Fear generalization modulated by shock intensity and protein synthesis inhibitor.

IF 3.5 3区 医学 Q2 NEUROSCIENCES
Psychopharmacology Pub Date : 2024-12-01 Epub Date: 2024-08-06 DOI:10.1007/s00213-024-06662-1
Xinwen Dong, Yunyun Wang, Yudan Liu, Yonghui Li
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引用次数: 0

Abstract

Rationale: Maladaptive fear responses, including sensitized threat reactions and overgeneralization, contribute to anxiety disorders such as generalized anxiety disorder and post-traumatic stress disorder. Although stress intensity influences the generation and extent of these maladaptive fears, the underlying mechanisms remain unclear.

Objectives: The present study examined whether varying footshock stress intensity and inhibition of protein synthesis have differential effect on fear sensitization and generalization in mice.

Methods: Mice were subjected to a classic fear conditioning protocol involving five different levels of footshock intensities. Prior to fear acquisition, the protein synthesis inhibitor cycloheximide (CHX) was administered intraperitoneally. Fear sensitization to white noise and fear generalization to tones with frequencies differing from the conditioned tone were assessed at either 2 or 4 days after fear acquisition.

Results: The results showed that, although varying shock intensities (except the lowest) led to a similar pattern of increased freezing during auditory cues in fear acquisition, the extent of both fear sensitization and generalization increased with the intensity of the footshock in the following days. As shock intensities increased, there was a proportional rise in sensitized fear to white noise and generalized freezing to tones with frequencies progressively closer to the conditioned stimulus. Mildest shocks did not induce discriminative conditioned fear memory, whereas the most intense shocks led to pronounced fear generalization. Administration of CHX before fear acquisition did not affect sensitized fear but reduced generalization of freezing to tones dissimilar from the conditioned stimulus in the group exposed to the most intense shock.

Conclusions: Our results suggest that maladaptive fear responses elicited by varying stress intensities exhibit distinct characteristics. The effect of CHX to prevent overgeneralization without affecting discriminative fear memory points to potential therapeutic approaches for fear-related disorders, suggesting the possibility of mitigating overgeneralization while preserving necessary fear discrimination.

Abstract Image

恐惧泛化受冲击强度和蛋白质合成抑制剂的调节
理论依据:适应不良的恐惧反应,包括敏感化威胁反应和过度泛化,是焦虑症(如广泛性焦虑症和创伤后应激障碍)的诱因。虽然压力强度会影响这些适应不良恐惧的产生和程度,但其潜在机制仍不清楚:本研究探讨了不同的足震应激强度和蛋白质合成抑制是否会对小鼠的恐惧敏化和泛化产生不同影响:方法:对小鼠进行经典的恐惧条件反射训练,包括五种不同强度的脚震。在获得恐惧之前,腹腔注射蛋白质合成抑制剂环己亚胺(CHX)。在获得恐惧后 2 天或 4 天评估对白噪声的恐惧敏感性和对频率与条件音不同的音调的恐惧泛化:结果表明,尽管不同的电击强度(除最低强度外)会导致恐惧获得过程中听觉线索引起的冻结增加的相似模式,但在随后的几天里,恐惧敏感化和泛化的程度会随着脚击强度的增加而增加。随着电击强度的增加,对白噪声的敏感恐惧和对频率逐渐接近条件刺激的音调的泛化冻结也成比例增加。最轻微的电击不会诱发辨别性条件恐惧记忆,而最强烈的电击则会导致明显的恐惧泛化。在获得恐惧之前服用CHX不会影响敏感化恐惧,但会减少受到最强烈冲击组的冻结泛化到与条件刺激不同的音调:我们的研究结果表明,不同应激强度引起的适应不良恐惧反应表现出不同的特征。CHX能防止过度泛化而不影响辨别性恐惧记忆,这为恐惧相关疾病的潜在治疗方法提供了可能,表明有可能在减轻过度泛化的同时保留必要的恐惧辨别能力。
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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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