CC..png    

16plus.png

Legal and postal addresses of the founder and publisher: Northern (Arctic) Federal University named after M.V. Lomonosov, Naberezhnaya Severnoy Dviny, 17, Arkhangelsk, 163002, Russian Federation

Editorial office address: Journal of Medical and Biological Research, 56 ul. Uritskogo, Arkhangelsk

Phone: (8182) 21-61-00, ext.18-20

E-mail: vestnik_med@narfu.ru
https://vestnikmed.ru/en/

ABOUT JOURNAL

Effects of Different Types of Exercise on Liver Function in Type 2 Diabetes in Mice (Review). P. 73-89

Версия для печати

Section: Review articles

Download (pdf, 1.3MB )

UDC

[616.36+59.084]:[616.379-008.64+612.766.1]

DOI

10.37482/2687-1491-Z271

Authors

Yuyfeng Yun* ORCID: https://orcid.org/0009-0005-8495-207X
Elena Yu. Dyakova* ORCID: https://orcid.org/0000-0001-7653-2386
Xianbo Qu* ORCID: https://orcid.org/0000-0002-0237-7915

*Tomsk State University
(Tomsk, Russia)

Corresponding author: Yuyfeng Yun, address: prosp. Lenina 36, Tomsk, 634050, Russia; e-mail: q634920875@163.com

Abstract

Type 2 diabetes mellitus (T2DM) is a chronic metabolic disorder that affects multiple organ systems. The liver serves as a central regulator of carbohydrate and lipid homeostasis and represents a major target of diabetic complications. Regular physical activity is acknowledged as an effective non-pharmacological intervention for improving metabolic control in diabetes. The purpose of this review was a comparative analysis of the effects of different exercise modalities on liver-related biomarkers in animals with T2DM. Materials and methods. A network meta-analysis of 38 randomized controlled trials with a total of 601 animals involved was conducted. The following databases were searched: Web of Science, PubMed, Scopus, CNKI and EBSCO. Six categories of exercise interventions were analysed: aerobic training, resistance training, swimming, high-intensity interval training, moderate-intensity continuous training, and voluntary wheel running. The initial assessment criteria included alanine aminotransferase (ALT), aspartate aminotransferase (AST), hepatic triglyceride, high-density lipoprotein (HDL) and low-density lipoprotein (LDL) levels as well as phosphoenolpyruvate carboxykinase (PEPCK) enzymatic activity. Results. High-intensity interval training showed the greatest effectiveness in reducing ALT and hepatic triglyceride levels as well as increasing HDL concentrations in mice with T2DM. Resistance training was most effective in lowering AST and LDL as well as in PEPCK activity. Swimming and moderate-intensity continuous training had a positive, albeit less pronounced, influence on certain biomarkers. The findings indicate that high-intensity interval training and resistance training can be more effective strategies for modulating hepatic metabolism in mice with T2DM. These results underscore the potential of physical exercise as a safe and accessible adjunct to the management of diabetes-induced liver dysfunction. However, additional clinical studies in human populations are needed to substantiate these effects.

Keywords

type 2 diabetes mellitus, liver function, lipid metabolism, resistance training, high-intensity interval training, network meta-analysis

