Ver registro no DEDALUS
Exportar registro bibliográfico

Metrics


Metrics:

The effects of exercise training associated with low-level laser therapy on biomarkers of adipose tissue transdifferentiation in obese women (2018)

  • Authors:
  • USP affiliated authors: BAGNATO, VANDERLEI SALVADOR - IFSC
  • USP Schools: IFSC
  • DOI: 10.1007/s10103-018-2465-1
  • Subjects: OBESIDADE; EXERCÍCIO FÍSICO; TREINAMENTO AERÓBIO; LASER
  • Keywords: Phototherapy; Physical exercise; Obesity; Adipose tissue; Browning
  • Agências de fomento:
  • Language: Inglês
  • Imprenta:
  • Source:
  • Acesso online ao documento

    Online accessDOI or search this record in
    Informações sobre o DOI: 10.1007/s10103-018-2465-1 (Fonte: oaDOI API)
    • Este periódico é de assinatura
    • Este artigo NÃO é de acesso aberto
    • Cor do Acesso Aberto: closed

    How to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas

    • ABNT

      CAMPOS, Raquel Munhoz da Silveira; DÂMASO, Ana Raimunda; MASQUIO, Deborah Cristina Landi; et al. The effects of exercise training associated with low-level laser therapy on biomarkers of adipose tissue transdifferentiation in obese women. Lasers in Medical Science, London, Springer, v. 33, n. 6, p. 1245-1254, 2018. Disponível em: < http://dx.doi.org/10.1007/s10103-018-2465-1 > DOI: 10.1007/s10103-018-2465-1.
    • APA

      Campos, R. M. da S., Dâmaso, A. R., Masquio, D. C. L., Duarte, F. O., Sene-Fiorese, M., Aquino Jr, A. E., et al. (2018). The effects of exercise training associated with low-level laser therapy on biomarkers of adipose tissue transdifferentiation in obese women. Lasers in Medical Science, 33( 6), 1245-1254. doi:10.1007/s10103-018-2465-1
    • NLM

      Campos RM da S, Dâmaso AR, Masquio DCL, Duarte FO, Sene-Fiorese M, Aquino Jr AE, Savioli FA, Quintiliano PCL, Kravchychyn ACP, Guimarães LI, Tock L, Oyama LM, Boldarine VT, Bagnato VS, Parizotto NA. The effects of exercise training associated with low-level laser therapy on biomarkers of adipose tissue transdifferentiation in obese women [Internet]. Lasers in Medical Science. 2018 ; 33( 6): 1245-1254.Available from: http://dx.doi.org/10.1007/s10103-018-2465-1
    • Vancouver

      Campos RM da S, Dâmaso AR, Masquio DCL, Duarte FO, Sene-Fiorese M, Aquino Jr AE, Savioli FA, Quintiliano PCL, Kravchychyn ACP, Guimarães LI, Tock L, Oyama LM, Boldarine VT, Bagnato VS, Parizotto NA. The effects of exercise training associated with low-level laser therapy on biomarkers of adipose tissue transdifferentiation in obese women [Internet]. Lasers in Medical Science. 2018 ; 33( 6): 1245-1254.Available from: http://dx.doi.org/10.1007/s10103-018-2465-1

