کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5553121 1557954 2017 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Suppressive effect of Spirulina fusiformis on diclofenac-induced hepato-renal injury and gastrointestinal ulcer in Wistar albino rats: A biochemical and histological approach
موضوعات مرتبط
علوم پزشکی و سلامت پزشکی و دندانپزشکی تومور شناسی
پیش نمایش صفحه اول مقاله
Suppressive effect of Spirulina fusiformis on diclofenac-induced hepato-renal injury and gastrointestinal ulcer in Wistar albino rats: A biochemical and histological approach
چکیده انگلیسی

ContextThe non-steroidal anti-inflammatory drug (NSAID), diclofenac causes hepato-renal toxicity and gastric ulcer. The aim of this study was to investigate the protective effect of Spirulina fusiformis on Diclofenac-induced toxicity in Wistar albino rats.MethodsRats were treated as follows: normal control (group I); diclofenac (50 mg/kg b.w., i.p.) treated rats (group II); diclofenac-induced (50 mg/kg b.w., i.p.) rats treated with Spirulina fusiformis (400 mg/kg b.w., p.o.) (group III); diclofenac-induced (50 mg/kg b.w., i.p.) rats treated with silymarin (25 mg/kg b.w., p.o.) (group IV); Spirulina fusiformis (400 mg/kg b.w., p.o.) alone treated rats (group V). Biochemical (liver and kidney functional markers) and antioxidant parameters (enzymic and non-enzymic antioxidants) were measured in the blood and tissue homogenates of the rats. Evaluation of intestinal ulcer score and assessment of liver and kidney histology were also done.DiscussionAlterations in the levels of biochemical and antioxidant assays and histopathological changes in liver and kidney proved the toxic effect of diclofenac. The ulcer score was significantly increased in the diclofenac treated rats. Spirulina fusiformis showed to reduce such changes and was able to restore normal antioxidant status in the rats.ConclusionOur study proves the hepato-renal and gastroprotective activity of Spirulina fusiformis in diclofenac-treated rats.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biomedicine & Pharmacotherapy - Volume 88, April 2017, Pages 11-18
نویسندگان
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