Dong Xinwen, Wang Yunyun, Liu Yudan, Li Yonghui
Key Laboratory of Mental Health, Institute of Psychology, Chinese Academy of Sciences, Beijing, China.
Department of Neuroendocrine Pharmacology, School of Pharmacy, China Medical University, Shenyang, China.
Psychopharmacology (Berl). 2024 Dec;241(12):2627-2637. doi: 10.1007/s00213-024-06662-1. Epub 2024 Aug 6.
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.
The present study examined whether varying footshock stress intensity and inhibition of protein synthesis have differential effect on fear sensitization and generalization in mice.
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.
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.
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.
适应不良的恐惧反应,包括敏感的威胁反应和过度泛化,会导致广泛性焦虑症和创伤后应激障碍等焦虑症。尽管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。
本研究探讨不同强度的足部电击应激和蛋白质合成抑制对小鼠恐惧敏感化和泛化是否有不同影响。
对小鼠进行经典的恐惧条件反射实验,涉及五种不同强度的足部电击。在恐惧习得前,腹腔注射蛋白质合成抑制剂环己酰亚胺(CHX)。在恐惧习得后2天或4天评估对白色噪音的恐惧敏感化以及对与条件刺激频率不同的音调的恐惧泛化。
结果表明,尽管不同强度的电击(除最低强度外)在恐惧习得期间的听觉提示过程中导致类似的僵立增加模式,但在随后几天,恐惧敏感化和泛化的程度均随足部电击强度的增加而增加。随着电击强度的增加,对白色噪音的敏感化恐惧以及对频率逐渐接近条件刺激的音调的僵立泛化呈比例上升。最轻微的电击未诱导出有区别的条件恐惧记忆,而最强的电击导致明显的恐惧泛化。在恐惧习得前给予CHX不影响敏感化恐惧,但在接受最强电击的组中,减少了对与条件刺激不同的音调的僵立泛化。
我们的结果表明,不同强度应激引发的适应不良恐惧反应表现出不同的特征。CHX在不影响有区别的恐惧记忆的情况下防止过度泛化的作用,为与恐惧相关的疾病指出了潜在的治疗方法,提示在保留必要的恐惧辨别能力的同时减轻过度泛化的可能性。