1. Fahed G, Aoun L, Bou Zerdan M, Allam S, Bou Zerdan M, Bouferraa Y, et al. Metabolic syndrome: updates on pathophysiology and management in 2021. Int J Mol Sci. 2022;23(2):786. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
2. Litwin M, Kułaga Z. Obesity, metabolic syndrome, and primary hypertension. Pediatr Nephrol. 2021;36(4):825-37. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
3. Gastaldelli A, Miyazaki Y, Pettiti M, Matsuda M, Mahankali S, Santini E, et al. Metabolic effects of visceral fat accumulation in type 2 diabetes. J Clin Endocrinol Metab. 2002;87(11):5098-103. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
4. Barré-Sinoussi F, Montagutelli X. Animal models are essential to biological research: issues and perspectives. Future Sci OA. 2015;1(4):FSO63. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
5. Benchoula K, Arya A, Parhar IS, Hwa WE. FoxO1 signaling as a therapeutic target for type 2 diabetes and obesity. European journal of pharmacology. 2021;891:173758. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
6. Xing Y-q, Li A, Yang Y, Li X-x, Zhang L-n, Guo H-c. The regulation of FOXO1 and its role in disease progression. Life sciences. 2018;193:124-31. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
7. Berlanga A, Guiu-Jurado E, Porras JA, Auguet T. Molecular pathways in non-alcoholic fatty liver disease. Clin Exp Gastroenterol. 2014;7:221-39. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
8. Li Y, Ma Z, Jiang S, Hu W, Li T, Di S, et al. A global perspective on FOXO1 in lipid metabolism and lipid-related diseases. Prog Lipid Res. 2017;66:42-9. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
9. Xiong X, Tao R, DePinho RA, Dong XC. Deletion of hepatic FoxO1/3/4 genes in mice significantly impacts on glucose metabolism through downregulation of gluconeogenesis and upregulation of glycolysis. PloS One. 2013;8(8):e74340. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
10. Yang D, Yang Y, Li Y, Han R. Physical exercise as therapy for type 2 diabetes mellitus: From mechanism to orientation. Ann Nutr Metab. 2019;74(4):313-21. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
11. Møller AB, Kampmann U, Hedegaard J, Thorsen K, Nordentoft I, Vendelbo MH, et al. Altered gene expression and repressed markers of autophagy in skeletal muscle of insulin resistant patients with type 2 diabetes. Sci Rep. 2017;7(1):43775. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
12. Changotra H, Kaur S, Yadav SS, Gupta GL, Parkash J, Duseja A. ATG5: A central autophagy regulator implicated in various human diseases. Cell Biochem Funct. 2022;40(7):650-67. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
13. Yang L, Li P, Fu S, Calay ES, Hotamisligil GS. Defective hepatic autophagy in obesity promotes ER stress and causes insulin resistance. Cell Metab. 2010;11(6):467-78. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
14. Xu Z, Wu Y, Wang F, Li X, Wang P, Li Y, et al. Fibroblast growth factor 1 ameliorates diabetes-induced liver injury by reducing cellular stress and restoring autophagy. Front Pharmacol. 2020;11:52. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
15. Amati F, Dubé JJ, Alvarez-Carnero E, Edreira MM, Chomentowski P, Coen PM, et al. Skeletal muscle triglycerides, diacylglycerols, and ceramides in insulin resistance: another paradox in endurance-trained athletes? Diabetes. 2011;60(10):2588-97. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
16. Shaw CS, Shepherd SO, Wagenmakers AJ, Hansen D, Dendale P, Van Loon LJ. Prolonged exercise training increases intramuscular lipid content and perilipin 2 expression in type I muscle fibers of patients with type 2 diabetes. Am J Physiol Endocrinol Metab. 2012;303(9):E1158-65. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