    Referências citadas na obra
    Gold MH, Khatri KA, Hails K, Weiss RA, Fournier N (2011) Reduction in thigh circumference and improvement in the appearance of cellulite with dual-wavelength, low-level laser energy and massage. J Cosmet Laser Ther 13:13–20. https://doi.org/10.3109/14764172.2011.552608
    Jackson RF, Dedo DD, Roche GC, Turok DI, Maloney RJ (2009) Low-level laser therapy as a non-invasive approach for body contouring: a randomized, controlled study. Lasers Surg Med 41:799–809. https://doi.org/10.1002/lsm.20855
    da Silveira Campos RM, Dâmaso AR, Masquio DC et al (2015) Low-level laser therapy (LLLT) associated with aerobic plus resistance training to improve inflammatory biomarkers in obese adults. Lasers Med Sci 30:1553–1563. https://doi.org/10.1007/s10103-015-1759-9
    Duarte FO, Sene-Fiorese M, de Aquino Junior AE et al (2015) Can low-level laser therapy (LLLT) associated with an aerobic plus resistance training change the cardiometabolic risk in obese women? A placebo-controlled clinical trial. J Photochem Photobiol B 153:103–110. https://doi.org/10.1016/j.jphotobiol.2015.08.026
    Sene-Fiorese M, Duarte FO, de Aquino Junior AE et al (2015) The potential of phototherapy to reduce body fat, insulin resistance and “metabolic inflexibility” related to obesity in women undergoing weight loss treatment. Lasers Surg Med 47:634–642. https://doi.org/10.1002/lsm.22395
    Elsen M, Raschke S, Tennagels N et al (2014) BMP4 and BMP7 induce the white-to-brown transition of primary human adipose stem cells. Am J Physiol Cell Physiol 306:C431–C440. https://doi.org/10.1152/ajpcell.00290.2013
    Ouellet V, Labbé SM, Blondin DP et al (2012) Brown adipose tissue oxidative metabolism contributes to energy expenditure during acute cold exposure in humans. J Clin Invest 122:545–552. https://doi.org/10.1172/JCI60433
    Stephens M, Ludgate M, Rees DA (2011) Brown fat and obesity: the next big thing? Clin Endocrinol 74:661–670. https://doi.org/10.1111/j.1365-2265.2011.04018.x
    Cypess AM, Lehman S, Williams G et al (2009) Identification and importance of brown adipose tissue in adult humans. N Engl J Med 360:1509–1517. https://doi.org/10.1056/NEJMoa0810780
    van Marken Lichtenbelt WD, Vanhommerig JW, Smulders NM et al (2009) Cold-activated brown adipose tissue in healthy men. N Engl J Med 360:1500–1508. https://doi.org/10.1056/NEJMoa0808718
    Saito M, Okamatsu-Ogura Y, Matsushita M et al (2009) High incidence of metabolically active brown adipose tissue in healthy adult humans: effects of cold exposure and adiposity. Diabetes 58:1526–1531. https://doi.org/10.2337/db09-0530
    Virtanen KA, Lidell ME, Orava J et al (2009) Functional brown adipose tissue in healthy adults. N Engl J Med 360:1518–1525. https://doi.org/10.1056/NEJMoa0808949
    Zingaretti MC, Crosta F, Vitali A et al (2009) The presence of UCP1 demonstrates that metabolically active adipose tissue in the neck of adult humans truly represents brown adipose tissue. FASEB J 23:3113–3120. https://doi.org/10.1096/fj.09-133546
    Nishida C, Ko GT, Kumanyika S (2010) Body fat distribution and noncommunicable diseases in populations: overview of the 2008 WHO expert consultation on waist circumference and waist-hip ratio. Eur J Clin Nutr 64:2–5. https://doi.org/10.1038/ejcn.2009.139
    Geloneze B, Repetto EM, Geloneze SR, Tambascia MA, Ermetice MN (2006) The threshold value for insulin resistance (HOMA-IR) in an admixtured population IR in the Brazilian Metabolic Syndrome Study. Diabetes Res Clin Pract 72:219–220
    Kraemer WJ, Ratamess NA, French DN (2002) Resistance training for health and performance. Curr Sports Med Rep 1:165–171
    Donnelly JE, Blair SN, Jakicic JM et al (2009) American College of Sports Medicine position stand. Appropriate physical activity intervention strategies for weight loss and prevention of weight regain for adults. Med Sci Sports Exerc 41:459–471. https://doi.org/10.1249/MSS.0b013e3181949333
    Min KH, Byun JH, Heo CY, Kim EH, Choi HY, Pak CS (2015) Effect of low-level laser therapy on human adipose-derived stem cells: in vitro and in vivo studies. Aesthet Plast Surg 39:778–782. https://doi.org/10.1007/s00266-015-0524-6
    Huang YY, Chen AC, Carroll JD, Hamblin MR (2009) Biphasic dose response in low level light therapy. Dose-Response 7:358–383. https://doi.org/10.2203/dose-response.09-027
