Category: Health

Glutathione and cellular health

Glutathione and cellular health

Martinou J. Cellular also has been described that γ-glutamylcysteine, Insulin pump technology intermediate of GSH Glutathione and cellular health, Glutathioone able to Glutathione and cellular health as crllular Gpx1 cofactor in mitochondrial H 2 O 2 detoxification, mimicking the physiological properties of GSH Quintana-Cabrera et al. CAS PubMed Google Scholar Marchetti P, Decaudin D, Macho A, Zamzami N, Hirsch T, Susin SA et al. The mechanism of how oral lavender works is a matter of conflict.

Glutathione and cellular health -

Free Radic Biol Med ; 37 : — Armstrong JS, Whiteman M, Yang H, Jones DP, Sternberg Jr P. Cysteine starvation activates the redox-dependent mitochondrial permeability transition in retinal pigment epithelial cells.

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J Biol Chem ; : — Botta D, Franklin CC, White CC, Krejsa CM, Dabrowski MJ, Pierce RH et al. Glutamate-cysteine ligase attenuates TNF-induced mitochondrial injury and apoptosis.

Fan Y, Wu D, Jin L, Yin Z. Human glutamylcysteine synthetase protects HEK cells against UV-induced cell death through inhibition of c-Jun NH2-terminal kinase. Cell Biol Int ; 29 : — Wild AC, Mulcahy RT. Regulation of gamma-glutamylcysteine synthetase subunit gene expression: Insights into transcriptional control of antioxidant defenses.

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Chanas SA, Jiang Q, McMahon M, McWalter GK, McLellan LI, Elcombe CR et al. Loss of the Nrf2 transcription factor causes a marked reduction in constitutive and inducible expression of the glutathione S-transferase Gsta1, Gsta2, Gstm1, Gstm2, Gstm3 and Gstm4 genes in the livers of male and female mice.

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Role of glutathione depletion and reactive oxygen species generation in apoptotic signaling in a human B lymphoma cell line. Cell Death Differ ; 9 : — Franco R, Panayiotidis MI, Cidlowski JA.

Glutathione depletion is necessary for apoptosis in lymphoid cells independent of reactive oxygen species formation. Franco R, Cidlowski JA.

Kirkland RA, Franklin JL. Evidence for redox regulation of cytochrome C release during programmed neuronal death: antioxidant effects of protein synthesis and caspase inhibition. J Neurosci ; 21 : — Wang X, Cederbaum AI. S-adenosyl-L-methionine attenuates hepatotoxicity induced by agonistic Jo2 Fas antibody following CYP2E1 induction in mice.

J Pharmacol Exp Ther ; : 44— Will Y, Kaetzel RS, Brown MK, Fraley TS, Reed DJ. In vivo reversal of glutathione deficiency and susceptibility to in vivo dexamethasone-induced apoptosis by N-acetylcysteine and Loxothiazolidinecarboxylic acid, but not ascorbic acid, in thymocytes from gamma-glutamyltranspeptidase-deficient knockout mice.

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Mitochondrial glutathione protects against cell death induced by oxidative and nitrative stress in astrocytes.

J Neurochem ; : — Xu F, Putt DA, Matherly LH, Lash LH. Modulation of expression of rat mitochondrial 2-oxoglutarate carrier in NRKE cells alters mitochondrial transport and accumulation of glutathione and susceptibility to chemically induced apoptosis. J Pharmacol Exp Ther ; : — Lash LH, Putt DA, Matherly LH.

Protection of NRKE cells, a rat renal proximal tubular cell line, from chemical-induced apoptosis by overexpression of a mitochondrial glutathione transporter. Colell A, Garcia-Ruiz C, Miranda M, Ardite E, Mari M, Morales A et al.

Selective glutathione depletion of mitochondria by ethanol sensitizes hepatocytes to tumor necrosis factor. Gastroenterology ; : — Zhao P, Kalhorn TF, Slattery JT.

Selective mitochondrial glutathione depletion by ethanol enhances acetaminophen toxicity in rat liver. Hepatology ; 36 : — Circu ML, Rodriguez C, Maloney R, Moyer MP, Aw TY. Contribution of mitochondrial GSH transport to matrix GSH status and colonic epithelial cell apoptosis.

