U-Bang-Haequi Tang: A Herbal Prescription that Prevents Acute Inflammation through Inhibition of NF-κB-Mediated Inducible Nitric Oxide Synthase

Author:

Hwangbo Min1,Jung Ji Yun2,Ki Sung Hwan3,Park Sang Mi2,Jegal Kyung Hwan2,Cho Il Je2ORCID,Lee Ju-Hee2,Kang Seung Ho4,Park Sun-Dong5,Ku Sae Kwang2,Kim Sang Chan2ORCID,Zhao Rong Jie26,Jee Seon Young1,Kim Young Woo25ORCID

Affiliation:

1. Department of Ophthalmology, Otolaryngology & Dermatology, Daegu Haany University, Daegu 706-828, Republic of Korea

2. Medical Research Center for Globalization of Herbal Formulation, College of Oriental Medicine, Daegu Haany University, Daegu 706-828, Republic of Korea

3. College of Pharmacy, Chosun University, Gwangju 501-759, Republic of Korea

4. Sunlin University, Pohang 791-712, Republic of Korea

5. College of Oriental Medicine, Dongguk University, Gyeongju 780-714, Republic of Korea

6. Department of Pharmacology, Mudanjiang Medical University, Mudanjiang 157011, China

Abstract

Since antiquity, medical herbs have been prescribed for both treatment and preventative purposes. Herbal formulas are used to reduce toxicity as well as increase efficacy in traditional Korean medicine.U-bang-haequi tang(UBT) is a herbal prescription containingArctii fructusandForsythia suspensaas its main components and has treated many human diseases in traditional Korean medicine. This research investigated the effects of UBT against an acute phase of inflammation. For this, we measured induction of nitric oxide (NO) and related proteins in macrophage cell line stimulated by lipopolysaccharide (LPS). Further, paw swelling was measured in carrageenan-treated rats. Carrageenan significantly induced activation of inflammatory cells and increases in paw volume, whereas oral administration of 0.3 or 1 g/kg/day of UBT inhibited the acute inflammatory response. In RAW264.7 cells, UBT inhibited mRNA and protein expression levels of iNOS. UBT treatment also blocked elevation of NO production, nuclear translocation of NF-κB, phosphorylation of Iκ-Bαinduced by LPS. Moreover, UBT treatment significantly blocked the phosphorylation of p38 and c-Jun NH2-terminal kinases by LPS. In conclusion, UBT prevented both acute inflammation in rats as well as LPS-induced NO and iNOS gene expression through inhibition of NF-κB in RAW264.7 cells.

Funder

National Research Foundation of Korea

Publisher

Hindawi Limited

Subject

Complementary and alternative medicine

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