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Review Article

Blood reflects tissue oxidative stress: a systematic review

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Pages 97-108 | Received 27 Nov 2014, Accepted 23 Dec 2014, Published online: 13 Jan 2015

References

  • Alkreathy H, Damanhouri ZA, Ahmed N, et al. (2010). Aged garlic extract protects against doxorubicin-induced cardiotoxicity in rats. Food Chem Toxicol 48:951–6
  • Argüelles S, García S, Maldonado M, et al. (2004). Do the serum oxidative stress biomarkers provide a reasonable index of the general oxidative stress status? Biochim Biophys Acta 1674:251–9
  • Aydin A, Sakrak O, Yilmaz TU, Kerem M. (2014). The effects of Hypericum perforatum on hepatic ischemia – reperfusion injury in rats. Bratisl Lek Listy 115:209–15
  • Barr RG, Rowe BH, Camargo Jr CA. (2003). Methylxanthines for exacerbations of chronic obstructive pulmonary disease: meta-analysis of randomised trials. BMJ 327:643
  • Baykan A, Narin N, Narin F, et al. (2008). The protective effect of melatonin on nicotine-induced myocardial injury in newborn rats whose mothers received nicotine. Anadolu Kardiyol Derg 8:243–8
  • Bayorh MA, Ganafa AA, Emmett N, et al. (2005). Alterations in aldosterone and angiotensin II levels in salt-induced hypertension. Clin Exp Hypertens 27:355–67
  • Block BM, Liu SS, Rowlingson AJ, et al. (2003). Efficacy of post-operative epidural analgesia: a meta-analysis. JAMA 290:2455–63
  • Calviello G, Palozza P, Franceschelli P, Bartoli GM. (1997). Low-dose eicosapentaenoic or docosahexaenoic acid administration modifies fatty acid composition and does not affect susceptibility to oxidative stress in rat erythrocytes and tissues. Lipids 32:1075–83
  • Cay M, Naziroğlu M, Simsek H, et al. (2001). Effects of intraperitoneally administered vitamin C on antioxidative defense mechanism in rats with diabetes induced by streptozotocin. Res Exp Med (Berl) 200:205–13
  • Cetinkale O, Konukoğlu D, Senel O, et al. (1999). Modulating the functions of neutrophils and lipid peroxidation by FK506 in a rat model of thermal injury. Burns 25:105–12
  • Chang L, Geng B, Yu F, et al. (2008). Hydrogen sulfide inhibits myocardial injury induced by homocysteine in rats. Amino Acids 34:573–85
  • Chang L, Zhao J, Li GZ, et al. (2004). Ghrelin protects myocardium from isoproterenol-induced injury in rats. Acta Pharmacol Sin 25:1131–7
  • Chen X, Tang J, Xie W, et al. (2013). Protective effect of the polysaccharide from Ophiopogon japonicus on streptozotocin-induced diabetic rats. Carbohydr Polym 94:378–85
  • Cheng J, Ma H, Fan C, et al. (2011). Effects of different copper sources and levels on plasma superoxide dismutase, lipid peroxidation, and copper status of lambs. Biol Trace Elem Res 144:570–9
  • Cong G, Cui L, Zang M, Hao L. (2013). Attenuation of renal ischemia/reperfusion injury by a polysaccharide from the roots of Dipsacus asperoides. Int J Biol Macromol 56:14–19
  • Cosar R, Yurut-Caloglu V, Eskiocak S, et al. (2012). Radiation-induced chronic oxidative renal damage can be reduced by amifostine. Med Oncol 29:768–75
  • Da Rocha RF, de Oliveira MR, Pasquali MA, et al. (2010). Vascular redox imbalance in rats submitted to chronic exercise. Cell Biochem Funct 28:190–6
  • Dalle-Donne I, Rossi R, Colombo R, et al. (2006). Biomarkers of oxidative damage in human disease. Clin Chem 52:601–23
  • Dalloz F, Maingon P, Cottin Y, et al. (1999). Effects of combined irradiation and doxorubicin treatment on cardiac function and antioxidant defenses in the rat. Free Radic Biol Med 26:785–800
  • Davies MJ, Hawkins CL. (2004). EPR spin trapping of protein radicals. Free Radic Biol Med 36:1072–86
