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Mapping NAD+ metabolism in the brain of ageing Wistar rats: potential targets for influencing brain senescence

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Abstract

Over the last decade, the importance of NAD+ has expanded beyond its role as an essential cofactor for energy metabolism. NAD+ has emerged as a major signalling molecule that serves as the sole substrate for several enzymatic reactions including the DNA repair enzyme, poly(ADP-ribose) polymerase (PARP), NAD-dependent protein deacetylases or CD38, and transcriptional factors by a new class of histone deacetylases known as sirtuins. NAD+ levels are regulated by the metabolic status and cellular stress caused by oxidative stress and DNA damage. Since a detailed study of NAD+ metabolism in the healthy ageing mammalian brain is nascent, we examined the effect of ageing on intracellular NAD+ metabolism in different brain regions in female Wistar rats in young (3 months), middle aged (12 months) and older adults (24 months). Our results are the first to show a significant decline in intracellular NAD+ levels and NAD:NADH ratio with ageing in the CNS, occurring in parallel to an increase in lipid peroxidation and protein oxidation (o- and m-tyrosine) and a decline in total antioxidant capacity. Hyperphosphorylation of H2AX levels was also observed together with increased PARP-1 and PARP-2 expression, and CD38 activity, concomitantly with reduced NAD+ and ATP levels and SIRT1 function in the cortex, brainstem, hippocampus and cerebellum. Reduced activity of mitochondrial complex I–IV and impaired maximum mitochondrial respiration rate were also observed in the ageing rat brain. Among the multiple physiological pathways associated with NAD+ catabolism, our discovery of CD38 as the major regulator of cellular NAD+ levels in rat neurons indicates that CD38 is a promising therapeutic target for the treatment of age-related neurodegenerative diseases.

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References

  • Aarhus R, Graeff RM, Dickey DM, Walseth TF, Lee HC (1995) ADP-ribosyl cyclase and CD38 catalyse the synthesis of a calcium-mobilizing metabolite from NADP. J Biol Chem 270(51):30327–30333

    Article  CAS  PubMed  Google Scholar 

  • Ahmed I, John A, Vijayasarathy C, Robin M, Raza H (2002) Differential modulation of growth and glutathione metabolism in cultured rat astrocytes by 4-hydroxynonenal and green tea polyphenol, epigallocatechin-3-gallate. Neurotoxicology 23:289–300

    Article  CAS  PubMed  Google Scholar 

  • Aksoy P, Escande C, White TA, Thompson M, Soares S, Benech JC, Chini EN (2006a) Regulation of SIRT 1 mediated NAD dependent deacetylation: a novel role for the multifunctional enzyme CD38. Biochem Biophys Res Commun 349(1):353–359

    Article  CAS  PubMed  Google Scholar 

  • Aksoy P, White TA, Thompson M, Chini EN (2006b) Regulation of intracellular levels of NAD: a novel role for CD38. Biochem Biophys Res Commun 345(4):1386–1392

    Article  CAS  PubMed  Google Scholar 

  • Akther S, Korshnova N, Zhong J, Liang M, Cherepanov SM, Lopatina O, Komleva YK, Salmina AB, Nishimura T, Fakhrul AA, Hirai H, Kato I, Yamamoto Y, Takasawa S, Okamoto H, Higashida H (2013) CD38 in the nucleus accumbens and oxytocin are related to paternal behavior in mice. Mol Brain 6(1):41

    Article  PubMed Central  PubMed  Google Scholar 

  • Alvarez-Gonzalez R, Zentgraf H, Frey M, Hilda M-A (2006) Functional interactions of PARP-1 with p53. Poly(ADP-ribosyl)ation. Springer, New York, pp 61–66

    Chapter  Google Scholar 

  • Anderson G, Maes M (2013) Neurodegeneration in Parkinson’s disease: interactions of oxidative stress, tryptophan catabolites and depression with mitochondria and sirtuins. Mol Neurobiol. doi:10.1007/s12035-013-8554-z

    Google Scholar 

  • Ashok BT, Ali R (1999) The aging paradox: free radical theory of aging. Exp Gerontol 34(3):293–303

