The goal of this two part proposal is to determine the effectiveness of a new pharmacologic agent, ritanserin, in the treatment of women with cocaine abuse. Compared to men, women exhibit a more rapid course of cocaine addiction and do worse in treatment. In addition, they are underrepresented in drug abuse studies. Ritanserin, a selective 5-HT2 serotonin antagonist, has been shown to decrease cocaine use in rats, decrease alcohol intake and depression in humans, and has a good safety profile. Additionally, it appears to have no abuse potential. Study 1 will evaluate the effects of ritanserin on cocaine self- administration in both depressed and non-depressed women with cocaine abuse. This study is a four week, double-blind trial of 84 depressed and 84 non-depressed subjects randomized into ritanserin or placebo conditions. Outcome will be determined by urine drug screens, drug use diaries and changes in craving and depression measures. Study 2 will determine the effect of ritanserin on relapse to cocaine use in a six month, double-blind, placebo-controlled trial of 100 depressed and 100 non-depressed women with cocaine abuse. A standardized psychosocial treatment component emphasizing relapse prevention is included in Study 2. Outcome measures include drug screen urinalysis, drug use diaries and changes on craving, depression and relapse scales. Hypotheses to be tested are: (1) ritanserin will decrease both the self- administration of cocaine and relapse to cocaine in both depressed and non-depressed women with a greater effect in depressed women; (2) ritanserin will decrease craving for cocaine; (3) ritanserin will decrease the frequency of relapses to cocaine and the consequences of relapse; and (4) depressive signs and symptoms will be decreased in ritanserin groups as compared to placebo. This work will test the efficacy of a new pharmacologic agent, ritanserin, in the treatment of cocaine abuse. It will also expand upon the limited knowledge of women with cocaine abuse.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Specialized Center (P50)
Project #
5P50DA009259-04
Application #
6238012
Study Section
Project Start
1997-09-30
Project End
1998-08-31
Budget Start
1996-10-01
Budget End
1997-09-30
Support Year
4
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Type
DUNS #
168559177
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Dickmann, Patricia J; Mooney, Marc E; Allen, Sharon S et al. (2009) Nicotine withdrawal and craving in adolescents: effects of sex and hormonal contraceptive use. Addict Behav 34:620-3
Mooney, Marc; Sofuoglu, Mehmet; Dudish-Poulsen, Susan et al. (2006) Preliminary observations of paranoia in a human laboratory study of cocaine. Addict Behav 31:1245-51
Sofuoglu, Mehmet; Dudish-Poulsen, Susan; Poling, James et al. (2005) The effect of individual cocaine withdrawal symptoms on outcomes in cocaine users. Addict Behav 30:1125-34
Hanson, Karen; Allen, Sharon; Jensen, Sue et al. (2003) Treatment of adolescent smokers with the nicotine patch. Nicotine Tob Res 5:515-26
Sofuoglu, Mehmet; Dudish-Poulsen, Susan; Brown, Scott B et al. (2003) Association of cocaine withdrawal symptoms with more severe dependence and enhanced subjective response to cocaine. Drug Alcohol Depend 69:273-82
Sofuoglu, Mehmet; Babb, David; Hatsukami, Dorothy K (2003) Labetalol treatment enhances the attenuation of tobacco withdrawal symptoms by nicotine in abstinent smokers. Nicotine Tob Res 5:947-53
Hatsukami, Dorothy K; Jensen, Joni; Brauer, Lisa H et al. (2003) Lack of effect of 5HT3 antagonist in mediating subjective and behavioral responses to cotinine. Pharmacol Biochem Behav 75:1-7
Sofuoglu, Mehmet; Babb, David A; Hatsukami, Dorothy K (2002) Effects of progesterone treatment on smoked cocaine response in women. Pharmacol Biochem Behav 72:431-5
Sofuoglu, M; Nelson, D; Babb, D A et al. (2001) Intravenous cocaine increases plasma epinephrine and norepinephrine in humans. Pharmacol Biochem Behav 68:455-9
Sofuoglu, M; Brown, S; Babb, D A et al. (2001) Depressive symptoms modulate the subjective and physiological response to cocaine in humans. Drug Alcohol Depend 63:131-7

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