Abstract |
Posterior pituitaries of obese mice (ob/ob) contained significantly more immunoreactive dynorphin (P less than .01) and leu-enkephalin (P less than .01) than their lean littermates. Drinking in obese mice was stimulated by 0.3%, and feeding by 10%, of the dose of ethylketocyclazocine, a kappa receptor agonist, needed to produce extra feeding and drinking in lean mice. Obese mice also showed greater and longer lasting suppression of ingestion after MR-2266, a kappa antagonist, than did lean mice. MR-2266 was much more effective than naloxone in suppressing schedule-induced polydipsia in rats. These results indicate that kappa receptors are involved in feeding and drinking and that obesity is associated with changes in these receptors and their ligands.
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Authors | M Ferguson-Segall, J J Flynn, J Walker, D L Margules |
Journal | Life sciences
(Life Sci)
1982 Nov 15-22
Vol. 31
Issue 20-21
Pg. 2233-6
ISSN: 0024-3205 [Print] Netherlands |
PMID | 6131356
(Publication Type: Journal Article, Research Support, U.S. Gov't, Non-P.H.S.)
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Chemical References |
- Analgesics, Opioid
- Benzomorphans
- Endorphins
- Morphinans
- Receptors, Opioid
- Receptors, Opioid, kappa
- MR 2266
- Ethylketocyclazocine
- Enkephalin, Leucine
- Dynorphins
- Cyclazocine
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Topics |
- Analgesics, Opioid
(pharmacology)
- Animals
- Benzomorphans
(analogs & derivatives, pharmacology)
- Cyclazocine
(analogs & derivatives, pharmacology)
- Drinking
(drug effects)
- Dynorphins
- Eating
(drug effects)
- Endorphins
(metabolism)
- Enkephalin, Leucine
(metabolism)
- Ethylketocyclazocine
- Female
- Mice
- Mice, Obese
- Morphinans
(pharmacology)
- Obesity
(physiopathology)
- Pituitary Gland, Posterior
(drug effects, metabolism)
- Receptors, Opioid
(drug effects, physiology)
- Receptors, Opioid, kappa
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