PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 22170706-7 2012 RESULTS: There was a significant inverse correlation between plasma beta-endorphin levels during exercise and catecholamine release during subsequent hypoglycemia. Catecholamines 110-123 proopiomelanocortin Homo sapiens 68-82 31765327-1 2019 Summary: ACTH-secreting pheochromocytoma is a very rare cause of Cushing"s syndrome, with a high morbidity and mortality risk due to both cortisol and catecholamines excess. Catecholamines 151-165 proopiomelanocortin Homo sapiens 9-13 29760304-4 2018 Moreover, his ACTH/cortisol ratio and catecholamine levels were extremely high, suggesting catecholamine-dominant ACTH-secreting pheochromocytoma. Catecholamines 91-104 proopiomelanocortin Homo sapiens 14-18 29760304-4 2018 Moreover, his ACTH/cortisol ratio and catecholamine levels were extremely high, suggesting catecholamine-dominant ACTH-secreting pheochromocytoma. Catecholamines 91-104 proopiomelanocortin Homo sapiens 114-118 26700559-1 2016 CONTEXT: Pheochromocytoma is a catecholamine-producing tumor that originates from adrenal chromaffin cells and is capable of secreting various hormones, including ACTH. Catecholamines 31-44 proopiomelanocortin Homo sapiens 163-167 26700559-3 2016 Endocrinological examinations demonstrated ectopic ACTH production with hypercortisolemia and excess urinary cortisol accompanied by elevated plasma and urine catecholamines. Catecholamines 159-173 proopiomelanocortin Homo sapiens 51-55 25228844-0 2014 Adrenocorticotropic hormone-independent macronodular adrenal hyperplasia with abnormal cortisol secretion mediated by catecholamines. Catecholamines 118-132 proopiomelanocortin Homo sapiens 0-27 2068891-3 1991 Histamine stimulates the secretion of ACTH, beta-endorphin (mediated by CRH and AVP), alpha-MSH (mediated by dopamine and peripheral catecholamines), and PRL (mediated by dopamine, serotonin and AVP), and participates in the stress-induced release of these hormones and possibly in the suckling- and estrogen-induced PRL release. Catecholamines 133-147 proopiomelanocortin Homo sapiens 86-95 21400210-0 2011 Catecholamine-resistant shock and hypoglycemic coma after cardiotomy in a patient with unexpected isolated ACTH deficiency. Catecholamines 0-13 proopiomelanocortin Homo sapiens 107-111 9621392-7 1998 A reduction in the modulatory effect of these catecholamines (by neurotoxic lesion, synthetic enzyme inhibitors or adrenergic receptor antagonists) resulted in an inhibition of nicotine-stimulated ACTH secretion. Catecholamines 46-60 proopiomelanocortin Homo sapiens 197-201 8806925-9 1996 In conclusion, neural and humoral mechanisms exert redundant control with regard to responses of catecholamines and pituitary hormones (growth hormone and adrenocorticotropic hormone). Catecholamines 97-111 proopiomelanocortin Homo sapiens 155-182 8383904-1 1993 In several animal species the catecholamines stimulate the release of alpha-MSH from the melanotrope cells of the pituitary neurointermediate lobe through beta-receptors. Catecholamines 30-44 proopiomelanocortin Homo sapiens 70-79 18234565-6 2008 Baseline values were different between the two groups, but an altered pattern of release was observed for TNFa, IL-6, IL-10 and beta-endorphin levels in patients treated with catecholamines. Catecholamines 175-189 proopiomelanocortin Homo sapiens 128-142 16786331-12 2006 CONCLUSION: In catecholamine-dependent septic shock patients managed with systematic glucocorticoid therapy the results of ACTH stimulation do not predict hemodynamic improvement. Catecholamines 15-28 proopiomelanocortin Homo sapiens 123-127 16138261-0 2005 Intranasal administration of ACTH(1-24) stimulates catecholamine secretion. Catecholamines 51-64 proopiomelanocortin Homo sapiens 29-33 12694379-1 2003 We investigated the role played by catecholamine-dependent pathways in modulating the ability of the nitric oxide (NO) donor 3-morpholino-sydnonimine (SIN-1) to release adrenocorticotropic hormone (ACTH) following its intracerebroventricular (i.c.v.) Catecholamines 35-48 proopiomelanocortin Homo sapiens 169-196 12153741-1 2002 OBJECTIVE: We describe a patient with an ACTH-producing phaeochromocytoma who initially presented with hypercortisolism and normal catecholamine concentrations, followed by near-normalisation of ACTH secretion and massive catecholamine secretion. Catecholamines 131-144 proopiomelanocortin Homo sapiens 41-45 12153741-1 2002 OBJECTIVE: We describe a patient with an ACTH-producing phaeochromocytoma who initially presented with hypercortisolism and normal catecholamine concentrations, followed by near-normalisation of ACTH secretion and massive catecholamine secretion. Catecholamines 222-235 proopiomelanocortin Homo sapiens 41-45 1646411-2 1991 This hypothesis has been tested here by investigating the effect of the met-enkephalin analog, DAMME (FK-33,824), on the elevation in serum cortisol induced by the catecholamine-releasing agent d-amphetamine (10 and 25 mg p.o.) Catecholamines 164-177 proopiomelanocortin Homo sapiens 72-86 2175252-9 1990 ACTH-like peptide in the brain may act as a neuromodulator, mainly in the NLT and the preoptic nucleus, and around the nuclei of the ventricular recesses containing serotonin and catecholamines. Catecholamines 179-193 proopiomelanocortin Homo sapiens 0-4 2169395-3 1990 Therefore, these studies investigated the role of catecholamines in nicotine-stimulated ACTH secretion. Catecholamines 50-64 proopiomelanocortin Homo sapiens 88-92 2138208-0 1990 Gamma 2-MSH in congestive heart failure: relation to atrial natriuretic peptide, arginine vasopressin and catecholamines. Catecholamines 106-120 proopiomelanocortin Homo sapiens 8-11 34756930-3 2021 All these cerebrovascular diseases may trigger pronounced catecholamine surges through diverse ways, including stimulation of hypothalamic-pituitary adrenal axis, dysregulation of autonomic system, and secretion of adrenocorticotropic hormone. Catecholamines 58-71 proopiomelanocortin Homo sapiens 215-242 2173366-4 1990 Reports differ as to whether circulating catecholamines can release ACTH in vivo by direct action on the pituitary. Catecholamines 41-55 proopiomelanocortin Homo sapiens 68-72 1968233-6 1990 This provides an explanation for some of the apparent contradictions in interpreting the data from previous studies on the effects of catecholamines on the secretion of ACTH. Catecholamines 134-148 proopiomelanocortin Homo sapiens 169-173 34345329-1 2021 Adrenocorticotropic hormone (ACTH)-producing pheochromocytoma can cause a variety of clinical manifestations of excess catecholamine and corticosteroid. Catecholamines 119-132 proopiomelanocortin Homo sapiens 0-27 34345329-1 2021 Adrenocorticotropic hormone (ACTH)-producing pheochromocytoma can cause a variety of clinical manifestations of excess catecholamine and corticosteroid. Catecholamines 119-132 proopiomelanocortin Homo sapiens 29-33 2537324-7 1989 On the other hand, met-enkephalin induced a dose-dependent increase in macrophage spreading, with a perimeter of 18.5 +/- 1.0 microns at 10(-8) M. Since catecholamines and opioids are simultaneously released from chromaffin cells of the adrenal, we examined the combinative effects due to treatment with both ligands. Catecholamines 153-167 proopiomelanocortin Homo sapiens 19-33 3335857-3 1988 Free Met-enkephalin immunoreactivity and total Met-enkephalin immunoreactivity, as determined by enzymatic digestion of large enkephalin-containing fragments, were coreleased with catecholamines. Catecholamines 180-194 proopiomelanocortin Homo sapiens 5-19 2850308-6 1988 It appears that the acute cardiovascular response to gamma-MSH administration depends primarily on the release of sympathetic terminal norepinephrine, though some contribution from other pressor systems such as adrenal catecholamines is possible. Catecholamines 219-233 proopiomelanocortin Homo sapiens 53-62 3335857-3 1988 Free Met-enkephalin immunoreactivity and total Met-enkephalin immunoreactivity, as determined by enzymatic digestion of large enkephalin-containing