Search Results - "Monks, T J"
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Histone H3 phosphorylation is coupled to poly-(ADP-ribosylation) during reactive oxygen species-induced cell death in renal proximal tubular epithelial cells
Published in Molecular pharmacology (01-08-2001)“…Although the cellular response to chemical-induced stress is relatively well characterized, particularly the response to DNA damage, factors that govern the…”
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2
Quinone chemistry and toxicity
Published in Toxicology and applied pharmacology (01-01-1992)Get more information
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Serotonergic Neurotoxicity of 3,4-(±)-Methylenedioxyamphetamine and 3,4-(±)-Methylendioxymethamphetamine (Ecstasy) Is Potentiated by Inhibition of γ-Glutamyl Transpeptidase
Published in Chemical research in toxicology (01-07-2001)“…Reactive metabolites play an important role in 3,4-(±)-methylenedioxyamphetamine (MDA) and 3,4-(±)-methylenedioxymethamphetamine (MDMA; ecstasy)-mediated…”
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4
Sequential oxidation and glutathione addition to 1,4-benzoquinone: correlation of toxicity with increased glutathione substitution
Published in Molecular pharmacology (01-12-1988)“…The chemical reaction of 1,4-benzoquinone with glutathione results in the formation of adducts that exhibit increasing degrees of glutathione substitution…”
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5
Symposium overview: the role of glutathione in neuroprotection and neurotoxicity
Published in Toxicological sciences (01-10-1999)“…Although the cytoprotective effects of glutathione (GSH) are well established, additional roles for GSH in brain function are being identified that provide a…”
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6
2,5- bis-(Glutathion- S-yl)-α-methyldopamine, a putative metabolite of (±)-3,4-methylenedioxyamphetamine, decreases brain serotonin concentrations
Published in European journal of pharmacology (04-04-1997)“…3,4-(±)-Methylenedioxyamphetamine (MDA) and 3,4-(±)-methylenedioxymethamphetamine (MDMA) are serotonergic neurotoxicants. However, when injected directly into…”
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Role of Quinones in Toxicology
Published in Chemical research in toxicology (01-03-2000)“…Quinones represent a class of toxicological intermediates which can create a variety of hazardous effects in vivo, including acute cytotoxicity,…”
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Evidence for DNA damage in amyotrophic lateral sclerosis
Published in Muscle & nerve (01-06-1996)Get full text
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9
Cytotoxicity and cell-proliferation induced by the nephrocarcinogen hydroquinone and its nephrotoxic metabolite 2,3,5-(tris-glutathion-S-yl)hydroquinone
Published in Carcinogenesis (New York) (01-12-1997)“…Hydroquinone, an intermediate used in the chemical industry and a metabolite of benzene, is a nephrocarcinogen in the 2-year National Toxicology Program…”
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10
The metabolism and toxicity of quinones, quinonimines, quinone methides, and quinone-thioethers
Published in Current drug metabolism (01-08-2002)“…Quinones are ubiquitous in nature and constitute an important class of naturally occurring compounds found in plants, fungi and bacteria. Human exposure to…”
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Formation of catechol estrogen glutathione conjugates and γ-glutamyl transpeptidase-dependent nephrotoxicity of 17β-estradiol in the golden Syrian hamster
Published in Carcinogenesis (New York) (01-03-1997)“…In an animal model of hormone-mediated carcinogenesis, male golden Syrian hamsters develop renal carcinoma following prolonged exposure to 17 beta -estradiol…”
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12
Differential Regulation of Redox Responsive Transcription Factors by the Nephrocarcinogen 2,3,5-Tris(glutathion-S-yl)hydroquinone
Published in Chemical research in toxicology (01-07-2001)“…2,3,5-Tris(glutathion-S-yl)hydroquinone [TGHQ] is a potent nephrotoxicant and nephrocarcinogen, and induces a spectrum of mutations in human and bacterial…”
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13
Glutathione conjugates of 2-bromohydroquinone are nephrotoxic
Published in Drug metabolism and disposition (01-09-1985)“…Incubation of either o-bromophenol or 2-bromohydroquinone with rat liver microsomes and 0.25 mM 35S-glutathione (GSH) gave rise to several isomeric 35S-GSH…”
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14
Metabolism as a determinant of species susceptibility to 2,3,5-(triglutathion-S-yl)hydroquinone-mediated nephrotoxicity. The role of N-acetylation and N-deacetylation
Published in Drug metabolism and disposition (01-10-1995)“…2,3,5-(Triglutathion-S-yl)hydroquinone [2,3,5-(triGSyl)HQ] is a potent nephrotoxicant when administered to male rats. We now report that significant species…”
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15
Quinol-glutathione conjugate-induced mutation spectra in the supF gene replicated in human AD293 cells and bacterial MBL50 cells
Published in Cancer research (Chicago, Ill.) (01-08-1999)“…Hydroquinone is a nephrocarcinogen in rats but generally tests negative in standard mutagenicity assays. However, 2,3,5-tris-(glutathion-S-yl)hydroquinone, a…”
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16
2-Bromo-(diglutathion-S-yl)hydroquinone nephrotoxicity: physiological, biochemical, and electrochemical determinants
Published in Molecular pharmacology (01-10-1988)“…2-Bromo-(diglutathion-S-yl)hydroquinone [2-Br-(diGSyl)HQ] causes severe necrosis of the proximal renal tubules in the rat, elevations in blood urea nitrogen…”
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2-hydroxy-4-glutathion-S-yl-17β-estradiol and 2-hydroxy-1-glutathion-S-yl-17β-estradiol produce oxidative stress and renal toxicity in an animal model of 17β-estradiol-mediated nephrocarcinogenicity
Published in Carcinogenesis (New York) (1998)“…Chronic exposure of male Syrian hamsters to a variety of estrogens has been linked with a high incidence of renal carcinoma. The basis of this species and…”
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Irreversible inhibition of rat glutathione S-transferase 1-1 by quinones and their glutathione conjugates : structure-activity relationship and mechanism
Published in Biochemical journal (15-06-1991)“…The irreversible inhibition of the rat glutathione S-transferase (GST) isoenzyme 1-1 by a series of halogenated 1,4-benzoquinones and their GSH conjugates was…”
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Toxicology of quinone-thioethers
Published in Critical reviews in toxicology (1992)“…Cytotoxicity associated with exposure to quinones has generally been attributed to either redox cycling, and the subsequent development of "oxidative stress,"…”
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Stimulation of N-methyl-D-aspartate receptor-mediated calcium entry into dissociated neurons by reduced and oxidized glutathione
Published in Molecular pharmacology (01-02-1992)“…The effects of GSH (gamma-glutamylcysteinylglycine) and GSSG on intracellular calcium levels ([Ca2+]i) were investigated using fura-2-loaded dissociated brain…”
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