Free Radic Biol Med ; 44 : — Blair IA. Endogenous glutathione adducts. Curr Drug Metab ; 7 : — Valko M, Morris H, Cronin MT. Metals, toxicity and oxidative stress.

Curr Med Chem ; 12 : — Hammond CL, Marchan R, Krance SM, Ballatori N. Glutathione export during apoptosis requires functional multidrug resistance-associated proteins.

Cole SP, Deeley RG. Transport of glutathione and glutathione conjugates by MRP1. Trends Pharmacol Sci ; 27 : — Verapamil and its derivative trigger apoptosis through glutathione extrusion by multidrug resistance protein MRP1.

Cancer Res ; 64 : — Marchan R, Hammond CL, Ballatori N. Multidrug resistance-associated protein 1 as a major mediator of basal and apoptotic glutathione release. Biochim Biophys Acta ; : — Li L, Meier PJ, Ballatori N.

Oatp2 mediates bidirectional organic solute transport: a role for intracellular glutathione. Mol Pharmacol ; 58 : — Mahagita C, Grassl SM, Piyachaturawat P, Ballatori N. Am J Physiol Gastrointest Liver Physiol ; : G—G Franklin CC, Krejsa CM, Pierce RH, White CC, Fausto N, Kavanagh TJ.

Caspasedependent cleavage of the glutamate-L-cysteine ligase catalytic subunit during apoptotic cell death. Am J Pathol ; : — Jungas T, Motta I, Duffieux F, Fanen P, Stoven V, Ojcius DM.

Glutathione levels and BAX activation during apoptosis due to oxidative stress in cells expressing wild-type and mutant cystic fibrosis transmembrane conductance regulator. Rana S, Dringen R. Gap junction hemichannel-mediated release of glutathione from cultured rat astrocytes.

Neurosci Lett ; : 45— Circu ML, Stringer S, Rhoads CA, Moyer MP, Aw TY. The role of GSH efflux in staurosporine-induced apoptosis in colonic epithelial cells.

Biochem Pharmacol ; 77 : 76— Paolicchi A, Dominici S, Pieri L, Maellaro E, Pompella A. Glutathione catabolism as a signaling mechanism. Biochem Pharmacol ; 64 : — Karp DR, Shimooku K, Lipsky PE.

Expression of gamma-glutamyl transpeptidase protects ramos B cells from oxidation-induced cell death. Armstrong JS, Jones DP. Glutathione depletion enforces the mitochondrial permeability transition and causes cell death in Bcl-2 overexpressing HL60 cells.

Faseb J ; 16 : — Varghese J, Khandre NS, Sarin A. Caspase-3 activation is an early event and initiates apoptotic damage in a human leukemia cell line. Apoptosis ; 8 : — Sato T, Machida T, Takahashi S, Iyama S, Sato Y, Kuribayashi K et al.

Fas-mediated apoptosome formation is dependent on reactive oxygen species derived from mitochondrial permeability transition in Jurkat cells. J Immunol ; : — Oxidative Bax dimerization promotes its translocation to mitochondria independently of apoptosis.

Faseb J ; 19 : — Brown GC, Borutaite V. Regulation of apoptosis by the redox state of cytochrome c. Vaughn AE, Deshmukh M. Glucose metabolism inhibits apoptosis in neurons and cancer cells by redox inactivation of cytochrome c. Nat Cell Biol ; 10 : — Martin SF, Sawai H, Villalba JM, Hannun YA.

Redox regulation of neutral sphingomyelinase-1 activity in HEK cells through a GSH-dependent mechanism. Lou H, Kaplowitz N.

Glutathione depletion down-regulates tumor necrosis factor alpha-induced NF-kappaB activity via IkappaB kinase-dependent and -independent mechanisms. Voehringer DW, Meyn RE. Redox aspects of Bcl-2 function. Antioxid Redox Signal ; 2 : — Ellerby LM, Ellerby HM, Park SM, Holleran AL, Murphy AN, Fiskum G et al.

