Biology Reference
In-Depth Information
31. Berczi I. Antigenic recognition by the brain: the brain as an immunocompetent organ.
In: Berczi I, editor. New insights to neuroimmune biology. Amsterdam: Elsevier; 2010.
p. 145-60.
32. Williams JM, Peterson RG, Shea PA, Schmedtje JF, Bauer DC, Felten DL. Sympathetic
innervation of murine thymus and spleen: evidence for a functional link between the ner-
vous and immune systems. Brain Res Bull 1981;6(1):83-94.
33. Jancso G, Katona M, Horvath V, Santa P, Nagy J. Sensory nerves as modulators of
cutaneous inflammatory reactions in health and disease. In: Jancso G, editor; Berczi I,
Szentivanyi A, series editors. Neurogenic inflammation in health and disease. Neuro-
immune biology, vol. 8. Amsterdam: Elsevier; 2008. p. 3-38.
34. McKay DM, Bienenstock J. The interaction between mast cells and nerves in the gastroin-
testinal tract. Immunol Today 1994;15(11):533-38.
35. Szentivanyi A. The beta adrenergic theory of the atopic abnormality in bronchial asthma.
J Allergy 1968;42:203-32.
36. Blatteis CM. Fever as a host defense mechanism. In: Arnason BG, Berczi I, editors;
Berczi I, series editor. The brain and host defense. Neuroimmune biology, vol. 9. Amst-
erdam: Elsevier; 2010.
37. Pavlov VA, Ulloa L, Metz CN. Infection and sepsis. In: Arnason BG, Berczi I, editors;
Berczi I, series editors. The brain and host defense. Neuroimmune biology, vol. 9. Amste-
rdam: Elsevier; 2010.
38. Berczi I, Nagy E, Kovacs K, Horvath E. Regulation of humoral immunity in rats by pitu-
itary hormones. Acta Endocrinol 1981;98:506-13.
39. Benigni F, Fantuzzi G, Sacco S, Sironi M, Pozzi P, Dinarello CA, et al. Six different
cytokines that share GP130 as a receptor subunit, induce serum amyloid A and potentiate
the induction of interleukin-6 and the activation of the hypothalamus-pituitary-adrenal
axis by interleukin-1. Blood 1996;87(5):1851-54.
40. Dhabhar FS. Enhancing versus suppressive effects of stress on immune function:
implications for immunoprotection and immunopathology. In: del Rey A, Chrousos
G, Besedovsky H, editors; Berczi I, Szentivanyi A, series editors. The hypothalamus-
pituitary-adrenal axis. Amsterdam: Elsevier; 2008. p. 207-24.
41. Chesnokova V, Melmed S. Minireview: neuro-immuno-endocrine modulation of the
hypothalamic-pituitary-adrenal (HPA) axis by gp130 signaling molecules. Endocrinology
2002;143(5):1571-74.
42. McCann SM, Kimura M, Walczewska A, Karanth S, Rettori V, Yu WH. Hypothalamic
control of FSH and LH by FSH-RF, LHRH, cytokines, leptin and nitric oxide. Neuroim-
munomodulation 1998;5(3-4):193-202.
43. Chikanza IC. Prolactin and neuroimmunomodulation: in vitro and in vivo observations.
Ann NY Acad Sci 1999;22(876):119-30.
44. Skurlova M, Stofkova A, Jurcovicova J. Exogenous IL-1beta induces its own expression,
but not that of IL-6 in the hypothalamus and activates HPA axis and prolactin release.
Endocr Regul 2006;40(4):125-28.
45. Cano P, Cardinali DP, Jimenez V, Alvarez MP, Cutrera RA, Esquifino AI. Effect of
interferon-gamma treatment on 24-hour variations in plasma ACTH, growth hor-
mone, prolactin, luteinizing hormone and follicle-stimulating hormone of male rats.
Neuroimmunomodulation 2005;12(3):146-51.
46. Perez Castro C, Carbia Nagashima A, Páez Pereda M, Goldberg V, Chervin A, Carrizo G,
et al. Effects of the gp130 cytokines ciliary neurotropic factor (CNTF) and interleukin-11
on pituitary cells: CNTF receptors on human pituitary adenomas and stimulation of pro-
lactin and GH secretion in normal rat anterior pituitary aggregate cultures. J Endocrinol
2001;169(3):539-47.
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