Alcohol ingestion activates the autonomic nervous system and the hypothalam
ic-pituitary-adrenal axis. This study examined naltrexone effects on alcoho
l-induced increases in physiological responses and their association with a
lcohol liking. Using a within-subjects design, heavy drinking men (N = 19)
were maintained on each of three naltrexone doses (0, 50, and 100 mg, p.o.)
over an 8-day inpatient stay. Within each naltrexone dose, subjects had th
ree alcohol challenge sessions (none, moderate, high) in random order. Auto
nomic, subjective and endocrine measurements were collected regularly prior
to and following alcohol administration. High-dose alcohol ingestion incre
ased heart rate, diastolic blood pressure, skin temperature, ACTH, cortisol
and liking of drink effects; responses following the moderate alcohol dose
were less consistent. Naltrexone significantly dampened alcohol-induced in
creases in heart rate, diastolic blood pressure, hormone levels and subject
ive liking of drink effects. This dampening of cardiovascular and hormonal
responses may contribute to the therapeutic effectiveness of naltrexone for
reducing alcohol liking and decreasing relapse in alcohol-dependent person
s.