Siebold Branch Extracts Attenuate NO and ROS Production via the Inhibition of p38 and JNK Phosphorylation.

Jae Min Kim, Moon-Hee Choi, Ji Hye Yang
Author Information
  1. Jae Min Kim: College of Pharmacy, Chosun University, Gwangju 61452, Republic of Korea.
  2. Moon-Hee Choi: Department of Biochemical Engineering, College of Engineering, Chosun University, Gwangju 61452, Republic of Korea. ORCID
  3. Ji Hye Yang: College of Korean Medicine, Dongshin University, Naju 58245, Republic of Korea.

Abstract

(CJ) is widely distributed in Asian countries like Korea, China, and Japan. Modern pharmacological studies have demonstrated that it exhibits various biological activities, including antioxidant and anti-inflammatory effects. However, most studies have confirmed the efficacy of its water extract but not that of its other extracts. Therefore, in this study, Siebold branches (CJB: 70% EtOH extract) were separated using hexane, chloroform, ethyl acetate (CJB3), butanol, and water. Then, their antioxidative activities and phenolic contents were measured. Results revealed that the antioxidant activities and phenolic contents of CJB3 were higher than those of the other extracts. Further, the inhibitory and anti-inflammatory effect of CJB3 on lipopolysaccharide (LPS)-induced reactive oxygen species (ROS) production and LPS-activated macrophages, respectively, was determined. CJB3 suppressed oxidative stress in LPS-activated cells and dose-dependently decreased LPS-stimulated ROS production. CJB3 reduced oxidative stress and reversed the glutathione decrease in LPS-activated RAW264.7 cells. The inhibitory and reducing effect of CJB3 on LPS-induced nitric oxide (NO) production and inducible NO synthase protein and messenger RNA levels, respectively, was investigated. CJB3 inhibited LPS-induced cytokine production and p38 and c-Jun N-terminal kinase (JNK) phosphorylation but not extracellular signal-regulated kinase phosphorylation. Overall, the study results suggest that CJB3 may exert its anti-inflammatory effects via the suppression of p38, JNK, and c-Jun activation.

Keywords

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Grants

  1. 2022R1A5A2029546/National Research Foundation of Korea (NRF), funded by the Ministry of Science and ICT

MeSH Term

Anti-Inflammatory Agents
Antioxidants
JNK Mitogen-Activated Protein Kinases
Lipopolysaccharides
NF-kappa B
Nitric Oxide
Nitric Oxide Synthase Type II
Phosphorylation
Reactive Oxygen Species
Plant Extracts
Cinnamomum

Chemicals

Anti-Inflammatory Agents
Antioxidants
JNK Mitogen-Activated Protein Kinases
Lipopolysaccharides
NF-kappa B
Nitric Oxide
Nitric Oxide Synthase Type II
Reactive Oxygen Species
Plant Extracts

Word Cloud

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