Literature DB >> 29417308

Burn-Induced Multiple Organ Injury and Protective Effect of Lutein in Rats.

Huda O AbuBakr1, Samira H Aljuaydi2, Shimaa M Abou-Zeid3, Amanallah El-Bahrawy4.   

Abstract

Thermal injury may lead to multiple organ dysfunction through release of proinflammatory mediators and reactive oxygen radicals. This study investigated the effects of thermal injury on remote organs of rats and the possible protective effect of lutein. Thermal trauma was induced in the back of rats by exposing them to 90 °C bath for 10 s. Rats were sacrificed 48 h after burn, and blood samples were collected to monitor liver and kidney functions. Tissue samples from liver, kidneys, and lungs were taken for studying oxidative stress parameters, gene expressions of TNF-α and Casp-3, besides histopathological examination. Skin scald injury caused significant elevations of liver and kidney function biomarkers in the serum. In tissue samples, increments of MDA, GPx, and 8-OHdG were recorded while GSH level and the activities of CAT and SOD were suppressed. The expressions of TNF-α and caspase-3 mRNA were increased, and histopathological results revealed remote organ injury. Oral administration of lutein (250 mg/kg) resulted in amelioration of the biochemical and molecular changes induced by burn as well as the histopathological alterations. According to the findings of the present study, lutein possesses anti-oxidant, anti-inflammatory, and anti-apoptotic effects that protect against burn-induced damage in remote organs.

Entities:  

Keywords:  Casp-3; TNF-α; lutein; oxidative stress; protection; scald

Mesh:

Substances:

Year:  2018        PMID: 29417308     DOI: 10.1007/s10753-018-0730-x

Source DB:  PubMed          Journal:  Inflammation        ISSN: 0360-3997            Impact factor:   4.092


  71 in total

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Journal:  Burns       Date:  2003-02       Impact factor: 2.744

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7.  [Effects of hydrogen-rich saline on liver of severely scalded rats with delayed resuscitation].

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4.  Protective effects of tiopronin against oxidative stress in severely burned patients.

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5.  Neutralization of interleukin-17A alleviates burn-induced intestinal barrier disruption via reducing pro-inflammatory cytokines in a mouse model.

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