
11 minute read
Treating the Body with Low Level Lasers
Treating the Body (Ref-1) dependent activator protein-1 (AP-1) (a heterodimer of c-Fos and c-Jun), nuclear factor kappa B (NF-κB), p53 activating with Low Level Lasers transcription factor/cAMP-response elementbinding protein (ATF/CREB) and hypoxiainducible factor (HIF)-1. 6 As a result of these changes, an increase is seen in cell Robert Sullivan explores the positive effect that proliferation and migration, and modulation in non-thermal low level lasers can have on the body the levels of transcription factor. 2-5 These transcription factors then cause through fat cell management protein synthesis that triggers further effects; cytokines, growth factors, inflammatory Non-thermal low-level laser therapy (NTLLLT) has been in clinical mediators, and increased tissue oxygenation. 2,3 Again, specific use since the late 1960s, 1 and for many years its method of action wavelengths also results in the release of the pro-inflammatory was not fully understood or appreciated. NTLLLT covers a broad cytokine TNF-a from the cells. 8 This leads to increased infiltration of medical spectrum which can be used to the benefit of our patients the tissues by leukocytes. NTLLLT also enhances the proliferation, and the expansion of our clinical practice. NTLLLT is also known maturation, and motility of fibroblasts, and increases the production simply as low-level laser, however the term NTLLLT will be used in of basic fibroblast growth factor. 9,10 According to Chung et al., this article as not all low-level lasers are non-thermal and some are lymphocytes become activated and proliferate more rapidly and misleadingly labelled as so. Patients are not just looking for ways to epithelial cells become more motile, which allow wound sites aesthetically modify their appearance, but many are also looking for to close more quickly, plus the ability of macrophages to act as ways of restoring, re-energising and revitalising their cells. Current phagocytes is also enhanced under the application of NTLLLT. 6 research, as presented in this article, suggests that beauty is no longer skin deep. This short article review demonstrates, in science, that Clinical studies NTLLLT possibly has the ability to restore, rejuvenate, revitalise, and A large number of animal model and clinical studies have re-energise the body, as well as being used for fat cell management. demonstrated highly beneficial NTLLLT effects on a variety of diseases and injuries, and it has been widely used in both chronic How NTLLLT works and acute conditions. NTLLLT may enhance neovascularisation, The biochemical mechanism underlying the therapeutic results of promote angiogenesis and increase collagen synthesis to NTLLLT has a wide range of effects at the molecular, cellular, and promote healing of acute and chronic wounds. 11,12 NTLLLT provided tissue levels. There is strong evidence to suggest that within the acceleration of cutaneous wound healing with a biphasic dose cell, NTLLLT acts on the mitochondria via cytochrome-c (COX) to response favouring lower doses. 13 It can also stimulate healing of increase adenosine triphosphate (ATP) production. This up-regulates deeper structures such as nerves, tendons, cartilage, bones, and mitochondrial respiration and is the energetic component that even internal organs, 14-18 as well as reduce pain, inflammation and produces an energy cascade and electron transport. 2-5 swelling caused by injuries, degenerative diseases or autoimmune Immune cells, in particular, appear to be strongly affected diseases. 19-21 There is an exponential increase in the numbers of by NTLLLT. Mast cells play a crucial role in the movement mitochondrial DNA, somatic stem cells and transcription factor as a of leukocytes and are of large importance in inflammation. result of the laser application, all of which decline in age. 6,22-24 Specific wavelengths of light can trigger mast cell degranulation, modulation of reactive oxygen species (ROS) and free nitric Body contouring and fat cell management oxide (NO), and the induction of transcription factors. Numerous More recently NTLLLT is being used in body contouring and fat cell transcription factors are regulated by changes in cellular redox management because there is no damage to the fat cell. 7 Because state. As described by Chung et al., among them are redox factor-1 fat cells are part of our endocrine system, the release of fat as
Case study The patient depicted in Figure 1 undertook a standard plan of nine treatments over 10 weeks (she was asked to maintain her current exercise and nutritional regiment), using a 532 nm non-thermal low-level green laser. It is important to say that this is a true laser, which is one that is collimated, monochromatic and unidirectional. It delivers a 532 nm linear rotating beam through six heads, four of which are moveable to achieve maximum area coverage. The laser was applied 11-15cm
Advertisement
Before After
Figure 1: A 47-year-old patient before and after eight sessions of NTLLLT treatment
from the skin surface. The heads were distributed to cover the stomach area and thighs, and after 20 minutes the patient is turned over and the heads repositioned in order to continue the treatment; this is a 40-minute protocol. This was carried out the same way for each session and measurements were taken before and after each session with results filed. The picture shows the condition of the patient at the inception of the treatment. As can be seen, there was well dispersed cellulite deposits, large amounts of fat to the stomach, lateral flanks and mid torso. The after image shows improved skin tone, reduction in cellulite and fat.
