Sirtuin Expression in Insulin-Sensitive Tissues of Rats with Impaired Glucose Tolerance is not Affected by Resistance Training or Zinc Supplementation.

Exercise Impaired glucose tolerance Sirtuins Zinc supplementation

Journal

Biological trace element research
ISSN: 1559-0720
Titre abrégé: Biol Trace Elem Res
Pays: United States
ID NLM: 7911509

Informations de publication

Date de publication:
01 Oct 2024
Historique:
received: 13 06 2024
accepted: 25 09 2024
medline: 1 10 2024
pubmed: 1 10 2024
entrez: 1 10 2024
Statut: aheadofprint

Résumé

While physical activity and zinc supplementation have shown benefits in diabetes management, little is known about their effect on less severe glucose homeostasis disorders, such as impaired glucose tolerance. On the other hand, sirtuins have an important role in glucose metabolism and insulin sensitivity, but to date, there is no information about the impact of zinc supplementation or physical activity on their regulation in individuals with impaired glucose homeostasis. The aim of this study was to assess the effect of supplemental zinc, muscle-resistance training, and their combination on the expression of selected sirtuins in insulin-sensitive tissues of rats with impaired glucose tolerance. Thirty male Wistar rats with impaired glucose tolerance were fed a high-fat diet for 12 weeks while subjected to zinc supplementation, resistance training, both, or none. Morphometric and metabolic evaluations were performed at the end of the experimental period, and gene expression of sirtuins 1, 2, 4, and 7 was assessed in liver, gastrocnemius muscle, and white adipose tissue. Results showed that zinc supplementation and/or resistance training did not improve metabolic parameters of rats with impaired glucose tolerance, nor did they affect the expression of selected sirtuins in any of the tissues evaluated. However, the expression of some sirtuins was associated with metabolic parameters in a tissue-specific manner. Additional studies are needed to evaluate whether zinc supplementation and/or resistance training can improve metabolic status or modulate sirtuins expression in advanced stages of impaired glucose homeostasis.

Identifiants

pubmed: 39352663
doi: 10.1007/s12011-024-04397-w
pii: 10.1007/s12011-024-04397-w
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : National Commission for Scientific and Technological Research (CONICYT)
ID : FONDECYT 1160792
Organisme : National Commission for Scientific and Technological Research (CONICYT)
ID : FONDECYT 1160792
Organisme : National Commission for Scientific and Technological Research (CONICYT)
ID : FONDECYT 1160792
Organisme : National Commission for Scientific and Technological Research (CONICYT)
ID : FONDECYT 1160792
Organisme : National Commission for Scientific and Technological Research (CONICYT)
ID : FONDECYT 1160792

