Volume 11, Issue 1 860970 pp. 788-800
Open Access

Antioxidant Activity of Artocarpus heterophyllus Lam. (Jack Fruit) Leaf Extracts: Remarkable Attenuations of Hyperglycemia and Hyperlipidemia in Streptozotocin-Diabetic Rats

Haidy S. Omar

Haidy S. Omar

Phytochemistry Department National Organization of Drug Control and Research Cairo, Egypt

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Hesham A. El-Beshbishy

Corresponding Author

Hesham A. El-Beshbishy

Medical Laboratories Technology Department Faculty of Applied Medical Sciences Taibah University Madinah, Saudi Arabia , taibahu.edu.sa

Biochemistry Department Faculty of Pharmacy Al-Azhar University Cairo, Egypt , azhar.edu.eg

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Ziad Moussa

Ziad Moussa

Chemistry Department Faculty of Science Taibah University Madinah, Saudi Arabia , taibahu.edu.sa

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Kamilia F. Taha

Kamilia F. Taha

Phytochemistry Department National Organization of Drug Control and Research Cairo, Egypt

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Abdel Nasser B. Singab

Abdel Nasser B. Singab

Pharmacognosy Department Faculty of Pharmacy Ain Shams University Cairo, Egypt , asu.edu.eg

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First published: 2011
Citations: 1
Academic Editor: Robert M. Cohen

Abstract

The present study examines the antioxidative, hypoglycemic, and hypolipidemic activities of Artocarpus heterophyllus (jack fruit) leaf extracts (JFEs). The 70% ethanol (JFEE), n-butanol (JFBE), water (JFWE), chloroform (JFCE), and ethyl acetate (JFEAE) extracts were obtained. Both JFEE and JFBE markedly scavenge diphenylpicrylhydrazyl radical and chelate Fe+2in vitro. A compound was isolated from JFBE and identified using 1D and 2D 1H- and 13C-NMR. The administration of JFEE or JFBE to streptozotocin (STZ)-diabetic rats significantly reduced fasting blood glucose (FBG) from 200 to 56 and 79 mg%, respectively; elevated insulin from 10.8 to 19.5 and 15.1 μU/ml, respectively; decreased lipid peroxides from 7.3 to 5.4 and 5.91 nmol/ml, respectively; decreased %glycosylated hemoglobin A1C (%HbA1C) from 6.8 to 4.5 and 5.0%, respectively; and increased total protein content from 2.5 to 6.3 and 5.7 mg%, respectively. Triglycerides (TG), total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), VLDL-C, and LDL/HDL ratio significantly declined by -37, -19, -23, -37, and -39%, respectively, in the case of JFEE; and by -31, -14, -17, -31, and -25%, respectively, in the case of JFBE; as compared to diabetic rats. HDL-C increased by +37% (JFEE) and by +11% (JFBE). Both JFEE and JFBE have shown appreciable results in decreasing FBG, lipid peroxides, %HbA1C, TC, LDL-C, and TG levels, and increasing insulin, HDL-C, and protein content. The spectrometric analysis confirmed that the flavonoid isolated from JFBE was isoquercitrin. We can conclude from this study that JFEE and JFBE exert hypoglycemic and hypolipidemic effects in STZ-diabetic rats through an antioxidative pathway that might be referred to their flavonoid contents.

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