Aydin Bahri, Dinç Erdem, Yilmaz S Necat, Altiparmak U Emrah, Yülek Fatma, Ertekin Sevda, Yilmaz Mustafa, Yakın Mehmet
Department of Ophthalmology, Faculty of Medicine, Gazi University , Ankara , Turkey .
Cutan Ocul Toxicol. 2014 Sep;33(3):192-6. doi: 10.3109/15569527.2013.832282. Epub 2013 Oct 22.
This study evaluates retinal toxicity due to endoillumination with the light-emitting diode (LED) light source in comparison to endoillumination with xenon light source.
Twenty-five eyes of 14 New Zealand pigmented rabbits were used in the study. The LED light (Omesis Medical Systems, Turkey) group was composed of 7 right eyes, while the other 7 right eyes constituted the xenon group (420 nm filter, 357mW/cm(2)) (Bright Star; DORC, Zuidland, Netherlands). Eleven untreated left eyes composed the control group. Twenty gauge pars plana incision 1.5 mm behind the limbus was performed in the right eyes. Twenty gauge bullet type fiberoptic endoilluminator was inserted into the eye from the incision without any pars plana vitrectomy. Fiberoptic endoilluminator was placed in such a way that it was directed toward visual streak of the rabbit retina with a 5 mm distance to retinal surface. Endoillumination was then applied for 20 min with a maximum light intensity for LED and xenon light. In left control eyes, no surgical procedure and no endoillumination were performed. One week after the endoillumination procedure, both eyes of the rabbits were enucleated following electroretinography. Sections stained with hematoxylin and eosin to evaluate morphologic changes. Retina tissues were assessed by active caspase-3 staining.
There was no difference in the shape of the waveforms recorded in the eyes endoilluminated with LED light and xenon light sources compared to control eyes both before and after endoillumination application (p > 0.05). Microscopic evaluation of the retinas with hematoxylin and eosin staining demonstrated that all study groups have normal histologic properties similar to control group. No apoptosis positive cells were found within all sections in all groups.
When the LED light source is used with maximum power and limited duration for endoillumination in rabbit eyes it does not produce phototoxic effects that may be detectable by electrophysiology and histology similar to xenon light.
本研究评估与氙光源眼内照明相比,发光二极管(LED)光源眼内照明引起的视网膜毒性。
本研究使用了14只新西兰有色家兔的25只眼。LED灯组(土耳其Omesis医疗系统公司)由7只右眼组成,另外7只右眼构成氙灯组(420nm滤光片,357mW/cm²)(Bright Star;荷兰 Zuidland的DORC公司)。11只未处理的左眼组成对照组。在右眼距角膜缘1.5mm处行20G的睫状体平坦部切口。在未行任何睫状体平坦部玻璃体切除术的情况下,将20G子弹型光纤眼内照明器从切口插入眼内。将光纤眼内照明器放置成指向兔视网膜的视条纹,距视网膜表面5mm。然后分别用LED和氙灯的最大光强度进行20分钟的眼内照明。在左侧对照眼中,未进行任何手术操作和眼内照明。眼内照明术后1周,在视网膜电图检查后摘除家兔的双眼。用苏木精和伊红染色切片以评估形态学变化。通过活性半胱天冬酶-3染色评估视网膜组织。
与对照组相比,在应用眼内照明前后,用LED灯和氙灯照明的眼所记录的波形形状没有差异(p>0.05)。用苏木精和伊红染色对视网膜进行显微镜评估表明,所有研究组的组织学特性均与对照组相似,均正常。所有组的所有切片中均未发现凋亡阳性细胞。
当在兔眼中以最大功率和有限持续时间使用LED光源进行眼内照明时,它不会产生类似于氙灯的、可通过电生理学和组织学检测到的光毒性作用。