Toxicity of Arsenicals Clark Lantz. Introduction Arsenic is widespread in the environment...
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![Page 1: Toxicity of Arsenicals Clark Lantz. Introduction Arsenic is widespread in the environment Occupational exposures can occur –Smelting industry –Coal fired.](https://reader035.fdocuments.us/reader035/viewer/2022062516/56649d7e5503460f94a61c11/html5/thumbnails/1.jpg)
Toxicityof Arsenicals
Clark Lantz
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Introduction
• Arsenic is widespread in the environment
• Occupational exposures can occur– Smelting industry– Coal fired power plants
• Epidemiological studies implicate arsenic as a carcinogen
• Inhalation is a common route of exposure
• Drinking water exposure can also lead to cancer
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History
• 50 ppb (g/L) has been the standard for arsenic in drinking water in US since 1942
• Adopted as an interim standard by US EPA in 1974
• SDWA 1986 required EPA to set a final standard
• In 1996, EPA was required by Congress to set a standard by 2000
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History
• Based on existing published data, EPA proposed a MCLG (maximum containment level goal) of 0 ppb and an MCL (maximum containment level of 5 ppb)– EPA was required to consider cost/benefit analysis in
setting the final rule
• EPA requested comments in summer of 2000– Could comment on the MCLG, or on an MCL of either 3,
5, 10 or 20 ppb
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History
• Just prior to the change in administration, EPA published the final rule as MCLG=0 ppb and MCL=10 ppb
• The new rule has been suspended by the Bush administration and is currently under re-review
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What data did EPA use to set the new rule?
• In 1960s, published data from Taiwan indicated that arsenic in drinking water could cause skin cancer
• These data and additional data collected from this region have been the primary sources of establishing arsenic in drinking water as a cause of skin, lung and bladder cancer
• Data have been supported by data from South American studies
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What data did EPA use to set the new rule?
• EPA also did a cost estimate of meeting the new rule standards
• Compared cost with the health benefits that would be obtained by lowering to 10 ppb (20-30 lives/year)
• Balance between cost and benefit, EPA arrived at 10 ppb for MCL. No change in MCLG of 0 ppb.
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Why all the uproar?Within the exposure range of 2-20 ppb
• Values are close to background exposure.
• Values are close to toxic events (small safety factor)
• Costs to remediate are greater as the value goes lower
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Why all the uproar? • Data showing cancer in Taiwan population was
obtained at high doses (100 - 2000 ppb).– Actual analysis showed that exposure above 400 ppb resulted
in cancer– EPA extrapolated from this point to low doses
• The shape of the dose-response curve may be sublinear– EPA assumed a linear dose-response curve extrapolated to
zero– Large percentage of investigators believe the dose-response
curve to be sublinear
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Setting the MCL (Effect of MCLG)
XPOD=400 ppb
MCLG=0 ppb
Can
cer
Arsenic levels in water
MCLG0 ppb
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Setting the MCL (Sublinear Dose-Response)
XPOD=400 ppb
MCLG=0 ppb
Can
cer
Arsenic levels in water
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Determining the mechanism of action
• Animal studies have been negative
• Not sure what form of arsenic is the carcinogenic species
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Arsenic Metabolism
Arsenate (V) Arsenite (III)GSH
ReductaseMMA(V)
MMA(III)DMA(V)
SAM
Methyltransferase
GSHReductase
Methyltransferase
SAM
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Multistage Carcinogenesis
NORMAL CELL INITIATED CELL
Single DNA mutation
DNA repair
CELL DEATH
CANCER
Growth factors
Cell cycle checkpoints
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Multistage Carcinogenesis
NORMAL CELL INITIATED CELL
Single DNA mutation
DNA repair
CELL DEATH
CANCER
Growth factors
Cell cycle checkpoints
Arsenic is not mutagenic
X
Arsenic is a co-carcinogen
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Proposed modes of action
• Alteration in DNA repair
• Changes in DNA methylation
• Suppression of cell cycle check point proteins (p53)
• Altered expression of growth factors
• Oxidative stress
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Arsenic-induced oxidative stress
• Arsenic may cycle between oxidative states, producing radicals
• Arsenic may interact with and reduce intracellular levels of antioxidants
• Arsenic may increase inflammation, leading to chronic presence of cells that produce radicals and/or growth factors
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OVERALL OBJECTIVES
• To determine if arsenicals will lead to oxidative stress
• To determine if exposure to arsenicals can lead to oxidative damage by initiating pulmonary inflammation.
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• Is there a correlation between inflammation and arsenic-induced genotoxic events?
• Does inflammatory cell oxygen radical production produce genotoxicity and cell proliferation?
• Will inhalation of environmental levels of arsenicals produce similar inflammation and genotoxicity?
• Is there synergism between arsenic and other pulmonary carcinogens?
• Does exposure to arsenic alter inflammatory mediator expression?
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Will inhalation of arsenicals lead to increased inflammation and oxidative stress?
• Male Syrian golden hamsters were exposed for 5 days by nose-only inhalation to 200 g/m3 TWA of either calcium arsenate, arsenic trisulfide or arsenic trioxide and/or primary cigarette smoke.
• BALF was analyzed for indicators of inflammation by determining total cell counts and TNF concentrations.
• PAM were analyzed for their ability to produce superoxide and TNF.
