国际眼科杂志
國際眼科雜誌
국제안과잡지
INTERNATIONAL JOURNAL OF OPHTHALMOLOGY
2015年
5期
764-766
,共3页
褪黑素%晶状体上皮细胞%氧化损伤
褪黑素%晶狀體上皮細胞%氧化損傷
퇴흑소%정상체상피세포%양화손상
melatonin%human lens epithelial cells%oxidative damage
目的:探讨褪黑素对过氧化氢诱导晶状体上皮细胞氧化损伤的保护作用。<br> 方法:晶状体上皮细胞传代培养后,分别加入不同浓度褪黑素预处理12h后,加入100μmol/L H2 O2继续孵育24h, MTT比色法检测褪黑素对H2 O2诱导的晶状体上皮细胞活力的影响,流式细胞仪检测细胞凋亡率,比色法检测凋亡相关因子Caspase-3及Caspase-9的活性。<br> 结果:MTT结果显示褪黑素对晶状体上皮细胞活性无影响,该药物可以抑制过氧化氢诱导的细胞活性的下降,流式细胞计数结果显示褪黑素可以抑制过氧化氢诱导的细胞凋亡,此外,褪黑素还可以减少过氧化氢所致晶状体上皮细胞内Caspase-3及Caspase-9的活性,并且,伴随褪黑素作用时间的延长其活性呈下降趋势。<br> 结论:褪黑素可以明显抑制过氧化氢诱导的晶状体上皮细胞的凋亡,从而为寻求有效的防治白内障药物提供可靠的实验依据。
目的:探討褪黑素對過氧化氫誘導晶狀體上皮細胞氧化損傷的保護作用。<br> 方法:晶狀體上皮細胞傳代培養後,分彆加入不同濃度褪黑素預處理12h後,加入100μmol/L H2 O2繼續孵育24h, MTT比色法檢測褪黑素對H2 O2誘導的晶狀體上皮細胞活力的影響,流式細胞儀檢測細胞凋亡率,比色法檢測凋亡相關因子Caspase-3及Caspase-9的活性。<br> 結果:MTT結果顯示褪黑素對晶狀體上皮細胞活性無影響,該藥物可以抑製過氧化氫誘導的細胞活性的下降,流式細胞計數結果顯示褪黑素可以抑製過氧化氫誘導的細胞凋亡,此外,褪黑素還可以減少過氧化氫所緻晶狀體上皮細胞內Caspase-3及Caspase-9的活性,併且,伴隨褪黑素作用時間的延長其活性呈下降趨勢。<br> 結論:褪黑素可以明顯抑製過氧化氫誘導的晶狀體上皮細胞的凋亡,從而為尋求有效的防治白內障藥物提供可靠的實驗依據。
목적:탐토퇴흑소대과양화경유도정상체상피세포양화손상적보호작용。<br> 방법:정상체상피세포전대배양후,분별가입불동농도퇴흑소예처리12h후,가입100μmol/L H2 O2계속부육24h, MTT비색법검측퇴흑소대H2 O2유도적정상체상피세포활력적영향,류식세포의검측세포조망솔,비색법검측조망상관인자Caspase-3급Caspase-9적활성。<br> 결과:MTT결과현시퇴흑소대정상체상피세포활성무영향,해약물가이억제과양화경유도적세포활성적하강,류식세포계수결과현시퇴흑소가이억제과양화경유도적세포조망,차외,퇴흑소환가이감소과양화경소치정상체상피세포내Caspase-3급Caspase-9적활성,병차,반수퇴흑소작용시간적연장기활성정하강추세。<br> 결론:퇴흑소가이명현억제과양화경유도적정상체상피세포적조망,종이위심구유효적방치백내장약물제공가고적실험의거。
?AlM: To investigate theprotective effect of melatonin against hydrogen peroxide ( H2 O2 )-induced oxidative damage to human lens epithelial cells. <br> ?METHODS: Sub-culture human lens epithelial cells preprocessed with different concentrations of melatonin for 12h and then 100 μmol/L H2 O2 for 24h. The impact of melatonin on H2 O2-induced lens epithelial cell viability was detected by MTT assay, rate of apoptosis was detected by flow cytometry instrument and activity of apoptosis-related factors, Caspase-3 and Caspase-9, were detected by colorimetric method. <br> ?RESULTS: MTT assay showed that melatonin had no effect on the activity of lens epithelial cells, and the drug can inhibit the decrease of H2 O2-induced cell activity, as well as flow cytometry showed that melatonin can inhibit H2 O2-induced apoptosis. ln addition, melatonin can also reduce H2 O2-induced Caspase-3 and Caspase-9 activity in lens epithelial cells, and their activity decreased with effect of melatonin along with extending time. <br> ?CONCLUSlON: Melatonin can obviously inhibit H2 O2 -induced apoptosis of human lens epithelial cells, which provide reliable experimental basis for drug on treatment of cataract.