Interleukin-4 increases cortisol release and decreases adrenal androgen release from bovine adrenal cells

Domestic Animal Endocrinology

Volumn 34, Issue 4, 2008, Pages 372-382

  Woods, Alison M ^a   Judd, Allan M ^a  

^a BRIGHAM YOUNG UNIVERSITY   (United States)

Author keywords

Adrenal; Androgen; Cortisol; Cytokine; Interleukin 4

Indexed keywords

ANDROGEN; HYDROCORTISONE; INTERLEUKIN 4; INTERLEUKIN 4 RECEPTOR;

ADRENAL CORTEX; ADRENAL GLAND; ANIMAL; ARTICLE; CATTLE; CELL CULTURE; DOSE RESPONSE; DRUG EFFECT; METABOLISM; SECRETION; STRESS; TIME; ZONA FASCICULATA;

ADRENAL GLANDS; ANDROGENS; ANIMALS; CATTLE; CELLS, CULTURED; DOSE-RESPONSE RELATIONSHIP, DRUG; HYDROCORTISONE; INTERLEUKIN-4; RECEPTORS, INTERLEUKIN-4; STRESS; TIME FACTORS; ZONA FASCICULATA; ZONA RETICULARIS;

BOVINAE;

EID: 42949096954     PISSN: 07397240     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.domaniend.2007.10.004     Document Type: Article

References (55)