17. Alvarez-Jimenez L, Morales-Palomo F, Moreno-Cabañas A, Ortega JF, Mora-Rodriguez R. Effects of statins on fat oxidation improvements after aerobic exercise training. J Clin Endocrinol Metab. 2023;108(5):e139-47. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
18. Cereijo L, Gullón P, Del Cura I, Valadés D, Bilal U, Badland H, et al. Exercise facilities and the prevalence of obesity and type 2 diabetes in the city of Madrid. Diabetologia. 2022;65(1):150-8. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
19. Bennetsen SL, Feineis CS, Legaard GE, Lyngbæk MP, Karstoft K, Ried-Larsen M. The impact of physical activity on glycemic variability assessed by continuous glucose monitoring in patients with type 2 diabetes mellitus: a systematic review. Front Endocrinol (Lausanne). 2020;11:486. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
20. Esefeld K, Kress S, Behrens M, Zimmer P, Stumvoll M, Thurm U, et al. Diabetes, sports and exercise. Experimental and Clinical Endocrinology & Diabetes. 2021;129(S 01):S52-S9. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
21. Yu H, Zhao X, Wu X, Yang J, Wang J, Hou L. High-intensity interval training versus moderate-intensity continuous training on patient quality of life in cardiovascular disease: A systematic review and meta-analysis. Sci Rep. 2023;13(1):13915. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
22. Umeno A, Horie M, Murotomi K, Nakajima Y, Yoshida Y. Antioxidative and antidiabetic effects of natural polyphenols and isoflavones. Molecules. 2016;21(6):708. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
23. Chiş I, Baltaru D, Dumitrovici A, Coseriu A, Radu B, Moldovan R, et al. Protective effects of quercetin from oxidative/nitrosative stress under intermittent hypobaric hypoxia exposure in the rat's heart. Physiol Int. 2018;105(3):233-46. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
24. Wang H, Zheng H, Zhang W, Yang L, Yu M, Li Z. A near-infrared aggregation-induced emission probe for imaging lipid droplet and in vivo visualization of diabetes-related viscosity variations. Sens Actuators B Chem. 2023;394:134347. [
View at Publisher] [
DOI] [
Google Scholar]
25. Veerapur V, Prabhakar K, Thippeswamy B, Bansal P, Srinivasan K, Unnikrishnan M. Antidiabetic effect of Ficus racemosa Linn. stem bark in high-fat diet and low-dose streptozotocin-induced type 2 diabetic rats: a mechanistic study. Food Chem. 2012;132(1):186-93. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
26. Pengam M, Goanvec C, Moisan C, Simon B, Albacète G, Féray A, et al. Moderate intensity continuous versus high intensity interval training: Metabolic responses of slow and fast skeletal muscles in rat. PloS One. 2023;18(10):e0292225. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
27. Dupas J, Feray A, Guernec A, Pengam M, Inizan M, Guerrero F, et al. Effect of personalized moderate exercise training on Wistar rats fed with a fructose enriched water. Nutr Metab (Lond). 2018;15(1):69. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
28. Yao Z, Gu Y, Zhang Q, Liu L, Meng G, Wu H, et al. Estimated daily quercetin intake and association with the prevalence of type 2 diabetes mellitus in Chinese adults. Eur J Nutr. 2019;58(2):819-30. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
29. Michala A-S, Pritsa A. Quercetin: a molecule of great biochemical and clinical value and its beneficial effect on diabetes and cancer. Diseases. 2022;10(3):37. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
30. Ansari P, Choudhury ST, Seidel V, Rahman AB, Aziz MA, Richi AE, et al. Therapeutic potential of quercetin in the management of type-2 diabetes mellitus. Life (Basel). 2022;12(8):1146. [
View at Publisher] [
DOI] [
PMID] [
Google Scholar]
31. Bahadoran Z, Golzarand M, Mirmiran P, Saadati N, Azizi F. The association of dietary phytochemical index and cardiometabolic risk factors in adults: Tehran Lipid and Glucose Study. J Hum Nutr Diet. 2013;26(s1):145-53. [
