Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 88

The DOI matches its Crossref record; 23 of the 23 references it cites were found in a registry or an index.

Zinc at the crossroads of exercise and proteostasis

Hernández-Camacho, Juan Diego, Vicente-García, Cristina, Parsons, Douglas S., Navas-Enamorado, Ignacio·2020·Redox Biology

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1016/j.redox.2020.101529

Cites

23 of 23 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 23 references

Research works printed but not linked: 158

  1. Raulin, 1869, Etudes chimiques sur la végétation, Ann. Sci. Nat. Bot. Biol. Veg., 11, 92
  2. Sommer, 1926, Evidence on the indispensable nature of zinc and boron for higher green plants, Plant Physiol., 1, 231, 10.1104/pp.1.3.231 · DOI
  3. Todd, 1934, Zinc in the nutrition of the rat, Am. J. Physiol., 107, 146, 10.1152/ajplegacy.1933.107.1.146 · DOI · Paper page
  4. Wastney, 1986, Kinetic analysis of zinc metabolism and its regulation in normal humans, Am. J. Physiol., 251, R398
  5. Jackson, 1982, Tissue zinc levels as an index of body zinc status, Clin. Physiol., 2, 333, 10.1111/j.1475-097X.1982.tb00038.x · DOI
  6. Barnett, 2013, Allosteric modulation of zinc speciation by fatty acids, Biochim. Biophys. Acta, 1830, 5456, 10.1016/j.bbagen.2013.05.028 · DOI
  7. Maret, 2009, Coordination dynamics of zinc in proteins, Chem. Rev., 109, 4682, 10.1021/cr800556u · DOI · Paper page
  8. Scott, 1938, The insulin and the zinc content of normal and diabetic pancreas, J. Clin. Invest., 17, 725, 10.1172/JCI101000 · DOI
  9. Keilin, 1939, Carbonic anhydrase, Nature, 144, 442, 10.1038/144442b0 · DOI
  10. Vallee, 1993, The biochemical basis of zinc physiology, Physiol. Rev., 73, 79, 10.1152/physrev.1993.73.1.79 · DOI · Paper page
  11. Brautigan, 1981, Phosphotyrosyl-protein phosphatase. Specific inhibition by Zn, J. Biol. Chem., 256, 6519, 10.1016/S0021-9258(19)69016-2 · DOI · Paper page
  12. Hanas, 1983, Xenopus transcription factor A requires zinc for binding to the 5 S RNA gene, J. Biol. Chem., 258, 14120, 10.1016/S0021-9258(17)43831-2 · DOI · Paper page
  13. Miller, 1985, Repetitive zinc-binding domains in the protein transcription factor IIIA from Xenopus oocytes, EMBO J., 4, 1609, 10.1002/j.1460-2075.1985.tb03825.x · DOI · Paper page
  14. Andreini, 2006, Zinc through the three domains of life, J. Proteome Res., 5, 3173, 10.1021/pr0603699 · DOI · Paper page
  15. Andreini, 2009, Metalloproteomes: a bioinformatic approach, Acc. Chem. Res., 42, 1471, 10.1021/ar900015x · DOI · Paper page
  16. Prasad, 2013, Discovery of human zinc deficiency: its impact on human health and disease, Adv. Nutr., 4, 176, 10.3945/an.112.003210 · DOI · Paper page
  17. Livingstone, 2015, Zinc: physiology, deficiency, and parenteral nutrition, Nutr. Clin. Pract., 30, 371, 10.1177/0884533615570376 · DOI · Paper page
  18. Atasoy, 2018, Zinc deficiency and its predictive capacity for anemia: unique model in school children, Pediatr. Int., 60, 703, 10.1111/ped.13603 · DOI
  19. Palacios, 2020, Zinc deficiency associated with anaemia among young children in rural Guatemala, Matern. Child Nutr., 16, 10.1111/mcn.12885 · DOI
  20. Adamo, 2019, Early developmental marginal zinc deficiency affects neurogenesis decreasing neuronal number and altering neuronal specification in the adult rat brain, Front. Cell. Neurosci., 13, 62, 10.3389/fncel.2019.00062 · DOI
