Intermittent fasting results in tissue-specific changes in bioenergetics and redox state

PLoS ONE

Volumn 10, Issue 3, 2015, Pages

  Chausse, Bruno ^a   Vieira Lara, Marcel A ^a   Sanchez, Angélica B ^a   Medeiros, Marisa H G ^a   Kowaltowski, Alicia J ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

CARBONYL DERIVATIVE; CATALASE; GLUTATHIONE PEROXIDASE; GLUTATHIONE REDUCTASE; REACTIVE OXYGEN METABOLITE;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BIOENERGY; BODY MASS; BRAIN TISSUE; CONTROLLED STUDY; DIET RESTRICTION; ENERGY CONVERSION; ENZYME ACTIVITY; HEART PROTECTION; INTERMITTENT FASTING; LIVER; MALE; MITOCHONDRIAL RESPIRATION; NONHUMAN; OXIDATION REDUCTION STATE; OXIDATIVE STRESS; RAT; TISSUE SPECIFICITY; ANIMAL; BRAIN; BRAIN INJURY; ENERGY METABOLISM; INJURIES; LIVER MITOCHONDRION; METABOLISM; OXIDATION REDUCTION REACTION; OXYGEN CONSUMPTION; PATHOLOGY; SPRAGUE DAWLEY RAT;

ANIMALIA; RATTUS;

ANIMALS; BRAIN; BRAIN INJURIES; ENERGY METABOLISM; FASTING; LIVER; MALE; MITOCHONDRIA, LIVER; OXIDATION-REDUCTION; OXYGEN CONSUMPTION; RATS; RATS, SPRAGUE-DAWLEY;

EID: 84929105141     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0120413     Document Type: Article

References (40)

