ZHANG Jie-ping, CHEN Xue-hua, YU Wen-zhen, et al. Effect of Compound Shihu Mixture Single-Dose Administration on Insulin Signaling in db/db Mice[J]. Chinese journal of experimental traditional medical formulae, 2017, 23(5): 147-151.
DOI:
ZHANG Jie-ping, CHEN Xue-hua, YU Wen-zhen, et al. Effect of Compound Shihu Mixture Single-Dose Administration on Insulin Signaling in db/db Mice[J]. Chinese journal of experimental traditional medical formulae, 2017, 23(5): 147-151. DOI: 10.13422/j.cnki.syfjx.2017050147.
Effect of Compound Shihu Mixture Single-Dose Administration on Insulin Signaling in db/db Mice
Objective: To study the effect of compound Shihu mixture(CSM) single-dose administration on insulin signaling in db/db mice.Method: According of the fasting blood glucose and body weight
30 male db/db mice of 14-16 weeks were randomly divided into model group
Chinese medicine group 1 and Chinese medicine group 2; another 10 db/m mice were selected as normal group. After single-dose administration of CSM1 and CSM2
glucose tolerance(OGTT) levels were determined from the overall aspect. The changes in levels of 6-phosphofructokinase-1 (PFK)
pyruvate dehydrogenase (PDH)
and expression levels of insulin receptor (InsR) and Akt phosphorylation were determined at 30 min and 60 min of administration.Result: As compared with the normal group
the blood glucose OGTT levels were significantly increased in model group at 0
30
60
120 min; activities of PFK and PDH in hepatic cells were significantly decreased; the protein expression levels of InsR and Akt were significantly reduced at 30 min and 60 min (P<0.01). As compared with the model group
the single-dose administration of both CSM1 and CSM2 could significantly reduce blood glucose OGTT levels at 60
120 min (P<0.05
P<0.01); increase the activities of PFK and PDH in hepatic cells
and promote the phosphorylation levels of InsR Tyr1150/1151
Akt Ser473 and Thr308 in a time-dependent manner(P<0.05
P<0.01).Conclusion: Single-dose administration of both CSM1 and CSM2 could improve the glucose tolerance in db/db mice and increase the activities of PFK and PDH in hepatic cells. The mechanism may be associated with improving insulin signal transduction and promoting the phosphorylation of InsR Tyr150/1151
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