Shift of the cellular oxidation-reduction potential in neural cells expressing Bcl J Neurochem ; 67 : — Zimmermann AK, Loucks FA, Schroeder EK, Bouchard RJ, Tyler KL, Linseman DA. Glutathione binding to the Bcl-2 homology-3 domain groove: A molecular basis for Bcl-2 antioxidant function at mitochondria.

Schor NF, Rudin CM, Hartman AR, Thompson CB, Tyurina YY, Kagan VE. Cell line dependence of Bclinduced alteration of glutathione handling. Oncogene ; 19 : — Bojes HK, Datta K, Xu J, Chin A, Simonian P, Nunez G et al. Bcl-xL overexpression attenuates glutathione depletion in FL5. Biochem J ; Pt 2 : — Redox modulation of the apoptogenic activity of thapsigargin.

Ann NY Acad Sci ; : — Chakravarthi S, Jessop CE, Bulleid NJ. The role of glutathione in disulphide bond formation and endoplasmic-reticulum-generated oxidative stress. EMBO Rep ; 7 : — Jessop CE, Bulleid NJ. Glutathione directly reduces an oxidoreductase in the endoplasmic reticulum of mammalian cells.

Cullinan SB, Diehl JA. PERK-dependent activation of Nrf2 contributes to redox homeostasis and cell survival following endoplasmic reticulum stress. McCullough KD, Martindale JL, Klotz LO, Aw TY, Holbrook NJ.

Gadd sensitizes cells to endoplasmic reticulum stress by down-regulating Bcl2 and perturbing the cellular redox state. Mol Cell Biol ; 21 : — Subcellular compartmentalization of glutathione: correlations with parameters of oxidative stress related to genotoxicity.

Mutagenesis ; 21 : — Higuchi Y. Glutathione depletion-induced chromosomal DNA fragmentation associated with apoptosis and necrosis. J Cell Mol Med ; 8 : — Kamada K, Goto S, Okunaga T, Ihara Y, Tsuji K, Kawai Y et al. Nuclear glutathione S-transferase pi prevents apoptosis by reducing the oxidative stress-induced formation of exocyclic DNA products.

Hollins DL, Suliman HB, Piantadosi CA, Carraway MS. Glutathione regulates susceptibility to oxidant-induced mitochondrial DNA damage in human lymphocytes. Free Radic Biol Med ; 40 : — Jones DP. Redefining oxidative stress.

Antioxid Redox Signal ; 8 : — Filomeni G, Aquilano K, Civitareale P, Rotilio G, Ciriolo MR. Activation of c-Jun-N-terminal kinase is required for apoptosis triggered by glutathione disulfide in neuroblastoma cells.

Free Radic Biol Med ; 39 : — Pias EK, Aw TY. Early redox imbalance mediates hydroperoxide-induced apoptosis in mitotic competent undifferentiated PC cells. Ho HY, Cheng ML, Chiu DT. Glucosephosphate dehydrogenase — from oxidative stress to cellular functions and degenerative diseases.

Redox Rep ; 12 : — Ayene IS, Biaglow JE, Kachur AV, Stamato TD, Koch CJ. Mutation in G6PD gene leads to loss of cellular control of protein glutathionylation: Mechanism and implication. J Cell Biochem ; : — Fico A, Paglialunga F, Cigliano L, Abrescia P, Verde P, Martini G et al. Glucosephosphate dehydrogenase plays a crucial role in protection from redox-stress-induced apoptosis.

Cell Death Differ ; 11 : — Gendron MC, Schrantz N, Metivier D, Kroemer G, Maciorowska Z, Sureau F et al. Oxidation of pyridine nucleotides during Fas- and ceramide-induced apoptosis in Jurkat cells: Correlation with changes in mitochondria, glutathione depletion, intracellular acidification and caspase 3 activation.

Banki K, Hutter E, Colombo E, Gonchoroff NJ, Perl A. Glutathione levels and sensitivity to apoptosis are regulated by changes in transaldolase expression. Delgado-Esteban M, Almeida A, Bolanos JP. D-Glucose prevents glutathione oxidation and mitochondrial damage after glutamate receptor stimulation in rat cortical primary neurons.

