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Intrathecal morphine slows gastrointestinal transit in rats
European Journal of Pharmacology
|December 17, 1985
Summary
Morphine administered intrathecally inhibits rat gastrointestinal transit. Spinal cord appears to be a target site for this morphine effect, as naloxone reversed it when given intrathecally.
Area of Science:
- Pharmacology
- Neuroscience
- Gastroenterology
Background:
- Opioid analgesics like morphine are known to affect gastrointestinal motility.
- The precise site of action for morphine's effects on gastrointestinal transit is not fully elucidated.
Purpose of the Study:
- To investigate the role of the spinal cord in mediating the gastrointestinal inhibitory effects of morphine.
- To compare the effects of intrathecal versus intraperitoneal morphine administration on gastrointestinal transit.
Main Methods:
- Rats received intrathecal or intraperitoneal injections of morphine at varying doses.
- Gastrointestinal transit was measured following morphine administration.
- Naloxone, an opioid antagonist, was administered intrathecally prior to morphine to assess the involvement of spinal receptors.
Main Results:
- Both intrathecal and intraperitoneal morphine administration produced a dose-dependent inhibition of gastrointestinal transit in rats.
- Intrathecal naloxone pretreatment successfully reversed the inhibitory effects of intrathecal morphine.
- However, intrathecal naloxone did not affect the gastrointestinal inhibitory response to intraperitoneal morphine.
Conclusions:
- The spinal cord is a significant site for the gastrointestinal inhibitory effects of intrathecally administered morphine.
- These findings suggest that the central nervous system, specifically the spinal cord, plays a crucial role in mediating morphine's impact on gut motility.