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Effect of Jiangtang Xiaoke Granule on liver glycogen content and hepatic glucose metabolism-related genes in type 2 diabetic mice
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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 NameAffiliationE-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 
Abstract
    [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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