The changes in opioid receptors (Op-R) caused by repeated administration of pentazocine and the effect of concomitant clonidine were investigated. Binding of [3H] naloxone was markedly decreased in the absence of Na+, but was increased in the presence of Na+ in the diencephalon-mesencephalon of chronic pentazocine-treated rats. No significant changes were observed in the cerebral cortex of pentazocine-treated rats. The pentazocine-induced changes in Op-R were abolished by the concurrent use of clonidine, an alpha-adrenergic agonist, which has been shown to relieve the withdrawal symptoms of morphine. This result indicated that the behavioral action of clonidine can also be observed at the Op-R level.</p
Morphine interacts with brain serotonergic (5-HT) systems; these systems have been implicated in mor...
Copyright material has been removed from the electronic version of this thesis. For access to the p...
1. The antinociceptive action of clonidine (Clon) and the interactions with α1, α2 adrenoceptor and ...
The changes in opioid receptors (Op-R) caused by repeated administration of pentazocine and the effe...
The changes in opioid receptors (Op-R) caused by repeated administration of pentazocine and the effe...
Clonidine, an alpha2 adrenoreceptor agonist, is used to treat opiate dependent individuals who are e...
Chronic opioid exposure induces neuroadaptative changes in several brain systems. Amongst others the...
An opioid withdrawal syndrome was induced in rats by repeated morphine administration and final nalo...
Opiates are known to produce various physiological effects. Our understanding of these effects has b...
Morphine, a mu-opiate agonist, and ethylketazocine, a kappa-opiate agonist, produce distinct behavio...
The molecular basis for the different pharmacological effects of (mu) (morphine-like) and k (ketazoc...
The effects of long-term treatment of rats with morphine sulfate were assessed upon the specific bin...
Recent studies showed that oxytocin and opioid peptides play important roles in pain modulation at d...
Morphine interacts with brain serotonergic (5-HT) systems; these systems have been implicated in mor...
Morphine interacts with brain serotonergic (5-HT) systems; these systems have been implicated in mor...
Morphine interacts with brain serotonergic (5-HT) systems; these systems have been implicated in mor...
Copyright material has been removed from the electronic version of this thesis. For access to the p...
1. The antinociceptive action of clonidine (Clon) and the interactions with α1, α2 adrenoceptor and ...
The changes in opioid receptors (Op-R) caused by repeated administration of pentazocine and the effe...
The changes in opioid receptors (Op-R) caused by repeated administration of pentazocine and the effe...
Clonidine, an alpha2 adrenoreceptor agonist, is used to treat opiate dependent individuals who are e...
Chronic opioid exposure induces neuroadaptative changes in several brain systems. Amongst others the...
An opioid withdrawal syndrome was induced in rats by repeated morphine administration and final nalo...
Opiates are known to produce various physiological effects. Our understanding of these effects has b...
Morphine, a mu-opiate agonist, and ethylketazocine, a kappa-opiate agonist, produce distinct behavio...
The molecular basis for the different pharmacological effects of (mu) (morphine-like) and k (ketazoc...
The effects of long-term treatment of rats with morphine sulfate were assessed upon the specific bin...
Recent studies showed that oxytocin and opioid peptides play important roles in pain modulation at d...
Morphine interacts with brain serotonergic (5-HT) systems; these systems have been implicated in mor...
Morphine interacts with brain serotonergic (5-HT) systems; these systems have been implicated in mor...
Morphine interacts with brain serotonergic (5-HT) systems; these systems have been implicated in mor...
Copyright material has been removed from the electronic version of this thesis. For access to the p...
1. The antinociceptive action of clonidine (Clon) and the interactions with α1, α2 adrenoceptor and ...