ZHANG Jie-ping, QING Chong-tao, YU Wen-zhen, et al. Effects of Jinkui Shenqi Wan on Expression of Insulin Receptor of Skeletal Muscle in Rats with Diabetes[J]. Chinese journal of experimental traditional medical formulae, 2014, 20(22): 165-168.
DOI:
ZHANG Jie-ping, QING Chong-tao, YU Wen-zhen, et al. Effects of Jinkui Shenqi Wan on Expression of Insulin Receptor of Skeletal Muscle in Rats with Diabetes[J]. Chinese journal of experimental traditional medical formulae, 2014, 20(22): 165-168. DOI: 10.13422/j.cnki.syfjx.2014220165.
Effects of Jinkui Shenqi Wan on Expression of Insulin Receptor of Skeletal Muscle in Rats with Diabetes
Objective:To investigate the effect of Jinkui Shenqi Wan(JKSQ) on insulin receptor (InsR) gene expression in skeletal muscle. Method: With 4 weeks fed high fat high sugar diet
male SD SPF rats of 6 weeks were induced diabete by intraperitoneal injection with streptozotocin. After 4 days the model rats were randomly divided into model group
metformin group
JKSQ low dose group and high dose group. The normal group and model group were given physiological saline
metformin group was given metformin (100 mg · kg-1)
JKSQ low dose group and high dose group were given JKSQ (10
20 g · kg-1) by gavage for 4 weeks. Hexokinase (HK)
6-phosphofructokinase-1(PFK) activity of skeletal muscle were detected. The mRNA and protein expression lever of InsR were detected with RT-PCR and Western blot. Result: As compared with normal group
HK and PFK activity decreased in model group (P<0.01)
the mRNA and protein expression of InsR were decreased markedly (P<0.01). During 4 weeks with drug treatment
as compared with the model group
medicine HK and PFK activity were significantly increased in positive control group
JKSQ low dose group and high dose group (P<0.05);while each of the above groups InsR expression on mRNA and protein were significantly increased (P<0.05). Conclusion: JKSQ can increase the mRNA and protein lever expression of InsR
and increas HK and PFK activity
to promote the oxidation of glucose utilization in skeletal muscle.
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