Oliveira Fabiana Aparecida Mayrink, Moraes Ana Carolina Meneghin, Paiva Amanda Povoa, Schinzel Vânia, Correa-Costa Matheus, Semedo Patricia, Castoldi Angêla, Cenedeze Marcos Antonio, Oliveira Roberto Sotto-Maior Fortes, Bastos Marcus Gomes, Câmara Niels Olsen Saraiva, Sanders-Pinheiro Helady
Division of Nephrology, Federal University of Juiz de Fora, Juiz de Fora (UFJF), Brazil.
Photomed Laser Surg. 2012 Dec;30(12):705-13. doi: 10.1089/pho.2012.3272. Epub 2012 Nov 7.
the purpose of this study was to investigate the effect of low-level laser therapy (LLLT) on chronic kidney disease (CKD) in a model of unilateral ureteral obstruction (UUO).
Regardless of the etiology, CKD involves progressive widespread tissue fibrosis, tubular atrophy, and loss of kidney function. This process also occurs in kidney allograft. At present, effective therapies for this condition are lacking. We investigated the effects of LLLT on the interstitial fibrosis that occurs after experimental UUO in rats.
The occluded kidney of half of the 32 Wistar rats that underwent UUO received a single intraoperative dose of LLLT (AlGaAs laser, 780 nm, 22.5 J/cm(2), 30 mW, 0.75 W/cm(2), 30 sec on each of nine points). After 14 days, renal fibrosis was assessed by Sirius red staining under polarized light. Immunohistochemical analyses quantitated the renal tissue cells that expressed fibroblast (FSP-1) and myofibroblast (α-SMA) markers. Reverse transcriptase polymerase chain reaction (RT-PCR) was performed to determine the mRNA expression of interleukin (IL)-6, monocyte chemotactic protein-1 (MCP-1), transforming growth factor (TGF)-β1 and Smad3.
The UUO and LLLT animals had less fibrosis than the UUO animals, as well having decreased expression inflammatory and pro-fibrotic markers.
For the first time, we showed that LLLT had a protective effect regarding renal interstitial fibrosis. It is conceivable that by attenuating inflammation, LLLT can prevent tubular activation and transdifferentiation, which are the two processes that mainly drive the renal fibrosis of the UUO model.
本研究旨在探讨低强度激光疗法(LLLT)对单侧输尿管梗阻(UUO)模型中慢性肾脏病(CKD)的影响。
无论病因如何,CKD都涉及进行性广泛的组织纤维化、肾小管萎缩和肾功能丧失。这种过程也发生在肾移植中。目前,针对这种病症缺乏有效的治疗方法。我们研究了LLLT对大鼠实验性UUO后发生的间质纤维化的影响。
32只接受UUO的Wistar大鼠中,一半大鼠的梗阻肾脏在术中接受单次剂量的LLLT(铝镓砷激光,780纳米,22.5焦耳/平方厘米,30毫瓦,0.75瓦/平方厘米,在九个点上各照射30秒)。14天后,通过偏振光下的天狼星红染色评估肾纤维化。免疫组织化学分析对表达成纤维细胞(FSP-1)和肌成纤维细胞(α-SMA)标志物的肾组织细胞进行定量。进行逆转录聚合酶链反应(RT-PCR)以确定白细胞介素(IL)-6、单核细胞趋化蛋白-1(MCP-1)、转化生长因子(TGF)-β1和Smad3的mRNA表达。
接受UUO和LLLT治疗的动物比仅接受UUO治疗的动物纤维化程度更低,炎症和促纤维化标志物的表达也降低。
我们首次表明LLLT对肾间质纤维化具有保护作用。可以想象,通过减轻炎症,LLLT可以预防肾小管激活和转分化,这是驱动UUO模型肾纤维化的两个主要过程。