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      Hesperidin, a citrus bioflavonoid, decreases the oxidative stress produced by carbon tetrachloride in rat liver and kidney

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      1 , 1 , 1 , 1 ,
      BMC Pharmacology
      BioMed Central

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          Abstract

          Background

          CCl 4 is a well-established hepatotoxin inducing liver injury by producing free radicals. Exposure to CCl 4 also induces acute and chronic renal injuries. The present study was designed to establish the protective effect of hesperidin (HDN), a citrus bioflavonoid, on CCl 4-induced oxidative stress and resultant dysfunction of rat liver and kidney.

          Methods

          Animals were pretreated with HDN (100 and 200 mg/kg orally) for one week and then challenged with CCl 4 (2 ml/kg/s.c.) in olive oil. Rats were sacrificed by carotid bleeding under ether anesthesia. Liver enzymes, urea and creatinine were estimated in serum. Oxidative stress in liver and kidney tissue was estimated using Thiobarbituric acid reactive substances (TBARS), glutathione (GSH) content, superoxide dismutase(SOD), and Catalase (CAT)

          Results

          CCl 4 caused a marked rise in serum levels of ALT and AST (P < 0.05). TBARS levels were significantly increased whereas GSH, SOD and CAT levels decreased in the liver and kidney homogenates of CCl 4 treated rats. HDN (200 mg/kg) successfully attenuated these effects of CCl 4

          Conclusion

          In conclusion, our study demonstrated a protective effect of HDN in CCl 4 induced oxidative stress in rat liver and kidney. This protective effect of HDN can be correlated to its direct antioxidant effect.

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          Most cited references40

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          Chemistry and pharmacology of the Citrus bioflavonoid hesperidin.

          Hesperidin, a bioflavonoid, is an abundant and inexpensive by-product of Citrus cultivation. A deficiency of this substance in the diet has been linked with abnormal capillary leakiness as well as pain in the extremities causing aches, weakness and night leg cramps. No signs of toxicity have been observed with the normal intake of hesperidin or related compounds. Both hesperidin and its aglycone hesperetin have been reported to possess a wide range of pharmacological properties. This paper reviews various aspects of hesperidin and its related compounds, including their occurrence, physical and chemical properties, analysis, pharmacokinetics, safety and toxicity and the marketed products available. A special emphasis has been laid on the pharmacological properties and medicinal uses of these compounds. Copyright 2001 John Wiley & Sons, Ltd.
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            Catalase, superoxide dismutase, and glutathione peroxidase activities in various rat tissues after carbon tetrachloride intoxication.

            The aim of this study was to determine the possible relationship between the activity of three different antioxidant enzymes--peroxidase superoxide dismutase, catalase, and glutathione peroxidase--and carbon tetrachloride-induced injury. Male Wistar rats weighing 200-250 g were used in the experiments. Rats of the experimental groups were given carbon tetrachloride 0.5 ml/kg i.p. in olive oil (5 mmol/kg body mass) for 1 or 3 days. Control group rats were injected with olive oil only for the same period. Brain, liver, kidney, and heart supernatants were used for measurement of superoxide dismutase (SOD), catalase, and glutathione peroxidase (GPX) activities. No statistically significant changes in SOD and GPX activities were observed in the liver after CCl4 administration, but catalase activity was significantly increased after 24 h and remained at that level during the course of the study. In the brain, SOD and catalase activities decreased after 24 h of experiment, but GPX activity statistically significantly increased at all time points studied. Increased activities of SOD, catalase, and GPX were found in heart after CCl4 intoxication. The CCl4 injection in our experiment caused a reduction of SOD and catalase activities and increased GPX activity in the kidney. The results suggest that change in antioxidant enzyme activities may be relevant to the ability of the liver and other investigated organs to cope with oxidative stress during CCl4 poisoning.
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              Protective effects of lemon flavonoids on oxidative stress in diabetic rats.

              The effects of lemon flavonoids, as crude flavonoids prepared from lemon juice, were investigated in diabetic rats. The oxidative stress of eriocitrin (eriodictyol 7-O-beta-rutinoside) and hesperidin (hesperetin 7-O-beta-rutinoside) on streptozotocin-induced diabetic rats was investigated. Diabetic rats were given a diet which contained 0.2% crude flavonoids, 0.2% eriocitrin, and 0.2% hesperidin. After the 28-d feeding period, the concentration of the thiobarbituric acid-reactive substance in the serum, liver, and kidney of diabetic rats administered crude flavonoids, eriocitrin, and hesperidin significantly decreased as compared with that of the diabetic group. The levels of 8-hydroxydeoxyguanosine, which is exchanged from deoxyguanosine owing to oxidative stress, in the urine of diabetic rats administered eriocitrin and hesperidin significantly decreased as compared with that of the diabetic rat group. Crude flavonoids, eriocitrin, and hesperidin suppressed the oxidative stress in the diabetic rats. These results demonstrated that dietary lemon flavonoids of eriocitrin and hesperidin play a role as antioxidant in vivo.
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                Author and article information

                Journal
                BMC Pharmacol
                BMC Pharmacology
                BioMed Central (London )
                1471-2210
                2005
                31 January 2005
                : 5
                : 2
                Affiliations
                [1 ]Pharmacology division, University Institute of Pharmaceutical Sciences, Panjab University, Chandigarh-160014, India
                Article
                1471-2210-5-2
                10.1186/1471-2210-5-2
                549532
                15683547
                42d70f59-1d84-43d4-af38-a2c8b1ea4f89
                Copyright © 2005 Tirkey et al; licensee BioMed Central Ltd.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 22 July 2004
                : 31 January 2005
                Categories
                Research Article

                Pharmacology & Pharmaceutical medicine
                Pharmacology & Pharmaceutical medicine

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