1. Beishuizen A., Thijs L.G., Haanen C., and Vermes I. Macrophage migration inhibitory factor and hypothalamo-pituitary-adrenal function during critical illness. J Clin Endocrinol Metab 86 6 (2001) 2811-2816
2. Beishuizen A., Thijs L.G., and Vermes I. Decreased levels of dehydroepiandrosterone sulphate in severe critical illness: a sign of exhausted adrenal reserve?. Crit Care 6 5 (2002) 434-438
3. Almeida P.E., Weber P.S., Burton J.L., and Zanella A.J. Depressed DHEA and increased sickness response behaviors in lame dairy cows with inflammatory foot lesions. Domest Anim Endcorinol 34 1 (2008) 89-99
4. Beishuizen A., and Thijs L.G. The immunoneuroendocrine axis in critical illness: beneficial adaptation or neuroendocrine exhaustion?. Curr Opin Crit Care 10 6 (2004) 461-467
5. Vermes I., and Beishuizen A. The hypothalamic-pituitary-adrenal response to critical illness. Best Pract Res Clin Endocrinol Metab 15 4 (2001) 495-511
6. Alesci S., and Bornstein S.R. Neuroimmunoregulation of androgens in the adrenal gland and the skin. Horm Res 54 5-6 (2000) 281-286
7. Parker C.R. Dehydsoepiandrosterone and dehydroepiandrosterone sulfate production in the human adrenal during development and aging. Steroids 64 9 (1999) 640-647
8. Straub R.H., Schuld A., Mullington J., Haack M., Scholmerich J., and Pollmacher T. The endotoxin-induced increase of cytokines is followed by an increase of cortisol relative to dehydroepiandrosterone (DHEA) in healthy male subjects. J Endocrinol 175 2 (2002) 467-474
9. Straub R.H., Lehle K., Herfarth H., Weber M., Falk W., Preuner J., et al. Dehydroepiandrosterone in relation to other adrenal hormones during an acute inflammatory stressful disease state compared with chronic inflammatory disease: role of interleukin-6 and tumour necrosis factor. Eur J Endocrinol 146 3 (2002) 365-374
10. Bornstein S.R., Rutkowski H., and Vrezas I. Cytokines and steroidogenesis. Mol Cell Endocrinol 215 1-2 (2004) 135-141
11. Ehrhart-Bornstein M., Hinson J.P., Bornstein S.R., Scherbaum W.A., and Vinson G.P. Intraadrenal interactions in the regulation of adrenocortical steroidogenesis. Endocr Rev 19 2 (1998) 101-143
12. Judd A.M. Cytokine expression in the rat adrenal cortex. Horm Metab Res 30 6-7 (1998) 404-410
13. Judd A.M., Call G.B., Barney M., McIlmoil C.J., Balls A.G., Adams A., et al. Possible function of IL-6 and TNF as intraadrenal factors in the regulation of adrenal steroid secretion. Ann N Y Acad Sci 917 (2000) 628-637
14. Cardoso E., Arzt E., Coumroglon M., Andrada E.C., and Andrada J.A. Alpha-interferon induces cortisol release by human adrenals in vitro. Int Arch Allergy Appl Immunol 93 2-3 (1990) 263-266
15. Koldzic-Zivanovic N., Tu H., Juelich T.L., Rady P.L., Tyring S.K., Hudnall S.D., et al. Regulation of adrenal glucocorticoid synthesis by interleukin-10: a preponderance of IL-10 receptor in the adrenal zona fasciculata. Brain Behav Immun 20 5 (2006) 460-468
16. Lo M.J., and Lee S.D. Direct effects of IL-15 on corticosterone secretion by rat adrenocortical cells. Immunol Cell Biol 84 1 (2006) 38-43
17. Michl P., Beikler T., Engelhardt D., and Weber M.M. Interleukin-3 and interleukin-6 stimulate bovine adrenal cortisol secretion through different pathways. J Neuroendocrinol 12 1 (2000) 23-28
18. Tominaga T., Fukata J., Naito Y., Usui T., Murakami N., Fukushima M., et al. Prostaglandin-dependent in vitro stimulation of adrenocortical ateroidogenesis by interleukins. Endocrinology 128 1 (1991) 526-531
19. Romero D.G., Vergara G.R., Zhu Z., Covington G.S., Plonczynski M.W., Yanes L.L., et al. Interleukin-8 synthesis, regulation, and steroidogenic role in H295R human adrenocortical cells. Endocrinology 147 2 (2006) 891-898
20. Sekiyama A., Ueda H., Kashiwamura S., and Okamura H. Stress induced, superoxide mediated caspase-1 activation causes plasma cytokines' elevation. Biol Psychiatry 57 8 (2005) 92S
21. Sekiyama A., Ueda H., Kashiwamura S., Sekiyama R., Takeda M., Rokutan K., et al. A stress-induced, superoxide-mediated caspase-1 activation pathway causes plasma IL-18 upregulation. Immunity 22 6 (2005) 669-677
22. Sekiyama A., Ueda H., Kashiwamura S., Nishida K., Yamaguchi S., Sasaki H., et al. A role of the adrenal gland in stress-induced up-regulation of cytokines in plasma. J Neuroimmunol 171 1-2 (2006) 38-44
23. Pinto J.G., Martins L.A., Cavalheiro J.S., Acorsi M.J., Pedrini S.C.B., Soares A.M.V.C., et al. Cytokine production in lungs and adrenal glands of high and low antibody producing mice infected with Paracoccidioides brasiliensis. Med Mycol 44 6 (2006) 505-514
24. Debinski W., Puri R.K., Kreitman R.J., and Pastan I. A wide-range of human cancers express interleukin-4 (IL4) receptors that can be targeted with chimeric toxin composed of IL4 and pseudomonas exotoxin. J Biol Chem 268 19 (1993) 14065-14070
25. Simard J., Ricketts M.L., Gingras B., Soucy P., Feltus F.A., and Melner M.H. Molecular biology of the 3 beta-hydroxysteroid dehydrogenase/delta(5)-delta(4) isomerase gene family. Endocr Rev 26 4 (2005) 525-582
26. Burke F., Relf M., Negus R., and Balkwill F. A cytokine profile of normal and malignant ovary. Cytokine 8 7 (1996) 578-585
27. Hashii K., Fujiwara H., Yoshioka S., Kataoka N., Yamada S., Hirano T., et al. Peripheral blood mononuclear cells stimulate progesterone production by luteal cells derived from pregnant and non-pregnant women: possible involvement of interleukin-4 and interleukin-10 in corpus luteum function and differentiation. Hum Reprod 13 10 (1998) 2738-2744
28. Evagelatou M., Peterson S.L., and Cooke B.A. Leukocytes modulate 11 beta-hydroxysteroid dehydrogenase (11 beta-HSD) activity in human granulosa-lutein cell cultures. Mol Cell Endocrinol 133 2 (1997) 81-88