    Yu HS, Chang KL, Yu CL, Chen JW, Chen GS (1996) Low-energy helium-neon laser irradiation stimulates interleukin-1 alpha and interleukin-8 release from cultured human keratinocytes. J Invest Dermatol 107:593–596
    Conlan MJ, Rapley JW, Cobb CM (1996) Biostimulation of wound healing by low-energy laser irradiation. A review. J Clin Periodontol 23:492–496
    Lo KA, Ng PY, Kabiri Z, Virshup D, Sun L (2016) Wnt inhibition enhances browning of mouse primary white adipocytes. Adipocyte 5:224–231. https://doi.org/10.1080/21623945.2016.1148834
    Jeon M, Rahman N, Kim YS (2016) Wnt/β-catenin signaling plays a distinct role in methyl gallate-mediated inhibition of adipogenesis. Biochem Biophys Res Commun 479:22–27. https://doi.org/10.1016/j.bbrc.2016.08.178
    Chung SS, Lee JS, Kim M (2012) Regulation of Wnt/β-catenin signaling by CCAAT/enhancer binding protein β during adipogenesis. Obesity (Silver Spring) 20:482–487. https://doi.org/10.1038/oby.2011.212
    Prestwich TC, Macdougald OA (2007) Wnt/beta-catenin signaling in adipogenesis and metabolism. Curr Opin Cell Biol 19:612–617
    Rosen ED, Walkey CJ, Puigserver P, Spiegelman BM (2000) Transcriptional regulation of adipogenesis. Genes Dev 14:1293–1307
    Wu Z, Rosen ED, Brun R et al (1999) Cross-regulation of C/EBP alpha and PPAR gamma controls the transcriptional pathway of adipogenesis and insulin sensitivity. Mol Cell 3:151–158
    He X, Semenov M, Tamai K, Zeng X (2004) LDL receptor-related proteins 5 and 6 in Wnt/beta-catenin signaling: arrows point the way. Development 131:1663–1677
    Kawai M, Mushiake S, Bessho K et al (2007) Wnt/Lrp/beta-catenin signaling suppresses adipogenesis by inhibiting mutual activation of PPARgamma and C/EBPalpha. Biochem Biophys Res Commun 363:276–282
    Kimelman D, Xu W (2006) Beta-catenin destruction complex: insights and questions from a structural perspective. Oncogene 25:7482–7491
    Herencia C, Martínez-Moreno JM, Herrera C (2012) Nuclear translocation of β-catenin during mesenchymal stem cells differentiation into hepatocytes is associated with a tumoral phenotype. PLoS One 7:e34656. https://doi.org/10.1371/journal.pone.0034656
    Liu C, Li Y, Semenov M et al (2002) Control of beta-catenin phosphorylation/degradation by a dual-kinase mechanism. Cell 108:837–847
    Gruden G, Landi A, Bruno G (2014) Natriuretic peptides, heart, and adipose tissue: new findings and future developments for diabetes research. Diabetes Care 37:2899–2908. https://doi.org/10.2337/dc14-0669
    Nishikimi T, Kuwahara K, Nakao K (2011) Current biochemistry, molecular biology, and clinical relevance of natriuretic peptides. J Cardiol 57:131–140. https://doi.org/10.1016/j.jjcc.2011.01.002
    Potter LR (2011) Natriuretic peptide metabolism, clearance and degradation. FEBS J 278:1808–1817. https://doi.org/10.1111/j.1742-4658.2011.08082.x
    Sellitti DF, Koles N, Mendonça MC (2011) Regulation of C-type natriuretic peptide expression. Peptides 32:1964–1971. https://doi.org/10.1016/j.peptides.2011.07.013
    Chen-Tournoux A, Khan AM, Baggish AL (2010) Effect of weight loss after weight loss surgery on plasma N-terminal pro-B-type natriuretic peptide levels. Am J Cardiol 106:1450–1455. https://doi.org/10.1016/j.amjcard.2010.06.076
    Bordicchia M, Liu D, Amri EZ et al (2012) Cardiac natriuretic peptides act via p38 MAPK to induce the brown fat thermogenic program in mouse and human adipocytes. J Clin Invest 122:1022–1036. https://doi.org/10.1172/JCI59701
    Miyashita K, Itoh H, Tsujimoto H et al (2009) Natriuretic peptides/cGMP/cGMP-dependent protein kinase cascades promote muscle mitochondrial biogenesis and prevent obesity. Diabetes 58:2880–2892. https://doi.org/10.2337/db09-0393
    Tsukamoto O, Fujita M, Kato M et al (2009) Natriuretic peptides enhance the production of adiponectin in human adipocytes and in patients with chronic heart failure. J Am Coll Cardiol 53(22):2070–2077. https://doi.org/10.1016/j.jacc.2009.02.038
    Osborn O, Olefsky JM (2012) The cellular and signaling networks linking the immune system and metabolism in disease. Nat Med 18:363–374. https://doi.org/10.1038/nm.2627
    El-Kadre LJ, Tinoco AC (2013) Interleukin-6 and obesity: the crosstalk between intestine, pancreas and liver. Curr Opin Clin Nutr Metab Care 16:564–568. https://doi.org/10.1097/MCO.0b013e32836410e6
    Böttcher RT, Niehrs C (2005) Fibroblast growth factor signaling during early vertebrate development. Endocr Rev 26:63–77
