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Early application of percutaneous neuromuscular electric stimulation in interfering motor function of limbs and difference in temperature of axilla of patients with ischemic stroke
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作者 Zhenhui Jiang Siyi Yin Na Bi Xiang He Fang Qu 《Neural Regeneration Research》 SCIE CAS CSCD 2006年第2期188-189,共2页
BACKGROUND: Temperature of axilla could be affected due to motor dysfunction of limbs and neural changes of vessel after ischemic stroke. OBJECTIVE: To observe the effect of percutaneous neuromuscular electric stimu... BACKGROUND: Temperature of axilla could be affected due to motor dysfunction of limbs and neural changes of vessel after ischemic stroke. OBJECTIVE: To observe the effect of percutaneous neuromuscular electric stimulation (PNES) on difference in temperature of axilla and analyze the relationship between function of limbs and difference in temperature of axilla. DESIGN: Randomized grouping and controlled observation SETTING: Department of Neurology, General Hospital of Shenyang Military Area Command of Chinese PLA PARTICIPANTS: Sixty patients with ischemic stroke were selected from Neurological Department of General Hospital of Shenyang Military Area Command of Chinese PLA from January to June 2003. All cases were diagnosed with clinical diagnosis criteria of ischemic stroke established by the Fourth Chinese Classification of Cerebrovasular Disease and CT examination and received neuromuscular electric stimulation (NES). Patients were randomly divided into control group and treatment group with 30 in each group. METHODS: Control group: Patients received routinely neurological therapy. Treatment group: Except routine therapy, patients suffered from NES at 48 hours after hospitalization. NMT-91 NES equipment was used to stimulated injured limbs with low frequency once 30 minutes a day in total of 10 times a course, especially extensor muscle of upper limb and flexor muscle of lower limb. Prescription of hemiplegia was internally decided by equipment with the output frequency of 200 Hz. Intensity of electric output could cause muscle contraction. The therapy needed two or three courses. Temperature of bilateral axilla was measured every day to calculate the difference with the formula of (temperature of axilla on the injured side - temperature of axilla on the healthy side). Motor function of limbs was measured with FugI-Meyer Motor Assessment (FMA) during hospitalization and at 2 and 4 hours after hospitalization. Among 90 points, upper and lower limb function was 54, equilibrium function 10, sensory function 10, and motion of joint 16. The higher the scores were, the better the function was. Correlation of data was dealt with linear correlation analysis. MAIN OUTCOME MEASURES : Assessment and correlation between difference in temperature of axilla and motor function of injured limbs during hospitalization and at 2 and 4 weeks after hospitalization. RESULTS: All 60 patients with ischemic stroke were involved in the final analysis. ① Difference in temperature: Difference of 2 and 4 weeks after hospitalization was lower than that in control group and at just hospitalization [treatment group: (0.056±0.000), (0.024±0.003) ℃; control group: (0.250±0.001), (0.131 ±0.001)℃; hospitalization; (0.513±0.001) ℃, P 〈 0.05-0,01]. ② FMA scores: Scores of 2 and 4 weeks after hospitalization were higher than those in control group and at just hospitalization [treatment group; (43.50±15.09), (67.97 ±18.21) points; control group: (33.33 ±13.54), (40.87±19.34) points; hospitalization: (26.43 ±11.87) points, P 〈 0.05-0.01]. ③ Correlation: Difference in temperature of axilla was negative correlation with FMA scores (c=- -0.255 1, P 〈 0.05). CONCLUSION: ① PNES can accelerate recovery of limb function and decrease temperature of axilla of patients with ischemic stroke. ② The lower the difference in temperature is, the better the functional recovery is. 展开更多
关键词 lim Early application of percutaneous neuromuscular electric stimulation in interfering motor function of limbs and difference in temperature of axilla of patients with ischemic stroke
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Nischarin-siRNA delivered by polyethyleniminealginate nanoparticles accelerates motor function recovery after spinal cord injury 被引量:2
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作者 Yue-min Ding Yu-ying Li +6 位作者 Chu Wang Hao Huang Chen-chen Zheng Shao-han Huang Yang Xuan Xiao-yi Sun Xiong Zhang 《Neural Regeneration Research》 SCIE CAS CSCD 2017年第10期1687-1694,共8页
A previous study by our group found that inhibition of nischarin promotes neurite outgrowth and neuronal regeneration in Neuro-2 a cells and primary cortical neurons.In recent years,more and more studies have shown th... A previous study by our group found that inhibition of nischarin promotes neurite outgrowth and neuronal regeneration in Neuro-2 a cells and primary cortical neurons.In recent years,more and more studies have shown that nanomaterials have good prospects in treatment of spinal cord injury.We proposed that small interfering RNA targeting nischarin(Nis-si RNA) delivered by polyethyleneimine-alginate(PEIALG) nanoparticles promoted motor function recovery in rats with spinal cord injury.Direct microinjection of 5 μL PEI-ALG/Nis-si RNA into the spinal cord lesion area of spinal cord injury rats was performed.From day 7 after surgery,Basso,Beattie and Bresnahan score was significantly higher in rats from the PEI-ALG/Nis-si RNA group compared with the spinal cord injury group and PEI-ALG/Control-si RNA group.On day 21 after injection,hematoxylin-eosin staining showed that the necrotic area was reduced in the PEI-ALG/Nis-si RNA group.Immunohistochemistry and western blot assay results confirmed successful inhibition of nischarin expression and increased protein expression of growth-associated protein-43 in the PEI-ALG/Nis-si RNA group.These findings suggest that a complex of PEI-ALG nanoparticles and Nis-si RNA effectively suppresses nischarin expression,induces expression of growth-associated protein-43,and accelerates motor function recovery after spinal cord injury. 展开更多
关键词 nerve regeneration spinal cord injury polyethylenimine alginate nanoparticles nischarin small interfering RNA necrotic area growth-associated protein-43 motor function neural regeneration
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