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Updated: Jun 18, 2025

A Protocol for Transcranial Photobiomodulation Therapy in Mice
Published on: November 18, 2018
Photobiomodulation therapy mitigates depressive-like behaviors by remodeling synaptic links and mitochondrial
Hongli Chen1, Xinyu Shi2, Na Liu2
1State Key Laboratry of Separation Membrane and Membrane Process & Tianjin Key Laboratory of Optoelectronic Detection Technology and Systems, School of Life Sciences, Tiangong University, Tianjin 300387, China; Academy of Medical Engineering and Translational Medicine, Medical College, Tianjin University, Tianjin 300072, China.
Photobiomodulation (PBM) using 468 nm light improved depression-like behaviors in mice by reducing neuroinflammation and apoptosis. This non-invasive treatment rejuvenates hippocampal synaptic function, offering a promising therapeutic approach for depression.
Area of Science:
- Neuroscience
- Biomedical Engineering
- Psychiatry
Background:
- Depression is a major public health concern with complex underlying mechanisms.
- Photobiomodulation (PBM) shows therapeutic potential for depression, but its cellular effects are not fully understood.
- The chronic unpredictable mild stress (CUMS) model is widely used to study depression-like behaviors in rodents.
Purpose of the Study:
- To investigate the effects of 468 nm Photobiomodulation (PBM) on depression-like behavior and neuronal damage in a CUMS mouse model.
- To explore the molecular and cellular mechanisms underlying PBM's efficacy in treating depression.
- To assess PBM's impact on neuroinflammation, apoptosis, and synaptic function in the hippocampus.
Main Methods:
- Utilized the chronic unpredictable mild stress (CUMS) murine model to induce depression-like phenotypes.
- Administered Photobiomodulation (PBM) with 468 nm light to CUMS mice.
- Conducted in vitro experiments on corticosterone-induced hippocampal neuron injury models.
- Assessed behavioral deficits, neuroinflammation, apoptosis, oxidative stress, mitochondrial function, and brain-derived neurotrophic factor (BDNF) signaling pathways.
Main Results:
- PBM treatment significantly ameliorated depression-like behaviors in CUMS mice.
- PBM inhibited neuroinflammation and apoptosis in the hippocampus.
- PBM rejuvenated hippocampal synaptic function, potentially via up-regulation of BDNF signaling pathways.
- In vitro studies showed PBM reduced oxidative stress and improved mitochondrial function in injured hippocampal neurons.
Conclusions:
- Photobiomodulation (PBM) with 468 nm light is a promising non-invasive treatment for depression.
- PBM exerts its therapeutic effects by mitigating neuroinflammation, apoptosis, and oxidative stress, while enhancing synaptic function and mitochondrial health.
- The findings provide insights into the biological mechanisms of PBM for depression and suggest its potential for clinical application.
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