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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Lee, Jin | - |
| dc.contributor.author | Lee, Hae-In | - |
| dc.contributor.author | Seo, Kown-Il | - |
| dc.contributor.author | Cho, Hyun Wook | - |
| dc.contributor.author | Kim, Myung-Joo | - |
| dc.contributor.author | Park, Eun-Mi | - |
| dc.contributor.author | Lee, Mi-Kyung | - |
| dc.date.accessioned | 2014-07-03T04:01:45Z | - |
| dc.date.available | 2014-07-03T04:01:45Z | - |
| dc.date.issued | 2014-07 | - |
| dc.identifier.issn | 0975-1009 (Online); 0019-5189 (Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/29041 | - |
| dc.description | 683-691 | en_US |
| dc.description.abstract | Ursolic acid (UA) is a pentacyclic triterpenoid compound that naturally occurs in fruits, leaves and flowers of medicinal herbs. This study investigated the dose-response efficacy of UA (0.01 and 0.05%) on glucose metabolism, the polyol pathway and dyslipidemia in streptozotocin/nicotinamide-induced diabetic mice. Supplement with both UA doses reduced fasting blood glucose and plasma triglyceride levels in non-obese type 2 diabetic mice. High-dose UA significantly lowered plasma free fatty acid, total cholesterol and VLDL-cholesterol levels compared with the diabetic control mice, while LDL-cholesterol levels were reduced with both doses. UA supplement effectively decreased hepatic glucose-6-phosphatase activity and increased glucokinase activity, the glucokinase/glucose-6-phosphatase ratio, GLUT2 mRNA levels and glycogen content compared with the diabetic control mice. UA supplement attenuated hyperglycemia-induced renal hypertrophy and histological changes. Renal aldose reductase activity was higher, whereas sorbitol dehydrogenase activity was lower in the diabetic control group than in the non-diabetic group. However, UA supplement reversed the biochemical changes in polyol pathway to normal values. These results demonstrated that low-dose UA had preventive potency for diabetic renal complications, which could be mediated by changes in hepatic glucose metabolism and the renal polyol pathway. High-dose UA was more effective anti-dyslipidemia therapy in non-obese type 2 diabetic mice. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | NISCAIR-CSIR, India | en_US |
| dc.rights | CC Attribution-Noncommercial-No Derivative Works 2.5 India | en_US |
| dc.source | IJEB Vol.52(07) [July 2014] | en_US |
| dc.subject | Dyslipidemia | en_US |
| dc.subject | Kidney | en_US |
| dc.subject | Liver | en_US |
| dc.subject | Polypol pathway | en_US |
| dc.subject | Ursolic acid | en_US |
| dc.title | Effects of ursolic acid on glucose metabolism, the polyol pathway and dyslipidemia in non-obese type 2 diabetic mice | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJEB Vol.52(07) [July 2014] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJEB 52(7) 683-691.pdf | 811.01 kB | Adobe PDF | View/Open |
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