PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 6099973-0 1984 Responsiveness of the rat vas deferens to catecholamines and electrical stimulation during an infection with Trypanosoma brucei. Catecholamines 42-56 arginine vasopressin Rattus norvegicus 26-29 6756553-1 1982 Catecholamine innervation of vasopressin and oxytocin neurons in the rhesus monkey hypothalamus. Catecholamines 0-13 arginine vasopressin Rattus norvegicus 29-40 6756553-7 1982 Oxytocin neurons were clustered in this relatively catecholamine poor region, whereas the vasopressin-containing neurons were more abundantly found in the catecholamine rich region. Catecholamines 155-168 arginine vasopressin Rattus norvegicus 90-101 6756553-10 1982 These observations confirm our earlier reports, in rat hypothalamus, that the norepinephrine innervation of the hypothalamic magnocellular neurons as seen with catecholamine histofluorescence favors the vasopressin-containing neurons over those located within the same nuclei which synthesize another neurohyphysial principal, oxytocin. Catecholamines 160-173 arginine vasopressin Rattus norvegicus 203-214 7084115-5 1982 Histofluorescence examination of additional explants revealed that endogenous catecholamine was still present on day 2 within varicosities in the supraoptic nucleus, but diminished by days 3 and 4, suggesting that endogenous NE could influence basal VP release. Catecholamines 78-91 arginine vasopressin Rattus norvegicus 250-252 500827-0 1979 Effect of central catecholamine depletion on the osmotic and nonosmotic stimulation of vasopressin (antidiuretic hormone) in the rat. Catecholamines 18-31 arginine vasopressin Rattus norvegicus 87-98 7040232-2 1982 Catecholamine depletion decreased blood pressure and stimulated vasopressin levels in all rats, but significantly more so in the anephric ones. Catecholamines 0-13 arginine vasopressin Rattus norvegicus 64-75 7040232-6 1982 Catecholamine levels were inversely correlated with those of plasma vasopressin, which were far greater in anephric rats through both stimulation and accumulation. Catecholamines 0-13 arginine vasopressin Rattus norvegicus 68-79 6274671-0 1981 Excitability ot beta-endorphin, morphine and catecholamines of the vas deferens of the rat at different stages of development. Catecholamines 45-59 arginine vasopressin Rattus norvegicus 67-70 110623-6 1979 Regional studies, utilizing microdissection techniques in combination with a sensitive radioenzymatic catecholamine assay, revealed a distinct pattern of effects on cerebral alpha-methyl-p-tyrosine methylester-induced catecholamine disappearance following intraventricular vasopressin administration in limbic midbrain structures. Catecholamines 218-231 arginine vasopressin Rattus norvegicus 273-284 487159-10 1979 Modulation of catecholamine turnover in specific brain areas after AVP administration may be related to this behavioral effect. Catecholamines 14-27 arginine vasopressin Rattus norvegicus 67-70 110623-8 1979 These results indicate that vasopressin modulates memory processes by modulation of neurotransmission in distinct catecholamine systems. Catecholamines 114-127 arginine vasopressin Rattus norvegicus 28-39 24737484-9 2014 In contrast, the contractile effects of histamine in the vas deferens were related to H2 receptor activation followed by release of catecholamines from sympathetic nerve endings. Catecholamines 132-146 arginine vasopressin Rattus norvegicus 57-60 219400-0 1979 Vasopressin modulates the activity of catecholamine containing neurons in specific brain regions. Catecholamines 38-51 arginine vasopressin Rattus norvegicus 0-11 219400-5 1979 The results support the hypothesis that vasopressin modulates catecholamine neurotransmission in specific brain regions of the rat. Catecholamines 62-75 arginine vasopressin Rattus norvegicus 40-51 744179-2 1978 It is concluded that in situations in which an increase of vasopressin release is expected, the posterior pituitary content of catecholamines will also be increased, and vice versa, which might imply their role in the release of vasopressin. Catecholamines 127-141 arginine vasopressin Rattus norvegicus 229-240 748009-0 1978 Catecholamine concentration and turnover in discrete regions of the brain of the homozygous Brattleboro rat deficient in vasopressin. Catecholamines 0-13 arginine vasopressin Rattus norvegicus 121-132 19556183-0 1977 Regional effects of vasopressin on rat