TY - JOUR
T1 - Plasma NPY concentrations during tryptophan and sham depletion in medication-free patients with remitted depression
AU - Czermak, Christoph
AU - Hauger, Richard
AU - Drevets, Wayne C.
AU - Luckenbaugh, David A.
AU - Geraci, Marilla
AU - Charney, Dennis S.
AU - Neumeister, Alexander
N1 - Funding Information:
Dr. Czermak received financial support for a postdoctoral fellowship at the Yale University School of Medicine from the Max Kade Foundation, New York. Dr. Hauger received support from a Department of Veterans Affairs Merit Review grant (#0015); the VA Mental Illness Research, Education and Clinical Center (MIRECC) of VISN22; the VA Center of Excellence for Stress and Mental Health, and NIH/NIA AG022982) and NIH/NIMH (MH074697) RO1 grants. This study was funded by the Intramural Research Program of the National Institute of Mental Health. None of the funding sources had further role in study design; in the collection, analysis and interpretation of data; in the writing of the report; and in the decision to submit the paper for publication.
PY - 2008/10
Y1 - 2008/10
N2 - Background: Neuropeptide Y (NPY) and serotonergic systems have been implicated in the pathophysiology of depression but have not yet been linked together. Methods: In a randomized, double-blind crossover study, 28 medication-free patients with remitted depression and 26 healthy control subjects underwent tryptophan depletion (TD) and sham depletion. Plasma NPY concentrations were determined at baseline and at + 5, + 7, and + 24 h during TD and sham depletion, respectively. Hamilton Depression Rating Scale (HDRS, 24-item) scores were assessed at baseline and at + 7 and + 24 h after TD and sham depletion, respectively. Results: There was no difference between healthy subjects and patients with remitted depression in baseline plasma NPY concentrations and in plasma NPY concentrations during TD and sham depletion, respectively. Plasma NPY concentrations did not differ between TD and sham depletion. At no time point there was an association between HDRS scores and plasma NPY concentrations in patients with remitted depression. Limitations: Plasma NPY concentrations in rMDD patients were not obtained during the symptomatic phase of the illness. Only peripheral measurements of NPY were used. Conclusions: Decreased plasma NPY concentrations, as described previously during a spontaneous episode of major depression, appear as state but not as trait marker in depression. No evidence was found for an involvement of plasma NPY in relapse during TD. There appears no direct functional link between serotonergic neurotransmission and plasma NPY concentrations.
AB - Background: Neuropeptide Y (NPY) and serotonergic systems have been implicated in the pathophysiology of depression but have not yet been linked together. Methods: In a randomized, double-blind crossover study, 28 medication-free patients with remitted depression and 26 healthy control subjects underwent tryptophan depletion (TD) and sham depletion. Plasma NPY concentrations were determined at baseline and at + 5, + 7, and + 24 h during TD and sham depletion, respectively. Hamilton Depression Rating Scale (HDRS, 24-item) scores were assessed at baseline and at + 7 and + 24 h after TD and sham depletion, respectively. Results: There was no difference between healthy subjects and patients with remitted depression in baseline plasma NPY concentrations and in plasma NPY concentrations during TD and sham depletion, respectively. Plasma NPY concentrations did not differ between TD and sham depletion. At no time point there was an association between HDRS scores and plasma NPY concentrations in patients with remitted depression. Limitations: Plasma NPY concentrations in rMDD patients were not obtained during the symptomatic phase of the illness. Only peripheral measurements of NPY were used. Conclusions: Decreased plasma NPY concentrations, as described previously during a spontaneous episode of major depression, appear as state but not as trait marker in depression. No evidence was found for an involvement of plasma NPY in relapse during TD. There appears no direct functional link between serotonergic neurotransmission and plasma NPY concentrations.
KW - Major depressive disorder
KW - Neurobiology
KW - Neuropeptide Y
KW - Serotonin
KW - Tryptophan depletion
UR - https://www.scopus.com/pages/publications/49949120001
U2 - 10.1016/j.jad.2008.01.014
DO - 10.1016/j.jad.2008.01.014
M3 - Article
C2 - 18281099
AN - SCOPUS:49949120001
SN - 0165-0327
VL - 110
SP - 277
EP - 281
JO - Journal of Affective Disorders
JF - Journal of Affective Disorders
IS - 3
ER -