free fatty acid has no adverse effect on our blood chemistry or triglyceride levels. 25,27 Caruso-Davis et al. conducted a study to examine the clinical effectiveness by which 635-680 nm NTLLLT acts as a non-invasive body contouring intervention method. Results of 40 participants showed a statistically significant cumulative girth loss of 2.15cm after eight 30-minute treatments over four weeks. As a secondary objective, in vitro assays were conducted to determine cell lysis, glycerol and triglyceride release. Three separate experiments were performed to evaluate whether fat loss was induced by irradiation with NTLLLT due to: 7
1. Laser activation of the complement cascade 2. Laser-induced adipocyte death 3. Laser-induced increased triglyceride release or lipolysis from adipocytes
Obtained from subcutaneous fat during abdominal surgery, human adipose-derived stem cells were plated and differentiated to form adipocytes. 28 In the first experiment, results showed that serum complement does lyse fat cells in both irradiated and non-irradiated adipocytes. Consequently, it was determined that NTLLLT does not activate the complement cascade to induce fat loss from adipocytes. 7 In the second experiment, researchers found that irradiation with NTLLLT does not kill adipocytes in both irradiated and non-irradiated groups. 7 The adipocytes maintained intact metabolic functions and the number of viable cells, as measured by the propidium iodide assay, remained the same. Through a dye injected into both groups, calcein levels were lower in the laser-treated group, suggesting reduction of cell-trapped calcein due to leakage. Finally, results of the last experiment showed that irradiation with NTLLLT increased triglyceride release, but not lipolysis from adipocytes. 21 The findings from these three in vitro experiments are consistent with the theory that NTLLLT create pores in adipocytes, and fat leaks into the interstitial space without inducing cell lysis, while further confirming the ability of the laser to influence fat loss. 7 NTLLLT has also shown to provide further clinical benefit to patients, including a reduction in both cholesterol and leptin levels. 1 According to Coll et al., an adipocyte-derived hormone called leptin influences appetite, energy expenditure, and neuroendocrine function. 29 In a two week trial (n=22), Maloney et al. demonstrated a 50% reduction, 29.49 to 14.60 points (P < 0001), in leptin levels after six total treatments of NTLLLT. 1
Summary As a scientist and clinician, I frequently hear patients reporting feelings of more energy, improved health, less pain and better sleep patterns as a result of an increase in cellular activity and function, with better internal body communication. Based on the scientific evidence presented in this article, it is plausible to conclude that NTLLLT improves cellular function and, as supported by the presented evidence, produces within the body, the ability to restore, re-energise and rejuvenate. As we age and lose energy and cellular function, we have within us the chemicals and biological agents for life, health and beauty. NTLLLT may be the way to empower our bodies for a better healthier life.
Robert Sullivan is a progressive podiatrist and surgeon, a Fellow of the Open College of Podiatry, and a Member of the College of Podiatry. He has worked for many years in the fields of non-thermal laser medicine, with experience including advanced education and support in body sculpting, fat loss and obesity management. Qual: DPMed., BSc.(Hons) Pod., MSc. Surg (Edin)., DSc. (IRL)., M.Inst,ChP., FCFhCSc., FIChPA., FSSChP.
REFERENCES
1. Maloney R, Shanks S, Jenney E. The reduction in cholesterol and tri-glyceride serum levels following low-level laser irradiation: A non-controlled, non-randomized pilot study.Laser Surg Med. 2009;21S:66. 2. Karu TI. Primary and secondary mechanisms of action of visible to near-IR radiation on cells. J Photochemical Photobiol B. 1999; 49:1–17. [PubMed: 10365442] 3. Chen AC-H, Arany PR, Huang Y-Y, Tomkinson EM, Saleem T, Yull FE, Blackwell TS, Hamblin MR. Low level laser therapy activates NF-κB via generation of reactive oxygen species in mouse embryonic fibroblasts. Proc SPIE. 2009; 7165:71650–71659. 4. Karu TI, Kolyakov SF. Exact action spectra for cellular responses relevant to phototherapy. Photomed
Laser Surg. 2005; 23:355–361. [PubMed: 16144476] 5. el Sayed OS, Dyson M. Effect of laser pulse repetition rate and pulse duration on mast cell number and degranulation. Lasers Surg Med. 1996; 19:433–437. [PubMed: 8983003] 6. Chung, H., Dai, T., Sharma, S.K. et al. The Nuts and Bolts of Low-level Laser (Light) Therapy. Ann