Informations de copyright

© 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Références

World Health Organization Diabetes. https://www.who.int/health-topics/diabetes . Accessed 16 Aug 2023
ElSayed NA, Aleppo G, Aroda VR et al (2023) 2. Classification and diagnosis of diabetes: standards of care in diabetes—2023. Diabetes Care 46:S19–S40. https://doi.org/10.2337/dc23-S002
Nathan DM, Davidson MB, DeFronzo RA et al (2007) Impaired fasting glucose and impaired glucose tolerance. Diabetes Care 30:753–759. https://doi.org/10.2337/dc07-9920
doi: 10.2337/dc07-9920 pubmed: 17327355
Rooney MR, Fang M, Ogurtsova K et al (2023) Global prevalence of prediabetes. Diabetes Care 46:1388–1394. https://doi.org/10.2337/dc22-2376
doi: 10.2337/dc22-2376 pubmed: 37196350 pmcid: 10442190
ElSayed NA, Aleppo G, Aroda VR et al (2023) 5. Facilitating positive health behaviors and well-being to improve health outcomes: Standards of Care in Diabetes—2023. Diabetes Care 46:S68–S96. https://doi.org/10.2337/dc23-S005
doi: 10.2337/dc23-S005 pubmed: 36507648
ElSayed NA, Aleppo G, Aroda VR et al (2023) 9. Pharmacologic approaches to glycemic treatment: Standards of Care in Diabetes—2023. Diabetes Care 46:S140–S157. https://doi.org/10.2337/dc23-S009
doi: 10.2337/dc23-S009 pubmed: 36507650
Kanaley JA, Colberg SR, Corcoran MH et al (2022) Exercise/physical activity in individuals with type 2 diabetes: a consensus statement from the American College of Sports Medicine. Med Sci Sports Exerc 54:353–368. https://doi.org/10.1249/MSS.0000000000002800
doi: 10.1249/MSS.0000000000002800 pubmed: 35029593 pmcid: 8802999
Pazmino L, Esparza W, Aladro-Gonzalvo AR, León E (2021) Impact of work and recreational physical activity on prediabetes condition among U.S. adults: NHANES 2015–2016. Int J Environ Res Public Health 18:1378. https://doi.org/10.3390/ijerph18041378
doi: 10.3390/ijerph18041378 pubmed: 33546150 pmcid: 7913268
Bahadoran Z, Mirmiran P, Shabani M, Azizi F (2023) Higher daily physical activity levels may facilitate pre-diabetes regression to normoglycemia: a longitudinal study among an Iranian population. Prev Med Rep 34:102233. https://doi.org/10.1016/j.pmedr.2023.102233
doi: 10.1016/j.pmedr.2023.102233 pubmed: 37288139 pmcid: 10241965
Huang L, Fang Y, Tang L (2021) Comparisons of different exercise interventions on glycemic control and insulin resistance in prediabetes: a network meta-analysis. BMC Endocr Disord 21:181. https://doi.org/10.1186/s12902-021-00846-y
doi: 10.1186/s12902-021-00846-y pubmed: 34488728 pmcid: 8422751
Zhang H, Guo Y, Hua G et al (2024) Exercise training modalities in prediabetes: a systematic review and network meta-analysis. Front Endocrinol 15:1308959. https://doi.org/10.3389/fendo.2024.1308959
doi: 10.3389/fendo.2024.1308959
Ruz M, Carrasco F, Rojas P et al (2013) Zinc as a potential coadjuvant in therapy for type 2 diabetes. Food Nutr Bull 34:215–221. https://doi.org/10.1177/156482651303400210
doi: 10.1177/156482651303400210 pubmed: 23964394
Emdin SO, Dodson GG, Cutfield JM, Cutfield SM (1980) Role of zinc in insulin biosynthesis: some possible zinc-insulin interactions in the pancreatic B-cell. Diabetologia 19:174–182. https://doi.org/10.1007/BF00275265
doi: 10.1007/BF00275265 pubmed: 6997118
Vardatsikos G, Pandey NR, Srivastava AK (2013) Insulino-mimetic and anti-diabetic effects of zinc. J Inorg Biochem 120:8–17. https://doi.org/10.1016/j.jinorgbio.2012.11.006
doi: 10.1016/j.jinorgbio.2012.11.006 pubmed: 23266931
Jansen J, Karges W, Rink L (2009) Zinc and diabetes — clinical links and molecular mechanisms. J Nutr Biochem 20:399–417. https://doi.org/10.1016/j.jnutbio.2009.01.009
doi: 10.1016/j.jnutbio.2009.01.009 pubmed: 19442898
Jayawardena R, Ranasinghe P, Galappatthy P et al (2012) Effects of zinc supplementation on diabetes mellitus: a systematic review and meta-analysis. Diabetol Metab Syndr 4:13. https://doi.org/10.1186/1758-5996-4-13
doi: 10.1186/1758-5996-4-13 pubmed: 22515411 pmcid: 3407731
Capdor J, Foster M, Petocz P, Samman S (2013) Zinc and glycemic control: a meta-analysis of randomised placebo controlled supplementation trials in humans. J Trace Elem Med Biol 27:137–142. https://doi.org/10.1016/j.jtemb.2012.08.001
doi: 10.1016/j.jtemb.2012.08.001 pubmed: 23137858
Wang X, Wu W, Zheng W et al (2019) Zinc supplementation improves glycemic control for diabetes prevention and management: a systematic review and meta-analysis of randomized controlled trials. Am J Clin Nutr 110:76–90. https://doi.org/10.1093/ajcn/nqz041
doi: 10.1093/ajcn/nqz041 pubmed: 31161192
Moniot S, Weyand M, Steegborn C (2012) Structures, substrates, and regulators of mammalian sirtuins – opportunities and challenges for drug development.  Front Pharmacol 3.  https://doi.org/10.3389/fphar.2012.00016
