TY - JOUR
T1 - The stability of plasma growth hormone and MHPG responses to repeated clonidine challenge in normal males
AU - Trestman, Robert L.
AU - Coccaro, Emil F.
AU - Lawrence, Timothy
AU - Knott, Peter
AU - Gabriel, Steven M.
AU - Siever, Larry J.
N1 - Funding Information:
Acknowledgments: This research was supported in part by grants from the National Institutes of Health, National Center for Research Resources, RR00071, to the Mt. Sinai Medical Center, National Institutes of Mental Health, R01-MH4113l , and Department of Veterans Affairs Merit Award 7609004. The authors gratefully wish to acknowledge Vivian Mitropoulou MA and Irene Lopez BA for their assistance in the preparation of this manuscript, and Ren~ Kahn M.D. for his thoughtful critique of an earlier version of this manuscript.
PY - 1994
Y1 - 1994
N2 - Clonidine is a centrally acting alpha2-adrenergic agonist used in many psychiatric studies to assess adrenergic functioning. The short- and long-term stability of plasma growth hormone (GH) and plasma 3-methoxy-4-hydroxy phenylglycol (MHPG) responses to clonidine (2 μg/kg IV) over a 60-min period were assessed in subsets of 13 male normal controls on 2 consecutive days (Study A; n = 11) and on 2 days separated by several months (Study B; n = 11). In Study A, no significant differences between consecutive days were found in either baseline plasma GH or MHPG or their responses to clonidine. The 60 minute plasma GH responses between consecutive days were highly correlated (r = 0.75, n = 11, p < .001), while the 60 min plasma MHPG responses were not. In Study B, no significant differences in baseline plasma GH or MHPG, or their responses to clonidine challenge, were found between the 2 test days. However, neither the plasma GH responses nor the plasma MHPG responses to clonidine at 60 min correlated significantly between the 2 study days separated by several months. Both in Study A and in Study B, 8 of 11 subjects had a stable GH response to clonidine across both study days when defined dichotomously (blunted < 4 ng/ml; otherwise, not blunted). These results suggest that the plasma GH response and plasma MHPG response to clonidine are unaffected by repeat clonidine challenge separated by 24 h, and that the plasma GH response to clonidine may be more stable over time than the plasma MHPG response to clonidine.
AB - Clonidine is a centrally acting alpha2-adrenergic agonist used in many psychiatric studies to assess adrenergic functioning. The short- and long-term stability of plasma growth hormone (GH) and plasma 3-methoxy-4-hydroxy phenylglycol (MHPG) responses to clonidine (2 μg/kg IV) over a 60-min period were assessed in subsets of 13 male normal controls on 2 consecutive days (Study A; n = 11) and on 2 days separated by several months (Study B; n = 11). In Study A, no significant differences between consecutive days were found in either baseline plasma GH or MHPG or their responses to clonidine. The 60 minute plasma GH responses between consecutive days were highly correlated (r = 0.75, n = 11, p < .001), while the 60 min plasma MHPG responses were not. In Study B, no significant differences in baseline plasma GH or MHPG, or their responses to clonidine challenge, were found between the 2 test days. However, neither the plasma GH responses nor the plasma MHPG responses to clonidine at 60 min correlated significantly between the 2 study days separated by several months. Both in Study A and in Study B, 8 of 11 subjects had a stable GH response to clonidine across both study days when defined dichotomously (blunted < 4 ng/ml; otherwise, not blunted). These results suggest that the plasma GH response and plasma MHPG response to clonidine are unaffected by repeat clonidine challenge separated by 24 h, and that the plasma GH response to clonidine may be more stable over time than the plasma MHPG response to clonidine.
UR - https://www.scopus.com/pages/publications/0028054795
U2 - 10.1016/0306-4530(94)90055-8
DO - 10.1016/0306-4530(94)90055-8
M3 - Article
C2 - 9210208
AN - SCOPUS:0028054795
SN - 0306-4530
VL - 19
SP - 13
EP - 20
JO - Psychoneuroendocrinology
JF - Psychoneuroendocrinology
IS - 1
ER -