Stressor-specific effects of sex on HPA axis hormones and activation of stress-related neurocircuitry

References

• Aloisi AM, Ceccarelli I, Lupo C. (1998). Behavioral and hormonal effects of restraint stress and formalin test in male and female rats. Brain Res Bull 47:57–62
   PubMedGoogle Scholar
• 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. Physiol Behav 55:1–5
   PubMedGoogle Scholar
• Babb JA, Masini CV, Day HEW, Campeau S. (2013). Sex differences in activated corticotropin-releasing factor neurons within stress-related neurocircuitry and hypothalamic-pituitary-adrenocortical axis hormones following restraint in rats. Neuroscience 234:40–52
   PubMedGoogle Scholar
• Bekker MH, van Mens-Verhulst J. (2007). Anxiety disorders: sex differences in prevalence, degree, and background, but gender-neutral treatment. Gend Med 4:S178–93
   PubMedGoogle Scholar
• Bielajew C, Konkle ATM, Kentner AC, Baker SL, Stewart A, Hutchins AA, Santa-Maria Barbagallo L, Fourirzos G. (2003). Strain and gender specific effects in the forced swim test: effects of previous stress exposure. Stress 6:269–80
   PubMed Web of Science ®Google Scholar
• Bowen GP, Lin D, Taylor MK, Ison JR. (2003). Auditory cortex lesions in the rat impair both temporal acuity and noise increment thresholds, revealing a common neural substrate. Cerebral Cortex 13:815–22
   PubMedGoogle Scholar
• Burow A, Day HE, Campeau S. (2005). A detailed characterization of loud noise stress: Intensity analysis of hypothalamo-pituitary-adrenocortical axis and brain activation. Brain Res 1062:63–73
   PubMedGoogle Scholar
• Campeau S, Akil H, Watson SJ. (1997). Lesions of the medial geniculate nuclei specifically block corticosterone release and induction of c-fos mRNA in the forebrain associated with audiogenic stress in rats. J Neurosci 17:5979–92
   PubMed Web of Science ®Google Scholar
• Campeau S, Nyhuis TJ, Sasse SK, Kryskow EM, Herlihy L, Masini CV, Babb JA, et al. (2010). Hypothalamic pituitary adrenal axis responses to low-intensity stressors are reduced after voluntary wheel running in rats. J Neuroendocrinol 22:872–88
   PubMedGoogle Scholar
• Campeau S, Watson SJ. (1997). Neuroendocrine and behavioral responses and brain pattern of c-fos induction associated with audiogenic stress. J Neuroendocrinol 9:577–88
   PubMed Web of Science ®Google Scholar
• Campeau S, Watson SJ. (2000). Connections of some auditory-responsive posterior thalamic nuclei putatively involved in activation of the hypothalamo-pituitary-adrenocortical axis in response to audiogenic stress in rats: an anterograde and retrograde tract tracing study combined with Fos expression. J Comp Neurol 423:474–91
   PubMed Web of Science ®Google Scholar
• Charitidi K, Meltser I, Canlon B. (2012). Estradiol treatment and hormonal fluctuations during the estrous cycle modulate the expression of estrogen receptors in the auditory system and the prepulse inhibition of acoustic startle response. Endocrinol 153:4412–21
   PubMedGoogle Scholar
• Chowdhury GM, Fujioka T, Nakamura S. (2000). Induction and adaptation of Fos expression in the rat brain by two types of acute restraint stress. Brain Res Bull 52:171–82
   PubMed Web of Science ®Google Scholar
• Critchlow V, Liebelt RA, Bar-Sela M, Mountcastle W, Lipscomb HS. (1963). Sex difference in resting pituitary-adrenal function in the rat. Am J Physiol 205:807–15
   PubMedGoogle Scholar
