Abstract
Administration of rutin (50 and 100 mg/kg) and pioglitazone (10 mg/kg) orally for 3 weeks treatment significantly improved body weight, reduced plasma glucose and glycosylated hemoglobin, pro-inflammatory cytokines (IL-6 and TNF-alpha), restored the depleted liver antioxidant status and serum lipid profile in high fat diet + streptozotocin induced type 2 diabetic rats. Rutin treatment also improved histo-architecture of beta islets and reversed hypertrophy of hepatocytes. Rutin exhibited significant antidiabetic activity, presumably by inhibiting inflammatory cytokines, improving antioxidant and plasma lipid profiles in High fat diet + streptozotocin induced type 2 diabetic model and may be useful as a diabetic modulator along with standard antidiabetic drugs. However, such effects need to be confirmed on human subjects in clinical condition.
MeSH terms
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Animals
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Antioxidants / metabolism*
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Biomarkers / metabolism
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Blood Glucose / analysis
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Body Weight / drug effects
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Diabetes Complications / drug therapy
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Diabetes Complications / etiology
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Diabetes Complications / metabolism
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Diabetes Mellitus, Experimental / complications
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Diabetes Mellitus, Experimental / drug therapy*
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Diabetes Mellitus, Experimental / metabolism
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Diabetes Mellitus, Type 2 / complications
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Diabetes Mellitus, Type 2 / drug therapy*
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Diabetes Mellitus, Type 2 / metabolism
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Diet, High-Fat / adverse effects
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Female
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Glycated Hemoglobin / analysis
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Hyperglycemia / drug therapy*
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Hyperglycemia / etiology
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Hyperglycemia / metabolism
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Hypoglycemic Agents / pharmacology
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Insulin / metabolism
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Insulin-Secreting Cells / metabolism
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Interleukin-6 / metabolism*
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Lipids / blood*
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Male
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Mice
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Pioglitazone
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Rats, Sprague-Dawley
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Rutin / pharmacology*
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Thiazolidinediones / pharmacology
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Tumor Necrosis Factor-alpha / metabolism*
Substances
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Antioxidants
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Biomarkers
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Blood Glucose
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Glycated Hemoglobin A
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Hypoglycemic Agents
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Insulin
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Interleukin-6
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Lipids
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Thiazolidinediones
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Tumor Necrosis Factor-alpha
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Rutin
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Pioglitazone