J Neurochem ; 75 : — Han D, Hanawa N, Saberi B, Kaplowitz N. Hydrogen peroxide and redox modulation sensitize primary mouse hepatocytes to TNF-induced apoptosis.

Free Radic Biol Med ; 41 : — Minich T, Riemer J, Schulz JB, Wielinga P, Wijnholds J, Dringen R. The multidrug resistance protein 1 Mrp1 , but not Mrp5, mediates export of glutathione and glutathione disulfide from brain astrocytes.

J Neurochem ; 97 : — Ryter SW, Kim HP, Hoetzel A, Park JW, Nakahira K, Wang X et al. Mechanisms of cell death in oxidative stress. Antioxid Redox Signal ; 9 : 49— Arthur JR. The glutathione peroxidases.

Cell Mol Life Sci ; 57 : — Kayanoki Y, Fujii J, Islam KN, Suzuki K, Kawata S, Matsuzawa Y et al. The protective role of glutathione peroxidase in apoptosis induced by reactive oxygen species.

J Biochem ; : — Yan W, Chen X. GPX2, a direct target of p63, inhibits oxidative stress-induced apoptosis in a pdependent manner. Crack PJ, Taylor JM, Flentjar NJ, de Haan J, Hertzog P, Iannello RC et al.

J Neurochem ; 78 : — Gouaze V, Mirault ME, Carpentier S, Salvayre R, Levade T, Andrieu-Abadie N. Glutathione peroxidase-1 overexpression prevents ceramide production and partially inhibits apoptosis in doxorubicin-treated human breast carcinoma cells.

Mol Pharmacol ; 60 : — Faucher K, Rabinovitch-Chable H, Cook-Moreau J, Barriere G, Sturtz F, Rigaud M. Overexpression of human GPX1 modifies Bax to Bcl-2 apoptotic ratio in human endothelial cells. Mol Cell Biochem ; : 81— Ran Q, Liang H, Gu M, Qi W, Walter CA, Roberts 2nd LJ et al.

Transgenic mice overexpressing glutathione peroxidase 4 are protected against oxidative stress-induced apoptosis. Ran Q, Gu M, Van Remmen H, Strong R, Roberts JL, Richardson A.

Glutathione peroxidase 4 protects cortical neurons from oxidative injury and amyloid toxicity. J Neurosci Res ; 84 : — Seiler A, Schneider M, Forster H, Roth S, Wirth EK, Culmsee C et al. Cell Metab ; 8 : — Savaskan NE, Borchert A, Brauer AU, Kuhn H. Role for glutathione peroxidase-4 in brain development and neuronal apoptosis: Specific induction of enzyme expression in reactive astrocytes following brain injury.

Free Radic Biol Med ; 43 : — Nomura K, Imai H, Koumura T, Kobayashi T, Nakagawa Y. Mitochondrial phospholipid hydroperoxide glutathione peroxidase inhibits the release of cytochrome c from mitochondria by suppressing the peroxidation of cardiolipin in hypoglycaemia-induced apoptosis.

Shen HM, Pervaiz S. TNF receptor superfamily-induced cell death: Redox-dependent execution. Faseb J ; 20 : — Devadas S, Hinshaw JA, Zaritskaya L, Williams MS. Fas-stimulated generation of reactive oxygen species or exogenous oxidative stress sensitize cells to Fas-mediated apoptosis.

Free Radic Biol Med ; 35 : — Gouaze V, Andrieu-Abadie N, Cuvillier O, Malagarie-Cazenave S, Frisach MF, Mirault ME et al. Glutathione peroxidase-1 protects from CDinduced apoptosis. Bajt ML, Ho YS, Vonderfecht SL, Jaeschke H.

Reactive oxygen as modulator of TNF and fas receptor-mediated apoptosis in vivo : studies with glutathione peroxidase-deficient mice. Antioxid Redox Signal ; 4 : — Han YH, Kim SZ, Kim SH, Park WH. Apoptosis in pyrogallol-treated Calu-6 cells is correlated with the changes of intracellular GSH levels rather than ROS levels.

