PubMed:15673851 JSONTXT 23 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T1 0-195 Sentence denotes The activation of spinal N-methyl-D-aspartate receptors may contribute to degeneration of spinal motor neurons induced by neuraxial morphine after a noninjurious interval of spinal cord ischemia.
T2 196-421 Sentence denotes We investigated the relationship between the degeneration of spinal motor neurons and activation of N-methyl-d-aspartate (NMDA) receptors after neuraxial morphine following a noninjurious interval of aortic occlusion in rats.
T3 422-509 Sentence denotes Spinal cord ischemia was induced by aortic occlusion for 6 min with a balloon catheter.
T4 510-783 Sentence denotes In a microdialysis study, 10 muL of saline (group C; n = 8) or 30 mug of morphine (group M; n = 8) was injected intrathecally (IT) 0.5 h after reflow, and 30 mug of morphine (group SM; n = 8) or 10 muL of saline (group SC; n = 8) was injected IT 0.5 h after sham operation.
T5 784-920 Sentence denotes Microdialysis samples were collected preischemia, before IT injection, and at 2, 4, 8, 24, and 48 h of reperfusion (after IT injection).
T6 921-1071 Sentence denotes Second, we investigated the effect of IT MK-801 (30 mug) on the histopathologic changes in the spinal cord after morphine-induced spastic paraparesis.
T7 1072-1219 Sentence denotes After IT morphine, the cerebrospinal fluid (CSF) glutamate concentration was increased in group M relative to both baseline and group C (P < 0.05).
T8 1220-1254 Sentence denotes This increase persisted for 8 hrs.
T9 1255-1406 Sentence denotes IT MK-801 significantly reduced the number of dark-stained alpha-motoneurons after morphine-induced spastic paraparesis compared with the saline group.
T10 1407-1564 Sentence denotes These data indicate that IT morphine induces spastic paraparesis with a concomitant increase in CSF glutamate, which is involved in NMDA receptor activation.
T11 1565-1675 Sentence denotes We suggest that opioids may be neurotoxic in the setting of spinal cord ischemia via NMDA receptor activation.