{"id":202,"date":"2025-11-06T09:17:26","date_gmt":"2025-11-06T09:17:26","guid":{"rendered":"https:\/\/doctoravida.com\/?p=202"},"modified":"2026-04-18T17:40:14","modified_gmt":"2026-04-18T17:40:14","slug":"terapia-luminica-de-baja-intensidad-fotobiomodulacion","status":"publish","type":"post","link":"https:\/\/doctoravida.com\/en\/terapia-luminica-de-baja-intensidad-fotobiomodulacion\/","title":{"rendered":"Low level light intensity therapy: photobiomodulation"},"content":{"rendered":"

More than 3,000 years ago, ancient Egyptian and Greek texts already referenced the healing properties of sunlight. Herodotus, the founder of heliotherapy, described the benefits of sunlight in treating vitiligo and psoriasis, and its preventative effect on rickets and depressive psychoses.<\/span><\/p>\n

Dr. Niels Ryberg Finsen's studies on the effects of sunlight on cutaneous tuberculosis, which led to his being awarded the Nobel Prize in Medicine in 1903, culminated in his receiving this award. He demonstrated a bactericidal effect of solar radiation along with a regenerative effect on tissues. He also warned of the harmful effects of excessively high doses of radiation on scars, inducing hyperpigmentation secondary to cellular damage in smallpox.<\/span><\/p>\n

In 1967, Hungarian physician Dr. Endre Mester, a few years after the first laser devices were invented, wanted to study whether laser radiation could cause skin cancer in mice. He shaved the backs of mice and then applied laser treatment with a low-power 694nm ruby \u200b\u200blaser. There were no cases of cancer, but he observed that hair grew back more quickly in the mice treated with the low-power laser than in the untreated control group. This was the first practical demonstration of laser biostimulation.\u00a0<\/span><\/p>\n

Subsequently, multiple studies in cell cultures, animal models, and humans have demonstrated that the response to light therapy is inversely dose-dependent: that is, low doses of light energy have a regenerative effect on cells, while high doses can have an inhibitory effect on the cellular response. For this reason, the English term LLLT (low-level light therapy) was coined to describe these therapies in which low doses of energy are converted into metabolic energy, subsequently modulating biological functions, as we will see in the next section. <\/span>Therapy light of low intensity acts by a mechanism of photobiomodulation.<\/span><\/i><\/p>\n

Starting in 1960, NASA researchers began studying the effects of low-intensity light therapy on astronauts subjected to the effects of weightlessness in space. Weightlessness causes slowed wound healing and muscle atrophy in astronauts, effects that could be partially mitigated with light therapy.<\/span><\/p>\n

Low-intensity light therapy is currently used in a wide range of clinical situations. In neonatal jaundice, 460nm blue light is used to accelerate bilirubin breakdown. Light therapy is also currently used in sports medicine, inflammatory joint diseases, neurological disorders, scar healing and skin regeneration, and inflammatory skin diseases.<\/span><\/p>\n

WHAT IS LOW INTENSITY LIGHT THERAPY?<\/strong><\/p>\n

Light is a type of electromagnetic radiation that, according to modern quantum physics, consists of both particles (photons, which are particles or quanta of energy) and waves. The energy of photons depends on the wavelength of the electromagnetic radiation. When photons interact with living tissue, they can be absorbed or reflected. Absorbed photons interact with organic molecules or chromophores, exciting them and causing an electron jump in the peripheral electrons of these chromophores. This energy change in cells is used to alter cellular functions. Low-intensity light therapy works by converting light energy into metabolic energy, with the subsequent modulation of cellular biological function. For this reason, low-intensity light therapy is called <\/span>photobiomodulation.<\/span><\/i> In this respect, it is important to distinguish this therapy from the effects of high-power lasers, in which the tissue absorbs high energies resulting in heating and cell destruction. The energy doses are not high enough to cause heating and cell destruction, but they are sufficient to modulate cellular functions.\u00a0<\/span><\/p>\n

