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Cellmed Orthocellular Medicine and Pharmaceutical Association (셀메드 세포교정의약학회)
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An alternative method to reduce anaphylaxis by moxibustion

  • Jeong, Hyun-Ja (Biochip Research Center and Inflammatory Disease Research Center, Hoseo University) ;
  • Nam, Sun-Young (Department of Pharmacology, College of Korean Medicine, Kyung Hee University) ;
  • Lee, Byong-Joo (Department of Pharmacology, College of Korean Medicine, Kyung Hee University) ;
  • Kim, Min-Gi (Department of Pharmacology, College of Korean Medicine, Kyung Hee University) ;
  • Kim, Jeong-Hwa (Graduate School of Social Welfare, Ewha Womans University) ;
  • Kim, Hyung-Min (Department of Pharmacology, College of Korean Medicine, Kyung Hee University)
  • Received : 2014.03.15
  • Accepted : 2014.05.08
  • Published : 2014.05.31
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Abstract

Epinephrine is a critical drug for patients at risk for anaphylaxis. Here, we suggest moxibustion as an alternative method to reduce anaphylaxis. Moxibustion was applied to the Shimen (CV5) acupoint and found to attenuate compound 48/80-induced mortality. Capsazepine, a transient receptor potential vanilloid (TRPV) 1 antagonist, significantly improved overall survival rates compared to groups treated with moxibustion or 2-aminoethoxydiphenyl borate (an activator of TRPV1, 2, and 3). Probenecid (a TRPV2 agonist) also increased survival rate and reduced histamine levels. Survival rates increased by moxibustion and probenecid were completely inhibited by ruthenium red (a TRPV2 and 3 antagonist) and gadolinium chloride (general TRPV antagonist), respectively. Passive cutaneous anaphylaxis and ear swelling were significantly reduced by moxibustion and probenecid (p < 0.05). In cardiomyocytes, TRPV2 was over-expressed by compound 48/80 and histamine but this increased TRPV2 expression decreased to baseline with moxibustion and probenecid treatment. In addition, intracellular calcium levels increased by compound 48/80 were reduced by probenecid. Overall, these findings suggest that the reduction of anaphylaxis caused by moxibustion could represent a new mechanism of moxibustion related to the regulation of TRPV2 activation and promotion of epinephrine secretion.

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