Effect of Agaricus blazei Murill on the Pulmonary Tissue of Animals with Streptozotocin-Induced Diabetes. (26th May 2010)

• Record Type: Journal Article
• Authors: Di Naso, Fábio Cangeri; de Mello, Rodrigo Noronha; Bona, Sílvia; Dias, Alexandre Simões; Porawski, Marilene; Ferraz, Alexandre de Barros Falcão; Richter, Marc François; Marroni, Norma Possa
• Other Names: Chakrabarti Subrata K. Academic Editor.
• Is Part Of: Experimental diabetes research. Volume 2010(2010)
• Publication Date: 2010-05-26
• Subjects: Diabetes -- Research -- Periodicals; Diabetes -- Research; Periodicals; 616.462
• DOI: 10.1155/2010/543926
• Languages: English
• ISSNs: 1687-5214

Abstract

Abstract : The present study was designed to evaluate the oxidative stress as well as the therapeutic effect of Agaricus blazei Muril ( A. Blazei ) in rats with streptozotocin-induced diabetes. We used 25 Wistar rats, and DM was induced by injecting streptozotocin (70 mg/Kg i.p.). Agaricus blazei Muril was administered daily starting 40 days after disease onset. A. Blazei was tested as an aqueous extract for its phytochemical composition, and its antioxidant activity in vitro was also evaluated. Lipoperoxidation (LPO), and superoxide dismutase (SOD), catalase, and glutathione peroxidase activities were measured in the pulmonary tissue, as well as the presence of inducible nitric oxide synthase (iNOS), through immunohistochemistry. An anatomopathologic study was also performed. Phytochemical screening of A. Blazei detected the presence of alkaloids and saponins. The extract exhibited a significant antioxidant activity in the DPPH-scavenging and the hipoxanthine/xanthine oxidase assays. Pulmonary LPO increased in diabetic animals (0.43 ± 0.09 ;P < .001 ) as compared to the control group (0.18 ± 0.02 ), followed by a reduction in the A. Blazei -treated group (0.33 ± 0.04 ;P < .05 ). iNOS was found increased in the lung in diabetic rats and reduced in the A. Blazei -treated group. The pulmonary tissue in diabetic rats showed oxidative alterations related to the streptozotocin treatment. The A. Blazei treatment effectively reduced the oxidative stress and contributed to tissue recovery.