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Effect of Jiangtang Xiaoke Granule on liver glycogen content and hepatic glucose metabolism-related genes in type 2 diabetic mice |
Hits 701 Download times 563 Received:September 28, 2021 |
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DOI
10.11656/j.issn.1672-1519.2022.01.22 |
Key Words
Jiangtang Xiaoke Granule;type 2 diabetes mellitus;hepatic glycometabolism;insulin receptor substrate-2;liver glycogen |
Author Name | Affiliation | E-mail | ZHANG Yi | Beijing Open University, Beijing 100081, China | | ZHAO Dandan | Beijing University of Chinese Medicine, Beijing 100029, China | | MO Fangfang | Beijing University of Chinese Medicine, Beijing 100029, China | | GAO Sihua | Beijing University of Chinese Medicine, Beijing 100029, China | gaosihua1216@163.com |
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Abstract
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[Objective] To investigate the effect of Jiangtang Xiaoke Granule (JTXKG) on liver glycogen content andhepatic insulin receptor substrate-2 (IRS-2) mRNA,protein kinase B,PKB/Akt (Akt) mRNA,glycogen synthase kinase 3α (GSK-3α) mRNA expression in type 2 diabetic KK-Ay mice. [Methods] KK-Ay mice,male,8 weeks old,were fed by high-fat-diet for 4 weeks,T2DM model were established by FBG≥13.9 mmol/L. The T2DM mice were then randomly divided into model group,pioglitazone group and JTXKG groups in low (1.75 g/kg),medium (3.50 g/kg),and high (7.00 g/kg) doses. The normal group had C57BL/6J in it and feed by normal diet. After 10-week treatment,the average daily food intake and the rate of weight gain were weighed and calculated. The liver glycogen was examined by Periodic Acid-Schiff stain. The expressions of GSK-3α was examined by real-time fluorescence quantitative PCR,and the effects of JTXKG on the above indexes were observed. [Results] Compared with model group,T2DM mice supplemented with 3.50 g/kg dose of JTXKG can lower GSK-3α mRNA expression (P<0.01) and raise IRS-2 mRNA (P<0.01),Akt mRNA (P<0.01) expression to restore more liver glycogen (P<0.05). The 7 g/kg dose of JTXKG also can raise IRS-2 mRNA and lower hepatic GSK-3α mRNA expression of T2DM mice significantly (P<0.01). [Conclusion] JTXKG can raised the liver glycogen synthetize and repertory function in T2DM mice by regulating hepatic glycometabolism related gene expressions. |
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