摘要
目的:建立糖尿病肥胖小鼠模型,观察降糖消脂片对模型小鼠胰腺胰岛素受体及底物表达的影响。方法:采用KK-Ay转基因小鼠,高脂饲料喂养造成糖尿病肥胖小鼠模型。对照组为同龄C57小鼠,成模的KK-Ay小鼠分为模型组、吡格咧酮组、降糖消脂片高、中、低剂量组(10,5,2.5 g.kg-1)(11只/组),连续灌胃给药(ig)8周。每周称体重及摄食量,隔周测血糖。药后8周取胰腺作病理切片,并取胰腺组织检测胰岛素受体及底物表达。结果:降糖消脂片各剂量组明显减轻糖尿病肥胖小鼠体重,降低血糖。病理结果显示:降糖消脂片可减少变性及凋亡的胰岛细胞。糖尿病肥胖模型组小鼠胰腺组织胰岛素受体β(insulin receptorβ,InsRβ)和胰岛素受体底物-1(insulin receptor substrate 1,IRS-1)的表达低于对照组。降糖消脂片可有效诱导InsRβ和IRS-1表达。结论:降糖消脂片对KK-Ay糖尿病肥胖小鼠有明显的治疗作用,并可诱导胰岛素受体及底物表达。
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.
出处
《中国实验方剂学杂志》
CAS
北大核心
2013年第3期175-179,共5页
Chinese Journal of Experimental Traditional Medical Formulae
基金
综合性中药新药研究开发技术大平台(2009ZX09301-005-007)
重大新药创制-中药医院制剂新药研发(2010ZX09102-213)