Expression of nitric oxide synthase isoforms in spinal cord in amyotrophiclateral sclerosis

Citation
Rk. Phul et al., Expression of nitric oxide synthase isoforms in spinal cord in amyotrophiclateral sclerosis, AMYOTROPH L, 1(4), 2000, pp. 259-267
Citations number
22
Categorie Soggetti
Neurology
Journal title
AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS
ISSN journal
14660822 → ACNP
Volume
1
Issue
4
Year of publication
2000
Pages
259 - 267
Database
ISI
SICI code
1466-0822(200009)1:4<259:EONOSI>2.0.ZU;2-S
Abstract
METHODS: Autoradiography with [H-3]nitro-L-arginine ((HL)-H-3-NNA) was used to quantify nitric oxide synthase (NOS), and immunocytochemistry to identi fy NOS isoforms, in spinal cord in amyotrophic lateral sclerosis (ALS) and controls. RESULTS: In controls NOS binding was marked only in the superficial dorsal horn, but in ALS tissue it was intense throughout the grey and white matter . A single population of binding sites was indicated in controls, but two p opulations in ALS. In the controls intense neuronal NOS (nNOS) immunoreacti vity was present in numerous cells in the dorsal horn, and faint immunoreac tivity in small and medium-sized cells in the ventral horn. Only weak immun oreactivity for inducible NOS (iNOS) and endothelial NOS (eNOS) was detecta ble in control tissue. In ALS, the pattern was broadly similar in the grey matter, but immunoreactivity for both nNOS and iNOS was present in white ma tter. CONCLUSION: Expression of abnormal variants of nNOS or increased expression of iNOS may have a role in motoneuron death in ALS.