Neuronal Nitric Oxide Synthase mRNA Upregulation in Rat Sensory Neurons after Spinal Nerve Ligation: Lack of a Role in Allodynia Development

• Published in: The Journal of neuroscience Vol. 19; no. 21; pp. 9201 - 9208
• Main Authors: Luo, Z. David, Chaplan, S. R, Scott, B. P, Cizkova, D, Calcutt, N. A, Yaksh, T. L
• Format: Journal Article
• Language: English
• Published: United States Soc Neuroscience 01.11.1999; Society for Neuroscience
• Subjects: Animals; Ganglia, Spinal - enzymology; Ganglia, Spinal - physiology; Ganglia, Spinal - physiopathology; Gene Expression Regulation, Enzymologic; Male; Neurons, Afferent - enzymology; Nitric Oxide Synthase - genetics; Nitric Oxide Synthase Type I; Pain - enzymology; Pain - physiopathology; Rats; Rats, Sprague-Dawley; RNA, Messenger - genetics; Species Specificity; Spinal Nerves - injuries; Spinal Nerves - physiology; Spinal Nerves - physiopathology; Time Factors; Transcription, Genetic
• ISSN: 0270-6474; 1529-2401
• DOI: 10.1523/jneurosci.19-21-09201.1999

Pharmacological evidence suggests a functional role for spinal nitric oxide (NO) in the modulation of thermal and/or inflammatory hyperalgesia. To assess the role of NO in nerve injury-induced tactile allodynia, we examined neuronal NO synthase (nNOS) expression in the spinal cord and dorsal root ganglia (DRG) of rats with tactile allodynia because of either tight ligation of the left fifth and sixth lumbar spinal nerves or streptozotocin-induced diabetic neuropathy. RNase protection assays indicated that nNOS mRNA (1) was upregulated in DRG, but not spinal cord, neurons on the injury side beginning 1 d after nerve ligation, (2) peaked (approximately 10-fold increase) at 2 d, and (3) remained elevated for at least 13 weeks. A corresponding increase in DRG nNOS protein was also observed and localized principally to small and occasionally medium-size sensory neurons. In rats with diabetic neuropathy, there was no significant change in DRG nNOS mRNA. However, similar increases in DRG nNOS mRNA were observed in rats that did not develop allodynia after nerve ligation and in rats fully recovered from allodynia 3 months after the nerve ligation. Systemic treatment with a specific pharmacological inhibitor of nNOS failed to prevent or reverse allodynia in nerve-injured rats. Thus, regulation of nNOS may contribute to the development of neuronal plasticity after specific types of peripheral nerve injury. However, upregulation of nNOS is not responsible for the development and/or maintenance of allodynia after nerve injury.