临床儿科杂志
臨床兒科雜誌
림상인과잡지
2014年
5期
476-479
,共4页
蔡成%裘刚%龚小慧%魏东%胡勇%赵焕虎
蔡成%裘剛%龔小慧%魏東%鬍勇%趙煥虎
채성%구강%공소혜%위동%호용%조환호
红霉素%高浓度氧%肺损伤%谷胱甘肽%γ-谷氨酰半胱氨酸合成酶
紅黴素%高濃度氧%肺損傷%穀胱甘肽%γ-穀氨酰半胱氨痠閤成酶
홍매소%고농도양%폐손상%곡광감태%γ-곡안선반광안산합성매
erythromycin%hyperoxia%lung injury%glutathione hormone%γ-glutamyl cysteine synthetase
目的:观察红霉素对高氧暴露下早产新生大鼠肺组织中的谷胱甘肽(GSH)和γ-谷氨酰半胱氨酸合成酶(γ-GCS)表达的影响,探讨红霉素对高氧肺损伤的干预作用。方法将孕第21天剖宫产生后1 d的新生SD大鼠随机分为4组:对照组、红霉素组、高氧组、红霉素高氧组。高氧组和红霉素高氧组持续暴露于常压氧舱中,对照组和红霉素组置于同一室常压空气中;红霉素组和红霉素高氧组每天尾静脉注射红霉素,高氧组和对照组注射生理盐水。四组分别于高氧暴露后第1、7、14天取肺组织标本,石蜡包埋切片行苏木精-伊红染色观察肺组织病理学变化,双抗体夹心酶联免疫吸附法分析GSH和γ-GCS的蛋白水平,半定量逆转录聚合酶链反应测定γ-GCS mRNA表达。结果高氧暴露后第1和7天,对照组、红霉素组、高氧组、红霉素高氧组四组间大鼠肺组织GSH、γ-GCS及γ-GCS mRNA表达的差异均有统计学意义(P<0.05)。其中,高氧组和红霉素高氧组的GSH、γ-GCS表达以及红霉素高氧组的γ-GCS mRNA表达均高于对照组和红霉素组,差异有统计学意义(P均<0.05)。第14天,四组间大鼠肺组织GSH、γ-GCS表达的差异无统计学意义(P均>0.05),而红霉素高氧组γ-GCS mRNA表达高于其余三组,差异有统计学意义(P<0.05)。结论氧化爆发能导致GSH与γ-GCS的表达异常。红霉素可能通过上调γ-GCS活性,提高GSH抗氧化,在减轻高氧肺损伤过程中发挥一定抗氧化作用。
目的:觀察紅黴素對高氧暴露下早產新生大鼠肺組織中的穀胱甘肽(GSH)和γ-穀氨酰半胱氨痠閤成酶(γ-GCS)錶達的影響,探討紅黴素對高氧肺損傷的榦預作用。方法將孕第21天剖宮產生後1 d的新生SD大鼠隨機分為4組:對照組、紅黴素組、高氧組、紅黴素高氧組。高氧組和紅黴素高氧組持續暴露于常壓氧艙中,對照組和紅黴素組置于同一室常壓空氣中;紅黴素組和紅黴素高氧組每天尾靜脈註射紅黴素,高氧組和對照組註射生理鹽水。四組分彆于高氧暴露後第1、7、14天取肺組織標本,石蠟包埋切片行囌木精-伊紅染色觀察肺組織病理學變化,雙抗體夾心酶聯免疫吸附法分析GSH和γ-GCS的蛋白水平,半定量逆轉錄聚閤酶鏈反應測定γ-GCS mRNA錶達。結果高氧暴露後第1和7天,對照組、紅黴素組、高氧組、紅黴素高氧組四組間大鼠肺組織GSH、γ-GCS及γ-GCS mRNA錶達的差異均有統計學意義(P<0.05)。其中,高氧組和紅黴素高氧組的GSH、γ-GCS錶達以及紅黴素高氧組的γ-GCS mRNA錶達均高于對照組和紅黴素組,差異有統計學意義(P均<0.05)。第14天,四組間大鼠肺組織GSH、γ-GCS錶達的差異無統計學意義(P均>0.05),而紅黴素高氧組γ-GCS mRNA錶達高于其餘三組,差異有統計學意義(P<0.05)。結論氧化爆髮能導緻GSH與γ-GCS的錶達異常。紅黴素可能通過上調γ-GCS活性,提高GSH抗氧化,在減輕高氧肺損傷過程中髮揮一定抗氧化作用。
목적:관찰홍매소대고양폭로하조산신생대서폐조직중적곡광감태(GSH)화γ-곡안선반광안산합성매(γ-GCS)표체적영향,탐토홍매소대고양폐손상적간예작용。방법장잉제21천부궁산생후1 d적신생SD대서수궤분위4조:대조조、홍매소조、고양조、홍매소고양조。고양조화홍매소고양조지속폭로우상압양창중,대조조화홍매소조치우동일실상압공기중;홍매소조화홍매소고양조매천미정맥주사홍매소,고양조화대조조주사생리염수。사조분별우고양폭로후제1、7、14천취폐조직표본,석사포매절편행소목정-이홍염색관찰폐조직병이학변화,쌍항체협심매련면역흡부법분석GSH화γ-GCS적단백수평,반정량역전록취합매련반응측정γ-GCS mRNA표체。결과고양폭로후제1화7천,대조조、홍매소조、고양조、홍매소고양조사조간대서폐조직GSH、γ-GCS급γ-GCS mRNA표체적차이균유통계학의의(P<0.05)。기중,고양조화홍매소고양조적GSH、γ-GCS표체이급홍매소고양조적γ-GCS mRNA표체균고우대조조화홍매소조,차이유통계학의의(P균<0.05)。제14천,사조간대서폐조직GSH、γ-GCS표체적차이무통계학의의(P균>0.05),이홍매소고양조γ-GCS mRNA표체고우기여삼조,차이유통계학의의(P<0.05)。결론양화폭발능도치GSH여γ-GCS적표체이상。홍매소가능통과상조γ-GCS활성,제고GSH항양화,재감경고양폐손상과정중발휘일정항양화작용。
