The distribution of Hypocretin/Orexin receptor mRNA in the mouse and human brain

Hypocretin (Hcrtr, HCRTR) / orexin (OX) receptors modulate a range of neurobiological functions and are drug targets for several disorders. Mapping the distribution of receptors in the brain can inform their function and guide targeting of specific disorders. Although studied in rodents, orexin rece...

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Main Authors: Sanjida Mir, Ryan J. Keenan, Romke Bron, Cameron J. Nowell, Catriona McLean, Leah C. Beauchamp, Laura J. Vella, Brian Dean, Daniel Hoyer, Laura H. Jacobson
Format: Article
Language:English
Published: Elsevier 2024-12-01
Series:Medicine in Drug Discovery
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Online Access:http://www.sciencedirect.com/science/article/pii/S2590098624000277
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author Sanjida Mir
Ryan J. Keenan
Romke Bron
Cameron J. Nowell
Catriona McLean
Leah C. Beauchamp
Laura J. Vella
Brian Dean
Daniel Hoyer
Laura H. Jacobson
author_facet Sanjida Mir
Ryan J. Keenan
Romke Bron
Cameron J. Nowell
Catriona McLean
Leah C. Beauchamp
Laura J. Vella
Brian Dean
Daniel Hoyer
Laura H. Jacobson
author_sort Sanjida Mir
collection DOAJ
description Hypocretin (Hcrtr, HCRTR) / orexin (OX) receptors modulate a range of neurobiological functions and are drug targets for several disorders. Mapping the distribution of receptors in the brain can inform their function and guide targeting of specific disorders. Although studied in rodents, orexin receptor distribution has remained relatively unexplored in humans, and thus there is also a paucity of comparative anatomy. The aim of this study was therefore to map the distribution of hypocretin/orexin receptor mRNA in selected regions of the mouse and human brain by non-radioactive in situ hybridization (ISH) using digoxigenin (DIG)-labelled cRNA anti-sense probes. Data revealed both distinct and overlapping patterns of distributions of Hcrtr1/HCRTR1 and Hcrtr2/HCRTR2 mRNA suggesting that the functions of the orexin system are mediated differently by each receptor. In the mouse brain, the highest expression of Hcrtr1 mRNA was in the locus coeruleus (LC) whereas Hcrtr2 mRNA was most abundant in the lateral hypothalamus (LH). The human caudate nuclei showed significant expression of both HCRTR1 and HCRTR2 mRNA, whereas the mouse predominantly expressed Hcrtr2 mRNA. The noradrenergic neurons of the human LC showed high signals for both HCRTR1 (71.7%) and HCRTR2 (81.5%) mRNA. Expression of HCRTR2 mRNA in non-noradrenergic human LC cells was also notable. The distribution pattern in mouse and human brains is consistent with the involvement of the orexin system in arousal and the sleep/wake cycle in both species, however, variations in receptor subtype expression profiles suggests that species differences in responses to orexin receptor ligands may be expected.