    Article  CAS  PubMed  Google Scholar 

  • Bagul PK, Banerjee SK (2013) Insulin resistance, oxidative stress and cardiovascular complications: role of sirtuins. Curr Pharm Des 19(32):5663–5677

    Article  CAS  PubMed  Google Scholar 

  • Bai P, Canto C (2012) The role of PARP-1 and PARP-2 enzymes in metabolic regulation and disease. Cell Metab 16(3):290–295

    CAS  PubMed  Google Scholar 

  • Balaban RS, Nemoto S, Finkel T (2005) Mitochondria, oxidants, and aging. Cell 120(4):483–495

    Article  CAS  PubMed  Google Scholar 

  • Ban TA (1975) Nicotinic acid in the treatment of schizophrenias. Practical and theoretical considerations. Neuropsychobiology 1(3):133–145

    Article  CAS  PubMed  Google Scholar 

  • Banerjee S, Walseth TF, Borgmann K, Wu L, Bidasee KR, Kannan MS, Ghorpade A (2008) CD38/cyclic ADP-ribose regulates astrocyte calcium signalling: implications for neuroinflammation and HIV-1-associated dementia. J Neuroimmune Pharmacol 3(3):154–164

    Article  PubMed  Google Scholar 

  • Beach TG, Adler C, Sue L, Vedders L, Lue L, White L (2010) Multi-organ distribution of phosphorylated alpha-synuclein histopathology in subjects with Lewy body disorders. Acta Neuropathol 119:689–702

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Berger F, Lau C, Ziegler M (2007) Regulation of poly(ADP-ribose) polymerase 1 activity by the phosphorylation state of the nuclear NAD biosynthetic enzyme NMN adenylyl transferase 1. Proc Natl Acad Sci USA 104(10):3765–3770

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Bernofsky C, Swan M (1973) An improved cycling assay for nicotinamide adenine dinucleotide. Anal Biochem 53:452–458

    Article  CAS  PubMed  Google Scholar 

  • Betarbet R, Sherer T, MacKenzie G, Garcia-Osuna M, Panov A, Greenamyre J (2000) Chronic systemic pesticide exposure reproduces features of Parkinson’s disease. Nat Neurosci 3:1301–1306

    Article  CAS  PubMed  Google Scholar 

  • Blalock EM, Grondin R, Chen KC, Thibault O, Thibault V, Pandya JD, Dowling A, Zhang Z, Sullivan P, Porter NM, Landfield PW (2010) Aging-related gene expression in hippocampus proper compared with dentate gyrus is selectively associated with metabolic syndrome variables in rhesus monkeys. J Neurosci 30(17):6058–6071

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Blalock EM, Buechel HM, Popovic J, Geddes JW, Landfield PW (2011) Microarray analyses of laser-captured hippocampus reveal distinct gray and white matter signatures associated with incipient Alzheimer’s disease. J Chem Neuroanat 42(2):118–126

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Blankfield A (2013) Kynurenine pathway pathologies: do nicotinamide and other pathway co-factors have a therapeutic role in reduction of symptom severity, including chronic fatigue syndrome (CFS) and fibromyalgia (FM). Int J Tryptophan Res 6(Suppl 1):39–45

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Bohr V (2002) Oxidative DNA damage and repair. Free Radic Biol Med 32(9):804–812

    Article  CAS  PubMed  Google Scholar 

  • Bouchard V, Rouleau M, Poirier GG (2003) PARP-1, a determinant of cell survival in response to DNA damage. Exp Hematol 31:446–454

    Article  CAS  PubMed  Google Scholar 

  • Bradford MM (1976) A rapid and sensitive method for quantitation of microgram quantities of protein utilising the principle of protein-dye binding. Anal Biochem 53:452–458

    Google Scholar 

  • Braidy N, Guillemin G, Grant R (2008) Promotion of cellular NAD(+) anabolism: therapeutic potential for oxidative stress in ageing and Alzheimer’s disease. Neurotox Res 13(3–4):173–184

