Влияние различных типов физической нагрузки на функциональное состояние печени мышей при диабете 2-го типа (обзор)
DOI:
https://doi.org/10.37482/2687-1491-Z271Ключевые слова:
сахарный диабет 2-го типа, функциональное состояние печени, липидный обмен, силовые тренировки, высокоинтенсивные интервальные тренировки, сетевой метаанализАннотация
Сахарный диабет 2-го типа вызывает комплексные системные нарушения, при этом печень, будучи центральным органом углеводного и липидного обмена, является одной из основных мишеней хронических диабетических осложнений. Регулярная физическая активность рассматривается как эффективное немедикаментозное средство коррекции метаболических расстройств, связанных с указанным заболеванием. Цель настоящего обзора – сравнительный анализ влияния различных форм физической активности на показатели функционального состояния печени у животных с экспериментальной моделью сахарного диабета 2-го типа. Материалы и методы. Выполнен сетевой метаанализ, охватывающий 38 рандомизированных контролируемых исследований (суммарно – с участием 601 мыши). Данные были собраны из баз Web of Science, PubMed, Scopus, CNKI и EBSCO. Рассматривались следующие виды нагрузок: аэробные и силовые тренировки, плавание, высокоинтенсивные интервальные тренировки, тренировки средней интенсивности, а также спонтанная двигательная активность. В качестве исходных критериев оценки учитывались уровни аланинаминотрансферазы (ALT), аспартатаминотрансферазы (AST), триглицеридов, липопротеинов высокой (ЛПВП) и низкой (ЛПНП) плотности, а также активность фосфоенолпируваткарбоксикиназы (PEPCK). Результаты. Анализ выявил, что высокоинтенсивные интервальные тренировки оказывали наиболее выраженное воздействие на функциональное состояние печени мышей с сахарным диабетом 2-го типа, обеспечивая значительное снижение уровней ALT и триглицеридов при одновременном повышении концентрации ЛПВП. Силовые тренировки продемонстрировали преимущество в снижении уровней AST, ЛПНП и активности PEPCK. Плавание и тренировки средней интенсивности также положительно влияли на ряд биомаркеров, однако их эффект был менее выраженным. На основании полученных данных можно сделать вывод, что высокоинтенсивные интервальные тренировки и силовые тренировки могут быть более эффективными стратегиями для регуляции метаболизма печени у мышей с сахарным диабетом 2-го типа. Эти результаты подчеркивают потенциал физической активности как безопасного и доступного метода коррекции диабетических нарушений печени, действенность которого требует дальнейшего подтверждения в клинических исследованиях.
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Tomic D., Shaw J.E., Magliano D.J. The Burden and Risks of Emerging Complications of Diabetes Mellitus // Nat. Rev. Endocrinol. 2022. Vol. 18, No 9. P. 525–539. https://doi.org/10.1038/s41574-022-00690-7
Lee C.-H., Lui D.T.W., Lam K.S.L. Non-Alcoholic Fatty Liver Disease and Type 2 Diabetes: An Update // J. Diabetes Investig. 2022. Vol. 13, No 6. P. 930–940. https://doi.org/10.1111/jdi.13756
Bergman R.N., Piccinini F., Kabir M., Kolka C.M., Ader M. Hypothesis: Role of Reduced Hepatic Insulin Clearance in the Pathogenesis of Type 2 Diabetes // Diabetes. 2019. Vol. 68, No 9. P. 1709–1716. https://doi.org/10.2337/db19-0098
