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Enhanced Anti-Diabetic Activity of a Combination of Chromium(III) Malate Complex and Propolis and its Acute Oral Toxicity Evaluation

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Abstract

In order to obtain the additional benefit of anti-diabetic activity and protective effects of liver injury for diabetes, the anti-diabetic effect and acute oral toxicity of a combination of chromium(III) malate complex (Cr2(LMA)3) and propolis were assessed. The anti-diabetic activity of the combination of the Cr2LMA3 and propolis was compared with Cr2(LMA)3 and propolis alone in alloxan-induced diabetic mice by daily oral gavage for a period of 2 weeks. Acute oral toxicity of the combination of the Cr2LMA3 and propolis was tested using ICR mice at the dose of 1.0–5.0 g/kg body mass by a single oral gavage and observed for a period of 2 weeks. The results of the anti-diabetic activity of the combination from the aspects of blood glucose level, liver glycogen level, and the activities of aspartate transaminase, alanine transaminase, and alkaline phosphatase indicated that the increased anti-diabetic activity and the protective efficacy of liver injury for diabetes were observed. In acute toxicity study, LD50 (median lethal dose) value for the combination was greater than 5.0 g/kg body mass. The combination of Cr2LMA3 and propolis might represent the nutritional supplement with potential therapeutic value to control blood glucose and exhibit protective efficacy of liver injury for diabetes and non-toxicity in acute toxicity.

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Acknowledgments

This work was supported financially by Specialized Research Fund for the Doctoral Program of Higher Education of China (20103227110004) and Graduate innovative projects in Jiangsu University (CX10B_019X). All authors thank Dr. Mohammed Takase for the language revising and polishing.

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Correspondence to Liu-Qing Yang.

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Wu, XY., Li, F., Zhao, T. et al. Enhanced Anti-Diabetic Activity of a Combination of Chromium(III) Malate Complex and Propolis and its Acute Oral Toxicity Evaluation. Biol Trace Elem Res 148, 91–101 (2012). https://doi.org/10.1007/s12011-012-9347-3

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  • DOI: https://doi.org/10.1007/s12011-012-9347-3

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