TY - JOUR
T1 - A study of gastrointestinal opiate receptors
T2 - The role of the Mu receptor on gastric emptying: concise communication
AU - Lamki, L.
AU - Sullivan, S.
PY - 1983
Y1 - 1983
N2 - Animal and in vitro experiments suggest that opiates exert their actions by interaction with possibly five different subtypes of opiate receptors, identified as mu (μ), kappa (κ), sigma (σ), delta (δ), and epsilon (ε). As yet there is no conclusive evidence for their existence in man. Our experiments on morphine and the enkephalin analog DAMME have suggested at least two types of opiate receptors involved in gastric secretion. In this study we have used the very powerful and nonselective opiate agonist etorphine to stimulate as many of the different opiate receptors as possible. We have then attempted to block selectively the μ receptor by administering a small dose of naloxone. Etorphine delayed gastric emptying whereas naloxone alone had no effect. In combination, the inhibitory effect of etorphine on gastric emptying was incompletely prevented while the subjective effects of etorphine were completely abolished. These results may indicate that μ receptors are important in the regulation of gastric emptying, but that other (non-μ) receptors are also involved. The radionuclide study of gastric emptying, as used here, is a potentially powerful tool in physiological research on the gastrointestinal tract.
AB - Animal and in vitro experiments suggest that opiates exert their actions by interaction with possibly five different subtypes of opiate receptors, identified as mu (μ), kappa (κ), sigma (σ), delta (δ), and epsilon (ε). As yet there is no conclusive evidence for their existence in man. Our experiments on morphine and the enkephalin analog DAMME have suggested at least two types of opiate receptors involved in gastric secretion. In this study we have used the very powerful and nonselective opiate agonist etorphine to stimulate as many of the different opiate receptors as possible. We have then attempted to block selectively the μ receptor by administering a small dose of naloxone. Etorphine delayed gastric emptying whereas naloxone alone had no effect. In combination, the inhibitory effect of etorphine on gastric emptying was incompletely prevented while the subjective effects of etorphine were completely abolished. These results may indicate that μ receptors are important in the regulation of gastric emptying, but that other (non-μ) receptors are also involved. The radionuclide study of gastric emptying, as used here, is a potentially powerful tool in physiological research on the gastrointestinal tract.
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M3 - Article
C2 - 6308189
AN - SCOPUS:0020962071
SN - 0161-5505
VL - 24
SP - 689
EP - 692
JO - Journal of Nuclear Medicine
JF - Journal of Nuclear Medicine
IS - 8
ER -