    Article  CAS  PubMed  Google Scholar 

  • Braidy N, Guillemin GMH, Chan-Ling T, Poljak A, Grant R (2011) Age related changes in NAD+ metabolism, oxidative stress and Sirt1 activity in wistar rats. PLOS One 6(4):e19194

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Braidy N, Jayasena T, Poljak A, Sachdev PS (2012) Sirtuins in cognitive ageing and Alzheimer’s disease. Curr Opin Psychiatry 25(3):226–230

    Article  PubMed  Google Scholar 

  • Brunetti E, Malavasi F (2012) CD38 and behavior: moving from correlation to causality? Biol Psychiatry 72(3):168–170

    Article  PubMed  Google Scholar 

  • Burkle A (2005) Poly(ADP-ribose). The most elaborate metabolite of NAD+. FEBS J 272(18):4576–4589

    Article  PubMed  Google Scholar 

  • Burkle A, Beneke S, Muiras ML (2004) Poly(ADP-ribosyl)ation and aging. Exp Gerontol 39(11–12):1599–1601

    Article  PubMed  Google Scholar 

  • Butterfield DA (2002) Amyloid beta-peptide (1-42)-induced oxidative stress and neurotoxicity: implications for neurodegeneration in Alzheimer’s disease brain. A review. Free Radic Res 36(12):1307–1313

    Article  CAS  PubMed  Google Scholar 

  • Butterfield DA, Draker J, Pocernich C, Categna A (2001) Evidence of oxidative damage in the Alzheimer’s Disease brain:central role of Amyloid β-peptide. Trends Mol Med 7:548–554

    Article  CAS  PubMed  Google Scholar 

  • Canevari L, Clark J, Bates T (1999) β-Amyloid fragment 25–35 selectively decreases complex IV activity in isolated mitochondria. FEBS Lett 457:131–134

    Article  CAS  PubMed  Google Scholar 

  • Chen Q, Fischer A, Reagan J, Yan L, Ames B (1995) Oxidative DNA damage and senescence of human diploid fibroblast cells. Proc Natl Acad Sci USA 92(10):4337–4341

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Chen KC, Blalock EM, Curran-Rauhut MA, Kadish I, Blalock SJ, Brewer L, Porter NM, Landfield PW (2013) Glucocorticoid-dependent hippocampal transcriptome in male rats: pathway-specific alterations with aging. Endocrinology 154(8):2807–2820

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Chidambaram N, Chang CF (1999) NADP+-dependent internalization of recombinant CD38 in CHO cells. Arch Biochem Biophys 363(2):267–272

    Article  CAS  PubMed  Google Scholar 

  • Collier TJ, Coleman PD (1991) Divergence of biological and chronological aging: evidence from rodent studies. Neurobiol Aging 12:685–693

    Article  CAS  PubMed  Google Scholar 

  • Craft S, Foster TC, Landfield PW, Maier SF, Resnick SM, Yaffe K (2012) Session III: mechanisms of age-related cognitive change and targets for intervention: inflammatory, oxidative, and metabolic processes. J Gerontol A 67(7):754–759

    Article  Google Scholar 

  • Davies S, Poljak A, Duncan M, Smythe G, Murphy M (2001) Measurements of protein carbonyls, ortho- and meta-tyrosine and oxidative phosphorylation complex activity in mitochondria from young and old rats. Free Radic Biol Med 31:181–190

    Article  CAS  PubMed  Google Scholar 

  • de Marcia G (1994) Poly(ADP-ribose) polymerase: a molecular nick sensor. Trends Biochem Sci 19:172–176

    Article  Google Scholar 

  • Erdelyi K, Bakondi E, Gergely P, Szabo C, Virag L (2005) Pathophysiologic role of oxidative stress-induced poly(ADP-ribose) polymerase-1 activation: focus on cell death and transcriptional regulation. Cell Mol Life Sci 62(7–8):751–759

    Article  CAS  PubMed  Google Scholar 

  • Escande C, Nin V, Price NL, Capellini V, Gomes AP, Barbosa MT, O’Neil L, White TA, Sinclair DA, Chini EN (2013) Flavonoid apigenin is an inhibitor of the NAD+ ase CD38: implications for cellular NAD+ metabolism, protein acetylation, and treatment of metabolic syndrome. Diabetes 62(4):1084–1093

