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Anti-inflammatory effects of a traditional Korean medicine: Ojayeonjonghwan.
Nam, Sun-Young; Kim, Kyu-Yeob; Kim, Mi Hye; Jang, Jae-Bum; Rah, So-Young; Chae, Hee Jeong; Lee, Jin-Man; Kim, Hyung-Min; Jeong, Hyun-Ja.
Affiliation
  • Nam SY; a Department of Pharmacology, College of Korean Medicine , Kyung Hee University , Seoul , Republic of Korea.
  • Kim KY; a Department of Pharmacology, College of Korean Medicine , Kyung Hee University , Seoul , Republic of Korea.
  • Kim MH; b Department of Food and Nutrition , Hoseo University , Asan , Chungnam , Republic of Korea.
  • Jang JB; c Department of Pharmaceutical Engineering , Hoseo University , Asan , Chungnam , Republic of Korea.
  • Rah SY; d Department of Biochemistry , Chonbuk National University , Jeonju , Republic of Korea.
  • Chae HJ; e Department of Food Science & Technology and Research Institute for Basic Science , Hoseo University , Asan , Chungnam , Republic of Korea.
  • Lee JM; e Department of Food Science & Technology and Research Institute for Basic Science , Hoseo University , Asan , Chungnam , Republic of Korea.
  • Kim HM; a Department of Pharmacology, College of Korean Medicine , Kyung Hee University , Seoul , Republic of Korea.
  • Jeong HJ; e Department of Food Science & Technology and Research Institute for Basic Science , Hoseo University , Asan , Chungnam , Republic of Korea.
Pharm Biol ; 55(1): 1856-1862, 2017 Dec.
Article in En | MEDLINE | ID: mdl-28614972
ABSTRACT

OBJECTIVE:

To study the anti-inflammatory properties of OJ. CONTEXT Ojayeonjonghwan (OJ) is a traditional Korean prescription, which has been widely used for the treatment of prostatitis. However, no scientific study has been performed of the anti-inflammatory effects of OJ. MATERIALS AND

METHODS:

Peritoneal macrophages were isolated 3-4 days after injecting a C57BL/6J mouse with thioglycollate. They were then treated with OJ water extract (0.01, 0.1, and 1 mg/mL) for 1 h and stimulated with lipopolysaccharide (LPS) for different times. Nitric oxide (NO), inducible nitric oxide synthase (iNOS) and cyclooxygenase (COX)-2, and proinflammatory cytokine levels were determined by NO assay, Western blotting, RT-PCR and ELISA.

RESULTS:

NO generation and iNOS induction were increased in the LPS-activated mouse peritoneal macrophages. However, NO generation and iNOS induction by LPS were suppressed by treatment with OJ for the first time. The IC50 value of OJ with respect to NO production was 0.09 mg/mL. OJ did not influence LPS-stimulated COX-2 induction, but did significantly decrease LPS-stimulated secretions and mRNA expressions of tumour necrosis factor (TNF)-α, interleukin (IL)-6, and IL-1ß. Inhibition rates of TNF-α, IL-6, and IL-1ß at an OJ concentration of 1 mg/mL were 77%, 88%, and 50%, respectively. OJ also suppressed the LPS-induced nuclear translocation of NF-κB. High-performance liquid chromatography showed schizandrin and gomisin A are major components of OJ.

CONCLUSIONS:

OJ reduces inflammatory response, and this probably explains its positive impact on the prostatitis associated inflammation.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polycyclic Compounds / Plant Extracts / Anti-Inflammatory Agents, Non-Steroidal / Gene Expression Regulation / Macrophages, Peritoneal / Lignans / Cyclooctanes / Dioxoles / Macrophage Activation Limits: Animals Language: En Journal: Pharm Biol Year: 2017 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polycyclic Compounds / Plant Extracts / Anti-Inflammatory Agents, Non-Steroidal / Gene Expression Regulation / Macrophages, Peritoneal / Lignans / Cyclooctanes / Dioxoles / Macrophage Activation Limits: Animals Language: En Journal: Pharm Biol Year: 2017 Type: Article