Eicosapentaenoic Acid Alleviates Inflammatory Response and Insulin Resistance in Pregnant Mice With Gestational Diabetes Mellitus

. 2024 Mar 11 ; 73 (1) : 57-68.

Jazyk angličtina Země Česko Médium print

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid38466005

This study investigated the effect of eicosapentaenoic acid (EPA) on insulin resistance in pregnant mice with gestational diabetes mellitus (GDM) and underlying mechanism. C57BL/6 mice fed with a high-fat diet for 4 weeks and the newly gestated were selected and injected with streptozotocin for GDM modeling. We demonstrated that the fasting insulin levels (FINS) and insulin sensitivity index (ISI) in serum and blood glucose level were significantly higher in GDM group than in normal control (NC) group. The low or high dose of EPA intervention reduced these levels, and the effect of high dose intervention was more significant. The area under the curve in GDM group was higher than that of NC group, and then gradually decreased after low or high dose of EPA treatment. The serum levels of TC, TG and LDL were increased in GDM group, while decreased in EPA group. GDM induced down-regulation of HDL level, and the low or high dose of EPA gradually increased this level. The levels of p-AKT2Ser, p-IRS-1Tyr, GLUT4, and ratios of pIRS-1Tyr/IRS-1 and pAKT2Ser/AKT2 in gastrocnemius muscle were reduced in GDM group, while low or high dose of EPA progressively increased these alterations. GDM enhanced TLR4, NF-kappaB p65, IL-1beta, IL-6 and TNF-alpha levels in placental tissues, and these expressions were declined at different dose of EPA, and the decrease was greater at high dose. We concluded that EPA receded the release of inflammatory factors in the placental tissues by inhibiting the activation of TLR4 signaling, thereby alleviating the IR.

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Alejandro EU, Mamerto TP, Chung G, Villavieja A, Gaus NL, Morgan E, Pineda-Cortel MRB. Gestational Diabetes Mellitus: A Harbinger of the Vicious Cycle of Diabetes. Int J Mol Sci. 2020;21:5003. doi: 10.3390/ijms21145003. PubMed DOI PMC

Phoswa WN, Khaliq OP. The Role of Oxidative Stress in Hypertensive Disorders of Pregnancy (Preeclampsia, Gestational Hypertension) and Metabolic Disorder of Pregnancy (Gestational Diabetes Mellitus) Oxid Med Cell Longev. 2021;2021:5581570. doi: 10.1155/2021/5581570. PubMed DOI PMC

Ali AM, Kunugi H. Intermittent Fasting, Dietary Modifications, and Exercise for the Control of Gestational Diabetes and Maternal Mood Dysregulation: A Review and a Case Report. Int J Environ Res Public Health. 2020;17:9379. doi: 10.3390/ijerph17249379. PubMed DOI PMC

Kijmanawat A, Panburana P, Reutrakul S, Tangshewinsirikul C. Effects of probiotic supplements on insulin resistance in gestational diabetes mellitus: A double-blind randomized controlled trial. J Diabetes Investig. 2019;10:163–170. doi: 10.1111/jdi.12863. PubMed DOI PMC

Chen SH, Liu XN, Peng Y. MicroRNA-351 eases insulin resistance and liver gluconeogenesis via the PI3K/AKT pathway by inhibiting FLOT2 in mice of gestational diabetes mellitus. J Cell Mol Med. 2019;23:5895–5906. doi: 10.1111/jcmm.14079. PubMed DOI PMC

Brinton EA, Mason RP. Prescription omega-3 fatty acid products containing highly purified eicosapentaenoic acid (EPA) Lipids Health Dis. 2017;16:23. doi: 10.1186/s12944-017-0415-8. PubMed DOI PMC

Gevariya N, Lachance G, Robitaille K, Joly Beauparlant C, Beaudoin L, Fournier E, Fradet Y, et al. Omega-3 Eicosapentaenoic Acid Reduces Prostate Tumor Vascularity. Mol Cancer Res. 2021;19:516–527. doi: 10.1158/1541-7786.MCR-20-0316. PubMed DOI

Trivedi K, Le V, Nelson JR. The case for adding eicosapentaenoic acid (icosapent ethyl) to the ABCs of cardiovascular disease prevention. Postgrad Med. 2021;133:28–41. doi: 10.1080/00325481.2020.1783937. PubMed DOI

