Hydrogen sulfide mediates the protection of dietary restriction against renal senescence in aged F344 rats

Scientific Reports

Volumn 6, Issue , 2016, Pages

  Wang, Wen Juan ^a,b   Cai, Guang Yan ^a   Ning, Yi Chun ^a,b   Cui, Jing ^a   Hong, Quan ^a   Bai, Xue Yuan ^a   Xu, Xiao Meng ^a,b   Bu, Ru ^a   Sun, Xue Feng ^a   Chen, Xiang Mei ^a  

^a CHINESE PLA GENERAL HOSPITAL   (China)

^b NANKAI UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CYSTATHIONINE BETA SYNTHASE; CYSTATHIONINE GAMMA LYASE; GLUTATHIONE; HYDROGEN SULFIDE;

AGING; ANIMAL; CALORIC RESTRICTION; CELL AGING; KIDNEY; LONGEVITY; METABOLISM; MITOCHONDRION; OXIDATIVE STRESS; PATHOLOGY; PATHOPHYSIOLOGY; PHYSIOLOGY; RAT;

AGING; ANIMALS; CALORIC RESTRICTION; CELLULAR SENESCENCE; CYSTATHIONINE BETA-SYNTHASE; CYSTATHIONINE GAMMA-LYASE; GLUTATHIONE; HYDROGEN SULFIDE; KIDNEY; LONGEVITY; MITOCHONDRIA; OXIDATIVE STRESS; RATS;

EID: 84979643003     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/srep30292     Document Type: Article

References (50)

