Persistent Neuroendocrine Changes in Multiple Hormonal Axes after a Single or Repeated Stressor Exposures

References

• Armario A., Hidalgo J., Giralt M. Evidence that the pituitary-adrenal axis does not cross-adapt to stressors: comparison to other physiological variables. Neuroendocrinology 1988; 47: 263–267
   PubMed Web of Science ®Google Scholar
• Bambino T. H, Hsueh A. J. Direct inhibitory effect of glucocorticoids upon testicular luteinizing hormone receptor and steroidogenesis in vivo and in vitro. Endocrinology 1981; 108: 2142–2148
   PubMed Web of Science ®Google Scholar
• Bianco A. C., Nunes M. T., Hell N. S, Maciel R. M. The role of glucocorticoids in the stress-induced reduction of extrathyroidal 3,5,3′-triiodothyronine generation in rats. Endocrinology 1987; 120: 1033–1038
   PubMed Web of Science ®Google Scholar
• Bidzinska B., Petraglia F., Angioni S., Genazzani A. D., Criscuolo M., Ficarra G., Gallinelli A., Trentini G. P, Genazzani A. R. Effect of different chronic intermittent stressors and acetyl-1-carnitine on hypothalamic beta-endorphin and GnRH and on plasma testosterone levels in male rats. Neuroendocrinology 1993; 57: 985–990
   PubMed Web of Science ®Google Scholar
• Chappell P. B., Smith M. A., Kilts C. D., Bissette G., Ritchie J., Anderson C., Nemeroff C. B. Alterations in corticotropin-releasing factor-like immunoreactivity in discrete rat brain regions after acute and chronic stress. J Neurosci. 1986; 6: 2908–2914
   PubMed Web of Science ®Google Scholar
• Collu R., Gibb W., Ducharme J. R. Effects of stress on the gonadal function. J Endocrinol. Invest. 1984; 7: 529–537
   PubMed Web of Science ®Google Scholar
• Fleshner M., Deak T., Spencer R. L., Laudenslager M. L., Watkins L. R., Maier S. F. A long-term increase in basal levels of corticosterone and a decrease in corticosteroid-binding globulin after acute stressor exposure. Endocrinology 1995; 136: 5336–5342
   PubMed Web of Science ®Google Scholar
• Herman J. P., Schafer K. H., Sladek C. D., Day R., Young E. A., Akil H., Watson S. J. Chronic electroconvulsive shock treatment elicits up-regulation of CRF and AVP mRNA in select populations of neuroendocrine neurons. Brain Res. 1989; 501: 235–246
   Google Scholar
• Herman J. P., Schäfer M. K., Young E. A., Thompson R., Douglass J., Akil H., Watson S. J. Evidence for hippocampal regulation of neuroendocrine neurons of the hypothalamo-pituitary-adrenocortical axis. J Neurosci. 1989; 9: 3072–3082
   PubMed Web of Science ®Google Scholar
• Huang H. F.S., Pogach L. M., Nathan E., Giglio W, Seebode J. Synergistic effects of FSH and testosterone upon the maintenance of spermiogenesis in hypophysectomized rats: relationship with androgen binding protein status. Endocrinology 1991; 128: 3152–3161
   Google Scholar
• Kant G. J., Bauman R. A., Anderson S. M., Mougey E. H. Effects of controllable vs. uncontrollable chronic stress on stress-responsive plasma hormones. Physiol. Behav. 1992; 51: 1285–1288
   PubMed Web of Science ®Google Scholar
• Kant G. J., Bunnell B. N., Mougey E. H., Pennington L. L., Meyerhoff J. L. Effects of repeated stress on pituitary cyclic AMP, and plasma prolactin, corticosterone and growth hormone in male rats. Pharmacol. Biochem. Behav. 1983; 18: 967–971
   PubMed Web of Science ®Google Scholar
• Kant G. J., Eggleston T., Landman R. L., Kenion C. C., Driver G. C., Meyerhoff J. L. Habituation to repeated stress is stressor specific. Pharmacol. Biochem. Behav. 1985; 22: 631–634
   PubMed Web of Science ®Google Scholar
• Kant G. J., Leu J. R., Anderson S. M., Mougey E. H. Effects of chronic stress on plasma corticosterone, ACTH and prolactin. Physiol. Behav. 1987; 40: 775–779
   PubMedGoogle Scholar
• Kant G. J., Mougey E. H., Pennington L. L., Meyerhoff J. L. Graded footshock stress elevates pituitary cyclic AMP and plasma beta-endorphin, beta-LPH corticosterone and prolactin. Life Sci. 1983; 33: 2657–2663
   PubMed Web of Science ®Google Scholar
• Katz R. J., Roth K. A., Carroll B. J. Acute and chronic stress effects on open field activity in the rat: implications for a model of depression. Neurosci. Biobehav. Rev. 1981; 5: 247–251
   PubMed Web of Science ®Google Scholar
• Konarska M., Stewart R. E., McCarty R. Habituation of sympathetic-adrenal medullary responses following exposure to chronic intermittent stress. Physiol. Behav. 1989; 45: 255–261
   PubMed Web of Science ®Google Scholar
• López-Calderon C. A., Gonzaléz Q. M., Tresguerres J. A., Ariznavarreta C. Role of LHRH in the gonadotrophin response to restraint stress in intact male rats. J Endocrinol. 1990; 124: 241–246
   Google Scholar
• Maric D., Kostic T., Kovacevic R. Effects of acute and chronic immobilization stress on rat Leydig cell steroidogenesis. J Steroid Biochem. Mol. Biol. 1996; 58: 351–355
   PubMed Web of Science ®Google Scholar
• Martí O., Armario A. Anterior pituitary response to stress: time-related changes and adaptation. Int. J. Dev. Neurosci. 1998; 16: 241–260
