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Effects of morphine on electrical activity of single myenteric neurons in cat small bowel
European Journal of Pharmacology
|February 15, 1978
Abstract:
Quantitative parameters of the discharge patterns of burst-type units and single-spike units were increased, decreased or unchanged after application of morphine. The results were the same when morphine was added in the presence of naloxone. The results suggest that morphine had no consistent effect on the spike discharge of continuously active neurons in Auerbach's plexus of cat small intestine.
Insights
Morphine did not consistently alter the firing patterns of neurons in the cat small intestine
Area of Science:
- Neuroscience
- Gastroenterology
- Pharmacology
Background:
- Auerbach's plexus, a component of the enteric nervous system, regulates gastrointestinal motility.
- Opioid receptors are present in the enteric nervous system, suggesting a potential role for morphine in modulating neuronal activity.
Purpose of the Study:
- To investigate the effect of morphine on the discharge patterns of neurons in Auerbach's plexus.
- To determine if naloxone, an opioid antagonist, alters morphine's effects on these neurons.
Main Methods:
- Quantitative analysis of neuronal discharge patterns (burst-type and single-spike units).
- Application of morphine to neurons in Auerbach's plexus of cat small intestine.
- Administration of morphine in the presence of naloxone.
Main Results:
- Morphine application resulted in varied effects on quantitative parameters of neuronal discharge, including increases, decreases, or no change.
- These varied effects were observed consistently even when morphine was administered with naloxone.
- No uniform or predictable change in spike discharge was noted across continuously active neurons.
Conclusions:
- Morphine does not exhibit a consistent effect on the spike discharge of continuously active neurons within the Auerbach's plexus of the cat small intestine.
- The presence of naloxone did not alter the inconsistent effects of morphine, further supporting the lack of a clear modulatory action on these specific neuronal populations.