fragments, were coreleased with catecholamines. Catecholamines 180-194 proopiomelanocortin Homo sapiens 47-61 2940358-3 1986 administration of synthetic human beta-endorphin to increase plasma catecholamine concentrations, presumably by acting at opioid receptors in the brain to stimulate the central sympathetic outflow to adrenal medulla and peripheral sympathetic nerve terminals. Catecholamines 68-81 proopiomelanocortin Homo sapiens 34-48 2963188-8 1987 The low correlation suggests a weak relationship between beta-endorphin and catecholamine responses during exercise. Catecholamines 76-89 proopiomelanocortin Homo sapiens 57-71 2890079-4 1987 Two to 4 weeks after surgery the responsiveness of their catecholaminergic neurons was tested by an injection of human beta-endorphin (20 micrograms/kg); it caused a rise in portal catecholamine levels equivalent to that seen in intact dogs. Catecholamines 57-70 proopiomelanocortin Homo sapiens 119-133 2822768-0 1987 Effects of catecholamines on secretion of adrenocorticotrophic hormone (ACTH) in man. Catecholamines 11-25 proopiomelanocortin Homo sapiens 72-76 2822310-11 1987 Increased pressor sensitivity to catecholamines during ACTH administration in man is not sodium-dependent. Catecholamines 33-47 proopiomelanocortin Homo sapiens 55-59 2940358-4 1986 This beta-endorphin-induced increase in plasma catecholamine concentration is dose-dependent, inhibited by naloxone and blocked by bilateral adrenal gland denervation or ganglionic blockade with chlorisondamine. Catecholamines 47-60 proopiomelanocortin Homo sapiens 5-19 2940358-6 1986 In this study we examined the possibility of central noradrenergic regulation of beta-endorphin-induced catecholamine secretion. Catecholamines 104-117 proopiomelanocortin Homo sapiens 81-95 2940358-15 1986 norepinephrine on beta-endorphin-induced catecholamine secretion. Catecholamines 41-54 proopiomelanocortin Homo sapiens 18-32 2940358-17 1986 norepinephrine at a dose insufficient to reduce beta-endorphin-induced catecholamine secretion in vehicle-treated rats prevented beta-endorphin-induced epinephrine and norepinephrine secretion in rats whose brains had been depleted of norepinephrine by prior 6-OHDA treatment. Catecholamines 71-84 proopiomelanocortin Homo sapiens 48-62 6091217-5 1984 Elevated serum beta-endorphin concentrations induced by exercise have been linked to several psychological and physiological changes, including mood state changes and "exercise-induced euphoria", altered pain perception, menstrual disturbances in female athletes, and the stress responses of numerous hormones (growth hormone, ACTH, prolactin, catecholamines and cortisol). Catecholamines 344-358 proopiomelanocortin Homo sapiens 15-29 2860247-0 1985 Photoaffinity labelling of MSH receptors on Anolis melanophores: effects of catecholamines, calcium and forskolin. Catecholamines 76-90 proopiomelanocortin Homo sapiens 27-30 2860247-1 1985 Photoaffinity labelling of MSH receptors on Anolis melanophores was used as a tool for studying the effects of catecholamines, calcium and forskolin on hormone-receptor interaction and receptor-adenylate cyclase coupling. Catecholamines 111-125 proopiomelanocortin Homo sapiens 27-30 2860247-2 1985 Covalent attachment of photoreactive alpha-MSH to its receptor was suppressed in calcium-free buffer but was hardly influenced by catecholamines or forskolin. Catecholamines 130-144 proopiomelanocortin Homo sapiens 43-46 2860247-4 1985 The suppression of pigment dispersion by catecholamines was blocked by the simultaneous presence of yohimbine but not prazosin, indicating that the catecholamines antagonize the alpha-MSH signal by inhibitory action on the adenylate cyclase system through an alpha-2 receptor. Catecholamines 41-55 proopiomelanocortin Homo sapiens 178-187 2860247-4 1985 The suppression of pigment dispersion by catecholamines was blocked by the simultaneous presence of yohimbine but not prazosin, indicating that the catecholamines antagonize the alpha-MSH signal by inhibitory action on