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Insulin Sensitizer and Antihyperlipidemic Effects of Cajanus Cajan (L.) Millsp. Root in Methylglyoxal-Induced Diabetic Rats

卡亚努斯 化学 胰岛素 二甲双胍 糖尿病 内科学 胰岛素抵抗 甘油三酯 药理学 内分泌学 生物化学 医学 胆固醇 生物 园艺
作者
Shu-Er Yang,Y.F. Lin,Jiunn‐Wang Liao,Jianting Chen,Chien‐Lin Chen,Chen-I Chen,Shih‐Lan Hsu,Tuzz‐Ying Song
出处
期刊:Chinese Journal of Physiology [Medknow Publications]
卷期号:65 (3): 125-135 被引量:7
标识
DOI:10.4103/cjp.cjp_88_21
摘要

Cajanus cajan (L.) Millsp., known as pigeon pea, is one of the major grain legume crops of the tropical world. It recognizes as an ethnomedicine to possess various functions, such as helping in healing wound and cancer therapy. We investigated whether 95% ethanol extracts from C. cajan root (EECR) protect against methylglyoxal (MGO)-induced insulin resistance (IR) and hyperlipidemia in male Wistar rats and explored its possible mechanisms. The hypoglycemic potential of EECR was evaluated using α-amylase, α-glucosidase activities, and advanced glycation end products (AGEs) formation. For in vivo study, the rats were divided into six groups and orally supplemented with MGO except for Group 1 (controls). Group 2 was supplemented with MGO only, Group 3: MGO + metformin, Group 4: MGO + Low dose-EECR (L-EECR; 10 mg/kg bw), Group 5: MGO + Middle dose-EECR (M-EECR; 50 mg/kg bw), and Group 6: MGO + High dose-EECR (H-EECR; 100 mg/kg bw). EECR possessed good inhibition of α-glucosidase, α-amylase activities, and AGEs formation (IC50 = 0.12, 0.32, and 0.50 mg/mL), respectively. MGO significantly increased serum levels of blood glucose (GLU), glycosylated hemoglobin, homeostasis model assessment of IR, AGEs, lipid biochemical values, and atherogenic index, whereas EECR decreased these levels in a dose-dependent manner. EECR can also act as an insulin sensitizer, which significantly decreased (47%, P < 0.05) the blood GLU levels after intraperitoneal injection of insulin in the insulin tolerance tests. The hypoglycemic and antihyperlipidemic mechanisms of EECR are likely through several possible pathways including the inhibition of carbohydrate-hydrolyzing enzymes (α-glucosidase and α-amylase) and the enhancement of MGO-trapping effects on inhibition of AGEs formation.

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