Abstract
Both morbidity and mortality due to cardiovascular diseases (CVDs) elevate with age. The elevated prevalence of cardiovascular risk factors with age and cardiovascular aging contribute to the relationship between aging and CVDs. Dietary restriction (DR) consisting of calorie restriction (CR) and alternate-day fasting (ADF) is an approved nutritional intervention and shows anti-aging impacts. Recent studies demonstrate that DR makes an active defense response in stressful states. At the core of this response are cardiovascular protective signals, which consist of the mammalian target of rapamycin (mTOR), AMP-activated kinase, sirtuins and endothelial nitric oxide synthase. These make a network with positive and negative feedback regulation. Hence, DR is a hopeful intervention for controlling cardiovascular aging and managing individuals with CVDs.
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References
Varady KA, Hellerstein MK (2007) Alternate-day fasting and chronic disease prevention: a review of human and animal trials. Am J Clin Nutr 86:7–13
Weindruch R, Sohal RS (1997) Caloric intake and aging. N Engl J Med 337:986–994
Mattison JA, Lane MA, Roth GS, Ingram DK (2003) Calorie restriction in rhesus monkeys. Exp Gerontol 38:35–46
Masoro EJ (2005) Overview of caloric restriction and ageing. Mech Ageing Dev 126:913–922
McCay CM, Crowell MF, Maynard LA (1989) The effect of retarded growth upon the length of life span and upon the ultimate body size. 1935. Nutrition 5:155–171
Shinmura K (2011) Cardiovascular protection afforded by caloric restriction: essential role of nitric oxide synthase. Geriatr Gerontol Int 11:143–156
Shinmura K (2013) Effects of caloric restriction on cardiac oxidative stress and mitochondrial bioenergetics: potential role of cardiac sirtuins. Oxidative Med Cell Longev 2013:528935
Speakman JR, Mitchell SE (2011) Caloric restriction. Mol Asp Med 32:159–221
Ungvari Z, Parrado-Fernandez C, Csiszar A, De Cabo R (2008) Mechanisms underlying caloric restriction and lifespan regulation. Circ Res 102:519–528
North BJ, Sinclair DA (2012) The intersection between aging and cardiovascular disease. Circ Res 110:1097–1108
Schroeder JE, Richardson JC, Virley DJ (2010) Dietary manipulation and caloric restriction in the development of mouse models relevant to neurological diseases. Biochim Biophys Acta 1802:840–846
Zanetti M, Cappellari GG, Burekovic I, Barazzoni R, Stebel M, Guarnieri G (2010) Caloric restriction improves endothelial dysfunction during vascular aging: effects on nitric oxide synthase isoforms and oxidative stress in rat aorta. Exp Gerontol 45:848–855
Lakatta EG (2003) Arterial and cardiac aging: major shareholders in cardiovascular disease enterprises. Circulation 107:490–497
Lakatta EG (2003) Arterial and cardiac aging: major shareholders in cardiovascular disease enterprises: part I: aging arteries: a “set up” for vascular disease. Circulation 107:490–497
Hammer S, Snel M, Lamb HJ, Jazet IM, van der Meer RW, Pijl H et al (2008) Prolonged caloric restriction in obese patients with type 2 diabetes mellitus decreases myocardial triglyceride content and improves myocardial function. J Am Coll Cardiol 52:1006–1012
Riordan MM, Weiss EP, Meyer TE, Ehsani AA, Racette SB, Villareal DT et al (2008) The effects of caloric restriction-and exercise-induced weight loss on left ventricular diastolic function. Am J Physiol Heart Circ Physiol 294:H1174–H1182
Holloszy JO, Fontana L (2007) Caloric restriction in humans. Exp Gerontol 42:709–712
Nisoli E, Tonello C, Cardile A, Cozzi V, Bracale R, Tedesco L et al (2005) Calorie restriction promotes mitochondrial biogenesis by inducing the expression of eNOS. Science 310:314–317
Donato AJ, Eskurza I, Silver AE, Levy AS, Pierce GL, Gates PE et al (2007) Direct evidence of endothelial oxidative stress with aging in humans: relation to impaired endothelium-dependent dilation and upregulation of nuclear factor-kappaB. Circ Res 100:1659–1666