    Article  CAS  PubMed  Google Scholar 

  • Farres J, Martin-Caballero J, Martinez C, Lozano JJ, Llacuna L, Ampurdanes C, Ruiz-Herguido C, Dantzer F, Schreiber V, Villunger A, Bigas A, Yelamos J (2013) Parp-2 is required to maintain hematopoiesis following sublethal gamma-irradiation in mice. Blood 122(1):44–54

    Article  CAS  PubMed  Google Scholar 

  • Finkel T (2005) Opinion: radical medicine: treating ageing to cure disease. Nat Rev Mol Cell Biol 6:971–976

    Article  CAS  PubMed  Google Scholar 

  • Floyd RA, Hensley K (2002) Oxidative stress in brain aging: implications for therapeutics of neurodegenerative diseases. Neurobiol Aging 23:795–807

    Article  CAS  PubMed  Google Scholar 

  • Grant RS, Kapoor V (1998) Murine glial cells regenerate NAD, after peroxide-induced depletion, using either nicotinic acid, nicotinamide, or quinolinic acid as substrates. J Neurochem 70:1759–1763

    Article  CAS  PubMed  Google Scholar 

  • Hara-Yokoyama M, Kukimoto I, Nishima H, Kontani K, Hirabayashi Y, Irie F, Sugiya H, Furuyama S, Katada T (1996) Inhibition of NAD+ glyohydrolase and ADP-ribosyl cyclase activities of leukocyte cell surface antigen CD38 by gangliosides. J Biol Chem 271:12951–12955

    Article  CAS  PubMed  Google Scholar 

  • Harman D (1956) Aging: a theory based on free radical and radiation chemistry. J Gerontol 11(3):298–300

    Article  CAS  PubMed  Google Scholar 

  • Harman D (2003) The free radical theory of aging. Antioxid Redox Signal 5(5):557–561

    Article  CAS  PubMed  Google Scholar 

  • Harper ME, Monemdjou S, Ramsey JJ, Weindruch R (1998) Age-related increase in mitochondrial proton leak and decrease in ATP turnover reactions in mouse hepatocytes. Am J Physiol 275:197–206

    Google Scholar 

  • Huang X, Tanaka T, Kurose A, Traganos F, Darzynkiewicz Z (2006) Constitutive histone H2AX phosphorylation on Ser-139 in cells untreated by genotoxic agents is cell-cycle phase specific and attenuated by scavenging reactive oxygen species. Int J Oncol 29:495–501

    CAS  PubMed  Google Scholar 

  • Infante J, Llorca J, Mateo I, Rodriguez-Rodriguez E, Sanchez-Quintana C, Sanchez-Juan P, Fernandez-Viadero C, Pena N, Berciano J, Combarros O (2007) Interaction between poly(ADP-ribose) polymerase 1 and interleukin 1A genes is associated with Alzheimer’s disease risk. Dement Geriatr Cogn Disord 23(4):215–218

    Article  CAS  PubMed  Google Scholar 

  • Kamata H, Hirata H (1999) Redox regulation of cellular signalling. Cell Signal 11(1):1–14

    Article  CAS  PubMed  Google Scholar 

  • Keller JN, Mattson MP (1998) Roles of lipid peroxidation in modulation of cellular signalling pathways, cell dysfunction, and death in the nervous system. Rev Neurosci 9(2):105–116

    Article  CAS  PubMed  Google Scholar 

  • Khan JA, Forouhar F, Tao X, Tong L (2007) Nicotinamide adenine dinucleotide metabolism as an attractive target for drug discovery. Expert Opin Ther Targets 11(5):695–705

    Article  CAS  PubMed  Google Scholar 

  • Kim MY, Zhang T, Kraus WL (2005) Poly(ADP-ribosyl)ation by PARP-1: ‘PAR-laying’ NAD+ into a nuclear signal. Genes Dev 19(17):1951–1967