Lung Cancer ; 59 : — Jacobson MD, Raff MC. Programmed cell death and Bcl-2 protection in very low oxygen. Nature ; : — Jiang S, Cai J, Wallace DC, Jones DP. Cytochrome c-mediated apoptosis in cells lacking mitochondrial DNA.

Signaling pathway involving release and caspase 3 activation is conserved. Han YH, Kim SH, Kim SZ, Park WH.

Apoptosis in arsenic trioxide-treated Calu-6 lung cells is correlated with the depletion of GSH levels rather than the changes of ROS levels. Janssen-Heininger YM, Mossman BT, Heintz NH, Forman HJ, Kalyanaraman B, Finkel T et al.

Redox-based regulation of signal transduction: principles, pitfalls, and promises. Free Radic Biol Med ; 45 : 1— Dalle-Donne I, Giustarini D, Colombo R, Milzani A, Rossi R. S-glutathionylation in human platelets by a thiol-disulfide exchange-independent mechanism.

Free Radic Biol Med ; 38 : — Sullivan DM, Wehr NB, Fergusson MM, Levine RL, Finkel T. Identification of oxidant-sensitive proteins: TNF-alpha induces protein glutathiolation. Biochemistry ; 39 : — Anathy V, Aesif SW, Guala AS, Havermans M, Reynaert NL, Ho YS et al. Redox amplification of apoptosis by caspase-dependent cleavage of glutaredoxin 1 and S-glutathionylation of Fas.

J Cell Biol ; : — Pan S, Berk BC. Glutathiolation regulates tumor necrosis factor-alpha-induced caspase-3 cleavage and apoptosis: key role for glutaredoxin in the death pathway. Circ Res ; : — Huang Z, Pinto JT, Deng H, Richie Jr JP.

Inhibition of caspase-3 activity and activation by protein glutathionylation. Biochem Pharmacol ; 75 : — Franco R, Bortner CD, Cidlowski JA. Potential roles of electrogenic ion transport and plasma membrane depolarization in apoptosis. J Membr Biol ; : 43— Yin W, Cheng W, Shen W, Shu L, Zhao J, Zhang J et al.

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Glutathione depletion and disruption of intracellular ionic homeostasis regulate lymphoid cell apoptosis. Google Scholar. Kourie JI. Interaction of reactive oxygen species with ion transport mechanisms.

Am J Physiol ; : C1— Cai S, Sauve R. J Membr Biol ; : — Gallogly MM, Mieyal JJ. Mechanisms of reversible protein glutathionylation in redox signaling and oxidative stress.

Curr Opin Pharmacol ; 7 : — Chrestensen CA, Starke DW, Mieyal JJ. Acute cadmium exposure inactivates thioltransferase Glutaredoxin , inhibits intracellular reduction of protein-glutathionyl-mixed disulfides, and initiates apoptosis.

Lillig CH, Berndt C, Holmgren A. Glutaredoxin systems. Meyer EB, Wells WW. Thioltransferase overexpression increases resistance of MCF-7 cells to adriamycin. Free Radic Biol Med ; 26 : — Lofgren S, Fernando MR, Xing KY, Wang Y, Kuszynski CA, Ho YS et al. Effect of thioltransferase glutaredoxin deletion on cellular sensitivity to oxidative stress and cell proliferation in lens epithelial cells of thioltransferase knockout mouse.

Invest Ophthalmol Vis Sci ; 49 : — Lillig CH, Lonn ME, Enoksson M, Fernandes AP, Holmgren A. Short interfering RNA-mediated silencing of glutaredoxin 2 increases the sensitivity of HeLa cells toward doxorubicin and phenylarsine oxide. Enoksson M, Fernandes AP, Prast S, Lillig CH, Holmgren A, Orrenius S.

Overexpression of glutaredoxin 2 attenuates apoptosis by preventing cytochrome c release. Dalle-Donne I, Milzani A, Gagliano N, Colombo R, Giustarini D, Rossi R. Molecular mechanisms and potential clinical significance of S-glutathionylation.

Antioxid Redox Signal ; 10 : — West MB, Hill BG, Xuan YT, Bhatnagar A. Protein glutathiolation by nitric oxide: an intracellular mechanism regulating redox protein modification. Klatt P, Pineda Molina E, Perez-Sala D, Lamas S. Novel application of S-nitrosoglutathione-Sepharose to identify proteins that are potential targets for S-nitrosoglutathione-induced mixed-disulphide formation.