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spelling doaj-art-9f4c6bbb7e4a49a9a8786c108d2f560f2024-11-22T07:38:49ZengElsevierMedicine in Drug Discovery2590-09862024-12-0124100202The distribution of Hypocretin/Orexin receptor mRNA in the mouse and human brainSanjida Mir0Ryan J. Keenan1Romke Bron2Cameron J. Nowell3Catriona McLean4Leah C. Beauchamp5Laura J. Vella6Brian Dean7Daniel Hoyer8Laura H. Jacobson9Department of Biochemistry and Pharmacology, University of Melbourne, Parkville, Victoria, AustraliaDepartment of Biochemistry and Pharmacology, University of Melbourne, Parkville, Victoria, Australia; The Florey Institute of Neuroscience and Mental Health, Parkville, Victoria, AustraliaDrug Discovery Biology, Monash Institutes of Pharmaceutical Sciences, Monash University, Parkville, Victoria, AustraliaDrug Discovery Biology, Monash Institutes of Pharmaceutical Sciences, Monash University, Parkville, Victoria, AustraliaVictorian Brain Bank, The Florey Institute of Neuroscience and Mental Health, Parkville, Victoria, Australia; Department of Pathology, The Alfred, Melbourne, Victoria, AustraliaThe Florey Institute of Neuroscience and Mental Health, Parkville, Victoria, AustraliaThe Florey Institute of Neuroscience and Mental Health, Parkville, Victoria, AustraliaThe Florey Institute of Neuroscience and Mental Health, Parkville, Victoria, AustraliaDepartment of Biochemistry and Pharmacology, University of Melbourne, Parkville, Victoria, Australia; The Florey Institute of Neuroscience and Mental Health, Parkville, Victoria, Australia; Department of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, USA; Corresponding authors at: Department of Biochemistry and Pharmacology, University of Melbourne, Parkville, Victoria, Australia; The Florey Institute of Neuroscience and Mental Health, Parkville, Victoria, Australia.Department of Biochemistry and Pharmacology, University of Melbourne, Parkville, Victoria, Australia; The Florey Institute of Neuroscience and Mental Health, Parkville, Victoria, Australia; Corresponding authors at: Department of Biochemistry and Pharmacology, University of Melbourne, Parkville, Victoria, Australia; The Florey Institute of Neuroscience and Mental Health, Parkville, Victoria, Australia.Hypocretin (Hcrtr, HCRTR) / orexin (OX) receptors modulate a range of neurobiological functions and are drug targets for several disorders. Mapping the distribution of receptors in the brain can inform their function and guide targeting of specific disorders. Although studied in rodents, orexin receptor distribution has remained relatively unexplored in humans, and thus there is also a paucity of comparative anatomy. The aim of this study was therefore to map the distribution of hypocretin/orexin receptor mRNA in selected regions of the mouse and human brain by non-radioactive in situ hybridization (ISH) using digoxigenin (DIG)-labelled cRNA anti-sense probes. Data revealed both distinct and overlapping patterns of distributions of Hcrtr1/HCRTR1 and Hcrtr2/HCRTR2 mRNA suggesting that the functions of the orexin system are mediated differently by each receptor. In the mouse brain, the highest expression of Hcrtr1 mRNA was in the locus coeruleus (LC) whereas Hcrtr2 mRNA was most abundant in the lateral hypothalamus (LH). The human caudate nuclei showed significant expression of both HCRTR1 and HCRTR2 mRNA, whereas the mouse predominantly expressed Hcrtr2 mRNA. The noradrenergic neurons of the human LC showed high signals for both HCRTR1 (71.7%) and HCRTR2 (81.5%) mRNA. Expression of HCRTR2 mRNA in non-noradrenergic human LC cells was also notable. The distribution pattern in mouse and human brains is consistent with the involvement of the orexin system in arousal and the sleep/wake cycle in both species, however, variations in receptor subtype expression profiles suggests that species differences in responses to orexin receptor ligands may be expected.http://www.sciencedirect.com/science/article/pii/S2590098624000277HypocretinOrexinhypocretin receptor mRNAOrexin receptorsIn situ hybridization
spellingShingle Sanjida Mir
Ryan J. Keenan
Romke Bron
Cameron J. Nowell
Catriona McLean
Leah C. Beauchamp
Laura J. Vella
Brian Dean
Daniel Hoyer
Laura H. Jacobson
The distribution of Hypocretin/Orexin receptor mRNA in the mouse and human brain
Medicine in Drug Discovery
Hypocretin
Orexin
hypocretin receptor mRNA
Orexin receptors
In situ hybridization
title The distribution of Hypocretin/Orexin receptor mRNA in the mouse and human brain
title_full The distribution of Hypocretin/Orexin receptor mRNA in the mouse and human brain
title_fullStr The distribution of Hypocretin/Orexin receptor mRNA in the mouse and human brain
title_full_unstemmed The distribution of Hypocretin/Orexin receptor mRNA in the mouse and human brain
title_short The distribution of Hypocretin/Orexin receptor mRNA in the mouse and human brain
title_sort distribution of hypocretin orexin receptor mrna in the mouse and human brain
topic Hypocretin
Orexin
hypocretin receptor mRNA
Orexin receptors
In situ hybridization
url http://www.sciencedirect.com/science/article/pii/S2590098624000277
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