References

  1. 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, рр. 525–539. https://doi.org/10.1038/s41574-022-00690-7
  2. 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, pp. 930–940. https://doi.org/10.1111/jdi.13756
  3. 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, pp. 1709–1716. https://doi.org/10.2337/db19-0098
  4. 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
  5. Duckworth W.C., Bennett R.G., Hamel F.G. Insulin Degradation: Progress and Potential. Endocr. Rev., 1998, vol. 19, no. 5, pp. 608–624. https://doi.org/10.1210/edrv.19.5.0349
  6. Fazio S., Linton M.F. Mouse Models of Hyperlipidemia and Atherosclerosis. Front. Biosci., 2001, vol. 6, pp. D515–D525. https://doi.org/10.2741/fazio
  7. 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
  8. 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, pp. 2074–2084. https://doi.org/10.2337/db19-0120
  9. 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, pp. 1706–1713. https://doi.org/10.2337/diacare.26.6.1706
  10. 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, pp. 2815–2829. https://doi.org/10.7150/ijbs.31781
  11. 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, pp. 241–252. https://doi.org/10.1113/jphysiol.2008.160275
  12. 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, pp. 353–368. https://doi.org/10.1249/MSS.0000000000002800
  13. 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
  14. 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, pp. 121–122. https://doi.org/10.1038/sj.ebd.6400831
  15. 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, pp. 2917–2926. https://doi.org/10.1002/jcp.23037
  16. 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, pp. 495–504. https://doi.org/10.2147/dmso.s70767
  17. 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 оbesus. Metabolism, 2004, vol. 53, no. 7, pp. 836–841. https://doi.org/10.1016/j.metabol.2004.02.001
  18. 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, pp. 981–987. https://doi.org/10.1002/hipo.20636
  19. 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
  20. 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
  21. 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, pp. 10930–10938. https://doi.org/10.1111/jcmm.16994
  22. 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
  23. 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, pp. 64–71. https://doi.org/10.1016/j.lfs.2015.01.031
  24. 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
  25. 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 R.S. 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, pp. 70–81. https://doi.org/10.1016/j.jnutbio.2017.09.021
  26. 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
  27. 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, pp. 426–430. https://doi.org/10.12047/j.cjap.5495.2017.103
  28. 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
  29. 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, pp. 199–204. https://doi.org/10.1002/cbf.1556
  30. 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, pp. 1012–1021. https://doi.org/10.1016/j.jep.2016.10.056
  31. 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, pp. 9–14. https://doi.org/10.1080/08977190701210693
  32. 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, pp. 262–266. https://doi.org/10.1016/j.ghir.2008.12.004
  33. 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, pp. 2069–2076. https://doi.org/10.1113/jphysiol.2008.164202
  34. 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
  35. 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
  36. 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, pp. 61–71. https://doi.org/10.1515/jbcpp-2017-0069
  37. 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, pp. 92–97. https://doi.org/10.1002/jcp.21833
  38. 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, pp. 317–324. https://doi.org/10.1007/s12011-010-8658-5
  39. 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, pp. 59–70. https://doi.org/10.1530/JOE-18-0567
  40. 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, pp. 2215–2224. https://doi.org/10.1007/s12011-020-02324-3
  41. 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, pp. 4262–4274. https://doi.org/10.1002/jcp.30882
  42. 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
  43. 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, pp. 503–510. https://doi.org/10.1016/j.biopha.2017.10.138
  44. 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
  45. 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, pp. E671–E682. https://doi.org/10.1152/ajpendo.90575.2008
  46. 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, pp. 537–544. https://doi.org/10.1007/s11332-022-01041-9
  47. 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, pp. 242–249. https://doi.org/10.1080/13813455.2018.1510968
  48. 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, pp. 379–387. https://doi.org/10.1007/s40200-019-00422-1
  49. 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, pp. 213–224. https://doi.org/10.1556/2060.106.2019.24
  50. 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
  51. 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, pp. 903–915. https://doi.org/10.1016/j.molmet.2015.09.006
  52. 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
  53. 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, pp. 1502–1512. https://doi.org/10.1530/EC-21-0414
  54. 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
  55. 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, pp. 1446–1459. https://doi.org/10.1111/obr.12719
  56. 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, pp. S502–S515. https://doi.org/10.1097/00005768-200106001-00021
  57. Najjar S.M., Caprio S., Gastaldelli A. Insulin Clearance in Health and Disease. Annu. Rev. Physiol., 2023, vol. 85, pp. 363–381. https://doi.org/10.1146/annurev-physiol-031622-043133
  58. 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, pp. 90–93. https://doi.org/10.1055/s-0040-1703770
  59. 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, pp. 414–421. https://doi.org/10.1016/j.hlc.2019.03.019
  60. 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, pp. S11–S14. https://doi.org/10.1038/sj.ijo.0801493
  61. 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, pp. 2018–2029. https://doi.org/10.1007/s10753-018-0845-0
  62. 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
  63. 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, pp. 191–198. https://doi.org/10.1111/j.1440-1746.2005.04233.x
  64. 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, pp. 1738–1745. https://doi.org/10.1002/hep.25548
  65. Taskinen M.R. Pathogenesis of Dyslipidemia in Type 2 Diabetes. Exp. Clin. Endocrinol. Diabetes, 2001, vol. 109, suppl. 2, pp. S180–S188. https://doi.org/10.1055/s-2001-18580
  66. 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, pp. 454–459. https://doi.org/10.1007/bf03346485
  67. 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
  68. Yki-Järvinen H. Liver Fat in the Pathogenesis of Insulin Resistance and Type 2 Diabetes. Dig. Dis., 2010, vol. 28, no. 1, pp. 203–209. https://doi.org/10.1159/000282087



Make a Submission


INDEXED IN: 

DOAJ_logo-colour.png

Elibrary.ru

logotype.png

infobaseindex

Логотип.png




Лань

OTHER NArFU JOURNALS: 

Vestnik of NArFU.
Series "Humanitarian and Social Sciences"

Forest Journal 
obl_les2023.jpg 

Arctic and North  

AiS.jpg

Продолжая просмотр сайта, я соглашаюсь с использованием файлов cookie владельцем сайта в соответствии с Политикой в отношении файлов cookie, в том числе на передачу данных, указанных в Политике, третьим лицам (статистическим службам сети Интернет).