Martinez-Ruiz A, Lamas S. Signalling by NO-induced protein S-nitrosylation and S-glutathionylation: convergences and divergences. Cardiovasc Res ; 75 : — Hess DT, Matsumoto A, Kim SO, Marshall HE, Stamler JS. Protein S-nitrosylation: purview and parameters.

Nat Rev Mol Cell Biol ; 6 : — Mannick JB, Schonhoff C, Papeta N, Ghafourifar P, Szibor M, Fang K et al. S-Nitrosylation of mitochondrial caspases. Kroemer G, Galluzzi L, Vandenabeele P, Abrams J, Alnemri ES, Baehrecke EH et al. Classification of cell death: recommendations of the Nomenclature Committee on Cell Death Cell Death Differ ; 16 : 3— Scherz-Shouval R, Shvets E, Fass E, Shorer H, Gil L, Elazar Z.

Reactive oxygen species are essential for autophagy and specifically regulate the activity of Atg4. EMBO J ; 26 : — Yuan H, Perry CN, Huang C, Iwai-Kanai E, Carreira RS, Glembotski CC et al. LPS-induced autophagy is mediated by oxidative signaling in cardiomyocytes and is associated with cytoprotection.

Am J Physiol Heart Circ Physiol ; : H—H Lai Y, Hickey RW, Chen Y, Bayir H, Sullivan ML, Chu CT et al. Autophagy is increased after traumatic brain injury in mice and is partially inhibited by the antioxidant gamma-glutamylcysteinyl ethyl ester.

J Cereb Blood Flow Metab ; 28 : — Troyano A, Sancho P, Fernandez C, de Blas E, Bernardi P, Aller P. The selection between apoptosis and necrosis is differentially regulated in hydrogen peroxide-treated and glutathione-depleted human promonocytic cells. Cell Death Differ ; 10 : — Davis MA, Flaws JA, Young M, Collins K, Colburn NH.

Effect of ceramide on intracellular glutathione determines apoptotic or necrotic cell death of JB6 tumor cells. Toxicol Sci ; 53 : 48— Estrela JM, Ortega A, Obrador E. Glutathione in cancer biology and therapy. Crit Rev Clin Lab Sci ; 43 : — Voehringer DW.

BCL-2 and glutathione: alterations in cellular redox state that regulate apoptosis sensitivity. Free Radic Biol Med ; 27 : — Benlloch M, Ortega A, Ferrer P, Segarra R, Obrador E, Asensi M et al.

Acceleration of glutathione efflux and inhibition of gamma-glutamyltranspeptidase sensitize metastatic B16 melanoma cells to endothelium-induced cytotoxicity.

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Mitochondrial impairment as an early event in the process of apoptosis induced by glutathione depletion in neuronal cells: relevance to Parkinson's disease.

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Indices of oxidative stress and mitochondrial function in individuals with incidental Lewy body disease. Ann Neurol ; 35 : 38— Offen D, Ziv I, Sternin H, Melamed E, Hochman A. Prevention of dopamine-induced cell death by thiol antioxidants: possible implications for treatment of Parkinson's disease.

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Neurobiol Dis ; 21 : 29— Kil IS, Park JW. Daily D, Vlamis-Gardikas A, Offen D, Mittelman L, Melamed E, Holmgren A et al. Glutaredoxin protects cerebellar granule neurons from dopamine-induced apoptosis by activating NF-kappa B via Ref Jaeschke H, Bajt ML.

Intracellular signaling mechanisms of acetaminophen-induced liver cell death. Toxicol Sci ; 89 : 31— Iimuro Y, Bradford BU, Yamashina S, Rusyn I, Nakagami M, Enomoto N et al. The glutathione precursor Loxothiazolidinecarboxylic acid protects against liver injury due to chronic enteral ethanol exposure in the rat.

Hepatology ; 31 : — Download references. We acknowledge Dr. Carl D Bortner, Dr. Robert H Oakley, and Dr. John B Pritchard critical comments of this manuscript. Owing to space considerations we apologize for not citing many important contributions to this field.