Ciardullo S., Perseghin G. Prevalence of Elevated Liver Stiffness in Patients with Type 1 and Type 2 Diabetes: A Systematic Review and Meta-Analysis // Diabetes Res. Clin. Pract. 2022. Vol. 190. Art. No 109981. https://doi.org/10.1016/j.diabres.2022.109981
Duckworth W.C., Bennett R.G., Hamel F.G. Insulin Degradation: Progress and Potential // Endocr. Rev. 1998. Vol. 19, No 5. P. 608–624. https://doi.org/10.1210/edrv.19.5.0349
Fazio S., Linton M.F. Mouse Models of Hyperlipidemia and Atherosclerosis // Front. Biosci. 2001. Vol. 6. P. D515–D525. https://doi.org/10.2741/fazio
Feng J., Zhang Q., Chen B., Chen J., Wang W., Hu Y., Yu J., Huang H. Effects of High-Intensity Intermittent Exercise on Glucose and Lipid Metabolism in Type 2 Diabetes Patients: A Systematic Review and Meta-Analysis // Front. Endocrinol. (Lausanne). 2024. Vol. 15. Art. No 1360998. https://doi.org/10.3389/fendo.2024.1360998
Galderisi A., Polidori D., Weiss R., Giannini C., Pierpont B., Tricò D., Caprio S. Lower Insulin Clearance Parallels a Reduced Insulin Sensitivity in Obese Youths and Is Associated with a Decline in β-Cell Function over Time // Diabetes. 2019. Vol. 68, No 11. P. 2074–2084. https://doi.org/10.2337/db19-0120
Gan S.K., Kriketos A.D., Ellis B.A., Thompson C.H., Kraegen E.W., Chisholm D.J. Changes in Aerobic Capacity and Visceral Fat but Not Myocyte Lipid Levels Predict Increased Insulin Action After Exercise in Overweight and Obese Men // Diabetes Care. 2003. Vol. 26, No 6. P. 1706–1713. https://doi.org/10.2337/diacare.26.6.1706
Gu L., Ding X., Wang Y., Gu M., Zhang J., Yan S., Li N., Song Z., Yin J., Lu L., Peng Y. Spexin Alleviates Insulin Resistance and Inhibits Hepatic Gluconeogenesis via the FoxO1/PGC-1α Pathway in High-Fat-Diet-Induced Rats and Insulin Resistant Cells // Int. J. Biol. Sci. 2019. Vol. 15, No 13. P. 2815–2829. https://doi.org/10.7150/ijbs.31781
Hoene M., Lehmann R., Hennige A.M., Pohl A.K., Häring H.U., Schleicher E.D., Weigert C. Acute Regulation of Metabolic Genes and Insulin Receptor Substrates in the Liver of Mice by One Single Bout of Treadmill Exercise // J. Physiol. 2009. Vol. 587, No 1. P. 241–252. https://doi.org/10.1113/jphysiol.2008.160275
Kanaley J.A., Colberg S.R., Corcoran M.H., Malin S.K., Rodriguez N.R., Crespo C.J., Kirwan J.P., Zierath J.R. Exercise/Physical Activity in Individuals with Type 2 Diabetes: A Consensus Statement from the American College of Sports Medicine // Med. Sci. Sports Exerc. 2022. Vol. 54, No 2. P. 353–368. https://doi.org/10.1249/MSS.0000000000002800
Kazeminasab F., Baharlooie M., Rezazadeh H., Soltani N., Rosenkranz S.K. The Effects of Aerobic Exercise on Liver Function, Insulin Resistance, and Lipid Profiles in Prediabetic and Type 2 Diabetic Mice // Physiol. Behav. 2023. Vol. 271. Art. No 114340. https://doi.org/10.1016/j.physbeh.2023.114340
Liu J.L. The Role of the Funnel Plot in Detecting Publication and Related Biases in Meta-Analysis // Evid. Based Dent. 2011. Vol. 12, No 4. P. 121–122. https://doi.org/10.1038/sj.ebd.6400831
Marinho R., Ropelle E.R., Cintra D.E., De Souza C.T., Da Silva A.S., Bertoli F.C., Colantonio E., D’Almeida V., Pauli J.R. Endurance Exercise Training Increases APPL1 Expression and Improves Insulin Signaling in the Hepatic Tissue of Diet-Induced Obese Mice, Independently of Weight Loss // J. Cell. Physiol. 2012. Vol. 227, No 7. P. 2917–2926. https://doi.org/10.1002/jcp.23037
