Effects of Herbal-Partitioned Moxibustion on DA/D1R Expression in the Colon and Central Nervous System using a Rat Model of Crohn's Disease
Yuan Lu, Tingting Lv, Manwen Xu, Zhe Ma, Zhijun Weng, Hui Feng, Luyi Wu, Fang Zhang, Guanghong Ding, Huangan Wu, Huirong Liu
(1. Shanghai Institute of Acupuncture-Moxibustion and Meridian. 650 South WanPing Road, Shanghai, China. 200030; 2. Department of Mechanics and Engineering Science, Fudan University. 220 Handan Road, Shanghai, China. 200433; 3.Longhua Hospital, Shanghai University of Traditional Chinese Medicine. 725 South WanPing Road, Shanghai, China. 200030; 4. Guanghua Hospital. 540 Xinhua Road,
Shanghai, China. 200052)
Abstract: Objective: To observe dopamine (DA)/dopamine receptor D1R in the colon, spinal dorsal horn and hypothalamus of a rat model of Crohn's disease (CD) by moxibustion at the Tian-shu(ST25)and Qihai(CV6)acupoints and to elucidate the mechanism of moxibustion in treating CD. Methods: The rats were randomly divided into the normal, model, herbal-partitioned moxibustion (Mox) and mesalazine (Mesa)groups. Damage in the colons was scored and observed by HE staining. DA/D1R expression in the colonic mucosa was detected by immunohistochemistry, which in the spinal dorsal horn and hypothalamus were measured by ELISA. D1R mRNA expression in the three sites was evaluated by real-time PCR. Results:Immunohistochemistry and ELISA results showed that DA/D1R expressions were significantly higher in themodel group than in the normal group (P<0.01), and decreased in the Mox and Mesa groups compared to the model group (P<0.01, P<0.05). PCR showed the same results of D1R mRNA expression as DA/D1R.. Conclusion: Moxibustion at the Tian-shu (ST25) and Qi-hai (CV6) acupoints can relieve colitis in a CD rat, decrease DA/D1R mRNA expression in the intestine, spinal dorsal horn and hypothalamus. The antiinflammatory effect may be important mechanisms underlying the efficacy of moxibustion on CD.
Key words:Acupuncture, Crohn's disease, Herbal-partitioned moxibustion, Dopamine, Dopaminereceptor