the adenylate cyclase system through an alpha-2 receptor. Catecholamines 148-162 proopiomelanocortin Homo sapiens 178-187 3524698-2 1986 As high amounts of catecholamines are released in the newborn at delivery, probably following the stress of parturition, a similar release of met-enkephalin and other pro-enkephalin A deriving peptides from the newborn chromaffin tissue may be hypothesized. Catecholamines 19-33 proopiomelanocortin Homo sapiens 142-156 3000912-6 1986 It is also possible that the increase in adrenal catecholamine secretion after ACTH may be due to ACTH augmentation of catecholamine secretion by endogenous opioids such as beta-endorphin. Catecholamines 49-62 proopiomelanocortin Homo sapiens 79-83 3000912-6 1986 It is also possible that the increase in adrenal catecholamine secretion after ACTH may be due to ACTH augmentation of catecholamine secretion by endogenous opioids such as beta-endorphin. Catecholamines 49-62 proopiomelanocortin Homo sapiens 98-102 3000912-6 1986 It is also possible that the increase in adrenal catecholamine secretion after ACTH may be due to ACTH augmentation of catecholamine secretion by endogenous opioids such as beta-endorphin. Catecholamines 119-132 proopiomelanocortin Homo sapiens 79-83 3000912-6 1986 It is also possible that the increase in adrenal catecholamine secretion after ACTH may be due to ACTH augmentation of catecholamine secretion by endogenous opioids such as beta-endorphin. Catecholamines 119-132 proopiomelanocortin Homo sapiens 98-102 3002132-9 1985 Since both the ACTH secretion and memory function may be dependent upon the intracerebral catecholamines, the present findings may reflect variations in central monoaminergic receptor function. Catecholamines 90-104 proopiomelanocortin Homo sapiens 15-19 6280799-1 1982 1 The primary effect of catecholamines was to lighten Anolis skin previously darkened by alpha-melanocyte-stimulating hormone (alpha-MSH). Catecholamines 24-38 proopiomelanocortin Homo sapiens 89-125 6885962-4 1983 As plasma catecholamines levels returned to the normal range after extirpation of tumors, met-enkephalin-LI and leu-enkephalin-LI in plasma became undetectable in these patients. Catecholamines 10-24 proopiomelanocortin Homo sapiens 90-104 6885962-7 1983 Plasma met-enkephalin-LI and leu-enkephalin-LI increased concomitantly with catecholamines after glucagon stimulation and during a spontaneous attack in a patient with pheochromocytoma. Catecholamines 76-90 proopiomelanocortin Homo sapiens 7-21 6885962-11 1983 It is concluded that met-enkephalin and leu-enkephalin are released concomitantly with catecholamines from pheochromocytomas. Catecholamines 87-101 proopiomelanocortin Homo sapiens 21-35 6306616-2 1983 We have reported that intracisternal administration of synthetic human beta-endorphin increases plasma concentration of catecholamines, apparently by acting at unknown brain sites to increase sympathetic outflow to the adrenal medulla and sympathetic nerves. Catecholamines 120-134 proopiomelanocortin Homo sapiens 71-85 6280799-1 1982 1 The primary effect of catecholamines was to lighten Anolis skin previously darkened by alpha-melanocyte-stimulating hormone (alpha-MSH). Catecholamines 24-38 proopiomelanocortin Homo sapiens 127-136 6280799-3 1982 Subsequent experiments were concerned with the effect of low catecholamine concentrations on alpha-MSH action. Catecholamines 61-74 proopiomelanocortin Homo sapiens 93-102 6280799-5 1982 3 alpha-MSH dose-response curves were shifted, in parallel, to the right in the presence of the catecholamines, noradrenaline, adrenaline and dopamine, and Lineweaver-Burke plots and Arunlakshana-Schild plots indicated that the catecholamines antagonized MSH action by a competitive mechanism. Catecholamines 96-110 proopiomelanocortin Homo sapiens 2-11 6280799-5 1982 3 alpha-MSH dose-response curves were shifted, in parallel, to the right in the presence of the catecholamines, noradrenaline, adrenaline and dopamine, and Lineweaver-Burke plots and Arunlakshana-Schild plots