临床内科杂志
臨床內科雜誌
림상내과잡지
JOURNAL OF CLINICAL INTERNAL MEDICINE
2015年
7期
487-490
,共4页
范临夏%潘辉%王小军%王红娟%刘华
範臨夏%潘輝%王小軍%王紅娟%劉華
범림하%반휘%왕소군%왕홍연%류화
支气管哮喘%大鼠%苦参碱%IL-4%干扰素-γ%细胞因子转导抑制因子 3
支氣管哮喘%大鼠%苦參堿%IL-4%榦擾素-γ%細胞因子轉導抑製因子 3
지기관효천%대서%고삼감%IL-4%간우소-γ%세포인자전도억제인자 3
Asthma%Rats%Matrine%IL-4%INF-γ%Suppressor of cytokine signaling 3
目的:观察苦参碱对哮喘大鼠 Th1/Th2失衡以及嗜酸细胞中细胞因子转导抑制因子3(SOCS3)表达的影响,探讨苦参碱治疗哮喘气道炎症的作用机制。方法以健康大鼠作为对照组,卵清蛋白致敏法构建大鼠哮喘模型后随机分为 A 组、B 组、C 组。A 组大鼠不接受任何治疗;B、C 组大鼠分别接受低剂量和高剂量的苦参碱治疗。分析各组大鼠肺组织中的嗜酸性粒细胞(EOS)计数、杯状细胞百分比、炎性细胞浸润积分。对比各组大鼠支气管肺泡灌洗液(BAFL)中IL-4、干扰素(INF)-γ水平,计算 INF-γ/IL4比值。荧光实时定量 PCR 技术(qRT-PCR)和蛋白质免疫印迹(Western blot)技术分析各组大鼠肺组织中 SOCS3 mRNA 与蛋白水平的表达变化。结果A 组大鼠出现明显的炎性反应,BAFL 中的 INF-γ水平低于对照组,IL-4水平高于对照组,差异均具有统计学意义。各组 INF-γ/IL-4比值分别为3.90±0.30、0.61±0.08、1.71±0.54、2.15±0.21,各组比较差异有统计学意义(P <0.05)。qRT-PCR 检测发现,与对照组比较,A 组大鼠肺组织 SOCS3的 mRNA 表达水平显著增高(P <0.05),而 B 组、C 组大鼠肺组织 SOCS3的 mRNA 表达水平明显低于 A 组(P <0.05)。SOCS3蛋白水平的变化与 mRNA 水平的变化一致。结论苦参碱可以抑制支气管哮喘大鼠炎症反应、调节 Th1/Th2免疫平衡,该作用的机制与 SOCS3的表达水平有关。
目的:觀察苦參堿對哮喘大鼠 Th1/Th2失衡以及嗜痠細胞中細胞因子轉導抑製因子3(SOCS3)錶達的影響,探討苦參堿治療哮喘氣道炎癥的作用機製。方法以健康大鼠作為對照組,卵清蛋白緻敏法構建大鼠哮喘模型後隨機分為 A 組、B 組、C 組。A 組大鼠不接受任何治療;B、C 組大鼠分彆接受低劑量和高劑量的苦參堿治療。分析各組大鼠肺組織中的嗜痠性粒細胞(EOS)計數、杯狀細胞百分比、炎性細胞浸潤積分。對比各組大鼠支氣管肺泡灌洗液(BAFL)中IL-4、榦擾素(INF)-γ水平,計算 INF-γ/IL4比值。熒光實時定量 PCR 技術(qRT-PCR)和蛋白質免疫印跡(Western blot)技術分析各組大鼠肺組織中 SOCS3 mRNA 與蛋白水平的錶達變化。結果A 組大鼠齣現明顯的炎性反應,BAFL 中的 INF-γ水平低于對照組,IL-4水平高于對照組,差異均具有統計學意義。各組 INF-γ/IL-4比值分彆為3.90±0.30、0.61±0.08、1.71±0.54、2.15±0.21,各組比較差異有統計學意義(P <0.05)。qRT-PCR 檢測髮現,與對照組比較,A 組大鼠肺組織 SOCS3的 mRNA 錶達水平顯著增高(P <0.05),而 B 組、C 組大鼠肺組織 SOCS3的 mRNA 錶達水平明顯低于 A 組(P <0.05)。SOCS3蛋白水平的變化與 mRNA 水平的變化一緻。結論苦參堿可以抑製支氣管哮喘大鼠炎癥反應、調節 Th1/Th2免疫平衡,該作用的機製與 SOCS3的錶達水平有關。
목적:관찰고삼감대효천대서 Th1/Th2실형이급기산세포중세포인자전도억제인자3(SOCS3)표체적영향,탐토고삼감치료효천기도염증적작용궤제。방법이건강대서작위대조조,란청단백치민법구건대서효천모형후수궤분위 A 조、B 조、C 조。A 조대서불접수임하치료;B、C 조대서분별접수저제량화고제량적고삼감치료。분석각조대서폐조직중적기산성립세포(EOS)계수、배상세포백분비、염성세포침윤적분。대비각조대서지기관폐포관세액(BAFL)중IL-4、간우소(INF)-γ수평,계산 INF-γ/IL4비치。형광실시정량 PCR 기술(qRT-PCR)화단백질면역인적(Western blot)기술분석각조대서폐조직중 SOCS3 mRNA 여단백수평적표체변화。결과A 조대서출현명현적염성반응,BAFL 중적 INF-γ수평저우대조조,IL-4수평고우대조조,차이균구유통계학의의。각조 INF-γ/IL-4비치분별위3.90±0.30、0.61±0.08、1.71±0.54、2.15±0.21,각조비교차이유통계학의의(P <0.05)。qRT-PCR 검측발현,여대조조비교,A 조대서폐조직 SOCS3적 mRNA 표체수평현저증고(P <0.05),이 B 조、C 조대서폐조직 SOCS3적 mRNA 표체수평명현저우 A 조(P <0.05)。SOCS3단백수평적변화여 mRNA 수평적변화일치。결론고삼감가이억제지기관효천대서염증반응、조절 Th1/Th2면역평형,해작용적궤제여 SOCS3적표체수평유관。
