Cited by 631Cannabis and Cannabinoid ResearchNeuroscience and Neuropharmacology ResearchNeuropeptides and Animal Physiology

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Localization of cannabinoid receptor mRNA in rat brain

Matsuda, Lisa A., Bonner, Tom I., Lolait, Stephen J.·1993·Journal of Comparative Neurology

DOI 10.1002/cne.903270406

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Abstract

Cannabinoid receptor mRNA was localized in adult rat brain by 35S-tailed oligonucleotide probes and in situ hybridization histochemistry. Labelling is described as uniform or non-uniform depending on the relative intensities of individual cells expressing cannabinoid receptor mRNA within a given region or nucleus. Uniform labelling was found in the hypothalamus, thalamus, basal ganglia, cerebellum and brainstem. Non-uniform labelling that resulted from the presence of cells displaying two easily distinguishable intensities of hybridization signals was observed in several regions and nuclei in the forebrain (cerebral cortex, hippocampus, amygdala, certain olfactory structures). Olfactory-associated structures, basal ganglia, hippocampus, and cerebellar cortex displayed the heaviest amounts of labelling. Many regions that displayed cannabinoid receptor mRNA could reasonably be identified as sources for cannabinoid receptors on the basis of well documented hodologic data. Other sites that were also clearly labelled could not be assigned as logical sources of cannabinoid receptors. The localization of cannabinoid receptor mRNA indicates that sensory, motor, cognitive, limbic, and autonomic systems should all be influenced by the activation of this receptor by either exogenous cannabimimetics, including marijuana, or the yet unknown endogenous "cannabinoid" ligand.

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Structure of a cannabinoid receptor and functional expression of the cloned cDNA
Matsuda, L. A., Lolait, S. J., Brownstein, M. J., Young, A. C., & Bonner, T. I. (1990) · Nature · doi:10.1038/346561a0 · Cited by 5,011
Self-citation
Handbook of Chemical Neuroanatomy
Stern, C. D. (1986) · Neurochemistry International · doi:10.1016/0197-0186(86)90021-5 · Cited by 4,160
Cerebellar Cortex
Palay, S. L., & Chan‐Palay, V. (1974) · Springer eBooks · doi:10.1007/978-3-642-65581-4 · Cited by 2,468
Determination and characterization of a cannabinoid receptor in rat brain
Devane, W. A., Dysarz, F. A., Johnson, M. R., Melvin, L. S., & Howlett, A. C. (1988) · Molecular Pharmacology · doi:10.1016/s0026-895x(25)09876-1 · Cited by 2,443
Cannabinoid receptor localization in brain.
Herkenham, M., Lynn, A. B., Little, M. D., Johnson, M. R., Melvin, L. S., de Costa, B. R., & Rice, K. C. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.5.1932 · Cited by 2,321
Characterization and localization of cannabinoid receptors in rat brain: a quantitative in vitro autoradiographic study
Herkenham, M., Lynn, A., Johnson, M., Melvin, L., de Costa, B., & Rice, K. (1991) · The Journal of Neuroscience · doi:10.1523/jneurosci.11-02-00563.1991 · Cited by 2,159
Cerebellar Cortex: Cytology and Organization
Palay, S. L., & Chan‐Palay, V. (1974) · Medical Entomology and Zoology · Cited by 1,679
The amygdalostriatal projection in the rat—an anatomical study by anterograde and retrograde tracing methods
Kelley, A. E., Domesick, V. B., & Nauta, W. J. H. (1982) · Neuroscience · doi:10.1016/0306-4522(82)90067-7 · Cited by 888
Retrograde axonal transport and the demonstration of non‐specific projections to the cerebral cortex and striatum from thalamic intralaminar nuclei in the rat, cat and monkey
Jones, E. G., & Leavitt, R. Y. (1974) · The Journal of Comparative Neurology · doi:10.1002/cne.901540402 · Cited by 882
Efferent connections of the habenular nuclei in the rat
Herkenham, M. A., & Nauta, W. J. H. (1979) · The Journal of Comparative Neurology · doi:10.1002/cne.901870103 · Cited by 855

