Supplementation with n-acetylcysteine and taurine failed to restore glutathione content in liver of streptozotocin-induced diabetics rats but protected from oxidative stress

Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman's reagent

Sedlak, J., & Lindsay, R. H. (1968) · Analytical Biochemistry · doi:10.1016/0003-2697(68)90092-4 · Cited by 8,092 · see citing works

[49] Determination of carbonyl content in oxidatively modified proteins

Levine, R. L., Garland, D. L., Oliver, C. N., Amici, A., Climent, I., Lenz, A.-G., Ahn, B. W., Shaltiel, S., & Stadtman, E. R. (1990) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(90)86141-h · Cited by 5,895 · see citing works

GLUTATHIONE

Meister, A., & Anderson, M. E. (1983) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.52.070183.003431 · Cited by 5,694 · see citing works

[43] Malondialdehyde determination as index of lipid Peroxidation

Draper, H. H., & Hadley, M. (1990) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(90)86135-i · Cited by 4,291 · see citing works

Advanced glycation end-products: A review

Singh, R., Barden, A., Mori, T., & Beilin, L. (2001) · Diabetologia · doi:10.1007/s001250051591 · Cited by 2,597 · see citing works

The antioxidant action of N-acetylcysteine: Its reaction with hydrogen peroxide, hydroxyl radical, superoxide, and hypochlorous acid

Aruoma, O. I., Halliwell, B. B., Hoey, B. M., & Butler, J. (1989) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(89)90066-x · Cited by 1,774 · see citing works

Glutathione and its role in cellular functions

Sies, H. (1999) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(99)00177-x · Cited by 1,735 · see citing works

Efficacy of Oral N-Acetylcysteine in the Treatment of Acetaminophen Overdose

Smilkstein, M. J., Knapp, G. L., Kulig, K. W., & Rumack, B. H. (1988) · New England Journal of Medicine · doi:10.1056/nejm198812153192401 · Cited by 1,102 · see citing works

The antioxidant action of taurine, hypotaurine and their metabolic precursors

Aruoma, O. I., Halliwell, B. B., Hoey, B. M., & Butler, J. (1988) · Biochemical Journal · doi:10.1042/bj2560251 · Cited by 580 · see citing works

TAURINE: BIOLOGICAL UPDATE

Wright, C. E., Tallan, H. H., Lin, Y. Y., & Gaull, G. E. (1986) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.55.070186.002235 · Cited by 575 · see citing works

High-performance liquid chromatography of thiols and disulfides: Dinitrophenol derivatives

Fariss, M. W., & Reed, D. J. (1987) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(87)43018-8 · Cited by 505 · see citing works

Simultaneous determination of tocopherols, ubiquinols, and ubiquinones in blood, plasma, tissue homogenates, and subcellular fractions

Lang, J. K., Gohil, K., & Packer, L. (1986) · Analytical Biochemistry · doi:10.1016/0003-2697(86)90203-4 · Cited by 493 · see citing works

Cloning and expression of cDNA for rat heme oxygenase.

Shibahara, S., Müller, R., Taguchi, H., & Yoshida, T. (1985) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.82.23.7865 · Cited by 452 · see citing works

Lipid peroxidation and activity of antioxidant enzymes in diabetic rats

Kakkar, R., Kalra, J., Mantha, S. V., & Prasad, K. (1995) · Molecular and Cellular Biochemistry · doi:10.1007/bf01322333 · Cited by 395 · see citing works

Xanthine Oxidase Is Involved in Free Radical Production in Type 1 Diabetes

Desco, C., Asensi, M. A., Márquez, R., Martínez-Valls, J. F., Vento, M., Pallardó, F. V., Sastre, J., & Viña, J. (2002) · Diabetes · doi:10.2337/diabetes.51.4.1118 · Cited by 391 · see citing works

Elevated Levels of Authentic Plasma Hydroperoxides in NIDDM

Nourooz‐Zadeh, J., Tajaddini-Sarmadi, J., McCarthy, S., Betteridge, D. J., & Wolff, S. P. (1995) · Diabetes · doi:10.2337/diab.44.9.1054 · Cited by 282 · see citing works

Lung Protection by a Thiol-Containing Antioxidant: N-Acetylcysteine

Moldéus, P., Cotgreave, I. A., & Berggren, M. M. (2009) · Respiration · doi:10.1159/000195086 · Cited by 262 · see citing works

Blood Glutathione Disulfide: In Vivo Factor or in Vitro Artifact?