Lepretti M, Martucciello S, Burgos Aceves MA, Putti R, Lionetti L. Omega-3 Fatty Acids and Insulin Resistance: Focus on the Regulation of Mitochondria and Endoplasmic Reticulum Stress. Nutrients. 2018;10:350. doi: 10.3390/nu10030350. PubMed DOI PMC

Li R, Zhou Y, Zhang S, Li J, Zheng Y, Fan X. The natural (poly)phenols as modulators of microglia polarization via TLR4/NF-kappaB pathway exert anti-inflammatory activity in ischemic stroke. Eur J Pharmacol. 2022;914:174660. doi: 10.1016/j.ejphar.2021.174660. PubMed DOI

Louwagie EJ, Larsen TD, Wachal AL, Baack ML. Placental lipid processing in response to a maternal high-fat diet and diabetes in rats. Pediatr Res. 2018;83:712–722. doi: 10.1038/pr.2017.288. PubMed DOI PMC

Hassan NF, Nada SA, Hassan A, El-Ansary MR, Al-Shorbagy MY, Abdelsalam RM. Saroglitazar Deactivates the Hepatic LPS/TLR4 Signaling Pathway and Ameliorates Adipocyte Dysfunction in Rats with High-Fat Emulsion/LPS Model-Induced Non-alcoholic Steatohepatitis. Inflammation. 2019;42:1056–1070. doi: 10.1007/s10753-019-00967-6. PubMed DOI

Xu W, Tang M, Wang J, Wang L. Anti-inflammatory activities of puerarin in high-fat diet-fed rats with streptozotocin-induced gestational diabetes mellitus. Mol Biol Rep. 2020;47:7537–7546. doi: 10.1007/s11033-020-05816-6. PubMed DOI PMC

Wang H, Chen X, Miao X, Lu K, He M, Wu X. Dendrobium mixture improves gestational diabetes mellitus through regulating Nrf2/HO1 signaling pathway. Biomed Pharmacother. 2022;155:113656. doi: 10.1016/j.biopha.2022.113656. PubMed DOI

Chen T, Zhang Y, Liu Y, Zhu D, Yu J, Li G, Sun Z, Wang W, Jiang H, Hong Z. MiR-27a promotes insulin resistance and mediates glucose metabolism by targeting PPAR-gamma-mediated PI3K/AKT signaling. Aging (Albany NY) 2019;11:7510–7524. doi: 10.18632/aging.102263. PubMed DOI PMC

Zhang XY, Chen J, Yi K, Peng L, Xie J, Gou X, Peng T, Tang L. Phlorizin ameliorates obesity-associated endotoxemia and insulin resistance in high-fat diet-fed mice by targeting the gut microbiota and intestinal barrier integrity. Gut Microbes. 2020;12:1–18. doi: 10.1080/19490976.2020.1842990. PubMed DOI PMC

Wu YT, Zhang CJ, Mol BW, Kawai A, Li C, Chen L, Wang Y, Sheng JZ, Fan JX, Shi Y. Early Prediction of Gestational Diabetes Mellitus in the Chinese Population via Advanced Machine Learning. J Clin Endocrinol Metab. 2021;106:e1191–e1205. doi: 10.1210/clinem/dgaa899. PubMed DOI PMC

Xu YXZ, Xi S, Qian X. Evaluating Traditional Chinese Medicine and Herbal Products for the Treatment of Gestational Diabetes Mellitus. J Diabetes Res. 2019;2019:9182595. doi: 10.1155/2019/9182595. PubMed DOI PMC

Wei HK, Deng Z, Jiang SZ, Song TX, Zhou YF, Peng J, Tao YX. Eicosapentaenoic acid abolishes inhibition of insulin-induced mTOR phosphorylation by LPS via PTP1B downregulation in skeletal muscle. Mol Cell Endocrinol. 2017;439:116–125. doi: 10.1016/j.mce.2016.10.029. PubMed DOI

Baek JY, Na E, Lim SY. Synthesis of Eicosapentaenoic Acid-enriched Phosphatidylcholine and its Effect on Pro-inflammatory Cytokine Expression. Comb Chem High Throughput Screen. 2022;25:97–102. doi: 10.2174/1386207324666210118100049. PubMed DOI

Ostadrahimi A, Mohammad-Alizadeh S, Mirgafourvand M, Yaghoubi S, Shahrisa E, Farshbaf-Khalili A. Effects of Fish Oil Supplementation on Gestational Diabetes Mellitus (GDM): A Systematic Review. Iran Red Crescent Med J. 2016;18:e24690. doi: 10.5812/ircmj.24690. PubMed DOI PMC

