Abstract | BACKGROUND: MATERIALS AND METHODS: Adult male Sprague-Dawley rats were randomized to receive I/R, I/R plus cepharanthine, or I/R plus cepharanthine plus the HO-1 activity inhibitor tin protoporphyrin (SnPP; n = 12 in each group). Sham control groups were run simultaneously. I/R was induced by applying rubber band tourniquets high around each thigh for 3 h followed by reperfusion for 24 h. RESULTS: Rats receiving I/R had significant increases in concentrations of nitric oxide, malondialdehyde (lipid peroxidation marker), and inflammatory molecules (including interleukin 6, macrophage inflammatory protein 2, and prostaglandin E2) in plasma, and the lungs, indicating that I/R caused significant oxidation and inflammation in rats. Rats receiving I/R also had significant increases in concentration of phosphorylated inhibitor-κB, indicating that I/R caused significant nuclear factor κB activation. Assays of arterial blood gas, biochemistry, and histopathology confirmed that I/R-induced significant lung injury in rats. Cepharanthine significantly reduced the oxidation, inflammation, nuclear factor κB activation, and lung injury induced by I/R. Of note, cepharanthine significantly enhanced pulmonary HO-1 expression after I/R. Moreover, these previously mentioned effects of cepharanthine were partially reversed by inhibiting the activity of HO-1. CONCLUSIONS:
Cepharanthine mitigates lung injury induced by bilateral lower limb I/R in rats. The mechanisms may involve its effects on reducing oxidation and inflammation. The mechanisms may also involve enhancing HO-1 expression.
|
Authors | Ming-Chang Kao, Chen-Hsien Yang, Wei-Chih Chou, Joen-Rong Sheu, Chun-Jen Huang |
Journal | The Journal of surgical research
(J Surg Res)
Vol. 199
Issue 2
Pg. 647-56
(Dec 2015)
ISSN: 1095-8673 [Electronic] United States |
PMID | 26193830
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Copyright | Copyright © 2015 Elsevier Inc. All rights reserved. |
Chemical References |
- Anti-Inflammatory Agents, Non-Steroidal
- Benzylisoquinolines
- I-kappa B Proteins
- Plant Extracts
- Nitric Oxide
- Malondialdehyde
- cepharanthine
- Heme Oxygenase-1
- Cyclooxygenase 2
- Ptgs2 protein, rat
|
Topics |
- Acute Lung Injury
(metabolism, pathology, prevention & control)
- Animals
- Anti-Inflammatory Agents, Non-Steroidal
(therapeutic use)
- Benzylisoquinolines
(therapeutic use)
- Blood Gas Analysis
- Bronchoalveolar Lavage Fluid
(cytology)
- Cyclooxygenase 2
(metabolism)
- Drug Evaluation, Preclinical
- Heme Oxygenase-1
(metabolism)
- I-kappa B Proteins
(metabolism)
- Lung
(metabolism, pathology)
- Male
- Malondialdehyde
(blood)
- Nitric Oxide
(blood)
- Phytotherapy
- Plant Extracts
(therapeutic use)
- Random Allocation
- Rats, Sprague-Dawley
- Reperfusion Injury
(metabolism, pathology, prevention & control)
- Stephania
(chemistry)
|