Rossi, R., Milzani, A., Dalle‐Donne, I., Giustarini, D., Lusini, L., Colombo, R., & Simplicio, P. D. (2002) · Clinical Chemistry · doi:10.1093/clinchem/48.5.742 · Cited by 254 · see citing works

N-Acetylcysteine and glutathione as inhibitors of tumor necrosis factor production

Peristeris, P., Clark, B. D., Gatti, S., Faggioni, R., Mantovani, A., Mengozzi, M., Orencole, S. F., Sironi, M., & Ghezzi, P. (1992) · Cellular Immunology · doi:10.1016/0008-8749(92)90205-4 · Cited by 236 · see citing works

Impaired antioxidant status in diabetic rat liver

Saxena, A. K., Srivastava, P., Kale, R. K., & Baquer, N. Z. (1993) · Biochemical Pharmacology · doi:10.1016/0006-2952(93)90124-f · Cited by 211 · see citing works

[23] Ratio of reduced to oxidized glutathione as indicator of oxidative stress status and DNA damage

Asensi, M. A., Sastre, J., Pallardó, F. V., Lloret, A., Lehner, M., de la Asunción, J. G., & Viña, J. (1999) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(99)99026-2 · Cited by 193 · see citing works

Antioxidant enzyme status in biliary obstructed rats: effects of N-acetylcysteine

Pastor, A., Collado, P. S., Almar, M., & González‐Gallego, J. (1997) · Journal of Hepatology · doi:10.1016/s0168-8278(97)80183-3 · Cited by 156 · see citing works

Role of Oxygen in Cross-Linking and Chemical Modification of Collagen by Glucose

Fu, M.-X., Wells‐Knecht, K. J., Thorpe, S. R., & Baynes, J. (1992) · Diabetes · doi:10.2337/diab.41.2.s42 · Cited by 149 · see citing works

Tumor Necrosis Factor Increases Hepatocellular Glutathione by Transcriptional Regulation of the Heavy Subunit Chain of γ-Glutamylcysteine Synthetase

Morales, A., García‐Ruiz, C., Miranda, M., Marı́, M., Colell, A., Ardite, E., & Fernández-Checa, J. C. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.48.30371 · Cited by 144 · see citing works

Increased Transcription of the Regulatory Subunit of γ-Glutamylcysteine Synthetase in Rat Lung Epithelial L2 Cells Exposed to Oxidative Stress or Glutathione Depletion

Tian, L., Shi, M. M., & Forman, H. J. (1997) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1997.9997 · Cited by 142 · see citing works

Long Exposure to High Glucose Concentration Impairs the Responsive Expression of γ-Glutamylcysteine Synthetase by Interleukin-1β and Tumor Necrosis Factor-α in Mouse Endothelial Cells

Urata, Y., Yamamoto, H., Goto, S., Tsushima, H., 赤澤昭一, Yamashita, S., Nagataki, S., & Kondo, T. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.25.15146 · Cited by 133 · see citing works

Mechanisms of endotoxin-induced haem oxygenase mRNA accumulation in mouse liver: synergism by glutathione depletion and protection by N-acetylcysteine

Rizzardini, M., Carelli, M., Porras, M. R. C., & Cantoni, L. (1994) · Biochemical Journal · doi:10.1042/bj3040477 · Cited by 103 · see citing works

Age-dependent increase of heme oxygenase–1 gene expression in the liver mediated by NFκB

Lavrovsky, Y., Song, C. S., Chatterjee, B., & Roy, A. K. (2000) · Mechanisms of Ageing and Development · doi:10.1016/s0047-6374(00)00087-7 · Cited by 84 · see citing works

Regulation of cysteine dioxygenase and γ-glutamylcysteine synthetase is associated with hepatic cysteine level

Lee, J.-I., Londono, M. P., Hirschberger, L. L., & Stipanuk, M. H. (2004) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2003.10.005 · Cited by 84 · see citing works

Lipid peroxidation, glutathione levels and changes in glutathione‐related enzyme activities in streptozotocin‐induced diabetic rats

Mukherjee, B., MUKHERJEE, J. R., & Chatterjee, M. (1994) · Immunology and Cell Biology · doi:10.1038/icb.1994.17 · Cited by 80 · see citing works

Effects of nonsulfur and sulfur amino acids on the regulation of hepatic enzymes of cysteine metabolism

