Autoradiographic localization of opiate receptors in rat brain. II. The brain stem
References (42)
- et al.
Monoaminergic mechanisms of stimulation-produced analgesia
Brain Research
(1975) - et al.
Antagonism of stimulation-produced analgesia byp-CPA, a serotonin synthesis inhibitor
Brain Research
(1972) - et al.
Inhibition of visceral pain by electrical stimulation of the periaqueductal gray matter
Pain
(1976) - et al.
On the central sites for the antinociceptive action of morphine and fentanyl
Neuropharmacology
(1970) - et al.
The periaqueductal gray: site of morphine analgesia and tolerance as shown by 2-way cross tolerance between systemic and intracerebral injections
Brain Research
(1976) - et al.
Pain reduction by focal electrical stimulation of the brain: an anatomical and behavioral analysis
Brain Research
(1974) - et al.
Effects of morphine on the turnover of brain catecholamines and serotonin in rats—acute morphine administration
Europ. J. Pharmacol.
(1975) - et al.
Site of morphine induced analgesia in the primate brain: relation to pain pathways
Pharmacol. Biochem. Behav.
(1975) - et al.
Identification of opiate receptor binding in intact animals
Life Sci.
(1975) - et al.
Morphine analgesia: blockade by raphe magus lesions
Brain Research
(1975)
Reduced effect of morphine in midbrain raphe lesioned rats
Europ. J. Pharmacol.
Differential projections of habenular nuclei
J. comp. Neurol.
Antagonism of stimulation-produced analgesia by naloxone, a narcotic antagonist
Science
Morphine tolerance, dependence and withdrawal and brain acetylcholine
Pharmacologist
Dose-dependent behavioral and analgesic effects produced by microinjection of morphine sulfate into the anterior thalamic nuclei
Pharmacologist
Morphine dependence and in vivo turnover of acetylcholine in mouse brain
J. Pharmacol. exp. Ther.
Brain acetylcholine in morphine pellet implanted rats given naloxone
Psychopharmacologia (Berl.)
The accessory optic fiber system in the rat
J. comp. Neurol.
Distribution of stereospecific binding of the potent narcotic analgesic etorphine in the human brain: predominance in the limbic system
Res. Commun chem. path. Pharmacol.
Cited by (481)
Immunolocalization of kappa opioid receptors in the axon initial segment of a group of embryonic mesencephalic dopamine neurons
2022, IBRO Neuroscience ReportsCitation Excerpt :On the other hand, we observed that KOR was highly localized in axonal tracts such as the anterior commissure, corpus callosum, and striatal streaks. Autoradiography assays performed in the brains of rats (Atweh and Kuhar, 1977) and guinea pigs (Foote, 1987) also found this KOR pattern, indicating that KOR localization in fiber tracts is transversal to rodent species and suggesting a pivotal role of KOR on the control of neuron activity directly on axons. Svingos et al. 2001, showed that KOR was preferentially located in terminals in the NAc.
Changes in opioid receptors, opioid peptides and morphine antinociception in mice subjected to early life stress
2020, European Journal of PharmacologyReview of the cytology and connections of the lateral habenula, an avatar of adaptive behaving
2017, Pharmacology Biochemistry and BehaviorOpioid administration following spinal cord injury: Implications for pain and locomotor recovery
2013, Experimental NeurologyCitation Excerpt :How locomotor function and pain are affected by opioids following SCI, however, has yet to be fully examined. Three classic opioid receptors, the μ-opioid receptor (MOR), δ-opioid receptor (DOR), and κ-opioid receptor (KOR) have been identified and are located throughout regions of the brain, brainstem, spinal cord, and periphery on both presynaptic (e.g. afferent fibers), postsynaptic (e.g. dorsal horn neurons), and glial cells (Arvidsson et al., 1995; Atweh and Kuhar, 1977a, 1977b, 1977c; Besse et al., 1990a, 1990b, 1991; Fields et al., 1980; Mansour et al., 1987; Pert and Snyder, 1973a, 1973b; Pert et al., 1973; Simon, 1973; Terenius, 1973; Yaksh, 1997; reviewed by Hutchinson et al., 2011; Stein et al., 1989; Yaksh and Noueihed, 1985). Traditionally, opioid receptor agonists are known for their analgesic (antinociceptive) and rewarding, hedonic properties.
Neurosurgical Approaches to Pain Management
2013, Practical Management of Pain: Fifth Edition