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Differences in peripheral nerve degeneration/regeneration between wild‐type and neuronal nitric oxide synthase knockout mice
Author(s) -
Keilhoff Gerburg,
Fansa Hisham,
Wolf Gerald
Publication year - 2002
Publication title -
journal of neuroscience research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.72
H-Index - 160
eISSN - 1097-4547
pISSN - 0360-4012
DOI - 10.1002/jnr.10229
Subject(s) - wallerian degeneration , regeneration (biology) , remyelination , axon , nitric oxide synthase , sciatic nerve , myelin , peripheral nervous system , knockout mouse , nerve guidance conduit , microbiology and biotechnology , context (archaeology) , biology , peripheral nerve injury , neuroscience , anatomy , nitric oxide , central nervous system , endocrinology , biochemistry , paleontology , receptor
Nitric oxide (NO), a unique biological messenger molecule, is synthesized by three isoforms of the enzyme NO synthase (NOS) and diffuses from the site of production across cellular membranes. A postulated role for NO in degeneration and regeneration of peripheral nerves has been explored in a sciatic nerve model comparing wild‐type mice and mice lacking neuronal NOS after transection and microsurgical repair. In NOS knockout mice, regenerative delay was observed, preceded by a decelerated Wallerian degeneration (WD). In the regenerated nerve, pruning of uncontrolled sprouts was disturbed, leading to an enhanced number of axons, whereas remyelination seemed to be less affected. Delayed regeneration was associated with a delayed recovery of sensor and motor function. In such a context, possible NO targets are neurofilaments and myelin sheaths of the interrupted axon, filopodia of the growth cone, newly formed neuromuscular endplates, and Schwann cells in the distal nerve stump. The results presented suggest that 1) local release of NO following peripheral nerve injury is a crucial factor in degeneration/regeneration, 2) success of fiber regeneration in the peripheral nervous system depends on a regular WD, and 3) manipulation of NO supply may offer interesting therapeutic options for treatment of peripheral nerve lesions. © 2002 Wiley‐Liss, Inc.