Gomes Lessandra Esper Abdala, Dalmarco Eduardo Monguilhott, André Edison Sanfelice
1 Laboratório de Fisioterapia Neurológica Experimental (LFNE), Departamento de Fisioterapia, Universidade Regional de Blumenau (FURB) , Blumenau, Brazil .
Photomed Laser Surg. 2012 Nov;30(11):642-7. doi: 10.1089/pho.2012.3242. Epub 2012 Sep 24.
A robust body of evidence has shown that low-level laser therapy (LLLT) improves peripheral nerve regeneration. However, the biochemical background triggered in this process is not yet fully understood.
The purpose of this study was to evaluate the mRNA expression of neurotrophic factors (brain-derived neurotrophic factor [BDNF], nerve growth factor [NGF], and neurotrophin-3, [NT-3]) and also an inflammatory marker (induced nitric oxide synthase [iNOS]) in an axonotmesis experimental model after low-level laser therapy.
Thirty-six adult male Wistar rats (250-350 g) were subjected to right sciatic nerve crush injury, and 24 h later, the animals in the three different experimental groups (n=18) were irradiated on a daily basis with helium-neon laser (collimated HeNe laser, continuous emission, wavelength: 632.8 nm, power density: 0.5 mW/cm(2), irradiation time: 20 sec, energy density: 10 J/cm(2)) during 7, 14, and 21 consecutive days, respectively. The control group (n=18) underwent the same procedures, but with the equipment turned off. At the end of the experiments, animals were killed with an overdose of anesthesia to remove samples from the sciatic nerve lesion epicenter to determine the mRNA expression of BDNF, NGF, NT-3 and iNOS enzyme.
Comparisons between groups showed that HeNe laser increased the mRNA expression of both BDNF and NGF factors after 14 days of LLLT, with peak expression at the 21st day. Increase in NT-3 mRNA expression was not observed. In addition, HeNe laser produced iNOS expression reduction, which played an important role in the inflammatory process.
The reported data could have a relevant practical value because LLLT is a noninvasive procedure, and have revealed significant increase in neurotrophic factor expressions and inflammatory process reduction, opening the possibility of using LLLT as an important aid to nerve regeneration process.
大量证据表明,低强度激光疗法(LLLT)可促进周围神经再生。然而,这一过程中引发的生化背景尚未完全明确。
本研究旨在评估低强度激光疗法后轴突断裂实验模型中神经营养因子(脑源性神经营养因子[BDNF]、神经生长因子[NGF]和神经营养素-3[NT-3])的mRNA表达以及一种炎症标志物(诱导型一氧化氮合酶[iNOS])。
36只成年雄性Wistar大鼠(250 - 350克)右侧坐骨神经遭受挤压损伤,24小时后,三个不同实验组(n = 18)的动物分别在连续7天、14天和21天每天接受氦氖激光照射(准直氦氖激光,连续发射,波长:632.8纳米,功率密度:0.5毫瓦/平方厘米,照射时间:20秒,能量密度:10焦/平方厘米)。对照组(n = 18)进行相同操作,但设备关闭。实验结束时,过量麻醉处死动物,从坐骨神经损伤中心采集样本,以测定BDNF、NGF、NT-3和iNOS酶的mRNA表达。
组间比较显示,低强度激光疗法14天后,氦氖激光增加了BDNF和NGF因子的mRNA表达,在第21天达到峰值表达。未观察到NT-3 mRNA表达增加。此外,氦氖激光使iNOS表达降低,这在炎症过程中起重要作用。
所报道的数据可能具有重要的实际价值,因为低强度激光疗法是一种非侵入性程序,且已显示神经营养因子表达显著增加以及炎症过程减轻,这为将低强度激光疗法用作神经再生过程的重要辅助手段开辟了可能性。