    Article  CAS  PubMed  Google Scholar 

  • Kraus WL, Hottiger MO (2013) PARP-1 and gene regulation: progress and puzzles. Mol Aspects Med 34(6):1109–1123

    Article  CAS  PubMed  Google Scholar 

  • Kruman I, Bruce-Keller A, Bredesen D, Waeg G, Mattson M (1997) Evidence that 4-hydroxynonenal mediates oxidative stress-induced neuronal apoptosis. J Neurosci 17:5089–5100

    CAS  PubMed  Google Scholar 

  • Kutuzov MM, Khodyreva SN, Ame JC, Ilina ES, Sukhanova MV, Schreiber V, Lavrik OI (2013) Interaction of PARP-2 with DNA structures mimicking DNA repair intermediates and consequences on activity of base excision repair proteins. Biochimie 95(6):1208–1215

    Article  CAS  PubMed  Google Scholar 

  • Landfield PW, Blalock EM, Chen KC, Porter NM (2007) A new glucocorticoid hypothesis of brain aging: implications for Alzheimer’s disease. Curr Alzheimer Res 4(2):205–212

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Latimer CS, Searcy JL, Bridges MT, Brewer LD, Popovic J, Blalock EM, Landfield PW, Thibault O, Porter NM (2011) Reversal of glial and neurovascular markers of unhealthy brain aging by exercise in middle-aged female mice. PLoS One 6(10):e26812

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Li J, Holbrook NJ (2003) Common mechanisms for declines in oxidative stress tolerance and proliferation with aging. Free Radic Biol Med 35(3):292–299

    Article  CAS  PubMed  Google Scholar 

  • Lopatina O, Inzhutova A, Salmina AB, Higashida H (2012) The roles of oxytocin and CD38 in social or parental behaviors. Front Neurosci 6:182

    PubMed Central  PubMed  Google Scholar 

  • Love S, Barber R, Wilcock GK (1999) Increased poly(ADP-ribosyl)ation of nuclear proteins in Azheimer’s Disease. Brain 122:247–253

    Article  PubMed  Google Scholar 

  • Maldonado PD, Chanez-Cardenas ME, Barrera D, Villeda-Hernandez J, Santamaria A, Pedraza-Chaverri J (2007) Poly(ADP-ribose) polymerase-1 is involved in the neuronal death induced by quinolinic acid in rats. Neurosci Lett 425(1):28–33

    Article  CAS  PubMed  Google Scholar 

  • Massudi H, Grant R, Guillemin GJ, Braidy N (2012) NAD+ metabolism and oxidative stress: the golden nucleotide on a crown of thorns. Redox Rep 17(1):28–46

    Article  CAS  PubMed  Google Scholar 

  • Mattson MP (2004) Pathway towards and away from Azheimer’s Disease. Nature 430:630–639

    Article  Google Scholar 

  • Merksamer PI, Liu Y, He W, Hirschey MD, Chen D, Verdin E (2013) The sirtuins, oxidative stress and aging: an emerging link. Aging (Albany NY) 5(3):144–150

    CAS  Google Scholar 

  • Miranda S, Opazo C, Larrondo LF, Munoz FJ, Ruiz F, Leighton F, Inestrosa NC (2000) The role of oxidative stress in the toxicity induced by amyloid beta-peptide in Alzheimer’s disease. Prog Neurobiol 62(6):633–648

    Article  CAS  PubMed  Google Scholar 

  • Moss NG, Vogel PA, Kopple TE, Arendshorst WJ (2013) Thromboxane-induced renal vasoconstriction is mediated by the ADP-ribosyl cyclase CD38 and superoxide anion. Am J Physiol Renal Physiol 305(6):830–838

    Article  Google Scholar 

  • Mutisya E, Bowling A, Beal M (2002) Cortical cytochrome oxidase activity is reduced in Alzheimer’s disease. J Neurochem 63(6):2179–2184

