PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 21368111-0 2011 Epigenetic control of vasopressin expression is maintained by steroid hormones in the adult male rat brain. Steroids 62-78 arginine vasopressin Rattus norvegicus 22-33 15927785-8 2005 We conclude that both the magnocellular and the parvocellular hypothalamic vasopressin systems are capable of expressing the steroid binding globulin, which is probably subject to axonal transport, along with the peptide hormone. Steroids 125-132 arginine vasopressin Rattus norvegicus 75-86 19383875-3 2009 In the bed nucleus of the stria terminalis (BST), AVP gene expression is tightly regulated by gonadal steroid hormones. Steroids 102-118 arginine vasopressin Rattus norvegicus 50-53 19383875-4 2009 However, the degree by which AVP is regulated by gonadal steroid hormones in the suprachiasmatic nucleus (SCN) and medial amygdala (MeA) is unclear. Steroids 57-73 arginine vasopressin Rattus norvegicus 29-32 18824073-1 2008 The sexually dimorphic vasopressin system of the bed nucleus of the stria terminalis (BNST) is the most sensitive neurotransmitter system regulated by sex steroids in rats and mice. Steroids 155-163 arginine vasopressin Rattus norvegicus 23-34 12047907-2 2002 Sex differences in water balance and differences in the effects of gonadal steroids on osmotic stimulation of vasopressin secretion have been reported. Steroids 75-83 arginine vasopressin Rattus norvegicus 110-121 14962079-2 2004 However, how these ovarian steroids interact to regulate the principal ACTH cosecretagogues, corticotropin-releasing hormone (CRH) and arginine vasopressin is not understood. Steroids 27-35 arginine vasopressin Rattus norvegicus 144-155 12121493-1 2002 Progestin receptor immunoreactivity is found in the same regions of the bed nucleus of stria terminalis (BST) and centromedial amygdala (CMA) as steroid-responsive vasopressin immunoreactive (AVP-ir) cells. Steroids 145-152 arginine vasopressin Rattus norvegicus 164-175 11495696-3 2001 Since sex differences may exist in the regulation of water balance by angiotensin II and differential sexual steroid modulation of vasopressin secretion, in response to osmotic stimulation have been reported, gonadotropin releasing hormone (GnRH)-degrading activity was also analysed in serum, neurohypophysis and adrenal glands of male and female rats. Steroids 109-116 arginine vasopressin Rattus norvegicus 131-142 10100486-0 1999 Principal cells of the vas deferens are involved in water transport and steroid synthesis in the adult rat. Steroids 72-79 arginine vasopressin Rattus norvegicus 23-26 10795920-0 2000 The role of steroid hormones in the regulation of vasopressin and oxytocin release and mRNA expression in hypothalamo-neurohypophysial explants from the rat. Steroids 12-28 arginine vasopressin Rattus norvegicus 50-61 10795920-8 2000 Thus, steroid inhibition of osmotically stimulated vasopressin secretion may reflect inhibition of mechanisms mediated by excitatory amino acids. Steroids 6-13 arginine vasopressin Rattus norvegicus 51-62 10795920-10 2000 Therefore, additional work is warranted to understand these effects of the steroid hormones on vasopressin and oxytocin secretion and to elucidate the potential contribution of these mechanisms to regulation of hormone release in vivo. Steroids 75-82 arginine vasopressin Rattus norvegicus 95-106 10385436-3 1999 In this study we evaluated androstenedione"s ability to maintain vasopressin peptide levels in the gonadal steroid-responsive vasopressin cells of the bed nucleus of the stria terminalis and the centromedial amygdala, and their projections. Steroids 107-114 arginine vasopressin Rattus norvegicus 126-137 10100486-12 1999 Use of anti-3beta-hydroxysteroid dehydrogenase antibody revealed an intense reaction over principal cells of the vas deferens, as well as over the blebs in the lumen of the vas deferens, which is indicative of the steroid synthesis performed by these cells. Steroids 25-32 arginine vasopressin Rattus norvegicus 113-116 10100486-12 1999 Use of anti-3beta-hydroxysteroid dehydrogenase antibody revealed an intense reaction over principal cells of the vas deferens, as well as over the blebs in the lumen of the vas deferens, which is indicative of the steroid synthesis performed by