Koreck A, Szechenyi A, Morocz M, Cimpean A, Bella Zs, Garaczi E, Raica M, Olariu T R, Rasko I, Kemeny L
Department of Dermatology and Allergology, University of Szeged, P.O. Box 427, H-6701 Szeged, Hungary.
J Photochem Photobiol B. 2007 Dec 14;89(2-3):163-9. doi: 10.1016/j.jphotobiol.2007.09.013. Epub 2007 Oct 5.
Rhinophototherapy has been shown to be effective in the treatment of allergic rhinitis. Considering that phototherapy with ultraviolet light (UV) induces DNA damage, it is of outstanding importance to evaluate the damage and repair process in human nasal mucosa.
We have investigated eight patients undergoing intranasal phototherapy using a modified Comet assay technique and by staining nasal cytology samples for cyclobutane pyrimidine dimers (CPDs), which are UV specific photoproducts.
Immediately after last treatment Comet assay of nasal cytology samples showed a significant increase in DNA damage compared to baseline. Ten days after the last irradiation a significant decrease in DNA damage was observed compared to data obtained immediately after finishing the treatment protocol. Difference between baseline and 10 days after last treatment was not statistically significant. Two months after ending therapy, DNA damage detected by Comet assay in patients treated with intranasal phototherapy was similar with that of healthy individuals. None of the samples collected before starting intranasal phototherapy stained positive for CPDs. In all samples collected immediately after last treatment strong positive staining for CPDs was detected. The number of positive cells significantly decreased 10 days after last treatment, but residual positive staining was present in all the examined samples. This finding is consistent with data reported in skin samples after UV irradiation. Cytology samples examined two months after ending therapy contained no CPD positive cells.
Our results suggest that UV damage induced by intranasal phototherapy is efficiently repaired in nasal mucosa.
鼻光疗已被证明在治疗过敏性鼻炎方面有效。鉴于紫外线(UV)光疗会诱导DNA损伤,评估人体鼻黏膜中的损伤和修复过程具有极其重要的意义。
我们使用改良彗星试验技术并通过对鼻细胞学样本进行环丁烷嘧啶二聚体(CPD)染色(CPD是紫外线特异性光产物),对8名接受鼻内光疗的患者进行了研究。
与基线相比,最后一次治疗后立即对鼻细胞学样本进行彗星试验显示DNA损伤显著增加。与完成治疗方案后立即获得的数据相比,最后一次照射后10天观察到DNA损伤显著减少。基线与最后一次治疗后10天之间的差异无统计学意义。治疗结束两个月后,经鼻内光疗治疗的患者通过彗星试验检测到的DNA损伤与健康个体相似。在开始鼻内光疗前采集的样本中,没有一个CPD染色呈阳性。在最后一次治疗后立即采集的所有样本中,均检测到CPD强阳性染色。最后一次治疗后10天,阳性细胞数量显著减少,但所有检测样本中仍存在残留的阳性染色。这一发现与紫外线照射后皮肤样本中报告的数据一致。治疗结束两个月后检查的细胞学样本中没有CPD阳性细胞。
我们的结果表明,鼻内光疗诱导的紫外线损伤在鼻黏膜中得到有效修复。