慢性应激诱导DPP-4表达及对脂肪炎症和代谢的影响

阿不来克木·马合木提, 买买提·依斯热依力, 艾克拜尔·艾力, 李义亮, 阿孜古丽·阿力木江, 闫晶, 克力木·阿不都热依木

中国临床解剖学杂志 ›› 2020, Vol. 38 ›› Issue (4) : 438-443.

中国临床解剖学杂志 ›› 2020, Vol. 38 ›› Issue (4) : 438-443. DOI: 10.13418/j.issn.1001-165x.2020.04.014
实验研究

慢性应激诱导DPP-4表达及对脂肪炎症和代谢的影响

  • 阿不来克木·马合木提1, 买买提·依斯热依力2,3, 艾克拜尔·艾力2,3, 李义亮3, 阿孜古丽·阿力木江2,  闫晶3, 克力木·阿不都热依木2,3
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The chronic stress induced expression of DPP-4 and its role in adipose inflammation and glucose metabolism

  • ABULAIKEMU·Mahemuti1, MAIMAITI·Yisireyili2,3, AIKEBAIER·Aili2,3, LI Yi-liang3, AZIGULI -Alimujiang2, YAN Jing3, KELIMU·Abudureyimu2,3
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摘要

目的 分析慢性应激诱导脂肪二肽基肽酶-4(DPP-4)表达及对脂肪炎症和糖代谢的影响。  方法 雄性SPF级小鼠20只随机分慢性应激(Stress)组和正常对照(Control)组。Stress组小鼠每天在自制式束缚器中限制活动2 h,实验持续14 d。采用免疫组化方法检测巨噬细胞表面标志物(CD11b)在脂肪中的表达,实时定量PCR法检测脂肪组织中DPP-4、细胞因子(Adiponectin、MCP-1、IL-6、TNF-α)及糖代谢(IRS-1、GLUT-4)等指标的mRNA的相对表达量;ELISA法检测DPP-4酶活性及GLP-1浓度。  结果 Stress小鼠腹部白色脂肪组织(WAT)与Control组相比显著的退缩及其重量显著降低(P<0.001)。Stress组WAT出现大量的单核细胞、中性粒细胞浸润反应和炎症性改变;Stress显著降低Adiponectin的表达,并显著增高MCP-1、IL-6、TNF-α的mRNA表达及其血液中的浓度(P<0.001);Stress组WAT组织中DPP-4 mRNA表达及其血液中的活性显著增高,而GLP-1血液中的浓度显著降低(P<0.001);Stress组WAT组织中IRS-1及GLUT-4的mRNA水平显著低于Control组(P<0.001)。  结论 慢性应激诱导脂肪DPP-4异常表达,进而引起脂肪炎症和糖代谢异常等反应。

Abstract

Objective To analyze chronic stress induced dipeptidyl peptidase-4 (DPP-4) expression and its role in adipose inflammation and glycometabolism. Methods 20 male SPF mice were randomly divided into two groups: a stress group and a control group. Mice in the stress group were restrained in our own restraint device for 2 hours per day and lasted for 14 days. The expression of macrophage surface marker (CD11b) in adipose tissue was detected by immunohistochemistry. The expression of DPP-4, adipocytokines (Adiponectin, MCP-1, IL-6, TNF-α) in adipose tissue and the expressions of glucose metabolism molecules (IRS-1, GLUT-4) were further detected by RT-PCR. The enzymatic activity of DPP-4 and the concentration of GLP-1 were detected by ELISA. Results The white adipose tissue (WAT) of the stress group mice significantly retracted and WAT weight significantly reduced (P<0.001). WAT in the stress group showed a large number of monocytes, neutrophils infiltration and inflammatory changes. Mice in the stress group significantly decreased the expression of Adiponectin and significantly increased the expression of MCP-1, IL-6 and TNF-α (P<0.001). DPP-4 expression in WAT tissues and its activity in blood increased significantly in the stress group, but the concentration of serum GLP-1 decreased significantly (P<0.001). The mRNA level of IRS-1 and mRNA level of GLUT-4 in WAT of the stress group were significantly lower than that of the control group (P<0.001). Conclusions Chronic stress induced abnormal expression of DPP-4 in adipose tissue, which can lead to adipose inflammation and abnormal glycometabolism.