  21. Sandstead, 1995, Requirements and toxicity of essential trace elements, illustrated by zinc and copper, Am. J. Clin. Nutr., 61, 621S, 10.1093/ajcn/61.3.621S · DOI
  22. Maret, 2006, Zinc requirements and the risks and benefits of zinc supplementation, J. Trace Elem. Med. Biol., 20, 3, 10.1016/j.jtemb.2006.01.006 · DOI · Paper page
  23. Wieringa, 2015, Determination of zinc status in humans: which indicator should we use?, Nutrients, 7, 3252, 10.3390/nu7053252 · DOI
  24. Khalid, 2014, A question mark on zinc deficiency in 185 million people in Pakistan--possible way out, Crit. Rev. Food Sci. Nutr., 54, 1222, 10.1080/10408398.2011.630541 · DOI
  25. Ackland, 2006, Zinc deficiency and its inherited disorders -a review, Genes Nutr., 1, 41, 10.1007/BF02829935 · DOI
  26. McClain, 1985, Zinc metabolism in malabsorption syndromes, J. Am. Coll. Nutr., 4, 49, 10.1080/07315724.1985.10720066 · DOI
  27. Solomons, 1977, Zinc deficiency in Crohn's disease, Digestion, 16, 87, 10.1159/000198059 · DOI
  28. Steel, 1985, Kinetics of zinc absorption by luminally and vascularly perfused rat intestine, Am. J. Physiol., 248, G46
  29. Hambidge, 2001, Interrelationships of key variables of human zinc homeostasis: relevance to dietary zinc requirements, Annu. Rev. Nutr., 21, 429, 10.1146/annurev.nutr.21.1.429 · DOI
  30. Sandstead, 1996, Deliberations and evaluations of approaches, endpoints and paradigms for determining zinc dietary recommendations, J. Nutr., 126, 2410S, 10.1093/jn/126.suppl_9.2410S · DOI
  31. Tang, 2017, Zinc bioavailability from phytate-rich foods and zinc supplements. Modeling the effects of food components with oxygen, nitrogen, and sulfur donor ligands, J. Agric. Food Chem., 65, 8727, 10.1021/acs.jafc.7b02998 · DOI
  32. Cassens, 1967, Zinc content and subcellular distribution in red vs. white porcine skeletal muscle, Am. J. Physiol., 212, 688, 10.1152/ajplegacy.1967.212.3.688 · DOI
  33. O'Leary, 1979, Effect of zinc deficiency on the weight, cellularity and zinc concentration of different skeletal muscles in the post-weanling rat, Br. J. Nutr., 42, 487, 10.1079/BJN19790140 · DOI
  34. Giugliano, 1984, Growth and zinc homeostasis in the severely zinc-deficient rat, Br. J. Nutr., 52, 545, 10.1079/BJN19840122 · DOI
  35. Irving, 1948, Order of stability of metal complexes, Nature, 162, 746, 10.1038/162746a0 · DOI · Paper page
  36. Krezel, 2016, The biological inorganic chemistry of zinc ions, Arch. Biochem. Biophys., 611, 3, 10.1016/j.abb.2016.04.010 · DOI · Paper page
  37. Krezel, 2007, Dual nanomolar and picomolar zinc(II) binding properties of metallothionein, J. Am. Chem. Soc., 129, 10911, 10.1021/ja071979s · DOI · Paper page
  38. Maret, 2015, Analyzing free zinc(II) ion concentrations in cell biology with fluorescent chelating molecules, Metall, 7, 202, 10.1039/C4MT00230J · DOI
  39. Kimura, 2016, The functions of metallothionein and ZIP and ZnT transporters: an overview and perspective, Int. J. Mol. Sci., 17, 336, 10.3390/ijms17030336 · DOI · Paper page
  40. Vasak, 2011, Chemistry and biology of mammalian metallothioneins, J. Biol. Inorg. Chem., 16, 1067, 10.1007/s00775-011-0799-2 · DOI · Paper page
  41. Andrews, 2001, Cellular zinc sensors: MTF-1 regulation of gene expression, Biometals, 14, 223, 10.1023/A:1012932712483 · DOI · Paper page
  42. Giles, 2003, Metal and redox modulation of cysteine protein function, Chem. Biol., 10, 677, 10.1016/S1074-5521(03)00174-1 · DOI · Paper page
  43. Wessels, 2017, Zinc as a gatekeeper of immune function, Nutrients, 9, 10.3390/nu9121286 · DOI · Paper page
