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类胡萝卜素对阿霉素诱导的心脏和肝脏毒性的改善作用。

Amelioration of doxorubicin induced cardio-and hepato-toxicity by carotenoids.

作者信息

Indu R, Azhar T S, Nair Arathy, Nair Cherupally Krishnan Krishnan

机构信息

Department of Radiation Biology, Pushpagiri Institute of Medical Sciences and Research Centre, Tiruvalla, Kerala, India.

出版信息

J Cancer Res Ther. 2014 Jan-Mar;10(1):62-7. doi: 10.4103/0973-1482.131370.

Abstract

AIM OF STUDY

The aim of this study is to explore the ability of the carotenoids (CARs) to offer protection against acute cardiotoxicity and hepatotoxicity induced by doxorubicin (DOX) (25 mg/kg) in tumor bearing Swiss albino mice.

MATERIALS AND METHODS

Tumor bearing Swiss albino mice administered with DOX (25 mg/kg, i.p) and two doses of CARs (50 and 100 μg/kg). 24 h after administration of the drugs, histopathological evaluation of tumor, liver and heart tissues carried out. Furthermore, various antioxidant parameters in these tissues were investigated. Serum marker enzymes for tissue injury were examined.

RESULTS

Administration of CARs prevented the depletion of antioxidants in the heart and liver, thereby protecting the tissue damage and release of marker enzymes. However, similar antioxidant depletion was not observed in the tumor tissue. CARs prevented DOX induced variation in tissue architecture in heart and liver tissues. However, CARs did not influence DOX induced alterations in the tumor.

CONCLUSION

Administration of CARs could prevent DOX induced acute toxicity to heart and liver.

摘要

研究目的

本研究旨在探讨类胡萝卜素(CARs)对荷瘤瑞士白化小鼠由阿霉素(DOX)(25mg/kg)诱导的急性心脏毒性和肝毒性的保护能力。

材料与方法

给荷瘤瑞士白化小鼠注射DOX(25mg/kg,腹腔注射)和两剂CARs(50和100μg/kg)。给药24小时后,对肿瘤、肝脏和心脏组织进行组织病理学评估。此外,还研究了这些组织中的各种抗氧化参数。检测了组织损伤的血清标志物酶。

结果

给予CARs可防止心脏和肝脏中抗氧化剂的消耗,从而保护组织损伤和标志物酶的释放。然而,在肿瘤组织中未观察到类似的抗氧化剂消耗。CARs可防止DOX诱导的心脏和肝脏组织结构变化。然而,CARs不影响DOX诱导的肿瘤改变。

结论

给予CARs可预防DOX诱导的心脏和肝脏急性毒性。

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