Psychopharmacology of Fear-Potentiated Startle in Humans
| Status: | Completed |
|---|---|
| Conditions: | Healthy Studies |
| Therapuetic Areas: | Other |
| Healthy: | No |
| Age Range: | 18 - 45 |
| Updated: | 10/8/2017 |
| Start Date: | August 15, 2002 |
| End Date: | September 17, 2013 |
The purpose of this study is to understand the effects of the drug alprazolam (Xanax ) on
anxiety.
To understand the effect of anxiety-relieving drugs on fear and anxiety, researchers often
have participants anticipate unpleasant stimuli. Anticipating unpleasant stimuli increases or
potentiates a simple reflex called the startle reflex. The so-called fear-potentiated startle
reflex (FPS) effect may be blocked or reduced by anxiety-relieving drugs. Evidence suggests
that the FPS can be mediated by two mechanisms that regulate the phasic- and sustained
enhancement of startle. This study will elicit phasic and sustained FPS in participants by
having them anticipate moderately painful stimuli that are administered predictably and
unpredictably. The main goal of this study is to assess the affect of alprazolam on the
phasic and sustained enhancement of startle.
This study comprises two pilot experiments and a main study. Participants in the study will
be screened with a psychiatric history, physical examination, electrocardiogram (EKG), and
blood and urine tests. Participants will four testing sessions separated by 5 to 10 days. At
each session, participants will be given one of two doses of alprazolam, diphenhydramine, or
placebo (an inactive pill). Questionnaires and other tests will be performed.
anxiety.
To understand the effect of anxiety-relieving drugs on fear and anxiety, researchers often
have participants anticipate unpleasant stimuli. Anticipating unpleasant stimuli increases or
potentiates a simple reflex called the startle reflex. The so-called fear-potentiated startle
reflex (FPS) effect may be blocked or reduced by anxiety-relieving drugs. Evidence suggests
that the FPS can be mediated by two mechanisms that regulate the phasic- and sustained
enhancement of startle. This study will elicit phasic and sustained FPS in participants by
having them anticipate moderately painful stimuli that are administered predictably and
unpredictably. The main goal of this study is to assess the affect of alprazolam on the
phasic and sustained enhancement of startle.
This study comprises two pilot experiments and a main study. Participants in the study will
be screened with a psychiatric history, physical examination, electrocardiogram (EKG), and
blood and urine tests. Participants will four testing sessions separated by 5 to 10 days. At
each session, participants will be given one of two doses of alprazolam, diphenhydramine, or
placebo (an inactive pill). Questionnaires and other tests will be performed.
Objective:
Recent breakthroughs in biomedical research have not improved the ability to identify
successful pharmacological treatments derived from novel candidate compounds. This is partly
due to the inability of the existing scientific approach to translate candidate anxiolytics
identified through the drug discovery process into efficient psychopharmacological treatment
of patients. A new drug development approach urgently needs to be implemented to improve
predictability and efficiency in translating the basic science explosion into validated drug
targets. A key approach to improve the selection of candidate anxiolytics for clinical trials
is to fill the gap between animal models and clinical studies in patients by implementing
tests in healthy humans with a predictive validity of subsequent clinical efficacy. As a step
towards this goal, we developed integrative experimental models of fear and anxiety in
non-clinical subjects. We now use these models to identify the anxiolytic and anxiogenic
properties of various compounds. The current specific objectives are to 1) further test the
psychopharmacological validity of the model using recognized anxiolytics (the SSRI
citalopram), 2) test the properties of compounds that are hypothesized to be anxiolytic or
anxiogenic (e.g., oxytocin, arginine vasopressin, hydrocortisone) and 3) examine the time
course of the anxiolytic effect of the benzodiazepine alprazolam on FPS.
Study population:
Medically and psychiatrically healthy males and females ages 18 to 45.
Design:
The study examines fear and anxiety elicited by unpleasant electric shock delivered
predictably and unpredictably, respectively. The following drugs will be tested:
1) Citalopram, 2) oxytocin and arginine vasopressin, 3) hydrocortisone, 4) alprazolam.
Outcome measures:
The primary outcome measure is the startle reflex. Secondary measures include the skin
conductance response, the heart rate, and subjective measures of anxiety.
Recent breakthroughs in biomedical research have not improved the ability to identify
successful pharmacological treatments derived from novel candidate compounds. This is partly
due to the inability of the existing scientific approach to translate candidate anxiolytics
identified through the drug discovery process into efficient psychopharmacological treatment
of patients. A new drug development approach urgently needs to be implemented to improve
predictability and efficiency in translating the basic science explosion into validated drug
targets. A key approach to improve the selection of candidate anxiolytics for clinical trials
is to fill the gap between animal models and clinical studies in patients by implementing
tests in healthy humans with a predictive validity of subsequent clinical efficacy. As a step
towards this goal, we developed integrative experimental models of fear and anxiety in
non-clinical subjects. We now use these models to identify the anxiolytic and anxiogenic
properties of various compounds. The current specific objectives are to 1) further test the
psychopharmacological validity of the model using recognized anxiolytics (the SSRI
citalopram), 2) test the properties of compounds that are hypothesized to be anxiolytic or
anxiogenic (e.g., oxytocin, arginine vasopressin, hydrocortisone) and 3) examine the time
course of the anxiolytic effect of the benzodiazepine alprazolam on FPS.
Study population:
Medically and psychiatrically healthy males and females ages 18 to 45.
Design:
The study examines fear and anxiety elicited by unpleasant electric shock delivered
predictably and unpredictably, respectively. The following drugs will be tested:
1) Citalopram, 2) oxytocin and arginine vasopressin, 3) hydrocortisone, 4) alprazolam.
Outcome measures:
The primary outcome measure is the startle reflex. Secondary measures include the skin
conductance response, the heart rate, and subjective measures of anxiety.
- INCLUSION CRITERIA:
Subjects will be healthy volunteers between 18-45 years old and free of current
psychopathology and organic central nervous system disorders.
EXCLUSION CRITERIA:
- Any significant medical or neurological problems (e.g. cardiovascular illness,
respiratory illness, neurologic illness, seizure, etc.)
- Adverse reactions to cortisol (cortisol study only)
- Adverse reactions to benzodiazepines or antihistamines (alprazolam study only)
- History of angioedema
- Osteoporosis (Hydrocortisone study only)
- High or low blood pressure
- History of fainting
- First degree relative with history of mania, schizophrenia, or other psychoses
- A history of mania, schizophrenia, or other psychoses
- Current migraine
- Use of herbal medicines or dietary supplements with psychoactive properties
(citalopram study only)
- Any current psychiatric disorders
- Past alcohol/drug dependence and alcohol/drug abuse in past one year
- Current use of psychotropic medication
- Impaired hearing
- Pregnancy
- Breast-feeding or currently taking contraceptive hormones (oxytocin/vasopressin study
only)
- Positive results of beta-human chorionic gonadotropin testing (females only)
- Neurological syndrome of the wrist (e.g., carpal tunnel syndrome)
We found this trial at
1
site
9000 Rockville Pike
Bethesda, Maryland 20892
Bethesda, Maryland 20892
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