临床医学工程
臨床醫學工程
림상의학공정
CLINICAL MEDICAL ENGINEERING
2014年
7期
837-839
,共3页
徐敏%刘勇军%闵闽%陈洪涛%徐莉%顾华群
徐敏%劉勇軍%閔閩%陳洪濤%徐莉%顧華群
서민%류용군%민민%진홍도%서리%고화군
天麻素%神经病理性疼痛%镇痛%P-ERK1/2通路
天痳素%神經病理性疼痛%鎮痛%P-ERK1/2通路
천마소%신경병이성동통%진통%P-ERK1/2통로
Gastrodin%Neuropathic pain%Analgesic%ERK1/2 pathways
目的:探讨天麻素对神经病理性疼痛大鼠的镇痛作用及其机制,为临床开发新的镇痛药物奠定基础。方法SD大鼠随机分为坐骨神经慢性压迫性损伤组(n=32)和假手术组(n=8),自术后第8天分别腹腔注射天麻素治疗,用电子Von-Frey测痛仪测定大鼠机械缩足反射阈值,热痛刺激仪测定大鼠热痛缩足反应潜伏期。取脊髓腰膨大及L4/L6背根神经节,采用Westem blotting法测定脊髓背角和背根神经节p-ERK1/2的表达。结果与假手术组相比,对照组和天麻素治疗组各时点机械缩足反射阈值降低、热痛缩足反应潜伏期缩短,脊髓背角及背根神经节p-ERK1/2均出现表达上调(P<0.05);与对照组相比,天麻素治疗组在给药后7d机械缩足反射阈值回升、热痛缩足反应潜伏期延长;在给药14d后脊髓背角及背根神经节p-ERK1/2表达下调(P<0.05)。结论天麻素可减轻大鼠神经病理性痛,其机制可能与抑制脊髓背角和背根神经节p-ERK1/2通路激活有关。
目的:探討天痳素對神經病理性疼痛大鼠的鎮痛作用及其機製,為臨床開髮新的鎮痛藥物奠定基礎。方法SD大鼠隨機分為坐骨神經慢性壓迫性損傷組(n=32)和假手術組(n=8),自術後第8天分彆腹腔註射天痳素治療,用電子Von-Frey測痛儀測定大鼠機械縮足反射閾值,熱痛刺激儀測定大鼠熱痛縮足反應潛伏期。取脊髓腰膨大及L4/L6揹根神經節,採用Westem blotting法測定脊髓揹角和揹根神經節p-ERK1/2的錶達。結果與假手術組相比,對照組和天痳素治療組各時點機械縮足反射閾值降低、熱痛縮足反應潛伏期縮短,脊髓揹角及揹根神經節p-ERK1/2均齣現錶達上調(P<0.05);與對照組相比,天痳素治療組在給藥後7d機械縮足反射閾值迴升、熱痛縮足反應潛伏期延長;在給藥14d後脊髓揹角及揹根神經節p-ERK1/2錶達下調(P<0.05)。結論天痳素可減輕大鼠神經病理性痛,其機製可能與抑製脊髓揹角和揹根神經節p-ERK1/2通路激活有關。
목적:탐토천마소대신경병이성동통대서적진통작용급기궤제,위림상개발신적진통약물전정기출。방법SD대서수궤분위좌골신경만성압박성손상조(n=32)화가수술조(n=8),자술후제8천분별복강주사천마소치료,용전자Von-Frey측통의측정대서궤계축족반사역치,열통자격의측정대서열통축족반응잠복기。취척수요팽대급L4/L6배근신경절,채용Westem blotting법측정척수배각화배근신경절p-ERK1/2적표체。결과여가수술조상비,대조조화천마소치료조각시점궤계축족반사역치강저、열통축족반응잠복기축단,척수배각급배근신경절p-ERK1/2균출현표체상조(P<0.05);여대조조상비,천마소치료조재급약후7d궤계축족반사역치회승、열통축족반응잠복기연장;재급약14d후척수배각급배근신경절p-ERK1/2표체하조(P<0.05)。결론천마소가감경대서신경병이성통,기궤제가능여억제척수배각화배근신경절p-ERK1/2통로격활유관。
Objective To investigate the analgesic effects and mechanism of gastrodin on the neuropathic pain in rats, and screen novel analgesics for clinical treatment of neuropathic pain diseases. Methods Forty male SD rats were randomly divided into 5 groups as sham operation group, control group, gastrodin 30 mg/kg group, gastrodin 60 mg/kg group, gastrodin120 mg/kg group. From the 8th day post-ligation, different doses of gastrodin were injected into abdominal cavity and the pain thresholds before and after intraperitoneal injection of the different doses of gastrodin were measured by the mechanical and hot stimulus. The expressions of p-ERK1/2 in L4/6 dorsal root ganglion neurons and dorsal horn was measured by the methods of Western blotting. Results Compared with sham operation group, the rats in CCI group developed a decrease in mechanical withdrawal threshold and thermal withdrawal latency associated with an increase in the activity of p-ERK1/2 in dorsal horn and dorsal root ganglion. Compared with CCI group, 7 day treatment with gastrodin significantly attenuated mechanical allodynia and thermal hyperalgesia, and these effects were correlated with inhibiting the hyper-activation of p-ERK1/2 after 14 days treatment with gastrodin. Conclusions Gastrodin has beneficial effects on neuropathic pain and the analgesic effects of gastrodin would be mediated by the ERK1/2 signaling pathways.