Objective To observe the effects of matrine on Th1 /Th2 balance and suppressor of cytokine signaling 3 (SOCS3)expression in eosinophil of asthmatic mats and to explore mechanisms of matrine in treating infectious airway of asthmatics.Methods Rats,ovalbumin-sensitized to establish asthma model,were randomly divided into three groups,vehicle(group A),low-dose matrine treatment (group B)and high-dose matrine treatment (group C).Normal rats were kept as control group.The eosinophil count,goblet cells percentage,inflammatory cell infiltration in rat lung were analyzed and scored by morphological examination.IL-4 and INF-γlevel in BALF were determined by ELISA and INF-γ/IL-4 ratio was further calculated.Furthermore,the expression of SOCS3 in mRNA and protein level was detected by qRT-PCR and Western blotting,respectively.Results Compare to control group,inflammation was evident in group A rats.Eosinophil count significantly elevated to 14.6 ±1.9 per high power field,with gob-let cells increased to (67.6 ±5.1)%,and inflammatory cell infiltration scored 3.7 ±0.7(all P <0.05). Eosinophil count,goblet cell percentage and inflammatory cell infiltration score were significantly lower in group B and C,compare to group A(P <0.05).Compared to control group,group A exhibited a lower INF-γlevel and a higher IL-4 level(P <0.05).INF-γlevel in group B and C were higher while IL-4 level were lower,compare to group A.The INF-γ/IL-4 ratio were 3.90 ±0.30,0.61 ±0.08,1.71 ±0.54,and 2.15 ±0.21 in group A,B and C,respectively.Meanwhile,SOCS3 mRNA level in rat lung tissue was elevated in group A,compare to control group.Matrine treatment decreased SOCS3 expression in group B and C.Similar trend was found in SOCS3 protein level.Conclusion Matrine may exhibit its anti-inflam-matory effect by inhibiting SOCS3 expression and maintaining Th1 /Th2 balance in asthmatic rats.