  44. Heffernan, 2019, The role of mineral and trace element supplementation in exercise and athletic performance: a systematic review, Nutrients, 11, 10.3390/nu11030696 · DOI · Paper page
  45. Dong, 2015, Balance between metallothionein and metal response element binding transcription factor 1 is mediated by zinc ions (review), Mol. Med. Rep., 11, 1582, 10.3892/mmr.2014.2969 · DOI
  46. Lichten, 2009, Mammalian zinc transporters: nutritional and physiologic regulation, Annu. Rev. Nutr., 29, 153, 10.1146/annurev-nutr-033009-083312 · DOI · Paper page
  47. Maltin, 1983, Effect of zinc deficiency on muscle fibre type frequencies in the post-weanling rat, Br. J. Nutr., 50, 597, 10.1079/BJN19830131 · DOI
  48. Chal, 2017, Making muscle: skeletal myogenesis in vivo and in vitro, Development, 144, 2104, 10.1242/dev.151035 · DOI · Paper page
  49. Kugelberg, 1976, Adaptive transformation of rat soleus motor units during growth, J. Neurol. Sci., 27, 269, 10.1016/0022-510X(76)90001-0 · DOI · Paper page
  50. Pfaender, 2016, Cellular zinc homeostasis contributes to neuronal differentiation in human induced pluripotent stem cells, Neural Plast., 10.1155/2016/3760702 · DOI
  51. O'Dell, 1989, Production and reversal of the neuromuscular pathology and related signs of zinc deficiency in Guinea pigs, J. Nutr., 119, 196, 10.1093/jn/119.2.196 · DOI
  52. O'Dell, 1958, Significance of dietary zinc for the growing chicken, J. Nutr., 65, 503, 10.1093/jn/65.4.503 · DOI
  53. Hurley, 1969, Zinc deficiency in the developing rat, Am. J. Clin. Nutr., 22, 1332, 10.1093/ajcn/22.10.1332 · DOI
  54. Huber, 1973, Effects of dietary zinc on zinc enzymes in the rat, J. Nutr., 103, 1175, 10.1093/jn/103.8.1175 · DOI
  55. Grider, 2007, Consumption of a moderately zinc-deficient and zinc-supplemented diet affects soluble protein expression in rat soleus muscle, J. Nutr. Biochem., 18, 753, 10.1016/j.jnutbio.2006.11.013 · DOI
  56. Sandow, 1962, Blockade of neuromuscular transmission by zinc, Nature, 193, 689, 10.1038/193689a0 · DOI
  57. Isaacson, 1963, Effects of zinc on responses of skeletal muscle, J. Gen. Physiol., 46, 655, 10.1085/jgp.46.4.655 · DOI
  58. Stanfield, 1975, The effect of zinc ions on the gating of the delayed potassium conductance of frog sartorius muscle, J. Physiol., 251, 711, 10.1113/jphysiol.1975.sp011118 · DOI
  59. Ragozzino, 2000, Zinc permeates mouse muscle ACh receptor channels expressed in BOSC 23 cells and affects channel function, J. Physiol., 529, 83, 10.1111/j.1469-7793.2000.00083.x · DOI
  60. Harrison, 1994, Zn2+: an endogenous modulator of ligand- and voltage-gated ion channels, Neuropharmacology, 33, 935, 10.1016/0028-3908(94)90152-X · DOI · Paper page
  61. Noh, 2015, The direct modulatory activity of zinc toward ion channels, Integr. Med. Res., 4, 142, 10.1016/j.imr.2015.07.004 · DOI
  62. Mnatsakanyan, 2018, Zinc uptake promotes myoblast differentiation via Zip7 transporter and activation of Akt signalling transduction pathway, Sci. Rep., 8, 10.1038/s41598-018-32067-0 · DOI
  63. Ohashi, 2015, Zinc promotes proliferation and activation of myogenic cells via the PI3K/Akt and ERK signaling cascade, Exp. Cell Res., 333, 228, 10.1016/j.yexcr.2015.03.003 · DOI
  64. Paskavitz, 2018, Differential expression of zinc transporters accompanies the differentiation of C2C12 myoblasts, J. Trace Elem. Med. Biol., 49, 27, 10.1016/j.jtemb.2018.04.024 · DOI