1. Zhou, X. J. et al. The aging kidney. Kidney international 74, 710-720, doi: 10.1038/ki.2008.319 (2008).
2. Musso, C. G., Oreopoulos, D. G. Aging and physiological changes of the kidneys including changes in glomerular filtration rate. Nephron. Physiology 119 Suppl 1, p1-5, doi: 10.1159/000328010 (2011).
3. Chung, H. Y. et al. Molecular inflammation: underpinnings of aging and age-related diseases. Ageing research reviews 8, 18-30, doi: 10.1016/j.arr.2008.07.002 (2009).
4. Harman, D. Aging: a theory based on free radical and radiation chemistry. Journal of gerontology 11, 298-300 (1956).
5. Sohal, R. S., Allen, R. G. Oxidative stress as a causal factor in differentiation and aging: a unifying hypothesis. Experimental gerontology 25, 499-522 (1990).
6. Harman, D. The aging process. Proceedings of the National Academy of Sciences of the United States of America 78, 7124-7128 (1981).
7. Liu, J. et al. Immobilization stress causes oxidative damage to lipid, protein, DNA in the brain of rats. FASEB journal: official publication of the Federation of American Societies for Experimental Biology 10, 1532-1538 (1996).
8. Bedard, K., Krause, K. H. The NOX family of ROS-generating NADPH oxidases: physiology and pathophysiology. Physiological reviews 87, 245-313, doi: 10.1152/physrev.00044.2005 (2007).
9. Qin, L., Liu, Y., Hong, J. S., Crews, F. T. NADPH oxidase and aging drive microglial activation, oxidative stress, dopaminergic neurodegeneration following systemic LPS administration. Glia 61, 855-868, doi: 10.1002/glia.22479 (2013).
10. Hao, C. M., Haase, V. H. Sirtuins and their relevance to the kidney. Journal of the American Society of Nephrology: JASN 21, 1620-1627, doi: 10.1681/asn.2010010046 (2010).
11. Kume, S. et al. Calorie restriction enhances cell adaptation to hypoxia through Sirt1-dependent mitochondrial autophagy in mouse aged kidney. The Journal of clinical investigation 120, 1043-1055, doi: 10.1172/jci41376 (2010).
12. Hine, C., Mitchell, J. R. Calorie restriction and methionine restriction in control of endogenous hydrogen sulfide production by the transsulfuration pathway. Experimental gerontology 68, 26-32, doi: 10.1016/j.exger.2014.12.010 (2015).
13. Fontana, L., Partridge, L., Longo, V. D. Extending healthy life span-from yeast to humans. Science 328, 321-326, doi: 10.1126/science.1172539 (2010).
14. Ruckenstuhl, C. et al. Lifespan extension by methionine restriction requires autophagy-dependent vacuolar acidification. PLoS Genet 10, e1004347, doi: 10.1371/journal.pgen.1004347 (2014).
15. Grandison, R. C., Piper, M. D., Partridge, L. Amino-acid imbalance explains extension of lifespan by dietary restriction in Drosophila. Nature 462, 1061-1064, doi: 10.1038/nature08619 (2009).
16. Miller, R. A. et al. Methionine-deficient diet extends mouse lifespan, slows immune and lens aging, alters glucose, T4, IGF-I and insulin levels, increases hepatocyte MIF levels and stress resistance. Aging cell 4, 119-125, doi: 10.1111/j.1474-9726.2005.00152.x (2005).
17. Cabreiro, F. et al. Metformin retards aging in C. elegans by altering microbial folate and methionine metabolism. Cell 153, 228-239, doi: 10.1016/j.cell.2013.02.035 (2013).
18. Ledford, H. Mice share yeast's ageing system. Nature 456, 433, doi: 10.1038/456433a (2008).
19. Mair, W. et al. Lifespan extension induced by AMPK and calcineurin is mediated by CRTC-1 and CREB. Nature 470, 404-408, doi: 10.1038/nature09706 (2011).
20. Harrison, D. E. et al. Rapamycin fed late in life extends lifespan in genetically heterogeneous mice. Nature 460, 392-395, doi: 10.1038/nature08221 (2009).
21. Sharples, A. P. et al. Longevity and skeletal muscle mass: the role of IGF signalling, the sirtuins, dietary restriction and protein intake. Aging cell 14, 511-523, doi: 10.1111/acel.12342 (2015).
22. Zhang, Y. et al. Hydrogen sulfide, the next potent preventive and therapeutic agent in aging and age-associated diseases. Molecular and cellular biology 33, 1104-1113, doi: 10.1128/mcb.01215-12 (2013).
23. Hine, C. et al. Endogenous hydrogen sulfide production is essential for dietary restriction benefits. Cell 160, 132-144, doi: 10.1016/j. cell.2014.11.048 (2015).
24. Zhang, X., Bian, J. S. Hydrogen sulfide: a neuromodulator and neuroprotectant in the central nervous system. ACS chemical neuroscience 5, 876-883, doi: 10.1021/cn500185g (2014).
25. Lobb, I., Sonke, E., Aboalsamh, G., Sener, A. Hydrogen sulphide and the kidney: important roles in renal physiology and pathogenesis and treatment of kidney injury and disease. Nitric oxide: biology and chemistry/official journal of the Nitric Oxide Society 46, 55-65, doi: 10.1016/j.niox.2014.10.004 (2015).
26. Xia, M., Chen, L., Muh, R. W., Li, P. L., Li, N. Production and actions of hydrogen sulfide, a novel gaseous bioactive substance, in the kidneys. The Journal of pharmacology and experimental therapeutics 329, 1056-1062, doi: 10.1124/jpet.108.149963 (2009).
27. Stipanuk, M. H., Ueki, I. Dealing with methionine/homocysteine sulfur: cysteine metabolism to taurine and inorganic sulfur. Journal of inherited metabolic disease 34, 17-32, doi: 10.1007/s10545-009-9006-9 (2011).
