Efficacy of fluoxetine and (R,S)-ketamine in attenuating conditioned fear behaviors in male mice.

IF 3.8 3区 医学 Q2 PHARMACOLOGY & PHARMACY Journal of Pharmacology and Experimental Therapeutics Pub Date : 2025-01-01 Epub Date: 2024-11-22 DOI:10.1124/jpet.124.002252
Megan Wells, Jan Hoffmann, Autumn Stage, Isabella Enger, Jayme Pomper, Lily Briggs, Amber LaCrosse
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Abstract

Post-traumatic stress disorder (PTSD) is caused by exposure to a traumatic or stressful event. Symptoms related to this disorder include persistent re-experiencing of memories and fear of generalization. Current pharmacological treatments for PTSD are insufficient, with fewer than 30% of patients reporting symptom remission. This study aims to determine the efficacy of acute (R,S)-ketamine and chronic fluoxetine (FLX) in reducing fear memory and fear generalization. In rodents, fear conditioning (FC) is commonly used in the literature to induce behaviors related to symptoms of PTSD, and the open field test (OFT) can assess anxiety and fear generalization behaviors during the exploration of a novel environment. In this study, FC consisted of a white noise cue stimulus and 4 inescapable foot shocks. Treatments began 4 hours after FC. Fear and anxiety behaviors were recorded during re-exposure to the FC stimuli at 24 hours and 2 weeks. The OFT was conducted 1 day before the last FC re-exposure. Results support the combined use of acute ketamine and chronic FLX as a treatment for reducing behaviors indicative of fear memory during re-exposure at 2 weeks, but not behaviors indicative of anxiety and fear generalization in the OFT. FLX alone was most effective in reducing behaviors related to fear generalization. This study contributes to the existing literature on pharmacological treatment for fear and anxiety behaviors relating to fear memory and fear generalization. Continued research is necessary to replicate results, optimize treatment protocols, and investigate the molecular adaptations to trauma and treatment. SIGNIFICANCE STATEMENT: Up to 6% of people in the United States will develop PTSD within their lifetime, and less than half of those individuals will find relief from their symptoms given the current therapeutic options. This study offers preliminary support for the efficacy of ketamine and FLX in reducing PTSD-like behaviors induced by fear-conditioning in mice. Compared with current standard treatments, the results of the current study indicate the potential for a more effective therapeutic option for those with stress-related disorders, such as PTSD.

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氟西汀和(R,S)-氯胺酮对雄性小鼠条件恐惧行为的抑制作用。
创伤后应激障碍(PTSD)是由于暴露于创伤或压力事件而引起的。与这种疾病相关的症状包括持续的记忆重现和对泛化的恐惧。目前创伤后应激障碍的药物治疗是不够的,只有不到30%的患者报告症状缓解。本研究旨在探讨急性(R,S)-氯胺酮和慢性氟西汀(FLX)在降低恐惧记忆和恐惧泛化方面的疗效。在啮齿动物中,文献中常用恐惧条件反射(FC)诱导与PTSD症状相关的行为,而开放场测试(OFT)可以评估探索新环境时的焦虑和恐惧泛化行为。在本研究中,FC由一个白噪声提示刺激和4个不可避免的足部冲击组成。FC后4小时开始治疗。分别于24小时和2周再次暴露于FC刺激时记录恐惧和焦虑行为。OFT在最后一次FC再暴露前1天进行。结果支持联合使用急性氯胺酮和慢性氟氯胺酮作为治疗,以减少2周后再次暴露时指示恐惧记忆的行为,但不能减少OFT中指示焦虑和恐惧泛化的行为。FLX在减少与恐惧泛化相关的行为方面是最有效的。本研究对恐惧记忆和恐惧泛化相关的恐惧和焦虑行为的药物治疗有一定的贡献。继续研究是必要的,以重复结果,优化治疗方案,并调查分子适应创伤和治疗。意义声明:在美国,高达6%的人会在他们的一生中患上PTSD,而在目前的治疗方案下,只有不到一半的人会从他们的症状中得到缓解。本研究初步支持氯胺酮和氟哌啶可减少小鼠恐惧条件反射诱导的ptsd样行为。与目前的标准治疗方法相比,目前的研究结果表明,对于那些与压力相关的疾病,如创伤后应激障碍,可能会有更有效的治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.90
自引率
0.00%
发文量
115
审稿时长
1 months
期刊介绍: A leading research journal in the field of pharmacology published since 1909, JPET provides broad coverage of all aspects of the interactions of chemicals with biological systems, including autonomic, behavioral, cardiovascular, cellular, clinical, developmental, gastrointestinal, immuno-, neuro-, pulmonary, and renal pharmacology, as well as analgesics, drug abuse, metabolism and disposition, chemotherapy, and toxicology.
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