Literature DB >> 3771837

3H-nicotine- and 125I-alpha-bungarotoxin-labeled nicotinic receptors in the interpeduncular nucleus of rats. II. Effects of habenular deafferentation.

P B Clarke, G S Hamill, N S Nadi, D M Jacobowitz, A Pert.   

Abstract

The cholinergic innervation of the interpeduncular nucleus (IPN) is wholly extrinsic and is greatly attenuated by bilateral habenular destruction. We describe changes in the labeling of putative nicotinic receptors within this nucleus at 3, 5, or 11 days after bilateral habenular lesions. Adjacent tissue sections of the rat IPN were utilized for 3H-nicotine and 125I-alpha-bungarotoxin (125I-BTX) receptor autoradiography. Compared to sham-operated controls, habenular destruction significantly reduced autoradiographic 3H-nicotine labeling in rostral (-25%), intermediate (-13%), and lateral subnuclei (-36%). Labeling in the central subnucleus was unchanged. Loss of labeling was maximal at the shortest survival time (3 days) and did not change thereafter. In order to establish whether this loss was due to a reduction in the number or the affinity of 3H-nicotine-binding sites, a membrane assay was performed on microdissected IPN tissue from rats that had received surgery 3 days previously. Bilateral habenular lesions produced a 35% reduction of high-affinity 3H-nicotine-binding sites, with no change in binding affinity. Bilateral habenular lesions reduced 125I-BTX labeling in the intermediate subnuclei, and a slight increase occurred in the rostral subnucleus. In the lateral subnuclei, 125I-BTX labeling was significantly reduced (27%) at 3 days but not at later survival times. In view of the known synaptic morphology of the habenulointerpeduncular tract, it is concluded that a subpopulation of 3H-nicotine binding sites within the IPN is located on afferent axons and/or terminals. This subpopulation, located within rostral, intermediate, and lateral subnuclei, may correspond to presynaptic nicotinic cholinergic receptors. Sites that bind 125I-BTX may include a presynaptic subpopulation located in the lateral and possibly the intermediate subnuclei.

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Year:  1986        PMID: 3771837     DOI: 10.1002/cne.902510311

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  15 in total

1.  Direct recording of nicotinic responses in presynaptic nerve terminals.

Authors:  J S Coggan; J Paysan; W G Conroy; D K Berg
Journal:  J Neurosci       Date:  1997-08-01       Impact factor: 6.167

2.  Professional biographical sketch.

Authors:  David M Jacobowitz
Journal:  Neurotox Res       Date:  2004       Impact factor: 3.911

Review 3.  Nicotinic modulation of synaptic transmission and plasticity in cortico-limbic circuits.

Authors:  Huibert D Mansvelder; Marjolijn Mertz; Lorna W Role
Journal:  Semin Cell Dev Biol       Date:  2009-01-22       Impact factor: 7.727

Review 4.  Molecular studies of the neuronal nicotinic acetylcholine receptor family.

Authors:  J Lindstrom; R Schoepfer; P Whiting
Journal:  Mol Neurobiol       Date:  1987       Impact factor: 5.590

5.  Effect of nicotine and tacrine on acetylcholine release from rat cerebral cortical slices.

Authors:  R E Loiacono; F J Mitchelson
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1990-07       Impact factor: 3.000

Review 6.  Nicotine and smoking: a perspective from animal studies.

Authors:  P B Clarke
Journal:  Psychopharmacology (Berl)       Date:  1987       Impact factor: 4.530

7.  Role of Ca2+ ions in nicotinic facilitation of GABA release in mouse thalamus.

Authors:  C Léna; J P Changeux
Journal:  J Neurosci       Date:  1997-01-15       Impact factor: 6.167

8.  Tethered agonist analogs as site-specific probes for domains of the human α7 nicotinic acetylcholine receptor that differentially regulate activation and desensitization.

Authors:  Jingyi Wang; Nicole A Horenstein; Clare Stokes; Roger L Papke
Journal:  Mol Pharmacol       Date:  2010-09-07       Impact factor: 4.436

9.  Rodent habenulo-interpeduncular pathway expresses a large variety of uncommon nAChR subtypes, but only the alpha3beta4* and alpha3beta3beta4* subtypes mediate acetylcholine release.

Authors:  Sharon R Grady; Milena Moretti; Michele Zoli; Michael J Marks; Alessio Zanardi; Luca Pucci; Francesco Clementi; Cecilia Gotti
Journal:  J Neurosci       Date:  2009-02-18       Impact factor: 6.167

10.  Effects of acute subcutaneous nicotine on attention, information processing and short-term memory in Alzheimer's disease.

Authors:  G M Jones; B J Sahakian; R Levy; D M Warburton; J A Gray
Journal:  Psychopharmacology (Berl)       Date:  1992       Impact factor: 4.530

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