  65. Kim, 2014, Regulation of the catabolic cascade in osteoarthritis by the zinc-ZIP8-MTF1 axis, Cell, 156, 730, 10.1016/j.cell.2014.01.007 · DOI · Paper page
  66. Huang, 2012, zinct7-null mice are more susceptible to diet-induced glucose intolerance and insulin resistance, J. Biol. Chem., 287, 33883, 10.1074/jbc.M111.309666 · DOI
  67. Wijesekara, 2010, Beta cell-specific Znt8 deletion in mice causes marked defects in insulin processing, crystallisation and secretion, Diabetologia, 53, 1656, 10.1007/s00125-010-1733-9 · DOI · Paper page
  68. Norouzi, 2018, Zinc stimulates glucose oxidation and glycemic control by modulating the insulin signaling pathway in human and mouse skeletal muscle cell lines, PloS One, 13, 10.1371/journal.pone.0191727 · DOI
  69. Wu, 2016, Zinc stimulates glucose consumption by modulating the insulin signaling pathway in L6 myotubes: essential roles of Akt-GLUT4, GSK3beta and mTOR-S6K1, J. Nutr. Biochem., 34, 126, 10.1016/j.jnutbio.2016.05.008 · DOI
  70. Norouzi, 2019, The zinc transporter Zip7 is downregulated in skeletal muscle of insulin-resistant cells and in mice fed a high-fat diet, Cells, 8, 10.3390/cells8070663 · DOI
  71. Myers, 2013, The zinc transporter, Slc39a7 (Zip7) is implicated in glycaemic control in skeletal muscle cells, PloS One, 8, 10.1371/journal.pone.0079316 · DOI
  72. Hardy, 2016, Comparative study of injury models for studying muscle regeneration in mice, PloS One, 11, 10.1371/journal.pone.0147198 · DOI · Paper page
  73. Jinno, 2014, Marginal zinc deficiency negatively affects recovery from muscle injury in mice, Biol. Trace Elem. Res., 158, 65, 10.1007/s12011-014-9901-2 · DOI
  74. Mukund, 2020, Skeletal muscle: a review of molecular structure and function, in health and disease, Wiley Interdiscip. Rev. Sys. Biol. Med., 12
  75. Chu, 2017, Plasma/serum zinc status during aerobic exercise recovery: a systematic review and meta-analysis, Sports Med., 47, 127, 10.1007/s40279-016-0567-0 · DOI
  76. Granell, 2014, Zinc and copper changes in serum and urine after aerobic endurance and muscular strength exercise, J. Sports Med. Phys. Fit., 54, 232
  77. Maynar, 2018, Influence of an acute exercise until exhaustion on serum and urinary concentrations of molybdenum, selenium, and zinc in athletes, Biol. Trace Elem. Res., 186, 361, 10.1007/s12011-018-1327-9 · DOI · Paper page
  78. Chu, 2016, Immediate effects of aerobic exercise on plasma/serum zinc levels: a meta-analysis, Med. Sci. Sports Exerc., 48, 726, 10.1249/MSS.0000000000000805 · DOI
  79. Anderson, 1984, Acute effects on chromium, copper, zinc, and selected clinical variables in urine and serum of male runners, Biol. Trace Elem. Res., 6, 327, 10.1007/BF02989240 · DOI
  80. Anderson, 1995, Acute exercise effects on urinary losses and serum concentrations of copper and zinc of moderately trained and untrained men consuming a controlled diet, Analyst, 120, 867, 10.1039/an9952000867 · DOI
  81. Volpe, 2007, Effect of maximal exercise on the short-term kinetics of zinc metabolism in sedentary men, Br. J. Sports Med., 41, 156, 10.1136/bjsm.2006.030346 · DOI
  82. van Rij, 1986, Changes in zinc metabolism following exercise in human subjects, Biol. Trace Elem. Res., 10, 99, 10.1007/BF02795562 · DOI
  83. Donath, 2010, Cytokine production by islets in health and diabetes: cellular origin, regulation and function, Trends Endocrinol. Metabol., 21, 261, 10.1016/j.tem.2009.12.010 · DOI
