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吴家鹏, 李学智, 汪 莹, 等.电针结合脑内注射VEGF修复大鼠脑缺血后再灌注损伤的机制研究.四川大学学报(医学版),2019,50(1):34-39
电针结合脑内注射VEGF修复大鼠脑缺血后再灌注损伤的机制研究
Effects of Electroacupuncture and Intracerebral Injection of VEGF on Caspase12, Caspase3, and GRP78 Genes in Rats with Cerebral Ischemia-Reperfusion Injury
  
中文关键词:  脑缺血后再灌注损伤 caspase12 caspase3 GRP78 电针 VEGF
英文关键词:Cerebral ischemia-reperfusion injury Caspase12 Caspase3 GRP78 Electroacupuncture VEGF
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中文摘要:
      目的 观察电针及电针结合脑内注射血管内皮生长因子(VEGF)对脑缺血后再灌注损伤大鼠caspase12、caspasse3、 葡萄糖调节蛋白-78 (GRP78)的影响,探讨电针结合脑内VEGF对脑缺血后再灌注损伤的修复机制。方法 将60只雄性SD大鼠随机分为假手术组、模型组、电针组、电针+VEGF组,每组15只。后3组采用线栓法进行大脑中动脉缺血(MCAO)法制作脑缺血后再灌注损伤模型。电针组及电针+VEGF组造模后1 d开始电针干预(穴位:百会、曲池、足三里),1次/d,每次30 min,共14 d。电针+VEGF组大鼠于造模成功后24 h行第一次电针干预后,向侧脑室内一次性注入10 μL VEGF165 (0.025 μg/μL)。每组于0 d(造模后1 d,开始电针干预前)、7 d、14 d时,各取5只大鼠进行神经功能评分(mNSS)后处死取材,尼氏染色观察脑梗死区组织形态,免疫组化法检测大鼠缺血脑组织GRP78活性,real-time PCR法检测大鼠缺血脑组织caspase12、caspase3、GRP78 mRNA表达量。结果 0 d、7 d、14 d时,与假手术组比较,模型组大鼠mNSS评分升高( P<0.05),镜下可见脑梗死征象(尼氏小体数量明显减少且排列混乱,结构不清晰),GRP78免疫阳性细胞数量增多,GRP78 mRNA表达升高( P<0.05),caspase12及caspase3 mRNA表达升高( P<0.05)。7 d和14 d时,与模型组比较,电针组以及电针+VEGF组大鼠的mNSS评分降低( P<0.05),镜下脑梗死征象减轻,GRP78免疫阳性细胞数量增多,GRP78 mRNA表达增多( P<0.05),caspase12、caspase3 mRNA表达降低( P<0.05),电针+VEGF组上述指标变化均较电针组明显( P<0.05)。假手术组各时点间上述指标差异无统计学意义( P>0.05),其余3组mNSS评分( P<0.05)、脑梗死征象、caspase12、caspase3 mRNA表达随治疗时间降低( P<0.05),GRP78免疫阳性细胞数量随治疗时间增多,GRP78 mRNA表达随治疗时间升高( P<0.05)。结论 电针结合脑内注射VEGF可促进脑缺血损伤组织修复,其机制可能与下调caspase12、caspase3基因,上调GRP78基因的表达有关,且其效果比单纯使用电针法更具优势。
英文摘要:
      Objective To determine the effects of electroacupuncture (EA) and intracerebral injection of vascular endothelial growth factor (VEGF) on caspase12, caspase3, and glucose regulated protein 78 kD (GRP78) genes of rats with cerebral ischemia reperfusion injury. Methods 60 SD rats were randomly divided into sham-operation group, model group, EA group and EA+VEGF group with 15 rats in each group. Middle cerebral artery occlusion (MCAO) method was used to establish the model of cerebral ischemia reperfusion injury. Electro-acupuncture intervention was introduced 1 day after the injury in the EA group and EA+VEGF group: 30 minutes each session and once a day for a total of 14 d 〔acupoint selection: Baihui (GV 20), Quchi(Li 11), Zusanli (ST36)〕. The rats in the EA+VEGF group were also injected with 10 μL of VEGF165 (0.025 μg/μL) into the lateral ventricle after the first session of EA. Five rats in each group were sacrificed after obtaining a neurological function score (mNSS) at day 0 (1 d after modeling, before EA intervention), day 7 and day 14, respectively. Nissl staining was used to observe the histomorphology of cerebral infarction areas. Immunohistochemistry was used to CM(155mm]detect GRP78 activity in the ischemic brain tissues. Real-time fluorescence quantitative PCR (real-time PCR) was used to detect the expressions of caspase12, caspase3 and GRP78 mRNA in the ischemic brain tissues. Results Compared with the sham-operation group, rats in the model group had higher mNSS scores ( P<0.05), showed signs of cerebral infarction (with reduced numbers of and disordered Nissl bodies and unclear structure), increased GRP78 immunopositive cells, increased expression of GRP78 mRNA ( P<0.05), and increased expressions of caspase12 and caspase3 mRNA ( P<0.05). Compared with the model group, EA and EA+VEGF decreased mNSS scores at day 7 and 14 ( P<0.05), showing alleviated signs of cerebral infarction, increased GRP78 immunopositive cells ( P<0.05), increased GRP78 mRNA expression ( P<0.05),and decreased caspase12 and caspase3 mRNA expressions ( P<0.05). The most obvious changes were found in the EA+VEGF group ( P<0.05). No significant changes were observed in the sham-operation group over time ( P<0.05). In comparison, mNSS scores, the signs of cerebral infarction, and the expressions of caspase12 and caspase3 decreased over time in the other groups ( P<0.05), accompanied with increased GRP78 immunopositive cells and the expression of GRP78 gene ( P<0.05). Conclusion Electroacupuncture and intracerebral injection of VEGF promote tissue repair of rats with cerebral ischemic injury, possibly through down-regulating the expressions of caspase12 and caspase3 genes and up-regulating the expression of GRP78 gene. The effect of electroacupuncture in combination with intracerebral injection of VEGF is superior to that of the single use of electroacupuncture.
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