[Effects of adipokine chemerin on the improvement of islet function in diabetic mice by aerobic exercise and its mechanisms].

Qi-Long Zhang, Jing Qu, Xiao-Hui Wang
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Abstract

Objective: To investigate the effects of adipokines chemerin on the improvement of islet function caused by exercise in mice with diabetes, and the possible mechanism of glucagon-like peptide 1 (GLP-1). Methods: Male ICR mice were randomly divided into a control group fed with normal diet (Con, n=6) and a diabetic modeling group fed with 60% kcal high-fat diet (n=44). After 6 weeks, the diabetic modeling group was once given a fasting intraperitoneal injection of streptozotocin (100 mg/kg). The successfully modeled mice were divided into diabetes group (DM), diabetes plus exercise group (EDM), and diabetes plus exercise and exogenous chemerin group (EDMC), 6 in each group. Mice in exercise groups participated in a six-week modest intensity treadmill running exercise with a gradually increased load. Mice in the EDMC group were intraperitoneally injected with exogenous chemerin (8 μg/kg) from the 4th week of the exercise period, six days per week, and one time per day. And the other groups were untreated. Adipose chemerin knockout mice were constructed. Then they and the control mice were divided into 6 groups (n=4): Normal diet control group (Con-ND), Normal diet chemerin knockout heterozygote mice group (Chemerin(+/-)-ND), Normal diet chemerin knockout homozygotes mice group(Chemerin(-/-)-ND), High-fat diet control group (Con-HFD), High-fat diet chemerin knockout heterozygote mice group (Chemerin(+/-)-HFD), High-fat diet chemerin knockout homozygotes mice group (Chemerin(-/-)-HFD). They were fed with normal or high-fat diet for 11 weeks and oral glucose tolerance test (OGTT) was conducted. After the mice of each group were executed under anesthesia, the samples such as pancreas and colon were collected. Fasting blood glucose (FBG) and fasting insulin (FINS) levels in mice were measured, and the insulin resistance index (HOMA-IR) was calculated. HE staining was used to observe the structure of islets. ELISA was used to detect the GLP-1 level in serum. The mRNA levels of proglucagon (GCG) and chemerin in the colon were measured by real-time PCR. And the protein levels of GCG and chemerin in the colon were detected by Western blot. Results: Compared with the DM group, the vacuolar degeneration and shrinkage of islet cells in the EDM group were reduced, the islet structure was improved, while the levels of FINS, HOMA-IR and FBG were decreased significantly (P<0.05 or P<0.01). The colon and serum chemerin levels were decreased significantly(P<0.05), while the colonic GCG mRNA and protein levels were increased significantly (P<0.05 or P<0.01). Compared with the EDM group, the islet cells in the EDMC group were shrunken, with unclear borders. The structure of the islets was damaged, and the levels of FINS, HOMA-IR and FBG were increased significantly (P<0.01), while the mRNA and protein levels of GCG were decreased significantly (P<0.05 or P<0.01). Compared with the Con-HFD group, the blood glucose at 30, 90 and 120 min after oral glucose in the chemerin (-/-)-HFD group was significantly lower (P<0.01), and the area under the blood glucose time curve was significantly lower (P<0.01). The islets had clear structure, regular shape and well-defined boundaries, while the serum GLP-1 and colonic GCG protein levels were increased significantly(P<0.05). Conclusion: Aerobic exercise improves the structure and function of pancreatic islets by reducing the level of chemerin in diabetes mice, which is related to the negative regulation of chemerin on GLP-1 level.

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脂肪因子趋化素对有氧运动改善糖尿病小鼠胰岛功能的影响及其机制
目的:探讨脂肪因子趋化素对运动所致糖尿病小鼠胰岛功能的改善作用,并探讨胰高血糖素样肽1 (GLP-1)的作用机制。方法:将雄性ICR小鼠随机分为正常对照组(Con, n=6)和糖尿病造模组(n=44),分别饲喂60% kcal高脂饲料。6周后,糖尿病造模组1次空腹腹腔注射链脲佐菌素(100 mg/kg)。将成功造模的小鼠分为糖尿病组(DM)、糖尿病+运动组(EDM)和糖尿病+运动+外源性趋化素组(EDMC),每组6只。运动组小鼠参加为期六周的中等强度的跑步机运动,逐渐增加负荷。EDMC组小鼠从运动期第4周开始腹腔注射外源性chemerin (8 μg/kg),每周6天,每天1次。而其他组则未经治疗。构建脂肪趋化素基因敲除小鼠。将其与对照组随机分为6组(n=4):正常饮食对照组(Con-ND)、正常饮食除化素杂合子组(chemerin (+/-)- nd)、正常饮食除化素纯合子组(chemerin (-/-)- nd)、高脂肪饮食对照组(Con-HFD)、高脂肪饮食除化素杂合子组(chemerin (+/-)- hfd)、高脂肪饮食除化素纯合子组(chemerin (-/-)- hfd)。分别饲喂正常或高脂饲料11周,并进行口服葡萄糖耐量试验(OGTT)。各组小鼠麻醉处死后,取胰腺、结肠等标本。测定小鼠空腹血糖(FBG)和空腹胰岛素(FINS)水平,计算胰岛素抵抗指数(HOMA-IR)。HE染色观察胰岛组织结构。ELISA法检测血清GLP-1水平。实时荧光定量PCR检测大鼠结肠胰高血糖素(GCG)和趋化素(chemerin) mRNA表达水平。Western blot法检测大鼠结肠组织中GCG和趋化素蛋白水平。结果:与DM组比较,EDM组胰岛细胞空泡变性和萎缩减轻,胰岛结构改善,FINS、HOMA-IR、FBG水平明显降低(P<0.05或P<0.01)。结肠和血清趋化素水平极显著降低(P<0.05),结肠GCG mRNA和蛋白水平极显著或极显著升高(P<0.05或P<0.01)。与EDM组比较,EDMC组胰岛细胞萎缩,边界不清。胰岛结构受损,FINS、HOMA-IR和FBG水平显著升高(P<0.01), GCG mRNA和蛋白水平显著或极显著降低(P<0.05或P<0.01)。与Con-HFD组相比,化疗素(-/-)- hfd组口服葡萄糖后30min、90min、120min血糖显著降低(P<0.01),血糖时间曲线下面积显著降低(P<0.01)。胰岛结构清晰、形状规则、边界明确,血清GLP-1和结肠GCG蛋白水平显著升高(P<0.05)。结论:有氧运动通过降低趋化素水平改善糖尿病小鼠胰岛结构和功能,这与趋化素对GLP-1水平的负调控有关。
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