Objectives To explore the effect of erythromycin on glutathione hormone (GSH) and γ-glutamyl cysteine synthetase (γ-GCS) in premature newborn rats exposed to hyperoxia, to study the intervention effect of erythromycin on hype-roxia-induced lung injury. Methods One-day old preterm SD rats were randomly divided into four groups:control group, eryth-romycin group, hyperoxia group, erythromycin+hyperoxia group. Hyperoxia group and hyperoxia+erythromycin group were continuously exposed to oxygen (oxygen concentration>0.85), control group and erythromycin group were in room air. Via cau-dal vein, the preterm rats was injected with erythromycin in erythromycin group and hyperoxia+erythromycin group, sodium chloride in control group and hyperoxia group daily. After 1,7,14 day(s) of hyperoxia (or air ) exposure, the preterm SD rats of four groups were killed, whole lung of these rats were isolated and histological changes were observed by hematoxylin-eosin (HE) staining, GSH andγ-GCS of pulmonary tissue homogenate were detected by double antibody sandwich enzyme linked im-munosorbent assay. Total lung RNA was extracted andγ-GCS mRNA was detected by reverse transcription polymerase chain re-action. Results The results showed that:After 1 and 7 day(s) of exposure, the expression of GSH、γ-GCS andγ-GCS mRNA in four groups showed significant differences(P<0.05). Among them, GSH expression in erythromycin + hyperoxia group was higher than that in the other three groups in 1,7,14 day(s) of exposure with significant differences (P<0.05);GSH expression in erythromycin+hyperoxia group and hyperoxia group reached the peak after 7 days of exposure. The expression ofγ-GCS andγ-GCS mRNA in erythromycin+hyperoxia group and hyperoxia group were higher than the other two groups after 1and 7 day(s) of exposure, the expression ofγ-GCS mRNA in erythromycin+hyperoxia group were higher than that of hyperoxia group with significant differences (P<0.05). Conclusions The expressions of GSH andγ-GCS in the lung of premature SD rats were abnor-mal by oxidation outbreak. Erythromycin may increase the activity ofγ-GCS, improve the anti-oxidation ability of GSH, and al-leviate hyperoxia mediated lung injury in premature rats.