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Nitric Oxide, 2020
Shortly after joint remobilization, inflammation is induced in the joint and aggravates joint contracture via subsequent fibrosis. However, the mechanisms involved in remobilization-induced inflammation are not yet fully understood. We hypothesized that joint immobilization followed by remobilization induces hypoxia/reoxygenation, initiating ...
Akinori, Kaneguchi +3 more
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Shortly after joint remobilization, inflammation is induced in the joint and aggravates joint contracture via subsequent fibrosis. However, the mechanisms involved in remobilization-induced inflammation are not yet fully understood. We hypothesized that joint immobilization followed by remobilization induces hypoxia/reoxygenation, initiating ...
Akinori, Kaneguchi +3 more
openaire +2 more sources
13. Anti-inflammatory role of L-NG-Nitroarginine Methyl Ester in a chronic model of depression
Brain, Behavior, and Immunity, 2013The role of nitric oxide (NO) in the neurodegenerative disorders is well illustrated. The close relationship of NO level and the inflammation points out the clinical relevance of NO in depressive disorder. Present study evaluated the neuroprotective role of L-NAME, a NO synthase blocker in chronic restraint hypoxia (CRH) induced depressive behaviour ...
S. DEEP +5 more
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Chronobiology International, 1998
Circadian changes in the interactions between L-NG-nitroarginine methyl ester (L-NAME), a nitric oxide synthase (NOS) inhibitor, and morphine-induced antinociception were investigated by the mouse hot-plate test. Both the basal pain sensitivity and morphine-induced analgesia undergo significant 24 h variations.
Uludag, O +6 more
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Circadian changes in the interactions between L-NG-nitroarginine methyl ester (L-NAME), a nitric oxide synthase (NOS) inhibitor, and morphine-induced antinociception were investigated by the mouse hot-plate test. Both the basal pain sensitivity and morphine-induced analgesia undergo significant 24 h variations.
Uludag, O +6 more
openaire +3 more sources
Journal of Neural Transmission, 1998
NG-Nitro-L-arginine methyl ester (L-NAME, an unspecific nitric oxide synthase inhibitor), applied at 1 and 40 mg/kg, did not influence the electroconvulsive threshold, but impaired the anticonvulsant activity of valproate (at 40 mg/kg) and phenobarbital (at 1 and 40 mg/kg). No effect was observed in the case of carbamazepine and diphenylhydantoin.
K K, Borowicz +3 more
openaire +2 more sources
NG-Nitro-L-arginine methyl ester (L-NAME, an unspecific nitric oxide synthase inhibitor), applied at 1 and 40 mg/kg, did not influence the electroconvulsive threshold, but impaired the anticonvulsant activity of valproate (at 40 mg/kg) and phenobarbital (at 1 and 40 mg/kg). No effect was observed in the case of carbamazepine and diphenylhydantoin.
K K, Borowicz +3 more
openaire +2 more sources

