Effect of Jiangtang Xiaozhi Tablets on Expression of Insulin Receptor and Insulin Receptor Substrate-1 in KK-A Transgenic Mice Model of Diabetes Mellitus
ZHENG Yong-qiu, GE Zheng-yan, JIN Long, et al. Effect of Jiangtang Xiaozhi Tablets on Expression of Insulin Receptor and Insulin Receptor Substrate-1 in KK-A Transgenic Mice Model of Diabetes Mellitus[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(3): 175-179.
ZHENG Yong-qiu, GE Zheng-yan, JIN Long, et al. Effect of Jiangtang Xiaozhi Tablets on Expression of Insulin Receptor and Insulin Receptor Substrate-1 in KK-A Transgenic Mice Model of Diabetes Mellitus[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(3): 175-179.DOI:
Objective:To observe effects of Jiangtang Xiaozhi(JTXZ) tablets on expression of insulin receptor β(InsRβ) and insulin receptor substrate-1(IRS-1) in KK-Ay transgenic mice model of diabetes mellitus (DM). Method: KK-Ay transgenic mice were used and fed with high-fat diet to induce hyperglycemia as a model of DM obesity. The C57mice with same age of KK-Ay transgenic mice were used as a control group. Thereafter
Fifty-five mice with DM obesity were divided into 5 groups (n=11) including model group without any treatment
pioglitazone hydrochloride tablets treatment group as a positive control group
and JTXZ tablets groups at high
middle and low treatment doses
and were continuously given JTXZ tablets by intragastric administration for 8 weeks. All mice were sacrificed after treatment of 8 weeks. The pathology examination of abdominal salivary gland was performed. The expression of InRβ and IRS-1 were deteced
respectively. Result: In the JTXZ tablets treatment group
compared with that in KK-Ay transgenic mice model with DM obesity
the pancreatic pathological changes were ameliorated significantly. Expression of InRβ and IRS-1 were increased in each treatment group by JTXZ tablets
respectively. Conclusion: JTXZ tablets have obvious effects of increasing levels of InRβ and IRS-1 in KK-Ay transgenic mice model with DM obesity.