  • De Oliveira SL, Diniz DB, Amaya-Farfan J. (2003). Carbohydrate-energy restriction may protect the rat brain against oxidative damage and improve physical performance. Br J Nutr 89:89–96
  • Deminice R, Portari GV, Vannucchi H, Jordao AA. (2009). Effects of creatine supplementation on homocysteine levels and lipid peroxidation in rats. Br J Nutr 102:110–16
  • Desco MC, Asensi M, Márquez R, et al. (2002). Xanthine oxidase is involved in free radical production in type 1 diabetes: protection by allopurinol. Diabetes 51:1118–24
  • Devika PT, Stanely Mainzen Prince P. (2008). Protective effect of (−)-epigallocatechin-gallate (EGCG) on lipid peroxide metabolism in isoproterenol induced myocardial infarction in male Wistar rats: a histopathological study. Biomed Pharmacother 62:701–8
  • Duarte J, Jiménez R, O’Valle F, et al. (2002). Protective effects of the flavonoid quercetin in chronic nitric oxide deficient rats. J Hypertens 20:1843–54
  • Eder K. (1999). The effects of a dietary oxidized oil on lipid metabolism in rats. Lipids 34:717–25
  • Engberg RM, Lauridsen C, Jensen SK, Jakobsen K. (1996). Inclusion of oxidized vegetable oil in broiler diets. Its influence on nutrient balance and on the antioxidative status of broilers. Poult Sci 75:1003–11
  • Fan Q, Chen M, Fang X, et al. (2013). Aging might augment reactive oxygen species (ROS) formation and affect reactive nitrogen species (RNS) level after myocardial ischemia/reperfusion in both humans and rats. Age (Dordr) 35:1017–26
  • Fébel H, Mézes M, Pálfy T, et al. (2008). Effect of dietary fatty acid pattern on growth, body fat composition and antioxidant parameters in broilers. J Anim Physiol Anim Nutr (Berl) 92:369–76
  • Forman HJ, Maiorino M, Ursini F. (2010). Signaling functions of reactive oxygen species. Biochemistry 49:835–42
  • Geng B, Chang L, Pan C, et al. (2004). Endogenous hydrogen sulfide regulation of myocardial injury induced by isoproterenol. Biochem Biophys Res Commun 318:756–63
  • Girard A, Madani S, El Boustani ES, et al. (2005). Changes in lipid metabolism and antioxidant defense status in spontaneously hypertensive rats and Wistar rats fed a diet enriched with fructose and saturated fatty acids. Nutririon 21:240–8
  • Giustarini D, Dalle-Donne I, Milzani A, Rossi R. (2011). Low molecular mass thiols, disulfides and protein mixed disulfides in rat tissues: influence of sample manipulation, oxidative stress and ageing. Mech Ageing Dev 132:141–8
  • Gunay N, Kose B, Demiryurek S, et al. (2008). Effects of a selective Rho-kinase inhibitor Y-27632 on oxidative stress parameters in acute dichlorvos poisoning in rats. Cell Biochem Funct 26:747–54
  • Guo CH, Hsia S, Chen PC. (2013). Distribution of selenium and oxidative stress in breast tumor-bearing mice. Nutrients 5:594–607
  • Halliwell B, Gutteridge J. (2007). Free radicals in biology and medicine. New York (NY): Oxford University Press
  • Haramizu S, Ota N, Hase T, Murase T. (2011). Aging-associated changes in physical performance and energy metabolism in the senescence-accelerated mouse. J Gerontol A Biol Sci Med Sci 66:646–55
  • Hermann J, Gulati R, Napoli C, et al. (2003). Oxidative stress-related increase in ubiquitination in early coronary atherogenesis. FASEB J 17:1730–2
  • Hou YJ, Zhao YY, Xiong B, et al. (2013). Mycotoxin-containing diet causes oxidative stress in the mouse. PLoS One 8:e60374
  • Hsu YC, Chiu YT, Lee CY, et al. (2004). Increases in fibrosis-related gene transcripts in livers of dimethylnitrosamine-intoxicated rats. J Biomed Sci 11:408–17
  • Hwang ES, Kim GH. (2007). Biomarkers for oxidative stress status of DNA, lipids, and proteins in vitro and in vivo cancer research. Toxicology 229:1–10
  • Itoh H, Ohkuwa T, Yamamoto T, et al. (1998). Effects of endurance physical training on hydroxyl radical generation in rat tissues. Life Sci 63:1921–9
