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also in protection against it. The hypophyseal–pituitary–adrenal axis in the brain and addiction In relation to addiction, far more attention has been paid to hypophyseal–pituitary–adrenal (HPA) components in the brain than to the systemic (i.e. blood
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diagnosis. Evaluation of the hypothalamic–pituitary–adrenal (HPA) axis is, however, missed in over two-thirds of the patients labeled as having SIAD ( 14 ). Clear estimates of the contribution of secondary AI to EuVHNa are hard to come by. We could locate
Division of Endocrinology, Division of Nephrology, Endocrine Research Laboratory, Department of Medicine
Division of Endocrinology, Division of Nephrology, Endocrine Research Laboratory, Department of Medicine
Division of Endocrinology, Division of Nephrology, Endocrine Research Laboratory, Department of Medicine
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Introduction The measurement of salivary cortisol has emerged as a first-line test in the evaluation of the hypothalamic–pituitary–adrenal (HPA) axis in humans and, in particular, for the diagnosis of endogenous hypercortisolism (Cushing
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Department of Physiology, Faculty of Science, Charles University, Prague, Czech Republic
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Department of Physiology, Faculty of Science, Charles University, Prague, Czech Republic
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Introduction Stress is a ubiquitous condition that affects both people and animals. It initiates a series of events, culminating in the activation of the hypothalamic–pituitary–adrenal (HPA) axis and sympathetic nervous system (SNS), including
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Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel
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Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel
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, prolactin and cortisol ( 15 , 16 , 17 ). The stimulation of the HPA axis by ghrelin is exerted predominantly at the hypothalamic level ( 18 ) through vasopressin stimulation ( 19 ) and indirect activation of CRH neurons ( 20 , 21 ). Direct effects of
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hoc analyses of multiple hormones in patients with obesity and T2DM followed up for 2 years after RYGB. We highlight the novel findings on the responses of GH and the hypothalamus–pituitary–adrenal (HPA) axis to oral glucose following RYGB. For the
Department of Clinical Research, University of Basel Hospital, Basel, Switzerland
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Department of Clinical Research, University of Basel Hospital, Basel, Switzerland
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Division of Endocrinology, Diabetes and Metabolism, University Department of Medicine, Kantonsspital Aarau, Aarau, Switzerland
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Division of Endocrinology, Diabetes and Metabolism, University Department of Medicine, Kantonsspital Aarau, Aarau, Switzerland
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Department of Clinical Research, University of Basel Hospital, Basel, Switzerland
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Department of Clinical Research, University of Basel Hospital, Basel, Switzerland
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leads to an increased activity of the hypothalamus–pituitary–adrenal (HPA) axis with excess of glucocorticoids which are known to increase the risk for metabolic complications and cardiovascular mortality ( 6 ). Interleukin-1β (IL-1β) is known to
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Department of Psychiatry, VU University Medical Center, Amsterdam, The Netherlands
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fetal hypothalamic–pituitary–adrenal (HPA) axis, which are protective in the short term, but might pose a risk in the long term ( 3 ). The development of the fetal HPA axis is, among other factors, influenced by the placental transfer of maternal GCs
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deficit. This focus complements the earlier study of IL-2’s suppressive effect on the gonadotropic axis in the same cohort of volunteers ( 6 ). Aging is also associated with increased systemic inflammation ( 7 ) and regulation of the HPA axis is age
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independent of the salivary flow rate (11) and that its response to Trier Social Stress Test (TSST) is predictive of the plasma catecholamine response to TSST (13) . Activation of the hypothalamo–pituitary–adrenal (HPA) axis by stress results in the