The Effect of Stress on Inflammation

References

• Aguilera G., Jessop D. S., Harbuz M. S., Kiss A., Lightman S. L. Differential regulation of hypothalamic pituitary corticotropin releasing hormone receptors during development of adjuvant-induced arthritis in the rat. J. Endocrinol. 1997; 153: 185–191
   PubMedGoogle Scholar
• Bonneau R. H., Sheridan J. F., Feng N., Glaser R. Stress induced suppression of herpes simplex virus (HSV)-specific cytotoxic T lymphocyte and natural killer cell activity and enhancement of acute pathogenesis following local HSV infection. Brain Behav. Immun. 1991; 5: 170–192
   PubMed Web of Science ®Google Scholar
• Broadhurst P. L. Experiments in Personality, H. J. Eysenck. Praeger, New York 1960; Vol. 1: 2
   Google Scholar
• Bruot B. C., Clemens J. W. Effects of adjuvant-induced arthritis on serum luteinizing hormone and testosterone concentrations in the male rat. Life. Sci. 1987; 41: 1559–1565
   PubMedGoogle Scholar
• Calogero A. E., Sternberg E. M., Bagdy G., Smith C., Bernardini R., Aksentijevich S., Wilder R. L., Gold P. W., Chrousos G. P. Neurotransmitter-induced hypothalamic-pituitary-adrenal axis responsiveness is defective in inflammatory disease-susceptible Lewis rats: in vivo and in vitro studies suggesting globally defective hypothalamic secretion of corticotropin-releasing hormone. Neuroendocrinology 1992; 55: 600–608
   PubMedGoogle Scholar
• Cash J. M., Crofford L. J., Gallucci W. T., Sternberg E. M., Gold P. W., Chrousos G. P., Wilder R. L. Pituitary-adrenal axis responsiveness to ovine corticotropin releasing hormone in patients with rheumatoid arthritis treated with low dose prednisone. J. Rheumatol. 1992; 19: 1692–1696
   PubMedGoogle Scholar
• Cavallo T., Granholm N. A. Lipopolysaccharide from gram-negative bacteria enhances polyclonal B cell activation and exacerbates nephritis in MRL/lpr mice. Clin. Exp. Immunol. 1990; 82: 515–521
   PubMed Web of Science ®Google Scholar
• Cerinic M. M., Konttinen Y., Gencrini S., Cutolo M. Neuropeptides and steroid hormones in arthritis. Curr. Opin. Rheumatol. 1998; 10: 220–235
   PubMedGoogle Scholar
• Chikanza I. C., Grossman A. B. Hypothalamic-pitutary-mediated immunomodulation: arginine vasopressin in a neuroendocrine immune mediator. Br J. Rheumatol. 1998; 37: 131–236
   PubMedGoogle Scholar
• Chover-Gonzalez A. J., Harbuz M. S., Tejedor-Real P., Gibert-Rahola J., Larsen P. J., Jessop D. S. Effects of stress on susceptibility and severity of inflammation in adjuvant-induced arthritis. Ann. N. Y. Acad. Sci. 1999; 876: 276–386
   PubMedGoogle Scholar
• Chover-Gonzalez A. J., Jessop D. S., Tejedor-Real P., Gibert-Rahola J., Harbuz M. S. Onset and severity of inflammation in rats exposed to the learned helplessness paradigm. Rheumatology 2000; 39: 764–771
   PubMed Web of Science ®Google Scholar
• Chover-Gonzalez A. J., Tejedor-Real P., Harbuz M. S., Gibert-Rahola J., Larsen P. J., Jessop D. S. A differential response to stress is not a prediction of susceptibility or severity in adjuvant-induced arthritis. Stress 1998; 2: 221–226
   PubMedGoogle Scholar
• Coe C. L., Rosenberg L. T., Levine S. Effect of maternal separation on the complement system and antibody responses in infant primates. Int. J. Neurosci. 1988; 40: 289–302
   PubMed Web of Science ®Google Scholar
