| WHAT IS LASER THERAPY
Low Level Laser Therapy (LLLT) is the application
of red light and near infrared radiation over injuries or
lesions to stimulate healing and relive pain without sensation
or side effects.
It is popularly used for the treatment of sports injuries,
several different chronic pain syndromes and non-healing wounds
such as venous and diabetic ulcers.
Many new applications for this treatment are being investigated
including nerve regeneration for spinal chord injuries, and
muscle atrophy for astronauts on long-term space missions.
The new official technical term adopted by NASA and US military
scientists is Photobiomodulation (PBM).
Sunlight ( many different colours)

LED: one colour (monochromatic) and waves
not in phase (non-coherent)

LASER: One colour (monochromatic) and waves
in phase (coherent)
HOW DOES IT WORK?
Tissue regeneration via improved cellular function.
To paraphrase NASA research:
Low-energy photon irradiation by light in the far-red to
near-IR spectral range with low-energy lasers or LED arrays
has been found to modulate various biological processes in
cell culture and animal models. This phenomenon of photobiomodulation
has been applied clinically in the treatment of soft tissue
injuries and the acceleration of wound healing. The mechanism
of photobiomodulation by red to near-IR light at the cellular
level has been ascribed to the activation of mitochondrial
respiratory chain components, resulting in initiation of a
signalling cascade that promotes cellular proliferation and
cytoprotection.
A growing body of evidence suggests that cytochrome oxidase
is a key photoacceptor of light in the far-red to near-IR
spectral range. Cytochrome oxidase is an integral membrane
protein that contains four redox active metal centers and
has a strong absorbance in the far-red to near-IR spectral
range detectable in vivo by near-IR spectroscopy.
Moreover, 660--680 nm of irradiation has been shown to increase
electron transfer in purified cytochrome oxidase, increase
mitochondrial respiration and ATP synthesis in isolated mitochondria,
and up-regulate cytochrome oxidase activity in cultured neuronal
cells.
LED photostimulation induces a cascade of signalling events
initiated by the initial absorption of light by cytochrome
oxidase. These signalling events may include the activation
of immediate early genes, transcription factors, cytochrome
oxidase subunit gene expression, and a host of other enzymes
and pathways related to increased oxidative metabolism.
In addition to increased oxidative metabolism, red to near-IR
light stimulation of mitochondrial electron transfer is known
to increase the generation of reactive oxygen species. These
mitochondrially generated reactive oxygen species may function
as signalling molecules to provide communication between mitochondria
and the cytosol and nucleus.
Therapeutic photobiomodulation for methanol-induced retinal
toxicity. Proceedings of the National Academy of Sciences
USA. 2003 Mar 18; 1 00(6):3439-44.
(Above) Harry Whelan (NASA) & Juanita Anders (US Navy
research)
PBM CLINICAL RESEARCH
WHY PBM IS A VALID MEANS OF TREATING ACUPOINTS
Acu-points / trigger points are traditionally deactivated
via massage, ischaemic pressure or acupressure techniques,
ice and stretch
PBM is an increasingly accepted form of non-invasive stimulation
of acu-points particularly in patients where risk factors
(HIV, nervousness, the young or blood conditions) restrict
the use of invasive techniques
PBM stimulates ATP, affects membrane permeability and calcium
ion concentrations. Simons and Trevell's trigger point model
suggests that PBM can therefore also be used as an alternative
form of stimulation or deactivation of acu-points.
CLINICAL APPLICATIONS
PAIN MANAGEMENT
SOFT TISSUE INJURIES
- HAEMATOMAS
- ACUTE BACK / NECK PAIN
- SPRAINS + STRAINS
JOINT CONDITIONS
RA
CAPSULITIS, BURSITIS
TENDONITIS, TENOSYNOVITIS
C.M.P
SI JOINT PAIN
FRACTURES
SMALL BONE
NONUNION
CLINICAL APPLICATIONS
CHRONIC PAIN / DYSFUNCTION
LUMBAR AND CERVICAL SPONDYLOSIS
RSI
PLANTAR FASCIITIS
BELLS PALSY
TRIGEMMINAL NEURALGIA
PHN
CARPAL / TARSAL TUNNEL SYNDROME
SHIN SPLINTS
FROZEN SHOULDER
TMJ SYNDROME
PHANTOM LIMB PAIN
METATARSALGIA
CLINICAL APPLICATIONS
WOUND MANAGEMENT
ULCERS
VARICOSE
DIABETIC
NEUROPATHIC
ISCHAEMIC
MALIGNANT
PRESSURE SORES
POST OP- SKIN GRAFTS
TENDON REPAIRS
NON-HEALING WOUNDS
POST OP OEDEMA
POST OP PAIN
INFECTED WOUNDS
BURNS
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