Abstract
Clinical reports suggest that females diagnosed with substance use disorder experience enhanced relapse vulnerability compared with males, particularly during stress. We previously demonstrated that a stressor (footshock) can potentiate cocaine seeking in male rats via glucocorticoid-dependent cannabinoid type-1 receptor (CB1R)-mediated actions in the prelimbic prefrontal cortex (PrL-PFC). Here, we investigated the influence of biological sex on stress-potentiated cocaine seeking. Despite comparable self-administration and extinction, females displayed a lower threshold for cocaine-primed reinstatement than males. Unlike males, footshock, tested across a range of intensities, failed to potentiate cocaine-primed reinstatement in females. However, restraint potentiated reinstatement in both sexes. While sex differences in stressor-induced plasma corticosterone (CORT) elevations and defensive behaviors were not observed, differences were evident in footshock-elicited ultrasonic vocalizations. CORT administration, at a dose which recapitulates stressor-induced plasma levels, reproduced stress-potentiated cocaine-primed reinstatement in both sexes. In females, CORT effects varied across the estrous cycle; CORT-potentiated reinstatement was only observed during diestrus and proestrus. As in males, CORT-potentiated cocaine seeking in females was localized to the PrL-PFC and both CORT- and restraint-potentiated cocaine seeking required PrL-PFC CB1R activation. In addition, ex vivo whole-cell electrophysiological recordings from female layer V PrL-PFC pyramidal neurons revealed CB1R-dependent CORT-induced suppression of inhibitory synaptic activity, as previously observed in males. These findings demonstrate that, while stress potentiates cocaine seeking via PrL-PFC CB1R in both sexes, sensitivity to cocaine priming injections is greater in females, CORT-potentiating effects vary with the estrous cycle, and whether reactivity to specific stressors may manifest as drug seeking depends on biological sex.
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References
Westermeyer J, Boedicker AE. Course, severity, and treatment of substance abuse among women versus men. Am J Drug Alcohol Abus. 2000;26:523–35.
Greenfield SF, Pettinati HM, O’Malley S, Randall PK, Randall CL. Gender differences in alcohol treatment: an analysis of outcome from the COMBINE study. Alcohol Clin Exp Res. 2010;34:1803–12.
Gallop RJ, Crits-Christoph P, Ten Have TR, Barber JP, Frank A, Griffin ML et al. Differential transitions between cocaine use and abstinence for men and women. J Consulting Clin Psychol. 2007;75:95–103.
Ong KC, Cheong GN, Prabhakaran L, Earnest A. Predictors of success in smoking cessation among hospitalized patients. Respirology. 2005;10:63–9.
Carpenter MJ, Upadhyaya HP, LaRowe SD, Saladin ME, Brady KT. Menstrual cycle phase effects on nicotine withdrawal and cigarette craving: a review. Nicotine Tob Res. 2006;8:627–38.
Back SE, Brady KT, Jackson JL, Salstrom S, Zinzow H. Gender differences in stress reactivity among cocaine-dependent individuals. Psychopharmacology. 2005;180:169–76.
Feltenstein MW, Henderson AR, See RE. Enhancement of cue-induced reinstatement of cocaine-seeking in rats by yohimbine: sex differences and the role of the estrous cycle. Psychopharmacology. 2011;216:53–62.
Fox HC, Morgan PT, Sinha R. Sex differences in guanfacine effects on drug craving and stress arousal in cocaine-dependent individuals. Neuropsychopharmacology. 2014;39:1527–37.
Furnari M, Epstein DH, Phillips KA, Jobes ML, Kowalczyk WJ, Vahabzadeh M, et al. Some of the people, some of the time: field evidence for associations and dissociations between stress and drug use. Psychopharmacology. 2015;232:3529–37.
Preston KL, Kowalczyk WJ, Phillips KA, Jobes ML, Vahabzadeh M, Lin JLL, et al. Exacerbated craving in the presence of stress and drug cues in drug-dependent patients. Neuropsychopharmacology. 2018;43:859–67.
