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Butorphanol precipitates abstinence in morphine dependent rats.
1Department of Pharmacology and Toxicology, University of Mississippi Medical Center, Jackson 39216.
European Journal of Pharmacology
|November 7, 1989
Summary
Butorphanol triggered opioid withdrawal in morphine-dependent rats, but with significantly less potency than naloxone. Qualitative differences were observed in the precipitated withdrawal syndromes.
Area of Science:
- Pharmacology
- Neuroscience
- Behavioral Science
Background:
- Opioid dependence is a major public health concern.
- Understanding opioid withdrawal is crucial for developing effective treatments.
- Butorphanol and naloxone are opioid receptor modulators with different pharmacological profiles.
Purpose of the Study:
- To investigate and compare the opioid withdrawal syndrome precipitated by butorphanol and naloxone in a rat model.
- To characterize the qualitative and quantitative differences in withdrawal behaviors induced by these two agents.
Main Methods:
- Continuous intracerebroventricular infusion of morphine to establish dependence in rats for three days.
- Challenge with butorphanol or naloxone to precipitate withdrawal.
- Observation and quantification of specific withdrawal behaviors (defecation, urination, teeth chattering, escape behavior, wet shake behavior).
Main Results:
- Butorphanol precipitated a withdrawal syndrome in morphine-dependent rats.
- The potency of butorphanol to induce withdrawal behaviors was 10-100 times less than naloxone on a molar basis.
- Wet shake behavior, a key feature of naloxone-precipitated withdrawal, was notably absent in butorphanol-challenged animals.
Conclusions:
- Butorphanol induces opioid withdrawal, but it is quantitatively less potent than naloxone.
- Qualitative differences exist between butorphanol- and naloxone-precipitated opioid withdrawal syndromes.
- These findings highlight distinct pharmacological actions of butorphanol and naloxone in the context of opioid dependence and withdrawal.