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GDNF overexpression fails to provoke muscle recovery from botulinum toxin poisoning: a preliminary study.

Abstract
Glial cell line-derived neurotrophic factor (GDNF) has potent axonal growth and survival effects on motoneurons. This study used transgenic Myo-GDNF mice to assess the effects of targeted GDNF overexpression on functional recovery after botulinum toxin type A (BTxA) chemodenervation. BTxA (0.1 U) was injected into the tibialis anterior (TA) muscle of wild-type CF1 and transgenic Myo-GDNF mice. On days 1, 7, 14, and 21 after injection, evoked muscle force production and muscle mass were measured (n = 6, for each group at each time point). Greater maximal tetanic force and calculated specific force were evoked in Myo-GDNF animals when compared with control CF1 animals at days 1, 7, and 21. However, the differences were not statistically significant. Similarly, modest reductions in muscle atrophy in the Myo-GDNF group at all time points were not statistically significant. Targeted overexpression of GDNF in the muscles of Myo-GDNF mice did not improve motor recovery in the first 21 days after BTxA chemodenervation.
AuthorsKenny F Lin, Hank H Sun, Matthew R Macewan, Susan E Mackinnon, Philip J Johnson
JournalMicrosurgery (Microsurgery) Vol. 32 Issue 5 Pg. 370-6 (Jul 2012) ISSN: 1098-2752 [Electronic] United States
PMID22473739 (Publication Type: Evaluation Study, Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2012 Wiley-Liss, Inc.
Chemical References
  • Gdnf protein, mouse
  • Glial Cell Line-Derived Neurotrophic Factor
  • Neuromuscular Agents
  • Botulinum Toxins, Type A
Topics
  • Animals
  • Botulinum Toxins, Type A (administration & dosage, pharmacology)
  • Glial Cell Line-Derived Neurotrophic Factor (metabolism, physiology)
  • Mice
  • Mice, Transgenic
  • Muscle Strength (drug effects, physiology)
  • Muscle, Skeletal (drug effects, metabolism, pathology, physiology)
  • Muscular Atrophy (chemically induced)
  • Nerve Block (methods)
  • Neuromuscular Agents (administration & dosage, pharmacology)
  • Organ Size
  • Recovery of Function (physiology)
  • Up-Regulation

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