Abstract
Previous studies demonstrated a bi-phasic time course with post-operative dissociation of blood levels of cortisol and ACTH in patients undergoing major surgery and critically ill patients. A possible role of endothelin and atrial natriuretic peptide (ANP) in the dissociation of concentrations of cortisol and ACTH in critically ill patients has been suggested. In the present study, we investigated the perioperative course of blood levels of endothelin, ANP, ACTH, and cortisol in 13 male patients undergoing cardiac surgery with cardiopulmonary bypass (CPB): group 1 consisted of 7 patients with an uneventful perioperative period and group 2 consisted of 6 patients with perioperative complications. Blood samples were taken pre-[T1], intra-[T2], post-operatively (on the day of surgery) [T3], as well as on the first [T4] and second [T5] post-operative days. Blood samples of endothelin, ANP, cortisol, and ACTH were measured using commercially available immunoassays. Perioperatively, a biphasic time course with post-operative dissociation of ACTH and cortisol concentrations was observed in all patients studied. Intraoperatively, during CPB, the highest levels of endothelin were found. Perioperatively, ANP and endothelin levels were elevated compared to pre-operative values up to the second post-operative day. On the second post-operative day, ANP concentrations were significantly higher in patients with complications in the perioperative period compared to those with an uneventful perioperative period. Our results suggest that: 1) plasma levels of ANP increased in patients with perioperative complications; 2) plasma levels of ANP may have prognostic value for patients undergoing cardiac surgery; and 3) the dissociation of ACTH and cortisol cannot solely be explained by the increase in endothelin-1 and ANP concentrations observed in patients undergoing major surgery.
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Naito Y., Fukata J., Tamai S., Seo N., Nakai Y., Mori K., Imura H. Biphasic changes in hypothalamo-pituitary-adrenal function during the early recovery period after major abdominal surgery. J. Clin. Endocrinol. Metab. 1991, 73: 111–117.
Roth-Isigkeit A., Schmucker P. Postoperative dissociation of blood levels of cortisol and adrenocorticotropin after coronary artery bypass grafting surgery. Steroids 1997, 62: 695–699.
Vermes I., Beishuizen A., Hampsink R.M., Haanen C. Dissociation of plasma adrenocorticotropin and cortisol levels in critically ill patients: possible role of endothelin and atrial natriuretic hormone. J. Clin. Endocrinol. Metab. 1995, 80: 1238–1242.
Jessop D.S. Central non-glucocorticoid inhibitors of the hypothalamo-pituitary-adrenal axis. J. Endocrinol. 1999, 160: 169–180.
Hinson J.P., Vinson G.P., Kapas S., Teja R. The role of endothelin in the control of adrenocortical function: stimulation of endothelin release by ACTH and the effects of endothelin-1 and endothelin-3 on steroidogenesis in rat and human adrenocortical cells. J. Endocrinol. 1991, 128: 275–280.
Calogero A.E., Raiti F., Nicolosi G., Burello N., D’Agata R., Mantero F. Effects of endothelin-1 and endothelin-3 on rat hy-pothalamic corticotropin-releasing hormone and pituitary ACTH release in vitro. J. Endocrinol. 1994, 140: 419–424.
Malendowicz L.K., Nussdorfer G.G., Meneghelli V., Nowak M., Markowska A., Majchrzak M. Effects of endothelin-1 on the rat pituitary-adrenocortical axis under basal and stressful conditions. Endocr. Res. 1997, 23: 349–364.
Vierhapper H., Hollenstein U., Roden M., Nowotny P. Effect of endothelin-1 in manimpact on basal and stimulated concentrations of luteinizing hormone, follicle-stimulating hormone, thyrotropin, growth hormone, corticotropin, and prolactin. Metabolism 1993, 42: 902–906.
Delarue C., Delton I., Fiorini F., Homo-Delarche F., Fasolo A., Braquet P., Vaudri H. Endothelin stimulates steroid secretion by frog adrenal gland in vitro: evidence for the involvement of prostaglandins and extracellular calcium in the mechanism of action of endothelin. Endocrinology 1990, 127: 2001–2008.
