机构地区:[1]辽宁中医药大学附属医院,辽宁沈阳110032
出 处:《中华中医药学刊》2013年第8期1670-1673,I0007,共5页Chinese Archives of Traditional Chinese Medicine
基 金:辽宁省教育厅资助项目(2009T067)
摘 要:目的:探讨泻火化瘀通窍法对耳蜗组织缺血再灌注损伤iNOSmRNA和MMP-2mRNA表达的影响。方法:健康豚鼠60只,随机分成5组,每组12只,即正常组、模型组、行气组、活血化瘀组、泻火化瘀通窍组,除正常组外,其余各组分别进行光化学诱导法造模,成功后正常组:予0.9%生理盐水4 mL/(只.d)灌胃;模型组:予0.9%生理盐水4 mL/(只.d)灌胃;行气组:予行气中药4 mL/(只.d)灌胃(含生药1 g);活血化瘀组:予活血化瘀药物4 mL/(只.d)灌胃(含生药2 g),共连续给药10天;泻火化瘀通窍组,予泻火化瘀通窍药物4 mL/(只.d)灌胃(含生药4 g),各组均每日分2次给药,共连续给药10 d。10 d后取耳蜗组织行实时荧光定量PCR检测iNOSmRNA及MMP-2mRNA。结果:正常组与各治疗组iNOSmRNA的表达均明显低于模型组P<0.05,且泻火化瘀通窍组iNOSmRNA的表达量与活血化瘀组接近P>0.05,模型组iNOSmRNA的表达约是行气组的1.3倍,约是活血化瘀组的4.7倍,约是泻火化瘀通窍组的4.6倍;各治疗组MMP-2mRNA的表达均明显低于模型组P<0.05,模型组MMP-2mRNA的表达是是行气组的1.5倍;是活血化瘀组的2.4倍;是泻火化瘀通窍组的7.3倍。结论:①泻火化瘀通窍法与活血化瘀法均能够抑制iNOS的表达,保护耳蜗组织的缺血损伤,明显优于行气法。②泻火化瘀通窍法、活血化瘀法与行气法均能够抑制MMP-2的表达,且泻火化瘀通窍法作用最强。Objective: To explore the effect of method of reducing fire and resolving stasis to dredge the orifice (RRDO) on iNOSmRNA and MMP- 2mRNA expressions of cochlea ischemia reperfusion injury. Method:60 healthy guinea pigs were randomly divided into 5 groups. Animal model and grouping: photochemical induction method was used in modeling, then the guinea pig models were divided into five groups, namely normal group, model group, qi - promo- ting group, blood - activating group and RRDO group, with 12 guinea pigs in each group. Experimental method: 2 mL of 0.9% normal saline twice a day for the normal group ; 2 mL of 0.9% normal saline twice a day for the model group 12 h after the operation ; and different treatments for the rest three groups. The specimens of the guinea pigs were sampled after quick decapitation on the 2nd day after administration of anesthesia, for RRDO group: 12 h after the operation, adminis- tration of the RRDO decoction, 2 mL, twice a day (amounting to 1 g/d for the raw medicine) ; for the blood - activating group: administration of the ingredients activating blood to resolve stasis in the RRDO decoction, 2 mL, twice a day (a- mounting to 2 g/d for the raw medicine) ; for the qi -promoting group: administration of the ingredients the qi -promo- ting simply in the RRDO decoction, 2 mL, twice a day (amounting to 4 g/d for the raw medicine). The course of treat- ment consisted of 10 days. Expressions of cochlear iNOSmRNA and MMP - 2mRNA were determined by using Real - Time PCR after 10 days. Results: In the normal group and all the 3 treatment groups, the expressions of iNOSmRNA were significantly lower than that in the model group (P 〈 0. 05). The expression of iNOSmRNA in the RRDO group was simi- lar with that in the blood - activating group (P 〉 0. 05 ). The expression of iNOSmRNA in the model group was about 1.3 times what it was in the qi - promoting group, about 4.7 times what it was in the blood - activating group, and about 4.6 times what it was i
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