• Deak T., Meriwether J. L., Fleshner M., Spencer R. L., Abouhamze A., Moldawer L. L., Grahn R. E., Watkins L. R., Maier S. F. Evidence that brief stress may induce the acute phase response in rats. Am. J. Physiol. 1997; 273: R1998–2004
   Google Scholar
• Derijk R., Berkenbosch F. The immune-hypothalamo-pituitary-adrenal axis and autoimmunity. Int. J. Neurosci. 1991; 59: 59–91
   Google Scholar
• Esterling B., Rabin B. S. Stress-induced alteration of T-lymphocyte subsets and humoral immunity in mice. Behav. Neurosci. 1987; 101: 115–119
   PubMed Web of Science ®Google Scholar
• Fleshner M., Laudenslager M. L., Simons L., Maier S. F. Reduced serum antibodies associated with social defeat in rats. Physiol. Behav. 1989; 45: 1183–1187
   PubMed Web of Science ®Google Scholar
• Goffin V., Bouchard B., Ormandy C. J., Weimann E., Ferrag F., Touraine P., Bole-Feysot C., Maaskant R. A., Clement-Lacroix P., Edery M., Binart N., Kelly P. A. Prolactin: a hormone at the crossroads of neuroimmunoendocrinology. Ann. N.Y. Acad. Sci. 1998; 840: 498–509
   PubMed Web of Science ®Google Scholar
• Gudbjornsson B., Skogseid B., Oberg K., Wide L., Hallgren R. Intact adrenocorticotropic hormone secretion but impaired Cortisol response in patients with active rheumatoid arthritis. Effect of glucocorticoids. J. Rheumatol. 1996; 23: 596–602
   PubMed Web of Science ®Google Scholar
• Harbuz M. S., Jessop D. S. Is there a defect in Cortisol production in rheumatoid arthritis?. Rheumatology 1999; 38: 298–302
   PubMed Web of Science ®Google Scholar
• Harbuz M. S., Marti O., Lightman S. L., Jessop D. S. Alteration of central serotonin modifies onset and severity of adjuvant-induced arthritis in the rat. Br. J. Rheumatol. 1998; 37: 1077–1083
   PubMedGoogle Scholar
• Harbuz M. S., Perveen-Gill Z., Lightman S. L., Jessop D. S. A protective role for testosterone in adjuvant-induced arthritis. Br. J. Rheumatol. 1995; 34: 1117–1122
   PubMedGoogle Scholar
• Harbuz M. S., Rees R. G., Eckland D., Jessop D. S., Brewerton D., Lightman S. L. Paradoxical responses of hypothalamic corticotropin-releasing factor (CRF) messenger ribonucleic acid (mRNA) and CRF-41 peptide and adenohypophysial proopiomelanocortin mRNA during chronic inflammatory stress. Endocrinology 1992; 130: 1394–1400
   PubMed Web of Science ®Google Scholar
• Harbuz M. S., Rees R. G., Lightman S. L. Hypothalamo-pituitary responses to acute stress and changes in circulating glucocorticoids during chronic adjuvant-induced arthritis in the rat. Am. J. Physiol. 1993; 264: R179–R185
   Google Scholar
• Harbuz M. S., Rooney C., Jones M., Ingram C. D. Hypothalamo-pituitary-adrenal axis responses to lipopolysaccharide in male and female rats with adjuvant-induced arthritis. Brain. Behav. Immun. 1999; 13: 335–347
   PubMedGoogle Scholar
• Hellhammer D. H., Rea M. A., Bell M., Belkien L., Ludwig M. Learned helplessness: effects on brain monoamines and the pituitary-gonadal axis. Pharmacol. Biochem. Behav. 1984; 21: 481–485
   PubMedGoogle Scholar
• Jann K., Jann B. Polysaccharide antigens of Escherichia coli. Rev. Infect. Dis. 1987; 9: S517–S526
   Google Scholar
• Jessop D. S. Neuropeptides: modulators of the immune system. Curr. Opin. Endocrinol. Diabetes 1998a; 5: 52–58
   Google Scholar