Mantsch JR, Baker DA, Funk D, Lê AD, Shaham Y. Stress-induced reinstatement of drug seeking: 20 years of progress. Neuropsychopharmacology. 2016;41:335–56.
Graf EN, Wheeler RA, Baker DA, Ebben AL, Hill JE, McReynolds JR, et al. Corticosterone acts in the nucleus accumbens to enhance dopamine signaling and potentiate reinstatement of cocaine seeking. J Neurosci. 2013;33:11800–10.
McReynolds JR, Doncheck EM, Li Y, Vranjkovic O, Graf EN, Ogasawara D, et al. Stress promotes drug seeking through glucocorticoid-dependent endocannabinoid mobilization in the prelimbic cortex. Biol Psychiatry. 2018;84:85–94.
Kalivas PW, Volkow ND. The neural basis of addiction: a pathology of motivation and choice. Am J Psychiatry. 2005;162:1403–13.
Park WK, Bari AA, Jey AR, Anderson SM, Spealman RD, Rowlett JK et al. Cocaine administered into the medial prefrontal cortex reinstates cocaine-seeking behavior by increasing AMPA receptor-mediated glutamate transmission in the nucleus accumbens. J Neurosci. 2002;22:2916–25.
Capriles N, Rodaros D, Sorge RE, Stewart J. A role for the prefrontal cortex in stress- and cocaine-induced reinstatement of cocaine seeking in rats. Psychopharmacology. 2003;168:66–74.
McFarland K, Lapish CC, Kalivas PW. Prefrontal glutamate release into the core of the nucleus accumbens mediates cocaine-induced reinstatement of drug-seeking behavior. J Neurosci. 2003;23:3531–7.
Stefanik MT, Moussawi K, Kupchik YM, Smith KC, Miller RL, Huff ML et al. Optogenetic inhibition of cocaine seeking in rats. Addiction Biol 2013;18:50–53.
Hill MN, McLaughlin RJ, Pan B, Fitzgerald ML, Roberts CJ, Lee TT, et al. Recruitment of prefrontal cortical endocannabinoid signaling by glucocorticoids contributes to termination of the stress response. J Neurosci. 2011;31:10506–15.
Li CSRS, Kosten TR, Sinha R. Sex differences in brain activation during stress imagery in abstinent cocaine users: a functional magnetic resonance imaging study. Biol Psychiatry. 2005;57:487–94.
Zhou L, Pruitt C, Shin CB, Garcia AD, Zavala AR, See RE. Fos expression induced by cocaine-conditioned cues in male and female rats. Brain Struct Funct. 2014;219:1831–40.
Bland ST, Schmid MJ, Der-Avakian A, Watkins LR, Spencer RL, Maier SF. Expression of c-fos and BDNF mRNA in subregions of the prefrontal cortex of male and female rats after acute uncontrollable stress. Brain Res. 2005;1051:90–99.
Henricks AM, Berger AL, Lugo JM, Baxter-Potter LN, Bieniasz KV, Petrie G, et al. Sex- and hormone-dependent alterations in alcohol withdrawal-induced anxiety and corticolimbic endocannabinoid signaling. Neuropharmacology. 2017;124:121–33.
Chiu CQ, Puente N, Grandes P, Castillo PE. Dopaminergic modulation of endocannabinoid-mediated plasticity at GABAergic synapses in the prefrontal cortex. J Neurosci. 2010;30:7236–48.
Rodriguez de Fonseca F, Cebeira M, Martin M, Fernandez-Ruiz JJ. Cannabinoid receptors in rat brain areas: sexual differences, fluctuations during estrous cycle and changes after gonadectomy and sex steroid replacement. Life Sci. 1994;54:159–70.
Doncheck EM, Urbanik LA, DeBaker MC, Barron LM, Liddiard GT, Tuscher JJ, et al. 17β-estradiol potentiates the reinstatement of cocaine seeking in female rats: role of the prelimbic prefrontal cortex and cannabinoid type-1 receptors. Neuropsychopharmacology. 2018;43:781–90.
Tinnikov AA. Responses of serum corticosterone and corticosteroid-binding globulin to acute and prolonged stress in the rat. Endocrine. 1999;11:145–50.