Goetz K.L., Wang B.C., Madwed J.B., Zhu J.L., Leadley R.J. Cardiovascular, renal, and endocrine responses to intravenous endothelin in conscious dogs. Am. J. Physiol. Endocrinol. Metab. 1988, 255: R1064–R1068.
Shirakami G., Segawa H., Shingu K., Saito Y., Magaribuchi T., Nakao K., Mori K. The effects of atrial natriuretic peptide infusion on hemodynamic, renal, and hormonal responses during gastrectomy. Anesth. Analg. 1997, 85: 907–912.
Brenner B.M., Ballermann B.J., Gunning M.E., Zeidel M.L. Diverse biological actions of atrial natriuretic peptide. Physiol. Rev. 1990, 70: 665–699.
Hu R.M., Lewin E.R., Pedram A., Frank H.J.L. Atrial natriuretic peptide inhibits the production and secretion of endothelin from cultured endothelial cells. Mediation through the C receptor. J. Biol. Chem. 1992, 267: 17384–17389.
Espiner E.A. Physiology of natriuretic peptides. J. Intern. Med. 1994, 235: 527–541.
Rubanyi G.M., Polokoff M.A. Endothelins: molecular biology, biochemistry, pharmacology, physiology, and pathophysiology. Pharmacol. Rev. 1994, 46: 325–415.
Fink G., Dow R.C., Casley D., Johnston C.I., Bennie J., Carroll S., Dick H. Atrial natriuretic peptide is involved in the ACTH response to stress and glucocorticoid negative feedback in the rat. J. Endocrinol. 1992, 135: 37–43.
Antoni F.A., Dayanithi G. Guanosine 3′:5′cyclic monophosphate and activators of guanylate cyclase inhibit secretagogue-induced corticotropin release by rat anterior pituitary cells. Biochem. Biophys. Res. Commun. 1989, 158: 824–830.
Kellner M., Wiedemann K., Holsboer F. Atrial natriuretic factor inhibits the CRH-stimulated secretion of ACTH and cortisol in man. Life Sci. 1992, 50: 1835–1842.
Fink G., Dow R.C., Casley D., Johnston C.I., Lim A.T., Copolov D.L., Bennie J., Carroll S., Dick H. Atrial natriuretic peptide is a physiological inhibitor of ACTH release: evidence from immunoneutraliza-tion in vivo. J. Endocrinol. 1991, 131: R9–R12.
Antoni F.A., Hunter E.F.M., Lowry P.J., Noble J.M., Seckl J.R. Atriopeptin: an endogenous corticotropin-release inhibiting hormone. Endocrinology 1992, 130: 1753–1755.
Shito M., Ueda M., Wakabayashi G., Endo M., Kitajima M. Pathophysiological response of cytokines and vasoactive agents in patients undergoing total gastrectomy. Eur. J. Surg. 1998, 164: 115–118.
Tanabe M., Ueda M., Endo M., Kitajima M. Effect of acute lung injury and coexisting disorders on plasma concentrations of atrial natriuretic peptide. Crit. Care Med. 1994, 22: 1762–1768.
Boldt J., Papsdorf M., Uphus D., Müller M., Hempelmann G. Changes in regulators of the circulation in patients undergoing lung surgery. Br. J. Anaesth. 1997, 79: 733–739.
Roth-Isigkeit A., Dibbelt L., Schmucker P. Blood levels of corticosteroid-binding globulin, total cortisol and unbound cortisol in patients undergoing coronary artery bypass grafting surgery with cardiopulmonary bypass. Steroids 2000, 65: 513–520.
Taylor K.M., Bain W.H., Jones J.V., Walker M.S. The effect of hemodilution on plasma levels of cortisol and free cortisol. J. Thorac. Cardiovasc. Surg. 1976, 72: 57–61.
Roth-Isigkeit A., Brechmann J., Dibbelt L., Sievers H.H., Raasch W., Schmucker P. Persistent endocrine stress response in patients undergoing cardiac surgery. J. Endocrinol. Invest. 1998, 21: 12–19.
