1988
DOI: 10.1172/jci113561
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Human corticotropin-releasing factor plus lysine vasopressin test during glucocorticoid therapy.

Abstract: Methods1.0 Ag/kg body wt human corticotropin-releasing factor (hCRF) and 0.005 IU/kg body wt lysine vasopressin (LVP) were administered in a bolus dose to patients receiving daily or alternate-day glucocorticoid therapy. In normal subjects with this hCRF-LVP test, the plasma ACTH increment was significantly greater (-2.5-fold) 15 min after injection than under the CRF test. In patients receiving daily glucocorticoid therapy (> 15 mg prednisolone or an equivalent daily dose), the plasma ACTH and cortisol respon… Show more

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Cited by 7 publications
(2 citation statements)
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“…Dose-response studies of intravenous AVP administration to normal humans have demonstrated that while a peripheral plasma AVP concentration of 60 pmol/1 does not stimulate ACTH and cortisol release [42], levels of 135 pmol/1 cause a significant rise in both ACTH and cortisol [43]. Considerably lower AVP concentrations of 5-10 pmol/1, achieved by hypertonic saline infusion, will augment the stimulatory effect of synthetic CRH in vivo [6,7], and this is consistent with reports that very low intra venous doses of AVP or LVP, which do not by themselves significantly increase ACTH levels above basal, still sub stantially increase the ACTH response to human or ovine 203 CRH [41,[44][45][46]. In the present study, plasma AVP levels were greater than 220 prnol/1 (considerably greater than the above threshold for ACTH release) 15 min prior to the peak ACTH responses (i.e., 10 min after AVP was admin istered) in all three tests in which active AVP was given.…”
Section: Discussionsupporting
confidence: 86%
“…Dose-response studies of intravenous AVP administration to normal humans have demonstrated that while a peripheral plasma AVP concentration of 60 pmol/1 does not stimulate ACTH and cortisol release [42], levels of 135 pmol/1 cause a significant rise in both ACTH and cortisol [43]. Considerably lower AVP concentrations of 5-10 pmol/1, achieved by hypertonic saline infusion, will augment the stimulatory effect of synthetic CRH in vivo [6,7], and this is consistent with reports that very low intra venous doses of AVP or LVP, which do not by themselves significantly increase ACTH levels above basal, still sub stantially increase the ACTH response to human or ovine 203 CRH [41,[44][45][46]. In the present study, plasma AVP levels were greater than 220 prnol/1 (considerably greater than the above threshold for ACTH release) 15 min prior to the peak ACTH responses (i.e., 10 min after AVP was admin istered) in all three tests in which active AVP was given.…”
Section: Discussionsupporting
confidence: 86%
“…Three previous studies used smaller doses of LVP (either 0.35 or 0.5 IU, but in the form of i.v. bolus injections) combined with 50-100 pg hCRH(Spath-Schwalbe, 1987;Hashimoto et al, 1988; Arai & Takabe, 1991).…”
mentioning
confidence: 99%