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The effect of transcutaneous application of carbon dioxide (CO 2) on skeletal muscle

► PGC-1α is up-regulated as a result of exercise such as mitochondrial biogenesis and muscle fiber-type switching, and up-regulation of VEGF. ► We demonstrated transcutaneous application of CO 2 up-regulated the gene expression of PGC-1α, SIRT1 and VEGF, and instance of muscle fiber switching. ► Tra...

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Published in:Biochemical and biophysical research communications 2011-04, Vol.407 (1), p.148-152
Main Authors: Oe, Keisuke, Ueha, Takeshi, Sakai, Yoshitada, Niikura, Takahiro, Lee, Sang Yang, Koh, Akihiro, Hasegawa, Takumi, Tanaka, Masaya, Miwa, Masahiko, Kurosaka, Masahiro
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cites cdi_FETCH-LOGICAL-c449t-5efe40e4d7694edc007b10dfcc2d89a5606f2bf105096103e336700c9b4c08b83
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creator Oe, Keisuke
Ueha, Takeshi
Sakai, Yoshitada
Niikura, Takahiro
Lee, Sang Yang
Koh, Akihiro
Hasegawa, Takumi
Tanaka, Masaya
Miwa, Masahiko
Kurosaka, Masahiro
description ► PGC-1α is up-regulated as a result of exercise such as mitochondrial biogenesis and muscle fiber-type switching, and up-regulation of VEGF. ► We demonstrated transcutaneous application of CO 2 up-regulated the gene expression of PGC-1α, SIRT1 and VEGF, and instance of muscle fiber switching. ► Transcutaneous application of CO 2 may cause similar effect to aerobic exercise in skeletal muscle. In Europe, carbon dioxide therapy has been used for cardiac disease and skin problems for a long time. However there have been few reports investigating the effects of carbon dioxide therapy on skeletal muscle. Peroxisome proliferators-activated receptor (PPAR)-gamma coactivator-1 (PGC-1α) is up-regulated as a result of exercise and mediates known responses to exercise, such as mitochondrial biogenesis and muscle fiber-type switching, and neovascularization via up-regulation of vascular endothelial growth factor (VEGF). It is also known that silent mating type information regulation 2 homologs 1 (SIRT1) enhances PGC-1α-mediated muscle fiber-type switching. Previously, we demonstrated transcutaneous application of CO 2 increased blood flow and a partial increase of O 2 pressure in the local tissue known as the Bohr effect. In this study, we transcutaneously applied CO 2 to the lower limbs of rats, and investigated the effect on the fast muscle, tibialis anterior (TA) muscle. The transcutaneous CO 2 application caused: (1) the gene expression of PGC-1α, silent mating type information regulation 2 homologs 1 (SIRT1) and VEGF, and increased the number of mitochondria, as proven by real-time PCR and immunohistochemistry, (2) muscle fiber switching in the TA muscle, as proven by isolation of myosin heavy chain and ATPase staining. Our results suggest the transcutaneous application of CO 2 may have therapeutic potential for muscular strength recovery resulting from disuse atrophy in post-operative patients and the elderly population.
