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Sulfuryl
fluoride ProFume - CAS No. 2699-79-8
Comments
on Sprando and Collins et. al. studies:
Effects in Control groups compared to NaF treated groups.
Appendix
B. Objections and Request for Hearing. Docket OPP-2005-0174.
Submitted to US EPA on sulfuryl fluoride pesticide residue tolerances.
September 13, 2005. |
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Return
to Main Submission
Appendix
B.
Comments on Sprando and Collins et. al. studies:
Effects in Control groups compared to NaF treated groups.
Tables
Include:
Table
1. August 2001 Study.
Effects: Control versus NaF treated groups.
Table
2. 1998 Study.
Effects: Control versus NaF treated groups.
Table 3.
1997 Study. Effects: Control versus NaF treated groups.
Table 4.
1995 Study. Effects: Control versus NaF treated groups.
Table 5. 1996 Study.
Effects: Control versus NaF treated groups.
Table 6. June 2001 Study. Control
versus NaF treated groups.
Table 7. Rat chow used in the 6 Sprando and Collins et al.
studies
Table 8. Rats used in the 6 Sprando and Collins et al. studies
Sprando, Collins
et al. published 6 papers on fluoride's effects in Food
and Chemical Toxicology
(1995, 1996, 1997, 1998, June 2001, August 2001).
The 1997 and 1998
studies were two of the four studies cited by ATSDR 2003 Toxicological
Profile for Fluorides, Hydrogen fluoride, and Fluorine to
counter the many studies which reported adverse effects on the
male reproductive system. The concern with the Sprando and Collins
et al. studies are:
• the high
number of adverse effects found in the Control group vs. the
Treated groups in the multigenerational studies
• the rats used in the 1997 and 1998 studies were bred
from the rat group used in the multigenerational studies (published
in 2001)
• the lack of published fluoride levels in blood, bone,
organs, and tissues in all these studies. Without this data
it is not possible to understand the high number of effects
reported for the Control groups.
In March 2004, Ellen
Connett of Fluoride Action Network spoke with Robert Collins,
one of the authors, about these studies. Dr. Collins stated
that samples of blood, bone, tissue, and organs, from all experiments
were given to a FDA researcher for analysis of fluoride levels.
However, the results of this analysis have not been published.
This is regrettable as other researchers have reported fluoride
levels, for example,
Messer et al. (1973),
used a "low fluoride" diet that varied from 0.1
to 0.3 ppm fluoride (compared to the Sprando &
Collins et. al. "low fluoride" diet of 7.95
pm fluoride) and published the fluoride levels in the
humeri of two generations. The authors state, "The concentration
of fluoride in the humeri of mice fed the low fluoride diet
was 70 to 80 times lower than in animals receiving 50 pppm
fluoride in their drinking water." - (page 1325).
Ref: Messer et al. (1973). Influence of fluoride intake on
reproduction in mice. Journal
of Nutrition 103:1319-1327
Table
1. August 2001 Study.
Effects: Control versus NaF treated groups.
Developmental toxicity of sodium fluoride measured during
multiple generations.
Collins TF, Sprando RL, Black TN, Shackelford ME, Olejnik
N, Ames MJ, Rorie JI, Ruggles DI.
Food Chem Toxicol. 2001 Aug;39(8):867-76. |
"This
study was done to determine any generational effects of
NaF on the development of the offspring." - page 872 |
| •
The treated groups were exposed to NaF in drinking water
at levels of
25 ppm, 100 ppm, 175 ppm, and 250 ppm.
• No Fluoride levels in blood, bone and tissue are
presented
• Skeletal variations are not identified by sex
• Incidence of specific soft -tissue variations are
not identified by sex
• Runts are not identified by sex
Incidence
of specific skeletal variations (excluding sternebral) are
presented for F2 fetuses (Table
7) -
25 Parameters were listed:
-
only the 175-ppm treated group had higher number of effects
than the Control (16 vs 6 respectively)
- the Control had higher number of effects compared to
the 250-ppm treated group (12 vs 10 respectively)
- the Control had higher number of effects compared to
the 100-ppm treated group (14 vs 8 respectively)
- the Control had higher number of effects compared to
the 25-ppm treated groups (12 vs 5 respectively)
-
in 5 of the 25 parameters, the Control group had the highest
number of effects
- in 3 of the 25 Parameters: 175-ppm treated group had
no effects listed
- in 4 of the 25 Parameters: 100-ppm treated group had
no effects listed
- in 5 of the 25 Parameters: Control
group had no effects listed
- in 6 of the 25 Parameters: 25-ppm treated group had
no effects listed
- in 6 of the 25 Parameters: 250-ppm treated group had
no effects listed
Analysis
of incidence of sternebral variations are presented only
for F2 fetuses
(Table 6)
Two of the 4 Parameters:
•
Fetuses with 2 + variation: Control group
had higher number of effects than 25-ppm and 250-pppm
treated groups.