Mattagajasingh I, Kim CS, Naqvi A, Yamamori T, Hoffman TA, Jung SB et al (2007) SIRT1 promotes endothelium-dependent vascular relaxation by activating endothelial nitric oxide synthase. Proc Natl Acad Sci U S A 104:14855–14860
Zhang QJ, Wang Z, Chen HZ, Zhou S, Zheng W, Liu G et al (2008) Endothelium-specific overexpression of class III deacetylase SIRT1 decreases atherosclerosis in apolipoprotein E-deficient mice. Cardiovasc Res 80:191–199
Mattson MP, Wan R (2005) Beneficial effects of intermittent fasting and caloric restriction on the cardiovascular and cerebrovascular systems. J Nutr Biochem 16:129–137
Mager DE, Wan R, Brown M, Cheng A, Wareski P, Abernethy DR et al (2006) Caloric restriction and intermittent fasting alter spectral measures of heart rate and blood pressure variability in rats. FASEB J 20:631–637
Heilbronn LK, de Jonge L, Frisard MI, DeLany JP, Larson-Meyer DE, Rood J et al (2006) Effect of 6-month calorie restriction on biomarkers of longevity, metabolic adaptation, and oxidative stress in overweight individuals: a randomized controlled trial. JAMA 295:1539–1548
Csiszar A, Labinskyy N, Jimenez R, Pinto JT, Ballabh P, Losonczy G et al (2009) Anti-oxidative and anti-inflammatory vasoprotective effects of caloric restriction in aging: role of circulating factors and SIRT1. Mech Ageing Dev 130:518–527
Fontana L, Meyer TE, Klein S, Holloszy JO (2004) Long-term calorie restriction is highly effective in reducing the risk for atherosclerosis in humans. Proc Natl Acad Sci U S A 101:6659–6663
Pearson KJ, Lewis KN, Price NL, Chang JW, Perez E, Cascajo MV et al (2008) Nrf2 mediates cancer protection but not prolongevity induced by caloric restriction. Proc Natl Acad Sci U S A 105:2325–2330
Varady KA, Bhutani S, Klempel MC, Kroeger CM, Trepanowski JF, Haus JM et al (2013) Alternate day fasting for weight loss in normal weight and overweight subjects: a randomized controlled trial. Nutr J 12:146
Taffet GE, Pham TT, Hartley CJ (1997) The age-associated alterations in late diastolic function in mice are improved by caloric restriction. J Gerontol A Biol Sci Med Sci 52:B285–B290
Shinmura K, Tamaki K, Sano M, Murata M, Yamakawa H, Ishida H et al (2011) Impact of long-term caloric restriction on cardiac senescence: caloric restriction ameliorates cardiac diastolic dysfunction associated with aging. J Mol Cell Cardiol 50:117–127
Dhahbi JM, Tsuchiya T, Kim HJ, Mote PL, Spindler SR (2006) Gene expression and physiologic responses of the heart to the initiation and withdrawal of caloric restriction. J Gerontol A Biol Sci Med Sci 61:218–231
Seymour EM, Parikh RV, Singer AA, Bolling SF (2006) Moderate calorie restriction improves cardiac remodeling and diastolic dysfunction in the Dahl-SS rat. J Mol Cell Cardiol 41:661–668
Ahmet I, Tae HJ, de Cabo R, Lakatta EG, Talan MI (2011) Effects of calorie restriction on cardioprotection and cardiovascular health. J Mol Cell Cardiol 51:263–271
Yan L, Gao S, Ho D, Park M, Ge H, Wang C et al (2013) Calorie restriction can reverse, as well as prevent, aging cardiomyopathy. Age (Dordr) 35:2177–2182
Dai DF, Karunadharma PP, Chiao YA, Basisty N, Crispin D, Hsieh EJ et al (2014) Altered proteome turnover and remodeling by short-term caloric restriction or rapamycin rejuvenate the aging heart. Aging Cell 13:529–539
Castello L, Froio T, Maina M, Cavallini G, Biasi F, Leonarduzzi G et al (2010) 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 48:47–54
Castello L, Maina M, Testa G, Cavallini G, Biasi F, Donati A et al (2011) Alternate-day fasting reverses the age-associated hypertrophy phenotype in rat heart by influencing the ERK and PI3K signaling pathways. Mech Ageing Dev 132:305–314
Ahmet I, Wan R, Mattson MP, Lakatta EG, Talan MI (2010) Chronic alternate-day fasting results in reduced diastolic compliance and diminished systolic reserve in rats. J Card Fail 16:843–853