  • Jones DP, Carlson JL, Samiec PS, et al. (1998). Glutathione measurement in human plasma. Evaluation of sample collection, storage and derivatization conditions for analysis of dansyl derivatives by HPLC. Clin Chim Acta 275:175–84
  • Kanko M, Maral H, Akbas MH, et al. (2005). Protective effects of clopidogrel on oxidant damage in a rat model of acute ischemia. Tohoku J Exp Med 205:133–9
  • Kasahara E, Kashiba M, Jikumaru M, et al. (2009). Dynamic aspects of ascorbic acid metabolism in the circulation: analysis by ascorbate oxidase with a prolonged in vivo half-life. Biochem J 421:293–9
  • Koksal GM, Sayilgan C, Aydin S, et al. (2004). Correlation of plasma and tissue oxidative stresses in intra-abdominal sepsis. J Surg Res 122:180–3
  • Küçükkurt I, Ince S, Keleş H, et al. (2010). Beneficial effects of Aesculus hippocastanum L. seed extract on the body’s own antioxidant defense system on subacute administration. J Ethnopharmacol 129:18–22
  • Kuzu N, Bahcecioglu IH, Dagli AF, et al. (2008). Epigallocatechin gallate attenuates experimental non-alcoholic steatohepatitis induced by high fat diet. J Gastroenterol Hepatol 23:e465–70
  • Leeuwenburgh C, Hollander J, Leichtweis S, et al. (1997). Adaptations of glutathione antioxidant system to endurance training are tissue and muscle fiber specific. Am J Physiol 272:R363–9
  • Leeuwenburgh C, Ji LL. (1996). Alteration of glutathione and antioxidant status with exercise in unfed and refed rats. J Nutr 126:1833–43
  • Leeuwenburgh C, Ji LL. (1995). Glutathione depletion in rested and exercised mice: biochemical consequence and adaptation. Arch Biochem Biophys 316:941–9
  • Leeuwenburgh C, Ji LL. (1998). Glutathone and glutathione ethyl ester supplementation of mice alter glutathione homeostasis during exercise. J Nutr 128:2420–6
  • Leeuwenburgh C, Leichtweis S, Hollander J, et al. (1996b). Effect of acute exercise on glutathione deficient heart. Mol Cell Biochem 156:17–24
  • Lew H, Quintanilha A. (1991). Effects of endurance training and exercise on tissue antioxidative capacity and acetaminophen detoxification. Eur J Drug Metab Pharmacokinet 16:59–68
  • Li TT, Zhang YS, He L, et al. (2011). Protective effect of phloroglucinol against myocardial ischaemia-reperfusion injury is related to inhibition of myeloperoxidase activity and inflammatory cell infiltration. Clin Exp Pharmacol Physiol 38:27–33
  • Loe SM, Sanchez-Ramos L, Kaunitz AM. (2005). Assessing the neonatal safety of indomethacin tocolysis: a systematic review with meta-analysis. Obstet Gynecol 106:173–9
  • Lykkesfeldt J, Trueba GP, Poulsen HE, Christen S. (2007). Vitamin C deficiency in weanling guinea pigs: differential expression of oxidative stress and DNA repair in liver and brain. Br J Nutr 98:1116–19
  • Mohamadin AM, Hammad LN, El-Bab MF, Abdel Gawad HS. (2007). Attenuation of oxidative stress in plasma and tissues of rats with experimentally induced hyperthyroidism by caffeic acid phenylethyl ester. Basic Clin Pharmacol Toxicol 100:84–90
  • Molinar-Toribio E, Pérez-Jiménez J, Ramos-Romero S, et al. (2014). Cardiovascular disease-related parameters and oxidative stress in shrob rats, a model for metabolic syndrome. PLoS One 9:e104637
  • Mujahid A, Furuse M. (2008). Central administration of corticotropin-releasing factor induces tissue specific oxidative damage in chicks. Comp Biochem Physiol A Mol Integr Physiol 151:664–9
  • Mujahid A, Furuse M. (2009). Oxidative damage in different tissues of neonatal chicks exposed to low environmental temperature. Comp Biochem Physiol A Mol Integr Physiol 152:604–8
  • Nandi D, Patra RC, Swarup D. (2005). Effect of cysteine, methionine, ascorbic acid and thiamine on arsenic-induced oxidative stress and biochemical alterations in rats. Toxicology 211:26–35