view at publisher] [
DOI] [
PMID] [
Google Scholar]
32. Kostić M, Korićanac G, Tepavčević S, Stanišić J, Romić S, Ćulafić T, et al. Low-intensity exercise affects cardiac fatty acid oxidation by increasing the nuclear content of pparα, foxo1, and lipin1 in fructose-fed rats. Metab Syndr Relat Disord. 2023;21(2):122-31. [
view at publisher] [
DOI] [
PMID] [
Google Scholar]
33. Pereira RM, da Cruz Rodrigues KC, Sant'Ana MR, da Rocha AL, Morelli AP, Veras AS, et al. FOXO1 is downregulated in obese mice subjected to short‐term strength training. J Cell Physiol. 2022;237(11):4262-74. [
view at publisher] [
DOI] [
PMID] [
Google Scholar]
34. Yarmohammadi M, Behboudi L, Eizadi M. The Effect of 12 Weeks Resistance Training on FOXO1 Expression in Hepatocytes, Glucose and Insulin in Diabetic Rats-A Brief-Report. Iranian journal of diabetes and obesity. 2020;11(3):193-5. [
view at publisher] [
DOI] [
Google Scholar]
35. Slopack D, Roudier E, Liu ST, Nwadozi E, Birot O, Haas TL. Forkhead BoxO transcription factors restrain exercise‐induced angiogenesis. J Physiol. 2014;592(18):4069-82. [
view at publisher] [
DOI] [
PMID] [
Google Scholar]
36. Sohaily S, Eizadi M, Tarmast D. Effect of resistance training on FOXO1 gene expression in subcutaneous fatty tissue in diabetic wistar rats. J Gorgan Univ Med Sci. 2019;21(4):53-9. [
view at publisher] [
Google Scholar]
37. Karimi M, Eizadi M. The effect of interval training on FOXO1 expression in pancreas tissue of diabetes rats with high fat diet and STZ. Razi Journal of Medical Sciences. 2019;26(6):95-104. [
view at publisher] [
Google Scholar]
38. Joodi M, Banaeifar A, Eizadia M, Arshadi S. The changes of serum insulin in response to resistance training with emphasis on FOXO1 in pancreas of diabetes rats. J Jiroft Univ Med Sci. 2021;7(4):480-8. [
view at publisher] [
Google Scholar]
39. Wu B, Xu C, Tian Y, Zeng Y, Yan F, Chen A, et al. Aerobic exercise promotes the expression of ATGL and attenuates inflammation to improve hepatic steatosis via lncRNA SRA. Sci Rep. 2022;12(1):5370. [
view at publisher] [
DOI] [
PMID] [
Google Scholar]
40. Kamagate A, Kim DH, Zhang T, Slusher S, Gramignoli R, Strom SC, et al. FoxO1 links hepatic insulin action to endoplasmic reticulum stress. Endocrinology. 2010;151(8):3521-35. [
view at publisher] [
DOI] [
PMID] [
Google Scholar]
41. Kazeminasab F, Baharlooie M, Rezazadeh H, Soltani N, Rosenkranz SK. The effects of aerobic exercise on liver function, insulin resistance, and lipid profiles in prediabetic and type 2 diabetic mice. Physiol Behav. 2023;271:114340 [
view at publisher] [
DOI] [
PMID] [
Google Scholar]
42. Daneshyar S, Pouyandeh Ravan A, Khosravi A, Fourotan Y. The Long-Term Effect of High Fat Diet and Regular Aerobic Exercise Training on Gene Expression of Isoforms of Mitochondrial Creatine Kinase (Ckmt1, 2) in White Adipose Tissue of Mice: An Experimental Study. J Rafsanjan Univ Med Sci. 2020;19(6):619-32. [
view at publisher] [
Google Scholar]
43. Pinto AP, da Rocha AL, Marafon BB, Rovina RL, Muñoz VR, da Silva LE, et al. Impact of different physical exercises on the expression of autophagy markers in mice. Int J Mol Sci. 2021;22(5):2635. [
view at publisher] [
DOI] [
PMID] [
Google Scholar]
44. Li Y, Zong W-X, Ding W-X. Recycling the danger via lipid droplet biogenesis after autophagy. Autophagy. 2017;13(11):1995-7. [
view at publisher] [
DOI] [
PMID] [
Google Scholar]
45. Kaur J, Debnath J. Autophagy at the crossroads of catabolism and anabolism. Nat Rev Mol Cell Biol. 2015;16(8):461-72. [
view at publisher] [
DOI] [
PMID] [
Google Scholar]
46. Zechner R, Madeo F, Kratky D. Cytosolic lipolysis and lipophagy: two sides of the same coin. Nat Rev Mol Cell Biol. 2017;18(11):671-84. [
view at publisher] [
DOI] [
PMID] [
Google Scholar]