Flagged first, then by citations

Show all 52 references

Research works printed but not linked: 5

Bayer S. A., 1985, The Rat Nervous System: Forebrain and Midbrain, 335
Bystrzycka E. K., 1985, The Rat Nervous System: Hindbrain and Spinal Cord, 95
Deadwyler S. A., 1992, Synthetic cannabinoid analogs enhance a fast potassium conductance in cultured hippocampal neurons, Soc. Neurosci. Abst., 15, 372
Heimer L., 1975, Golgi Centennial Symposium, Proceedings, 177
Matsuda L. A., The Biological Basis of Substance Abuse and its Treatment

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Engler, B., Freiman, I., Urbanski, M. J., & Szabó, B. (2006) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.105.092718 · Cited by 58
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McLaughlin, C. R., & Abood, M. E. (1993) · Developmental Brain Research · doi:10.1016/0165-3806(93)90124-s · Cited by 58
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Puente, N., Elezgarai, I., Lafourcade, M., Reguero, L., Marsicano, G., Georges, F. E., Manzoni, O. J., & Grandes, P. (2010) · PLoS ONE · doi:10.1371/journal.pone.0008869 · Cited by 63
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Robinson, S. A., Loiacono, R. E., Christopoulos, A., Sexton, P. M., & Malone, D. T. (2010) · Brain Research · doi:10.1016/j.brainres.2010.04.031 · Cited by 57
GABAB and CB1 cannabinoid receptor expression identifies two types of septal cholinergic neurons
Nyíri, G., Szabadits, E., Cserép, C., Mackie, K., Shigemoto, R., & Freund, T. F. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04146.x · Cited by 55
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Koch, J. E., & Matthews, S. M. (2001) · Nutritional Neuroscience · doi:10.1080/1028415x.2001.11747361 · Cited by 57
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Suárez, J., Romero‐Zerbo, S., Rivera, P., Bermúdez‐Silva, F. J., Pérez, J., de Fonseca, F. R., & Fernández‐Llebrez, P. (2010) · The Journal of Comparative Neurology · doi:10.1002/cne.22382 · Cited by 57
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Hoozen, B. E. V., & Cross, C. E. (1997) · Clinical Reviews in Allergy & Immunology · doi:10.1007/bf02737700 · Cited by 56
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Onaivi, E. S., Chakrabarti, A. K., & Chaudhuri, G. (1996) · Progress in Neurobiology · doi:10.1016/0301-0082(95)00044-5 · Cited by 55
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Perra, S., Pillolla, G., Luchicchi, A., & Pistis, M. (2008) · Alcoholism Clinical and Experimental Research · doi:10.1111/j.1530-0277.2007.00588.x · Cited by 49
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Authors: Matsuda, L. A., Bonner, T. I., & Lolait, S. J.
Affiliations: National Institute of Mental Health (US)
Corresponding author: Matsuda, Lisa A.
ORCID: Lolait, Stephen J.
Venue: Journal of Comparative Neurology
Publisher: Wiley
Published: 1993-01-22
Volume: 327
Issue: 4
Pages: 535-550
ISSN: 0021-9967 (ISSN-L)
1096-9861
DOI: 10.1002/cne.903270406
OpenAlex: W2025390026
Cited by: 631
References: 52
Citations by year: 2026: 2 · 2025: 6 · 2024: 4 · 2023: 8 · 2022: 10 · 2021: 15 · 2020: 20 · 2019: 11 · 2018: 21 · 2017: 19 · 2016: 16 · 2015: 20 · 2014: 14 · 2013: 25 · 2012: 22
FWCI: 9.64
Type: journal article
Language: en
Open access: closed
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor, 4278 d)
Locations: The Journal of Comparative Neurology (publishedVersion)
PubMed (publishedVersion)
Funders: National Alliance for Research on Schizophrenia and Depression
Topics: Health Sciences › Medicine › Pharmacology (medical) › Cannabis and Cannabinoid Research
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
Keywords: cannabinoid receptors, mRNA localization, rat brain, hypothalamus, thalamus, basal ganglia, cerebellum, brainstem, cerebral cortex, hippocampus, amygdala, endocannabinoids, cannabis
MeSH terms: Animals, Brain Chemistry, Male, Mesencephalon, Receptors, Drug, Rhombencephalon, RNA, Messenger, Prosencephalon, Rats, Sprague-Dawley, Receptors, Cannabinoid, Rats

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Localization of cannabinoid receptor mRNA in rat brain

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