  • Nandi D, Patra RC, Swarup D. (2006). Oxidative stress indices and plasma biochemical parameters during oral exposure to arsenic in rats. Food Chem Toxicol 44:1579–84
  • Naziroğlu M, Cay M. (2001). Protective role of intraperitoneally administered vitamin E and selenium on the antioxidative defense mechanisms in rats with diabetes induced by streptozotocin. Biol Trace Elem Res 79:149–59
  • Nikolaidis MG, Jamurtas AZ. (2009). Blood as a reactive species generator and redox status regulator during exercise. Arch Biochem Biophys 490:77–84
  • Nikolaidis MG, Kyparos A, Dipla K, et al. (2012a). Exercise as a model to study redox homeostasis in blood: the effect of protocol and sampling point. Biomarkers 17:28–35
  • Nikolaidis MG, Kyparos A, Spanou C, et al. (2012b). Redox biology of exercise: an integrative and comparative consideration of some overlooked issues. J Exp Biol 215:1615–25
  • Nikolaidis MG, Margaritelis NV, Paschalis V, et al. (2014). Common questions and tentative answers on how to assess oxidative stress after antioxidant supplementation and exercise. In: Lamprecht M, ed. Antioxidants in sports nutrition. New York: CRC Press. 221--246
  • Ohkuwa T, Sato Y, Naoi M. (1997). Glutathione status and reactive oxygen generation in tissues of young and old exercised rats. Acta Physiol Scand 159:237–44
  • Orozco TJ, Wang JF, Keen CL. (2003). Chronic consumption of a flavanol- and procyanindin-rich diet is associated with reduced levels of 8-hydroxy-2′-deoxyguanosine in rat testes. J Nutr Biochem 14:104–10
  • Otto DM, Moon TW. (1995). 3,3′,4,4′-tetrachlorobiphenyl effects on antioxidant enzymes and glutathione status in different tissues of rainbow trout. Pharmacol Toxicol 77:281–7
  • Ozkan F, Senayli Y, Ozyurt H, et al. (2012). Antioxidant effects of propofol on tourniquet-induced ischemia-reperfusion injury: an experimental study. J Surg Res 176:601–7
  • Ozyurt H, Ozyurt B, Koca K, Ozgocmen S. (2007). Caffeic acid phenethyl ester (CAPE) protects rat skeletal muscle against ischemia-reperfusion-induced oxidative stress. Vascul Pharmacol 47:108–12
  • Padmanabhan M, Prince PS. (2006). Preventive effect of S-allylcysteine on lipid peroxides and antioxidants in normal and isoproterenol-induced cardiotoxicity in rats: a histopathological study. Toxicology 224:128–37
  • Palace VP, Hill MF, Farahmand F, Singal PK. (1999). Mobilization of antioxidant vitamin pools and hemodynamic function after myocardial infarction. Circulation 99:121–6
  • Punithavathi VR, Stanely Mainzen Prince P. (2011). The cardioprotective effects of a combination of quercetin and α-tocopherol on isoproterenol-induced myocardial infarcted rats. J Biochem Mol Toxicol 25:28–40
  • Pushpavalli G, Kalaiarasi P, Veeramani C, Pugalendi KV. (2010). Effect of chrysin on hepatoprotective and antioxidant status in d-galactosamine-induced hepatitis in rats. Eur J Pharmacol 631:36–41
  • Quiroz Y, Ferrebuz A, Romero F, et al. (2008). Melatonin ameliorates oxidative stress, inflammation, proteinuria, and progression of renal damage in rats with renal mass reduction. Am J Physiol Renal Physiol 294:336–44
  • Rajadurai M, Stanely Mainzen Prince P. (2006). Preventive effect of naringin on lipid peroxides and antioxidants in isoproterenol-induced cardiotoxicity in Wistar rats: biochemical and histopathological evidences. Toxicology 228:259–68
  • Reilly ME, Patel VB, Peters TJ, Preedy VR. (2000). In vivo rates of skeletal muscle protein synthesis in rats are decreased by acute ethanol treatment but are not ameliorated by supplemental alpha-tocopherol. J Nutr 130:3045–9
  • Richman JM, Liu SS, Courpas G, et al. (2006). Does continuous peripheral nerve block provide superior pain control to opioids? A meta-analysis. Anesth Analg 102:248–57
