Skin sensitization to linalyl hydroperoxide: support for radical intermediates.

Abstract:

:In order to better understand the skin sensitization mechanism of allylic hydroperoxides, linalyl hydroperoxide (1) and several of its potential rearrangement products-epoxylinalool (2), epoxynerol (3), epoxygeraniol (4), and furan (5) and pyran (6) derivatives-were synthesized. The sensitizing properties of these molecules have been screened on mice using the local lymph node assay (LLNA) and further evaluated on guinea pigs using the Freund's complete adjuvant test (FCAT). Linalyl hydroperoxide (1) and linalyl epoxide (2) were found to be sensitizers, while the other compounds were classified as mild sensitizers or nonsensitizers. In the guinea pigs, no cross-reactions were observed between skin sensitizers 1 and 2. Radical-trapping experiments were carried out on linalyl hydroperoxide (1) using TTBP as trapping agent and Fe(3+)-TPP as radical inducer. The major reaction taking place is the formation of a furan ring by intramolecular reaction of the oxygen-centered radical with the isoprenyl double bond with the formation of a tertiary radical. Reaction of this intermediate with radicals derived from TTBP gave compounds 10a,b in 25% yield. The second important reaction, accounting for 14%, is taking place on the allylic double bond with the formation of a less stable primary radical which is not trapped by a TTBP-derived radical but by a hydroxy radical to give a mixture of epoxides 3 and 4. These results are in favor of the formation of a carbon-centered reactive radical as intermediate in the skin sensitization to linalyl hydroperoxide.

journal_name

Chem Res Toxicol

authors

Bezard M,Karlberg AT,Montelius J,Lepoittevin JP

doi

10.1021/tx970014r

subject

Has Abstract

pub_date

1997-09-01 00:00:00

pages

987-93

issue

9

eissn

0893-228X

issn

1520-5010

pii

tx970014r

journal_volume

10

pub_type

杂志文章
  • Identification and characterization of a reaction product of 2'-deoxyoxanosine with glycine.

    abstract::2'-Deoxyoxanosine (dOxo) is a novel DNA lesion produced from dGuo by reaction with nitrous acid or nitric oxide [Suzuki, T., Yamaoka, R., Nishi, M., Ide, H., and Makino, K. (1996) J. Am. Chem. Soc. 118, 2515-2516]. We investigated the reaction of dOxo with glycine (Gly) under physiological conditions. When 5 mM dOxo w...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx990164x

    authors: Suzuki T,Yamada M,Ide H,Kanaori K,Tajima K,Morii T,Makino K

    更新日期:2000-04-01 00:00:00

  • Chemical modification of lysozyme, glucose 6-phosphate dehydrogenase, and bovine eye lens proteins induced by peroxyl radicals: role of oxidizable amino acid residues.

    abstract::Chemical and structural alterations to lysozyme (LYSO), glucose 6-phosphate dehydrogenase (G6PD), and bovine eye lens proteins (BLP) promoted by peroxyl radicals generated by the thermal decomposition of 2,2'-azobis(2-amidinopropane) hydrochloride (AAPH) under aerobic conditions were investigated. SDS-PAGE analysis of...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx300372t

    authors: Arenas A,López-Alarcón C,Kogan M,Lissi E,Davies MJ,Silva E

    更新日期:2013-01-18 00:00:00

  • Chalcone inhibition of anthracycline secondary alcohol metabolite formation in rabbit and human heart cytosol.

    abstract::Antineoplastic therapy with anthracyclines like doxorubicin (DOX) and daunorubicin (DNR) is limited by the possible development of a dose-related cardiomyopathy. Secondary alcohol metabolites like doxorubicinol (DOXol) and daunorubicinol (DNRol), formed by cytoplasmic two-electron reductases, have been implicated as p...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx060159a

    authors: Silvestrini A,Meucci E,Vitali A,Giardina B,Mordente A

    更新日期:2006-11-01 00:00:00

  • T-Cell Activation by Low Molecular Weight Drugs and Factors That Influence Susceptibility to Drug Hypersensitivity.