  84. Maynar, 2019, Influence of a 6-month physical training program on serum and urinary concentrations of trace metals in middle distance elite runners, J. Int. Soc. Sports. Nutr., 16, 53, 10.1186/s12970-019-0322-7 · DOI
  85. Somboonwong, 2015, Moderate-intensity exercise training elevates serum and pancreatic zinc levels and pancreatic zincT8 expression in streptozotocin-induced diabetic rats, Life Sci., 139, 46, 10.1016/j.lfs.2015.08.008 · DOI
  86. Song, 2009, Zinc deficiency affects DNA damage, oxidative stress, antioxidant defenses, and DNA repair in rats, J. Nutr., 139, 1626, 10.3945/jn.109.106369 · DOI
  87. Rakhra, 2017, Effect of physical activity and age on plasma copper, zinc, iron, and magnesium concentration in physically active healthy males, Nutrition, 43–44, 75, 10.1016/j.nut.2017.06.005 · DOI
  88. Kwon, 2020, Elevation of hepatic autophagy and antioxidative capacity by endurance exercise is associated with suppression of apoptosis in mice, Ann. Hepatol., 19, 69, 10.1016/j.aohep.2019.08.010 · DOI
  89. Koury, 2005, Effect of the period of resting in elite judo athletes: hematological indices and copper/zinc-dependent antioxidant capacity, Biol. Trace Elem. Res., 107, 201, 10.1385/BTER:107:3:201 · DOI
  90. Koury, 2004, Zinc and copper biochemical indices of antioxidant status in elite athletes of different modalities, Int. J. Sport Nutr. Exerc. Metabol., 14, 358, 10.1123/ijsnem.14.3.358 · DOI
  91. Bicer, 2012, Effect of zinc supplementation on lipid peroxidation and lactate levels in rats with diabetes induced by streptozotocin and subjected to acute swimming exercise, Bratisl. Lek. Listy, 113, 199
  92. Gouzi, 2019, Additional effects of nutritional antioxidant supplementation on peripheral muscle during pulmonary rehabilitation in COPD patients: a randomized controlled trial, Oxid. Med. Cell. Longev., 10.1155/2019/5496346 · DOI · Paper page
  93. Cinar, 2018, The effect of 6-week zinc supplement and weight training on the blood lipids of the sedentaries and athletes, Cell. Mol. Biol., 64, 1, 10.14715/cmb/2018.64.11.1 · DOI
  94. Ozturk, 2003, Effects of zinc deficiency and supplementation on malondialdehyde and glutathione levels in blood and tissues of rats performing swimming exercise, Biol. Trace Elem. Res., 94, 157, 10.1385/BTER:94:2:157 · DOI
  95. Lukaski, 2005, Low dietary zinc decreases erythrocyte carbonic anhydrase activities and impairs cardiorespiratory function in men during exercise, Am. J. Clin. Nutr., 81, 1045, 10.1093/ajcn/81.5.1045 · DOI
  96. Van Loan, 1999, The effects of zinc depletion on peak force and total work of knee and shoulder extensor and flexor muscles, Int. J. Sport Nutr., 9, 125, 10.1123/ijsn.9.2.125 · DOI
  97. Giolo De Carvalho, 2012, Evidence of zinc deficiency in competitive swimmers, Nutrition, 28, 1127, 10.1016/j.nut.2012.02.012 · DOI
  98. McClung, 2019, Iron, zinc, and physical performance, Biol. Trace Elem. Res., 188, 135, 10.1007/s12011-018-1479-7 · DOI
  99. King, 2000, Zinc homeostasis in humans, J. Nutr., 130, 1360S, 10.1093/jn/130.5.1360S · DOI · Paper page
  100. Lighthouse, 2019, Exercise promotes a cardioprotective gene program in resident cardiac fibroblasts, JCI Insight, 4, 10.1172/jci.insight.92098 · DOI
  101. Bobillier Chaumont, 2001, Effect of exercise training on metallothionein levels of hypertensive rats, Med. Sci. Sports Exerc., 33, 724, 10.1097/00005768-200105000-00007 · DOI
  102. Saxena, 2010, Hypoxia preconditioning by cobalt chloride enhances endurance performance and protects skeletal muscles from exercise-induced oxidative damage in rats, Acta Physiol., 200, 249, 10.1111/j.1748-1716.2010.02136.x · DOI