  • Rodriguez DA, Kalko S, Puig-Vilanova E, et al. (2012). Muscle and blood redox status after exercise training in severe COPD patients. Free Radic Biol Med 52:88–94
  • Rossi R, Milzani A, Dalle-Donne I, et al. (2002). Blood glutathione disulfide: in vivo factor or in vitro artifact? Clin Chem 48:742–53
  • Sahin S, Oter S, Burukoğlu D, Sutken E. (2013). The effects of carnosine in an experimental rat model of septic shock. Med Sci Monit Basic Res 19:54–61
  • Salehi I, Mohammadi M, Mirzaei F, Soufi FG. (2012). Amlodipine attenuates oxidative stress in the heart and blood of high-cholesterol diet rabbits. Cardiovasc J Afr 23:18–22
  • Saoudi M, Abdelmouleh A, Kammoun W, et al. (2008). Toxicity assessment of the puffer fish Lagocephalus lagocephalus from the Tunisian coast. C R Biol 331:611–16
  • Sen V, Güzel A, Selimoğlu Şen H, et al. (2014). Preventive effects of dexmedetomidine on the liver in a rat model of acid-induced acute lung injury. Biomed Res Int 2014:621827
  • Sheehy PJ, Morrissey PA, Flynn A. (1993). Influence of heated vegetable oils and alpha-tocopheryl acetate supplementation on alpha-tocopherol, fatty acids and lipid peroxidation in chicken muscle. Br Poult Sci 34:367–81
  • Shukla K, Dikshit P, Tyagi MK, et al. (2012). Ameliorative effect of Withania coagulans on dyslipidemia and oxidative stress in nicotinamide-streptozotocin induced diabetes mellitus. Food Chem Toxicol 50:3595–9
  • Sibel S, Enis YM, Hüseyin S, et al. (2014). Analysis of grayanatoxin in Rhododendron honey and effect on antioxidant parameters in rats. J Ethnopharmacol 156:155--61. pii: S0378-8741(14)00621-7
  • Singh AK, Pandey SK, Naresh Kumar G. (2014). Pyrroloquinoline quinone-secreting probiotic Escherichia coli Nissle 1917 ameliorates ethanol-induced oxidative damage and hyperlipidemia in rats. Alcohol Clin Exp Res 38:2127–37
  • Sohal RS, Orr WC. (2012). The redox stress hypothesis of aging. Free Radic Biol Med 52:539–55
  • Sudhahar V, Kumar SA, Varalakshmi P. (2006). Role of lupeol and lupeol linoleate on lipemic-oxidative stress in experimental hypercholesterolemia. Life Sci 78:1329–35
  • Sumien N, Forster MJ, Sohal RS. (2003). Supplementation with vitamin E fails to attenuate oxidative damage in aged mice. Exp Gerontol 38:699–704
  • Sun F, Iwaguchi K, Shudo R, et al. (1999). Change in tissue concentrations of lipid hydroperoxides, vitamin C and vitamin E in rats with streptozotocin-induced diabetes. Clin Sci (Lond) 96:185–90
  • Sun Q, Kang Z, Cai J, et al. (2009). Hydrogen-rich saline protects myocardium against ischemia/reperfusion injury in rats. Exp Biol Med (Maywood) 234:1212–19
  • Taleb-Senouci D, Ghomari H, Krouf D, et al. (2009). Antioxidant effect of Ajuga iva aqueous extract in streptozotocin-induced diabetic rats. Phytomedicine 16:623–31
  • Tanaka K, Hashimoto T, Tokumaru S, et al. (1997). Interactions between vitamin C and vitamin E are observed in tissues of inherently scorbutic rats. J Nutr 127:2060–4
  • Tandon N, Roy M, Roy S, Gupta N. (2012). Protective effect of Psidium guajava in arsenic-induced oxidative stress and cytological damage in rats. Toxicol Int 19:245–9
  • Tas S, Sarandol E, Ayvalik SZ, et al. (2007). Vanadyl sulfate, taurine, and combined vanadyl sulfate and taurine treatments in diabetic rats: effects on the oxidative and antioxidative systems. Arch Med Res 38:276–83
  • Tasanarong A, Kongkham S, Itharat A. (2014). Antioxidant effect of Phyllanthus emblica extract prevents contrast-induced acute kidney injury. BMC Complement Altern Med 14:138
  • Terada Y, Okura Y, Kikusui T, Takenaka A. (2011). Dietary vitamin E deficiency increases anxiety-like behavior in juvenile and adult rats. Biosci Biotechnol Biochem 75:1894–9
