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660nm 和 808nm 低水平激光疗法对骨关节炎实验模型的影响。

Effects of low-level laser therapy at wavelengths of 660 and 808 nm in experimental model of osteoarthritis.

机构信息

Post Graduation Program for Health and Development of the Central-West Region, Federal University of Mato Grosso do Sul, Campo Grande, Mato Grosso do Sul, Brazil.

出版信息

Photochem Photobiol. 2012 Jan-Feb;88(1):161-6. doi: 10.1111/j.1751-1097.2011.01032.x. Epub 2011 Dec 16.

Abstract

The aim of the present study was to analyze the influence of low-level laser radiation at wavelengths of 660 and 808 nm in an experimental model of osteoarthritis (OA). The sample was composed of 36 male adult Wistar rats divided into three groups (G1, G2 and G3). For the induction of cartilage injury, three injections of 4% papain and 10 μL of a cysteine solution were performed at right knee of the hind leg. Two weeks after the last injection, group G1 was treated with InGaAlP (660 nm, 100 mW, 3.57 W cm(-2), 40 s) and G2 was treated with AsGaAl (808 nm, 100 mW, 3.57 W cm(-2), 40 s) both with energy of 4 J. There were significant differences in the type of squamous epithelium between days 7 and 14 in G2 (P < 0.05) and on day 14 between G1 and G2 (P < 0.05). Moreover, statistically significant differences were found in the formation of new blood vessels between G1 and G3 on days 7 and 21 as well as between G2 and G3 on day 21. The formation of fibrotic tissue was greater in G3 (P < 0.05). In conclusion, laser therapy, especially at a wavelength of 808 nm, stimulated angiogenesis and reduced the formation of fibrosis in an experimental model of OA.

摘要

本研究旨在分析低水平激光辐射(波长分别为 660nm 和 808nm)对骨关节炎(OA)实验模型的影响。样本由 36 只雄性成年 Wistar 大鼠组成,分为三组(G1、G2 和 G3)。为了诱导软骨损伤,在后腿的右膝关节处进行了三次 4%木瓜蛋白酶和 10 μL 半胱氨酸溶液的注射。最后一次注射后两周,G1 组接受 InGaAlP(660nm,100mW,3.57W/cm(-2),40s)治疗,G2 组接受 AsGaAl(808nm,100mW,3.57W/cm(-2),40s)治疗,能量均为 4J。G2 组在第 7 天和第 14 天之间以及 G1 组和 G2 组之间在第 14 天之间的鳞状上皮类型存在显著差异(P<0.05)。此外,在第 7 天和第 21 天以及 G2 组和 G3 组之间在第 21 天之间,G1 组和 G3 组之间在新血管形成方面存在统计学显著差异。G3 组的纤维组织形成更大(P<0.05)。总之,激光治疗,特别是波长为 808nm 的激光治疗,在 OA 实验模型中刺激血管生成并减少纤维化的形成。

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