Brust K.B., Corbell K.A., Al-Nakkash L., Babu J.R., Broderick T.L. Expression of Gluconeogenic Enzymes and 11β-Hydroxysteroid Dehydrogenase Type 1 in Liver of Diabetic Mice After Acute Exercise // Diabetes Metab. Syndr. Obes. 2014. Vol. 7. P. 495–504. https://doi.org/10.2147/dmso.s70767
Heled Y., Shapiro Y., Shani Y., Moran D.S., Langzam L., Barash V., Sampson S.R., Meyerovitch J. Physical Exercise Enhances Hepatic Insulin Signaling and Inhibits Phosphoenolpyruvate Carboxykinase Activity in Diabetes-Prone Psammomys obesus // Metabolism. 2004. Vol. 53, No 7. P. 836–841. https://doi.org/10.1016/j.metabol.2004.02.006
Gomes R.J., de Oliveira C.A.M., Ribeiro C., de Alencar Mota C.S., Moura L.P., Cesar Tognoli L.M.M., de Almeida Leme J.A.C., Luciano E., de Mello M.A.R. Effects of Exercise Training on Hippocampus Concentrations of Insulin and IGF-1 in Diabetic Rats // Hippocampus. 2009. Vol. 19, No 10. P. 981–987. https://doi.org/10.1002/hipo.20636
Stevanović-Silva J., Beleza J., Coxito P., Oliveira P.J., Ascensão A., Magalhães J. Gestational Exercise Antagonises the Impact of Maternal High-Fat High-Sucrose Diet on Liver Mitochondrial Alterations and Quality Control Signalling in Male Offspring // Int. J. Environ. Res. Public Health. 2023. Vol. 20, No 2. Art. No 1388. https://doi.org/10.3390/ijerph20021388
Lin X., Qu J., Yin L., Wang R., Wang X. Aerobic Exercise-Induced Decrease of Chemerin Improved Glucose and Lipid Metabolism and Fatty Liver of Diabetes Mice Through Key Metabolism Enzymes and Proteins // Biochim. Biophys. Acta Mol. Cell Biol. Lipids. 2023. Vol. 1868, No 12. Art. No 159409. https://doi.org/10.1016/j.bbalip.2023.159409
Zhang Y., Ye T., Zhou P., Li R., Liu Z., Xie J., Hua T., Sun Q. Exercise Ameliorates Insulin Resistance and Improves ASK1-Mediated Insulin Signalling in Obese Rats // J. Cell. Mol. Med. 2021. Vol. 25, No 23. P. 10930–10938. https://doi.org/10.1111/jcmm.16994
Moura L.P., Puga G.M., Beck W.R., Teixeira I.P., Ghezzi A.C., Silva G.A., Mello M.A.R. Exercise and Spirulina Control Non-Alcoholic Hepatic Steatosis and Lipid Profile in Diabetic Wistar Rats // Lipids Health Dis. 2011. Vol. 10. Art. No 77. https://doi.org/10.1186/1476-511X-10-77
Lima T.I., Monteiro I.C., Valença S., Leal-Cardoso J.H., Fortunato R.S., Carvalho D.P., Teodoro B.G., Ceccatto V.M. Effect of Exercise Training on Liver Antioxidant Enzymes in STZ-Diabetic Rats // Life Sci. 2015. Vol. 128. P. 64–71. https://doi.org/10.1016/j.lfs.2015.01.031
Kuga G.K., Gaspar R.C., Muñoz V.R., Nakandakari S.C.B.R., Breda L., Sandoval B.M., Caetano F.H., Leme J.A.C.A., Pauli J.R., Gomes R.J. Physical Training Reverses Changes in Hepatic Mitochondrial Diameter of Alloxan-Induced Diabetic Rats // Einstein (São Paulo). 2018. Vol. 16, No 3. Art. No eAO4353. https://doi.org/10.1590/S1679-45082018AO4353
de Bem G.F., da Costa C.A., da Silva Cristino Cordeiro V., Santos I.B., de Carvalho L.C.R.M., de Andrade Soares R., Ribeiro J.H., de Souza M.A.V., da Cunha Sousa P.J., Ognibene D.T., Resende A.C., de Moura RS. Euterpe oleracea Mart. (açaí) Seed Extract Associated with Exercise Training Reduces Hepatic Steatosis in Type 2 Diabetic Male Rats // J. Nutr. Biochem. 2018. Vol. 52. P. 70–81. https://doi.org/10.1016/j.jnutbio.2017.09.021