  103. Evers-van Gogh, 2015, Electric pulse stimulation of myotubes as an in vitro exercise model: cell-mediated and non-cell-mediated effects, Sci. Rep., 5, 10.1038/srep10944 · DOI
  104. Ni, 2011, Effects of forced running exercise on cognitive function and its relation to zinc homeostasis-related gene expression in rat hippocampus, Biol. Trace Elem. Res., 142, 704, 10.1007/s12011-010-8793-z · DOI
  105. Hashimoto, 2009, Exercise induces metallothioneins in mouse spinal cord, Neuroscience, 163, 244, 10.1016/j.neuroscience.2009.05.067 · DOI
  106. Podhorska-Okolow, 2006, Expression of metallothionein in renal tubules of rats exposed to acute and endurance exercise, Folia Histochem. Cytobiol., 44, 195
  107. Powers, 2016, Exercise-induced oxidative stress: past, present and future, J. Physiol., 594, 5081, 10.1113/JP270646 · DOI · Paper page
  108. Nam, 2018, Link of impaired metal ion homeostasis to mitochondrial dysfunction in neurons, Curr. Opin. Chem. Biol., 43, 8, 10.1016/j.cbpa.2017.09.009 · DOI
  109. Musci, 2018, Targeting mitochondrial function and proteostasis to mitigate dynapenia, Eur. J. Appl. Physiol., 118, 1, 10.1007/s00421-017-3730-x · DOI
  110. Bechet, 2005, Lysosomal proteolysis in skeletal muscle, Int. J. Biochem. Cell Biol., 37, 2098, 10.1016/j.biocel.2005.02.029 · DOI
  111. Hung, 2013, Dopamine- and zinc-induced autophagosome formation facilitates PC12 cell survival, Cell Biol. Toxicol., 29, 415, 10.1007/s10565-013-9261-2 · DOI
  112. Liuzzi, 2013, Role of zinc in the regulation of autophagy during ethanol exposure in human hepatoma cells, Biol. Trace Elem. Res., 156, 350, 10.1007/s12011-013-9816-3 · DOI
  113. Lee, 2010, Roles of zinc and metallothionein-3 in oxidative stress-induced lysosomal dysfunction, cell death, and autophagy in neurons and astrocytes, Mol. Brain, 3, 30, 10.1186/1756-6606-3-30 · DOI
  114. Hwang, 2010, Zinc(II) ion mediates tamoxifen-induced autophagy and cell death in MCF-7 breast cancer cell line, Biometals, 23, 997, 10.1007/s10534-010-9346-9 · DOI
  115. Bian, 2018, Zinc prevents mitochondrial superoxide generation by inducing mitophagy in the setting of hypoxia/reoxygenation in cardiac cells, Free Radic. Res., 52, 80, 10.1080/10715762.2017.1414949 · DOI
  116. Wang, 2009, A non-canonical MEK/ERK signaling pathway regulates autophagy via regulating Beclin 1, J. Biol. Chem., 284, 21412, 10.1074/jbc.M109.026013 · DOI · Paper page
  117. Song, 2019, Zinc oxide nanoparticles induce autophagy and apoptosis via oxidative injury and pro-inflammatory cytokines in primary astrocyte cultures, Nanomaterials, 9, 10.3390/nano9071043 · DOI
  118. Roy, 2014, Zinc oxide nanoparticles induce apoptosis by enhancement of autophagy via PI3K/Akt/mTOR inhibition, Toxicol. Lett., 227, 29, 10.1016/j.toxlet.2014.02.024 · DOI
  119. Li, 2015, ZNF32 inhibits autophagy through the mTOR pathway and protects MCF-7 cells from stimulus-induced cell death, Sci. Rep., 5, 9288, 10.1038/srep09288 · DOI
  120. Wei, 2018, Zinc reduces hepatic lipid deposition and activates lipophagy via zinc(2+)/MTF-1/PPARalpha and Ca(2+)/CaMKKbeta/AMPK pathways, Faseb. J., 10.1096/fj.201800463 · DOI
  121. Liuzzi, 2014, Zinc and autophagy, Biometals, 27, 1087, 10.1007/s10534-014-9773-0 · DOI
  122. Guo, 2020, Cathepsin-B dependent autophagy ameliorates steatoheaptitis in chronic exercise rats, Histol. Histopathol.
