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Nesfatin-1对肥胖大鼠糖脂代谢的影响研究

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为了探究Nesfatin-1 对肥胖大鼠糖脂代谢的影响,试验首先将 40 只 8 周龄健康SPF级SD大鼠随机分为对照组(n=8)和模型组(n=32),对照组饲喂维持日粮,模型组饲喂高脂日粮,连续饲喂 10 周,当模型组体重(空腹条件下)较对照组增加 20%以上视为造模成功;将造模成功的 32 只大鼠随机分为模型对照组(n=8)和模型试验组[Nesfatin-1 低剂量组(n=8)、Nesfatin-1 中剂量组(n=8)和Nesfatin-1 高剂量组(n=8)],Nesfatin-1 低、中、高剂量组按体重分别尾静脉注射 1,10,100 μg/kg 的 Nesfatin-1,每天 1 次,连续给药 5 周;对照组和模型对照组按体重10 mL/kg注射生理盐水,每天 1 次,连续注射 5 周。试验结束后,采用ELISA方法检测各组血清游离脂肪酸(free fatty acids,FFA)、总胆固醇(total cholesterol,TC)、三酰甘油(triglyceride,TG)、肿瘤坏死因子-α(tumor necrosis factor-α,TNF-α)和白细胞介素-10(interleukin-10,IL-10)浓度,采集各组大鼠肝脏组织进行称重,采用实时荧光定量PCR方法检测各组肝脏中与糖脂代谢相关的miR-122、miR-802 的表达水平及肩胛骨脂肪组织中解偶联蛋白-1(uncoupling protein-1,UCP-1)基因 mRNA的表达,并采用BCA法测定对照组、模型对照组及与模型对照组肩胛骨脂肪组织中UCP-1 基因mRNA表达水平有显著差异的模型试验组UCP-1 蛋白浓度。结果表明:与对照组相比,模型对照组血清FFA、TC、TG、TNF-α浓度,肝脏重量及肝脏组织miR-122、miR-802 的相对表达量显著升高(P<0。05),血清IL-10 浓度、肩胛骨脂肪组织UCP-1 基因mRNA相对表达量显著降低(P<0。05),脂肪组织UCP-1 蛋白表达水平差异不显著(P>0。05);与模型对照组相比,Nesfatin-1 低剂量组血清FFA浓度显著降低(P<0。05),Nesfatin-1 中、高剂量组差异不显著(P>0。05);Nesfatin-1 低、中、高剂量组血清TC浓度均显著降低(P<0。05);Nesfatin-1 中、高剂量组血清TG浓度显著降低(P<0。05),Nesfatin-1 低剂量组差异不显著(P>0。05);Nesfatin-1 低、中、高剂量组血清TNF-α浓度均显著降低(P<0。05),IL-10 浓度均显著升高(P<0。05);Nesfatin-1 中、高剂量组肝脏重量显著降低(P<0。05),Nesfatin-1低剂量组差异不显著(P>0。05);Nesfatin-1 低、高剂量组肝脏组织 miR-122 的相对表达量显著降低(P<0。05),Nesfatin-1 中剂量组差异不显著(P<0。05);Nesfatin-1 低、中、高剂量组肝脏组织miR-802 的相对表达量均显著降低(P<0。05);Nesfatin-1 高剂量组脂肪组织UCP-1 基因 mRNA相对表达量显著升高(P<0。05),Nesfatin-1 低、中剂量组差异不显著(P>0。05);Nesfatin-1 高剂量组脂肪组织UCP-1 蛋白表达水平显著升高(P<0。05)。说明Nesfatin-1 对机体糖脂代谢具有促进作用。
Study on the effects of Nesfatin-1 on glycolipid metabolism in obese rats
In order to explore the effects of Nesfatin-1 on glucose and lipid metabolism in obese rats,40 healthy SPF SD rats aged eight weeks were randomly divided into control group(n=8)and model group(n=32).The control group was fed a maintenance diet,while the model group was fed a high-fat diet for 10 weeks.When the body weight of the model group(under fasting condition)increased by more than 20%compared with that of the control group,the modeling was considered successful.The successfully modeled rats were further randomly divided into model control group(n=8)and model experimental group,which was subdivided into Nesfatin-1 low-dose group(n=8,1 μg/kg),Nesfatin-1 medium-dose group(n=8,10 μg/kg)and Nesfatin-1 high-dose group(n=8,100 μg/kg).The experimental groups received daily tail vein injections with 1,10,100 μg/kg respectively once a day for 5 weeks,while the control group and the model control group were injected with normal saline at the weight of 10 mL/kg once a day for 5 weeks.At the end of the experiment,serum FFA,TC,TG,TNF-α and IL-10 concentrations in each group were detected by ELISA,and liver tissues of each group were collected and weighed.Real-time quantitative PCR was used to detect miR-122 and miR-802 related to fat metabolism in liver as well as the expression level of UCP-1 gene mRNA in scapularadipose tissue of each group.UCP-1 protein concentration in the scapular adipose tissue was determined by BCA method in the control,model control group,and model experimental groups that had significant differences in UCP-1 mRNA expression level.The results showed that,compared with the control group,the serum FFA,TC,TG,TNF-α concentrations,liver weight and the relative expression levels of miR-122 and miR-802 in liver tissue were significantly increased in model control group(P<0.05),while the serum IL-10 concentration and UCP-1 mRNA levels in scapular adipose tissue were significantly decreased(P<0.05).There was no significant difference in UCP-1 protein expression in adipose tissue(P>0.05).Compared with model control group,the serum FFA concentration in Nesfatin-1 low dose group was significantly decreased(P<0.05),while no significant differences were observed in Nesfatin-1 medium and high dose groups(P>0.05).The serum TC concentration in all Nesfatin-1 groups was significantly decreased(P<0.05).The serum TG concentration in Nesfatin-1 medium and high dose groups was significantly decreased(P<0.05),with no significant difference in Nesfatin-1 low dose group(P>0.05).The serum TNF-α concentration was significantly decreased(P<0.05)and IL-10 concentration was significantly increased(P<0.05)in all Nesfatin-1 groups.The liver weight of Nesfatin-1 medium and high dose groups was significantly decreased(P<0.05),while no significant difference was observed in Nesfatin-1 low dose group(P>0.05).The relative expression levels of miR-122 in liver tissues were significantly decreased in Nesfatin-1 low and high dose groups(P<0.05),with no significant difference in Nesfatin-1 medium dose group(P>0.05).The relative expression levels of miR-802 in liver tissues were significantly decreased in low,medium and high dose Nesfatin-1 groups(P<0.05).The relative expression level of UCP-1 gene mRNA in adipose tissue was significantly increased in Nesfatin-1 high dose group(P<0.05),while no significant differences were observed in Nesfatin-1 low and medium dose groups(P>0.05).The UCP-1 protein expression level in adipose tissue was significantly increased in Nesfatin-1 high dose group(P<0.05).These results indicated that Nesfatin-1 could promote the metabolism of glucose and lipid in the body.

Nesfatin-1obesityglycolipid metabolismmiR-122miR-802

王亚楠、么宏强、李泽旭、温馨、陈碧君、玉斯日古楞

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内蒙古农业大学 兽医学院农业部动物疾病临床诊疗技术重点实验室,呼和浩特 010011

Nesfatin-1 肥胖 糖脂代谢 miR-122 miR-802

2025

黑龙江畜牧兽医
黑龙江省畜牧兽医学会

黑龙江畜牧兽医

北大核心
影响因子:0.402
ISSN:1004-7034
年,卷(期):2025.(1)