Cariporide pretreatment attenuated warm ischemia/reperfusion injury in an isolated rat lung: a study on antioxidative mechanism.
- Author:
Xinzhu LIN
1
;
Meiting LI
;
Ronghua ZHOU
;
Hai YU
;
Leng ZHOU
;
Qian LI
;
Bin LIU
Author Information
1. Department of Anesthesiology, West China Hospital, Sichuan University, Chengdu 610041, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Antioxidants;
pharmacology;
Guanidines;
pharmacology;
In Vitro Techniques;
Ischemic Preconditioning;
Lung;
blood supply;
Male;
Rats;
Rats, Sprague-Dawley;
Reperfusion Injury;
etiology;
prevention & control;
Sodium-Hydrogen Exchangers;
antagonists & inhibitors;
Sulfones;
pharmacology;
Superoxide Dismutase;
metabolism;
Warm Ischemia
- From:
Journal of Biomedical Engineering
2010;27(1):132-137
- CountryChina
- Language:Chinese
-
Abstract:
This experimental study was designed to explore the possible mechanisms of Cariporide, a kind of Na+/H+ exchanger inhibitor, for protecting the lung from warm ischemia/reperfusion injury (WI/RI) of isolated rat lung model. Thirty isolated rat lungs were established on the Langendorff apparatus and randomly divided to three groups (n = 10, each): control group (C group), ischemia/reperfusion group (IR group) and Cariporide group (CP group). Mean pulmonary artery pressure (MPAP) and peak airway pressure (pAwP) were monitored continuously. At the end of reperfusion, right bronchoalveolar lavage was performed, bronchoalveolar lavage fluid (BALF) recovery rate (BALFRR) was recorded, and protein content in BALF was measured. Lung water content (LWC), malondialdehyde (MDA) and superoxide dismutase (SOD)of left lung tissue were measured; histomorphology evaluation was performed under light microscope and transmission electron microscope. In comparison with the data from IR group, BALF protein concentration, LWC, MDA content and MPAP content of reperfusion were significantly decreased, but SOD activity was increased in CP group. Histomorphologic feature also showed that pathological change significantly reduced in CP group. In this rat WI/RI model, the mechanism by which the selective Na+/H+ exchanger inhibitor (Cariporide) attenuates lipid peroxidation induced by WI/IR may be: preventing Ca2+ overload via inhibiting the transport of Na+/H2 exchanger-1 (NHE1) in the context of the coupled exchanger, thereby reducing the activation of xanthine oxidase pathway and oxygen free radical liberation which is dependent on certain intracellular Ca2+ concentration, and lastly promoting the endogenous antioxidative mechanism.