Bella, D. L., Hahn, C., & Stipanuk, M. H. (1999) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1999.277.1.e144 · Cited by 76 · see citing works

Beta-carotene suppresses UVA-induced HO-1 gene expression in cultured FEK4

Trekli, M. C., Riss, G., Góralczyk, R., & Tyrrell, R. M. (2003) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(02)01303-5 · Cited by 49 · see citing works

Isolation and characterization of a cDNA for rat liver cysteine dioxygenase

Hosokawa, Y., Matsumoto, A., Oka, J., Itakura, H., & Yamaguchi, K. (1990) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(90)92345-z · Cited by 49 · see citing works

Renal Cortical Expression of mRNAs for Antioxidant Enzymes in Normal and Diabetic Rats

Reddi, A. S., & Bollineni, J. S. (1997) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1997.6836 · Cited by 48 · see citing works

Protective effect of N-acetylcysteine on reduced glutathione, reduced glutathione-related enzymes and lipid peroxidation in methanol intoxication

Skrzydlewska, E., & Farbiszewski, R. (1999) · Drug and Alcohol Dependence · doi:10.1016/s0376-8716(99)00040-x · Cited by 47 · see citing works

Lipoperoxidation in hepatic subcellular compartments of diabetic rats

Traverso, N., Menini, S., Odetti, P. R., Pronzato, M. A., Cottalasso, D., & Marinari, U. M. (1999) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(98)00238-x · Cited by 42 · see citing works

Effects of Antihypertensive Drugs or Glycemic Control on Antioxidant Enzyme Activities in Spontaneously Hypertensive Rats with Diabetes

Tang, Z. Z., Shou, I., Wang, L. N., Fukui, M., & Tomino, Y. (2008) · The Nephron journals/Nephron journals · doi:10.1159/000190199 · Cited by 25 · see citing works

Decrease of Rat Liver Cysteine Dioxygenase (Cysteine Oxidase) Activity Mediated by Glucagon

Hosokawa, Y., Yamaguchi, K., Kohashi, N., Yoshihiko, K. O. R. I., & Ueda, I. (1978) · The Journal of Biochemistry · doi:10.1093/oxfordjournals.jbchem.a132142 · Cited by 22 · see citing works

Effect of Acute Ethanol Administration on S-Amino Acid Metabolism: Increased Utilization of Cysteine for Synthesis of Taurine Rather Than Glutathione

Jung, Y. S., Kwak, H. E., Choi, K., & Kim, Y. C. (2003) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-0077-3_31 · Cited by 11 · see citing works

Protective Effect of Oral Acetylcysteine against the Hepatorenal Toxicity of Carbon Tetrachloride Potentiated by Ethyl Alcohol

Simko, V., Michael, S., Katz, J., Oberstein, E., & Popescu, A. (1992) · Alcoholism Clinical and Experimental Research · doi:10.1111/j.1530-0277.1992.tb00681.x · Cited by 10 · see citing works

Functions of ROS in Macrophages and Antimicrobial Immunity

Herb, M., & Schramm, M. (2021) · Antioxidants · doi:10.3390/antiox10020313 · Cited by 633 · see citing works

The central role of glutathione in the pathophysiology of human diseases

Franco, R., Schoneveld, O., Pappa, A., & Panayiotidis, M. I. (2007) · Archives of Physiology and Biochemistry · doi:10.1080/13813450701661198 · Cited by 536 · see citing works

N-Acetyl Cysteine Functions as a Fast-Acting Antioxidant by Triggering Intracellular H2S and Sulfane Sulfur Production

Ezeriņa, D., Takano, Y., Hanaoka, K., Urano, Y., & Dick, T. P. (2018) · Cell chemical biology · doi:10.1016/j.chembiol.2018.01.011 · Cited by 405 · see citing works

Role of antioxidant activity of taurine in diabetesThis article is one of a selection of papers from the NATO Advanced Research Workshop on Translational Knowledge for Heart Health (published in part 1 of a 2-part Special Issue).

