Abstract

The conditioned fear learning and memory occurs when a neutral conditioned stimulus (CS) is paired with an aversive unconditioned stimulus (US). This process is critically dependent on the amygdala and inevitably involves blood pressure (BP) alterations. We hypothesized that BP variations could instantaneously reveal individual steps during conditioned fear learning and memory. An implanted telemetric probe was used to monitor the BP real-time in rats during training and testing sessions of the fear-potentiated startle. Our results showed that (i) the conditioned fear learning during the training sessions was reflected by light (CS)-induced rapid BP elevations and by electric shock (US)-evoked sympathetic tone elevations; (ii) these two BP-related parameters were not only negatively correlated with each other but also coupled to each other in the training session trials; (iii) both parameters closely predicted the performance of fear-potentiated startle on the next day; and (iv) although local blocking of one of the two fear-conditioned pathways in the training session partially inhibited fear learning, the fear memory retrieval still used both pathways. Altogether, real-time blood pressure variations faithfully revealed the critical steps involved in conditioned fear learning and memory, and our results supported a coupling between the cued learning and the post-shock calmness.

Highlights

  • Classical fear conditioning occurs when a neutral stimulus is paired with an aversive stimulus, such as an electric shock

  • Performance of Fear-Potentiated Startle In order to investigate the learning curve of fear-potentiated startle, we reduced the standard training session from 10,15 repeated conditioned stimulus (CS)-unconditioned stimulus (US) pairs to only 7 pairs

  • PCS/PA was defined as the post-CS blood pressure (BP) (PCS; 3-s mean value) divided by the pre-CS BP (PA; 3-s mean value) in each trial; it served as an index for the CS-induced rapid elevation of BP

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Summary

Introduction

Classical fear conditioning occurs when a neutral stimulus (the conditioned stimulus, CS) is paired with an aversive stimulus (unconditioned stimulus, US), such as an electric shock. The previously neutral stimulus is able to elicit a variety of autonomic, hormonal, and skeletal responses that accompany the fear experience. The amygdala is an important site for associative memory storage during fear conditioning [1,2,3,4,5,6]. It is widely believed that conditioned fear stimuli activate the basolateral nucleus of the amygdala (BLA) projection neurons which send afferents to two distinct target areas, i.e., the central (CeA) and the medial (MeA) nuclei of the amygdala [7,8]. The ventromedial nucleus of the hypothalamus (VMH), a downstream target of MeA, is involved in fear responses [9,10,11,12,13]. It is tempting to monitor blood pressure (BP)-related parameters real-time to reveal the individual steps of fear learning and memory

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