  123. Kawamata, 2017, Zinc starvation induces autophagy in yeast, J. Biol. Chem., 292, 8520, 10.1074/jbc.M116.762948 · DOI
  124. Filfan, 2017, Autophagy in aging and disease, Rom. J. Morphol. Embryol., 58, 27
  125. Liuzzi, 2018, Effect of zinc intake on hepatic autophagy during acute alcohol intoxication, Biometals, 31, 217, 10.1007/s10534-018-0077-7 · DOI
  126. Nanao, 2015, Cellular localization and tissue distribution of endogenous DFCP1 protein, Biomed. Res., 36, 121, 10.2220/biomedres.36.121 · DOI
  127. Ding, 2017, Zinc deficiency: an unexpected trigger for autophagy, J. Biol. Chem., 292, 8531, 10.1074/jbc.H116.762948 · DOI
  128. Du, 2004, Activation of caspase-3 is an initial step triggering accelerated muscle proteolysis in catabolic conditions, J. Clin. Invest., 113, 115, 10.1172/JCI18330 · DOI · Paper page
  129. Costelli, 2005, Ca(2+)-dependent proteolysis in muscle wasting, Int. J. Biochem. Cell Biol., 37, 2134, 10.1016/j.biocel.2005.03.010 · DOI
  130. Kinbara, 1997, Muscle-specific calpain, p94, interacts with the extreme C-terminal region of connecting, a unique region flanked by two immunoglobulin C2 motifs, Arch. Biochem. Biophys., 342, 99, 10.1006/abbi.1997.0108 · DOI
  131. Carbone, 2014, Effects of short-term energy deficit on muscle protein breakdown and intramuscular proteolysis in normal-weight young adults, Appl. Physiol. Nutr. Metabol., 39, 960, 10.1139/apnm-2013-0433 · DOI
  132. Wang, 2010, Caspase-3 cleaves specific 19 S proteasome subunits in skeletal muscle stimulating proteasome activity, J. Biol. Chem., 285, 21249, 10.1074/jbc.M109.041707 · DOI · Paper page
  133. Eron, 2018, Multiple mechanisms of zinc-mediated inhibition for the apoptotic caspases-3, -6, -7, and -8, ACS Chem. Biol., 13, 1279, 10.1021/acschembio.8b00064 · DOI
  134. Velez, 2017, Moderate and sustained exercise modulates muscle proteolytic and myogenic markers in gilthead sea bream (Sparus aurata), Am. J. Physiol. Regul. Integr. Comp. Physiol., 312, R643, 10.1152/ajpregu.00308.2016 · DOI
  135. Kramerova, 2018, Calpain 3 and CaMKIIbeta signaling are required to induce HSP70 necessary for adaptive muscle growth after atrophy, Hum. Mol. Genet., 27, 1642, 10.1093/hmg/ddy071 · DOI
  136. Wang, 2006, The ubiquitin-proteasome system and its role in inflammatory and autoimmune diseases, Cell. Mol. Immunol., 3, 255
  137. Schwartz, 2009, Targeting proteins for destruction by the ubiquitin system: implications for human pathobiology, Annu. Rev. Pharmacol. Toxicol., 49, 73, 10.1146/annurev.pharmtox.051208.165340 · DOI · Paper page
  138. Nakajima, 2014, Activation of the mitochondrial caspase pathway and subsequent calpain activation in monkey RPE cells cultured under zinc depletion, Eye, 28, 85, 10.1038/eye.2013.239 · DOI
  139. Adebayo, 2015, Protective roles of selenium and zinc against postnatal protein-undernutrition-induced alterations in Ca(2+)-homeostasis leading to cognitive deficits in Wistar rats, Int. J. Dev. Neurosci., 43, 1, 10.1016/j.ijdevneu.2015.03.007 · DOI
  140. Tamada, 2007, Contribution of calpain to cellular damage in human retinal pigment epithelial cells cultured with zinc chelator, Curr. Eye Res., 32, 565, 10.1080/02713680701359633 · DOI
  141. Yan, 2010, Differential response to zinc-induced apoptosis in benign prostate hyperplasia and prostate cancer cells, J. Nutr. Biochem., 21, 687, 10.1016/j.jnutbio.2009.04.002 · DOI
