Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters










Database
Publication year range
1.
J Neurosurg Anesthesiol ; 22(1): 46-52, 2010 Jan.
Article in English | MEDLINE | ID: mdl-19996767

ABSTRACT

BACKGROUND: Remote ischemic preconditioning (RIPC) may protect the spinal cord from ischemic injury. This randomized clinical trial was designed to assess whether a large clinical trial testing the effect of RIPC on neurologic outcome in patients undergoing spine surgery is warranted. This trial was registered with ClinicalTrials.gov, number NCT00778323. METHODS: Forty adult cervical spondylotic myelopathy patients undergoing elective decompression surgery were randomly assigned to either the RIPC group (n=20) or the control group (n=20). Limb RIPC consisted of three 5-minutes cycles of upper right limb ischemia with intervening 5-minute periods of reperfusion. Neuron-specific enolase and S-100B levels were measured in serum at set time points. Median nerve somatosensory-evoked potentials (SEPs) were also recorded. Neurologic recovery rate was evaluated using a Japanese Orthopaedic Association scale. RESULTS: RIPC significantly reduced serum S-100B release at 6 hours and 1 day after surgery, and reduced neuron-specific enolase release at 6 hours, and then at 1, 3, and 5 days after surgery. No differences were observed in SEP measurements or the incidence of SEP changes during surgery between the control and RIPC groups. Recovery rate at 7 days, and at 1 and 3 months after surgery was higher in the RIPC group than in the control group (P<0.05). CONCLUSIONS: Our results for markers of neuronal ischemic injury and rate of recovery suggest that a clinical trial with sufficient statistical power to detect an effect of RIPC on the incidence of neurologic complications (paresis, palsy, etc) due to spinal cord ischemia-reperfusion injury after spine surgery is warranted [corrected].


Subject(s)
Cervical Vertebrae/surgery , Decompression, Surgical/methods , Evoked Potentials, Somatosensory , Ischemic Preconditioning/methods , Nerve Growth Factors/blood , Phosphopyruvate Hydratase/blood , Reperfusion Injury/prevention & control , S100 Proteins/blood , Biomarkers/blood , China , Elective Surgical Procedures , Female , Humans , Male , Median Nerve , Middle Aged , Prospective Studies , S100 Calcium Binding Protein beta Subunit , Spondylosis/surgery , Treatment Outcome , Upper Extremity
2.
Neurol Res ; 31(8): 853-8, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19278575

ABSTRACT

OBJECTIVE: This study investigates the effects of electroacupuncture (EA) preconditioning on blood-brain barrier (BBB) integrity and matrix metalloproteinase-9 (MMP-9) expression in subsequent ischemic hemisphere. METHODS: Focal cerebral ischemia was induced by middle cerebral artery occlusion (MCAO) in rats. Animals were randomly divided into four groups: normal, sham-operated, MCAO and EA groups. In EA group, rats received electroacupuncture stimuli at the Baihui acupoint (GV 20) 30 minutes/day for 5 days. Twenty-four hours after last treatment, the MCAO was performed. The brain water content and BBB permeability were measured 24 hours after MCAO. MMP-9 expression and activity were measured at 6, 12 and 24 hours after MCAO. RESULTS: The results showed that the brain water content of ischemic hemisphere was lower in EA group (81.45 +/- 1.09%) compared with MCAO group (83.98 +/- 1.30%; p<0.05). Similarly, the Evans blue content in EA group (4.90 +/- 1.77 microg/g) was lower compared with MCAO group (9.41 +/- 2.87 microg/g; p<0.05). The protein expression and enzyme activity of MMP-9 increased and reached maximum at 24 hours after reperfusion. However, the protein expression was lower in EA group at 12 and 24 hours after reperfusion (p<0.01, versus MCAO group), and enzyme activity was lower in EA group only at 24 hours (p<0.01, versus MCAO group). DISCUSSION: EA preconditioning could attenuate brain edema and BBB disruption caused by subsequent cerebral ischemia. EA preconditioning could decrease MMP-9 expression and activity, which may be an important mechanism of cerebral ischemic tolerance.


Subject(s)
Brain Ischemia/enzymology , Brain Ischemia/therapy , Electroacupuncture , Infarction, Middle Cerebral Artery/enzymology , Infarction, Middle Cerebral Artery/therapy , Matrix Metalloproteinase 9/metabolism , Animals , Blood-Brain Barrier/physiopathology , Blotting, Western , Body Water/metabolism , Brain/enzymology , Brain/pathology , Brain/physiopathology , Brain Edema/physiopathology , Brain Ischemia/physiopathology , Capillary Permeability/physiology , Electrophoresis, Polyacrylamide Gel , Evans Blue , Infarction, Middle Cerebral Artery/physiopathology , Male , Random Allocation , Rats , Rats, Sprague-Dawley , Severity of Illness Index , Time Factors
3.
Zhongguo Wei Zhong Bing Ji Jiu Yi Xue ; 20(11): 641-4, 2008 Nov.
Article in Chinese | MEDLINE | ID: mdl-19000414

ABSTRACT

OBJECTIVE: To investigate the neuroprotective effects and dose-response relation by combining JAK-STAT signal pathway inhibitor (AG490) with free radical scavenger dimethylthiourea (DMTU) in rats subjected to focal cerebral ischemia/reperfusion (I/R) injury. METHODS: In all rats, the middle cerebral artery occlusion (MCAO) was produced by occlusion of right internal carotid artery with a nylon monofilament. One hundred male Sprague-Dawley (SD) rats were divided into ten groups according to random digits table, 10 rats were in each group. The first experiment involved I/R model control, dimethyl sulfoxide (DMSO) control, normal saline (NS) control, AG490, DMTU and combination of AG490 and DMTU (A+D) groups. The second experiment involved model group and three experimental groups in which various doses of DMTU and AG490 were administered. The neurological behavior scores (NBS) were assessed at 24, 48 and 72 hours after reperfusion respectively in both experiments, and all the animals were then decapitated to determine the brain infarct volume after 72 hours. RESULTS: The values of NBS in A+D group, AG490 group and DMTU group were higher than those in model group at 24, 48 and 72 hours after I/R, and their brain infarct volumes were obviously smaller than model group as well (all P<0.05). The brain infarct volume in A+D group was obviously smaller compared with AG490 and DMTU alone (all P<0.05). The values of NBS were higher and the brain infarct volumes were smaller in both high dose and medium dose combination groups than those in low dose combination and model groups respectively (all P<0.05). In addition, brain infarct volumes in high dose group were smaller than medium dose group (P<0.05), but there was no statistically significant difference between low dose and model groups. CONCLUSION: The combined application of AG490 and DMTU produces a dose-dependent synergistic neuroprotective effect.


Subject(s)
Brain Ischemia/drug therapy , Enzyme Inhibitors/therapeutic use , Free Radical Scavengers/therapeutic use , Reperfusion Injury/drug therapy , Thiourea/analogs & derivatives , Tyrphostins/therapeutic use , Animals , Brain/pathology , Brain Ischemia/metabolism , Brain Ischemia/pathology , Disease Models, Animal , Dose-Response Relationship, Drug , Male , Neuroprotective Agents/therapeutic use , Random Allocation , Rats , Rats, Sprague-Dawley , Reperfusion Injury/metabolism , Reperfusion Injury/pathology , Signal Transduction/drug effects , Thiourea/therapeutic use
SELECTION OF CITATIONS
SEARCH DETAIL
...