Sunlight is polychromatic, meaning it's a mixture of different wavelengths, ranging from ultraviolet waves, which have shorter wavelengths and penetrate tissue less deeply, to infrared waves, which have longer wavelengths and greater penetrating power. Low-intensity light therapy uses lasers or LEDs (light-emitting diodes) of a specific wavelength that is absorbed by a chromophore, or specific cellular structure, triggering the modulation of biological functions. Lasers are monochromatic, meaning they emit light of a very specific wavelength in a coherent manner (the waves are emitted simultaneously, exhibiting spatial and temporal synchronization). This has the advantage of increasing tissue penetration. LEDs, on the other hand, emit nearly monochromatic light within a narrow wavelength range, typically between 4 and 10 nm. This light is incoherent, meaning waves of the same wavelength are emitted at different times. The incoherence of LED light can be advantageous in low-intensity light therapy because it allows tissue exposure to therapeutic wavelengths at low energy densities for a sufficient duration to modulate cellular metabolism. Another significant advantage of LEDs is their ability to treat much larger areas than lasers. Low-intensity light therapy utilizes wavelengths from the visible spectrum without employing the ultraviolet radiation present in sunlight, which is responsible for skin cancer.<\/span><\/p>\n

In the past, there had been conflicting results regarding the effectiveness of low-intensity light therapy because either energy densities that were too low or too high, irradiances measured in Watts per cm\u00b2 that were too high, exposure times, or wavelengths that were unsuitable. Currently, there is sufficient evidence that if the appropriate light parameters are used, based on the physicochemical properties of the tissue in question, the therapy is effective.<\/span><\/p>\n

It is very important to keep in mind that the effectiveness of the therapy in relation to the energy doses used follows an inverted U-shape. That is, minimum doses are needed to stimulate the cell, but as the dose increases, there comes a point where the effect reverses and an inhibitory effect occurs, as can be seen in the graph.<\/span><\/p>\n

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The most effective energy doses range between 1 and 7 J\/cm2 with irradiances of 5-100 mW\/cm2.<\/span><\/p>\n

MECHANISM OF ACTION<\/strong><\/p>\n

Nature has designed systems to harness electromagnetic radiation for the maintenance of biological functions. The use of electromagnetic radiation is fundamental for the maintenance of life on Earth. Light energy emits photons that, when interacting with certain cellular biomolecules, excite them and thus trigger metabolic processes. Within cells there are <\/span>chromophores<\/span><\/i> that will absorb photonic energy. A chromophore is a molecule or part of a molecule that gives a specific color to the compound it is part of and that will interact with light energy. Examples of chromophores are chlorophyll (used by plants for photosynthesis), hemoglobin in red blood cells, cytochrome c oxidase (the mitochondrial enzyme responsible for converting ADP into ATP used in the Krebs cycle to generate energy), myoglobin in muscles, flavoproteins, and porphyrins. It is interesting to note that all these chromophores share a basic chemical structure similar to that of protoporphyrin. The diagram shows how electromagnetic radiation interacts with chlorophyll in the case of plants and with the mitochondrial enzyme cytochrome c oxidase in the case of animals to stimulate a photochemical reaction that will culminate in photosynthesis in the case of plants and in the mitochondria of animal cells in the generation of energy in the form of ATP.\u00a0<\/span><\/p>\n

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Red or infrared wavelengths are those that produce the greatest biological effect due to their greater absorption by mitochondrial cytochrome c oxidase.\u00a0<\/span><\/p>\n

Studies by Tina Karu and subsequent work have demonstrated that low-intensity light therapy, in addition to increasing cellular ATP, alters the cell's redox potential. This change, in turn, signals the activation of nuclear gene expression, leading to the production of growth factors, cytokines, and enzymes. Light has been found to activate 111 genes. In simplified terms, light activates the mitochondrial enzyme cytochrome oxidase, causing a change in redox potential that stimulates both ATP production and, at low doses, the generation of free radicals. The increase in ATP results in an increase in cAMP and calcium, which, along with free radicals, act as second messengers, stimulating gene expression at the nuclear level. These genes are responsible for the formation of growth factors, anti-inflammatory cytokines, decreased apoptosis (cell death), and increased or decreased activity of various enzymes. So, will light stimulate cellular functions in all cells? No, only cells with a reduced redox state (low or acidic intracellular pH) will respond markedly, while cells in an optimal redox state will not. Therefore, the mechanism of action of this therapy is called photomodulation because it acts by regulating altered cellular functions.\u00a0<\/span><\/p>\n

CLINICAL APPLICATION OF LOW INTENSITY LIGHT THERAPY.<\/strong><\/p>\n

We have observed that light therapy through photobiomodulation regulates metabolism, cell migration, cell proliferation, cellular inflammation, and the synthesis and secretion of various proteins. These properties have been used clinically to stimulate tissue regeneration, treat skin aging, and reduce inflammation and pain.<\/span><\/p>\n