Biomed Eng 40, 516–533 (2012). https://doi.org/10.1007/s10439-011-0454-7 7. Caruso-Davis MK, Guillot TS, Podichetty VK, et al. Efficacy of low-levellaser therapy for body contouring and spot fat reduction.Obes Surg.2011;21:722-729. 8. Walsh LJ, Trinchieri G, Waldorf HA, Whitaker D, Murphy GF. Human dermal mast cells contain and release tumor necrosis factor-alpha which induces endothelial leukocyte adhesion molecule-1. Proc
Natl Acad Sci USA. 1991; 88:4220–4224. [PubMed: 1709737] 9. Hawkins D, Abrahamse H. Biological effects of helium-neon laser irradiation on normal and wounded human skin fibroblasts. Photomed Laser Surg. 2005; 23:251–259. [PubMed: 15954811] 10. Medrado AR, Pugliese LS, Reis SR, Andrade ZA. Influence of low level laser therapy on wound healing and its biological action upon myofibroblasts. Lasers Surg Med. 2003; 32:239–244. [PubMed: 12605432] 11. Hopkins JT, McLoda TA, Seegmiller JG, and David Baxter G. 2004. Low-level laser therapy facilitates superficial wound healing in humans: a triple-blind, sham-controlled study. J Athl Train 39:223-229. 12. Yu W, Naim JO, and Lanzafame RJ. 1994. The effect of laser irradiation on the release of bFGF from 3T3 fibroblasts. Photochem Photobiol 59:167-70. 13. Corazza AV, Jorge J, Kurachi C, and Bagnato VS. 2007. Photobiomodulation on the angiogenesis of skin wounds in rats using different light sources. Photomed Laser Surg 25:102-6. 14. Robecchi MG. 2004. Low-power laser biostimulation enhances nerve repair after end- to-side neurorrhaphy: a double-blind randomized study in the rat median nerve model. Lasers Med Sci 19:57-65. 15. Fillipin LI, Mauriz JL, Vedovelli K, Moreira AJ, Zettler CG, Lech O, Marroni NP, and Gonzalez- Gallego J. 2005. Low-level laser therapy (LLLT) prevents oxidative stress and reduces fibrosis in rat traumatized
Achilles tendon. Lasers Surg Med 37:293-300. 16. Morrone G, Guzzardella GA, Torricelli P, Rocca M, Tigani D, Brodano GB, Fini M, and Giardino R. 2000.
Osteochondral lesion repair of the knee in the rabbit after low-power diode Ga-Al-As laser biostimulation: an experimental study. Artif Cells Blood Substit Immobil Biotechnol 28:321-36. 17. Weber JB, Pinheiro AL, de Oliveira MG, Oliveira FA, and Ramalho LM. 2006. Laser therapy improves healing of bone defects submitted to autologous bone graft. Photomed Laser Surg 24:38-44 18. Shao XH, Yang YP, Dai J, Wu JF, and Bo AH. 2005. Effects of He-Ne laser irradiation on chronic atrophic gastritis in rats. World J Gastroenterol 11:3958-61. 19. Bjordal JM, Johnson MI, Lopes-Martins RA, Bogen B, Chow R, and Ljunggren AE. 2007. Short-term efficacy of physical interventions in osteoarthritic knee pain. A systematic review and meta- analysis of randomised placebo-controlled trials. BMC Musculoskelet Disord 8:51. 20. Bjordal JM, Lopes-Martins RA, and Iversen VV. 2006b. A randomised, placebo controlled trial of low level laser therapy for activated Achilles tendinitis with microdialysis measurement of peri- tendinous prostaglandin E2 concentrations. Br J Sports Med 40:76-80; discussion 76-80. 21. Carati CJ, Anderson SN, Gannon BJ, and Piller NB. 2003. Treatment of postmastectomy lymphedema with low-level laser therapy: a double blind, placebo-controlled trial. Cancer 98:1114-22. 22. Farfara, Dorit & Tuby, Hana & Trudler, Dorit & Doron-Mandel, Ella & Maltz, Lidya & Vassar, Robert &
Frenkel, Dan & Oron, Uri. (2014). Low-Level Laser Therapy Ameliorates Disease Progression in a
Mouse Model of Alzheimer’s Disease. Journal of molecular neuroscience: MN. 55. 10.1007/s12031- 014-0354-z. 23. Sun N, Youle RJ, Finkel T. The Mitochondrial Basis of Aging. Mol Cell. 2016 Mar 3;61(5):654-666. doi: 10.1016/j.molcel.2016.01.028. PMID: 26942670; PMCID: PMC4779179. 24. Ciccarone, F., Di Leo, L., Lazzarino, G. et al. Aconitase 2 inhibits the proliferation of MCF-7 cells promoting mitochondrial oxidative metabolism and ROS/FoxO1-mediated autophagic response. Br J
Cancer 122, 182–193 (2020). https://doi.org/10.1038/s41416-019-0641-0 25. Neira R, Arroyave J, Ramirez H, et al. Fat liquefaction: Effect of low-level laser energy on adipose tissue.Plast Reconstr Surg. 2002;110:912-922.26. 26. Karu TI, Afanasyeva NI. Cytochrome c oxidase as primary photoaccep-tor for cultured cells in visible and near IR regions.Dokl Akad Nauk(Mosc). 1995;342:693-695 27. Coelho M, Oliveira T, Fernandes R. Biochemistry of adipose tissue: an endocrine organ. Arch Med
Sci. 2013;9(2):191–200. doi:10.5114/aoms.2013.33181 28. Tsuji W, Rubin JP, Marra KG. Adipose-derived stem cells: Implications in tissue regeneration. World J
Stem Cells. 2014;6(3):312–321. doi:10.4252/wjsc.v6.i3.312 29. Coll AP, Farooqi IS, O’Rahilly S. The hormonal control of food intake. Cell. 2007;129(2):251–262. doi:10.1016/j.cell.2007.04.001