brain catecholamine metabolism. Catecholamines 45-58 arginine vasopressin Rattus norvegicus 20-31 5726781-0 1968 The effects of drugs inhibiting catecholamine uptake on tyramine and noradrenaline-induced contractions of the isolated rat vas deferens. Catecholamines 32-45 arginine vasopressin Rattus norvegicus 124-127 7918-0 1976 The effect of prolonged vasopressin administration on the level and metabolism of catecholamines in the rat brain and kidneys. Catecholamines 82-96 arginine vasopressin Rattus norvegicus 24-35 941687-0 1976 Turnover of catecholamines in some regions of the rat brain during prolonged vasopressin administration and after its withdrawal. Catecholamines 12-26 arginine vasopressin Rattus norvegicus 77-88 22886838-1 2012 BACKGROUND: Vasopressin is frequently used to treat catecholamine-resistant vasodilatory shock. Catecholamines 52-65 arginine vasopressin Rattus norvegicus 12-23 22886838-2 2012 It enhances the vasoconstrictor effects of catecholamines at concentrations of vasopressin that have none or only minimal intrinsic pressor effects. Catecholamines 43-57 arginine vasopressin Rattus norvegicus 79-90 22886838-18 2012 The apparent divergent roles of these pathways in mediating NE- versus VP-augmented pressor responses could potentially lead to new targeted therapies in catecholamine-resistant shock. Catecholamines 154-167 arginine vasopressin Rattus norvegicus 71-73 2511501-2 1989 Stimulation within the A1 catecholamine cell group in the ventrolateral medulla also activates supraoptic neurons and releases vasopressin. Catecholamines 26-39 arginine vasopressin Rattus norvegicus 127-138 22831701-0 2012 Intact catecholamine inputs to the forebrain are required for appropriate regulation of corticotrophin-releasing hormone and vasopressin gene expression by corticosterone in the rat paraventricular nucleus. Catecholamines 7-20 arginine vasopressin Rattus norvegicus 125-136 15363956-5 2004 In the present study, therefore, we attempted to identify which pathway is involved in the vasopressin-induced release of both catecholamines from adrenal medulla using urethane-anesthetized rats. Catecholamines 127-141 arginine vasopressin Rattus norvegicus 91-102 12460640-4 2002 The vasopressin (0.2 nmol/animal)-induced elevation of both catecholamines was significantly attenuated by [d(CH(2))(5)(1),Tyr(Me)(2),Arg(8)]-vasopressin, a selective vasopressin V(1) receptor antagonist, in a dose-dependent manner (0.1 and 0.2 nmol/animal, i.c.v.). Catecholamines 60-74 arginine vasopressin Rattus norvegicus 4-15 12460640-4 2002 The vasopressin (0.2 nmol/animal)-induced elevation of both catecholamines was significantly attenuated by [d(CH(2))(5)(1),Tyr(Me)(2),Arg(8)]-vasopressin, a selective vasopressin V(1) receptor antagonist, in a dose-dependent manner (0.1 and 0.2 nmol/animal, i.c.v.). Catecholamines 60-74 arginine vasopressin Rattus norvegicus 142-153 12460640-4 2002 The vasopressin (0.2 nmol/animal)-induced elevation of both catecholamines was significantly attenuated by [d(CH(2))(5)(1),Tyr(Me)(2),Arg(8)]-vasopressin, a selective vasopressin V(1) receptor antagonist, in a dose-dependent manner (0.1 and 0.2 nmol/animal, i.c.v.). Catecholamines 60-74 arginine vasopressin Rattus norvegicus 142-153 12460640-10 2002 The vasopressin-induced elevation of catecholamines was abolished by indomethacin, an inhibitor of cyclooxygenase (1.2 micromol/animal, i.c.v.). Catecholamines 37-51 arginine vasopressin Rattus norvegicus 4-15 9629270-3 1998 In turn, CRF and VP synthesis and/or release is modulated by catecholamines, prostaglandins (PGs), and nitric oxide (NO). Catecholamines 61-75 arginine vasopressin Rattus norvegicus 17-19 8287440-2 1993 Vasopressin is an abundantly available neuropeptide having well known interactions with catecholamines in vascular smooth muscle. Catecholamines 88-102 arginine vasopressin Rattus norvegicus 0-11 8264854-2 1993 The subpopulation of corticotropin-releasing hormone (CRH) neurosecretory cells that contains vasopressin (VP) is selectively activated by several types of stress (immobilization, hypoglycemia, and intracerebroventricular, i.c.v., colchicine), and is located in a catecholamine-rich area of the hypothalamic paraventricular nucleus. Catecholamines 264-277 arginine vasopressin Rattus norvegicus 94-105 8264854-2 1993 The subpopulation of corticotropin-releasing hormone (CRH) neurosecretory cells that contains vasopressin (VP) is selectively activated