    Cuevas-Ramos D, Almeda-Valdes P, Aguilar-Salinas CA, Cuevas-Ramos G, Cuevas-Sosa AA, Gomez-Perez FJ (2009) The role of fibroblast growth factor 21 (FGF21) on energy balance, glucose and lipid metabolism. Curr Diabetes Rev 5:216–220
    Inagaki T, Dutchak P, Zhao G et al (2007) Endocrine regulation of the fasting response by PPARα-mediated induction of fibroblast growth factor 21. Cell Metab 5:415–425
    Fisher FM, Kleiner S, Douris N et al (2012) FGF21 regulates PGC-1α and browning of white adipose tissues in adaptive thermogenesis. Genes Dev 26:271–281. https://doi.org/10.1101/gad.177857.111
    Hondares E, Iglesias R, Giralt A, Gonzalez FJ, Giralt M, Mampel T, Villarroya F (2011) Thermogenic activation induces FGF21 expression and release in brown adipose tissue. J Biol Chem 286:12983–12990. https://doi.org/10.1074/jbc.M110.215889
    Kim KH, Kim SH, Min YK, Yang HM, Lee JB, Lee MS (2013) Acute exercise induces FGF21 expression in mice and in healthy humans. PLoS One 8:e63517. https://doi.org/10.1371/journal.pone.0063517
    Roca-Rivada A, Castelao C, Senin LL et al (2013) FNDC5/irisin is not only a myokine but also an adipokine. PLoS One 8:e60563. https://doi.org/10.1371/journal.pone.0060563
    Boström P, Wu J, Jedrychowski MP et al (2012) PGC1-α-dependent myokine that drives brown-fat-like development of white fat and thermogenesis. Nature 481:463–468. https://doi.org/10.1038/nature10777
    Cuevas-Ramos D, Almeda-Valdés P, Meza-Arana CE et al (2012) Exercise increases serum fibroblast growth factor 21 (FGF21) levels. PLoS One 7:e38022. https://doi.org/10.1371/journal.pone.0038022
    Campos RMS, Masquio DCL, Aquino AE Jr (2016) The role of FGF-21/NPY pathway on weight loss therapy in obese women. In: 13th International Congress on Obesity, 2016, Vancouver. Abstracts of the 13th International Congress on Obesity 1–4 May 2016 Vancouver, Canada, 2016. v. 17. pp 1–213
    Tilg H, Moschen AR (2008) Inflammatory mechanisms in the regulation of insulin resistance. Mol Med 14:222–231. https://doi.org/10.2119/2007-00119.Tilg
    Tangvarasittichai S, Pongthaisong S, Tangvarasittichai O (2016) Tumor necrosis factor-Α, Interleukin-6, C-reactive protein levels and insulin resistance associated with type 2 diabetes in abdominal obesity women. Indian J Clin Biochem 31:68–74. https://doi.org/10.1007/s12291-015-0514-0
    Moreno-Navarrete JM, Ortega F, Serrano M (2013) Irisin is expressed and produced by human muscle and adipose tissue in association with obesity and insulin resistance. J Clin Endocrinol Metab 98:E769–E778. https://doi.org/10.1210/jc.2012-2749
    Houreld NN (2014) Shedding light on a new treatment for diabetic wound healing: a review on phototherapy. Sci World J 2014:398412. https://doi.org/10.1155/2014/398412
    Masha RT, Houreld NN, Abrahamse H (2013) Low-intensity laser irradiation at 660 nm stimulates transcription of genes involved in the electron transport chain. Photomed Laser Surg 31:47–53. https://doi.org/10.1089/pho.2012.3369
    Silveira PC, Silva LA, Fraga DB, Freitas TP, Streck EL, Pinho R (2009) Evaluation of mitochondrial respiratory chain activity in muscle healing by low-level laser therapy. J Photochem Photobiol B 95:89–92. https://doi.org/10.1016/j.jphotobiol.2009.01.004
    Aquino AE Jr, Sene-Fiorese M, Castro CA (2015) Can low-level laser therapy when associated to exercise decrease adipocyte area? J Photochem Photobiol B 149:21–26. https://doi.org/10.1016/j.jphotobiol.2015.04.033
    Nurković J, Zaletel I, Nurković S et al (2017) Combined effects of electromagnetic field and low-level laser increase proliferation and alter the morphology of human adipose tissue-derived mesenchymal stem cells. Lasers Med Sci 32:151–160. https://doi.org/10.1007/s10103-016-2097-2
    Karu TI (2008) Mitochondrial signaling in mammalian cells activated by red and near-IR radiation. Photochem Photobiol 84:1091–1099. https://doi.org/10.1111/j.1751-1097.2008.00394.x
    Lavi R, Shainberg A, Friedmann H et al (2003) Low energy visible light induces reactive oxygen species generation and stimulates an increase of intracellular calcium concentration in cardiac cells. J Biol Chem 278:40917–40922
    Hu WP, Wang JJ, Yu CL, Lan CC, Chen GS, Yu HS (2007) Helium-neon laser irradiation stimulates cell proliferation through photostimulatory effects in mitochondria. J Invest Dermatol 127:2048–2057
    AlGhamdi KM, Kumar A, Moussa NA (2012) Low-level laser therapy: a useful technique for enhancing the proliferation of various cultured cells. Lasers Med Sci 27:237–249. https://doi.org/10.1007/s10103-011-0885-2