Wednesday, April 17, 2013

Wet Cupping Therapy/Bekam done on the foot of a Gout patient (Singapore)




Google Videos - Cupping Therapy





Wet Cupping Therapy/Bekam done on the foot of a Gout patient (Singapore)




We Are Providing Wet Cupping Therapy/Bekam Darah in Singapore::: Male & Female Therapists Available. A gout patient should also perform ...

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HubMed - Laser Acupuncture





ST36 laser acupuncture reduces pain-related behavior in rats: involvement of the opioidergic and serotonergic systems.



Lasers Med Sci. 2013 Jan 5;
Erthal V, da Silva MD, Cidral-Filho FJ, Santos AR, Nohama P

Laser acupuncture is a modality of low-level light therapy used as an alternative to needling for the past three decades. Although it has proved effective for the treatment of various conditions, the mechanisms underlying its effects are not fully understood. To contribute to this understanding, this study was designed to (1) evaluate the antinociceptive effect of ST36 laser acupuncture (830 nm, 3 J/cm(2)) in rat models of acute nociception and (2) to investigate the opioidergic and serotonergic systems involvement in this effect. Our results demonstrate that ST36 laser acupuncture inhibited (36 ± 2 %) acetic acid-induced abdominal constrictions and both neurogenic (48 ± 7 %) and inflammatory (phase IIA 42 ± 8 % and phase IIB 83 ± 6 %) phases of formalin-induced nociceptive behavior. Moreover, the antinociceptive activity of laser irradiation in the acetic acid test was significantly reversed by preadministration of naloxone (1 mg/kg, nonselective opioid receptor antagonist), pindolol (1 mg/kg, subcutaneous; nonselective 5-HT 1A/B receptor antagonist), and ketanserin (1 mg/kg; selective 5-HT2A receptor antagonist) but not by ondansetron (1 mg/kg, selective 5-HT3 receptor antagonist). Taken together, our data demonstrate, for the first time, that (1) ST36 laser acupuncture elicited significant antinociceptive effect against acetic acid- and formalin-induced behavior in rats and that (2) this effect is mediated by activation of the opioidergic and serotonergic (5-HT1 and 5-HT2A receptors) systems.







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