Roth-Isigkeit A., Dibbelt L., Schmucker P., Seyfarth M. The immune-endocrine interaction varies with the duration of the inflammatory process in cardiac surgery patients. J. Neuroendocrinol. 2000, 12: 546–552.
Geny B., Piquard F., Follenius M., Thiranos J.C., Charpentier A., Epailly E., Levy F., Kretz J.G., Eisenmann B., Haberey P. Endothelin participates in increased circulating atrial natriuretic peptide early after human heart transplantation. J. Heart Lung Transplant. 1998, 17: 167–175.
Pasaoglu I., Erbas B., Varoglu E., Yorgancioglu C., Hazan E., Koray Z., Bekdik C., Bozer Y.A. Changes in the circulating endothelin and atrial natriuretic peptide levels during coronary artery bypass surgery. Jpn. Heart J. 1993, 34: 693–706.
Roth-Isigkeit A., v. Borstel T., Seyfarth M., Schmucker P. Perioperative serum levels of tumour-necrosis-factor alpha (TNF-α), IL-1β, IL-6, IL-10 and soluble IL-2 receptor in patients undergoing cardiac surgery with cardiopulmonary bypass without and with correction for haemodilution. Clin. Exp. Immunol. 1999, 118: 242–246.
Hasdai D., Erez E., Gil-Ad I., Raanani E., Sclarovsky S., Barak Y., Sulkes J., Vidne B.A. Is the heart a source for elevated circulating endothelin levels during aorta-coronary artery bypass grafting surgery in human beings? J. Thorac. Cardiovasc. Surg. 1996, 112: 531–536.
Haak T., Matheis G., Kohleisen M., Ngo H., Beyersdorf F., Usadel K.H. Endothelin during cardiovascular surgery: the effect of diltiazem and nitroglycerin. J. Cardiovasc. Pharmacol. 1995, 26 (Suppl. 3): 5494–5496.
Matheis G., Haak T., Beyersdorf F., Baretti R., Polywka C., Winkelmann B.R. Circulating endothelin in patients undergoing coronary artery bypass grafting. Eur. J. Cardiothorac. Surg. 1995, 9: 269–274.
Mair P., Mair J., Bleier J., Waldenberger F., Furtwaengler W., Balogh D., Puschendorf B. Coronary sinus endothelin-1 concentrations after cardioplegic cardiac arrest. Coron. Artery Dis. 1995, 6: 533–537.
Ferri C., De Marzio P., Desideri G., Baldoncini R., Bellini C., Morelli S., Santucci A. Plasma endothelin-1 levels during transient acute myocardial ischaemia in men: effects of coronary revascularization. Eur. J. Clin. Invest. 1997, 27: 526–532.
Kullmer T., Jungmann E., Haak T., Usadel K.H. Modification of the responses of endothelin-1 to exhaustive physical exercise under stimulated high-altitude conditions with acute hypoxia. Metabolism 1995, 44: 8–9.
Michael J.R., Markewitz B.A., Kohan D.E. Oxidant stress regulates basal endothelin-1 production by cultured rat pulmonary endothelial cells. Am. J. Physiol. 1997, 273: L768–L774.
Hynynen M., Saijonmaa O., Tikkanen I., Heinonen J., Fyhrquist F. Increased plasma endothelin immunoreactivity during cardiopulmonary bypass: a preliminary observation. J. Thorac. Cardiovasc. Surg. 1992, 103: 1024–1025.
Skvorak J.P., Nazian S.J., Dietz J.R. Endothelin acts as a paracrine regulator of stretch-induced atrial natriuretic peptide release. Am. J. Physiol. 1995, 269: R1093–R1098.
Omland T., Aarsland T., Aakvaag A., Lie R.T., Dickstein K. Prognostic value of plasma atrial natriuretic factor, norepinephrine and epinephrine in acute myocar-dial infarction. Am. J. Cardiol. 1993, 72: 255–259.