Katar M., Gevrek F. Relation of the Intense Physical Exercise and Asprosin Concentrations in Type 2 Diabetic Rats // Tissue Cell. 2024. Vol. 90. Art. No 102501. https://doi.org/10.1016/j.tice.2024.102501
Lin X.-J., Yang H.-F., Wang X.-H. Effects of Aerobic Exercise and Dieting on Chemerin and Its Receptor CMKLR1 in the Livers of Type 2 Diabetic Rats // Zhongguo Ying Yong Sheng Li Xue Za Zhi. 2017. Vol. 33, No 5. P. 426–430. https://doi.org/10.12047/j.cjap.5495.2017.103
Yi X., Cao S., Chang B., Zhao D., Gao H., Wan Y., Shi J., Wei W., Guan Y. Effects of Acute Exercise and Chronic Exercise on the Liver Leptin-AMPK-ACC Signaling Pathway in Rats with Type 2 Diabetes // J. Diabetes Res. 2013. Vol. 2013. Art. No 946432. https://doi.org/10.1155/2013/946432
Gomes R.J., de Almeida Leme J.A.C., de Moura L.P., de Araújo M.B., Rogatto G.P., de Moura R.F., Luciano E., de Mello MA.R. Growth Factors and Glucose Homeostasis in Diabetic Rats: Effects of Exercise Training // Cell Biochem. Funct. 2009. Vol. 27, No 4. P. 199–204. https://doi.org/10.1002/cbf.1556
Baldissera G., Sperotto N.D.M., Rosa H.T., Henn J.G., Peres V.F., Moura D.J., Roehrs R., Denardin E.L.G., Dal Lago P., Nunes R.B., Saffi J. Effects of Crude Hydroalcoholic Extract of Syzygium сumini (L.) Skeels Leaves and Continuous Aerobic Training in Rats with Diabetes Induced by a High-Fat Diet and Low Doses of Streptozotocin // J. Ethnopharmacol. 2016. Vol. 194. P. 1012–1021. https://doi.org/10.1016/j.jep.2016.10.076
de Almeida Leme J.A.C., Gomes R.J., de Mello M.A.R., Caetano F.H., Luciano E. Effects of Short-Term Physical Training on the Liver IGF-I in Diabetic Rats // Growth Factors. 2007. Vol. 25, No 1. P. 9–14. https://doi.org/10.1080/08977190701210693
Leme J.A.C.A., Silveira R.F., Gomes R.J., Moura R.F., Sibuya C.A., Mello M.A., Luciano E. Long-Term Physical Training Increases Liver IGF-I in Diabetic Rats // Growth Horm. IGF Res. 2009. Vol. 19, No 3. P. 262–266. https://doi.org/10.1016/j.ghir.2008.12.004
Ropelle E.R., Pauli J.R., Cintra D.E., Frederico M.J.S., de Pinho R.A., Velloso L.A., De Souza C.T. Acute Exercise Modulates the Foxo1/PGC-1α Pathway in the Liver of Diet-Induced Obesity Rats // J. Physiol. 2009. Vol. 587, No 9. P. 2069–2076. https://doi.org/10.1113/jphysiol.2008.164202
Kolieb E., Maher S.A., Shalaby M.N., Alsuhaibani A.M., Alharthi A., Hassan W.A., El-Sayed K. Vitamin D and Swimming Exercise Prevent Obesity in Rats Under a High-Fat Diet via Targeting FATP4 and TLR4 in the Liver and Adipose Tissue // Int. J. Environ. Res. Public Health. 2022. Vol. 19, No 21. Art. No 13740. https://doi.org/10.3390/ijerph192113740
Huang L., Yue P., Wu X., Yu T., Wang Y., Zhou J., Kong D., Chen K. Combined Intervention of Swimming Plus Metformin Ameliorates the Insulin Resistance and Impaired Lipid Metabolism in Murine Gestational Diabetes Mellitus // PLoS One. 2018. Vol. 13, No 4. Art. No e0195609. https://doi.org/10.1371/journal.pone.0195609
Sakr H.F., Abbas A.M., Haidara M.A. Swimming, but Not Vitamin E, Ameliorates Prothrombotic State and Hypofibrinolysis in a Rat Model of Nonalcoholic Fatty Liver Disease // J. Basic Clin. Physiol. Pharmacol. 2018. Vol. 29, No 1. P. 61–71. https://doi.org/10.1515/jbcpp-2017-0069