1. Redman LM, Ravussin E. Caloric restriction in humans: impact on physiological, psychological, and behavioral outcomes. Antioxid Redox Signal. 2011; 14: 275-287. doi: 10.1089/ars.2010.3253 PMID: 20518700
2. Speakman JR, Mitchell SE. Caloric restriction. Mol Aspects Med. 2011; 32: 159-221. doi: 10.1016/j.mam.2011.07.001 PMID: 21840335
3. Nisoli E, Tonello C, Cardile A, Cozzi V, Bracale R, Tedesco L, et al. Calorie restriction promotes mitochondrial biogenesis by inducing the expression of eNOS. Science. 2005; 310: 314-317. PMID: 16224023
4. Kowaltowski AJ. Caloric restriction and redox state: does this diet increase or decrease oxidant production? Redox Rep. 2011; 16: 237-241. doi: 10.1179/1351000211Y.0000000014 PMID: 22195991
5. Walsh ME, Shi Y, Van Remmen H. The effects of dietary restriction on oxidative stress in rodents. Free Radic Biol Med. 2014; 66: 88-99. doi: 10.1016/j.freeradbiomed.2013.05.037 PMID: 23743291
6. Anson RM, Jones B, de Cabo R. The diet restriction paradigm: a brief review of the effects of every-other-day feeding. Age (Dordr). 2005; 27: 17-25. doi: 10.1007/s11357-005-3286-2 PMID: 23598600
7. Cerqueira FM, Kowaltowski AJ. Commonly adopted caloric restriction protocols often involve malnutrition. Ageing Res Rev. 2010; 9: 424-430. doi: 10.1016/j.arr.2010.05.002 PMID: 20493280
8. Carlson AJ, Hoelzel F. Apparent prolongation of the life span of rats by intermittent fasting. J Nutr. 1946; 31: 363-375. PMID: 21021020
9. Goodrick CL, Ingram DK, Reynolds MA, Freeman JR, Cider N. Effects of intermittent feeding upon body weight and lifespan in inbred mice: interaction of genotype and age. Mech Ageing Dev. 1990; 55: 69-87. PMID: 2402168
10. Pearson KJ, Baur JA, Lewis KN, Peshkin L, Price NL, Labinskyy N et al. Resveratrol delays age-related deterioration and mimics transcriptional aspects of dietary restriction without extending lifespan. Cell Metab. 2008; 8: 157-168. doi: 10.1016/j.cmet.2008.06.011 PMID: 18599363
11. Martin B, Mattson MP, Maudsley S. Caloric restriction and intermittent fasting: two potential diets for successful brain aging. Ageing Res Rev. 2006; 5: 332-353. PMID: 16899414
12. Johnson JB, Summer W, Cutler RG, Martin B, Hyun DH, Dixit VDet al. Alternate day calorie restriction improves clinical findings and reduces markers of oxidative stress and inflammation in overweight adults with moderate asthma. Free Radic Biol Med. 2007; 42: 665-674. PMID: 17291990
13. Cerqueira FM, da Cunha FM, Caldeira da Silva CC, Chausse B, Romano RL, Garcia CC et al. Long-term intermittent feeding, but not caloric restriction, leads to redox imbalance, insulin receptor nitration, and glucose intolerance. Free Radic Biol Med. 2011; 51: 1454-1460. doi: 10.1016/j.freeradbiomed.2011.07.006 PMID: 21816219
14. Anson RM, Guo Z, de Cabo R, Lyun T, Rios M, Hagepanos A et al. Intermittent fasting dissociates beneficial effects of dietary restriction on glucose metabolism and neuronal resistance to injury from calorie intake. Proc Natl Acad Sci USA. 2003; 10: 6216-6220. PMID: 12724520
15. Tahara EB, Navarete FD, Kowaltowski AJ. Tissue-, substrate-, and site-specific characteristics of mitochondrial reactive oxygen species generation. Free Radic Biol Med. 2009; 46: 1283-1297. doi: 10.1016/j.freeradbiomed.2009.02.008 PMID: 19245829
16. Ferranti R, da Silva MM, Kowaltowski AJ. Mitochondrial ATP-sensitive K+ channel opening decreases reactive oxygen species generation. FEBS Lett. 2003; 536: 51-55. PMID: 12586337
17. Hütter E, Unterluggauer H, Garedew A, Jansen-Dürr P, Gnaiger E. High-resolution respirometry-a modern tool in aging research. Exp Gerontol. 2006; 41: 103-109. PMID: 16309877
18. Srere PA. Citrate synthase. Methods Enzymol. 1969; 13: 3-11.
19. Shacter E, Williams JA, Lim M, Levine RL. Differential susceptibility of plasma proteins to oxidative modification: examination by western blot immunoassay. Free Radic Biol Med. 1994; 17: 429-437. PMID: 7835749
20. Esworthy RS, Chu FF, Doroshow JH. Analysis of glutathione-related enzymes. In: Current Protocols in Toxicology. Wiley, 1999; Chapter 7.
21. Smith IK, Vierheller TL, Thorne CA. Assay of glutathione reductase in crude tissue homogenates using 5, 5′-dithiobis (2-nitrobenzoic acid). Anal Biochem. 1988; 175: 408-413. PMID: 3239770