Kirry AJ, Durigan DJ, Twining RC, Gilmartin MR. Estrous cycle stage gates sex differences in prefrontal muscarinic control of fear memory formation. Neurobiol Learn Mem. 2019;161:26–36.
Colom-Lapetina J, Li AJ, Pelegrina-Perez TC, Shansky RM. Behavioral diversity across classic rodent models is sex-dependent. Front Behav Neurosci. 2019;13:45.
Barker DJ, Simmons SJ, West MO. Ultrasonic vocalizations as a measure of affect in preclinical models of drug abuse: a review of current findings. Curr Neuropharmacol. 2015;13:193–210.
Mittal N, Thakore N, Bell RL, Maddox WT, Schallert T, Duvauchelle CL. Sex-specific ultrasonic vocalization patterns and alcohol consumption in high alcohol-drinking (HAD-1) rats. Physiol Behav. 2019;203:81–90.
Van der Kloot W. The regulation of quantal size. Prog Neurobiol. 1991;36:93–130.
Gruene TM, Flick K, Stefano A, Shea SD, Shansky RM. Sexually divergent expression of active and passive conditioned fear responses in rats. eLife. 2015;4:e11352.
Roth ME, Carroll ME. Sex differences in the escalation of intravenous cocaine intake following long- or short-access to cocaine self-administration. Pharmacol Biochem Behav. 2004;78:199–207.
Jackson LR, Robinson TE, Becker JB. Sex differences and hormonal influences on acquisition of cocaine self-administration in rats. Neuropsychopharmacology. 2006;31:129–38.
Carroll ME, Lynch WJ. How to study sex differences in addiction using animal models. Addiction Biol. 2016;21:1007–29.
Becker JB, Koob GF. Sex differences in animal models: focus on addiction. Pharmacol Rev. 2016;68:242–63.
Moran-Santa Maria MM, McRae-Clark A, Baker NL, Ramakrishnan V, Brady KT. Yohimbine administration and cue-reactivity in cocaine-dependent individuals. Psychopharmacology. 2014;231:4157–65.
Moran LM, Kowalczyk WJ, Phillips KA, Vahabzadeh M, Lin JLL, Mezghanni M, et al. Sex differences in daily life stress and craving in opioid-dependent patients. Am J Drug Alcohol Abus. 2018;44:512–23.
Lu J, Wu XYY, Zhu QBB, Li J, Shi LGG, Wu JLL, et al. Sex differences in the stress response in SD rats. Behavioural Brain Res. 2015;284:231–7.
Bertholomey ML, Nagarajan V, Torregrossa MM. Sex differences in reinstatement of alcohol seeking in response to cues and yohimbine in rats with and without a history of adolescent corticosterone exposure. Psychopharmacology. 2016;233:2277–87.
Bowers JM, Perez-Pouchoulen M, Edwards NOS, McCarthy MM. Foxp2 mediates sex differences in ultrasonic vocalization by rat pups and directs order of maternal retrieval. J Neurosci. 2013;33:3275–83.
Zala SM, Reitschmidt D, Noll A, Balazs P, Penn DJ. Sex-dependent modulation of ultrasonic vocalizations in house mice (Mus musculus musculus). PLoS ONE. 2017;12:e0188647.
Blanchard RJ, Agullana R, McGee L, Weiss S, Blanchard DC. Sex differences in the incidence and sonographic characteristics of antipredator ultrasonic cries in the laboratory rat (Rattus norvegicus). J Comp Psychol. 1992;106:270–7.
Knutson B, Burgdorf J, Panksepp J. High-frequency ultrasonic vocalizations index conditioned pharmacological reward in rats. Physiol Behav. 1999;66:639–43.
Bello NT, Walters AL, Verpeut JL, Caverly J. Dietary-induced binge eating increases prefrontal cortex neural activation to restraint stress and increases binge food consumption following chronic guanfacine. Pharmacol Biochem Behav. 2014;125:21–8.