Lima A.F., Ropelle E.R., Pauli J.R., Cintra D.E., Frederico M.J.S., Pinho R.A., Velloso L.A., De Souza C.T. Acute Exercise Reduces Insulin Resistance-Induced TRB3 Expression and Amelioration of the Hepatic Production of Glucose in the Liver of Diabetic Mice // J. Cell. Physiol. 2009. Vol. 221, No 1. P. 92–97. https://doi.org/10.1002/jcp.21833
Bicer M., Gunay M., Akil M., Avunduk M.C., Mogulkoc R., Baltaci A.K. Effect of Long-Term Intraperitoneal Zinc Administration on Liver Glycogen Levels in Diabetic Rats Subjected to Acute Forced Swimming // Biol. Trace Elem. Res. 2011. Vol. 139, No 3. P. 317–324. https://doi.org/10.1007/s12011-010-8658-5
Pereira R.M., da Cruz Rodrigues K.C., Anaruma C.P., Sant’Ana M.R., Pereira de Campos T.D., Gaspar R.S., Canciglieri R.S., de Melo D.G., Mekary R.A., Ramos da Silva A.S., Cintra D.E., Ropelle E.R., Pauli J.R., de Moura L.P. Short-Term Strength Training Reduces Gluconeogenesis and NAFLD in Obese Mice // J. Endocrinol. 2019. Vol. 241, No 1. P. 59–70. https://doi.org/10.1530/JOE-18-0567
Vivero A., Ruz M., Rivera M., Miranda K., Sacristán C., Espinosa A., Codoceo J., Inostroza J., Vásquez K., Pérez Á., García-Díaz D., Arredondo M. Zinc Supplementation and Strength Exercise in Rats with Type 2 Diabetes: Akt and PTP1B Phosphorylation in Nonalcoholic Fatty Liver // Biol. Trace Elem. Res. 2021. Vol. 199, No 6. P. 2215–2224. https://doi.org/10.1007/s12011-020-02324-3
Pereira R.M., da Cruz Rodrigues K.C., Sant’Ana M.R., da Rocha A.L., Morelli A.P., Veras A.S.C., Gaspar R.S., da Costa Fernandes C.J., Teixeira G.R., Simabuco F.M., da Silva A.S.R., Cintra D.E., Ropelle E.R., Pauli J.R., de Moura L.P. FOXO1 Is Downregulated in Obese Mice Subjected to Short-Term Strength Training // J. Cell. Physiol. 2022. Vol. 237, No 11. P. 4262–4274. https://doi.org/10.1002/jcp.30882
Júnior A.S.S., Aidar F.J., Dos Santos J.L., Dos Santos Estevam C., Dos Santos J.D.M., de Oliveira e Silva A.M., Lima F.B., De Araújo S.S., Marçal A.C. Effects of Resistance Training and Turmeric Supplementation on Reactive Species Marker Stress in Diabetic Rats // BMC Sports Sci. Med. Rehabil. 2020. Vol. 12. Art. No 45. https://doi.org/10.1186/s13102-020-00194-9
Zarrinkalam E., Ranjbar K., Salehi I., Vakili M., Kheiripour N., Komaki A. Resistance Training and Hawthorn Extract Ameliorate Cognitive Deficits in Streptozotocin-Induced Diabetic Rats // Biomed. Pharmacother. 2018. Vol. 97. P. 503–510. https://doi.org/10.1016/j.biopha.2017.10.138
Dehghan F., Hajiaghaalipour F., Yusof A., Muniandy S., Hosseini S.A., Heydari S., Salim L.Z.A., Azarbayjani M.A. Saffron with Resistance Exercise Improves Diabetic Parameters Through the GLUT4/AMPK Pathway in-vitro and in-vivo // Sci. Rep. 2016. Vol. 6. Art. No 25139. https://doi.org/10.1038/srep25139
Király M.A., Campbell J., Park E., Bates H.E., Yue J.T.Y., Rao V., Matthews S.G., Bikopoulos G., Rozakis-Adcock M., Giacca A., Vranic M., Riddell M.C. Exercise Maintains Euglycemia in Association with Decreased Activation of c-Jun NH2-Terminal Kinase and Serine Phosphorylation of IRS-1 in the Liver of ZDF Rats // Am. J. Physiol. Endocrinol. Metab. 2010. Vol. 298, No 3. P. E671–E682. https://doi.org/10.1152/ajpendo.90575.2008
