The neuroendocrine response to stress under the effect of drugs: Negative synergy between amphetamine and stressors

There have been numerous studies into the interaction between stress and addictive drugs, yet few have specifically addressed how the organism responds to stress when under the influence of psychostimulants. Thus, we studied the effects of different acute stressors (immobilization, interleukin-1β and forced swimming) in young adult male rats simultaneously exposed to amphetamine (AMPH, 4 mg/kg SC), evaluating classic biological markers. AMPH administration itself augmented the plasma hypothalamic-pituitary-adrenal (HPA) hormones, adrenocorticotropin (ACTH) and corticosterone, without affecting plasma glucose levels. By contrast, this drug dampened the peripheral HPA axis, as well as the response of glucose to the three stressors. We also found that AMPH administration completely blocked the forced swim-induced expression of the corticotropin-releasing hormone (hnCRH) and it partially reduced c-fos expression in the paraventricular nucleus of the hypothalamus (PVN). Indeed, this negative synergy in the forced swim test could even be observed with a lower dose of AMPH (1mg/kg, SC), a dose that is usually received in self-administration experiments. In conclusion, when rats that receive AMPH are subjected to stress, a negative synergy occurs that dampens the prototypic peripheral physiological response to stress and activation of the PVN.

[1]  J. Herman,et al.  Dissociation of ACTH and glucocorticoids , 2008, Trends in Endocrinology & Metabolism.

[2]  T. Robinson,et al.  Environmental modulation of amphetamine-induced c-fos expression in D1 versus D2 striatal neurons , 1999, Behavioural Brain Research.

[3]  G. Paxinos,et al.  The Rat Brain in Stereotaxic Coordinates , 1983 .

[4]  J. Hardin,et al.  Generalized Estimating Equations , 2002 .

[5]  W. Fratta,et al.  Sex differences in addictive disorders , 2014, Frontiers in Neuroendocrinology.

[6]  T. Robinson,et al.  Amphetamine-Induced Behavior, Dopamine Release, and c-fos mRNA Expression: Modulation by Environmental Novelty , 1998, The Journal of Neuroscience.

[7]  K. Miczek,et al.  Stress in adolescence and drugs of abuse in rodent models: Role of dopamine, CRF, and HPA axis , 2013, Psychopharmacology.

[8]  R. Spencer,et al.  Acute Glucocorticoid Pretreatment Suppresses Stress‐Induced Hypothalamic‐Pituitary‐Adrenal Axis Hormone Secretion and Expression of Corticotropin‐Releasing Hormone hnRNA but Does Not Affect c‐fos mRNA or Fos Protein Expression in the Paraventricular Nucleus of the Hypothalamus , 2003, Journal of neuroendocrinology.

[9]  T. Robinson,et al.  Environmental context modulates the ability of cocaine and amphetamine to induce c-fos mRNA expression in the neocortex, caudate nucleus, and nucleus accumbens , 2001, Brain Research.

[10]  G. Koob,et al.  Corticotropin releasing factor: A key role in the neurobiology of addiction , 2014, Frontiers in Neuroendocrinology.

[11]  Antonio Armario,et al.  What can We Know from Pituitary–Adrenal Hormones About the Nature and Consequences of Exposure to Emotional Stressors? , 2012, Cellular and Molecular Neurobiology.

[12]  K. Frantz,et al.  Age- and sex-dependent amphetamine self-administration in rats , 2007, Psychopharmacology.

[13]  Jane Stewart,et al.  Stress-induced relapse to heroin and cocaine seeking in rats: a review , 2000, Brain Research Reviews.

[14]  A. Armario,et al.  Forced swimming test in rats: effect of desipramine administration and the period of exposure to the test on struggling behavior, swimming, immobility and defecation rate. , 1988, European journal of pharmacology.

[15]  A. Armario,et al.  Dopamine D1 and D2 dopamine receptors regulate immobilization stress-induced activation of the hypothalamus-pituitary-adrenal axis , 2009, Psychopharmacology.

[16]  G. Breese,et al.  Rapid down regulation of beta adrenergic receptors by combining antidepressant drugs with forced swim: a model of antidepressant-induced neural adaptation. , 1985, The Journal of pharmacology and experimental therapeutics.