Schaffer, S. W., AZUMA, J., & Mozaffari, M. S. (2009) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y08-110 · Cited by 307 · see citing works

Long-Term N-Acetylcysteine and l -Arginine Administration Reduces Endothelial Activation and Systolic Blood Pressure in Hypertensive Patients With Type 2 Diabetes

Martina, V., Masha, A., Gigliardi, V. R., Brocato, L., Manzato, E., Berchio, A., Massarenti, P., Settanni, F., Casa, L. D., Bergamini, S., et al. (2008) · Diabetes Care · doi:10.2337/dc07-2251 · Cited by 137 · see citing works

Impact of Supplementary Amino Acids, Micronutrients, and Overall Diet on Glutathione Homeostasis

Gould, R. L., & Pazdro, R. (2019) · Nutrients · doi:10.3390/nu11051056 · Cited by 134 · see citing works

The role of antioxidants and other agents in alleviating hyperglycemia mediated oxidative stress and injury in liver

Dey, A., & Lakshmanan, J. (2013) · Food & Function · doi:10.1039/c3fo30317a · Cited by 133 · see citing works

Hypoglycaemic, antioxidative and nephroprotective effects of taurine in alloxan diabetic rabbits

Winiarska, K., Szymanski, K., Górniak, P., Dudziak, M., & Bryła, J. (2008) · Biochimie · doi:10.1016/j.biochi.2008.09.006 · Cited by 115 · see citing works

Taurine supplementation and diabetes mellitus

Franconi, F., Loizzo, A., Ghirlanda, G., & Seghieri, G. (2005) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/01.mco.0000196141.65362.46 · Cited by 95 · see citing works

Reactive Oxygen Species: Not Omnipresent but Important in Many Locations

Herb, M., Gluschko, A., & Schramm, M. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.716406 · Cited by 88 · see citing works

Glutathione depletion activates mitogen-activated protein kinase (MAPK) pathways that display organ-specific responses and brain protection in mice

Limón-Pacheco, J. H., Hernández, N. A. H., Fanjul‐Moles, M. L., & Gonsebatt, M. E. (2007) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2007.06.028 · Cited by 82 · see citing works

Dietary flaxseed oil and fish oil modulates expression of antioxidant and inflammatory genes with alleviation of protein glycation status and inflammation in liver of streptozotocin–nicotinamide induced diabetic rats

Jangale, N. M., Devarshi, P. P., Dubal, A. A., Ghule, A. E., Koppikar, S. J., Bodhankar, S. L., Chougale, A. D., Kulkarni, M. J., & Harsulkar, A. (2013) · Food Chemistry · doi:10.1016/j.foodchem.2013.03.001 · Cited by 76 · see citing works

Nutrient Metabolism, Subcellular Redox State, and Oxidative Stress in Pancreatic Islets and β-Cells

Roma, L. P., & Jonas, J. (2019) · Journal of Molecular Biology · doi:10.1016/j.jmb.2019.10.012 · Cited by 75 · see citing works

A Diterpenoid, 14-Deoxy-11, 12-Didehydroandrographolide, in Andrographis paniculata Reduces Steatohepatitis and Liver Injury in Mice Fed a High-Fat and High-Cholesterol Diet

Liu, Y.-T., Chen, H., Lii, C., Jhuang, J.-H., Huang, C., Li, M., & Yao, H. (2020) · Nutrients · doi:10.3390/nu12020523 · Cited by 67 · see citing works

Effects of lemongrass oil and citral on hepatic drug-metabolizing enzymes, oxidative stress, and acetaminophen toxicity in rats

Li, C., Yu, H.-F., Chang, C.-H., Liu, Y.-T., & Yao, H. (2017) · Journal of Food and Drug Analysis · doi:10.1016/j.jfda.2017.01.008 · Cited by 59 · see citing works

Taurine Prevents Oxidative Damage of High Glucose-Induced Cataractogenesis in Isolated Rat Lenses

Hee-Young, S. O. N., Kim, H., & Kwon, Y. H. (2007) · Journal of Nutritional Science and Vitaminology · doi:10.3177/jnsv.53.324 · Cited by 55 · see citing works

Sparing of Methionine Requirements: Evaluation of Human Data Takes Sulfur Amino Acids Beyond Protein

Fukagawa, N. K. (2006) · Journal of Nutrition · doi:10.1093/jn/136.6.1676s · Cited by 54 · see citing works

Role of Nrf2, HO-1 and GSH in Neuroblastoma Cell Resistance to Bortezomib

Furfaro, A. L., Piras, S., Domenicotti, C., Fenoglio, D., Luigi, A. D., Salmona, M., Moretta, L., Marinari, U. M., Pronzato, M. A., Traverso, N., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0152465 · Cited by 52 · see citing works