    abstract::Drug hypersensitivity reactions adversely affect treatment outcome, increase the length of patients' hospitalization, and limit the prescription options available to physicians. In addition, late stage drug attrition and the withdrawal of licensed drugs cost the pharmaceutical industry billions of dollars. This signif...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章,评审

    doi:10.1021/acs.chemrestox.9b00327

    authors: Hammond S,Thomson PJ,Ogese MO,Naisbitt DJ

    更新日期:2020-01-21 00:00:00

  • Ethical guidelines to publication of chemical research. American Chemical Society.

    abstract::The guidelines embodied in this document were revised by the editors of the Publication Division of the American Chemical Society in January 1994 and endorsed by the Society Committee on Publications. ...

    journal_title:Chemical research in toxicology

    pub_type: 指南,杂志文章

    doi:

    authors:

    更新日期:1994-07-01 00:00:00

  • Chemoavailability of Organic Electrophiles: Impact of Hydrophobicity and Reactivity on Their Aquatic Excess Toxicity.

    abstract::Organic electrophiles have been recognized as important components of the exposome that can be characterized as cumulative totality of exposure in the organism in response to environmental perturbation. For such compounds, chemical reactivity may contribute significantly to the toxicological profile through covalent a...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/acs.chemrestox.5b00398

    authors: Böhme A,Laqua A,Schüürmann G

    更新日期:2016-06-20 00:00:00

  • Formation of deoxyguanosine cross-links from calf thymus DNA treated with acrolein and 4-hydroxy-2-nonenal.

    abstract::Acrolein (AC) and 4-hydroxy-2-nonenal (HNE) are endogenous bis-electrophiles that arise from the oxidation of polyunsaturated fatty acids. AC is also found in high concentrations in cigarette smoke and automobile exhaust. These reactive α,β-unsaturated aldehyde (enal) covalently modify nucleic acids, to form exocyclic...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx100179g

    authors: Kozekov ID,Turesky RJ,Alas GR,Harris CM,Harris TM,Rizzo CJ

    更新日期:2010-11-15 00:00:00

  • Computational prediction of the chromosome-damaging potential of chemicals.

    abstract::We report on the generation of computer-based models for the prediction of the chromosome-damaging potential of chemicals as assessed in the in vitro chromosome aberration (CA) test. On the basis of publicly available CA-test results of more than 650 chemical substances, half of which are drug-like compounds, we gener...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx060136w

    authors: Rothfuss A,Steger-Hartmann T,Heinrich N,Wichard J

    更新日期:2006-10-01 00:00:00

  • Acrylamide Induces Senescence in Macrophages through a Process Involving ATF3, ROS, p38/JNK, and a Telomerase-Independent Pathway.

    abstract::Senescence, which is irreversible cell cycle arrest, is induced by various types of DNA damage, including genotoxic stress. Senescent cells show dysregulation of tumor suppressor genes and other regulators of cellular proliferation. Activating transcription factor 3 (ATF3) plays a pleiotropic role in biological proces...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx500341z

    authors: Kim KH,Park B,Rhee DK,Pyo S

    更新日期:2015-01-20 00:00:00

  • Decomposition and quality control considerations in biological work with fecapentaene preparations.

    abstract::Solutions of synthetic fecapentaene 12 (FP-12) intended for carcinogenicity studies were found to decompose extremely rapidly during customary dosage procedures. Apparent half-lives as short as 15 min were observed. While rates and even the qualitative course of decomposition were surprisingly variable in replicate ex...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx00009a007

    authors: Streeter AJ,Donovan PJ,Anjo T,Ohannesian L,Sheffels PR,Wu PP,Keefer LK,Andrews AW,Bradford WW 3rd,Reist EJ

    更新日期:1989-05-01 00:00:00

  • In vitro metabolism of 2-acetylbenzothiophene: relevance to zileuton hepatotoxicity.

    abstract::Zileuton, an inhibitor of 5-lipooxygenase, the initial enzyme in the leukotriene pathway, was marketed as a new treatment for asthma. This drug has been associated with liver toxicity, which has limited its clinical usefulness. We provide evidence here that the liver toxicity likely involves a sequence of biotransform...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx0341409

    authors: Joshi EM,Heasley BH,Chordia MD,Macdonald TL

    更新日期:2004-02-01 00:00:00

  • Chlorine dioxide oxidations of tyrosine, N-acetyltyrosine, and dopa.

