Effects of Smoking on Opioid Receptor Binding: A PET Study

Sponsor

National Institute on Drug Abuse (NIDA) (NIH)

Overall Status

Completed

CT.gov ID

NCT00618631

Collaborator

Johns Hopkins University (Other)

Enrollment

Locations

83.7

Duration (Months)

Patients Per Site

0.2

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Background:

Tobacco smoking is one of the most preventable causes of morbidity and mortality in the world, but the addictive property of nicotine is such that fewer than 10 percent of people who attempt to quit smoking remain tobacco-free after 1 year. Researchers are studying the addictive properties of nicotine in an attempt to develop more successful medication therapies for smoking cessation.
Nicotine acts on chemical receptors in the brain, including opioid receptors that affect the perception of pain. Repeated nicotine administration can cause adaptations in the brain s opioid receptors, which heightens the addictive properties of nicotine and increases the likelihood and severity of withdrawal symptoms associated with smoking cessation. Researchers are interested in using positron emission tomography (PET) scanning to study brain chemical responses to nicotine in current smokers and nonsmokers.

Objectives:

To study brain chemical activity related to cigarette smoking and nicotine administration.
To compare the brain chemical activity of current daily smokers with that of nonsmokers.

Eligibility:

Individuals 21 to 50 years of age who are either current smokers (10 to 25 cigarettes daily for at least 2 years) or have had some exposure to tobacco but have never smoked regularly (may have had a maximum of 20 cigarettes in their lifetime and none in past year).

Design:

Eligible participants will undergo initial medical and psychological screening and neuropsychological testing before beginning the main phase of the study. Participants will be required to abstain from alcohol and drugs (except caffeine, nicotine, and prescription drugs) for 24 hours before each session, and smokers will refrain from smoking after midnight on the night before each session.
Session 1: Participants will answer questions about nicotine craving and withdrawal symptoms, followed by a magnetic resonance imaging (MRI) scan to provide baseline information about brain activity.
Session 2 and 3: Participants will answer questions about nicotine craving and withdrawal symptoms, and then will smoke one cigarette (either active nicotine or placebo). Researchers will document participants consumption of the cigarette. After the cigarette is smoked, participants will have a PET scan. Blood samples will be drawn during the PET session.

Condition or Disease	Intervention/Treatment	Phase
Substance-related Discorder	Drug: Nicotine Drug: Carfentanil	Phase 1

Detailed Description

Objective: To determine whether nicotine, at the dose delivered through a cigarette (1-2 mg), will increase the release of endogenous opioids, measured by the displacement of the mu-opioid PET receptor radioligand [(11)C]carfentanil and to determine whether smokers have adaptations in the opioid system compared with nonsmokers.

Study Population: 20 current, daily smoikers and 20 never-smokers who have smoked between 1 and 20 cigarettes in their lifetime.

Design: Double-blind, placebo-controlled, parallel groups design.

Outcome Measures: 1) displacement [(11)C]carfentanil binding, secondary to the release of endorphins by nicotine; 2) upregulation of [(11)C]carfentanil specific binding in smokers compared with nonsmokers; 3) [(11)C]carfentanil specific binding as a function of the mu-opioid receptor A118G polymorphism; and 4) correlation between self-report measures of nicotine effect and [(11)C]carfentanil binding profile.

Study Design

Study Type:

Interventional

Actual Enrollment :

26 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Primary Purpose:

Screening

Official Title:

Effects of Smoking on Opioid Receptor Binding Using [(11)C]Carfentanil: An Imaging PET Study

Study Start Date :

Jan 17, 2008

Actual Study Completion Date :

Jan 8, 2015

Outcome Measures

Primary Outcome Measures

Changes in carfentanil binding. []

Secondary Outcome Measures

Cardiovascular and subjective responses to smoking one cigarette. []

Eligibility Criteria

Criteria

Ages Eligible for Study:

21 Years to 50 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Yes

INCLUSION CRITERIA FOR SMOKERS:

21-50 year old males and females
smoke 10 cigarettes per day on average for at least 2 years
urine cotinine level greater than or equal to 200 ng/ml (NicAlert reading greater than or equal to 4)
estimated IQ score greater than or equal to 85 (competent to give informed consent)
medically and psychologically healthy as determined by screening criteria.

EXCLUSION CRITERIA FOR SMOKERS:

interest in reducing or quitting tobacco use
treatment for nicotine dependence in the past 3 months
current drug or alcohol abuse or dependence
consumption of more than 15 alcoholic drinks per week during the past month
any opiate use in the past 6 months
marijuana use greater than one time per week on an average during the past month
other drug use greater than 2 time per month on average during the past 3 months.
current use of any medication that would interfere with the protocol
under the influence of a drug or alcohol at experimental sessions
HIV positive
history of psychotropic medications
history of head injury with unconscious longer than 5 minutes
implantable device or foreign body that would make an MRI examination unobtainable
MRI abnormality judged clinically significant by the PI
use of any investigational medication or device within the previous 30 days
donation at least 450 ml of blood or equivalent levels of plasma within the previous 30 days
exposure to ionizing radiation that, in combination with the study tracer, would result in a cumulative exposure exceeding 5 rem in one calendar year
any subject judged by the PI to be inappropriate for the study.
chronic pulmonary disease, including COPD, bronchitis, asthma, and emphysema
pregnant, nursing, or become pregnant during the study

INCLUSION CRITERIA FOR NONSMOKERS:

21-50 year old males and females
smoked 1-20 cigarettes in their life and none in past year
urine cotinine level less than 30 ng/ml (NicAlert reading less than or equal to 1)
estimated IQ score greater than or equal to 85 (competent to give informed consent)
medically and psychologically healthy as determined by screening criteria.

EXCLUSION CRITERIA FOR NONSMOKERS:

use of any tobacco products in the past year
current drug or alcohol abuse or dependence
consumption of more than 15 alcoholic drinks per week during the past month
any opiate use in the past 6 months
marijuana use greater than one time per week on average during past month
other drug use greater than two times per month on average during past three months.
current use of any medication that would interfere with the protocol
under the influence of a drug or alcohol at experimental sessions
HIV positive
history of psychotropic medications
history of head injury with unconscious longer than 5 minutes
implantable device or foreign body that would make an MRI examination unobtainable
MRI abnormality judged clinically significant by the PI
use of any investigational medication or device within the previous 30 days
donation of at least 450 ml of blood or equivalent levels of plasma within the previous 30 days
exposure to ionizing radiation that, in combination with the study tracer, would result in a cumulative exposure exceeding 5 rem in one calendar year
any subject judged by the PI to be inappropriate for the study.
chronic pulmonary disease, including COPD, bronchitis, asthma, and emphysema
pregnant, nursing, or become pregnant during the study