Autoradiographic distribution of mu and delta opiate receptors in rat brain using highly selective ligands
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Place preferences induced by electrical stimulation of the external lateral parabrachial subnucleus in a sequential learning task: Place preferences induced by NLPBe stimulation
2020, Behavioural Brain ResearchCitation Excerpt :In these studies, place preferences were induced using a concurrent procedure, in which the animals could move freely in the maze and intracranial electrical stimulation was associated with their voluntary stay in one of the two maze compartments. It has been observed that place preferences induced by NLPBe stimulation by means of this procedure are blocked by naloxone administration [9,13], reflecting the high density of opioid receptors in this region [6,8,14–16]. Interestingly, preferences induced by stimulating the lateral hypothalamus are not inhibited by naloxone administration [17].
Bioanalytical method development and validation of corynantheidine, a kratom alkaloid, using UPLC-MS/MS, and its application to preclinical pharmacokinetic studies
2020, Journal of Pharmaceutical and Biomedical AnalysisNaloxone blocks the aversive effects of electrical stimulation of the parabrachial complex in a place discrimination task
2016, Neurobiology of Learning and MemoryOpioid-induced redistribution of 6TM and 7TM mu opioid receptors: A hypothesized mechanistic facilitator model of opioid-induced hyperalgesia
2016, Pharmacological ReportsCitation Excerpt :MOR is distributed widely in the CNS. Caudate and putamen are the locations with the highest density of MOR exhibiting a patchy pattern; cortex, nucleus accumbens (NAc), thalamus, hippocampus, and amygdale have high levels of MOR; periaqueductal gray (PAG) matter and raphe nuclei have moderate MOR density; and preoptic area, hypothalamus, and globus pallidus are the areas with low levels of MOR; and in the spinal cord, MOR is mainly presented in the superficial layers of the dorsal horn [56]. MOR majorly locates perisynaptically including both pre- and post-synaptic terminals.
Molecular Changes in Opioid Addiction: The Role of Adenylyl Cyclase and cAMP/PKA System
2016, Progress in Molecular Biology and Translational ScienceSpinal and supraspinal N-methyl-d-aspartate and melanocortin-1 receptors contribute to a qualitative sex difference in morphine-induced hyperalgesia
2015, Physiology and BehaviorCitation Excerpt :Furthermore, previous studies have also suggested that a multitude of these areas involved in morphine antinociception are also implicated in MIH. Specifically relevant to opioid-induced nociception are the dorsal horn, and reciprocal connections between the PAG and RVM [15,17,23–30]. However, the contribution of spinal and supraspinal loci to the qualitative sex differences characterizing MIH remains unknown.