these cells. Steroids 25-32 arginine vasopressin Rattus norvegicus 173-176 10100486-15 1999 In summary, principal cells of the vas deferens appear to be involved in synthesis and secretion of steroids and in eliminating water from the lumen of the vas deferens. Steroids 100-108 arginine vasopressin Rattus norvegicus 35-38 10074805-3 1998 Interestingly, this VP system is sexually dimorphic and the VP synthesis in this system depends on circulating gonadal steroids. Steroids 119-127 arginine vasopressin Rattus norvegicus 20-22 10074805-3 1998 Interestingly, this VP system is sexually dimorphic and the VP synthesis in this system depends on circulating gonadal steroids. Steroids 119-127 arginine vasopressin Rattus norvegicus 60-62 10074777-6 1998 This system is also extremely responsive to gonadal steroids as it only produces VP in the presence of gonadal steroids. Steroids 52-60 arginine vasopressin Rattus norvegicus 81-83 9359583-12 1997 Because the ACTH data confirmed an activational effect of E2, we sought to determine whether this steroid regulated levels of corticotropin-releasing factor (CRF) and arginine vasopressin (AVP) mRNAs in the paraventricular nucleus of the hypothalamus (PVN). Steroids 98-105 arginine vasopressin Rattus norvegicus 176-187 9442352-17 1997 Taking into consideration that stress and AVP may play a role in neurogenic hypertension, the possibility of sexual dimorphisms in AVP control may be important to assess the role of sex hormones in stress and steroid-derived hypertension. Steroids 209-216 arginine vasopressin Rattus norvegicus 131-134 8949926-0 1996 Differential regulation of oxytocin and vasopressin messenger ribonucleic acid levels by gonadal steroids in postpartum rats. Steroids 97-105 arginine vasopressin Rattus norvegicus 40-51 9112409-0 1997 Gonadal steroid modulation of vasopressin secretion in response to osmotic stimulation. Steroids 8-15 arginine vasopressin Rattus norvegicus 30-41 9154434-1 1997 The vasopressin (VP)-containing projections from the cells of the bed nucleus of the stria terminalis to the lateral septum (LS) are sexually dimorphic and dependent on gonadal steroids. Steroids 177-185 arginine vasopressin Rattus norvegicus 4-15 9154434-1 1997 The vasopressin (VP)-containing projections from the cells of the bed nucleus of the stria terminalis to the lateral septum (LS) are sexually dimorphic and dependent on gonadal steroids. Steroids 177-185 arginine vasopressin Rattus norvegicus 17-19 9100560-1 1997 There is increasing evidence that ovarian steroids inhibit vascular responsiveness to the neurohypophysial hormone vasopressin. Steroids 42-50 arginine vasopressin Rattus norvegicus 115-126 9100560-12 1997 This provides further evidence for the existence of an important inhibitory interaction between ovarian steroids and vasopressin. Steroids 104-112 arginine vasopressin Rattus norvegicus 117-128 9100560-13 1997 The initial decrease in heart rate observed in pro-oestrous and steroid-treated OVX LE rats after haemorrhage also appears to be related to an ovarian steroid-vasopressin interaction. Steroids 64-71 arginine vasopressin Rattus norvegicus 159-170 9389154-0 1996 [Effects of gonadal steroid hormones on hypothalamic vasopressin mRNA level in male and female rats]. Steroids 20-27 arginine vasopressin Rattus norvegicus 53-64 8616539-1 1996 A sexual dimorphism in the pressor responsiveness to the neurohypophysial hormone vasopressin may be associated with a peripheral interaction between ovarian steroids and the neurohypophysial hormone. Steroids 158-166 arginine vasopressin Rattus norvegicus 82-93 8616539-2 1996 Indeed, the ovarian steroids may inhibit the vasopressin-dependent component of the pressor response to haemorrhage. Steroids 20-28 arginine vasopressin Rattus norvegicus 45-56 7612074-8 1993 These data refute the hypothesis that lactation is characterized by persistently elevated hypothalamic cytoplasmic OT and AVP mRNAs produced as a result of continuous stimulation by suckling and suggest that ovarian steroids may exert a modulatory effect on hypothalamic OT and AVP expression during early lactation. Steroids 216-224 arginine vasopressin Rattus norvegicus 278-281 8801532-1 1996 The dose and time relationships of testosterone treatment on arginine-vasopressin (AVP) concentrations of steroid-dependent vasopressinergic extrahypothalamic neurons were studied in the castrated male rat. Steroids 106-113 arginine vasopressin Rattus norvegicus 70-81 8801532-1 1996 The dose and time relationships of testosterone treatment on arginine-vasopressin (AVP) concentrations of steroid-dependent vasopressinergic extrahypothalamic neurons were studied in the castrated male rat. Steroids 106-113 arginine vasopressin Rattus norvegicus 83-86 8748118-1 1995 Vasopressin messenger RNA (AVP mRNA) expression in the medial amygdala and bed nucleus of the stria terminalis (BST) is almost completely dependent on gonadal steroids. Steroids 159-167 arginine vasopressin Rattus norvegicus 0-11 8748118-1 1995 Vasopressin messenger RNA (AVP mRNA) expression in the medial amygdala and bed nucleus of the stria terminalis (BST) is almost completely dependent on gonadal steroids. Steroids 159-167 arginine vasopressin Rattus norvegicus 27-30 8748118-2 1995 In the BST, the effects of gonadal steroids on AVP mRNA expression are sexually dimorphic. Steroids 35-43 arginine vasopressin Rattus norvegicus 47-50 8748118-8 1995 The pattern of steroid effects on AVP mRNA expression in the MA was similar in both sexes. Steroids 15-22 arginine vasopressin Rattus norvegicus 34-37 7530652-1 1995 Vasopressin (VP) neurons in the bed nucleus of the stria terminalis (BNST) are steroid sensitive and sexually dimorphic. Steroids 79-86 arginine vasopressin Rattus norvegicus 0-11 7530652-1 1995 Vasopressin (VP) neurons in the bed nucleus of the stria terminalis (BNST) are steroid sensitive and sexually dimorphic. Steroids 79-86 arginine vasopressin Rattus norvegicus 13-15 7854039-4 1994 In agreement with previous reports, adrenal steroid regulation of AVP and CRH mRNA was found to be mediated primarily through the Type II receptor. Steroids 44-51 arginine vasopressin Rattus norvegicus 66-69 7931009-4 1994 We have found that the ability of IL-1 beta to increase plasma AVP is strongly influenced by circulating levels of glucocorticoid steroids. Steroids 130-138 arginine vasopressin Rattus norvegicus 63-66 7783853-1 1995 We previously reported that gonadal steroids modify the expression of arginine vasopressin (AVP) in the hypothalamus of rats administered 2% sodium chloride solution for 5 days. Steroids 36-44 arginine vasopressin Rattus norvegicus 79-90 7783853-1 1995 We previously reported that gonadal steroids modify the expression of arginine vasopressin (AVP) in the hypothalamus of rats administered 2% sodium chloride solution for 5 days. Steroids 36-44 arginine vasopressin Rattus norvegicus 92-95 7652597-0 1995 [Effect of glucocorticoids and other steroids on arginine vasopressin release from rat hypothalamic slices]. Steroids 37-45 arginine vasopressin Rattus norvegicus 58-69 7652597-2 1995 The effect of glucocorticoids (GC) and other steroids on AVP release was investigated. Steroids 45-53 arginine vasopressin Rattus norvegicus 57-60 8126571-1 1994 Male rats have about two times as many steroid-responsive vasopressin-immunoreactive (AVP-ir) neurons in the bed nucleus of the stria terminalis (BST) as female rats. Steroids 39-46 arginine vasopressin Rattus norvegicus 58-69 8126571-1 1994 Male rats have about two times as many steroid-responsive vasopressin-immunoreactive (AVP-ir) neurons in the bed nucleus of the stria terminalis (BST) as female rats. Steroids 39-46 arginine vasopressin Rattus norvegicus 86-89 7968245-3 1994 We recently reported that gonadal steroid hormones modify the accumulation of hypothalamic AVP mRNA during sustained hypernatremia (12). Steroids 34-41 arginine vasopressin Rattus norvegicus 91-94 8243294-5 1993 Replacement with gonadal steroids restored the up-regulation in OT and AVP gene expression in gonadectomized animals rendered hyperosmolar. Steroids 25-33 arginine vasopressin Rattus norvegicus 71-74 8243294-0 1993 Gonadal steroid modulation of oxytocin and vasopressin gene expression in the hypothalamus of the osmotically stimulated rat. Steroids 8-15 arginine vasopressin Rattus norvegicus 43-54 8243294-1 1993 We investigated the modulatory role of gonadal steroids on the expression of oxytocin (OT) and vasopressin (AVP) cytoplasmic mRNAs in the paraventricular nucleus and supraoptic nucleus of the osmotically stimulated