• Day HE, Nebel S, Sasse S, Campeau S. (2005). Inhibition of the central extended amygdala by loud noise and restraint stress. Eur J Neurosci 21:441–54
   PubMed Web of Science ®Google Scholar
• Dhabhar FS, McEwen BS, Spencer RL. (1993). Stress response, adrenal steroid receptor levels and corticosteroid-binding globulin levels – a comparison between Sprague-Dawley, Fischer 344 and Lewis rats. Brain Res 616:89–98
   PubMed Web of Science ®Google Scholar
• Ehlert U, Gaab J, Heinrichs M. (2001). Psychoneuroendocrinological contributions to the etiology of depression, posttraumatic stress disorder, and stress-related bodily disorders: the role of the hypothalamus-pituitary-adrenal axis. Biol Psych 57:141–52
   Google Scholar
• Figueiredo HF, Ulrich-Lai YM, Choi DC, Herman JP. (2007). Estrogen potentiates adrenocortical responses to stress in female rats. Am J Physiol Endocrinol Metab 292:E1173–82
   PubMed Web of Science ®Google Scholar
• Gamaro GD, Xavier MH, Denardin JD, Pilger JA, Ely DR, Ferreira MB, Dalmaz C. (1998). The effects of acute and repeated restraint stress on the nociceptive response in rats. Physiol Behav 63:693–7
   PubMed Web of Science ®Google Scholar
• Heinsbroek RP, Van Haaren F, Feenstra MG, Endert E, Van De Poll, N. (1991). Sex- and time-dependent changes in neurochemical and hormonal variables induced by predictable and unpredictable footshock. Physiol Behav 49:1251–6
   PubMed Web of Science ®Google Scholar
• Hurley RW, Adams MCB. (2008). Sex, Gender, and Pain: An overview of a complex field. Anesthes Analges 107:309–17
   PubMed Web of Science ®Google Scholar
• Ison JR, O’Connor K, Bowen GP, Bocirnea A. (1991). Temporal resolution of gaps in noise by the rat is lost with functional decortication. Behav Neurosci 105:33–40
   PubMedGoogle Scholar
• Jovanovic T, Szilagyi S, Chakravorty S, Fiallos AM, Lewison BJ, Parwani A, Schwartz MP, et al. (2004). Menstrual cycle phase effects on prepulse inhibition of acoustic startle. Psychophysiol 41:401–6
   PubMed Web of Science ®Google Scholar
• Kelly JB, Rooney BJ, Phillips DP. (1996). Effects of bilateral auditory cortical lesions on gap-detection thresholds in the ferret (Mustela putorius). Behav Neurosci 110:542–50
   PubMedGoogle Scholar
• Kessler RC, Berglund P, Demler O, Jin R, Merikangas KR, Walters EE. (2005). Lifetime prevalence and age-of-onset distributions of DSM-IV disorders in the National Comorbidity Survey Replication. Arch Gen Psychiatry 62:593–602
   PubMed Web of Science ®Google Scholar
• Kitay JI. (1961). Sex differences in adrenal cortical secretion in the rat. Endocrinol 68:818–24
   PubMed Web of Science ®Google Scholar
• Kitay JI. (1963). Pituitary-adrenal function in the rat after gonadectomy and gonadal hormone replacement. Endocrinol 73:253–60
   PubMed Web of Science ®Google Scholar
• Le Mevel JC, Abitbol S, Beraud G, Maniey J. (1979). Temporal changes in plasma adrenocorticotropin concentration after repeated neurotropic stress in male and female rats. Endocrinol 105:812–17
   PubMed Web of Science ®Google Scholar
• Linzer M, Spitzer R, Kroenke K, Williams JB, Hahn S, Brody D, deGruy F. (1996). Gender, quality of life, and mental disorders in primary care: results from the PRIME-MD 1000 study. Am J Med 101:526–33
   PubMed Web of Science ®Google Scholar
• Masini CV, Babb JA, Nyhuis TJ, Day HEW, Campeau S. (2012). Auditory cortex lesions do not disrupt habituation of HPA axis responses to repeated noise stress. Brain Res 1443:1–9
