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PMID: 2747911 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Immunohistochemical analysis of the neurotoxic effects of DSP-4 identifies two populations of noradrenergic axon terminals.

Neuroscience ·Vol. 30 ·No. 1 ·1989-00-00 ·Pages 181-97

Fritschy JM, Grzanna R

Abstract

N-(2-chloroethyl)-N-ethyl-2-bromobenzylamine (DSP-4) is a potent and highly selective neurotoxin which induces degeneration of noradrenergic axons. The effects of DSP-4 vary considerably in different brain regions: the drug produces nearly complete depletion of noradrenaline in neocortex, hippocampus, cerebellum and spinal cord, but only partial depletion in hypothalamus and brainstem. In this study we have employed an immunohistochemical method to assess the neurotoxic effects of DSP-4 on the structural integrity of central noradrenergic neurons in the rat, and to identify those noradrenergic axons that remain in the central nervous system 2-4 weeks after DSP-4 treatment. The staining results identified noradrenergic axon terminals as the principal site of action of DSP-4; noradrenergic cell bodies and preterminal axons were not noticeably affected. DSP-4 produced an almost all or none neurotoxic effect on noradrenergic axon terminals in different brain regions. Nearly all noradrenergic axon terminals were destroyed in the neocortex, hippocampus, olfactory bulb, thalamus, tectum, cerebellum and spinal cord dorsal horn. In contrast, most noradrenergic axons were unaffected in the basal forebrain, hypothalamus, reticular formation, brainstem motor nuclei and spinal cord ventral horn. These remaining noradrenergic axon terminals differed morphologically from sensitive axons by their thickness, size and spacing of their varicosities and their dense arborizations within terminal fields. The distribution of noradrenergic axons susceptible to DSP-4 correlates very closely with the distribution of locus coeruleus axons and possibly all regions in which noradrenergic terminals are unaffected by DSP-4 receive their major noradrenergic input from non-locus coeruleus neurons. This study provides the first direct evidence that DSP-4 destroys noradrenergic axon terminals from the locus coeruleus, but not those from non-locus coeruleus neurons. This profound differential sensitivity of noradrenergic axons to DSP-4 is matched by distinct differences in their morphology and their topographic projections. The results support the view that locus coeruleus and non-locus coeruleus noradrenergic neurons constitute two separate subsystems, which differ not only in their projections but also with respect to the pharmacological properties of their axon terminals.

MeSH Terms
Animals Benzylamines/toxicity Central Nervous System/cytology,drug effects,metabolism Dose-Response Relationship, Drug Immunohistochemistry Locus Coeruleus/cytology,drug effects,metabolism Male Nerve Endings/drug effects,metabolism Neurotoxins/pharmacology Norepinephrine/metabolism Rats Rats, Inbred Strains
Chemicals
Benzylamines Neurotoxins DSP 4 Norepinephrine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Fritschy J M
Johns Hopkins University School of Medicine, Department of Neuroscience, Baltimore, MD 21205.
Grzanna R
Article Info
Journal
Neuroscience
Abbr.
Neuroscience
ISSN
0306-4522
Published
1989-00-00
Pages
181-97
Language
English
Region
United States
NLM ID
7605074
Subset
IM
Grants
NIMH NIH HHS · MH-41977 · United States
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