rat. Steroids 47-55 arginine vasopressin Rattus norvegicus 95-106 8284023-4 1993 Manipulation of circulating gonadal steroids by castration and T replacement was found to regulate the expression of VP mRNA in the bed nucleus of the stria terminalis and medial amygdala of LE and HET rats, but does not appear to modify the absence of VP mRNA in neurons in these nuclei in the HOM rat. Steroids 36-44 arginine vasopressin Rattus norvegicus 117-119 8243294-1 1993 We investigated the modulatory role of gonadal steroids on the expression of oxytocin (OT) and vasopressin (AVP) cytoplasmic mRNAs in the paraventricular nucleus and supraoptic nucleus of the osmotically stimulated rat. Steroids 47-55 arginine vasopressin Rattus norvegicus 108-111 8680418-0 1993 Regulation of vasopressin (VP) gene expression in the bed nucleus of the stria terminalis: gonadal steroid-dependent changes in VP mRNA accumulation are associated with alterations in mRNA poly (A) tail length but are independent of the rate of VP gene transcription. Steroids 99-106 arginine vasopressin Rattus norvegicus 14-25 8680418-0 1993 Regulation of vasopressin (VP) gene expression in the bed nucleus of the stria terminalis: gonadal steroid-dependent changes in VP mRNA accumulation are associated with alterations in mRNA poly (A) tail length but are independent of the rate of VP gene transcription. Steroids 99-106 arginine vasopressin Rattus norvegicus 27-29 8680418-0 1993 Regulation of vasopressin (VP) gene expression in the bed nucleus of the stria terminalis: gonadal steroid-dependent changes in VP mRNA accumulation are associated with alterations in mRNA poly (A) tail length but are independent of the rate of VP gene transcription. Steroids 99-106 arginine vasopressin Rattus norvegicus 128-130 8680418-0 1993 Regulation of vasopressin (VP) gene expression in the bed nucleus of the stria terminalis: gonadal steroid-dependent changes in VP mRNA accumulation are associated with alterations in mRNA poly (A) tail length but are independent of the rate of VP gene transcription. Steroids 99-106 arginine vasopressin Rattus norvegicus 128-130 8680418-1 1993 Forebrain vasopressin (VP) neurons of the bed nucleus of the stria terminalis (BNST) contrast with hypothalamic VP neurons in exhibiting nuclear gonadal steroid receptors which may directly effect steroid-induced changes in VP gene expression observed in BNST cells. Steroids 153-160 arginine vasopressin Rattus norvegicus 112-114 8680418-2 1993 A transcription and Northern mRNA analysis has been performed to determine the mechanism through which gonadal steroids regulate VP gene expression in the BNST. Steroids 111-119 arginine vasopressin Rattus norvegicus 129-131 8680418-5 1993 A post-transcriptional mechanism therefore appears to underlie the gonadal steroid-regulated changes in VP gene expression in the BNST. Steroids 75-82 arginine vasopressin Rattus norvegicus 104-106 8284023-4 1993 Manipulation of circulating gonadal steroids by castration and T replacement was found to regulate the expression of VP mRNA in the bed nucleus of the stria terminalis and medial amygdala of LE and HET rats, but does not appear to modify the absence of VP mRNA in neurons in these nuclei in the HOM rat. Steroids 36-44 arginine vasopressin Rattus norvegicus 253-255 8284269-3 1993 This study investigated the effects of androgens and estrogen in the steroid-dependent expression of VP mRNA in the bed nucleus of the stria terminalis (BNST). Steroids 69-76 arginine vasopressin Rattus norvegicus 101-103 2055176-13 1991 These results support the finding that gonadal steroids are essential in maintaining the biosynthetic integrity of VP neurons in the BNST and AME. Steroids 47-55 arginine vasopressin Rattus norvegicus 115-117 8341419-5 1993 Ovariectomized rats that were not pretreated with colchicine showed enhanced staining (increased cell number and staining intensity of both cell bodies and terminals in the posterior pituitary) for each of the peptides that was found to co-exist in vasopressinergic neurons after treatment with estradiol; staining for vasopressin was similar in steroid- and oil-treated animals. Steroids 346-353 arginine vasopressin Rattus norvegicus 249-260 7687506-4 1993 Testosterone stimulates GAL gene expression in the same neurons