Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 Mar 1:275:114456.
doi: 10.1016/j.physbeh.2024.114456. Epub 2024 Jan 3.

Acute stress facilitates habitual behavior in female rats

Affiliations

Acute stress facilitates habitual behavior in female rats

Russell Dougherty et al. Physiol Behav. .

Abstract

Instrumental behavior can reflect the influence of goal-directed and habitual systems. Contemporary research suggests that stress may facilitate control by the habitual system under conditions where the behavior would otherwise reflect control by the goal-directed system. However, it is unclear how stress modulates the influence of these systems on instrumental responding to achieve this effect, particularly in females. Here, we examine whether a mild psychogenic stressor experienced before acquisition training (Experiment 1), or prior to the test of expression (Experiment 2) would influence goal-directed and habitual control of instrumental responding in female rats. In both experiments, rats acquired an instrumental nose-poke response for a sucrose reward. This was followed by a reinforcer devaluation phase in which half the rats in Stressed and Non-Stressed conditions received pairings of the sucrose pellet with illness induced by lithium chloride until they rejected the pellet when offered. The remaining rats received a control treatment consisting of pellets and illness on separate days (Unpaired). Control by goal-directed and habitual systems was evaluated in a subsequent nonreinforced test of nose poking. The results of Experiment 1 indicated that the Non-Stressed Paired group reduced nose-poking compared to the Unpaired controls, identifying the response as goal directed, whereas the Stressed Paired and Unpaired groups made a similar number of nose pokes identifying the response as habitual despite a similar amount of training. Results from Experiment 2 indicated habitual control of nose-poke responding was present when stress was experienced just prior to the test. Collectively, these data suggest that stress may facilitate habitual control by altering the relative influence of goal-directed and habitual processes underpinning instrumental behavior. These results may be clinically relevant for understanding the contributions of stress to dysregulated instrumental behavior in compulsive pathologies.

Keywords: Action sequences; Females, Reinforcer devaluation; Goal-directed action; Habit; Stress.

PubMed Disclaimer

Figures

Figure 1.
Figure 1.. Experimental Timeline
Note. A) Experimental timeline for Experiment 1: Stress before acquisition. B) Experimental timeline for Experiment 2: Stress before test.
Figure 2.
Figure 2.. Results of Experiment 1
Note. A) Mean nose-poke rates (responses per minute) over the two sessions of training on a VI 30-s schedule. B) Mean number of sucrose pellets consumed by Paired condition animals during each cycle of the outcome devaluation phase. C) Mean nose-poke rates during the test as a proportion of nose-poke rate in the final VI 30-s session (proportion of baseline). D) Mean food-cup entry rates during the test as a proportion of baseline. E) Mean nose-pokes per minute during the reacquisition test as a proportion of baseline. Error bars denote standard error of the mean.
Figure 3.
Figure 3.. Results of Experiment 1 response sequence analyses
Note. A) Graphic depicting independent nose-poke responses and nose-poke to food-cup entry sequences. B) Mean nonreinforced (NR) independent nose-poke responses per minute during the final VI 30-s training session. C) Mean NR nose-poke to food-cup entry sequences per minute during the final VI 30-s training session. D) Mean independent nose-poke responses per minute during the test as a proportion of the independent response rates from the final VI 30-s training session (proportion of baseline). E) Mean nose-poke to food-cup entry sequences as a proportion of mean sequence rate in the final VI 30-s training session (proportion of baseline). Error bars denote standard error of the mean.
Figure 4.
Figure 4.. Results of Experiment 2
Note. A) Mean nose-poke rates (responses per minute) in the two VI 30-s training sessions. B) Mean number of sucrose pellets consumed by Paired condition animals during each cycle of the outcome devaluation phase. C) Mean nose-poke rates during the test as a proportion of nose-poke rate in the final VI 30-s training session (proportion of baseline). D) Mean food-cup entries per minute during the test as a proportion food-cup rates in the final VI 30-s training session. E) Mean nose-pokes per minute during the reacquisition test as a proportion of baseline. Error bars denote standard error of the mean.
Figure 5.
Figure 5.. Results of Experiment 2 response sequence analyses
Note. A) Mean NR independent nose-poke responses per minute during in the final VI 30-s training session. B) Mean NR nose-poke to food-cup entry sequences per minute during the final VI 30-s training session. C) Mean independent nose-poke responses per minute during the test as a proportion of baseline independent response rates from the final VI 30-s training session. D) Mean nose-poke to food-cup entry sequences as a proportion of baseline sequence rates from the final VI 30-s training session. Error bars denote standard error of the mean.

Similar articles

Cited by

References

    1. Adams CD (1982). Variations in the Sensitivity of Instrumental Responding to Reinforcer Devaluation. The Quarterly Journal of Experimental Psychology Section B, 34(2b), 77–98. 10.1080/14640748208400878 - DOI
    1. Adams CD, & Dickinson A (1981). Instrumental Responding following Reinforcer Devaluation. The Quarterly Journal of Experimental Psychology Section B, 33(2b), 109–121. 10.1080/14640748108400816 - DOI
    1. Aloisi AM, Steenbergen HL, van de Poll NE, & Farabollini F (1994). Sex-dependent effects of restraint on nociception and pituitary-adrenal hormones in the rat. Physiology & Behavior, 55(5), 789–793. 10.1016/0031-9384(94)90061-2 - DOI - PubMed
    1. Babb JA, Masini CV, Day HEW, & Campeau S (2013). Stressor-specific effects of sex on HPA axis hormones and activation of stress-related neurocircuitry. Stress (Amsterdam, Netherlands), 16(6), 664–677. 10.3109/10253890.2013.840282 - DOI - PMC - PubMed
    1. Balleine BW, & Dezfoub A (2019). Hierarchical Action Control: Adaptive Collaboration Between Actions and Habits. Frontiers in Psychology, 10, 2735. 10.3389/fpsyg.2019.02735 - DOI - PMC - PubMed

LinkOut - more resources