2003
DOI: 10.1016/s0041-008x(02)00072-8
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Acrylamide axonopathy revisited

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Cited by 162 publications
(89 citation statements)
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“…It was fi rst synthesized in United States in 1950s and used in several industrial fi elds such as textile, paper and cosmetics. ACR is neurotoxic, genotoxic and highly carcinogenic to humans and animals (2,3). The experimental research shows that administering acrylamide in certain doses and periods may have toxic and carcinogenic effects on animals and humans (2)(3)(4)(5).…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…It was fi rst synthesized in United States in 1950s and used in several industrial fi elds such as textile, paper and cosmetics. ACR is neurotoxic, genotoxic and highly carcinogenic to humans and animals (2,3). The experimental research shows that administering acrylamide in certain doses and periods may have toxic and carcinogenic effects on animals and humans (2)(3)(4)(5).…”
Section: Introductionmentioning
confidence: 99%
“…ACR is neurotoxic, genotoxic and highly carcinogenic to humans and animals (2,3). The experimental research shows that administering acrylamide in certain doses and periods may have toxic and carcinogenic effects on animals and humans (2)(3)(4)(5). It has been proven that cooking foods at high temperature leads to high level of acrylamide to form and this fact has been an important milestone for studies related to acrylamide (6,7).…”
Section: Introductionmentioning
confidence: 99%
“…AA is neuro-toxic, 3 ) clastogenic , 4 ) and mutagenic in somatic and germ cells in rodents 4 , 5 ) and is considered as a probable carcinogen in humans.…”
mentioning
confidence: 99%
“…LoPachin et al [21] reported that the cumulative neurotoxicity produced by ACR exposure was linked to nerve terminal damage in the central nervous system (CNS) and peripheral nervous system (PNS). At the molecular level, this presynaptic toxicity appears to be mediated by the formation of sulfhydryl adducts on the cysteine residues of many proteins [22] .…”
Section: Discussionmentioning
confidence: 99%
“…The dissociation between neurological dysfunction and the presumed underlying morphological lesion suggests that axonopathy might not be importantly involved in the pathophysiological process leading to ACR neurotoxicity. Nerve terminals have been suggested as an alternative site of ACR action based on early structural and functional changes as in PNS and CNS [21] .…”
Section: Discussionmentioning
confidence: 99%