  142. Varshavsky, 2012, The ubiquitin system, an immense realm, Annu. Rev. Biochem., 81, 167, 10.1146/annurev-biochem-051910-094049 · DOI · Paper page
  143. Bodine, 2014, Skeletal muscle atrophy and the E3 ubiquitin ligases MuRF1 and MAFbx/atrogin-1, Am. J. Physiol. Endocrinol. Metab., 307, E469, 10.1152/ajpendo.00204.2014 · DOI · Paper page
  144. Budenholzer, 2017, Proteasome structure and assembly, J. Mol. Biol., 429, 3500, 10.1016/j.jmb.2017.05.027 · DOI · Paper page
  145. Kim, 2004, Pyrrolidine dithiocarbamate and zinc inhibit proteasome-dependent proteolysis, Exp. Cell Res., 298, 229, 10.1016/j.yexcr.2004.04.017 · DOI
  146. Verma, 2002, Role of Rpn11 metalloprotease in deubiquitination and degradation by the 26S proteasome, Science, 298, 611, 10.1126/science.1075898 · DOI · Paper page
  147. Prasad, 2019, Molecular mechanisms of zinc as a pro-antioxidant mediator: clinical therapeutic implications, Antioxidants, 8, 10.3390/antiox8060164 · DOI · Paper page
  148. Olechnowicz, 2018, Zinc status is associated with inflammation, oxidative stress, lipid, and glucose metabolism, J. Physiol. Sci., 68, 19, 10.1007/s12576-017-0571-7 · DOI · Paper page
  149. Li, 2014, Zinc is essential for the transcription function of Nrf2 in human renal tubule cells in vitro and mouse kidney in vivo under the diabetic condition, J. Cell Mol. Med., 18, 895, 10.1111/jcmm.12239 · DOI
  150. Hadwan, 2014, Study of the effects of oral zinc supplementation on peroxynitrite levels, arginase activity and NO synthase activity in seminal plasma of Iraqi asthenospermic patients, Reprod. Biol. Endocrinol., 12, 1, 10.1186/1477-7827-12-1 · DOI
  151. Ogawa, 2011, High glucose increases metallothionein expression in renal proximal tubular epithelial cells, Exp. Diabetes Res., 2011, 10.1155/2011/534872 · DOI
  152. Bashandy, 2018, Role of zinc oxide nanoparticles in alleviating hepatic fibrosis and nephrotoxicity induced by thioacetamide in rats, Can. J. Physiol. Pharmacol., 96, 337, 10.1139/cjpp-2017-0247 · DOI
  153. Sefi, 2020, Zinc alleviates maneb-induced kidney injury in adult mice through modulation of oxidative stress, genotoxicity, and histopathological changes, Environ. Sci. Pollut. Res. Int., 10.1007/s11356-019-07175-7 · DOI
  154. Teixeira, 2019, Regular exercise participation contributes to better proteostasis, inflammatory and vasoactive profiles in patients with hypertension, Am. J. Hypertens.
  155. Fernandez-Sanchez, 2011, Inflammation, oxidative stress, and obesity, Int. J. Mol. Sci., 12, 3117, 10.3390/ijms12053117 · DOI · Paper page
  156. Prasad, 2014, Zinc is an antioxidant and anti-inflammatory agent: its role in human health, Front Nutr, 1, 14, 10.3389/fnut.2014.00014 · DOI · Paper page
  157. Amin, 2020, Increased oxidative stress, altered trace elements, and macro-minerals are associated with female obesity, Biol. Trace Elem. Res., 10.1007/s12011-019-02002-z · DOI
  158. Jung, 2015, The relationship between zinc status and inflammatory marker levels in rural Korean adults aged 40 and older, PloS One, 10, 10.1371/journal.pone.0130016 · DOI

Cited by

Metadata

Authors
Hernández-Camacho, J. D., Vicente-García, C., Parsons, D. S., & Navas-Enamorado, I.
Venue
Redox Biology
Publisher
Elsevier BV
Published
2020-08
Volume
35
Pages
101529
ISSN
2213-2317
Cited by
88
References
23
Language
en
Licence
Funders
  • Association Française contre les Myopathies (22450)
  • Ministerio de Educación, Cultura y Deporte (FPU16/03264)

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.