Sulfane sulfur – new findings on an old topic

Iciek, M., Bilska‐Wilkosz, A., & Górny, M. (2019) · Acta Biochimica Polonica · doi:10.18388/abp.2019_2909 · Cited by 52 · see citing works

Effect of taurine supplementation on cytochrome P450 2E1 and oxidative stress in the liver and kidneys of rats with streptozotocin-induced diabetes

Yao, H., Lin, P., Chang, Y.-W., Chen, C., Chiang, M., Chang, L., Kuo, Y.-C., Tsai, H.-T., & Yeh, T. (2009) · Food and Chemical Toxicology · doi:10.1016/j.fct.2009.04.030 · Cited by 50 · see citing works

N-Acetyl-L-Cysteine Protects Liver and Kidney Against Chromium(VI)-Induced Oxidative Stress in Mice

Boşgelmez, İ. İ., & Güvendik, G. (2016) · Biological Trace Element Research · doi:10.1007/s12011-016-0901-2 · Cited by 49 · see citing works

Taurine attenuates maternal and embryonic oxidative stress in a streptozotocin-diabetic rat model

Shivananjappa, M. M., & ., M. (2012) · Reproductive BioMedicine Online · doi:10.1016/j.rbmo.2012.01.016 · Cited by 41 · see citing works

N-Acetylcysteine Serves as Substrate of 3-Mercaptopyruvate Sulfurtransferase and Stimulates Sulfide Metabolism in Colon Cancer Cells

Zuhra, K., Tomé, C. S., Masi, L., Giardina, G., Paulini, G., Malagrinò, F., Forte, E., Vicente, J. B., & Giuffrè, A. (2019) · Cells · doi:10.3390/cells8080828 · Cited by 37 · see citing works

Cocoa intake ameliorates hepatic oxidative stress in young Zucker diabetic fatty rats

Cordero‐Herrera, I., Martín, M. Á., Goya, L., & Ramos, S. (2015) · Food Research International · doi:10.1016/j.foodres.2014.12.039 · Cited by 35 · see citing works

Cysteine becomes conditionally essential during hypobaric hypoxia and regulates adaptive neuro-physiological responses through CBS/H2S pathway

Mishra, S., Kumar, G., Chhabra, A., Sethy, N. K., Jain, N. F., Meena, R. N., Tulsawani, R., Prasad, D. N., Kumar, B., & Sharma, M. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2020.165769 · Cited by 34 · see citing works

Changes in Prooxidant–Antioxidant Balance in Tissues of Rats Following Long-term Hyperglycemic Status

Karaağaç, N., Salman, F., Doğru‐Abbasoğlu, S., & Uysal, M. (2011) · Endocrine Research · doi:10.3109/07435800.2011.566237 · Cited by 21 · see citing works

Melatonin is more effective than taurine and 5‐hydroxytryptophan against hyperglycemia‐induced kidney‐cortex tubules injurya

Derlacz, R., Śliwińska, M. A., Piekutowska, A., Winiarska, K., Drożak, J., & Bryła, J. (2006) · Journal of Pineal Research · doi:10.1111/j.1600-079x.2006.00405.x · Cited by 20 · see citing works

Chitosan oligosaccharides reduce acetaminophen-induced hepatotoxicity by suppressing CYP-mediated bioactivation

Yao, H., Luo, M.-N., & Li, C. (2014) · Journal of Functional Foods · doi:10.1016/j.jff.2014.11.014 · Cited by 17 · see citing works

Beyond Protein Building Blocks: A Review of Biological Roles and Therapeutic Potential of Free Amino Acids

Petkova, D., Stoyanova, S., Dinkov, G., & Bogdanov, M. G. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262311264 · Cited by 16 · see citing works

N-acetylcysteine treatment mitigates loss of cortical parvalbumin-positive interneuron and perineuronal net integrity resulting from persistent oxidative stress in a rat TBI model

Hameed, M. Q., Hodgson, N., Lee, H. H. C., Pascual-Leone, A., MacMullin, P., Jannati, A., Dhamne, S. C., Hensch, T. K., & Rotenberg, A. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac327 · Cited by 14 · see citing works

Beneficial effects of N -acetylcysteine on hepatic oxidative stress in streptozotocin-induced diabetic rats

Rosa, L. R. D. O., Kaga, A. K., Barbanera, P. O., Queiroz, P. M., do Carmo, N. O. L., & Fernandes, A. A. H. (2018) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2017-0559 · Cited by 13 · see citing works