indicated that the catecholamines antagonized MSH action by a competitive mechanism. Catecholamines 228-242 proopiomelanocortin Homo sapiens 2-11 196270-0 1977 Catecholamine turnover measurement and ACTH-induced short-term changes of catecholamine levels in individual brain nuclei. Catecholamines 74-87 proopiomelanocortin Homo sapiens 39-43 6270584-6 1981 administration of human beta-endorphin (25 microgram or 7.25 nmol) produced much greater plasma responses of all three catecholamines than seen with DALA. Catecholamines 119-133 proopiomelanocortin Homo sapiens 24-38 6270584-8 1981 dose of naloxone, which had been shown previously to inhibit the plasma catecholamine responses to beta-endorphin, failed to inhibit plasma catecholamine responses to DALA. Catecholamines 72-85 proopiomelanocortin Homo sapiens 99-113 6263592-6 1981 These beta-endorphin effects on plasma catecholamines were inhibited by intraarterial naloxone (1.1 mumol/kg), supporting mediation at opioid receptors. Catecholamines 39-53 proopiomelanocortin Homo sapiens 6-20 6263592-7 1981 Pretreatment with the ganglionic blocking agent chlorisondamine inhibited the responses of all three catecholamines to intracisternal beta-endorphin. Catecholamines 101-115 proopiomelanocortin Homo sapiens 134-148 6263592-9 1981 Prior intracisternal administration of hemicholinium-3 blocked the plasma responses of all three catecholamines to intracisternal beta-endorphin, providing evidence for the involvement of central cholinergic neurons in the mechanism mediating beta-endorphin-induced increases in plasma catecholamines. Catecholamines 97-111 proopiomelanocortin Homo sapiens 130-144 6263592-9 1981 Prior intracisternal administration of hemicholinium-3 blocked the plasma responses of all three catecholamines to intracisternal beta-endorphin, providing evidence for the involvement of central cholinergic neurons in the mechanism mediating beta-endorphin-induced increases in plasma catecholamines. Catecholamines 286-300 proopiomelanocortin Homo sapiens 130-144 6263592-9 1981 Prior intracisternal administration of hemicholinium-3 blocked the plasma responses of all three catecholamines to intracisternal beta-endorphin, providing evidence for the involvement of central cholinergic neurons in the mechanism mediating beta-endorphin-induced increases in plasma catecholamines. Catecholamines 286-300 proopiomelanocortin Homo sapiens 243-257 6112047-1 1981 Synthetic human beta-endorphin, 7.25 nmol intracisternally, in unanesthetized, freely moving, chronically cannulated, adult male rats increased plasma concentrations of all 3 catecholamines: epinephrine, norepinephrine and dopamine, for the 2 h period studied. Catecholamines 175-189 proopiomelanocortin Homo sapiens 16-30 196270-1 1977 The effect of acute ACTH treatment on catecholamine content of various brain nuclei was followed by radioenzymatic assay. Catecholamines 38-51 proopiomelanocortin Homo sapiens 20-24 4378153-0 1967 [The effect of sulfonyl urea, ACTH, and Metopirone on the end products of catecholamine metabolism in diabetes mellitus]. Catecholamines 74-87 proopiomelanocortin Homo sapiens 30-34 4374068-0 1974 The role of brain catecholamines in the regulation of ACTH secretion. Catecholamines 18-32 proopiomelanocortin Homo sapiens 54-58 29549-0 1977 Catecholamines: effects of ACTH and adrenal corticoids. Catecholamines 0-14 proopiomelanocortin Homo sapiens 27-31 29551-0 1977 Neurotransmitters involved in ACTH secretion: catecholamines. Catecholamines 46-60 proopiomelanocortin Homo sapiens 30-34 4346812-0 1973 ACTH-induced alterations in catecholamine metabolism in man. Catecholamines 28-41 proopiomelanocortin Homo sapiens 0-4 4318385-0 1970 Effect of adrenocorticotropic hormone and corticosteroid on release of catecholamine from adrenal medulla. Catecholamines 71-84 proopiomelanocortin Homo sapiens 10-37 14919100-0 1952 Excretion of catechol amines during administration of ACTH, cortisone and desoxycorticosterone acetate. Catecholamines 13-28 proopiomelanocortin Homo sapiens 54-58