doi_str_mv 10.1016/j.bbrc.2011.02.128
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In Europe, carbon dioxide therapy has been used for cardiac disease and skin problems for a long time. However there have been few reports investigating the effects of carbon dioxide therapy on skeletal muscle. Peroxisome proliferators-activated receptor (PPAR)-gamma coactivator-1 (PGC-1α) is up-regulated as a result of exercise and mediates known responses to exercise, such as mitochondrial biogenesis and muscle fiber-type switching, and neovascularization via up-regulation of vascular endothelial growth factor (VEGF). It is also known that silent mating type information regulation 2 homologs 1 (SIRT1) enhances PGC-1α-mediated muscle fiber-type switching. Previously, we demonstrated transcutaneous application of CO 2 increased blood flow and a partial increase of O 2 pressure in the local tissue known as the Bohr effect. In this study, we transcutaneously applied CO 2 to the lower limbs of rats, and investigated the effect on the fast muscle, tibialis anterior (TA) muscle. 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In Europe, carbon dioxide therapy has been used for cardiac disease and skin problems for a long time. However there have been few reports investigating the effects of carbon dioxide therapy on skeletal muscle. Peroxisome proliferators-activated receptor (PPAR)-gamma coactivator-1 (PGC-1α) is up-regulated as a result of exercise and mediates known responses to exercise, such as mitochondrial biogenesis and muscle fiber-type switching, and neovascularization via up-regulation of vascular endothelial growth factor (VEGF). It is also known that silent mating type information regulation 2 homologs 1 (SIRT1) enhances PGC-1α-mediated muscle fiber-type switching. Previously, we demonstrated transcutaneous application of CO 2 increased blood flow and a partial increase of O 2 pressure in the local tissue known as the Bohr effect. In this study, we transcutaneously applied CO 2 to the lower limbs of rats, and investigated the effect on the fast muscle, tibialis anterior (TA) muscle. The transcutaneous CO 2 application caused: (1) the gene expression of PGC-1α, silent mating type information regulation 2 homologs 1 (SIRT1) and VEGF, and increased the number of mitochondria, as proven by real-time PCR and immunohistochemistry, (2) muscle fiber switching in the TA muscle, as proven by isolation of myosin heavy chain and ATPase staining. 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In Europe, carbon dioxide therapy has been used for cardiac disease and skin problems for a long time. However there have been few reports investigating the effects of carbon dioxide therapy on skeletal muscle. Peroxisome proliferators-activated receptor (PPAR)-gamma coactivator-1 (PGC-1α) is up-regulated as a result of exercise and mediates known responses to exercise, such as mitochondrial biogenesis and muscle fiber-type switching, and neovascularization via up-regulation of vascular endothelial growth factor (VEGF). It is also known that silent mating type information regulation 2 homologs 1 (SIRT1) enhances PGC-1α-mediated muscle fiber-type switching. Previously, we demonstrated transcutaneous application of CO 2 increased blood flow and a partial increase of O 2 pressure in the local tissue known as the Bohr effect. In this study, we transcutaneously applied CO 2 to the lower limbs of rats, and investigated the effect on the fast muscle, tibialis anterior (TA) muscle. The transcutaneous CO 2 application caused: (1) the gene expression of PGC-1α, silent mating type information regulation 2 homologs 1 (SIRT1) and VEGF, and increased the number of mitochondria, as proven by real-time PCR and immunohistochemistry, (2) muscle fiber switching in the TA muscle, as proven by isolation of myosin heavy chain and ATPase staining. Our results suggest the transcutaneous application of CO 2 may have therapeutic potential for muscular strength recovery resulting from disuse atrophy in post-operative patients and the elderly population.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>21371433</pmid><doi>10.1016/j.bbrc.2011.02.128</doi><tpages>5</tpages></addata></record>
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ispartof Biochemical and biophysical research communications, 2011-04, Vol.407 (1), p.148-152
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source ScienceDirect Journals
subjects 60 APPLIED LIFE SCIENCES
Administration, Cutaneous
Animals
ATROPHY
BLOOD FLOW
CARBON DIOXIDE
Carbon Dioxide - administration & dosage
EXERCISE
FIBERS
Gene Expression - drug effects
GENE REGULATION
GENES
GROWTH FACTORS
LIMBS
Male
MATING
MITOCHONDRIA
Mitochondria, Muscle - drug effects
Mitochondrial biogenesis
Muscle fiber changing
Muscle, Skeletal - drug effects
Muscle, Skeletal - physiology
Muscle, Skeletal - ultrastructure
MUSCLES
Muscular Atrophy - drug therapy
MYOSIN
Myosin Heavy Chains - genetics
Myosin Heavy Chains - metabolism
PATIENTS
Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
PGC-1α
POLYMERASE CHAIN REACTION
RATS
Rats, Sprague-Dawley
RECEPTORS
RNA-Binding Proteins - genetics
Sirtuin 1 - genetics
SKELETAL DISEASES
SKIN
THERAPY
Transcription Factors - genetics
Transcutaneous application of carbon dioxide
Vascular Endothelial Growth Factor A - genetics
title The effect of transcutaneous application of carbon dioxide (CO 2) on skeletal muscle
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