中华眼视光学与视觉科学杂志
中華眼視光學與視覺科學雜誌
중화안시광학여시각과학잡지
CHINESE JOURNAL OF OPTOMETRY OPHTHALMOLOGY AND VISUAL SCIENCE
2011年
5期
328-331
,共4页
陈灿%蓝卫忠%林丽霞%王延东%付东%杨智宽
陳燦%藍衛忠%林麗霞%王延東%付東%楊智寬
진찬%람위충%림려하%왕연동%부동%양지관
多巴胺%光谱%色素上皮,眼%近视%户外活动
多巴胺%光譜%色素上皮,眼%近視%戶外活動
다파알%광보%색소상피,안%근시%호외활동
Dopamine%Spectrum%Pigment epithelium of eye%Myopia%Outdoor activity
目的 探索不同光谱组成的光照射对体外培养的视网膜色素上皮(RPE)细胞分泌多巴胺功能的影响.方法 实验研究.在细胞培养箱内建立光照系统后,将体外培养的RPE细胞分别放置于无光照(对照组)、全光谱低强度光照、红绿蓝(RGB)光谱低强度光照、全光谱高强度光照、RGB光谱高强度光照环境中进行培养,连续光照24、48 h后进行检测.利用WST-1法检测各处理组之间RPE 细胞增殖率的改变,用高效液相色谱法(HPLC)检测多巴胺分泌水平.用one-way ANOVA对实验数据进行统计学分析.结果 WST-1检测结果显示:连续光照24h后,低强度光照下的全光谱光照与RGB 光谱光照对RPE细胞增殖率的影响差异无统计学意义:而在高强度光照下,全光谱光照组的RPE细胞增殖率低于RGB光谱光照组(P<0.05).连续光照48 h后,无论在哪种光照强度下,全光谱光照比RGB光谱光照更能抑制RPE细胞的增殖(P均<0.01).HPLC检测结果显示:连续光照24 h后,低强度光照下的全光谱光照与RGB光谱光照相比,对RPE细胞分泌多巴胺功能的影响差异无统计学意义;而在高强度光照下,全光谱光照组的RPE细胞分泌多巴胺的水平高于RGB光谱光照组(P<0.01).连续光照48 h后,同一光照强度下,全光谱光照组RPE细胞分泌多巴胺的水平高于RGB光谱光照组(P均<0.05).结论 光的光谱组成也是调控RPE细胞分泌多巴胺的重要因素之一,这种调控作用与光照强度和光照时间密切相关.在评估光延缓近视发生发展的作用时应该考虑光的光谱组成.
目的 探索不同光譜組成的光照射對體外培養的視網膜色素上皮(RPE)細胞分泌多巴胺功能的影響.方法 實驗研究.在細胞培養箱內建立光照繫統後,將體外培養的RPE細胞分彆放置于無光照(對照組)、全光譜低彊度光照、紅綠藍(RGB)光譜低彊度光照、全光譜高彊度光照、RGB光譜高彊度光照環境中進行培養,連續光照24、48 h後進行檢測.利用WST-1法檢測各處理組之間RPE 細胞增殖率的改變,用高效液相色譜法(HPLC)檢測多巴胺分泌水平.用one-way ANOVA對實驗數據進行統計學分析.結果 WST-1檢測結果顯示:連續光照24h後,低彊度光照下的全光譜光照與RGB 光譜光照對RPE細胞增殖率的影響差異無統計學意義:而在高彊度光照下,全光譜光照組的RPE細胞增殖率低于RGB光譜光照組(P<0.05).連續光照48 h後,無論在哪種光照彊度下,全光譜光照比RGB光譜光照更能抑製RPE細胞的增殖(P均<0.01).HPLC檢測結果顯示:連續光照24 h後,低彊度光照下的全光譜光照與RGB光譜光照相比,對RPE細胞分泌多巴胺功能的影響差異無統計學意義;而在高彊度光照下,全光譜光照組的RPE細胞分泌多巴胺的水平高于RGB光譜光照組(P<0.01).連續光照48 h後,同一光照彊度下,全光譜光照組RPE細胞分泌多巴胺的水平高于RGB光譜光照組(P均<0.05).結論 光的光譜組成也是調控RPE細胞分泌多巴胺的重要因素之一,這種調控作用與光照彊度和光照時間密切相關.在評估光延緩近視髮生髮展的作用時應該攷慮光的光譜組成.
목적 탐색불동광보조성적광조사대체외배양적시망막색소상피(RPE)세포분비다파알공능적영향.방법 실험연구.재세포배양상내건립광조계통후,장체외배양적RPE세포분별방치우무광조(대조조)、전광보저강도광조、홍록람(RGB)광보저강도광조、전광보고강도광조、RGB광보고강도광조배경중진행배양,련속광조24、48 h후진행검측.이용WST-1법검측각처리조지간RPE 세포증식솔적개변,용고효액상색보법(HPLC)검측다파알분비수평.용one-way ANOVA대실험수거진행통계학분석.결과 WST-1검측결과현시:련속광조24h후,저강도광조하적전광보광조여RGB 광보광조대RPE세포증식솔적영향차이무통계학의의:이재고강도광조하,전광보광조조적RPE세포증식솔저우RGB광보광조조(P<0.05).련속광조48 h후,무론재나충광조강도하,전광보광조비RGB광보광조경능억제RPE세포적증식(P균<0.01).HPLC검측결과현시:련속광조24 h후,저강도광조하적전광보광조여RGB광보광조상비,대RPE세포분비다파알공능적영향차이무통계학의의;이재고강도광조하,전광보광조조적RPE세포분비다파알적수평고우RGB광보광조조(P<0.01).련속광조48 h후,동일광조강도하,전광보광조조RPE세포분비다파알적수평고우RGB광보광조조(P균<0.05).결론 광적광보조성야시조공RPE세포분비다파알적중요인소지일,저충조공작용여광조강도화광조시간밀절상관.재평고광연완근시발생발전적작용시응해고필광적광보조성.
Objective To investigate the effect of different spectral compositions of light on the release of dopamine by human retinal pigment epithelial (RPE) cells in vitro.Methods Experimental study.Cultured human RPE cells (RPE-19) were exposed to either full spectrum light or red,green,blue (RGB) spectrum light in the intensities of either 4000 lx or 1000 lx.Cells exposed to no light irradiation were used as the control.Cells were assayed at 24 hours and 48 hours for the secretion of dopamine using high performance liquid chromatography (HPLC) and cell viability by WST-1 (a sodium salt of 4-[3-4-iodophynyl)-2-(4-nitrophenyl)-2H-5-tetrazolio]-1,3-benzene disulfonate assay).Data were analyzed using one-way ANOVA.Results There was no statistical significance in the difference of proliferation rates between the full spectrum group and the RGB group at 1000 lx for the first 24 hours,while the difference was statistically significant at the 4000 lx level (P<0.05).In contrast,full spectrum light significantly suppressed the proliferation of cells compared to RGB light at 48 hours,both in the low and high light intensities (both P<0.01).After 24 hours treatment,the difference in the concentration of dopamine was not significant between the full spectrum group and the RGB group at an intensity of 1000 lx,while the difference was statistically significant at 4000 lx (P<0.01).Furthermore,the concentration of dopamine at 48 hours was higher in the full spectrum groups than in the RGB groups at both intensity levels (both P<0.05).Conclusion The present study found that the spectral composition of light is involved in regulating the release of dopamine by RPE and the effect was closely correlated with light intensity and time.These results demonstrate the importance of considering spectral composition when investigating sunlight's protective effect against the development of myopia.