Trentani A, Kuipers SD, te Meerman GJ, Beekman J, ter Horst GJ, den Boer JA Immunohistochemical changes induced by repeated footshock stress: revelations of gender-based differences. Neurobiology Dis. 2003;14:602–18.
Anker JJ, Carroll ME. Females are more vulnerable to drug abuse than males: evidence from preclinical studies and the role of ovarian hormones. Current Topics Behavioral. Curr Top Behav Neurosci. 2011;8:73–96.
Kippin TE, Fuchs RA, Mehta RH, Case JM, Parker MP, Bimonte-Nelson HA et al. Potentiation of cocaine-primed reinstatement of drug seeking in female rats during estrus. Psychopharmacology. 2005;182:245–52.
Feltenstein MW, See RE. Plasma progesterone levels and cocaine-seeking in freely cycling female rats across the estrous cycle. Drug Alcohol Depend. 2007;89:183–9.
Larson EB, Carroll ME. Estrogen receptor beta, but not alpha, mediates estrogen’s effect on cocaine-induced reinstatement of extinguished cocaine-seeking behavior in ovariectomized female rats. Neuropsychopharmacology. 2007;32:1334–45.
Sofuoglu M, Babb DA, Hatsukami DK. Effects of progesterone treatment on smoked cocaine response in women. Pharmacol Biochem Behav. 2002;72:431–5.
Sinha R, Fox H, Hong KII, Sofuoglu M, Morgan PT, Bergquist KT. Sex steroid hormones, stress response, and drug craving in cocaine-dependent women: implications for relapse susceptibility. Exp Clin Psychopharmacol. 2007;15:445–52.
Critchlow V, Liebelt RA, Bar-Sela M, Mountcastle W, Lipscomb HS. Sex difference in resting pituitary-adrenal function in the rat. Am J Physiol. 1963;205:807–15.
Windle RJ, Wood SA, Lightman SL, Ingram CD. The pulsatile characteristics of hypothalamo-pituitary-adrenal activity in female Lewis and Fischer 344 rats and its relationship to differential stress responses. Endocrinology. 1998;139:4044–52.
Choleris E, Cazzin L, Lymer JM, Amor TR, Lu R, Kavaliers M et al. Acute corticosterone sexually dimorphically facilitates social learning and inhibits feeding in mice. Neuropharmacology. 2013;75:191–200.
Droste SK, de Groote L, Atkinson HC, Lightman SL, Reul JMHM, Linthorst AC. Corticosterone levels in the brain show a distinct ultradian rhythm but a delayed response to forced swim stress. Endocrinology. 2008;149:3244–53.
Sze Y, Gill AC, Brunton PJ. Sex-dependent changes in neuroactive steroid concentrations in the rat brain following acute swim stress. J Neuroendocrinol. 2018;30:e12644.
McReynolds JR, Doncheck EM, Vranjkovic O, Ganzman GS, Baker DA, Hillard CJ et al. CB1 receptor antagonism blocks stress-potentiated reinstatement of cocaine seeking in rats. Psychopharmacology 2016;233:99–109.
Xi ZX, Gilbert JG, Peng XQ, Pak AC, Li X, Gardner EL. Cannabinoid CB1 receptor antagonist AM251 inhibits cocaine-primed relapse in rats: role of glutamate in the nucleus accumbens. J Neurosci. 2006;26:8531–6.
Tabatadze N, Huang G, May RM, Jain A, Woolley CS. Sex differences in molecular signaling at inhibitory synapses in the hippocampus. J Neurosci. 2015;35:11252–65.
Acknowledgements
We would like to thank Drs Hershel Raff and Paul Gasser for validation of and advice concerning CORT assays, Adam Kirry for instruction on footshock reactivity analyses, and Dr Robert Twining for advice concerning USVs.
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Doncheck, E.M., Liddiard, G.T., Konrath, C.D. et al. Sex, stress, and prefrontal cortex: influence of biological sex on stress-promoted cocaine seeking. Neuropsychopharmacol. 45, 1974–1985 (2020). https://doi.org/10.1038/s41386-020-0674-3
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DOI: https://doi.org/10.1038/s41386-020-0674-3
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