Mansoori Z., Jahromi M.K., Daryanoosh F., Forouhari S. High Intensity Interval Training Is More Effective Than Moderate Intensity Continuous Training in Ameliorating the Influence of Acute Noise Stress on Coagulation Factors // Sport Sci. Health. 2023. Vol. 19, No 2. P. 537–544. https://doi.org/10.1007/s11332-022-01041-9
Kalaki-Jouybari F., Shanaki M., Delfan M., Gorgani-Firuzjae S., Khakdan S. High-Intensity Interval Training (HIIT) Alleviated NAFLD Feature via miR-122 Induction in Liver of High-Fat High-Fructose Diet Induced Diabetic Rats // Arch. Physiol. Biochem. 2020. Vol. 126, No 3. P. 242–249. https://doi.org/10.1080/13813455.2018.1510968
Mohammad P., Esfandiar K.Z., Abbas S., Ahoora R. Effects of Moderate-Intensity Continuous Training and High-Intensity Interval Training on Serum Levels of Resistin, Chemerin and Liver Enzymes in Streptozotocin-Nicotinamide Induced Type-2 Diabetic Rats // J. Diabetes Metab. Disord. 2019. Vol. 18, No 2. P. 379–387. https://doi.org/10.1007/s40200-019-00422-1
Amri J., Parastesh M., Sadegh M., Latifi S.A., Alaee M. High-Intensity Interval Training Improved Fasting Blood Glucose and Lipid Profiles in Type 2 Diabetic Rats More Than Endurance Training; Possible Involvement of Irisin and Betatrophin // Physiol. Int. 2019. Vol. 106, No 3. P. 213–224. https://doi.org/10.1556/2060.106.2019.24
Sini Z.K., Afzalpour M.E., Ahmadi M.M., Sardar M.A., Khaleghzadeh H., Gorgani-Firuzjaee S., Hofmeister M., Akaras E., Azimkhani A. Comparison of the Effects of High-Intensity Interval Training and Moderate-Intensity Continuous Training on Indices of Liver and Muscle Tissue in High-Fat Diet-Induced Male Rats with Non-Alcoholic Fatty Liver Disease // Egypt. Liver J. 2022. Vol. 12. Art. No 63. https://doi.org/10.1186/s43066-022-00229-5
Marcinko K., Sikkema S.R., Samaan M.C., Kemp B.E., Fullerton M.D., Steinberg G.R. High Intensity Interval Training Improves Liver and Adipose Tissue Insulin Sensitivity // Mol. Metab. 2015. Vol. 4, No 12. P. 903–915. https://doi.org/10.1016/j.molmet.2015.09.006
Li W., Wang Y., He F., Liu Z., Dong J., Zhang Y., Li T., Liu S., Chen E. Association Between Triglyceride– Glucose Index and Nonalcoholic Fatty Liver Disease in Type 2 Diabetes Mellitus // BMC Endocr. Disord. 2022. Vol. 22, No 1. Art. No 261. https://doi.org/10.1186/s12902-022-01172-7
Gong R., Luo G., Wang M., Ma L., Sun S., Wei X. Associations Between TG/HDL Ratio and Insulin Resistance in the US Population: A Cross-Sectional Study // Endocr. Connect. 2021. Vol. 10, No 11. P. 1502–1512. https://doi.org/10.1530/EC-21-0414
Liu H., Liu J., Liu J., Xin S., Lyu Z., Fu X. Triglyceride to High-Density Lipoprotein Cholesterol (TG/HDL-C) Ratio, a Simple but Effective Indicator in Predicting Type 2 Diabetes Mellitus in Older Adults // Front. Endocrinol. (Lausanne). 2022. Vol. 13. Art. No 828581. https://doi.org/10.3389/fendo.2022.828581
Sargeant J.A., Gray L.J., Bodicoat D.H., Willis S.A., Stensel D.J., Nimmo M.A., Aithal G.P., King J.A. The Effect of Exercise Training on Intrahepatic Triglyceride and Hepatic Insulin Sensitivity: A Systematic Review and Meta-Analysis // Obes. Rev. 2018. Vol. 19, No 10. P. 1446–1459. https://doi.org/10.1111/obr.12719
