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Centrally mediated intestinal stimulation by morphine
Summary
Intraventricular morphine increases feline small intestine activity via a central mechanism, blocked by naloxone. This effect is distinct from the central emetic response.
Area of Science:
- Neurogastroenterology
- Pharmacology
Background:
- The central nervous system influences gastrointestinal motility.
- Opioid receptors in the brain can modulate gut activity.
Purpose of the Study:
- To investigate the effects of central administration of morphine, apomorphine, and epinephrine on feline small intestinal electrical activity.
- To determine if central opioid-induced gut effects are mediated by the emetic pathway.
Main Methods:
- Adult cats were surgically implanted with electrodes along the small intestine and a cannula into the cerebral ventricle.
- Drugs (morphine, apomorphine, epinephrine, naloxone) were administered intraventricularly (i.vt.) or intraperitoneally (i.p.).
- Small intestinal spike potentials were recorded and analyzed.
Main Results:
- Intraventricular morphine significantly increased spike potentials in the proximal small intestine.
- This effect was abolished by intraventricular naloxone, indicating central opioid receptor involvement.
- Apomorphine and epinephrine, potent emetic agents, did not alter intestinal activity when given centrally.
Conclusions:
- Central administration of morphine enhances small intestinal activity through a naloxone-sensitive, central mechanism.
- This effect is independent of the central emetic pathways activated by apomorphine and epinephrine.