• Whole lung GSH levels and DNA oxidation were used to evaluate oxidative stress
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BALF Cell Counts after 5 day inhalation exposure
0
2
4
6
8
10
12
14
none Ca3(AsO4)2 As2S3 As2O3
Arsenical
Cel
ls (
X10
^4/m
l)
As
As/smoke
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Glutathione and DNA oxidation following 5 days inhalation exposure
00.2
0.40.6
0.81
1.21.4
Glutathione DNA Oxidation
Rel
ativ
e to
Con
trol
Val
ues
control
ars/smoke
A
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Will inhalation of arsenicals lead to increased inflammation and oxidative stress?
• Inhalation of arsenicals at realistic environmental exposure levels does not lead to inflammation
• PAM lavages from animals after 5 day exposure do not show any differences in superoxide or TNF production compared to controls.
• Combined exposure to arsenic and cigarette does not lead to increased inflammatory response. However, it does lead to decreased GSH levels.
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Will inhalation of arsenicals lead to increased inflammation and oxidative stress?
• Male Syrian golden hamsters were exposed for 28 days by nose-only inhalation to 200 g/m3 TWA of arsenic trioxide and/or primary cigarette smoke.
• BALF was analyzed for indicators of inflammation by determining total cell counts. Histological tissue sections were also examined for signs of inflammation.
• Levels of total, reduced and oxidized glutathione were determined.
• DNA oxidation was determined as an indicator of genotoxicity.
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Control Arsenic Smoke Ars/Smoke0
5
10
15
Treatment
Cel
l Cou
nt
Cell Counts after 28 day inhalation exposure
A
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Control Arsenic Smoke Ars/Smoke0.000.25
0.500.751.00
1.251.50
Treatment
Glu
tath
ione
(nm
oles
/mg
tissu
e)
Total Glutathione after 28 day inhalation exposure
A
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DNA Oxidation after 28 day inhalation exposure
0
200
400
600
Treatment
DN
A O
xida
tion control
arsenic
smoke
ars/smoke
A
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Will inhalation of arsenicals lead to increased inflammation and oxidative stress?
• Inhalation of arsenicals at realistic environmental exposure levels does not lead to inflammation
• Inhalation of arsenicals or cigarette smoke alone at the exposures studied, does not lead to alterations in GSH or in DNA oxidation.
• Combined exposure to arsenicals and cigarette smoke significantly reduces GSH as early as 5 days after beginning exposure.
• Significant increases in DNA oxidation are seen after 28 day exposures.
• Effects of combined exposure to arsenic and cigarette smoke does not appear to be due to increased inflammatory response.
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Can arsenic activate oxidative stress sensitive transcription factors?
• Rat lung slices were exposed to arsenite (0.1 to 100 M) for up to 24 hr.
• Nuclear proteins were isolated and analyzed transcription factors c-Jun/AP-1 and p65 NFB by Western and EMSA
• HSP protein expression was also analyzed (HSP-32, 60, 72 and 90)
• Immunohistochemistry was used to identify the cells affected by the arsenic exposure
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Levels of expressionArsenic Dose-Response
0
250
500
750
0.1 1 10 100
Arsenic Concentration (M)
Nor
mal
ized
Res
pons
e
c-Jun
NFkB
HSP-32
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CONTROL ARSENIC
AP-1
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CONTROL ARSENIC
NFB
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Can arsenic activate oxidative stress sensitive transcription factors?
• c-Jun/AP-1 was activated at 1 M.
• p65 NFB was not translocated to the nucleus
• HSP-32 (HOX-1) was upregulated
• Other HSPs were either not affected of only increased at high arsenic concentrations
• Up regulation of AP-1 and HSP-32 were seen in PAM, EPII and endothelial cells.
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Effect of arsenic exposure in vitro on PGE2 production
Arsenic Dose-Response
0
250
500
750
0.1 1 10 100
Arsenic Concentration (M)
Nor
mal
ized
Res
pons
e
PGE2
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Overall Conclusions• Arsenic at environmentally relevant levels does cause
oxidative stress in the lung – Changes in GSH– Activation of oxidative stress sensitive transcription factors– Expression of HOX-1– Is not due to release of oxygen radicals by inflammatory cells
• Exposure to arsenic can potentiate the response following exposure to a second toxicant.
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Levels of expressionArsenic Dose-Response
0
250
500
750
0.1 1 10 100
Arsenic Concentration (M)
Nor
mal
ized
Res
pons
e
c-Jun
NFkB
HSP-32
PGE2
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Future Questions• What is the cellular site(s) of action that lead to
synergistic effects?
• Does the response depend on the chemical form of arsenic?
• What is the time course for development of the responses?
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Other concerns with EPA rule
• Taiwan data used “ecological” values for the dose
• US based studies (Utah study) have not demonstrated increased cancer associated with arsenic in the water (0-100 ppb)
• EPA underestimated costs associated with treatment, particularly in the Southwest
• EPA proposed best treatment will probably not work for Southwestern US water treatment
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Issues for Arizona water companies
• The economic effect will depend on the location within the state. – Only about 10% of Tucson Water wells exceed 10 ppb– However, some companies in the Phoenix area are
already having problems meeting 50 ppb– Cost of treatment would be prohibitive for small
companies– Small companies may be abandoned
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Lantz labGrace ParlimanGuan Jie ChenPadma SundareshanJayanthika Wijeweera
Carter labDr. Dean CarterDavid BarberMichael KopplinFelix Ayala
Witten labDr. Mark WittenAllison HaysMadel Balagtas
Funded byNIH R01ES05561NIH P30ES06694ADCRC 9703