29. Sakumoto R., Komatsu T., Kasuya E., Saito T., and Okuda K. Expression-of mRNAs for interleukin-4, interleukin-6 and their receptors in porcine corpus luteum during the estrous cycle. Domest Anim Endocrinol 31 3 (2006) 246-257
30. Barney M., Call G.B., McIlmoil C.J., Husein O.F., Adams A., Balls A.G., et al. Stimulation by interleukin-6 and inhibition by tumor necrosis factor of cortisol release from bovine adrenal zona fasciculata cells through their receptors. Endocrine 13 3 (2000) 369-377
31. Call G.B., Husein O.F., McIlmoil C.J., Adams A., Heckmann R.A., and Judd A.M. Bovine adrenal cells secrete interleukin-6 and tumor necrosis factor in vitro. Gen Comp Endocrinol 118 2 (2000) 249-261
32. Wallenstein S., Zucker C.L., and Fleiss J.L. Some statistical-methods useful in circulation research. Circ Res 47 1 (1980) 1-9
33. Nelms K., Keegan A.D., Zamorano J., Ryan J.J., and Paul W.E. The IL-4 receptor: signaling mechanisms and biologic functions. Annu Rev Immunol 17 (1999) 701-738
34. Hwang H., Choi S.Y., and Kim T.Y. IL-4 suppresses UVB-induced apoptosis in skin. J Biochem Mol Biol 40 1 (2007) 36-43
35. Finnegan A., Grusby M.J., Kaplan C.D., O'Neill S.K., Eibel H., Koreny T., et al. IL-4 and IL-12 regulate proteoglycan-induced arthritis through stat-dependent mechanisms. J Immunol 169 6 (2002) 3345-3352
36. Steinke J.W., and Borish L. Th2 cytokines and asthma. Interleukin-4: its role in the pathogenesis of asthma, and targeting it for asthma treatment with interleukin-4 receptor antagonists. Resp Res 2 2 (2001) 66-70
37. Walch L., Massade L., Dufilho M., Brunet A., and Rendu F. Pro-atherogenic effect of interleukin-4 in endothelial cells: modulation of oxidative stress, nitric oxide and monocyte chernoattractant protein-1 expression. Atherosclerosis 187 2 (2006) 285-291
38. Fang V.S. Cytotoxic activity of 1-(o-chlorophenyl)-1-(p-chlorophenyl)-2,2-dichloroethane (mitotane) and its analogs on feminizing adrenal neoplastic cells in culture. Cancer Res 39 1 (1979) 139-145
39. Wang S.M., Lei H.Y., Huang M.C., Su L.Y., Lin H.C., Yu C.K., et al. Modulation of cytokine production by intravenous immunoglobulin in patients with enterovirus 71-associated brainstem encephalitis. J Clin Virol 37 1 (2006) 47-52
40. Zhang Y.C., Li J., Zhan Y.L., Wu L.Q., Yu X.Y., Zhang W.J., et al. Analysis of serum cytokines in patients with severe acute respiratory syndrome. Infect Immun 72 8 (2004) 4410-4415
41. Viveros-Paredes J.M., Puebla-Perez A.M., Gutierrez-Coronado O., Sandoval-Ramirez L., and Villasenor-Garcia M.M. Dysregulation of the Th1/Th2 cytokine profile is associated with immunosuppression induced by hypothalamic-pituitary-adrenal axis activation in mice. Int Immunopharmacol 6 5 (2006) 774-781
42. Flynn R.J., Mannion C., Golden O., Hacariz O., and Mulcahy G. Experimental Fasciola hepatica infection alters responses to tests used for diagnosis of bovine tuberculosis. Infect Immun 75 3 (2007) 1373-1381
43. Rosbottom A., Guy C.S., Gibney E.H., Smith R.F., Valarcher J.F., Taylor G., et al. Peripheral immune responses in pregnant cattle following Neospora caninum infection. Parasite Immunol 29 4 (2007) 219-228
44. Thom M.L., Hope J.C., McAulay M., Villarreal-Ramos B., Coffey T.J., Stephens S., et al. The effect of tuberculin testing on the development of cell-mediated immune responses during mycobacterium bovis infection. Vet Immunol Immunopathol 114 1-2 (2006) 25-36
45. Breslow M.J. Regulation of adrenal-medullary and cortical blood-flow. Am J Physiol 262 5 (1992) H1317-H1330
46. Tagawa N., Hidaka Y., Takano T., Shimaoka Y., Kobayashi Y., and Amino N. Serum concentrations of androstenediol and androstenediol sulfate, and their relation to cytokine production during and after normal pregnancy. Steroids 69 10 (2004) 675-680
47. Tagawa N., Hidaka Y., Takano T., Shimaoka Y., Kobayashi Y., and Amino N. Serum concentrations of dehydroepiandrosterone and dehydroepiandrosterone sulfate and their relation to cytokine production during and after normal pregnancy. Clin Chim Acta 340 1-2 (2004) 187-193
48. Mueller M., Atanasov A., Cima I., Corazza N., Schoonjans K., and Brunner T. Differential regulation of glucocorticoid synthesis in murine intestinal epithelial versus adrenocortical cell lines. Endocrinology 148 3 (2007) 1445-1453
49. Sapolsky R.M., Romero L.M., and Munck A.U. How do glucocorticoids influence stress responses? Integrating permissive, suppressive, stimulatory, and preparative actions. Endocr Rev 21 1 (2000) 55-89
50. Saponaro S., Guarnieri V., Pescarmona G.P., and Silvagno F. Long-term exposure to dehydroepiandrosterone affects the transcriptional activity of the glucocorticoid receptors. J Steroid Biochem Mol Biol 103 2 (2007) 129-136
51. Kim S.K., Shin M.S., Jung B.K., Shim J.Y., Won H.S., Lee P.R., et al. Effect of dehydroepiandrosterone on lipopolysaccharide-induced interleukin-6 production in DH82 cultured canine macrophage cells. J Reprod Immunol 70 1-2 (2006) 71-81
52. Kawano H., Yasue H., Kitagawa A., Hirai N., Yoshida T., Soejima H., et al. Dehydroepiandrosterone supplementation improves endothelial function and insulin sensitivity in men. J Clin Endocrinol Metab 88 7 (2003) 3190-3195
53. Olech E., and Merrill J.T. DHEA supplementation: the claims in perspective. Clev Clin J Med 72 11 (2005) 965-984
54. Chen F., Knecht K., Birzin E., Fisher J., Wilkinson H., Mojena M., et al. Direct agonist/antagonist functions of dehydroepiandrosterone. Endocrinology 146 11 (2005) 4568-4576
55. Webb S.J., Geoghegan T.E., and Prough R.A. The biological actions of dehydroepiandrosterone involves multiple receptors. Drug Metab Rev 38 1-2 (2006) 89-116