Show simple item record

The role of corticosterone in human hypothalamic– pituitary–adrenal axis feedback

dc.contributor.authorRaubenheimer, Peter J.en_US
dc.contributor.authorYoung, Elizabeth A.en_US
dc.contributor.authorAndrew, Ruthen_US
dc.contributor.authorSeckl, Jonathan R.en_US
dc.date.accessioned2010-06-01T19:08:36Z
dc.date.available2010-06-01T19:08:36Z
dc.date.issued2006-07en_US
dc.identifier.citationRaubenheimer, Peter J.; Young, Elizabeth A.; Andrew, Ruth; Seckl, Jonathan R. (2006). "The role of corticosterone in human hypothalamic– pituitary–adrenal axis feedback." Clinical Endocrinology 65(1): 22-26. <http://hdl.handle.net/2027.42/72329>en_US
dc.identifier.issn0300-0664en_US
dc.identifier.issn1365-2265en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/72329
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=16817814&dopt=citationen_US
dc.description.abstractObjective  In humans, the glucocorticoid corticosterone circulates in blood at 10–20-fold lower levels than cortisol, but is found in higher relative amounts in postmortem brain samples. Access of cortisol and corticosterone to the central nervous system may not be equal. Additionally, the relative affinities for the glucocorticoid and mineralocorticoid receptors differ, such that corticosterone may play a significant role in human brain function. Design  We measured cortisol and corticosterone levels in paired plasma and cerebrospinal fluid (CSF) samples. To test the relative potency of cortisol vs. corticosterone on hypothalamic–pituitary–adrenal (HPA) feedback, subjects underwent a three-phase, single-blind, randomized study assessing the postmetyrapone ACTH response over 3 h to an intravenous bolus of vehicle, cortisol or corticosterone (0·15 mg/kg and 0·04 mg/kg). Participants  Outpatients undergoing diagnostic lumbar puncture who were subsequently deemed to be free of disease. Feedback was tested in healthy male volunteers. Measurements  Plasma and CSF corticosterone to cortisol ratio was calculated and the ACTH response over time after the bolus glucocorticoid measured. Results  Plasma corticosterone : cortisol was 0·069 ± 0·007; CSF corticosterone : cortisol was 0·387 ± 0·050 ( P <  0·001). Cortisol and corticosterone (0·15 mg/kg) suppressed ACTH vs. vehicle ( P =  0·002); there was no difference between corticosterone and cortisol. The 0·04 mg/kg dose had no effect on ACTH despite supraphysiological plasma corticosterone levels. Conclusions  Corticosterone contributes almost 40% of total active glucocorticoids (cortisol and corticosterone) in the CSF. Significant effects on HPA axis suppression were only seen with supraphysiological levels of corticosterone, suggesting that corticosterone is not important in this model of nonstress-induced ACTH hypersecretion, in which the effect of cortisol predominates.en_US
dc.format.extent145384 bytes
dc.format.extent3109 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing Ltden_US
dc.rights© 2006 The Authors Journal compilation © 2006 Blackwell Publishing Ltden_US
dc.titleThe role of corticosterone in human hypothalamic– pituitary–adrenal axis feedbacken_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationum† Department of Psychiatry and Mental Health Research Institute, University of Michigan, Ann Arbor, MI, USAen_US
dc.contributor.affiliationother* Department of Endocrinology, University of Edinburgh, Centre for Cardiovascular Science, The Queen's Medical Research Institute, Edinburgh, UK anden_US
dc.identifier.pmid16817814en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/72329/1/j.1365-2265.2006.02540.x.pdf
dc.identifier.doi10.1111/j.1365-2265.2006.02540.xen_US
dc.identifier.sourceClinical Endocrinologyen_US
