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己基氨基乙酰丙酸诱导的原卟啉IX在大鼠膀胱癌中的体内光漂白动力学及上皮生物分布

In vivo photobleaching kinetics and epithelial biodistribution of hexylaminolevulinate-induced protoporphyrin IX in rat bladder cancer.

作者信息

El Khatib Sami

机构信息

Department of Biological Sciences, Lebanese International University, Bekaa Campus, Khiyara, Lebanon.

出版信息

Curr Urol. 2021 Mar;15(1):2-10. doi: 10.1097/CU9.0000000000000004. Epub 2021 Mar 29.

DOI:10.1097/CU9.0000000000000004
PMID:34084115
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8137026/
Abstract

In a previous paper, we showed that rat bladder instillations with 8 or 16 mM of hexyl aminolevulinate (hALA) result in diametrically opposed photodynamic therapy efficiency. Although the same fluorescent intensities were detected spectroscopically and by fluorescent microscopy in both conditions, while a given light dose resulted in tumor necrosis with an intact bladder wall after 8 mM hALA, bladders instilled with 16 mM showed total wall necrosis without impact on the tumor. The current study investigated the photobleaching and localization pattern of protoporphyrin IX (PpIX) after both hALA intravesical instillations in tumor-bearing rat bladders. The total PpIX content was evaluated by the extraction of postmortem whole bladders. Photobleaching was evaluated in vivo by fluorescent spectroscopy. Cryosections of bladders were subjected to fluorescent microscopy for cellular localization of the photosensitizer. PpIX extraction showed identical amounts of photosensitizer in tumor-bearing bladders at both concentrations. Photobleaching experiments revealed mono-exponential decay curves in both situations but with a two times faster decay constant in 16 mM bladders. Fluorescent microscopy showed an identical fluorescent pattern for normal bladders at both concentrations and tumor bladders at 8 mM with bright spots. Tumor bladders at 16 mM exhibited a more diffuse cytoplasmatic fluorescent distribution. The different response to photodynamic therapy with regard to the initial pro-drug concentration can thus be attributed to the different cellular localizations.

摘要

在之前的一篇论文中,我们表明用8或16毫摩尔的己基氨基乙酰丙酸(hALA)对大鼠膀胱进行灌注会导致截然不同的光动力治疗效果。尽管在这两种情况下通过光谱学和荧光显微镜检测到相同的荧光强度,然而当给予一定光剂量时,8毫摩尔hALA灌注后肿瘤坏死而膀胱壁完整,而灌注16毫摩尔hALA的膀胱则显示全壁坏死且对肿瘤无影响。本研究调查了在荷瘤大鼠膀胱中进行两种hALA膀胱内灌注后原卟啉IX(PpIX)的光漂白和定位模式。通过对死后整个膀胱的提取来评估总PpIX含量。通过荧光光谱法在体内评估光漂白情况。对膀胱冷冻切片进行荧光显微镜检查以确定光敏剂的细胞定位。PpIX提取显示两种浓度下荷瘤膀胱中的光敏剂含量相同。光漂白实验在两种情况下均显示单指数衰减曲线,但在16毫摩尔膀胱中的衰减常数快两倍。荧光显微镜检查显示两种浓度下正常膀胱以及8毫摩尔肿瘤膀胱具有相同的荧光模式,有亮点。16毫摩尔肿瘤膀胱呈现出更弥散的细胞质荧光分布。因此,对于初始前药浓度,光动力治疗的不同反应可归因于不同的细胞定位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a46/8137026/11ba9055c9c9/curr-urol-15-02-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a46/8137026/3c0bb8092d39/curr-urol-15-02-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a46/8137026/622c3f159e4c/curr-urol-15-02-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a46/8137026/480aa277ed83/curr-urol-15-02-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a46/8137026/7041242c1962/curr-urol-15-02-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a46/8137026/cb74959a01ce/curr-urol-15-02-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a46/8137026/d1d802508985/curr-urol-15-02-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a46/8137026/11ba9055c9c9/curr-urol-15-02-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a46/8137026/3c0bb8092d39/curr-urol-15-02-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a46/8137026/622c3f159e4c/curr-urol-15-02-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a46/8137026/480aa277ed83/curr-urol-15-02-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a46/8137026/7041242c1962/curr-urol-15-02-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a46/8137026/cb74959a01ce/curr-urol-15-02-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a46/8137026/d1d802508985/curr-urol-15-02-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a46/8137026/11ba9055c9c9/curr-urol-15-02-g007.jpg

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