Bedalov A, Chowdhury S, Simon JA (2016) Biology, chemistry, and pharmacology of sirtuins. Methods Enzymol  574:183–211. Elsevier
Wu Q-J, Zhang T-N, Chen H-H et al (2022) The sirtuin family in health and disease. Signal Transduct Target Ther 7:402. https://doi.org/10.1038/s41392-022-01257-8
doi: 10.1038/s41392-022-01257-8 pubmed: 36581622 pmcid: 9797940
Lavu S, Boss O, Elliott PJ, Lambert PD (2008) Sirtuins — novel therapeutic targets to treat age-associated diseases. Nat Rev Drug Discov 7:841–853. https://doi.org/10.1038/nrd2665
doi: 10.1038/nrd2665 pubmed: 18827827
Wang Y, He J, Liao M et al (2019) An overview of Sirtuins as potential therapeutic target: structure, function and modulators. Eur J Med Chem 161:48–77. https://doi.org/10.1016/j.ejmech.2018.10.028
doi: 10.1016/j.ejmech.2018.10.028 pubmed: 30342425
Houtkooper RH, Pirinen E, Auwerx J (2012) Sirtuins as regulators of metabolism and healthspan. Nat Rev Mol Cell Biol 13:225–238. https://doi.org/10.1038/nrm3293
doi: 10.1038/nrm3293 pubmed: 22395773 pmcid: 4872805
Song J, Yang B, Jia X et al (2018) Distinctive roles of sirtuins on diabetes, protective or detrimental? Front Endocrinol 9:724. https://doi.org/10.3389/fendo.2018.00724
doi: 10.3389/fendo.2018.00724
Zhang H-H, Ma X-J, Wu L-N et al (2015) SIRT1 attenuates high glucose-induced insulin resistance via reducing mitochondrial dysfunction in skeletal muscle cells. Exp Biol Med 240:557–565. https://doi.org/10.1177/1535370214557218
doi: 10.1177/1535370214557218
Gomes P, Fleming Outeiro T, Cavadas C (2015) Emerging role of Sirtuin 2 in the regulation of mammalian metabolism. Trends Pharmacol Sci 36:756–768. https://doi.org/10.1016/j.tips.2015.08.001
doi: 10.1016/j.tips.2015.08.001 pubmed: 26538315
Parihar P, Solanki I, Mansuri ML, Parihar MS (2015) Mitochondrial sirtuins: emerging roles in metabolic regulations, energy homeostasis and diseases. Exp Gerontol 61:130–141. https://doi.org/10.1016/j.exger.2014.12.004
doi: 10.1016/j.exger.2014.12.004 pubmed: 25482473
Kurylowicz A, Owczarz M, Polosak J et al (2016) SIRT1 and SIRT7 expression in adipose tissues of obese and normal-weight individuals is regulated by microRNAs but not by methylation status. Int J Obes 40:1635–1642. https://doi.org/10.1038/ijo.2016.131
doi: 10.1038/ijo.2016.131
García-Díaz D, Campión J, Milagro FI, Martínez JA (2007) Adiposity dependent apelin gene expression: relationships with oxidative and inflammation markers. Mol Cell Biochem 305:87–94. https://doi.org/10.1007/s11010-007-9531-5
doi: 10.1007/s11010-007-9531-5 pubmed: 17594060
Garcia-Diaz DF, Arellano AV, Milagro FI et al (2011) Glucose and insulin modify thrombospondin 1 expression and secretion in primary adipocytes from diet-induced obese rats. J Physiol Biochem 67:453–461. https://doi.org/10.1007/s13105-011-0081-7
doi: 10.1007/s13105-011-0081-7 pubmed: 21394550
Soto-Covasich J, Reyes-Farias M, Torres RF et al (2020) A polyphenol-rich calafate (Berberis microphylla) extract rescues glucose tolerance in mice fed with cafeteria diet. J Funct Foods 67:103856. https://doi.org/10.1016/j.jff.2020.103856
doi: 10.1016/j.jff.2020.103856
Reeves PG, Nielsen FH, Fahey GC (1993) AIN-93 purified diets for Laboratory rodents: final report of the American Institute of Nutrition Ad Hoc Writing Committee on the reformulation of the AIN-76A Rodent Diet. J Nutr 123:1939–1951. https://doi.org/10.1093/jn/123.11.1939
doi: 10.1093/jn/123.11.1939 pubmed: 8229312
Institute of Medicine (2001) Dietary reference intakes for Vitamin A, Vitamin K, Arsenic, Boron, Chromium, Copper, Iodine, Iron, Manganese, Molybdenum, Nickel, Silicon, Vanadium, and Zinc. National Academies, Washington, D.C.
Thirupathi A, Da Silva Pieri BL, Queiroz JAMP et al (2019) Strength training and aerobic exercise alter mitochondrial parameters in brown adipose tissue and equally reduce body adiposity in aged rats. J Physiol Biochem 75:101–108. https://doi.org/10.1007/s13105-019-00663-x
doi: 10.1007/s13105-019-00663-x pubmed: 30712161
Avila-George K, Ramos-Olivares K, Vasquez-Munoz K et al (2017) Chemically induced hypoxia promotes differential outcomes over preadipocyte– or adipocyte–macrophage communication. Arch Physiol Biochem 123:175–181. https://doi.org/10.1080/13813455.2017.1285318
doi: 10.1080/13813455.2017.1285318 pubmed: 28276712
Pfaffl MW (2001) A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res 29:45e–445. https://doi.org/10.1093/nar/29.9.e45
doi: 10.1093/nar/29.9.e45
Vivero A, Ruz M, Rivera M et al (2021) Zinc supplementation and Strength Exercise in rats with type 2 diabetes: akt and PTP1B phosphorylation in nonalcoholic fatty liver. Biol Trace Elem Res 199:2215–2224. https://doi.org/10.1007/s12011-020-02324-3
