TY - JOUR
T1 - Expression of Mu Opioid Receptor in Dorsal Diencephalic Conduction System: New Insights for the Medial Habenula
AU - Gardon, O.
AU - Faget, Lauren
AU - Chu Sin Chung, P.
AU - Matifas, A.
AU - Massotte, D.
AU - Kieffer, B. L.
N1 - Copyright © 2014 IBRO. Published by Elsevier Ltd. All rights reserved.
PY - 2014/9/26
Y1 - 2014/9/26
N2 - The habenular complex, encompassing medial (MHb) and lateral (LHb) divisions, is a highly conserved epithalamic structure involved in the dorsal diencephalic conduction system (DDC). These brain nuclei regulate information flow between the limbic forebrain and the mid- and hindbrain, integrating cognitive with emotional and sensory processes. The MHb is also one of the strongest expression sites for mu opioid receptors (MORs), which mediate analgesic and rewarding properties of opiates. At present however, anatomical distribution and function of these receptors have been poorly studied in MHb pathways. Here we took advantage of a newly generated MOR-mcherry knock-in mouse line to characterize MOR expression sites in the DDC.
MOR-mcherry fluorescent signal is weak in the LHb, but strong expression is visible in the MHb, fasciculus retroflexus (fr) and interpeduncular nucleus (IPN), indicating that MOR is mainly present in the MHb–IPN pathway. MOR-mcherry cell bodies are detected both in basolateral and apical parts of MHb, where the receptor co-localizes with cholinergic and substance P (SP) neurons, respectively, representing two main MHb neuronal populations. MOR-mcherry is expressed in most MHb-SP neurons, and is present in only a subpopulation of MHb-cholinergic neurons. Intense diffuse fluorescence detected in lateral and rostral parts of the IPN further suggests that MOR-mcherry is transported to terminals of these SP and cholinergic neurons. Finally, MOR-mcherry is present in septal regions projecting to the MHb, and in neurons of the central and intermediate IPN.
Together, this study describes MOR expression in several compartments of the MHb–IPN circuitry. The remarkably high MOR density in the MHb–IPN pathway suggests that these receptors are in a unique position to mediate analgesic, autonomic and reward responses.
AB - The habenular complex, encompassing medial (MHb) and lateral (LHb) divisions, is a highly conserved epithalamic structure involved in the dorsal diencephalic conduction system (DDC). These brain nuclei regulate information flow between the limbic forebrain and the mid- and hindbrain, integrating cognitive with emotional and sensory processes. The MHb is also one of the strongest expression sites for mu opioid receptors (MORs), which mediate analgesic and rewarding properties of opiates. At present however, anatomical distribution and function of these receptors have been poorly studied in MHb pathways. Here we took advantage of a newly generated MOR-mcherry knock-in mouse line to characterize MOR expression sites in the DDC.
MOR-mcherry fluorescent signal is weak in the LHb, but strong expression is visible in the MHb, fasciculus retroflexus (fr) and interpeduncular nucleus (IPN), indicating that MOR is mainly present in the MHb–IPN pathway. MOR-mcherry cell bodies are detected both in basolateral and apical parts of MHb, where the receptor co-localizes with cholinergic and substance P (SP) neurons, respectively, representing two main MHb neuronal populations. MOR-mcherry is expressed in most MHb-SP neurons, and is present in only a subpopulation of MHb-cholinergic neurons. Intense diffuse fluorescence detected in lateral and rostral parts of the IPN further suggests that MOR-mcherry is transported to terminals of these SP and cholinergic neurons. Finally, MOR-mcherry is present in septal regions projecting to the MHb, and in neurons of the central and intermediate IPN.
Together, this study describes MOR expression in several compartments of the MHb–IPN circuitry. The remarkably high MOR density in the MHb–IPN pathway suggests that these receptors are in a unique position to mediate analgesic, autonomic and reward responses.
KW - acetylcholine
KW - interpeduncular nucleus
KW - knock-in mice
KW - medial habenula
KW - mu opioid receptor
KW - substance P
UR - https://doi.org/10.1016/j.neuroscience.2014.07.053
U2 - 10.1016/j.neuroscience.2014.07.053
DO - 10.1016/j.neuroscience.2014.07.053
M3 - Article
C2 - 25086313
VL - 277
SP - 595
EP - 609
JO - Neuroscience
JF - Neuroscience
ER -