Muscarinic acetylcholine receptor immunoreactivity after hippocampal commissural/associational pathway lesions: Evidence for multiple presynaptic receptor subtypes

The present study addressed the hypothesis that differential localization of m1–m4 subtypes in the inner one‐third of the dentate molecular layer is due to selective presynaptic expression of the receptor proteins on the hippocampal commissural/associational pathways. Physical and chemical lesions o...

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Published in:Journal of comparative neurology (1911) Vol. 380; no. 3; pp. 382 - 394
Main Authors: Rouse, Susan T., Levey, Allan I.
Format: Journal Article
Language:English
Published: New York John Wiley & Sons, Inc 14-04-1997
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Summary:The present study addressed the hypothesis that differential localization of m1–m4 subtypes in the inner one‐third of the dentate molecular layer is due to selective presynaptic expression of the receptor proteins on the hippocampal commissural/associational pathways. Physical and chemical lesions of the commissural and associational pathways were used to denervate afferent terminals in the inner one‐third of the molecular layer, and fluid injections were used to lesion granule cells, their postsynaptic target. Immunocytochemistry utilizing muscarine acetylcholine receptor (mAChR) subtype‐specific antibodies was used to identify changes in expression patterns in the molecular layer postlesion. m1 immunoreactivity in the molecular layer did not change after commissural/associational pathway lesions. m2 immuno‐reactivity in the inner one‐third of the molecular layer was attenuated only after lesions involving the associational pathway. In contrast, m3 and m4 immunoreactivity in the inner one‐third of the molecular layer was almost completely abolished by lesions of both pathways simultaneously. Granule cell lesions greatly attenuated m1 and m3 immunoreactivity in the molecular layer, with little to no diminution of m2 and m4 immunoreactivity. The results indicate that, in the inner one‐third of the molecular layer, m1 and m3 are mainly postsynaptic on granule cells, whereas m2 and m4 are presynaptic on the commissural/associational pathways. This study provides direct anatomical evidence for the diversity of molecular subtypes presynaptically on the commissural/associational pathways. J. Comp. Neurol. 380:382–394, 1997. © 1997 Wiley‐Liss, Inc.
Bibliography:Council on Tobacco Research USA
ark:/67375/WNG-7TWSRPX4-C
NIMH - No. F31 MH11186-01
istex:8ECD3BE52C376535C26BD7DD79F639D0B51749BF
ArticleID:CNE7
NIH - No. RO1 NS30454; No. RO1 NS34876
ObjectType-Article-2
SourceType-Scholarly Journals-1
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content type line 23
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ISSN:0021-9967
1096-9861
DOI:10.1002/(SICI)1096-9861(19970414)380:3<382::AID-CNE7>3.0.CO;2-Z