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首页> 外文期刊>Photodiagnosis and Photodynamic Therapy >Influence of non-irradiated and ultraviolet-A-irradiated N,N-dialanyl protoporphyrin and diarginine diprotoporphyrinate on the neutrophil respiratory burst in vitro
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Influence of non-irradiated and ultraviolet-A-irradiated N,N-dialanyl protoporphyrin and diarginine diprotoporphyrinate on the neutrophil respiratory burst in vitro

机译:非辐照和紫外线A辐照的N,N-二丙氨酰原卟啉和双精氨酸二原卟啉对体外嗜中性粒细胞呼吸爆发的影响

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摘要

N,N-Dialanyl protoporphyrin (PP(Ala)_2) and diarginine diprotoporphyrinate (PP(Arg)_2) are porphyrin photosensitizers that are currently being used in the photodynamic therapy (PDT) of cancer. In the present study, the effects of these agents on the neutrophil respiratory burst in vitro were investigated. In the case of non-stimulated neutrophils, the respiratory burst was significantly increased in the presence of PP(Ala)_2 in concentration 5.0 mg/l, while in the presence of PP(Arg)_2 in the same concentration it did not change. By contrast, both photosensitizers decreased a respiratory burst by neutrophils stimulated with opsonized zymosan. Pre-irradiation of solutions of PP(Ala)_2 and PP(Arg)_2 with ultraviolet A did not alter the observed responses. The prooxidative effect of PP(Ala)_2 is probably due to the stimulation of protein kinase C, which plays a key role in the respiratory burst of non-stimulated cells, whereas the antioxidant effect of both photosensitizers may be explained by their inhibitory effect on EGFR tyrosine kinase, which plays an important role in the respiratory burst of cells stimulated by opsonized zymosan. The lack of effect of the two dyes after UV-A pre-irradiation may be due to rapid self-quenching of UV-A-excited dye molecules to the ground state. The results of this study provide a starting point for experiments in animal models aimed at determining the clinical importance of the observed effects in cancer diagnosis and therapy.
机译:N,N-二丙氨酰原卟啉(PP(Ala)_2)和精氨酸二原卟啉(PP(Arg)_2)是卟啉光敏剂,目前正用于癌症的光动力疗法(PDT)。在本研究中,研究了这些药物对体外嗜中性粒细胞呼吸爆发的影响。在非刺激性中性粒细胞的情况下,在浓度为5.0 mg / l的PP(Ala)_2存在下,呼吸爆发明显增加,而在浓度相同的PP(Arg)_2存在下,呼吸爆发没有改变。相比之下,两种光敏剂均减少了由调理酵母聚糖刺激的嗜中性粒细胞的呼吸爆发。 PP(Ala)_2和PP(Arg)_2溶液用紫外线A的预辐照不会改变观察到的响应。 PP(Ala)_2的促氧化作用可能是由于蛋白激酶C的刺激,蛋白激酶C在非刺激细胞的呼吸爆发中起关键作用,而这两种光敏剂的抗氧化作用可能是由于它们的抑制作用所致。 EGFR酪氨酸激酶,在调理性酵母聚糖刺激的细胞呼吸爆发中起重要作用。 UV-A预辐照后两种染料的作用不足可能是由于UV-A激发的染料分子快速自淬灭至基态。这项研究的结果为动物模型中的实验提供了一个起点,旨在确定观察到的效应在癌症诊断和治疗中的临床重要性。

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