    abstract::The reactions of aqueous ClO2 with tyrosine, N-acetyltyrosine, and dopa (3,4-dihydroxyphenylalanine) are investigated from pH 4 to 7. The reaction rates increase greatly with pH to give a series of oxidized products. Tyrosine and N-acetyltyrosine have similar reactivities with second-order rate constants (25.0 degrees...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx049697i

    authors: Napolitano MJ,Green BJ,Nicoson JS,Margerum DW

    更新日期:2005-03-01 00:00:00

  • Thickness of multiwalled carbon nanotubes affects their lung toxicity.

    abstract::Two samples of highly pure multiwalled carbon nanotubes (MWCNTs) similar in hydrophobicity and surface reactivity were prepared with similar length, <5 μm, but markedly different diameter (9.4 vs 70 nm). The samples were compared for their cytotoxic activity, uptake, and ability to induce oxidative stress (ROS product...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx200255h

    authors: Fenoglio I,Aldieri E,Gazzano E,Cesano F,Colonna M,Scarano D,Mazzucco G,Attanasio A,Yakoub Y,Lison D,Fubini B

    更新日期:2012-01-13 00:00:00

  • Metabonomic evaluation of Schaedler altered microflora rats.

    abstract::Previously, we identified two distinct metabonomic phenotypes in Sprague-Dawley rats sourced from two different rooms (colonies) in the Charles River, Raleigh facility [Robosky, L. C., Wells, D. F., Egnash, L. A., Manning, M. L., Reily, M. D., and Robertson, D. G. (2005) Metabonomic identification of two distinct phen...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx700184u

    authors: Rohde CM,Wells DF,Robosky LC,Manning ML,Clifford CB,Reily MD,Robertson DG

    更新日期:2007-10-01 00:00:00

  • Hepatotoxicity after 3'-hydroxyacetanilide administration to buthionine sulfoximine pretreated mice.

    abstract::The administration of 3'-hydroxyacetanilide, a regioisomer of acetaminophen, to mice failed to produce hepatotoxicity even after the administration of diethyl maleate. In contrast, hepatotoxicity did occur when 3'-hydroxyacetanilide was administered to buthionine sulfoximine pretreated mice. Although the administratio...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx00020a014

    authors: Tirmenstein MA,Nelson SD

    更新日期:1991-03-01 00:00:00

  • Mechanism-based inactivation of human cytochromes p450s: experimental characterization, reactive intermediates, and clinical implications.

    abstract::The P450 type cytochromes are responsible for the metabolism of a wide variety of xenobiotics and endogenous compounds. Although P450-catalyzed reactions are generally thought to lead to detoxication of xenobiotics, the reactions can also produce reactive intermediates that can react with cellular macromolecules leadi...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章,评审

    doi:10.1021/tx7002504

    authors: Hollenberg PF,Kent UM,Bumpus NN

    更新日期:2008-01-01 00:00:00

  • Bezafibrate induces a mitochondrial derangement in human cell lines: a PPAR-independent mechanism for a peroxisome proliferator.

    abstract::Bezafibrate is a hypolipidemic drug that belongs to the group of peroxisome proliferators because it binds to peroxisome proliferator-activated receptors type alpha (PPARs). Peroxisome proliferators produce a myriad of extraperoxisomal effects, which are not necessarily dependent on their interaction with PPARs. An in...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx0341052

    authors: Scatena R,Bottoni P,Vincenzoni F,Messana I,Martorana GE,Nocca G,De Sole P,Maggiano N,Castagnola M,Giardina B

    更新日期:2003-11-01 00:00:00

  • Hplc/electrospray ionization mass spectrometric analysis of the heterocyclic aromatic amine carcinogen 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine in human milk.