    Article  Google Scholar 

  • Nadal-Serrano M, Pons DG, Sastre-Serra J, Blanquer-Rossello Mdel M, Roca P, Oliver J (2013) Genistein modulates oxidative stress in breast cancer cell lines according to ERalpha/ERbeta ratio: effects on mitochondrial functionality, sirtuins, uncoupling protein 2 and antioxidant enzymes. Int J Biochem Cell Biol 45(9):2045–2051

    Article  CAS  PubMed  Google Scholar 

  • Nakae D, Akai H, Kishida H, Kusuoka O, Tsutsumi M, Konishi Y (2000) Age and organ dependent spontaneous generation of nuclear 8-hydroxyguanosine in male Fischer 344 rats. Lab Invest 80(2):249–261

    Article  CAS  PubMed  Google Scholar 

  • Nipp RD, Volkheimer AD, Davis ED, Chen Y, Weinberg JB, Friedman DR (2013) CD38 variation as a prognostic factor in chronic lymphocytic leukemia. Leuk Lymphoma. doi:10.3109/10428194.2013.786070

    PubMed  Google Scholar 

  • Poljak A, Pamphlett R, Gurney M, Duncan M (2000) Measurement of o- and m-tyrosine as markers of oxidative damage in motor neuron disease. Redox Rep 5:137–140

    Article  CAS  PubMed  Google Scholar 

  • Poljak A, Dawes I, Ingelse B, Duncan M, Smythe G, Grant C (2003) Oxidative damage to proteins in yeast cells exposed to adaptive levels of H(2)O(2). Redox Rep 8:371–377

    Article  CAS  PubMed  Google Scholar 

  • Quarona V, Zaccarello G, Chillemi A, Brunetti E, Singh VK, Ferrero E, Funaro A, Horenstein AL, Malavasi F (2013) CD38 and CD157: a long journey from activation markers to multifunctional molecules. Cytometry B Clin Cytom 84(4):207–217

    Article  PubMed  Google Scholar 

  • Rebrin I, Sohal R (2004) Comparison of thiol redox state of mitochondria and homogenates of various tissues between two strains of mice with different longevities. Exp Gerontol 39:1513–1519

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Retz W, Gsell W, Munch L, Riedier P (1998) Free radicals in Alzheimer’s disease. J Neurol Transm Suppl 54:221–236

    Article  CAS  Google Scholar 

  • Romero FJ, Bosch-Morell F, Romero MJ, Jareno EJ, Romero B, Marin N, Roma J (1998) Lipid peroxidation products and antioxidants in human disease. Environ Health Perspect 106(Suppl 5):1229–1234

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Rudin DO (1981) The major psychoses and neuroses as omega-3 essential fatty acid deficiency syndrome: substrate pellagra. Biol Psychiatry 16(9):837–850

    CAS  PubMed  Google Scholar 

  • Sauve AA, Wolberger C, Schramm VL, Boeke JD (2006) The biochemistry of sirtuins. Annu Rev Biochem 75:435–465

    Article  CAS  PubMed  Google Scholar 

  • Savaskan D, Yurtseven N, Tuygun AK, Aksoy P, Canik S (2006) The effects of insulin given prior to release of cross-clamp on coronary sinus lactate levels in coronary artery surgery. Anadolu Kardiyol Derg 6(3):248–252

    PubMed  Google Scholar 

  • Schapira A, Cooper J, Dexter D, Jenner P, Marsden C (1989) Mitochondrial complex I deficiency in Parkinson’s disease. Lancet 1:1269

    Article  CAS  PubMed  Google Scholar 

  • Schreiber V, Dantzer F, Ame JC, de Murcia G (2006) Poly(ADP-ribose): novel functions for an old molecule. Nat Rev Mol Cell Biol 7(7):517–528

    Article  CAS  PubMed  Google Scholar 

  • Shinmura K (2013) Effects of caloric restriction on cardiac oxidative stress and mitochondrial bioenergetics: potential role of cardiac sirtuins. Oxid Med Cell Longev 2013:528935

    Article  PubMed Central  PubMed  Google Scholar 

  • Sieck G, White T, Thompson M, Pabelick C, Wylam M, Prakash Y (2008) Regulation of store-operated Ca2+ entry by CD38 in human airway smooth muscle. AJP-Lung Cell Mol Physiol 294:L378–L385