Meyer TE, Kovács SJ, Ehsani AA, Klein S, Holloszy JO, Fontana L (2006) Long-term caloric restriction ameliorates the decline in diastolic function in humans. J Am Coll Cardiol 47:398–402
Abete P, Testa G, Ferrara N, De Santis D, Capaccio P, Viati L et al (2002) Cardioprotective effect of ischemic preconditioning is preserved in food-restricted senescent rats. Am J Physiol Heart Circ Physiol 282:H1978–H1987
Broderick TL, Driedzic WR, Gillis M, Jacob J, Belke T (2001) Effects of chronic food restriction and exercise training on the recovery of cardiac function following ischemia. J Gerontol A Biol Sci Med Sci 56:B33–B37
Chandrasekar B, Nelson JF, Colston JT, Freeman GL (2001) Calorie restriction attenuates inflammatory responses to myocardial ischemia-reperfusion injury. Am J Physiol Heart Circ Physiol 280:H2094–H2102
Edwards AG, Donato AJ, Lesniewski LA, Gioscia RA, Seals DR, Moore RL (2010) Life-long caloric restriction elicits pronounced protection of the aged myocardium: a role for AMPK. Mech Ageing Dev 131:739–742
Long P, Nguyen Q, Thurow C, Broderick TL (2002) Caloric restriction restores the cardioprotective effect of preconditioning in the rat heart. Mech Ageing Dev 123:1411–1413
Peart JN, See Hoe L, Pepe S, Johnson P, Headrick JP (2012) Opposing effects of age and calorie restriction on molecular determinants of myocardial ischemic tolerance. Rejuvenation Res 15:59–70
Shinmura K, Tamaki K, Bolli R (2005) Short-term caloric restriction improves ischemic tolerance independent of opening of ATP-sensitive K+ channels in both young and aged hearts. J Mol Cell Cardiol 39:285–296
Shinmura K, Tamaki K, Bolli R (2008) Impact of 6-mo caloric restriction on myocardial ischemic tolerance: possible involvement of nitric oxide-dependent increase in nuclear Sirt1. Am J Physiol Heart Circ Physiol 295:H2348–H2355
Shinmura K, Tamaki K, Saito K, Nakano Y, Tobe T, Bolli R (2007) Cardioprotective effects of short-term caloric restriction are mediated by adiponectin via activation of AMP-activated protein kinase. Circulation 116:2809–2817
Sung MM, Soltys CL, Masson G, Boisvenue JJ, Dyck JR (2011) Improved cardiac metabolism and activation of the RISK pathway contributes to improved post-ischemic recovery in calorie restricted mice. J Mol Med (Berl) 89:291–302
Ahmet I, Wan R, Mattson MP, Lakatta EG, Talan M (2005) Cardioprotection by intermittent fasting in rats. Circulation 112:3115–3121
Katare RG, Kakinuma Y, Arikawa M, Yamasaki F, Sato T (2009) Chronic intermittent fasting improves the survival following large myocardial ischemia by activation of BDNF/VEGF/PI3K signaling pathway. J Mol Cell Cardiol 46:405–412
Sloan C, Tuinei J, Nemetz K, Frandsen J, Soto J, Wride N et al (2011) Central leptin signaling is required to normalize myocardial fatty acid oxidation rates in caloric-restricted ob/ob mice. Diabetes 60:1424–1434
AlGhatrif M, Watts VL, Niu X, Halushka M, Miller KL, Vandegaer K et al (2013) Beneficial cardiac effects of caloric restriction are lost with age in a murine model of obesity. J Cardiovasc Transl Res 6:436–445
van der Meer RW, Rijzewijk LJ, Diamant M, Hammer S, Schär M, Bax JJ et al (2008) The ageing male heart: myocardial triglyceride content as independent predictor of diastolic function. Eur Heart J 29:1516–1522
Stein PK, Soare A, Meyer TE, Cangemi R, Holloszy JO, Fontana L (2012) Caloric restriction may reverse age-related autonomic decline in humans. Aging Cell 11:644–650
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Abiri, B., Vafa, M. (2019). Dietary Restriction, Cardiovascular Aging and Age-Related Cardiovascular Diseases: A Review of the Evidence. In: Guest, P. (eds) Reviews on Biomarker Studies in Aging and Anti-Aging Research. Advances in Experimental Medicine and Biology(), vol 1178. Springer, Cham. https://doi.org/10.1007/978-3-030-25650-0_7
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DOI: https://doi.org/10.1007/978-3-030-25650-0_7
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