dc.identifier.citedreferenceUnderwood, R.H. & Williams, G.H. ( 1972 ) The simultaneous measurement of aldosterone, cortisol, and corticosterone in human peripheral plasma by displacement analysis. Journal of Laboratory and Clinical Medicine, 79, 848 – 862.en_US
dc.identifier.citedreferenceWest, C.D., Mahajan, D.K., Chavre, V.J., Nabors, C.J. & Tyler, F.H. ( 1973 ) Simultaneous measurement of multiple plasma steroids by radioimmunoassay demonstrating episodic secretion. Journal of Clinical Endocrinology and Metabolism, 36, 1230 – 1236.en_US
dc.identifier.citedreferenceNishida, S., Matsumura, S., Horino, M., Oyama, H. & Tenku, A. ( 1977 ) The variations of plasma corticosterone/cortisol ratios following ACTH stimulation or dexamethasone administration in normal men. Journal of Clinical Endocrinology and Metabolism, 45, 585 – 588.en_US
dc.identifier.citedreferenceSeckl, J.R., Campbell, J.C., Edwards, C.R., Christie, J.E., Whalley, L.J., Goodwin, G.M. & Fink, G. ( 1990 ) Diurnal variation of plasma corticosterone in depression. Psychoneuroendocrinology, 15, 485 – 488.en_US
dc.identifier.citedreferenceCordon-Cardo, C., O’Brien, J.P., Casals, D., Rittman-Grauer, L., Biedler, J.L., Melamed, M.R. & Bertino, J.R. ( 1989 ) Multidrug-resistance gene (P-glycoprotein) is expressed by endothelial cells at blood–brain barrier sites. Proceedings of the National Academy of Sciences of the United States of America, 86, 695 – 698.en_US
dc.identifier.citedreferenceMeijer, O.C., de Lange, E.C.M., Breimer, D.D., de Boer, A.G., Workel, J.O. & de Kloet, E.R. ( 1998 ) Penetration of dexamethasone into brain glucocorticoid targets is enhanced in mdr1A P-glycoprotein knockout mice. Endocrinology, 139, 1789 – 1793.en_US
dc.identifier.citedreferenceKarssen, A.M., Meijer, O.C., van der Sandt, I.C.J., Lucassen, P.J., de Lange, E.C.M., de Boer, A.G. & de Kloet, E.R. ( 2001 ) Multidrug resistance P-glycoprotein hampers the access of cortisol but not of corticosterone to mouse and human brain. Endocrinology, 142, 2686 – 2694.en_US
dc.identifier.citedreferenceBrooksbank, B.W., Brammall, M.A. & Shaw, D.M. ( 1973 ) Estimation of cortisol, cortisone and corticosterone in cerebral cortex, hypothalamus and other regions of the human brain after natural death and after death by suicide. Steroids and Lipids Research, 4, 162 – 183.en_US
dc.identifier.citedreferenceKeller-Wood, M.E. & Dallman, M.F. ( 1984 ) Corticosteroid inhibition of ACTH secretion. Endocrine Reviews, 5, 1 – 24.en_US
dc.identifier.citedreferenceMcEwen, B.S., Weiss, J.M. & Schwartz, L.S. ( 1968 ) Selective retention of corticosterone by limbic structures in rat brain. Nature, 220, 911 – 912.en_US
dc.identifier.citedreferenceDe Kloet, R., Wallach, G. & McEwen, B.S. ( 1975 ) Differences in corticosterone and dexamethasone binding to rat brain and pituitary. Endocrinology, 96, 598 – 609.en_US
dc.identifier.citedreferenceReul, J.M. & de Kloet, E.R. ( 1985 ) Two receptor systems for corticosterone in rat brain: microdistribution and differential occupation. Endocrinology, 117, 2505 – 2511.en_US
dc.identifier.citedreferenceIwasaki, E. ( 1987 ) Hydrocortisone succinate and hydrocortisone simultaneously determined in plasma by reversed-phase liquid chromatography, and their pharmacokinetics in asthmatic children. Clinical Chemistry, 33, 1412 – 1415.en_US
dc.identifier.citedreferenceSpencer, R.L., Young, E.A., Choo, P.H. & McEwen, B.S. ( 1990 ) Adrenal steroid type I and type II receptor binding: estimates of in vivo receptor number, occupancy, and activation with varying level of steroid. Brain Research, 514, 37 – 48.en_US
dc.identifier.citedreferenceSpencer, R.L., Miller, A.H., Moday, H., Stein, M. & McEwen, B.S. ( 1993 ) Diurnal differences in basal and acute stress levels of type I and type II adrenal steroid receptor activation in neural and immune tissues. Endocrinology, 133, 1941 – 1950.en_US