22. Goldstein DB. A method for assay of catalase with the oxygen cathode. Anal Biochem. 1968; 24: 431-437. PMID: 5723299
23. Rahman I, Kode A, Biswas SK. Assay for quantitative determination of glutathione and glutathione disulfide levels using enzymatic recycling method. Nat Protoc. 2007; 1: 3159-3165.
24. Tatum VL, Ghangchit C, Chow CK. Measurement of malonaldehyde by high performance liquid chromatography with fluorescence detection. Lipids. 1990; 25: 226-229.
25. Chausse B, Solon C, Caldeira da Silva CC, Masselli Dos Reis IG, Manchado-Gobatto FB, et al. Intermittent fasting induces hypothalamic modifications resulting in low feeding efficiency, low body mass and overeating. Endocrinology. 2014; 155: 2456-2466. doi: 10.1210/en.2013-2057 PMID: 24797627
26. Caro P, Gómez J, López-Torres M, Sánchez I, Naudi A, Portero-Otín M, et al. Effect of every other day feeding on mitochondrial free radical production and oxidative stress in mouse liver. Rej Res. 2008; 11: 621-629. doi: 10.1089/rej.2008.0704 PMID: 18593280
27. Nicholls DG, Ferguson SJ. Bioenergetics 3. Academic Press: San Diego - CA, 2002; Chapter 5.
28. Cardoso AR, Chausse B, da Cunha FM, Luévano-Martínez LA, Marazzi TB, Pessoa PS et al. Mitochondrial compartmentalization of redox processes. Free Radic Biol Med. 2012; 52: 2201-2208. doi: 10.1016/j.freeradbiomed.2012.03.008 PMID: 22564526
29. Valko M, Leibfritz D, Moncol J, Cronin MT, Mazur M, Tesler J. Free radicals and antioxidants in normal physiological functions and human disease. Int J Biochem Cell Biol. 2007; 39: 44-84. PMID: 16978905
30. Cerqueira FM, Kowaltowski AJ. Mitochondrial metabolism in aging: effect of dietary interventions. Ageing Res Rev. 2012; 12: 22-28. doi: 10.1016/j.arr.2012.03.009 PMID: 22504406
31. Sanz A, Caro P, Ibañez J, Gómez J, Gredilla R, Barja G. Dietary restriction at old age lowers mitochondrial oxygen radical production and leak at complex I and oxidativeDNA damage in rat brain. J Bioenerg Biomembr. 2005; 37: 83-90. PMID: 15906153
32. Hyun DH, Emerson SS, Jo DG, Mattson MP, de Cabo R. Calorie restriction up-regulates the plasma membrane redox system in brain cells and suppresses oxidativestress during aging. Proc Natl Acad Sci USA. 2006; 103: 19908-19912. PMID: 17167053
33. Mattson MP, Wan R. () Beneficial effects of intermittent fasting and caloric restriction on the cardiovascular and cerebrovascular systems. J Nutr Biochem. 2005; 16: 129-137. PMID: 15741046
34. Wolf FI, Fasanella S, Tedesco B, Cavallini G, Donati A, Bergamini E et al. Peripheral lymphocyte 8-OHdG levels correlate with age-associated increase of tissue oxidative DNA damage in Sprague-Dawley rats. Protective effects of caloric restriction. Exp Gerontol. 2005; 40: 181-188. PMID: 15763395
35. Sharma S, Singh R, Kaur M, Kaur G. Late-onset dietary restriction compensates for age-related increase in oxidative stress and alterations of HSP 70 and synapsin 1 protein levels in male Wistar rats. Biogerontology. 2010; 11: 197-209. doi: 10.1007/s10522-009-9240-4 PMID: 19609710
36. Chandrasekar B, Nelson JF, Colston JT, Freeman GL. Calorie restriction attenuates inflammatory responses to myocardial ischemia-reperfusion injury. Am J Physiol Heart Circ Physiol. 2001; 280: 2094-2102.
37. Castello L, Froio T, Maina M, Cavallini G, Biasi F, Leonarduzzi G et al. Alternate-day fasting protects the rat heart against age-induced inflammation and fibrosis by inhibiting oxidative damage and NF-kB activation. Free Radic Biol Med. 2010; 48: 47-54. doi: 10.1016/j.freeradbiomed.2009.10.003 PMID: 19818847
38. Kaneko T, Tahara S, Matsuo M. Retarding effect of dietary restriction on the accumulation of 8-hydroxy-2′-deoxyguanosine in organs of Fischer 344 rats during aging. Free Radic Biol Med. 1997; 23: 76-81. PMID: 9165299
39. Radák Z, Takahashi R, Kumiyama A, Nakamoto H, Ohno H, Ookawara T et al. Effect of aging and late onset dietary restriction on antioxidant enzymes and proteasome activities, and protein carbonylation of rat skeletal muscle and tendon. Exp Gerontol. 2002; 37: 1423-1430. PMID: 12559411
40. Armeni T, Pieri C, Marra M, Saccucci F, Principato G. Studies on the life prolonging effect of food restriction: glutathione levels and glyoxalase enzymes in rat liver. Mech Ageing Dev. 1998; 101: 101-110. PMID: 9593316