    Article  CAS  Google Scholar 

  • Smyth LM, Breen LT, Yamboliev IA, Mutafova-Yambolieva VN (2006) Novel localization of CD38 in perivascular sympathetic nerve terminals. Neuroscience 139(4):1467–1477

    Article  CAS  PubMed  Google Scholar 

  • Sobko EA, Kraposhina A, Demko IV, Salmina AB (2013) CD38/ADP-ribosyl cyclase, a marker of endothelial dysfunction in bronchial asthma. Klin Med (Mosk) 91(2):34–38

    CAS  Google Scholar 

  • Thibault O, Anderson KL, Demoll C, Brewer LD, Landfield PW, Porter NM (2013) Hippocampal calcium dysregulation at the nexus of diabetes and brain aging. Eur J Pharmacol 719(1–3):34–43

    Article  CAS  PubMed  Google Scholar 

  • Torti M, Bertoni A, Canobbio I, Sinigaglia F, Balduini C (1999) Hydrolysis of NADP+ by platelet CD38 in the absence of synthesis and degradation of cyclic ADP-ribose 2′-phosphate. FEBS Lett 455(3):359–363

    Article  CAS  PubMed  Google Scholar 

  • Virag L, Salzman AL, Szabo C (1998) Poly(ADP-ribose) synthetase activation mediates mitochondrial injury during oxidant-induced cell death. J Immunol 161:3753–3759

    CAS  PubMed  Google Scholar 

  • Weidele K, Kunzmann A, Schmitz M, Beneke S, Burkle A (2010) Ex vivo supplementation with nicotinic acid enhances cellular poly(ADP-ribosyl)ation and improves cell viability in human peripheral blood mononuclear cells. Biochem Pharmacol 80(7):1103–1112

    Article  CAS  PubMed  Google Scholar 

  • Wu M, Neilson A, Swift A, Moran R, Tamagnine J, Parslow D, Armistead S, Lemire K, Orrell J, Teich J, Chomicz S, Ferrick D (2007) Multiparameter metabolic analysis reveals a close link between attenuated mitochondrial bioenergetic function and enhances glycolysis dependency in human tumor cells. Am J Physiol Cell Physiol 292:C125–C136

    Article  CAS  PubMed  Google Scholar 

  • Xiong J, Xia M, Yi F, Abais JM, Li N, Boini KM, Li PL (2013) Regulation of renin release via cyclic ADP-ribose-mediated signalling: evidence from mice lacking CD38 gene. Cell Physiol Biochem 31(1):44–55

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Xu M, Li XX, Ritter JK, Abais JM, Zhang Y, Li PL (2013) Contribution of NADPH oxidase to membrane CD38 internalization and activation in coronary arterial myocytes. PLoS One 8(8):e71212

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Zarkovic K (2003) 4-Hydroxynonenal and neurodegenerative diseases. Mol Aspects Med 24(4–5):293–303

    Article  CAS  PubMed  Google Scholar 

  • Zhang J (2003) Are poly(ADP-ribosyl)ation by PARP-1 and deacetylation by Sir2 linked? Bioessays 25(8):808–814

    Article  CAS  PubMed  Google Scholar 

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Acknowledgments

This work was supported by a National Health & Medical Research Council of Australia Capacity Building Grant and a UNSW Faculty of Medicine Research Grant. NB is the recipient of an Alzheimer’s Australia Viertel Foundation Postdoctoral Research Fellowship at the University of New South Wales. TJ is a recipient of the University of New South Wales Postgraduate Award (UPA). The authors thank the Rebecca Cooper Medical Research Foundation for their ongoing financial support and staff of the Bioanalytical Mass Spectrometry Facility at the University of New South Wales for assistance with GC–MS experiments.

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Correspondence to Perminder Sachdev.

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Braidy, N., Poljak, A., Grant, R. et al. Mapping NAD+ metabolism in the brain of ageing Wistar rats: potential targets for influencing brain senescence. Biogerontology 15, 177–198 (2014). https://doi.org/10.1007/s10522-013-9489-5

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