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Published on: June 2, 2014
Morphine initiates migrating myoelectric complexes by acting on peripheral opioid receptors
Abstract:
The role of peripheral and central opioid receptors in morphine-induced migrating myoelectric complexes (MMECs) was studied in conscious dogs implanted with silver-silver chloride electrodes. In normal fasted dogs morphine (100-200 micrograms/kg iv) initiated phase III of the MMEC in the duodenum. Once initiated the MMEC propagated distally. This effect of morphine was blocked by the opioid receptor antagonists naloxone (2 mg/kg iv) and N,N-diallylnormorphinium bromide (4 mg/kg iv). Higher doses of morphine (300-600 micrograms/kg iv) initiated phase III activity in fed dogs as early as 20 min after feeding, while lower doses (150 micrograms/kg iv) initiated phase III activity routinely when administered 100 min after feeding. In dogs with bilateral vagotomies and bilateral thoracolumbar sympathetic chain ganglionectomies, morphine (150 micrograms/kg iv) initiated phase III activity in the duodenum, which then migrated distally. This study demonstrates that morphine initiates phase III of the MMEC by acting through peripheral opioid receptors.
Insights
Morphine triggers gut contractions, known as migrating myoelectric complexes (MMECs), by acting on peripheral opioid receptors. This effect was observed in dogs and could be blocked by opioid antagonists.
Area of Science:
- Gastroenterology
- Pharmacology
- Neuroscience
Background:
- Morphine is known to affect gastrointestinal motility.
- Migrating myoelectric complexes (MMECs) are important for gut clearance.
- The specific receptors involved in morphine's effect on MMECs are not fully understood.
Purpose of the Study:
- To investigate the role of peripheral and central opioid receptors in morphine-induced MMECs.
- To determine the site of action for morphine's effect on the initiation of phase III of the MMEC.
Main Methods:
- Conscious dogs were surgically implanted with electrodes to record myoelectric activity.
- Morphine was administered intravenously at various doses to fasted and fed dogs.
- Opioid receptor antagonists (naloxone and N,N-diallylnormorphinium bromide) were used to block morphine's effects.
- Studies were conducted in dogs with vagotomies and sympathetic denervation.
Main Results:
- Morphine initiated phase III of the MMEC in the duodenum, which then propagated distally.
- The effect of morphine was blocked by opioid receptor antagonists.
- Morphine induced phase III activity in both fasted and fed states, with dose and timing adjustments.
- Morphine's effect persisted even after vagotomies and sympathetic denervation.
Conclusions:
- Morphine initiates phase III of the migrating myoelectric complex (MMEC) by acting through peripheral opioid receptors.
- Central opioid receptors are not essential for morphine-induced MMEC initiation.
- These findings clarify the peripheral mechanism of morphine's prokinetic effect on the gastrointestinal tract.
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