• Jessop D. S. Beta-endorphin in the immune system- mediator of pain and stress?. Lancet 1998b; 351: 1828–1829
   PubMed Web of Science ®Google Scholar
• Jiang C. G., Morrow-Tesch J. L., Beller D. S., Levy E. M., Black P. H. Immune suppression in mice induced by cold water stress. Brain Behav. Immun. 1990; 4: 278–291
   PubMed Web of Science ®Google Scholar
• Jorgensen C., Bressot N., Bologna C., Sany J. Dysregulation of the hypothalamo-pituitary axis in rheumatoid arthritis. J. Rheumatol. 1995; 22: 1829–1833
   PubMedGoogle Scholar
• Kanik K. S., Chrousos G. P., Schumacher H. R., Crane M. L., Yarboro C. H., Wilder R. L. Adrenocorticotropin, glucocorticoid, and androgen secretion in patients with new onset synovitis/rheumatoid arthritis: relations with indices of inflammation. J. Clin. Endocrinol. Metab. 2000; 85: 1461–1466
   PubMed Web of Science ®Google Scholar
• Keller S. E., Weiss J. M., Schleifer S. J., Miller N. E., Stein M. Stress-induced suppression of immunity in adrenalectomized rats. Science 1983; 221: 1301–1304
   PubMed Web of Science ®Google Scholar
• Madden K. S., Felten D. L. Experimental basis for neural-immune interactions. Physiol. Rev. 1995; 75: 75–77
   Google Scholar
• Maier S. F., Goehler L. E., Fleshner M. L.R., Watkins. The role of the vagus nerve in cytokine-to-brain communication. Ann. N. Y. Acad. Sci. 1998; 840: 289–300
   PubMed Web of Science ®Google Scholar
• Marti O., Garcia A., Valles A., Harbuz M. S., Armario A. Evidence that a single exposure to aversive stimuli triggers long-lasting effects in the hypothalamus-pituitary-adrenal axis that consolidate with time. Eur. J. Neurosci. 2001; 13: 13–129
   Google Scholar
• Masi A. T. Hormonal and immunological risk factors for the development of arthritis: an integrative physiopathogenetic perspective. Neuroendocr. Mech. Rheum. Dis. 2000; 26: 775–803
   Google Scholar
• Masi A. T. Sex hormones and rheumatoid arthritis: cause or effect relationship in a complex pathophysiology?. Clin. Exp. Rheumatol. 1995; 13: 227–240
   PubMed Web of Science ®Google Scholar
• Masi A. T., Josipovic D. B., Jefferson W. E. Low adrenal androgenic-anabolic steroids in women with rheumatoid arthritis. Semin. Arthritis Rheum. 1984; 14: 1–23
   PubMed Web of Science ®Google Scholar
• Mason D. Genetic variation in the stress response: susceptibility to experimental allergic encephalomyelitis and implications for human inflammatory disease. Immunol. Today 1991; 12: 57–60
   PubMedGoogle Scholar
• Moynihan J., Brenner G., Koota D., Breneman S., Cohen N., Ader R. The effect of handling on antibody production, mitogen responses, spleen cell number, and lymphocyte subpopulations. Life Sci. 1990; 46: 1937–1944
   PubMed Web of Science ®Google Scholar
• Moynihan J., Koota D., Brenner G., Cohen N., Ader R. Repeated intraperitoneal injections of saline attenuate the antibody response to a subsequent intraperitoneal injection of antigen. Brain Behav. Immun. 1989; 3: 90–96
   PubMedGoogle Scholar
• Nankai M., Yamada S., Muneoka K., Toru M. Increased 5-HT2 receptor-mediated behavior 11 days after shock in learned helplessness rats. Eur. J. Pharmacol. 1995; 281: 123–130
   PubMed Web of Science ®Google Scholar
• Petty F., Davis L. L., Kabel D., Kramer G. L. Serotonin dysfunction disorders: a behavioral neurochemistry perspective. J. Clin. Psychiatry 1996; 57: 11–16