    abstract::A new procedure has been developed for the extraction of 2-amino-1-methyl-6-phenyl-imidazo[4,5-b]pyridine (PhIP) and other heterocyclic aromatic amines from human breast milk samples. Extracts were analyzed by high-performance liquid chromatography/electrospray ionization/tandem mass spectrometry (HPLC/ESI-MS/MS) with...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx0601861

    authors: Scott KA,Turesky RJ,Wainman BC,Josephy PD

    更新日期:2007-01-01 00:00:00

  • Biochemical investigations into the mutagenic potential of 8-oxo-2'-deoxyguanosine using nucleotide analogues.

    abstract::8-Oxo-2'-deoxyguanosine (OdG) is an abundant DNA lesion produced during oxidative damage to DNA. It can form relatively stable base pairs with both dC and dA that mimic natural dG:dC and dT:dA base pairs, respectively. Thus, when in the template strand, OdG can direct the insertion of either dCTP or dATP during replic...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx300365g

    authors: Hamm ML,Crowley KA,Ghio M,Lindell MA,McFadden EJ,Silberg JS,Weaver AM

    更新日期:2012-11-19 00:00:00

  • Future of toxicology--lipid peroxidation in the future: from biomarker to etiology.

    abstract::On the basis of a large number of reports concerning the detection of lipid peroxidation products as biomarkers in human diseases, there is no doubt that their steady-state levels increase under pathophysiological states associated with oxidative stress. The key question is whether they play any causative roles. This ...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx600304n

    authors: Uchida K

    更新日期:2007-01-01 00:00:00

  • Oxanosine Monophosphate Is a Covalent Inhibitor of Inosine 5'-Monophosphate Dehydrogenase.

    abstract::Reactive nitrogen species (RNS) are produced during infection and inflammation, and the effects of these agents on proteins, DNA, and lipids are well recognized. In contrast, the effects of RNS damaged metabolites are less appreciated. 5-Amino-3-β-(d-ribofuranosyl)-3 H-imidazo-[4,5- d][1,3]oxazine-7-one (oxanosine) an...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/acs.chemrestox.8b00342

    authors: Yu R,Kim Y,Maltseva N,Braunstein P,Joachimiak A,Hedstrom L

    更新日期:2019-03-18 00:00:00

  • Identification and quantification of DNA adducts in the oral tissues of mice treated with the environmental carcinogen dibenzo[a,l]pyrene by HPLC-MS/MS.

    abstract::Tobacco smoking is one of the leading causes for oral cancer. Dibenzo[a,l]pyrene (DB[a,l]P), an environmental pollutant and a tobacco smoke constituent, is the most carcinogenic polycyclic aromatic hydrocarbon (PAH) tested to date in several animal models (target organs: skin, lung, ovary, and mammary tissues). We hav...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx200188j

    authors: Zhang SM,Chen KM,Aliaga C,Sun YW,Lin JM,Sharma AK,Amin S,El-Bayoumy K

    更新日期:2011-08-15 00:00:00

  • Internalization of carbon black and maghemite iron oxide nanoparticle mixtures leads to oxidant production.

    abstract::The risk of potential human exposure to mixed nanomaterials in consumer, occupational, and medicinal settings is increasing as nanomaterials enter both the workplace and the marketplace. In this study, we investigated the toxicity of mixed engineered carbon black (ECB) and maghemite iron oxide (Fe(2)O(3)) nanoparticle...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx100307h

    authors: Berg JM,Ho S,Hwang W,Zebda R,Cummins K,Soriaga MP,Taylor R,Guo B,Sayes CM

    更新日期:2010-12-20 00:00:00

  • Lauric acid as a model substrate for the simultaneous determination of cytochrome P450 2E1 and 4A in hepatic microsomes.

    abstract::In vitro techniques have been utilized to investigate the microsomal enzymes involved in the metabolism of lauric acid and to establish conditions in which it can be used as a model substrate for both cytochrome P450 4A and cytochrome P450 2E1 in human liver microsomes. Studies of enzyme kinetics of lauric acid omega-...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx00042a018

    authors: Clarke SE,Baldwin SJ,Bloomer JC,Ayrton AD,Sozio RS,Chenery RJ

    更新日期:1994-11-01 00:00:00

  • Covalent binding of N-hydroxy-N-acetyl-2-aminofluorene and N-hydroxy-N-glycolyl-2-aminofluorene to rat hepatocyte DNA: in vitro and cell-suspension studies.