dc.identifier.citedreferencede Kloet, E.R., Vreugdenhil, E., Oitzl, M.S. & Joels, M. ( 1998 ) Brain corticosteroid receptor balance in health and disease. Endocrine Reviews, 19, 269 – 301.en_US
dc.identifier.citedreferenceBradbury, M.J., Akana, S.F. & Dallman, M.F. ( 1994 ) Roles of type I and II corticosteroid receptors in regulation of basal activity in the hypothalamo–pituitary–adrenal axis during the diurnal trough and the peak: evidence for a nonadditive effect of combined receptor occupation. Endocrinology, 134, 1286 – 1296.en_US
dc.identifier.citedreferenceYoung, E.A., Lopez, J.F., Murphy-Weinberg, V., Watson, S.J. & Akil, H. ( 1998 ) The role of mineralocorticoid receptors in hypothalamic–pituitary–adrenal axis regulation in humans. Journal of Clinical Endocrinology and Metabolism, 83, 3339 – 3345.en_US
dc.identifier.citedreferencede Kloet, E.R., Veldhuis, H.D., Wagenaars, J.L. & Bergink, E.W. ( 1984 ) Relative binding affinity of steroids for the corticosterone receptor system in rat hippocampus. Journal of Steroid Biochemistry, 21, 173 – 178.en_US
dc.identifier.citedreferenceArriza, J.L., Weinberger, C., Cerelli, G., Glaser, T.M., Handelin, B.L., Housman, D.E. & Evans, R.M. ( 1987 ) Cloning of human mineralocorticoid receptor complementary DNA: structural and functional kinship with the glucocorticoid receptor. Science, 237, 268 – 275.en_US
dc.identifier.citedreferenceRaven, P.W., Checkley, S.A. & Taylor, N.F. ( 1995 ) Extra-adrenal effects of metyrapone include inhibition of the 11-oxoreductase activity of 11-beta-hydroxysteroid dehydrogenase: a model for 11-HSD I deficiency. Clinical Endocrinology, 43, 637 – 644.en_US
dc.identifier.citedreferenceSheehan, D.V., Lecrubier, Y., Sheehan, K.H., Amorim, P., Janavs, J., Weiller, E., Hergueta, T., Baker, R. & Dunbar, G.C. ( 1998 ) The Mini-International Neuropsychiatric Interview (M.I.N.I.): the development and validation of a structured diagnostic psychiatric interview for DSM-IV and ICD-10. Journal of Clinical Psychiatry, 59 ( Suppl. 20 ), 22 – 33.en_US
dc.identifier.citedreferenceSeckl, J.R., Campbell, J.C., Edwards, C.R.W., Christie, J.E., Whalley, L.J., Goodwin, G.M. & Fink, G. ( 1990 ) Diurnal variation of plasma corticosterone in depression. Psychoneuroendocrinology, 15, 485 – 488.en_US
dc.identifier.citedreferenceStroupe, S.D., Harding, G.B., Forsthoefel, M.W. & Westphal, U. ( 1978 ) Kinetic and equilibrium studies on steroid interaction with human corticosteroid-binding globulin. Biochemistry, 17, 177 – 182.en_US
dc.identifier.citedreferenceMartensz, N.D., Herbert, J. & Stacey, P.M. ( 1983 ) Factors regulating levels of cortisol in cerebrospinal fluid of monkeys during acute and chronic hypercortisolemia. Neuroendocrinology, 36, 39 – 48.en_US
dc.identifier.citedreferenceFehm, H.L., Voigt, K.H., Kummer, G., Lang, R. & Pfeiffer, E.F. ( 1979 ) Differential and integral corticosteroid feedback effects on ACTH secretion in hypoadrenocorticism. Journal of Clinical Investigation, 63, 247 – 253.en_US
dc.identifier.citedreferenceWolf, O.T., Convit, A., de Leon, M.J., Caraos, C. & Qadri, S.F. ( 2002 ) Basal hypothalamo–pituitary–adrenal axis activity and corticotropin feedback in young and older men: relationships to magnetic resonance imaging-derived hippocampus and cingulate gyrus volumes. Neuroendocrinology, 75, 241 – 249.en_US
dc.identifier.citedreferenceBoscaro, M., Paoletta, A., Scarpa, E., Barzon, L., Fusaro, P., Fallo, F. & Sonino, N. ( 1998 ) Age-related changes in glucocorticoid fast feedback inhibition of adrenocorticotropin in man. Journal of Clinical Endocrinology and Metabolism, 83, 1380 – 1383.en_US
dc.identifier.citedreferenceBerger, T.S., Parandoosh, Z., Perry, B.W. & Stein, R.B. ( 1992 ) Interaction of glucocorticoid analogues with the human glucocorticoid receptor. Journal of Steroid Biochemistry and Molecular Biology, 41, 733 – 738.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.