that have previously been shown to exhibit steroid regulation of vasopressin gene expression. Steroids 107-114 arginine vasopressin Rattus norvegicus 129-140 1504830-1 1992 The biosynthetic activity of extra-hypothalamic vasopressin (VP) neurons in the bed nucleus of the stria terminalis (BNST) is regulated by gonadal steroids. Steroids 147-155 arginine vasopressin Rattus norvegicus 48-59 1504830-1 1992 The biosynthetic activity of extra-hypothalamic vasopressin (VP) neurons in the bed nucleus of the stria terminalis (BNST) is regulated by gonadal steroids. Steroids 147-155 arginine vasopressin Rattus norvegicus 61-63 1737959-3 1992 Both steroids also inhibited forskolin-induced CRF, AVP and oxytocin responses to PMA. Steroids 5-13 arginine vasopressin Rattus norvegicus 52-55 1834756-1 1991 It has been shown that surgical ovariectomy of the rat results in a fall in plasma vasopressin concentrations suggesting that ovarian steroids may influence hormone release. Steroids 134-142 arginine vasopressin Rattus norvegicus 83-94 7681457-1 1993 Vasopressin (VP) neurons in the bed nucleus of the stria terminalis (BNST) and medial amygdala (AMe) exhibit sexual dimorphism and steroid dependency. Steroids 131-138 arginine vasopressin Rattus norvegicus 0-11 7681457-1 1993 Vasopressin (VP) neurons in the bed nucleus of the stria terminalis (BNST) and medial amygdala (AMe) exhibit sexual dimorphism and steroid dependency. Steroids 131-138 arginine vasopressin Rattus norvegicus 13-15 1813922-4 1991 Although we are aware of some properties of VP systems, e.g., gonadal steroid dependency in the rat, major gaps characterize our knowledge of its anatomy. Steroids 70-77 arginine vasopressin Rattus norvegicus 44-46 1665802-6 1991 Conversely, AVP may enhance the steroid secretory capacity only in adrenocortical cells in which the maintenance of the steroidogenic machinery is assured by normal levels of circulating ACTH. Steroids 32-39 arginine vasopressin Rattus norvegicus 12-15 2313218-0 1990 Effect of ovariectomy and treatment with ovarian steroids on vasopressin release and fluid balance in the rat. Steroids 49-57 arginine vasopressin Rattus norvegicus 61-72 2394985-1 1990 Vasopressin (AVP) immunoreactivity in cells and projections of the bed nucleus of the stria terminalis (BST) and medial amygdaloid nucleus (MA) depends on gonadal steroids. Steroids 163-171 arginine vasopressin Rattus norvegicus 0-11 2139822-2 1990 Furthermore, receptors for the gonadal steroid hormones are located in centers in the brain involved in the control of vasopressin release and in cardiovascular regulation. Steroids 39-55 arginine vasopressin Rattus norvegicus 119-130 19210385-1 1990 Abstract Vasopressin (VP) cells in the bed nucleus of the stria terminalis, medial amygdaloid nucleus and supraoptic and paraventricular nuclei are influenced by gonadal steroids. Steroids 170-178 arginine vasopressin Rattus norvegicus 9-20 2313218-5 1990 The change in vasopressin concentrations observed on steroid treatment depended upon both the dose and the duration. Steroids 53-60 arginine vasopressin Rattus norvegicus 14-25 3698894-1 1986 Recent evidence indicates that the plasma vasopressin concentration is higher in males than in females and that this may be due to sexually dimorphic effects of the gonadal steroids. Steroids 173-181 arginine vasopressin Rattus norvegicus 42-53 2472572-8 1989 It is likely that steroid hormones mediate the action of enkephalin on vasopressin secretion in a specific manner. Steroids 18-34 arginine vasopressin Rattus norvegicus 71-82 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. Steroids 102-109 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. Steroids 85-93 arginine vasopressin Rattus norvegicus 0-3 2850158-0 1988 Effect of ovarian steroids on cyclic adenosine 3":5"-monophosphate production stimulated by arginine vasopressin in rat renal monolayer cultured cells. Steroids 18-26 arginine vasopressin Rattus norvegicus 101-112 2850158-2 1988 In order to study possible involvement of ovarian steroids in this mechanism, their effect on cyclic adenosine 3":5"-monophosphate (cAMP) response to arginine vasopressin (AVP) was examined utilizing rat and human renal medullary cells in monolayer culture. Steroids 50-58 arginine vasopressin Rattus