Beutel Julia, Schroder Christina, von Hof Katharina, Rades Dirk, Kosmehl Hartwig, Wedel Thilo, Sieg Peter, Geerling Gerd, Hakim Samer George
Department of Ophthalmology, University Hospital Schleswig-Holstein, Luebeck, Germany.
Graefes Arch Clin Exp Ophthalmol. 2007 Sep;245(9):1347-55. doi: 10.1007/s00417-007-0548-y. Epub 2007 Feb 21.
To evaluate the radioprotective effect of lidocaine, amifostine and pilocarpine on lacrimal glands.
Twenty-five rabbits were randomized into five groups: the control, irradiated/sham-treated, irradiated/lidocaine-pretreated, irradiated/amifostine-pretreated and irradiated/pilocarpine-pretreated groups. One week before irradiation, 72 h and 1 month afterward, the inferior lacrimal gland was investigated histomorphologically, immunohistochemically [tenascin-C and alpha smooth muscle actin (alpha-SMA)] and functionally using scintigraphy and the Schirmer test.
Compared with control animals, the lacrimal ejection fraction (LEF) in the irradiated/sham-treated group was significantly reduced 72 h afterwards. Pilocarpine- as well as amifostine-pretreated animals showed a slightly lower reduction. Lidocaine stabilized the LEF. Immunohistochemically, a significant loss of alpha-SMA and an up-regulation of tenascin-C expression in irradiated/untreated glands were evident. Pretreatment with lidocaine and amifostine-but not with pilocarpine-induced lower up-regulation of TN-C expression 72 h after radiation. One month after irradiation a reduction of the immunhistochemical changes at all was found. Ultrastructural damage was observed in irradiated/non-treated and pilocarpine-pretreated glands, whereas lidocaine and amifostine preserved the ultrastructure.
Morphologic and functional findings could prove a prevailing protection profile of amifostine and especially of lidocaine on lacrimal glands. This may provide a prophylactic approach in the radioprotection of the lacrimal glands during radiotherapy of the orbital region.
评估利多卡因、氨磷汀和毛果芸香碱对泪腺的辐射防护作用。
将25只兔子随机分为五组:对照组、照射/假处理组、照射/利多卡因预处理组、照射/氨磷汀预处理组和照射/毛果芸香碱预处理组。在照射前一周、照射后72小时和1个月,对泪腺进行组织形态学、免疫组织化学(肌腱蛋白-C和α平滑肌肌动蛋白(α-SMA))研究,并通过闪烁扫描和Schirmer试验进行功能研究。
与对照动物相比,照射/假处理组的泪腺排出分数(LEF)在72小时后显著降低。毛果芸香碱和氨磷汀预处理的动物降低幅度略小。利多卡因使LEF稳定。免疫组织化学显示,照射/未处理的腺体中α-SMA显著减少,肌腱蛋白-C表达上调。利多卡因和氨磷汀预处理,但毛果芸香碱预处理未诱导辐射后72小时TN-C表达上调幅度降低。照射后1个月,发现免疫组织化学变化总体减少。在照射/未处理和毛果芸香碱预处理的腺体中观察到超微结构损伤,而利多卡因和氨磷汀保留了超微结构。
形态学和功能学研究结果可证明氨磷汀,尤其是利多卡因对泪腺具有显著的保护作用。这可能为眼眶区域放射治疗期间泪腺的辐射防护提供一种预防性方法。