ENKEPHALIN RECEPTORS IN THE EMETIC CHEMORECEPTOR TRIGGER ZONE OF THE DOG

• Published in: British journal of pharmacology Vol. 72; no. 3; pp. 471 - 475
• Main Authors: BHARGAVA, K.P., DIXIT, K.S., GUPTA, Y.K.
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01.03.1981
• Subjects: Animals; Apomorphine - pharmacology; Chemoreceptor Cells - drug effects; Dogs; Emetics - administration & dosage; Emetics - pharmacology; Enkephalins - pharmacology; Female; Injections, Intraventricular; Male; Morphine - pharmacology; Naloxone - pharmacology; Receptors, Opioid - drug effects
• ISSN: 0007-1188; 1476-5381
• DOI: 10.1111/j.1476-5381.1981.tb10998.x

1 The emetic action of Met‐enkephalin, morphine and naloxone was studied following their administration into the cerebral ventricles of dogs through chronically implanted cannulae and the effect on the responses of ablating the chemoreceptor trigger zone (CTZ) was investigated. The opiate antagonist, naloxone, was used to determine the role of enkephalin receptors in emetic responses. 2 Administration of Met‐enkephalin (1.0 μg/kg) into the IVth ventricle regularly evoked emesis with an average latency of 35 s. A dose of morphine (2.5 μg/kg) which was five times larger was required for a consistent emetic response when introduced into the lateral cerebral ventricle (i.c.v.) as compared to the dose required by the IVth ventricular route. The latency of emetic responses by the latter route of injection of morphine was shorter. This is in accord with an action of morphine on the emetic CTZ. 3 After bilateral ablation of the CTZ, intraventricular injections of Met‐enkephalin and morphine failed to produce emesis even when given in doses that were 5 to 10 times the dose which regularly elicited emesis in animals with intact CTZ. The emesis produced in dogs by intraventricular Met‐enkephalin and morphine is thus fully accounted for by an action on the CTZ. 4 Naloxone (i.c.v.) in doses up to 10.0 μg/kg did not cause emesis. However, higher doses of naloxone elicited dose‐dependent emesis in dogs. The 100% emetic dose of naloxone was found to be 160 μg/kg and the latency of emesis was 180 s. Unlike Met‐enkephalin and morphine, naloxone continued to elicit emesis in CTZ‐ablated animals. 5 Pretreatment with intraventricular naloxone (1 to 8 μg/kg) blocked the emetic responses induced by intraventricular Met‐enkephalin and morphine but not that to apomorphine. The selective protective action of the opiate antagonist against Met‐enkephalin and morphine supports the presence of enkephalin receptors in the emetic CTZ.