[17]  L. Herlihy,et al.  Conditioned fear inhibits c-fos mRNA expression in the central extended amygdala , 2008, Brain Research.

[18]  S. Maier,et al.  Activation of serotonin-immunoreactive cells in the dorsal raphe nucleus in rats exposed to an uncontrollable stressor , 1999, Brain Research.

[19]  S. Watson,et al.  Rapid regulation of corticotropin-releasing hormone gene transcription in vivo. , 1992, Molecular endocrinology.

[20]  G. Laviola,et al.  Peculiar response of adolescent mice to acute and chronic stress and to amphetamine: evidence of sex differences , 2002, Behavioural Brain Research.

[21]  S. R. Searle,et al.  Generalized, Linear, and Mixed Models , 2005 .

[22]  R. Sapolsky,et al.  Interleukin-1 stimulates the secretion of hypothalamic corticotropin-releasing factor. , 1987, Science.

[23]  H. Akil,et al.  Pattern and time course of immediate early gene expression in rat brain following acute stress , 1995, Neuroscience.

[24]  N. Swerdlow,et al.  Pituitary-adrenal axis responses to acute amphetamine in the rat , 1993, Pharmacology Biochemistry and Behavior.

[25]  J. Crane,et al.  Patterns of neuronal activation in the rat brain and spinal cord in response to increasing durations of restraint stress , 2005, Stress.

[26]  A. Armario,et al.  Adaptation of the hypothalamic-pituitary-adrenal axis and glucose to repeated immobilization or restraint stress is not influenced by associative signals , 2011, Behavioural Brain Research.

[27]  A. Deutch,et al.  Stress selectively increases fos protein in dopamine neurons innervating the prefrontal cortex. , 1991, Cerebral cortex.

[28]  R. Porsolt,et al.  Depression: a new animal model sensitive to antidepressant treatments , 1977, Nature.

[29]  A. Armario Activation of the hypothalamic-pituitary-adrenal axis by addictive drugs: different pathways, common outcome. , 2010, Trends in pharmacological sciences.

[30]  P. Kalivas,et al.  Dopamine transmission in the initiation and expression of drug- and stress-induced sensitization of motor activity , 1991, Brain Research Reviews.

[31]  T. Robinson,et al.  Environmental Novelty Differentially Affects c-fosmRNA Expression Induced by Amphetamine or Cocaine in Subregions of the Bed Nucleus of the Stria Terminalis and Amygdala , 2001, The Journal of Neuroscience.

[32]  A. Armario,et al.  A single exposure to immobilization causes long-lasting pituitary-adrenal and behavioral sensitization to mild stressors , 2008, Hormones and Behavior.

[33]  T. Robinson,et al.  Opposite effects of amphetamine self-administration experience on dendritic spines in the medial and orbital prefrontal cortex. , 2004, Cerebral cortex.

[34]  M. Le Moal,et al.  The role of stress in drug self-administration. , 1998, Trends in pharmacological sciences.

[35]  Dennis C. Choi,et al.  Central mechanisms of stress integration: hierarchical circuitry controlling hypothalamo–pituitary–adrenocortical responsiveness , 2003, Frontiers in Neuroendocrinology.

[36]  A. Armario,et al.  Differential effects of stress and amphetamine administration on Fos‐like protein expression in corticotropin releasing factor‐neurons of the rat brain , 2007, Developmental neurobiology.

[37]  A. Armario,et al.  Long‐term effects of a single exposure to immobilization stress on the hypothalamic–pituitary–adrenal axis: transcriptional evidence for a progressive desensitization process , 2003, The European journal of neuroscience.

[38]  S. Campeau,et al.  Inhibition of the central extended amygdala by loud noise and restraint stress , 2005, The European journal of neuroscience.

[39]  A. Armario,et al.  The brain pattern of c-fos induction by two doses of amphetamine suggests different brain processing pathways and minor contribution of behavioural traits , 2010, Neuroscience.

[40]  M. Marinelli,et al.  Interaction between glucocorticoid hormones, stress and psychostimulant drugs * , 2002, The European journal of neuroscience.