   PubMed Web of Science ®Google Scholar
• Martí O., Gavaldà A., Jolín T., Armario A. Effect of regularity of exposure to chronic immobilization stress on the circadian pattern of pituitary adrenal hormones, growth hormone, and thyroid stimulating hormone in the adult male rat. Psychoneuroendocrinology 1993; 18: 67–77
   PubMed Web of Science ®Google Scholar
• Martf O., Gavaldà A., Jolín T., Armario A. Acute stress attenuates but does not abolish circadian rhythmicity of serum thyrotrophin and growth hormone in the rat. Eur. J Endocrinol 1996; 135: 703–708
   Google Scholar
• Millard W. J., Reppert S. M., Sagar S. M., Martin J. B. Light-dark entrainment of the growth hormone ultradian rhythm in the rat is mediated by the arcuate nucleus. Endocrinology 1981; 108: 2394–2396
   PubMed Web of Science ®Google Scholar
• Moldow R. L., Fischman A. J. Hypothalamic CRF-like immunoreactivity in the rat after hypophysectomy or adrenalectomy. Peptides 1982; 3: 143–147
   Google Scholar
• Moldow R. L., Fischman A. J. Cocaine induced secretion of ACTH, beta-endorphin, and corticosterone. Peptides 1987; 8: 819–822
   PubMed Web of Science ®Google Scholar
• Natelson B. H., Ottenweller J. E., Cook J. A., Pitman D., McCarty R., Tapp W. N. Effect of stressor intensity on habituation of the adrenocortical stress response. Physiol. Behav. 1988; 43: 41–46
   PubMed Web of Science ®Google Scholar
• Natelson B. H., Ottenweller J. E., Pitman D., Tapp W. N. An assessment of prolactin's value as an index of stress. Life Sci. 1988; 42: 1597–1602
   Google Scholar
• Ottenweller J. E., Natelson B. H., Pitman D. L., Drastal S. D. Adrenocortical and behavioral responses to repeated stressors: toward an animal model of chronic stress and stress-related mental illness. Biol. Psychiatry 1989; 26: 829–841
   PubMed Web of Science ®Google Scholar
• Ottenweller J. E., Servatius R. J., Natelson B. H. Repeated stress persistently elevates morning, but not evening, plasma corticosterone levels in male rats. Physiol. Behav. 1994; 55: 337–340
   PubMed Web of Science ®Google Scholar
• Ottenweller J. E., Servatius R. J., Tapp W. N., Drastal S. D., Bergen M. T., Natelson B. H. A chronic stress state in rats: effects of repeated stress on basal corticosterone and behavior. Physiol. Behav. 1992; 51: 689–698
   PubMed Web of Science ®Google Scholar
• Pamenter R. W., Hedge G. A. Inhibition of thyrotropin secretion by physiological levels of corticosterone. Endocrinology 1980; 106: 162–166
   PubMed Web of Science ®Google Scholar
• Pitman D. L., Ottenweller J. E., Natelson B. H. Effect of stressor intensity on habituation and sensitization of glucocorticoid responses in rats. Behavioral Neuroscience 1990; 104: 28–36
   PubMed Web of Science ®Google Scholar
• Schmidt E. D., Janszen A. W.J.W., Wouterland F. G., Tilders F. J.H. Interleukin-1-induced long-lasting changes in hypothalamic corticotropin-releasing hormone (CRH)-Neurons and hyperresponsiveness of the hypofhalamus-pituitary-adrenal axis. J Neurosci. 1995; 15: 7417–7426
   PubMed Web of Science ®Google Scholar
• Servatius R. J., Ottenweller J. E., Bergen M. T., Soldan S., Natelson B. H. Persistent stress-induced sensitization of adrenocortical and startle responses. Physiol. Behav. 1994; 56: 945–954
   PubMed Web of Science ®Google Scholar
• Servatius R. J., Ottenweller J. E., Gross J. L., Natelson B. H. Persistent plasma cholesterol elevations are produced by one or three stressor exposures in rats fed a normal laboratory diet. Physiol. Behav. 1993; 53: 1101–1104
   PubMed Web of Science ®Google Scholar
• Servatius R. J., Ottenweller J. E., Natelson B. H. A comparison of the effects of repeated stressor exposures and corticosterone injections on plasma cholesterol, thyroid hormones and corticosterone levels in rats. Life Sci. 1994; 55: 1611–1617
   PubMed Web of Science ®Google Scholar
• Stone E. A., McCarty R. Adaptation to stress: tyrosine hydroxylase activity and catecholamine release. Neurosci. Biobehav. Rev. 1983; 7: 29–34
   PubMed Web of Science ®Google Scholar
• Tache Y., Du Ruisseau P., Ducharme J. R., Collu R. Pattern of adenohypophyseal hormone changes in male rats following chronic stress. Neuroendocrinology 1978; 26: 208–219
   PubMedGoogle Scholar
• Tilders F. J.H., Schmidt E. D., DeGoeij D. C.E. Phenotypic plasticity of CRH neurons during stress. Ann NY Acad Sci. 1993; 697: 39–52
   Web of Science ®Google Scholar
• Tohei A., Tomabechi T., Mamada M., Akai M., Watanabe G., Taya K. Effects of repeated ether stress on the hypothalamic-pituitary-testes axis in adult rats with special reference to inhibin secretion. J Vet. Med. Sci. 1997; 59: 329–334
   Web of Science ®Google Scholar
• Wartofsky L., Burman K. D. Alterations in thyroid function in patients with systemic illness: the “euthyroid sick syndrome”. Endocr. Rev. 1982; 3: 164–217
   PubMed Web of Science ®Google Scholar