doi: 10.1007/s12011-020-02324-3 pubmed: 32939643
Kahn SE (2001) The importance of β-Cell failure in the development and progression of type 2 diabetes. J Clin Endocrinol Metab 86:4047–4058. https://doi.org/10.1210/jcem.86.9.7713
doi: 10.1210/jcem.86.9.7713 pubmed: 11549624
King A, Austin A (2017) Animal Models of Type 1 and Type 2 Diabetes Mellitus. Animal Models for the Study of Human Disease. Elsevier, pp 245–265. https://doi.org/10.1016/B978-0-12-809468-6.00010-3
doi: 10.1016/B978-0-12-809468-6.00010-3
Singh R, Gholipourmalekabadi M, Shafikhani SH (2024) Animal models for type 1 and type 2 diabetes: advantages and limitations. Front Endocrinol 15:1359685. https://doi.org/10.3389/fendo.2024.1359685
doi: 10.3389/fendo.2024.1359685
Gheibi S, Kashfi K, Ghasemi A (2017) A practical guide for induction of type-2 diabetes in rat: incorporating a high-fat diet and streptozotocin. Biomed Pharmacother 95:605–613. https://doi.org/10.1016/j.biopha.2017.08.098
doi: 10.1016/j.biopha.2017.08.098 pubmed: 28881291
Kottaisamy CPD, Raj DS, Prasanth Kumar V, Sankaran U (2021) Experimental animal models for diabetes and its related complications—a review. Lab Anim Res 37:23. https://doi.org/10.1186/s42826-021-00101-4
doi: 10.1186/s42826-021-00101-4 pubmed: 34429169 pmcid: 8385906
Milazzo G, Mercatelli D, Di Muzio G et al (2020) Histone Deacetylases (HDACs): evolution, specificity, role in Transcriptional Complexes, and pharmacological actionability. Genes 11:556. https://doi.org/10.3390/genes11050556
doi: 10.3390/genes11050556 pubmed: 32429325 pmcid: 7288346
Min J, Landry J, Sternglanz R, Xu R-M (2001) Crystal structure of a SIR2 Homolog–NAD complex. Cell 105:269–279. https://doi.org/10.1016/S0092-8674(01)00317-8
doi: 10.1016/S0092-8674(01)00317-8 pubmed: 11336676
Chen L, Feng Y, Zhou Y et al (2010) Dual role of Zn2 + in maintaining structural integrity and suppressing deacetylase activity of SIRT1. J Inorg Biochem 104:180–185. https://doi.org/10.1016/j.jinorgbio.2009.10.021
doi: 10.1016/j.jinorgbio.2009.10.021 pubmed: 19923004
Rosenkranz E, Metz CHD, Maywald M et al (2016) Zinc supplementation induces regulatory T cells by inhibition of Sirt-1 deacetylase in mixed lymphocyte cultures. Mol Nutr Food Res 60:661–671. https://doi.org/10.1002/mnfr.201500524
doi: 10.1002/mnfr.201500524 pubmed: 26614004
Liang J, Huang G, Liu X et al (2022) The ZIP8/SIRT1 axis regulates alveolar progenitor cell renewal in aging and idiopathic pulmonary fibrosis. J Clin Invest 132:e157338. https://doi.org/10.1172/JCI157338
doi: 10.1172/JCI157338 pubmed: 35389887 pmcid: 9151700
Jiang D, Yang X, Ge M et al (2023) Zinc defends against Parthanatos and promotes functional recovery after spinal cord injury through SIRT3 -mediated anti‐oxidative stress and mitophagy. CNS Neurosci Ther 29:2857–2872. https://doi.org/10.1111/cns.14222
doi: 10.1111/cns.14222 pubmed: 37063066 pmcid: 10493669
Xu C, Zhou Z, Zhao H et al (2023) Zinc promotes spinal cord Injury Recovery by blocking the activation of NLRP3 inflammasome through SIRT3-Mediated autophagy. Neurochem Res 48:435–446. https://doi.org/10.1007/s11064-022-03762-2
doi: 10.1007/s11064-022-03762-2 pubmed: 36152137
Marfe G, Manzi V, Tafani M et al (2012) The modulation of sirtuins and apoptotic proteins in rats after exhaustive exercise. Open J Mol Integr Physiol 02:65–74. https://doi.org/10.4236/ojmip.2012.23010
doi: 10.4236/ojmip.2012.23010
Liu H-W, Kao H-H, Wu C-H (2019) Exercise training upregulates SIRT1 to attenuate inflammation and metabolic dysfunction in kidney and liver of diabetic db/db mice. Nutr Metab 16:22. https://doi.org/10.1186/s12986-019-0349-4
doi: 10.1186/s12986-019-0349-4
Vargas-Ortiz K, Pérez-Vázquez V, Macías-Cervantes MH (2019) Exercise and sirtuins: a way to mitochondrial health in skeletal muscle. Int J Mol Sci 20:2717. https://doi.org/10.3390/ijms20112717
doi: 10.3390/ijms20112717 pubmed: 31163574 pmcid: 6600260
Min Z, Gao J, Yu Y (2019) The roles of mitochondrial SIRT4 in Cellular Metabolism. Front Endocrinol 9:783. https://doi.org/10.3389/fendo.2018.00783
doi: 10.3389/fendo.2018.00783
Ford E, Voit R, Liszt G et al (2006) Mammalian Sir2 homolog SIRT7 is an activator of RNA polymerase I transcription. Genes Dev 20:1075–1080. https://doi.org/10.1101/gad.1399706
doi: 10.1101/gad.1399706 pubmed: 16618798 pmcid: 1472467
Wronska A, Lawniczak A, Wierzbicki PM, Kmiec Z (2016) Age-related changes in Sirtuin 7 expression in calorie-restricted and refed rats. Gerontology 62:304–310. https://doi.org/10.1159/000441603
doi: 10.1159/000441603 pubmed: 26595207
Stott NL, Marino JS (2020) High Fat Rodent models of type 2 diabetes: from Rodent to Human. Nutrients 12:3650. https://doi.org/10.3390/nu12123650
doi: 10.3390/nu12123650 pubmed: 33261000 pmcid: 7761287