    abstract::Two 2-aminofluorene-derived hydroxamic acids that differ only in the nature of the N-acyl group were examined for their relative abilities to undergo covalent binding to nucleic acids. Studies of the bioactivation of N-hydroxy-N-acetyl-2-aminofluorene (N-OH-AAF) and N-hydroxy-N-glycolyl-2-aminofluorene (N-OH-GAF) were...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx00001a008

    authors: Corbett MD,Lim LO,Corbett BR,Johnston JJ,Wiebkin P

    更新日期:1988-01-01 00:00:00

  • Inhibition of 2,5-hexanedione-induced protein cross-linking by biological thiols: chemical mechanisms and toxicological implications.

    abstract::n-Hexane is metabolized to the gamma-diketone 2,5-hexanedione (2,5-HD), a derivative that covalently binds to lysine residues in neurofilament (NF) protein to yield 2,5-dimethylpyrrole adducts. Studies comparing the pyrrole-forming potential and neurotoxic potency of gamma-diketones have demonstrated that pyrrolylatio...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx00047a017

    authors: Zhu M,Spink DC,Yan B,Bank S,DeCaprio AP

    更新日期:1995-07-01 00:00:00

  • Distinct Orchestration and Dynamic Processes on γ-H2AX and p-H3 for Two Major Types of Genotoxic Chemicals Revealed by Mass Spectrometry Analysis.

    abstract::Genotoxic chemicals act by causing DNA damage, which, if left unrepaired, can have deleterious consequences for cell survival. DNA damage response (DDR) gets activated to repair or mitigate the effects of DNA damage. Histone H2AX and H3 phosphorylation biomarkers (γ-H2AX and p-H3) have attracted great attention as the...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/acs.chemrestox.0c00104

    authors: Qu M,Xu H,Chen J,Zhang Y,Xu B,Guo L,Xie J

    更新日期:2020-08-17 00:00:00

  • Synthesis and 32P-postlabeling/high-performance liquid chromatography separation of diastereomeric 1,N2-(1,3-propano)-2'-deoxyguanosine 3'-phosphate adducts formed from 4-hydroxy-2-nonenal.

    abstract::4-Hydroxy-2-nonenal (HNE), a major electrophilic byproduct of lipid peroxidation, is mutagenic and cytotoxic. The two pairs of HNE-derived diastereomeric 1,N2-propanodeoxyguanosine 3'-monophosphate adducts were synthesized from reaction of HNE with 2'-deoxyguanosine 3'-monophosphate. After HPLC separation, these adduc...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx970100r

    authors: Yi P,Zhan D,Samokyszyn VM,Doerge DR,Fu PP

    更新日期:1997-11-01 00:00:00

  • Comparative evaluation of the bioreactivity and mutagenic spectra of acrolein-derived alpha-HOPdG and gamma-HOPdG regioisomeric deoxyguanosine adducts.

    abstract::Acrolein is a bifunctional electrophile, present as an ubiquitous environmental pollutant and an endogenous cellular product of lipid peroxidation. Reaction of acrolein with deoxyguanosine produces two regioisomeric DNA adducts, specifically gamma-hydroxypropanodeoxyguanosine (gamma-HOPdG) and alpha-hydroxypropanodeox...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx034066u

    authors: Sanchez AM,Minko IG,Kurtz AJ,Kanuri M,Moriya M,Lloyd RS

    更新日期:2003-08-01 00:00:00

  • Cytochrome P450 enzymes involved in acetaminophen activation by rat and human liver microsomes and their kinetics.

    abstract::Acetaminophen (APAP), a commonly used analgesic, is catalyzed by cytochrome P450 (P450) enzymes to a toxic intermediate which can be trapped by glutathione. Using this approach, involvement of enzymes in the activation of APAP and their kinetics were studied. With human liver microsomes, there were three apparent Km v...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx00034a019

    authors: Patten CJ,Thomas PE,Guy RL,Lee M,Gonzalez FJ,Guengerich FP,Yang CS

    更新日期:1993-07-01 00:00:00