Sk. Teoh et al., COCAINE EFFECTS ON PULSATILE SECRETION OF ACTH IN MEN, The Journal of pharmacology and experimental therapeutics, 270(3), 1994, pp. 1134-1138
The effects of cocaine on pulsatile secretion of adrenocorticotropic h
ormone (ACTH) in men were studied under controlled clinical research w
ard conditions. Eight men with a Diagnostic and Statistical Manual of
the American Psychiatric Association Version III, revised, diagnosis o
f concurrent cocaine and opioid dependence provided their informed con
sent for participation in this study. After an overnight fast, a chall
enge dose of cocaine (30 mg i.v.) or placebo was administered under si
ngle-blind conditions in a randomized order on 2 study days. Blood sam
ples were collected at 2-min intervals for 76 min during base line and
for an additional 76 min after i.v. administration of the challenge d
ose. Peak plasma cocaine levels of 313.8 +/- 46.5 ng/ml were detected
within 2 min after cocaine administration. The cluster analysis progra
m originally described by Veldhuis and Johnson (1986) was used to char
acterize ACTH pulsatile secretion (Iran-manesh et al., 1990). Acute co
caine administration (30 mg i.v.) significantly increased ACTH mean pe
ak amplitude (P < .05), mean percent increase in peak amplitude, (P <.
05), mean peak area (P < .04), total peak area (P < .04) and increment
al peak height (P < .04). Mean ACTH valley levels (P < .02) and mean v
alley nadir (P < .02) were also significantly increased after cocaine
administration. We postulate that cocaine stimulates the release of co
rticotropin releasing factor and that the cocaine-induced secretion of
corticotropin releasing factor increases the amplitude of ACTH pulses
, because ACTH pulse frequency was not altered by cocaine.