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PMID: 15026251 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Intraocular injection of dibutyryl cyclic AMP promotes axon regeneration in rat optic nerve.

Experimental neurology ·Vol. 186 ·No. 2 ·2004-04-00 ·Pages 124-33

Monsul NT, Geisendorfer AR, Han PJ, Banik R, Pease ME, Skolasky RL, Hoffman PN

Abstract

The optic nerve is a CNS pathway containing molecules capable of inhibiting axon elongation. The growth program in embryonic retinal ganglion cell (RGC) neurons enables axons to regenerate in the optic nerve through at least two mechanisms. Namely, high cyclic AMP (cAMP) levels abrogate the ability of CNS molecules to inhibit elongation, and the pattern of gene expression enables axons to undergo rapid, sustained, and lengthy elongation. In adult mammals, recovery of visual function after optic nerve injury is limited by both the death of most RGC neurons and the inability of surviving axons to regenerate. We now report that a single intraocular injection of the membrane-permeable cAMP analogue dibutyryl cAMP (db cAMP) promotes the regeneration of RGC axons in the optic nerves of adult rats, but does not prevent the death of RGC neurons. This regeneration in optic nerves crushed within the orbit (2 mm from the eye) was equally effective either 1 day before or 1 day after db cAMP injection. The number of regenerating axons, which was maximal 14 days after crush, declined with increasing time after injury (i.e., 28, 56, and 112 days) and distance beyond the crush site (i.e., 0.25, 0.5, and 1.0 mm). Thus, db cAMP promotes optic nerve regeneration without increasing the survival of axotomized RGC neurons. Furthermore, since db cAMP does not enable axons to undergo rapid, sustained, and lengthy elongation, strategies that increase survival and promote these changes in elongation may critically complement the ability of db cAMP to promote regeneration.

MeSH Terms
Animals Axons/drug effects Bucladesine/pharmacology Cell Count/methods Cell Survival/drug effects Cholera Toxin/metabolism Dose-Response Relationship, Drug Female Fluorescent Dyes/metabolism Horseradish Peroxidase/metabolism Nerve Crush/methods Nerve Regeneration/drug effects Optic Nerve/cytology,drug effects Orbit/drug effects Rats Rats, Sprague-Dawley Retinal Ganglion Cells/metabolism Stilbamidines/metabolism Time Factors
Chemicals
2-hydroxy-4,4'-diamidinostilbene, methanesulfonate salt Fluorescent Dyes Stilbamidines cholera toxin, B subunit-horseradish peroxidase Bucladesine Cholera Toxin Horseradish Peroxidase
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Monsul Nicholas T
Department of Neurology, The Johns Hopkins School of Medicine, Baltimore, MD 21287-6953, USA.
Geisendorfer Abram R
Han Paul J
Banik Rudrani
Pease Mary Ellen
Skolasky Richard L
Hoffman Paul N
Article Info
Journal
Experimental neurology
Abbr.
Exp Neurol
ISSN
0014-4886
Published
2004-04-00
Pages
124-33
Language
English
Region
United States
NLM ID
0370712
Subset
IM
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