Fonseca Adenilson S, Moreira Thiago O, Paixão Deise L, Farias Fernanda M, Guimarães Oscar R, de Paoli Severo, Geller Mauro, de Paoli Flavia
Departamento de Ciências Fisiológicas, Instituto Biomédico, Universidade Federal do Estado do Rio de Janeiro, Rua Frei Caneca, 94, Rio de Janeiro 20211040, Brazil.
Lasers Surg Med. 2010 Aug;42(6):481-8. doi: 10.1002/lsm.20921.
Whereas the biostimulative effect on tissues using low intensity laser therapy for treating many diseases has been described, the photobiological basis and adverse effects are not well understood. The aim of this study, using experimental models, is to observe the combined effect of physical damage (laser) and a chemical agent (hydrogen peroxide) on Escherichia coli cultures and bacterial plasmids.
Survival of E. coli AB1157 (wild type) and BW9091 (xth(-)) cultures were used as an experimental model to assess the effect of agents on DNA, also agarose gel electrophoretic profile of bacterial plasmids for studying single and double strand breaks in DNA exposed to laser irradiation and in DNA pre-exposed to laser and subsequently incubated with hydrogen peroxide.
Data indicate low intensity laser: (i) did not alter the survival of E. coli cultures, (ii) pre-exposure had a protective effect against lethal action of hydrogen peroxide on E. coli cultures, and (iii) did not alter the electrophoretic profile and action of hydrogen peroxide on plasmids. This suggests that low intensity therapeutic red laser doses at different emission modes induces sub-lethal effects on E. coli wild type and exonuclease III mutant cultures inducing protective mechanisms against lethal action of hydrogen peroxide. Laser action on bacterial plasmids is related to lesions other than single or double DNA strands breaks.
This study shows a protective effect or DNA repair mechanism induction by pre-exposure to low intensity red laser on the lethal action of oxidant agents and, therefore, laser therapy protocol should consider fluencies, wavelength and tissue conditions before beginning treatment.
尽管低强度激光疗法对组织的生物刺激作用已被用于多种疾病的治疗,但光生物学基础和不良反应仍未得到充分理解。本研究旨在通过实验模型观察物理损伤(激光)和化学试剂(过氧化氢)对大肠杆菌培养物和细菌质粒的联合作用。
使用大肠杆菌AB1157(野生型)和BW9091(xth(-))培养物的存活率作为实验模型来评估试剂对DNA的影响,同时利用细菌质粒的琼脂糖凝胶电泳图谱研究暴露于激光照射的DNA以及预先暴露于激光并随后与过氧化氢孵育的DNA中的单链和双链断裂情况。
数据表明低强度激光:(i)未改变大肠杆菌培养物的存活率,(ii)预先暴露对过氧化氢对大肠杆菌培养物的致死作用具有保护作用,(iii)未改变过氧化氢对质粒的电泳图谱和作用。这表明不同发射模式下的低强度治疗性红色激光剂量对大肠杆菌野生型和核酸外切酶III突变体培养物产生亚致死效应,诱导针对过氧化氢致死作用的保护机制。激光对细菌质粒的作用与单链或双链DNA断裂以外的损伤有关。
本研究表明预先暴露于低强度红色激光对氧化剂的致死作用具有保护作用或诱导DNA修复机制,因此,激光治疗方案在开始治疗前应考虑通量、波长和组织状况。