关键词

慢性应激 /   /   / 二肽基肽酶-4 /   /   / 脂肪细胞因子 /   /   / 炎症 /   /   / 糖代谢

Key words

Chronic stress /  Dipeptidyl peptidase-4 /  Adipocytokine /  Inflammation / Glycometabolism

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阿不来克木·马合木提, 买买提·依斯热依力, 艾克拜尔·艾力, 李义亮, 阿孜古丽·阿力木江, 闫晶, 克力木·阿不都热依木. 慢性应激诱导DPP-4表达及对脂肪炎症和代谢的影响[J]. 中国临床解剖学杂志. 2020, 38(4): 438-443 https://doi.org/10.13418/j.issn.1001-165x.2020.04.014
ABULAIKEMU·Mahemuti, MAIMAITI·Yisireyili, AIKEBAIER·Aili, LI Yi-liang, AZIGULI -Alimujiang, YAN Jing, KELIMU·Abudureyimu. The chronic stress induced expression of DPP-4 and its role in adipose inflammation and glucose metabolism[J]. Chinese Journal of Clinical Anatomy. 2020, 38(4): 438-443 https://doi.org/10.13418/j.issn.1001-165x.2020.04.014
中图分类号:      R335.9   

参考文献

[1]  Carrier A. Metabolic syndrome and oxidative stress: a complex relat-ionship[J]. Antioxid Redox Signal, 2017, 26 (9):429-431. 
[2]  Liu YZ, Wang YX, Jiang CL. Inflammation: the common pathway of stress-related diseases[J]. Front Hum Neurosci, 2017, 11: 316.
[3] Secrest MH, Udell JA, Filion KB. The cardiovascular safety trials of DPP-4 inhibitors, GLP-1 agonists, and SGLT2 inhibitors[J]. Trends Cardiovasc Med, 2017, 27(3):194-202. 
[4] Dandekar A, Mendez R,  Zhang K. Cross Talk Between ER Stress, Oxidative Stress, and Inflammation in Health and Disease[J]. Methods Mol Biol, 2015,1292(3):205-214. 
[5]  Sharma D, Verma S, Vaidya S, et al. Recent updates on GLP-1 agonists: Current advancements & challenges[J]. Biomed Pharmacother, 2018, 108(88):952-962. 
[6] Yisireyili M, Uchida Y, Yamamoto K, et al. Angiotensin receptor blocker irbesartan reduces stress-induced intestinal inflammation via AT1a signaling and ACE2-dependent mechanism in mice[J]. Brain Behav Immun, 2018, 69 (010):167-179.
[7]  Yisireyili M, Takeshita K, Hayashi M, et al. Dipeptidyl peptidase- IV inhibitor alogliptin improves stress-induced insulin resistance and prothrombotic state in a murine model[J]. Psychoneuroendocrinology, 2016, 73(4):186-195.
[8] Takayanagi R, Uchida T, Kimura K, et al. Evaluation of drug efficacy of GLP-1 receptor agonists and DPP-4 inhibitors based on target molecular binding occupancy[J]. Biol Pharm Bull, 2018, 41(2):153-157. 
[9]  Senyigit A, Tabak O, Orhanoglu T, et al. Glucagon-like peptide-1 levels and dipeptidyl peptidase-4 activity in type 2 diabetes[J]. Clin Invest Med, 2017, 40(5):E188-E199.
[10] 买买提·依斯热依力, 买买提艾力·艾则孜, 吾布力卡斯木·吾拉木,等. 慢性束缚应激诱导脂肪Nox-4表达及其在脂肪炎症发生中的作用[J]. 中华内分泌代谢杂志, 2019, 35(5) : 410-416. 
[11] 胡仁明,谢颖,鹿斌,等. 2型糖尿病患者高发“代谢性炎症综合征”[J]. 中华内分泌代谢杂志,2016,32(1): 27-30.
[12] Burhans MS, Hagman DK, Kuzma JN, et al. Contribution of adipose tissue inflammation to the development of type 2 diabetes mellitus[J]. Compr Physiol, 2018, 9(1):1-58. 
[13] Yahagi K, Kolodgie FD, Lutter C, et al. Pathology of human coronary and carotid artery atherosclerosis and vascular calcification in diabetes mellitus[J]. Arterioscler Thromb Vasc Biol, 2017, 37(2):191-204. 
[14] Kacso T, Bondor CI, Rusu CC, et al. Adiponectin is related to markers of endothelial dysfunction and neoangiogenesis in diabetic patients[J].  Int Urol Nephrol, 2018, 50 (9):1661-1666. 
[15] 买买提·依斯热依力,阿孜古丽·阿力木江,吾布力卡斯木·吾拉木,等.Nox-4在慢性束缚应激致小鼠胃黏膜炎症损伤发生中的作用[J]. 中华行为医学与脑科学杂志, 2019, 28(4):316-321.
[16] Yisireyili M, Hayashi M, Wu H, et al. Xanthine oxidase inhibition by febuxostat attenuates stress-induced hyperuricemia, glucose dysmetabolism, and prothrombotic state in mice[J]. Sci Rep, 2017, 7(1):1266. 

基金

新疆维吾尔自治区自然科学基金(2018D01C134);新疆维吾尔自治区引进高层次人才天池百人计划项目(201939)

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