by several types of stress (immobilization, hypoglycemia, and intracerebroventricular, i.c.v., colchicine), and is located in a catecholamine-rich area of the hypothalamic paraventricular nucleus. Catecholamines 264-277 arginine vasopressin Rattus norvegicus 107-109 8386972-0 1993 Evaluation for roles of brain prostaglandins in the catecholamine-induced vasopressin secretion in conscious rats. Catecholamines 52-65 arginine vasopressin Rattus norvegicus 74-85 11033330-13 2000 Both CRF and vasopressin have effects in the same direction on behavior, learning and memory processes and stress responses (release of catecholamines and ACTH). Catecholamines 136-150 arginine vasopressin Rattus norvegicus 13-24 9200738-0 1997 Long-lasting effect of catecholamine deficiency on differentiating vasopressin and oxytocin neurons in the rat supraoptic nucleus. Catecholamines 23-36 arginine vasopressin Rattus norvegicus 67-78 9200738-1 1997 According to our earlier study, the catecholamine depletion in neonatal rats resulted in stimulation of the vasopressin and oxytocin gene expression in the neurons of the supraoptic nucleus. Catecholamines 36-49 arginine vasopressin Rattus norvegicus 108-119 9200738-2 1997 The present study extends this line, evaluating whether the catecholamine deficiency provides a long-lasting effect on the differentiating vasopressin and oxytocin neurons of the supraoptic nucleus. Catecholamines 60-73 arginine vasopressin Rattus norvegicus 139-150 9200738-7 1997 Conversely, the catecholamine deficiency resulted in an increased content of the vasopressin-immunoreactive material in cell bodies and processes. Catecholamines 16-29 arginine vasopressin Rattus norvegicus 81-92 9200738-10 1997 Thus, the catecholamine deficiency in the course of the neuron differentiation resulted in a long-lasting augmentation of the intracellular content of vasopressin and oxytocin but did not influence the vasopressin and oxytocin gene expression. Catecholamines 10-23 arginine vasopressin Rattus norvegicus 151-162 7633891-0 1995 Vasopressin and oxytocin gene expression in intact rats and under catecholamine deficiency during ontogenesis. Catecholamines 66-79 arginine vasopressin Rattus norvegicus 0-11 1639176-0 1992 Catecholamine metabolism in the vas deferens and the adrenal gland with special reference to the central catecholamine-depleted state. Catecholamines 0-13 arginine vasopressin Rattus norvegicus 32-35 1639176-1 1992 Experiments were carried out to elucidate the role of central catecholamines in regulating catecholamine metabolism in the vas deferens and adrenal gland of the rat. Catecholamines 62-76 arginine vasopressin Rattus norvegicus 123-126 1639176-1 1992 Experiments were carried out to elucidate the role of central catecholamines in regulating catecholamine metabolism in the vas deferens and adrenal gland of the rat. Catecholamines 62-75 arginine vasopressin Rattus norvegicus 123-126 1666613-4 1991 Stress, catecholamines sharply increased the sensitivity of coronary vessels of old rats to vasopressin. Catecholamines 8-22 arginine vasopressin Rattus norvegicus 92-103 2147376-3 1990 Autoradiographic studies have shown that some V1 receptors are localized presynaptically on catecholaminergic neuronal terminals in the mouse lateral septum, suggesting that vasopressin may act via modulation of catecholamine release. Catecholamines 92-105 arginine vasopressin Rattus norvegicus 174-185 3237322-1 1988 The effects of acetylcholine, arginine vasopressin (AVP) and oxytocin (OXT) on both catecholamine and steroid secretion have been investigated using the isolated rat adrenal gland perfused in situ. Catecholamines 84-97 arginine vasopressin Rattus norvegicus 52-55 3237322-4 1988 AVP at 100 nmol/l but not at 1 nmol/l significantly stimulated the secretion of both steroids and catecholamines. Catecholamines 98-112 arginine vasopressin Rattus norvegicus 0-3 6527741-9 1984 The opposite effects of vasopressin and oxytocin on catecholamine metabolism could be related to the opposite effects of the two peptides on behaviour, neuroendocrine and autonomic regulation. Catecholamines 52-65 arginine vasopressin Rattus norvegicus 24-35 2906609-8 1988 These results suggest that renal alpha 2-adrenoceptors may mediate the inhibition of the renal action of vasopressin by adrenal catecholamines. Catecholamines 128-142 arginine vasopressin Rattus norvegicus 105-116 3231703-7 1988 It is concluded that