ANTI-NOCICEPTIVE EFFECT OF MORPHINE, OPIOID ANALGESICS AND HALOPERIDOL INJECTED INTO THE CAUDATE-NUCLEUS OF THE RAT

被引:22
作者
JURNA, I
HEINZ, G
机构
[1] Institut für Pharmacologie und Toxikologie der Universität des Saarlandes, Homburg/Saar
关键词
Apomorphine; Haloperidol; Morphine; Naloxone; Nociceptive reflex; Opioid analgesics;
D O I
10.1007/BF00501222
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The effect of intracaudate (i.c.) microinjections of morphine, opioid analgesics and haloperidol was determined on the tail-flick response evoked by radiant heat in rats. Bilateral injections (0.2 μl on each side) into the caudate nuclei of morphine 5 μg, pethidine 50 μg, levorphanol 4 μg, dextrorphan 10 μg and haloperidol 5 μg significantly increased the reaction time of the tail-flick response. The antinociceptive effect of an i.c. injection of morphine or levorphanol was abolished by an intraperitoneal (i.p.) injection of naloxone 0.2 mg/kg or apomorphine 2 mg/kg. The anti-nociceptive effect of pethidine, dextrorphan and haloperidol was reduced but not abolished by an i.p. injection of naloxone 0.2 mg/kg. An i.p. injection of apomorphine 2 mg/kg abolished the effect of an i.c. injection of haloperidol. A bilateral i.c. injection of naloxone 5 μg or apomorphine 10 μg reduced the anti-nociceptive effect of an i.p. injection of morphine 2 mg/kg or haloperidol 2 mg/kg, but did not abolish it. It is concluded that (1) an anti-nociceptive effect can be achieved by an action on the caudate nucleus of the drugs tested; (2) the anti-nociceptive effect exerted by morphine and levorphanol in the caudate nucleus is due to a specific action mediated by opiate receptors, whilst that produced by pethidine and dextrorphan is due to a specific and/or unspecific action; (3) the anti-nociceptive effect of haloperidol in the caudate nucleus is due to an impairment of dopaminergic impulse transmission, which is also involved in the effect of morphine and levorphanol. © 1979 Springer-Verlag.
引用
收藏
页码:145 / 151
页数:7
相关论文
共 49 条
[1]   ANATOMICAL SPECIFICITY AS CRITICAL DETERMINANT OF INTERRELATIONSHIP BETWEEN RAPHE LESIONS AND MORPHINE ANALGESIA [J].
ADLER, M ;
KOSTOWSKI, W ;
RECCHIA, M ;
SAMANIN, R .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1975, 32 (01) :39-44
[2]   EVIDENCE FOR DOPAMINE RECEPTOR STIMULATION BY APOMORPHINE [J].
ANDEN, NE ;
RUBENSON, A ;
FUXE, K ;
HOKFELT, T .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1967, 19 (09) :627-&
[3]   AUTORADIOGRAPHIC LOCALIZATION OF OPIATE RECEPTORS IN RAT-BRAIN .3. TELENCEPHALON [J].
ATWEH, SF ;
KUHAR, MJ .
BRAIN RESEARCH, 1977, 134 (03) :393-405
[4]   PERMEATION OF MORPHINE-LIKE ACTING SUBSTANCES TO THEIR SITES OF ANTINOCICEPTIVE ACTION IN BRAIN AFTER INTRAVENOUS AND INTRAVENTRICULAR APPLICATION AND DEPENDENCE UPON LIPID-SOLUBILITY [J].
CUBE, BV ;
TESCHEMA.HJ ;
HERZ, A ;
HESS, R .
NAUNYN-SCHMIEDEBERGS ARCHIV FUR PHARMAKOLOGIE, 1970, 265 (05) :455-&
[5]   NALOXONE AS A GABA ANTAGONIST - EVIDENCE FROM IONTOPHORETIC, RECEPTOR-BINDING AND CONVULSANT STUDIES [J].
DINGLEDINE, R ;
IVERSEN, LL ;
BREUKER, E .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1978, 47 (01) :19-27
[6]   IMMUNOHISTOCHEMICAL STUDIES USING ANTIBODIES TO LEUCINE-ENCEPHALIN - INITIAL OBSERVATIONS ON NERVOUS-SYSTEM OF RAT [J].
ELDE, R ;
HOKFELT, T ;
JOHANSSON, O ;
TERENIUS, L .
NEUROSCIENCE, 1976, 1 (04) :349-&
[7]   MODE OF ACTION OF APOMORPHINE AND DEXAMPHETAMINE ON GNAWING COMPULSION IN RATS [J].
ERNST, AM .
PSYCHOPHARMACOLOGIA, 1967, 10 (04) :316-316
[8]  
FELTZ P, 1969, J PHYSIOL-LONDON, V205, pP8
[9]  
FIFKOVA E, 1967, ELECTROPHYSIOLOGICAL, P653
[10]   ORIGIN AND DISTRIBUTION OF GLUTAMATE DECARBOXYLASE IN SUBSTANTIA NIGRA OF CAT [J].
FONNUM, F ;
GROFOVA, I ;
RINVIK, E ;
STORMMAT.J ;
WALBERG, F .
BRAIN RESEARCH, 1974, 71 (01) :77-92