Auteurs

D Garcia-Díaz (D)

Department of Nutrition, Faculty of Medicine, University of Chile, Independencia 1027, Santiago, Chile.

A Pérez (A)

Department of Nutrition, Faculty of Medicine, University of Chile, Independencia 1027, Santiago, Chile.

A Barham (A)

Department de Kinesiology, Faculty of Medicine, University of Chile, Santiago, Chile.

M Cano-Cappellacci (M)

Department de Kinesiology, Faculty of Medicine, University of Chile, Santiago, Chile.

K Vásquez (K)

Department of Nutrition, Faculty of Medicine, University of Chile, Independencia 1027, Santiago, Chile.

F Pérez-Bravo (F)

Department of Nutrition, Faculty of Medicine, University of Chile, Independencia 1027, Santiago, Chile.

J Inostroza (J)

Department of Nutrition, Faculty of Medicine, University of Chile, Independencia 1027, Santiago, Chile.

J Codoceo (J)

Department of Nutrition, Faculty of Medicine, University of Chile, Independencia 1027, Santiago, Chile.

J Orellana (J)

School of Nutrition and Dietetics, Faculty of Medicine, University of Chile, Santiago, Chile.

S Samman (S)

School of Life and Environmental Sciences, University of Sydney, Sydney, Australia.

Manuel Ruz (M)

Department of Nutrition, Faculty of Medicine, University of Chile, Independencia 1027, Santiago, Chile. mruz@uchile.cl.

Classifications MeSH