norvegicus 159-170 3325130-5 1987 The results establish that CRF is contained within the long descending projections of the PVH, and are consistent with the view that adrenal steroid withdrawal preferentially enhances the expression of CRF and vasopressin in parvocellular neurosecretory neurons. Steroids 141-148 arginine vasopressin Rattus norvegicus 210-221 3553442-0 1987 Adrenalectomy-induced enhancement of CRF and vasopressin immunoreactivity in parvocellular neurosecretory neurons: anatomic, peptide, and steroid specificity. Steroids 138-145 arginine vasopressin Rattus norvegicus 45-56 34927288-3 2022 However, sex differences in social cognitive behaviors highlight an important interplay between OT, AVP and the sex steroids. Steroids 116-124 arginine vasopressin Rattus norvegicus 100-103 2589530-7 1989 These results suggest gonadal steroid hormones influence adrenoreceptor-mediated control of vasopressin secretion, MABP, and HR. Steroids 30-37 arginine vasopressin Rattus norvegicus 92-103 2791993-0 1989 Steroid dependency of vasopressin neurons in the bed nucleus of the stria terminalis by in situ hybridization. Steroids 0-7 arginine vasopressin Rattus norvegicus 22-33 2791993-1 1989 Recent immunocytochemical studies have suggested that vasopressin (VP) neurons in the bed nucleus of the stria terminalis (BNST) of the rat are gonadal steroid sensitive. Steroids 152-159 arginine vasopressin Rattus norvegicus 54-65 2791993-1 1989 Recent immunocytochemical studies have suggested that vasopressin (VP) neurons in the bed nucleus of the stria terminalis (BNST) of the rat are gonadal steroid sensitive. Steroids 152-159 arginine vasopressin Rattus norvegicus 67-69 3670566-0 1987 Oxytocin and arginine vasopressin stimulate steroid secretion by the isolated perfused rat adrenal gland. Steroids 44-51 arginine vasopressin Rattus norvegicus 22-33 2938937-11 1986 These results suggest that AVP secretion into pituitary stalk blood is under the inhibitory influence of the adrenal steroids, and the increased concentration of AVP found in portal blood may be partially responsible for the elevated levels of ACTH after ADX. Steroids 117-125 arginine vasopressin Rattus norvegicus 27-30 4017961-0 1985 Vasopressin release in male and female rats: effects of gonadectomy and treatment with gonadal steroid hormones. Steroids 95-111 arginine vasopressin Rattus norvegicus 0-11 7072450-0 1982 Effects of orchidectomy and sex steroids on vasopressin response to dehydration. Steroids 32-40 arginine vasopressin Rattus norvegicus 44-55 6726343-9 1984 Taken together, our findings indicate that the glucocorticoid receptor deficit in the Brattleboro rat probably represents a vasopressin-influenced defect in the synthesis or degradation of the receptor, whereas in the aged rat the deficit originates from loss of both receptor per neuron and the steroid-concentrating neurons themselves, and thus is most likely a permanent and pharmacologically insensitive deficit. Steroids 296-303 arginine vasopressin Rattus norvegicus 124-135 7072450-1 1982 The secretion of vasopressin has been shown recently to be influenced by gonadal steroids. Steroids 81-89 arginine vasopressin Rattus norvegicus 17-28 6103767-0 1980 A study of the effects of steroids on alpha-adrenoceptor-mediated contraction of the rat vas deferens. Steroids 26-34 arginine vasopressin Rattus norvegicus 89-92 7012656-0 1981 Adrenal steroid inhibition of the vasopressin-neurophysin neurosecretory system to the median eminence of the rat. Steroids 8-15 arginine vasopressin Rattus norvegicus 34-45 7415756-0 1980 Effects of arginine vasotocin, oxytocin, and arginine vasopressin on steroid-induced surges of luteinizing hormone and prolactin in ovariectomized rats. Steroids 69-76 arginine vasopressin Rattus norvegicus 54-65 744129-0 1978 Plasma neurophysin and vasopressin in the rat: response to adrenalectomy and steroid replacement. Steroids 77-84 arginine vasopressin Rattus norvegicus 23-34 187379-7 1976 In steroid depleted conditions the cyclic AMP medicate efflux of mitochondrial calcium ions, that occurs at low doses of vasopressin, may prevent the release of membrane bound calcium ions and thus inhibit the water permeability effect of the hormone. Steroids 3-10 arginine vasopressin Rattus norvegicus 121-132