Targeting Thioredoxin Reductase by Ibrutinib Promotes Apoptosis of SMMC-7721 Cells

Han, X., Zhang, J., Shi, D., Wu, Y., Liu, R., Liu, T., Xu, J., Yao, X., & Fang, J. (2019) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.118.254862 · Cited by 12 · see citing works

Effects of Bu-Zhong-Yi-Qi-Tang on hepatic drug-metabolizing enzymes and plasma tolbutamide concentration in rats

Yao, H., Chang, Y.-W., Uramaru, N., Watanabe, Y., Kitamura, S., Kuo, Y., Lii, C., & Yeh, T. (2012) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2012.04.024 · Cited by 10 · see citing works

Hydrogen sulfide: From a toxic gas to a potential therapy for COVID-19 and inflammatory disorders

Kumar, M. (2023) · Nitric Oxide · doi:10.1016/j.niox.2023.08.002 · Cited by 4 · see citing works

The Protective Effect of N-acetylcysteine against Deltamethrin-Induced Hepatotoxicity in Mice

Ameri, A., Rahmati, A., Soroushfar, S., Lalehzari, M., Dehghani, T., Haghi‐Aminjan, H., Shamseddin, J., & Omidi, M. (2024) · Avicenna Journal of Medical Biotechnology · doi:10.18502/ajmb.v16i2.14859 · Cited by 3 · see citing works

Egg white-derived metabolic regulatory peptide AD-IR10 promotes diabetic wound healing via Keap1/Nrf2/Irg1-mediated macrophage metabolic reprogramming

Sun, D., Su, T., Niu, X., He, Y., Wang, X., Sumampouw, F., Wu, C., Lu, F., Chang, Q., & Dong, Z. (2026) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2026.03.005 · Cited by 2 · see citing works

Voltage dependent anion channel and its interaction with N-acetyl-L-Cysteine (NAC) under oxidative stress on planar lipid bilayer

Siddiqui, S. I., Malik, C., & Ghosh, S. (2023) · Biochimie · doi:10.1016/j.biochi.2023.02.005 · Cited by 2 · see citing works

Evaluation of the Actions of Metformin and Taurine, Singly and in Combination, on Metabolic and Oxidative Alterations Caused by Diabetes in Rat Erythrocytes and Plasma

Budhram, R., Pandya, K. G., & Lau‐Cam, C. A. (2015) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-15126-7_21 · Cited by 2 · see citing works

PIKfyve Inhibition Controls Inflammatory Gene Expression Networks and Activates TFEB via Oxidative Stress

Mercer, M. (2024) · doi:10.32920/26052754

PIKfyve Inhibition Controls Inflammatory Gene Expression Networks and Activates TFEB via Oxidative Stress

Mercer, M. (2024) · doi:10.32920/26052754.v1

Antioxidant effects of sulfane sulfur

Hyšpler, R., Tichá, A., & Zadák, Z. (2022) · Klinická biochemie a metabolismus · doi:10.61568/kbm.2022.015

Impaired synthesis contributes to diabetes-induced decrease in liver glutathione

Traverso, N. (2012) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2012.915 · Cited by 35 · see citing works

Beneficial effects of N -acetylcysteine on hepatic oxidative stress in streptozotocin-induced diabetic rats

Rosa, L. R. D. O., Kaga, A. K., Barbanera, P. O., Queiroz, P. M., do Carmo, N. O. L., & Fernandes, A. A. H. (2018) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2017-0559 · Cited by 13 · see citing works

Tissue oxidative stress of diabetic rats treated with N-acetylcysteine

Ribeiro, G. L. (2010) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)

THE EFFECTS OF N-ACETYL-L-CYSTEINE ON OXIDATIVE PARAMETERS in TESTICULAR TISSUE OF STREPTOZOTOCIN INDUCED DIABETIC RATS

BERKTAŞ, Ö. A., & Keskin, A. (2022) · GOBEKLITEPE Saglik Bilimleri Dergisi · doi:10.55433/gsbd.126

Treatment with N-acetylcysteine does not alter blood glucose levels and the oxidative stress status in diabetic rats

de Bairros, A. V., de Freitas, F., Leal, M. B., Mazzanti, C. M. D. A., Moreira, A. P., Morsch, V. M., Ribeiro, G. L., Roehrs, M., & Tonello, R. (2013) · Journal of Pharmaceutical Negative Results · doi:10.4103/0976-9234.116755 · Cited by 2 · see citing works