Leon A.S., Sanchez O.A. Response of Blood Lipids to Exercise Training Alone or Combined with Dietary Intervention // Med. Sci. Sports Exerc. 2001. Vol. 33, No 6. P. S502–S515. https://doi.org/10.1097/00005768-200106001-00021
Najjar S.M., Caprio S., Gastaldelli A. Insulin Clearance in Health and Disease // Annu. Rev. Physiol. 2023. Vol. 85. P. 363–381. https://doi.org/10.1146/annurev-physiol-031622-043133
Philip R., Mathias M., Sucheta Kumari N., Damodara Gowda K.M., Jayaprakash Shetty K. Evaluation of Relationship Between Markers of Liver Function and the Onset of Type 2 Diabetes // J. Health Allied Sci. NU. 2014. Vol. 4, No 2. P. 90–93. https://doi.org/10.1055/s-0040-1703770
Sultani R., Tong D.C., Peverelle M., Lee Y.S., Baradi A., Wilson A.M. Elevated Triglycerides to High-Density Lipoprotein Cholesterol (TG/HDL-C) Ratio Predicts Long-Term Mortality in High-Risk Patients // Heart Lung Circ. 2020. Vol. 29, No 3. P. 414–421. https://doi.org/10.1016/j.hlc.2019.03.019
Reitman M.L., Gavrilova O. A-ZIP/F-1 Mice Lacking White Fat: A Model for Understanding Lipoatrophic Diabetes // Int. J. Obes. 2000. Vol. 24, suppl. 4. P. S11–S14. https://doi.org/10.1038/sj.ijo.0801493
Liu Q., Zhang L., Zhang W., Hao Q., Qiu W., Wen Y., Li X. Inhibition of NF-κB Reduces Renal Inflammation and Expression of PEPCK in Type 2 Diabetic Mice // Inflammation. 2018. Vol. 41, No 6. P. 2018–2029. https://doi.org/10.1007/s10753-018-0845-0
Shamsoddini A., Sobhani V., Ghamar Chehreh M.E., Alavian S.M., Zaree A. Effect of Aerobic and Resistance Exercise Training on Liver Enzymes and Hepatic Fat in Iranian Men with Nonalcoholic Fatty Liver Disease // Hepat. Mon. 2015. Vol. 15, No 10. Art. No e31434. https://doi.org/10.5812/hepatmon.31434
Sreenivasa Baba C., Alexander G., Kalyani B., Pandey R., Rastogi S., Pandey A., Choudhuri G. Effect of Exercise and Dietary Modification on Serum Aminotransferase Levels in Patients with Nonalcoholic Steatohepatitis // J. Gastroenterol. Hepatol. 2006. Vol. 21, No 1, pt. 1. P. 191–198. https://doi.org/10.1111/j.1440-1746.2005.04233.x
Sullivan S., Kirk E.P., Mittendorfer B., Patterson B.W., Klein S. Randomized Trial of Exercise Effect on Intrahepatic Triglyceride Content and Lipid Kinetics in Nonalcoholic Fatty Liver Disease // Hepatology. 2012. Vol. 55, No 6. P. 1738–1745. https://doi.org/10.1002/hep.25548
Taskinen M.R. Pathogenesis of Dyslipidemia in Type 2 Diabetes // Exp. Clin. Endocrinol. Diabetes. 2001. Vol. 109, suppl. 2. P. S 180–S188. https://doi.org/10.1055/s-2001-18580
Wan X.D., Yang W.B., Xia Y.Z., Wang J.F., Wang Y.J., Zhang Y.L. Disruption of Glucose Homeostasis and Induction of Insulin Resistance by Elevated Free Fatty Acids in Human L02 Hepatocytes // J. Endocrinol. Invest. 2009. Vol. 32, No 5. P. 454–459. https://doi.org/10.1007/bf03346485
Warner S.O., Yao M.V., Cason R.L., Winnick J.J. Exercise-Induced Improvements to Whole Body Glucose Metabolism in Type 2 Diabetes: The Essential Role of the Liver // Front. Endocrinol. (Lausanne). 2020. Vol. 11. Art. No 567. https://doi.org/10.3389/fendo.2020.00567
Yki-Järvinen H. Liver Fat in the Pathogenesis of Insulin Resistance and Type 2 Diabetes // Dig. Dis. 2010. Vol. 28, No 1. P. 203–209. https://doi.org/10.1159/000282087