  • Tomlinson CW, Godin DV, Rabkin SW. (1985). Adriamycin cardiomyopathy: implications of cellular changes in a canine model with mild impairment of left ventricular function. Biochem Pharmacol 34:4033–41
  • Turedi S, Yilmaz SE, Mentese A, et al. (2013). The diagnostic value of serum ischemia-modified albumin levels in experimentally induced carbon monoxide poisoning and their correlation with poisoning severity. Acad Emerg Med 20:652–8
  • Uthus EO, Yokoi K, Davis CD. (2002). Selenium deficiency in Fisher-344 rats decreases plasma and tissue homocysteine concentrations and alters plasma homocysteine and cysteine redox status. J Nutr 132:1122–8
  • Valko M, Leibfritz D, Moncol J, et al. (2007). Free radicals and antioxidants in normal physiological functions and human disease. Int J Biochem Cell Biol 39:44–84
  • Van der Loo B, Bachschmid M, Spitzer V, et al. (2003). Decreased plasma and tissue levels of vitamin C in a rat model of aging: implications for antioxidative defense. Biochem Biophys Res Commun 303:483–7
  • Vázquez-Medina JP, Crocker DE, Forman HJ, Ortiz RM. (2010). Prolonged fasting does not increase oxidative damage or inflammation in postweaned northern elephant seal pups. J Exp Biol 213:2524–30
  • Vennila L, Pugalendi KV. (2010). Protective effect of sesamol against myocardial infarction caused by isoproterenol in Wistar rats. Redox Rep 15:36–42
  • Veskoukis AS, Kyparos A, Nikolaidis MG, et al. (2012). The antioxidant effects of a polyphenol-rich grape pomace extract in vitro do not correspond in vivo using exercise as an oxidant stimulus. Oxid Med Cell Longev 2012:185867
  • Veskoukis AS, Nikolaidis MG, Kyparos A, et al. (2008). Effects of xanthine oxidase inhibition on oxidative stress and swimming performance in rats. Appl Physiol Nutr Metab 33:1140–54
  • Veskoukis AS, Nikolaidis MG, Kyparos A, Kouretas D. (2009). Blood reflects tissue oxidative stress depending on biomarker and tissue studied. Free Radic Biol Med 47:1371–4
  • Voljc M, Frankic T, Levart A, et al. (2011). Evaluation of different vitamin E recommendations and bioactivity of α-tocopherol isomers in broiler nutrition by measuring oxidative stress in vivo and the oxidative stability of meat. Poult Sci 90:1478–88
  • Vollaard NB, Shearman JP, Cooper CE. (2005). Exercise-induced oxidative stress: myths, realities and physiological relevance. Sports Med 35:1045–62
  • Yonar ME. (2013). Protective effect of lycopene on oxidative stress and antioxidant status in Cyprinus carpio during cypermethrin exposure. Environ Toxicol 28:609–16
  • Yonar ME, Yonar SM, Çoban MZ, Eroğlu M. (2014). Antioxidant effect of propolis against exposure to chromium in Cyprinus carpio. Environ Toxicol 29:155–64
  • You T, Goldfarb AH, Bloomer RJ, et al. (2005). Oxidative stress response in normal and antioxidant supplemented rats to a downhill run: changes in blood and skeletal muscles. Can J Appl Physiol 30:677–89
  • Yousef MI, Saad AA, El-Shennawy LK. (2009). Protective effect of grape seed proanthocyanidin extract against oxidative stress induced by cisplatin in rats. Food Chem Toxicol 47:1176–83
  • Zhang T, Gao J, Jin ZY, et al. (2014). Protective effects of polysaccharides from Lilium lancifolium on streptozotocin-induced diabetic mice. Int J Biol Macromol 65:436–40
  • Zhong R, Xiao W, Ren G, et al. (2011). Dietary tea catechin inclusion changes plasma biochemical parameters, hormone concentrations and glutathione redox status in goats. Asian-Aust J Anim Sci 24:1681–9
  • Zhu MJ, Sun LJ, Liu YQ, et al. (2008). Blood F2-isoprostanes are significantly associated with abnormalities of lipid status in rats with steatosis. World J Gastroenterol 14:4677–83

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