28. Koning, A. M., Frenay, A. R., Leuvenink, H. G., van Goor, H. Hydrogen sulfide in renal physiology, disease and transplantation-the smell of renal protection. Nitric oxide: biology and chemistry/official journal of the Nitric Oxide Society 46, 37-49, doi: 10.1016/j. niox.2015.01.005 (2015).
29. Song, K. et al. Hydrogen sulfide inhibits the renal fibrosis of obstructive nephropathy. Kidney international 85, 1318-1329, doi: 10.1038/ki.2013.449 (2014).
30. Aminzadeh, M. A., Vaziri, N. D. Downregulation of the renal and hepatic hydrogen sulfide (H2S)-producing enzymes and capacity in chronic kidney disease. Nephrology, dialysis, transplantation: official publication of the European Dialysis and Transplant Association-European Renal Association 27, 498-504, doi: 10.1093/ndt/gfr560 (2012).
31. Della Coletta Francescato, H. et al. Inhibition of hydrogen sulphide formation reduces cisplatin-induced renal damage. Nephrology, dialysis, transplantation: official publication of the European Dialysis and Transplant Association-European Renal Association 26, 479-488, doi: 10.1093/ndt/gfq447 (2011).
32. Bos, E. M. et al. Cystathionine gamma-lyase protects against renal ischemia/reperfusion by modulating oxidative stress. Journal of the American Society of Nephrology: JASN 24, 759-770, doi: 10.1681/asn.2012030268 (2013).
33. Striker, G. E. The aging kidney phenotype and systemically derived stem cells. Journal of the American Society of Nephrology: JASN 22, 1958-1960, doi: 10.1681/asn.2011090946 (2011).
34. Wulfert, F. M. et al. Age-dependent role of microvascular endothelial and polymorphonuclear cells in lipopolysaccharide-induced acute kidney injury. Anesthesiology 117, 126-136, doi: 10.1097/ALN.0b013e31825b57c9 (2012).
35. Cui, J. et al. Age-related changes in the function of autophagy in rat kidneys. Age 34, 329-339, doi: 10.1007/s11357-011-9237-1 (2012).
36. Ning, Y. C. et al. Short-term calorie restriction protects against renal senescence of aged rats by increasing autophagic activity and reducing oxidative damage. Mechanisms of ageing and development 134, 570-579, doi: 10.1016/j.mad.2013.11.006 (2013).
37. Ning, Y. C. et al. Beneficial effects of short-term calorie restriction against cisplatin-induced acute renal injury in aged rats. Nephron. Experimental nephrology 124, 19-27, doi: 10.1159/000357380 (2013).
38. Pincemail, J., Ricour, C., Defraigne, J. O., Petermans, J. [Oxidative stress, antioxydants and the ageing process]. Revue medicale de Liege 69, 270-275 (2014).
39. Aydin, S. et al. Comparison of oxidative stress biomarkers in renal tissues of D-galactose induced, naturally aged and young rats. Biogerontology 13, 251-260, doi: 10.1007/s10522-011-9370-3 (2012).
40. Modis, K., Coletta, C., Erdelyi, K., Papapetropoulos, A., Szabo, C. Intramitochondrial hydrogen sulfide production by 3-mercaptopyruvate sulfurtransferase maintains mitochondrial electron flow and supports cellular bioenergetics. FASEB journal: official publication of the Federation of American Societies for Experimental Biology 27, 601-611, doi: 10.1096/fj.12-216507 (2013).
41. Olson, K. R. et al. Thiosulfate: a readily accessible source of hydrogen sulfide in oxygen sensing. American journal of physiology. Regulatory, integrative and comparative physiology 305, R592-603, doi: 10.1152/ajpregu.00421.2012 (2013).
42. Muyzer, G., Stams, A. J. The ecology and biotechnology of sulphate-reducing bacteria. Nature reviews. Microbiology 6, 441-454, doi: 10.1038/nrmicro1892 (2008).
43. Yu, L. et al. Melatonin receptor-mediated protection against myocardial ischemia/reperfusion injury: role of SIRT1. Journal of pineal research 57, 228-238, doi: 10.1111/jpi.12161 (2014).
44. Wu, D. et al. Hydrogen sulfide protects against apoptosis under oxidative stress through SIRT1 pathway in H9c2 cardiomyocytes. Nitric oxide: biology and chemistry/official journal of the Nitric Oxide Society 46, 204-212, doi: 10.1016/j.niox.2014.11.006 (2015).
45. Xie, Z. Z. et al. Sulfhydration of p66Shc at cysteine59 mediates the antioxidant effect of hydrogen sulfide. Antioxidants & redox signaling 21, 2531-2542, doi: 10.1089/ars.2013.5604 (2014).
46. Yang, G. et al. Hydrogen sulfide protects against cellular senescence via S-sulfhydration of Keap1 and activation of Nrf2. Antioxidants & redox signaling 18, 1906-1919, doi: 10.1089/ars.2012.4645 (2013).
47. Nishida, M. et al. Hydrogen sulfide anion regulates redox signaling via electrophile sulfhydration. Nature chemical biology 8, 714-724, doi: 10.1038/nchembio.1018 (2012).
48. Mustafa, A. K. et al. Hydrogen sulfide as endothelium-derived hyperpolarizing factor sulfhydrates potassium channels. Circulation research 109, 1259-1268, doi: 10.1161/circresaha.111.240242 (2011).
49. Bazzi, C., Petrini, C., Rizza, V., Arrigo, G., D'Amico, G. A modern approach to selectivity of proteinuria and tubulointerstitial damage in nephrotic syndrome. Kidney international 58, 1732-1741, doi: 10.1046/j.1523-1755.2000.00334.x (2000).
50. Debelle, F. D. et al. Aristolochic acids induce chronic renal failure with interstitial fibrosis in salt-depleted rats. Journal of the American Society of Nephrology: JASN 13, 431-436 (2002).