1.Effects of different durations of warm-tube moxibustion by using near infrared spectroscopy
Masamichi NAKAMURA ; Tsuyoshi WADA ; Tomoki TSUJI ; Koji TAKEDA ; Tokiko KAWANO ; Masaki OKUBO ; Ayumi SAKAMOTO
Journal of the Japan Society of Acupuncture and Moxibustion 2013;63(4):260-267
[Objective]Although warm-tube moxibustion is easy-to-use in acupuncture therapy, the timing of moxa removal varies among practitioners. In the present study, we used near infrared spectroscopy (NIRS) to compare effects of different durations of moxibustion stimulation on improvement in local circulation as measured by changes in blood oxygenation dynamics in muscle tissue.
[Methods]Twelve healthy adults underwent warm-tube moxibustion with a single cone applied to the upper right shoulder region;measurements of tissue blood oxygenation dynamics (ΔOxy-Hb, ΔTotal-Hb) were obtained at intervals of 0.5 s. Control measurements were first taken for 15 min without intervention (Control);then, subjects received moxibustion 2 min after the start of measurement and had the moxa removed at the following time points: 30 s after patients experienced heat pain (Removal 30, moxibustion group); 45 s after heat pain (Removal 45, moxibustion group);or did not have the moxa removed (Continuous moxibustion group). These 4 different conditions were compared. Additionally, we determined the burning temperature of moxa and the skin temperature and intensity of heat pain sensation at the site of moxibustion.
[Results]Compared with the Control, the Removal 30, Removal 45, and Continuous moxibustion groups had significant increases in ΔOxy-Hb, ΔTotal-Hb, and skin temperature, with no significant differences among the moxibustion groups. No significant difference in the intensity of heat pain sensation was observed among the moxibustion groups. All moxibustion groups began to show rapid increases in both ΔTotal-Hb and ΔOxy-Hb around the time when subjects began to feel heat pain, suggesting that the axon reflex evoked by noxious stimuli of heat pain increased blood volume and arterial blood flow.
[Conclusion]Hemodynamic improvement in muscle tissue through the use of continuous warm-tube moxibustion for 30 s or longer after the occurrence of heat pain was confirmed.
2.A Practice Report of a “health of the Elderly People Using a Hot Spring, and Improvement-of-Physical-Strength Classroom” Enterprise About the Result of a “Clouds-of-Steam Health Class” Movement Continuation Person
Chikara NAGANO ; Tomoki SHONO ; Hiroaki HIRAMATSU ; Hitoshi HORI ; Chinatsu MORIWAKI
The Journal of The Japanese Society of Balneology, Climatology and Physical Medicine 2013;77(1):35-35
3.Intradiscal Injection of Autologous Platelet-Rich Plasma Releasate to Treat Discogenic Low Back Pain: A Preliminary Clinical Trial.
Koji AKEDA ; Kohshi OHISHI ; Koichi MASUDA ; Won C. BAE ; Norihiko TAKEGAMI ; Junichi YAMADA ; Tomoki NAKAMURA ; Toshihiko SAKAKIBARA ; Yuichi KASAI ; Akihiro SUDO
Asian Spine Journal 2017;11(3):380-389
STUDY DESIGN: Preliminary clinical trial. PURPOSE: To determine the safety and initial efficacy of intradiscal injection of autologous platelet-rich plasma (PRP) releasate in patients with discogenic low back pain. OVERVIEW OF LITERATURE: PRP, which is comprised of autologous growth factors and cytokines, has been widely used in the clinical setting for tissue regeneration and repair. PRP has been shown in vitro and in vivo to potentially stimulate intervertebral disc matrix metabolism. METHODS: Inclusion criteria for this study included chronic low back pain without leg pain for more than 3 months; one or more lumbar discs (L3/L4 to L5/S1) with evidence of degeneration, as indicated via magnetic resonance imaging (MRI); and at least one symptomatic disc, confirmed using standardized provocative discography. PRP releasate, isolated from clotted PRP, was injected into the center of the nucleus pulposus. Outcome measures included the use of a visual analog scale (VAS) and the Roland-Morris Disability Questionnaire (RDQ), as well as X-ray and MRI (T2-quantification). RESULTS: Data were analyzed from 14 patients (8 men and 6 women; mean age, 33.8 years). The average follow-up period was 10 months. Following treatment, no patient experienced adverse events or significant narrowing of disc height. The mean pain scores before treatment (VAS, 7.5±1.3; RDQ, 12.6±4.1) were significantly decreased at one month, and this was generally sustained throughout the observation period (6 months after treatment: VAS, 3.2±2.4, RDQ; 3.6±4.5 and 12 months: VAS, 2.9±2.8; RDQ, 2.8±3.9; p<0.01, respectively). The mean T2 values did not significantly change after treatment. CONCLUSIONS: We demonstrated that intradiscal injection of autologous PRP releasate in patients with low back pain was safe, with no adverse events observed during follow-up. Future randomized controlled clinical studies should be performed to systematically evaluate the effects of this therapy.
Cytokines
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Female
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Follow-Up Studies
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Humans
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In Vitro Techniques
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Intercellular Signaling Peptides and Proteins
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Intervertebral Disc
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Intervertebral Disc Degeneration
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Leg
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Low Back Pain*
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Magnetic Resonance Imaging
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Male
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Metabolism
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Outcome Assessment (Health Care)
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Platelet-Rich Plasma*
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Regeneration
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Visual Analog Scale