   PubMedGoogle Scholar
• Masini CV, Day HEW, Campeau S. (2008). Long-term habituation to repeated loud noise is impaired by relatively short interstressor intervals in rats. Behav Neurosci 122:210–23
   PubMed Web of Science ®Google Scholar
• Olff M, Langeland W, Draijer N, Gersons BP. (2007). Gender differences in posttraumatic stress disorder. Psychol Bull 133:183–204
   PubMed Web of Science ®Google Scholar
• Panagiotaropoulous T, Papaioannou A, Pondiki S, Prokopiou A, Stylianopoulou F, Gerozissis K. (2004). Effect of neonatal handling and sex on basal and chronic stress-induced corticosterone and leptin secretion. Neuroendocrinology 79:109–18
   PubMedGoogle Scholar
• Parham K, Willott JF. (1988). Acoustic startle response in young and aging C57BL/6J and CBA/J mice. Behav Neurosci 102:881–6
   PubMedGoogle Scholar
• Paxinos G, Watson C. (2005). The rat brain in stereotaxic coordinates, 5th edition. Burlington, MA: Elsevier Academic Press
   Google Scholar
• Rivier C. (1991). Gender, sex steroids, corticotrophin-releasing factor, nitric oxide, and HPA response to stress. Pharmacol Biochem Behav 64:739–51
   Google Scholar
• Seale JV, Wood SA, Atkinson HC, Bate E, Lightman SL, Ingram CD, Jessop DS, Harbuz MS. (2004a). Gonadectomy reverses the sexually diergic patterns of circadian and stress-induced hypothalamic-pituitary-adrenal axis activity in male and female rats. J Neuroendocrinol 16:516–24
   PubMed Web of Science ®Google Scholar
• Seale JV, Wood SA, Atkinson HC, Harbuz MS, Lightman SL. (2004b). Gonadal steroid replacement reverses gonadectomy-induced changes in the corticosterone pulse profile and stress-induced hypothalamic-pituitary-adrenal axis activity of male and female rats. J Neuroendocrinol 16:989–98
   PubMed Web of Science ®Google Scholar
• Stein MB, Walker JR, Forde DR. (2000). Gender differences in susceptibility to posttraumatic stress disorder. Behav Res Ther 38:619–28
   PubMed Web of Science ®Google Scholar
• Ström JO, Theodorsson E, Theodorsson A. (2008). Order of magnitude differences between methods for maintaining physiological 17beta-oestradiol concentrations in ovariectomized rats. Scan J Clin Lab Investig 68:814–22
   PubMed Web of Science ®Google Scholar
• Tolin DF, Foa EB. (2006). Sex differences in trauma and posttraumatic stress disorder: a quantitative review of 25 years of research. Psychol Bull 132:959–92
   PubMed Web of Science ®Google Scholar
• Vesga-Lopez O, Schneier FR, Wang S, Heimberg RG, Liu S-M, Hasin DS, Blanco C. (2008). Gender differences in generalized anxiety disorder: results from the National Epidemiologic Survey on Alcohol and Related Conditions (NESARC). J Clin Psychiatry 69:1606–16
   PubMed Web of Science ®Google Scholar
• Viau V, Bingham B, Davis J, Lee P, Wong M. (2005). Gender and puberty interact on the stress-induced activation of parvocellular neurosecretory neurons and CRH mRNA expression in the rat. Endocrinol 146:137–46
   PubMed Web of Science ®Google Scholar
• Viau V, Meaney MJ. (1991). Variations in the hypothalamic-pituitary-adrenal response to stress during the estrous cycle in the rat. Endocrinology 129:2503–11
   PubMed Web of Science ®Google Scholar
• Willott JF, Carlson S, Chen H. (1994). Prepulse inhibition of the startle response in mice: relationship to hearing loss and auditory system plasticity. Behav Neurosci 108:703–13
   PubMed Web of Science ®Google Scholar