the contractures induced by Na+ depletion result from the stimulation of postjunctional alpha-adrenoceptors by endogenously released catecholamines from the adrenergic nerve terminals innervating the vas deferens smooth muscle. Catecholamines 154-168 arginine vasopressin Rattus norvegicus 221-224 3409269-0 1988 Vasopressin and 1-deamino-8-D-arginine-vasopressin (DDAVP) reduce elevated plasma catecholamine levels in rats with hypothalamic deafferentation. Catecholamines 82-95 arginine vasopressin Rattus norvegicus 0-11 3409269-0 1988 Vasopressin and 1-deamino-8-D-arginine-vasopressin (DDAVP) reduce elevated plasma catecholamine levels in rats with hypothalamic deafferentation. Catecholamines 82-95 arginine vasopressin Rattus norvegicus 39-50 3389051-0 1988 Central effects of catecholamine antagonists on angiotensin-induced vasopressin secretion in conscious rats. Catecholamines 19-32 arginine vasopressin Rattus norvegicus 68-79 3125946-0 1988 Depletion of central catecholamines reduces pressor responses to arginine vasopressin. Catecholamines 21-35 arginine vasopressin Rattus norvegicus 74-85 3125946-1 1988 Previous reports that central administration of arginine vasopressin (AVP) increases turnover of brain catecholamines raise the possibility that the pressor responses which follow central administration of AVP may be mediated, in part, by central catecholamines. Catecholamines 103-117 arginine vasopressin Rattus norvegicus 48-68 3125946-1 1988 Previous reports that central administration of arginine vasopressin (AVP) increases turnover of brain catecholamines raise the possibility that the pressor responses which follow central administration of AVP may be mediated, in part, by central catecholamines. Catecholamines 103-117 arginine vasopressin Rattus norvegicus 70-73 3125946-1 1988 Previous reports that central administration of arginine vasopressin (AVP) increases turnover of brain catecholamines raise the possibility that the pressor responses which follow central administration of AVP may be mediated, in part, by central catecholamines. Catecholamines 103-117 arginine vasopressin Rattus norvegicus 206-209 3125946-1 1988 Previous reports that central administration of arginine vasopressin (AVP) increases turnover of brain catecholamines raise the possibility that the pressor responses which follow central administration of AVP may be mediated, in part, by central catecholamines. Catecholamines 247-261 arginine vasopressin Rattus norvegicus 48-68 3125946-1 1988 Previous reports that central administration of arginine vasopressin (AVP) increases turnover of brain catecholamines raise the possibility that the pressor responses which follow central administration of AVP may be mediated, in part, by central catecholamines. Catecholamines 247-261 arginine vasopressin Rattus norvegicus 70-73 3125946-1 1988 Previous reports that central administration of arginine vasopressin (AVP) increases turnover of brain catecholamines raise the possibility that the pressor responses which follow central administration of AVP may be mediated, in part, by central catecholamines. Catecholamines 247-261 arginine vasopressin Rattus norvegicus 206-209 3125946-3 1988 Following a one week recovery, these conscious rats, fitted with indwelling arterial catheters, were given intraventricular injections of AVP; the increases in arterial pressure and heart rate were significantly reduced in the catecholamine-depleted animals. Catecholamines 227-240 arginine vasopressin Rattus norvegicus 138-141 3125946-4 1988 These data support the hypothesis that the pressor and tachycardia responses to intraventricular AVP are mediated, in part, by central catecholamine-containing neurons. Catecholamines 135-148 arginine vasopressin Rattus norvegicus 97-100 3830349-0 1985 Central vasopressin in the modulation of catecholamine release in conscious rats. Catecholamines 41-54 arginine vasopressin Rattus norvegicus 8-19 3978417-6 1985 It is suggested that DMK-cut decreases the activity of the catecholaminergic system originating in A1 and terminating in PVN, where it causes catecholamine accumulation and may be involved in vasopressin release and thereby contribute to hypertension. Catecholamines 59-72 arginine vasopressin Rattus norvegicus 192-203 3156386-0 1985 Androgens and effects of opioids and catecholamines on the smooth muscle of the rat vas deferens. Catecholamines 37-51 arginine vasopressin Rattus norvegicus 84-87