The supplemental data contain a list of these important works. Cellular Health: Glutathione is crucial for maintaining healthy cells. It helps preserve cellular structures, supports DNA repair, and regulates cell proliferation and death, contributing to overall cellular health and longevity.

Energy Production: Glutathione is involved in various metabolic processes, including the production of adenosine triphosphate ATP , which is the primary energy currency of cells. Adequate levels of glutathione can contribute to improved energy levels. Anti-Aging Benefits: As an antioxidant, glutathione helps protect cells from damage, which can slow down the aging process and reduce the appearance of aging-related signs like wrinkles and fine lines.

Cardiovascular Health: Glutathione helps maintain healthy blood vessels and can protect against the damage caused by oxidative stress in the cardiovascular system, reducing the risk of heart disease. Respiratory Health: Glutathione is essential for maintaining healthy lung function and protecting lung tissues from damage caused by pollution, smoke, or other harmful substances.

Liver Support: The liver is a major organ involved in detoxification, and glutathione plays a critical role in supporting its function, protecting it from damage, and promoting optimal liver health. Sulfur-Rich Foods: Glutathione contains the sulfur-containing amino acid cysteine, which is a crucial component for its synthesis.

Foods rich in sulfur can help support glutathione production. Examples of sulfur-rich foods include garlic, onions, cruciferous vegetables broccoli, cauliflower, cabbage , and allium vegetables leeks, shallots. Protein-Rich Foods: Adequate protein intake provides the necessary amino acids, including cysteine, to support glutathione synthesis.

Good sources of protein include fish, poultry, lean meats, eggs, and legumes. High-Antioxidant Foods: Consuming a variety of antioxidant-rich foods helps reduce oxidative stress and preserve existing glutathione levels.

Include fruits berries, citrus fruits, kiwi and vegetables spinach, kale, bell peppers in your diet. Vitamin C: Vitamin C is essential for glutathione recycling, which means it helps to regenerate oxidized glutathione back to its active form. Foods rich in vitamin C include Kakadu plum, Acerola cherries, oranges, strawberries, kiwi, bell peppers, and broccoli.

Selenium: Selenium is another important mineral that supports glutathione function. Brazil nuts are an excellent source of selenium. Other sources include seafood, meat, poultry, and eggs.

Milk Thistle: This herb contains a compound called silymarin, which may help increase glutathione levels and protect the liver.

Curcumin Turmeric : Curcumin, the active compound in turmeric, has been shown to boost glutathione levels and possess potent antioxidant properties. N-Acetylcysteine NAC Supplements: NAC is a precursor to cysteine and has been shown to support glutathione synthesis. Share this Patient Testimonial Great as always!

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Ecllular GSH is the Gluttahione non-protein thiol in cells whose functions amd Glutathione and cellular health on Glutatione Glutathione and cellular health thiol of its cysteine moiety Glutarhione serves Glutatthione a cofactor for Glutathione and cellular health number of antioxidant and dellular enzymes. While synthesized exclusively Healt the cytosol from Fuel your potential with hydration constituent amino acids, GSH is hwalth in Pilates exercises compartments, including mitochondria where its concentration in the vellular equals that of the cytosol. This feature and its negative charge healtb physiological pH imply the existence of specific carriers to import GSH from the cytosol to the mitochondrial matrix, where it plays a key role in defense against respiration-induced reactive oxygen species and in the detoxification of lipid hydroperoxides and electrophiles. Moreover, as mitochondria play a central strategic role in the activation and mode of cell death, mitochondrial GSH has been shown to critically regulate the level of sensitization to secondary hits that induce mitochondrial membrane permeabilization and release of proteins confined in the intermembrane space that once in the cytosol engage the molecular machinery of cell death. Glutathione GSHthe major intracellular thiol compound, is a ubiquitous tripeptide produced by most mammalian cells and it is the main mechanism of antioxidant defense against reactive oxygen species ROS and electrophiles. GSH γ-glutamyl-cysteinyl-glycine is synthesized de novo in two sequential enzymatic ATP-dependent reactions. Glutathione and cellular health

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