Protective effect of astaxanthin against cisplatin-induced gastrointestinal toxicity in rats
Autor: | Levent Tumkaya, Tolga Mercantepe, Yeliz Yilmaz, Kerimali Akyildiz |
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Rok vydání: | 2020 |
Předmět: |
Cisplatin
medicine.medical_specialty Antioxidant business.industry medicine.medical_treatment Glutathione Malondialdehyde Small intestine Lipid peroxidation 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Endocrinology medicine.anatomical_structure chemistry Astaxanthin 030220 oncology & carcinogenesis Internal medicine medicine Immunohistochemistry 030211 gastroenterology & hepatology Surgery business medicine.drug |
Zdroj: | European Surgery. 54:32-38 |
ISSN: | 1682-4016 1682-8631 |
DOI: | 10.1007/s10353-020-00643-2 |
Popis: | The aim of the present study was to demonstrate astaxanthin’s attenuating effects against cisplatin (CIS)-induced gastrointestinal toxicity in a rat model. Thirty-two Wistar rats (weight 200–250 g) were divided into four groups (8 rats/group): control group, CIS group, astaxanthin 25 (ASTA25) group, and astaxanthin 75 (ASTA75) group. Tissue samples of small intestine extracted from rats were histopathologically and immunohistochemically analyzed. Histopathological findings were graded with the Duodenal Histopathological Damage Score. Evaluation of enterocytes showing caspase‑3 positivity was performed using the Immunohistochemistry Positivity Score. Intestinal glutathione (GSH) shows the endogenous antioxidant level. Lipid peroxidation in the intestinal tissue was evaluated by measuring the level of malondialdehyde (MDA), which is the end product of lipid peroxidation. In the ASTA25 group, we observed a significant decrease in the number of necrotic enterocytes, mucosal ulceration, and inflammation. In the ASTA75 group, enterocytes with normal microvilli were noticeable. According to the immunohistochemical results, in the ASTA25 and ASTA75 groups, caspase‑3 positivity scores in enterocytes were lower than the CIS group. Astaxanthin administration significantly inhibited MDA increase in intestinal tissue (p |
Databáze: | OpenAIRE |
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