Jamilian M, Samimi M, Mirhosseini N, Afshar Ebrahimi F, Aghadavod E, Taghizadeh M, Asemi Z. A Randomized Double-Blinded, Placebo-Controlled Trial Investigating the Effect of Fish Oil Supplementation on Gene Expression Related to Insulin Action, Blood Lipids, and Inflammation in Gestational Diabetes Mellitus-Fish Oil Supplementation and Gestational Diabetes. Nutrients. 2018;10:163. doi: 10.3390/nu10020163. PubMed DOI PMC

Guo X, Sun W, Luo G, Wu L, Xu G, Hou D, Hou Y, Guo X, Mu X, Qin L. Panax notoginseng saponins alleviate skeletal muscle insulin resistance by regulating the IRS1-PI3K-AKT signaling pathway and GLUT4 expression. FEBS Open Bio. 2019;9:1008–1019. doi: 10.1002/2211-5463.12635. PubMed DOI PMC

Radzicka S, Pietryga M, Iciek R, Brazert J. The role of visfatin in pathogenesis of gestational diabetes (GDM) Ginekol Pol. 2018;89:518–521. doi: 10.5603/GP.a2018.0088. PubMed DOI

Khondkaryan L, Margaryan S, Poghosyan D, Manukyan G. Impaired Inflammatory Response to LPS in Type 2 Diabetes Mellitus. Int J Inflam. 2018;2018:2157434. doi: 10.1155/2018/2157434. PubMed DOI PMC

Pena-Cano MI, Valencia-Ortega J, Morales-Avila E, Diaz-Velazquez MF, Gomez-Diaz R, Saucedo R. Omentin-1 and its relationship with inflammatory factors in maternal plasma and visceral adipose tissue of women with gestational diabetes mellitus. J Endocrinol Invest. 2022;45:453–462. doi: 10.1007/s40618-021-01671-9. PubMed DOI

Zheng XD, Huang Y, Li H. Regulatory role of Apelin-13-mediated PI3K/AKT signaling pathway in the glucose and lipid metabolism of mouse with gestational diabetes mellitus. Immunobiology. 2021;226:152135. doi: 10.1016/j.imbio.2021.152135. PubMed DOI

Aldhafiri FK. Investigating the Role of EPA and DHA on Cellular Oxidative Stress; Profiling Antidiabetic and Antihypertensive Potential. J Pharm Bioallied Sci. 2022;14:178–185. doi: 10.4103/jpbs.jpbs_383_22. PubMed DOI PMC

De Luccia TPB, Ono E, Menon R, Borbely AU, Mattar R, Richardson L, da Silva ALM, Botelho RM, da Rocha M, Daher S. The effect of Gestational Diabetes Mellitus on the fetal compartment. J Reprod Immunol. 2021;145:103314. doi: 10.1016/j.jri.2021.103314. PubMed DOI

Li YX, Long DL, Liu J, Qiu D, Wang J, Cheng X, Yang X, Li RM, Wang G. Gestational diabetes mellitus in women increased the risk of neonatal infection via inflammation and autophagy in the placenta. Medicine (Baltimore) 2020;99:e22152. doi: 10.1097/MD.0000000000022152. PubMed DOI PMC

Lee TC, Ivester P, Hester AG, Sergeant S, Case LD, Morgan T, Kouba EO, Chilton FH. The impact of polyunsaturated fatty acid-based dietary supplements on disease biomarkers in a metabolic syndrome/diabetes population. Lipids Health Dis. 2014;13:196. doi: 10.1186/1476-511X-13-196. PubMed DOI PMC

Dasu MR, Devaraj S, Park S, Jialal I. Increased toll-like receptor (TLR) activation and TLR ligands in recently diagnosed type 2 diabetic subjects. Diabetes Care. 2010;33:861–868. doi: 10.2337/dc09-1799. PubMed DOI PMC

Nakanishi S, Nagano C, Miyahara M, Sawano F. Sex Differences in the Association between the Eicosapentaenoic Acid/Arachidonic Acid Ratio and the Visceral Fat Area among Patients with Type 2 Diabetes. Intern Med. 2016;55:1269–1274. doi: 10.2169/internalmedicine.55.5624. PubMed DOI

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