   PubMedGoogle Scholar
• Pousset E, Fournier J., Legoux P., Keane P., Shire D., Soubrie P. Effect of serotonin on cytokine mRNA expression in rat hippocampal astrocytes. Brain Res. Mol. Brain Res. 1996; 38: 54–62
   PubMedGoogle Scholar
• Rabin B. S., Lyte M., Epstein L. H., Caggiula A. R. Alteration of immune competency by number of mice housed per cage. Ann. N Y. Acad. Sci. 1987; 496: 492–500
   PubMedGoogle Scholar
• Rietschel E. T., Kirikae T. F.U.S., Mamat U., Schmidt G., Loppnow H., Ulmer A. J., Zahringer U., Seudel U., Di Padova F. Bacterial endotoxin: molecular relationships of structure to activity and function. FASEB J. 1994; 8: 217–225
   PubMed Web of Science ®Google Scholar
• Schmidt E. D., Binnekade R., Janszen A. W., Tilders F. J. Short stressor induced long-lasting increases of vasopressin stores in hypothalamic corticotropin-releasing hormone (CRH) neurons in adult rats. J. Neuroendocrinal. 1996; 8: 703–712
   PubMedGoogle Scholar
• Shanks N., Windle R. J., Perks P., Harbuz M. S., Jessop D. S., Ingram C. D., Lightman S. L. Early life exposure to endotoxin alters hypothalamic-pituitary-adrenal function and predisposition to inflammation. Proc. Natl. Acad. Sci. U.S.A. 2000; 97: 5645–5650
   PubMed Web of Science ®Google Scholar
• Sternberg E. M., Hill J. M., Chrousos G. P., Kamilaris T., Listwak S. J., Gold P. W., Wilder R. L. Inflammatory mediator-induced hypothalamic-pituitary-adrenal axis activation is defective in streptococcal cell wall arthritis-susceptible Lewis rats. Proc. Natl. Acad. Sci. U.S.A. 1989; 86: 2374–2378
   PubMed Web of Science ®Google Scholar
• Steward A., Bayley D. L. Effects of androgens in models of rheumatoid arthritis. Agents Actions 1992; 35: 268–272
   PubMedGoogle Scholar
• Tilders F. J.H., Schmidt E. D., De Vries T. J., Vandersceuren L. J.M., Schoffelmeer A. N.M., Jansen A. S.P. Mechanisms in neuroendocrine stress sensitization. Neuropsychopharmacology 2000; 23: S32
   Google Scholar
• Tilders F. J.H., Schmidt E. D., Hoodedijk W. J.G., Swaab D. F. Delayed effects of stress and immune activation. Baillieres Clin. Endocrinol. Metab. 1999; 13: 523–540
   PubMed Web of Science ®Google Scholar
• van den Brink H. R., Blankenstein M. A., Koppeschaar H. P., Bijlsma J. W. Influence of disease activity on steroid hormone levels in peripheral blood of patients with rheumatoid arthritis. Clin. Exp. Rheumatol. 1993; 11: 649–652
   PubMedGoogle Scholar
• Walker J. G., Littlejohn G. O., McMurray N. E., Cutolo M. Stress system response and rheumatoid arthritis: a multilevel approach. Rheumatology 1999; 38: 1050–1057
   PubMed Web of Science ®Google Scholar
• Willner P. The validity of animal models of depression. Psychopharmacology 1984; 83: 1–16
   PubMed Web of Science ®Google Scholar
• Yokochi T., Fujii Y., Nakashima I., Asai J., Kiuchi M., Kojima K., Kato N. A murine model of experimental autoimmune lens-induced uveitis using Klebsiella O3 lipopolysaccharide as a potent immunological adjuvant. Int. J. Exp. Pathol. 1993; 74: 573–582
   PubMedGoogle Scholar
• Yoshino S., Sasatomi E., Ohsawa M. Bacterial lipopolysaccharide acts as an adjuvant to induce autoimmune arthritis in mice. Immunology 2000; 99: 607–614
   PubMed Web of Science ®Google Scholar