Omland T., Bonarjee V.V.S., Lie R.T., Caidahl K. Neurohumoral measurements as indicators of long-term prognosis after acute myocardial infarction. Am. J. Cardiol. 1995, 76: 230–235.
Hall C., Rouleau J.L., Moye L., de Champlain J., Bichet D., Klein M., Sussex B., Packer M., Rouleau J., Arnold M.O., Lamas G.A., Sestier F., Gottlieb S.S. Wun C.C., Pfeffer M.A. N-terminal proatrial natriuretic factor. An independent predictor of long-term prognosis after myocardial infarction. Circulation 1994, 89: 1934–1942.
De Groote P., Millaire A., Pigny P., Nugue O., Racadot A., Ducloux G. Plasma levels of atrial natriuretic peptide at peak exercise: a prognostic marker of cardiovascular-related death and heart transplantation in patients with moderate congestive heart failure. J. Heart Lung Transpl. 1997, 16: 956–963.
Hillege H.L., Girbes A.R.J., de Kam P.J., Boomsma F., de Zeeuw D., Charlesworth A., Hampton J.R., van Veldhuisen D.J. Renal function, neurohormonal activation, and survival in patients with chronic heart failure. Circulation 2000, 102: 203–210.
Mulligan R.S., Livesey J.H., Evans M.J., Ellis M.J., Donald R.A. Atrial natriuretic peptide and C-type natriuretic pep-tide do not acutely inhibit the release of adreno-corticotropin from equine pituitary cells in vitro. Neuroendocrinology 1997, 65: 64–69.
Bowman M.E., Robinson P.J., Smith R. Atrial natriuretic peptide, cyclic GMP analogues and modulation of guanylyl cyclase do not alter stimulated POMC peptide release from perifused rat or sheep corticotrophs. J. Neuroendocrinol. 1997, 9: 929–936.
Ambrosi B., Sala C., Bochicchio D., Colombo P., Gazzano G., Fadin C., Morganti A., Faglia G. Effect of atrial natriuretic factor infusion on basal and CRH-stimulated ACTH, cortisol and aldosterone levels in patients with Cushing’s or Addison’s disease. Clin. Endocrinol. (Oxf.) 1994, 40: 589–594.
Kellner M., Herzog L., Holsboer F., Wiedemann K. Circadian changes in the sensitivity of the corticotropin-releasing hormone-stimulated HPA system after arginine vasopressin and atrial natriuretic hormone in human male controls. Psychoneuroendocrinology 1995, 20: 515–524.
Dallman M.F., Akana S.F., Scribner K.A., Bradbury M.J., Walker C.D., Stark A.M., Cascio C.S. Stress, feedback and facilitation in the hypothalamo-pituitary-adrenal axis. J. Neuroendocrinol. 1992, 4: 517–526.
Bierwolf C., Burgemeister A., Lüthke K., Born J., Fehm H.L. Influence of exogenous atrial natriuretic peptide on the pituitary-adrenal response to corticotropin-releasing hormone and vasopressin in healthy man. J. Clin. Endocrinol. Metab. 1998, 83: 1151–1157.
Yasin S., Costa A., Navarra P., Pozzoli G., Kostoglou-Athanassiou I., Forsling M., Grossman A. Endothelin-1 stimulates the in vitro release of neurohypophyseal hormones, but not corticotropin-releasing hormone, via ETA receptors. Neuroendocrinology 1994, 60: 553–558.
Urquhart J. Adrenal blood flow and adrenocortical response to corticotropin. Am. J. Physiol. 1965, 209: 1162–1168.
Wood C.E., Shinsako M.J., Dallman M.F. Comparison of canine corticosteroid responses to mean and phasic increases in ACTH. Am. J. Physiol. 1982, 242: E102–E108.
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Roth-Isigkeit, A., Dibbelt, L., Eichler, W. et al. Blood levels of atrial natriuretic peptide, endothelin, cortisol and ACTH in patients undergoing coronary artery bypass grafting surgery with cardiopulmonary bypass. J Endocrinol Invest 24, 777–785 (2001). https://doi.org/10.1007/BF03343927
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DOI: https://doi.org/10.1007/BF03343927