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光生物调节与氧化应激:980nm 半导体激光调节线粒体活性和活性氧产生。

Photobiomodulation and Oxidative Stress: 980 nm Diode Laser Light Regulates Mitochondrial Activity and Reactive Oxygen Species Production.

机构信息

Faculty of Dentistry, Department of Orthopaedic Dentistry, First Moscow State Medical University (Sechenov University), 119991 Moscow, Russia.

Laser Therapy Centre, Department of Surgical and Diagnostic Sciences, University of Genoa, 16132 Genoa, Italy.

出版信息

Oxid Med Cell Longev. 2021 Mar 3;2021:6626286. doi: 10.1155/2021/6626286. eCollection 2021.

DOI:10.1155/2021/6626286
PMID:33763170
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7952159/
Abstract

Photobiomodulation with 808 nm laser light electively stimulates Complexes III and IV of the mitochondrial respiratory chain, while Complexes I and II are not affected. At the wavelength of 1064 nm, Complexes I, III, and IV are excited, while Complex II and some mitochondrial matrix enzymes seem to be not receptive to photons at that wavelength. Complex IV was also activated by 633 nm. The mechanism of action of wavelengths in the range 900-1000 nm on mitochondria is less understood or not described. Oxidative stress from reactive oxygen species (ROS) generated by mitochondrial activity is an inescapable consequence of aerobic metabolism. The antioxidant enzyme system for ROS scavenging can keep them under control. However, alterations in mitochondrial activity can cause an increment of ROS production. ROS and ATP can play a role in cell death, cell proliferation, and cell cycle arrest. In our work, bovine liver isolated mitochondria were irradiated for 60 sec, in continuous wave mode with 980 nm and powers from 0.1 to 1.4 W (0.1 W increment at every step) to generate energies from 6 to 84 J, fluences from 7.7 to 107.7 J/cm, power densities from 0.13 to 1.79 W/cm, and spot size 0.78 cm. The control was equal to 0 W. The activity of the mitochondria's complexes, Krebs cycle enzymes, ATP production, oxygen consumption, generation of ROS, and oxidative stress were detected. Lower powers (0.1-0.2 W) showed an inhibitory effect; those that were intermediate (0.3-0.7 W) did not display an effect, and the higher powers (0.8-1.1 W) induced an increment of ATP synthesis. Increasing the power (1.2-1.4 W) recovered the ATP production to the control level. The interaction occurred on Complexes III and IV, as well as ATP production and oxygen consumption. Results showed that 0.1 W uncoupled the respiratory chain and induced higher oxidative stress and drastic inhibition of ATP production. Conversely, 0.8 W kept mitochondria coupled and induced an increase of ATP production by increments of Complex III and IV activities. An augmentation of oxidative stress was also observed, probably as a consequence of the increased oxygen consumption and mitochondrial isolation experimental conditions. No effect was observed using 0.5 W, and no effect was observed on the enzymes of the Krebs cycle.

摘要

808nm 激光的光生物调节选择性地刺激线粒体呼吸链的复合物 III 和 IV,而复合物 I 和 II 不受影响。在 1064nm 的波长下,复合物 I、III 和 IV 被激发,而复合物 II 和一些线粒体基质酶似乎对该波长的光子没有反应。633nm 也能激活复合物 IV。对线粒体在 900-1000nm 范围内的波长的作用机制了解较少或尚未描述。线粒体活动产生的活性氧物质(ROS)引起的氧化应激是有氧代谢不可避免的后果。ROS 清除的抗氧化酶系统可以控制它们。然而,线粒体活动的改变会导致 ROS 产生的增加。ROS 和 ATP 可以在细胞死亡、细胞增殖和细胞周期停滞中发挥作用。在我们的工作中,牛肝分离的线粒体在连续波模式下用 980nm 照射 60 秒,功率从 0.1 到 1.4W(每步增加 0.1W),产生 6 到 84J 的能量,7.7 到 107.7J/cm 的剂量,0.13 到 1.79W/cm 的功率密度,以及 0.78cm 的光斑大小。对照为 0W。检测了线粒体复合物的活性、三羧酸循环酶、ATP 产生、耗氧量、ROS 的产生和氧化应激。较低的功率(0.1-0.2W)显示出抑制作用;中等功率(0.3-0.7W)没有显示出效果,而较高的功率(0.8-1.1W)诱导 ATP 合成的增加。增加功率(1.2-1.4W)使 ATP 产生恢复到对照水平。这种相互作用发生在复合物 III 和 IV 以及 ATP 产生和耗氧量上。结果表明,0.1W 解偶联呼吸链并诱导更高的氧化应激和 ATP 产生的急剧抑制。相反,0.8W 使线粒体保持偶联,并通过增加复合物 III 和 IV 的活性来增加 ATP 的产生。氧化应激的增加也被观察到,可能是由于耗氧量增加和线粒体分离实验条件的结果。使用 0.5W 时没有观察到效果,三羧酸循环的酶也没有观察到效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dac/7952159/054186a7cf53/OMCL2021-6626286.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dac/7952159/24f47f47f3a3/OMCL2021-6626286.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dac/7952159/9a83c946eb25/OMCL2021-6626286.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dac/7952159/cc65f5df98db/OMCL2021-6626286.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dac/7952159/3af5ed0e18de/OMCL2021-6626286.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dac/7952159/054186a7cf53/OMCL2021-6626286.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dac/7952159/24f47f47f3a3/OMCL2021-6626286.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dac/7952159/9a83c946eb25/OMCL2021-6626286.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dac/7952159/cc65f5df98db/OMCL2021-6626286.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dac/7952159/3af5ed0e18de/OMCL2021-6626286.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dac/7952159/054186a7cf53/OMCL2021-6626286.005.jpg

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