中国组织工程研究
中國組織工程研究
중국조직공정연구
Journal of Clinical Rehabilitative Tissue Engineering Research
2014年
11期
1700-1705
,共6页
陈宣煌%李荣议%张国栋%林海滨%吴献伟%林宇进%郑锋
陳宣煌%李榮議%張國棟%林海濱%吳獻偉%林宇進%鄭鋒
진선황%리영의%장국동%림해빈%오헌위%림우진%정봉
组织构建%组织工程%坐骨神经损伤%神经再生%胆囊收缩素%神经生长因子%诱导型一氧化氮合酶%超氧化物歧化酶%丙二醛%细胞凋亡
組織構建%組織工程%坐骨神經損傷%神經再生%膽囊收縮素%神經生長因子%誘導型一氧化氮閤酶%超氧化物歧化酶%丙二醛%細胞凋亡
조직구건%조직공정%좌골신경손상%신경재생%담낭수축소%신경생장인자%유도형일양화담합매%초양화물기화매%병이철%세포조망
sciatic nerve%cholecystokinin%apoptosis%nerve growth factor
背景:前期实验发现,八肽胆囊收缩素能促进大鼠坐骨神经损伤后的再生,但具体机制仍不清楚。<br> 目的:筛选有效指标,尝试从神经生长因子及神经再生微环境的角度分析八肽胆囊收缩素促进大鼠坐骨神经再生的机制。<br> 方法:选择健康SD大鼠,制备坐骨神经单侧离断伤模型后随机分为2组,八肽胆囊收缩素治疗组造模后连续7 d腹腔注射八肽胆囊收缩素8 nmol/kg,对照组腹腔注射等量生理盐水。检测两组大鼠局部神经生长因子蛋白表达、脊髓诱导型一氧化氮合酶水平、血清超氧化物歧化酶活性和丙二醛浓度,同时检测脊髓凋亡细胞数。<br> 结果与结论:八肽胆囊收缩素治疗组大鼠局部神经生长因子蛋白表达高于对照组(P <0.01),脊髓诱导型一氧化氮合酶和凋亡细胞数低于对照组(P <0.01),血清超氧化物歧化酶活性高于对照组且丙二醛浓度低于对照组(P<0.01,0.05)。说明胆囊收缩素促进坐骨神经再生的可能机制包括保护神经元、抗细胞凋亡、抑制炎性反应、抗NO及氧化反应、抗丙二醛减轻自由基损伤等方面外,还可刺激神经生长因子的表达和释放。
揹景:前期實驗髮現,八肽膽囊收縮素能促進大鼠坐骨神經損傷後的再生,但具體機製仍不清楚。<br> 目的:篩選有效指標,嘗試從神經生長因子及神經再生微環境的角度分析八肽膽囊收縮素促進大鼠坐骨神經再生的機製。<br> 方法:選擇健康SD大鼠,製備坐骨神經單側離斷傷模型後隨機分為2組,八肽膽囊收縮素治療組造模後連續7 d腹腔註射八肽膽囊收縮素8 nmol/kg,對照組腹腔註射等量生理鹽水。檢測兩組大鼠跼部神經生長因子蛋白錶達、脊髓誘導型一氧化氮閤酶水平、血清超氧化物歧化酶活性和丙二醛濃度,同時檢測脊髓凋亡細胞數。<br> 結果與結論:八肽膽囊收縮素治療組大鼠跼部神經生長因子蛋白錶達高于對照組(P <0.01),脊髓誘導型一氧化氮閤酶和凋亡細胞數低于對照組(P <0.01),血清超氧化物歧化酶活性高于對照組且丙二醛濃度低于對照組(P<0.01,0.05)。說明膽囊收縮素促進坐骨神經再生的可能機製包括保護神經元、抗細胞凋亡、抑製炎性反應、抗NO及氧化反應、抗丙二醛減輕自由基損傷等方麵外,還可刺激神經生長因子的錶達和釋放。
배경:전기실험발현,팔태담낭수축소능촉진대서좌골신경손상후적재생,단구체궤제잉불청초。<br> 목적:사선유효지표,상시종신경생장인자급신경재생미배경적각도분석팔태담낭수축소촉진대서좌골신경재생적궤제。<br> 방법:선택건강SD대서,제비좌골신경단측리단상모형후수궤분위2조,팔태담낭수축소치료조조모후련속7 d복강주사팔태담낭수축소8 nmol/kg,대조조복강주사등량생리염수。검측량조대서국부신경생장인자단백표체、척수유도형일양화담합매수평、혈청초양화물기화매활성화병이철농도,동시검측척수조망세포수。<br> 결과여결론:팔태담낭수축소치료조대서국부신경생장인자단백표체고우대조조(P <0.01),척수유도형일양화담합매화조망세포수저우대조조(P <0.01),혈청초양화물기화매활성고우대조조차병이철농도저우대조조(P<0.01,0.05)。설명담낭수축소촉진좌골신경재생적가능궤제포괄보호신경원、항세포조망、억제염성반응、항NO급양화반응、항병이철감경자유기손상등방면외,환가자격신경생장인자적표체화석방。
BACKGROUND:Previous studies have found that cholecystokinin octapeptide (CCK-8) can promote the regeneration after sciatic nerve injury in rats, but the exact mechanism remains unclear. <br> OBJECTIVE:To screen effective indicators and analyze the mechanism of CCK-8 promoting sciatic nerve regeneration from the perspective of nerve growth factor and nerve regeneration microenvironment. <br> METHODS:Healthy Sprague-Dawley rats, for the preparation of unilateral sciatic nerve transection injury model, were randomly divided into two groups. In the CCK-8 group, the animal model received intraperitoneal injection of CCK-8 (8 nmol/kg) for consecutive 7 days, while the control group was injected with equal volume of normal saline. The nerve growth factor expression, inducible nitric oxide synthase in the spinal cord, serum superoxide dismutase activity and malondialdehyde concentration, as wel as apoptotic cel s in spinal cord were al detected. <br> RESULTS AND CONCLUSION:In the CCK-8 group, nerve growth factor expression was higher than that in the control group (P<0.01), while inducible nitric oxide synthase and the number of apoptotic cel s were lower (P<0.01), serum superoxide dismutase activity was higher but malondialdehyde concentrations was lower (P<0.01, 0.05). The mechanisms of CCK-8 promoting sciatic nerve regeneration include protecting neurons, anti-apoptosis, inhibiting inflammatory response, anti-NO and anti-oxidation, reducing malondialdehyde, and al eviating free radical damage, as wel as stimulating nerve growth factor expression and release.