Meridian medicine, such as acupuncture, acupressure, and Qigong, have been commonly used to treat a variety of diseases and disorders; however, the potency of these alternative methods has not been widely accepted by mainstream due to a lack of scientific evidence. Although substantial evidences have been accumulated that acupuncture has prominent analgesic effect; there is no systemic research regarding signaling pathways mediated by acupuncture in treating diseases. Recently, we have found that acupuncture treatment lead to significant anti-inflammatory as well as vasodilatory modulation in animal models. We hypothesize that acupuncture analgesia might function partially by its direct and/or indirect inhibition of inflammation, since pain is frequently associated with inflammation and acupuncture has been successfully used to treat a number of human inflammatory diseases. We have also found that cholinergic pathway may play an important role in acupuncture-mediated anti-inflammatory effects and other therapeutic benefits in the animal model as demonstrated by microarray using a rat oligo set containing 6,000 probes. The purposes of this proposal are 1), to further determine cellular and molecular mechanisms by which acupuncture attenuates inflammation in vivo in rats; and 2), to identify the signaling pathways by which acupuncture mediates anti-inflammatory and vasodilatory effects in the animal model. This study represents an unexplored area of research and would provide important insight into how acupuncture technology can be linked to modern concept of gene regulation in biological systems and may further offer a feasible strategy to increase understanding the molecular biology of alternative medicine in meridian therapies. We believe that our studies may open new era towards molecular understanding of acupuncture treatment in pain, inflammation, as well as a variety of vascular diseases in humans.

Agency
National Institute of Health (NIH)
Institute
National Center for Complementary & Alternative Medicine (NCCAM)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21AT002140-01A1
Application #
6870758
Study Section
Special Emphasis Panel (ZAT1-DB (15))
Program Officer
Jackson, Morgan
Project Start
2005-02-15
Project End
2007-01-31
Budget Start
2005-02-15
Budget End
2006-01-31
Support Year
1
Fiscal Year
2005
Total Cost
$187,500
Indirect Cost
Name
Baylor College of Medicine
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030
Garcia, Gabriela E; Truong, Luan D; Chen, Jiang-Fan et al. (2011) Adenosine A(2A) receptor activation prevents progressive kidney fibrosis in a model of immune-associated chronic inflammation. Kidney Int 80:378-88
Wu, Huaizhu; Ghosh, Sudip; Perrard, Xiaoyuan Dai et al. (2007) T-cell accumulation and regulated on activation, normal T cell expressed and secreted upregulation in adipose tissue in obesity. Circulation 115:1029-38
Garcia, Gabriela E; Ma, Sheng-Xing; Feng, Lili (2005) Acupuncture and kidney disease. Adv Chronic Kidney Dis 12:282-91