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The physiological and pathophysiological roles of the Urocortins Krisztina Kárpáti and Hélène Rivière JPEMS 2015 2015-10-8 Content • Introduction • Physiological roles of the urocortins: Regulation of stress response Energy balance and expenditure Gastrointestinal motility and function Immune function Cardiovascular function • Pathophysiological roles: Anxiety Depression • Therapy CRF and CRF-related peptides • CRF (1981) CRFR1 in stress response - PVN of hypothalamus • Ucn 1 (1995): - structure similar to CRF - 100-fold higher affinity to CRFR2 - Edinger-Westphal nucleus • Ucn 2 and 3 (2001): CRFR2 selective ligands • CRF binding protein • These petides have different localisations and differents affinity for the receptors different physiological and pathophysiological functions Physiological roles Regulation of the neuroendocrine response to stress • Dualism of CRF/Ucn2 and 3 • CFR/CRFR1 control the initiation of stress, by the activation of the HPA axis: production of glucocorticoids Increase the blood sugar availability • Ucn 2,3/CRFR2 control the recovery from stress, by the inhibition of the HPA axis essential to maintain body and mental health under environmental threating conditions Role on energy balance and expenditure • Ucns stimulate the energy expenditure and decrease the food intake. • Mediated by brain CRFR2 and mainly by Ucn1 • To enhance the energy expenditure Ucn 1 elevate the arterial pressure, body temperature, stimulate the fat utilization and block the effect of orexigen peptides • Leptin is an anorexigen peptide which: - contributes to the catabolic functions of the Ucns - provide assistance for the peripheral Ucn 1 to get into the central compartment - stimulate the expression of brain CRFR2 Roles on the immune system: the dualistic action of Urocortin 1 • Exogenous administration: reduce inflammation - Inhibit cytokines and TNF release - Have palliative effects in experimental models of autoimmune diseases • - Endogenous Ucn1: pro-inflammatory effect Ucn1 stimulates IL-1beta and IL-6 secretion by immune cells. Mediated by CRFR1 Rheumatoid arthritis, endometriosis, asthma, gastritis, psoriasis, etc • CRFR2: protective against CRFR1 deleterious effects ? -the stomach is richer in CRFR2 than in CRFR1, and Ucn1 injection within the stomach seems to repair gastric mucosa from injury. Role on gastrointestinal motility and function • Ucns inhibit gastric motility - the gastric emptying is reduced - responsible for the anorectic effects of Ucns? - Mediated by brain CRFR2 (vagal efferents which inhibit gastric contractions) and gut CRFR2 • Ucns stimulate colonic motor function - colonic motility , colonic transit time - watery diarrhea - Mediated by CRFR1 • Ucns participate in the “irritable bowel syndrome” - painful gastrointestinal stimuli - Nociception is increased by CRFR1 and reduced by CRFR2. Protective and undesired effects on cardiovascular function • Inotropic effects: cardiac contractility, heart rate and aortic blood flow • Vasodilatory effects via CRFR2. • Cardioprotective effect: in hypoxic stress in heart failure: - Ucn 1 stimulate the synthesize of Atrial Natriuretic Peptide (ANP) - ANP causes hemodynamic adaptations to heart failure, mediated by CRFR2. • Undesired hypertrophic effects: Ucn1 expression is elevated in hypertrophic cardiomyopathy and dilated cardiomyopathy Pathophysiological roles Anxiety • CRF HPA-axis stress, anxiety • CRF deficiency aberrant stress response • In mice: CRFR1 antagonist antalarmin anxiolisis • Ucn 1: - exogenous administration: increased anxiety - endogenous Ucn1: minor importance • Ucn 2 and 3: • CRFR2: anxiogenesis or no change • homeostasis Depression • disturbances in HPA axis and aberrant stress coping • increased level of CRF in CSF in suicide victims • decreased level CRFR1 in suicide victims • Ucn 2 and 3: • antidepressant-like • Ucn 2 or CRFR2 deficiency depression (altered recovery) • Ucn 2 – serotonin level: • Administration of Ucn 2 depressive-like behavior • Localization-dependant effect Therapeutical possibilities • further researches • anxiety and depression-like disorders CRFR1 antagonists • obesity: Ucn 1 CRFR2 increased energy expenditure • cardioprotective effects: through CRFR2 reduce heart failure • GI tract: CRFR2 antagonists gastric motility increase • inflammatory disorders • cancer: • CRF receprors expression are increased • agonists may inhibit proliferaton Acknowledegment Department of Pathophysiology, University of Szeged • Zsolt Bagosi M.D., Ph.D. • Professor Dr. habil Gyula Szabó, M.D., Ph.D., D.Sc