 NEUROSCIENCES Psychopharmacology Pub Date : 2024-08-20 DOI:10.1007/s00213-024-06667-w
V Kafetzopoulos, N Kokras, Filippos Katsaitis, N Sousa, H Leite-Almeida, I Sotiropoulos, C Dalla
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Abstract

Rationale: Depression is a serious psychiatric disease, which is diagnosed twice as frequently in women than men. We have recently shown that lesioning or inactivation of the nucleus reuniens (RE), which interconnects the prefrontal cortex (PFC) and hippocampus, promoted resilience to stress in males, exerts an antidepressant effect in the Forced Swim Test (FST) and prevents the development of behavioral and neurobiological alterations induced by the chronic mild stress model of depression.

Objectives: In this study, we expand our findings on the FST in female rats and we investigate whether RE lesion presents sex differences following treatment with two distinct antidepressants, a selective serotonin reuptake inhibitor, i.e. sertraline and a tricyclic antidepressant, i.e. clomipramine.

Methods: Male and female rats received either a surgical lesion of the RE or sham operation, then treated with vehicle, sertraline (10mg/kg) or clomipramine (10mg/kg) and were subjected to the FST. Activation of key brain areas of interest (PFC, Hippocampus and RE) were measured by c-Fos immunoreactivity.

Results: RE lesion induced an antidepressant-like phenotype in both female and male rats, confirming its crucial role in the stress response. Similarly to RE lesion, sertraline treatment resulted in increased swimming and decreased immobility duration, as well as enhanced head shake frequency, in both sexes. Notably, climbing behavior was increased only following clomipramine treatment. RE area was less active in females compared to male rats and in clomipramine-treated males compared to their corresponding vehicle-group. Activation of the PFC and the CA1 hippocampal area was reduced in clomipramine-treated females, in comparison to vehicle-treated female rats. This effect was not evident in males, which exhibited less activation in the PFC and the hippocampus than females.

Conclusion: Re lesion proves equally effective in female and male rats, but sex is highlighted as a pivotal factor in behavioral and treatment response in FST, as well as in related circuit connectivity and activation.

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大鼠前额叶皮层-重聚核-海马体网络对压力和抗抑郁治疗表现出性别差异反应
理由抑郁症是一种严重的精神疾病,女性确诊抑郁症的比例是男性的两倍。我们最近的研究表明,对连接前额叶皮层(PFC)和海马的团圆核(RE)进行损伤或使其失活,可促进雄性大鼠对压力的恢复能力,在强迫游泳测试(FST)中发挥抗抑郁作用,并防止慢性轻度压力抑郁模型诱发的行为和神经生物学改变的发展:在本研究中,我们扩展了对雌性大鼠FST的研究结果,并探讨了两种不同的抗抑郁药(一种是选择性5-羟色胺再摄取抑制剂舍曲林,另一种是三环类抗抑郁药氯米帕明)治疗后RE病变是否存在性别差异:雄性和雌性大鼠分别接受RE手术损伤或假手术,然后接受药物、舍曲林(10毫克/千克)或氯米帕明(10毫克/千克)治疗,并进行FST试验。通过c-Fos免疫反应测量主要相关脑区(前区、海马和RE)的激活情况:结果:RE损伤可诱导雌性和雄性大鼠出现类似抗抑郁的表型,这证实了它在应激反应中的关键作用。与RE损伤相似,舍曲林治疗也会导致雌雄大鼠游泳时间增加、静止时间减少以及摇头频率增加。值得注意的是,只有在氯米帕明治疗后,攀爬行为才会增加。与雄性大鼠相比,雌性大鼠RE区域的活性较低,与相应的车辆组相比,氯米帕明治疗的雄性大鼠RE区域的活性较低。与接受药物治疗的雌性大鼠相比,接受氯米帕明治疗的雌性大鼠PFC和CA1海马区的激活程度降低。这种效应在雄性大鼠中并不明显,雄性大鼠的前脑功能区和海马区的激活程度低于雌性大鼠:结论:Re 损伤对雌性和雄性大鼠同样有效,但性别是影响 FST 行为和治疗反应以及相关回路连接和激活的关键因素。
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来源期刊
Psychopharmacology
Psychopharmacology 医学-精神病学
CiteScore
7.10
自引率
5.90%
发文量
257
审稿时长
2-4 weeks
期刊介绍: Official Journal of the European Behavioural Pharmacology Society (EBPS) Psychopharmacology is an international journal that covers the broad topic of elucidating mechanisms by which drugs affect behavior. The scope of the journal encompasses the following fields: Human Psychopharmacology: Experimental This section includes manuscripts describing the effects of drugs on mood, behavior, cognition and physiology in humans. The journal encourages submissions that involve brain imaging, genetics, neuroendocrinology, and developmental topics. Usually manuscripts in this section describe studies conducted under controlled conditions, but occasionally descriptive or observational studies are also considered. Human Psychopharmacology: Clinical and Translational This section comprises studies addressing the broad intersection of drugs and psychiatric illness. This includes not only clinical trials and studies of drug usage and metabolism, drug surveillance, and pharmacoepidemiology, but also work utilizing the entire range of clinically relevant methodologies, including neuroimaging, pharmacogenetics, cognitive science, biomarkers, and others. Work directed toward the translation of preclinical to clinical knowledge is especially encouraged. The key feature of submissions to this section is that they involve a focus on clinical aspects. Preclinical psychopharmacology: Behavioral and Neural This section considers reports on the effects of compounds with defined chemical structures on any aspect of behavior, in particular when correlated with neurochemical effects, in species other than humans. Manuscripts containing neuroscientific techniques in combination with behavior are welcome. We encourage reports of studies that provide insight into the mechanisms of drug action, at the behavioral and molecular levels. Preclinical Psychopharmacology: Translational This section considers manuscripts that enhance the confidence in a central mechanism that could be of therapeutic value for psychiatric or neurological patients, using disease-relevant preclinical models and tests, or that report on preclinical manipulations and challenges that have the potential to be translated to the clinic. Studies aiming at the refinement of preclinical models based upon clinical findings (back-translation) will also be considered. The journal particularly encourages submissions that integrate measures of target tissue exposure, activity on the molecular target and/or modulation of the targeted biochemical pathways. Preclinical Psychopharmacology: Molecular, Genetic and Epigenetic This section focuses on the molecular and cellular actions of neuropharmacological agents / drugs, and the identification / validation of drug targets affecting the CNS in health and disease. We particularly encourage studies that provide insight into the mechanisms of drug action at the molecular level. Manuscripts containing evidence for genetic or epigenetic effects on neurochemistry or behavior are welcome.
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