• Fetuses with 1 + variation: Control
group had higher number of effects than 25-ppm treated
group.
Incidence
of specific sternebral variation are presented for F2 fetuses
(Table 5)
Three of the 6 Parameters:
•
Bipartite: Controls had higher number
of effects than 250-ppm treated group.
• Reduced Ossification: Control
group and 250-ppm treated group had same number of effects.
Control group had higher number of effects than 25-ppm
treated group.
• Non-ossified: Control group had
higher number of effects than 25-ppm and 250-ppm treated
groups
•
The authors commented that one Control fetus with fused
sternebrae was not presented in this Table.
Analysis
of incidence of skeletal variations in F2 fetuses
(Table 8).
The six Parameters:
•
Litters with fetuses with
1 + variations: Control
group had highest number of effects compared to all treated
groups.
• Fetuses with 2 + variations:
Control group had higher number of effects compared to
25-ppm, 100-ppm, and 175-ppm treated groups.
• Fetuses with 1 + variations:
Control group had higher number of effects compared to
25-ppm and 100-ppm treated groups.
• Litters with fetuses with 2 + variations:
Control group had higher number of effects compared to
25-ppm and 100-ppm treated groups.
• Fetuses with 3 + variations:
Control group had same number of effects as 100-ppm treated
group.
• Litters with fetuses with 3 + variations:
Control group had higher number of effects compared to
25-ppm and 100-ppm treated groups.
• of 6 Parameters:
Control group had higher
number of effects than 25-ppm treated group
• of 5 Parameters: Control group
had higher number of effects than 100-ppm treated group
(for 6th parameter both Control and 100-ppm treated group
had same number of effects)
Incidence
of specific soft-tissue variations in F2 fetuses
(Table 9):
Three of the 7 Parameters:
•
Severe Enlarged ureter or kidney: Control
group had same number of effects as 100-ppm treated group.
• Moderate Enlarged ureter or kidney:
Control group had higher number of effects compared to
250-ppm treated group.
• Hemorrhage, internal: Control
group had higher number of effects compared to 25-ppm
and 250-ppm treated groups.
While
the authors give definitions for early and late deaths,
the statistics presented are grouped as one.
Early
deaths were defined as Deciduomas
(brownish
impantation sites without placenta)
Late Deaths
are defined: Implantation sites
with placentas and with complete but non-viable fetuses
that were of subnormal size, that showed retarded development,
or were in a macerated condition.
The
authors state
•
The single statistically significant decrease
in crown-rump length of F2
females at 175 ppm was considered
random.
Note:
In a 2003 sodium fluoride teratogen study, Goh and Neff
reported:
"The most prominent malformations caused by sodium
fluoride are reduction in the
head-tail lengths and dysfunction
of the neuromuscular system of the tadpoles... the
observed teratogenic action of sodium fluoride
on frog embryos would indicate a strong possibility that
sodium fluoride may also act directly on developing mammalian
fetuses to cause malformation."
Ref: Effects of fluoride on Xenopus embryo development.
Food Chem Toxicol. 2003 Nov;41(11):1501-8.
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Table
2. 1998 Study.
Effects: Control versus NaF treated groups.
Testing the potential of sodium fluoride to affect spermatogenesis:
a morphometric study.
Sprando RL, Collins TX, Black T, Olejnik N, Rorie J.
Food and Chemical Toxicology 36 (1998) 1117-1124. |
"This
study provides quantitative information on the effect
of sodium fluoride (NaF) on the testes of F1 generation
male rats exposed in utero and during lactation
to NaF at one of four concentraitons (25, 100, 175, 250
ppm)..." - page 1117
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In
this study, the authors cite the lack of statistical signficance
for several parameters for NaF-treated groups compared to
the control. The public have no way to determine the lack
of significance without the blood fluoride levels in the
control and treated groups.
•
Statistically significant differences in testis weight,
testicular volume or testicular specifric gravity were
not observed between the control and NaF-treated animals.
•
"The seminiferous tubules from the controls and NaF-treated
groups occupied approximately 87-88% of the total testis
volume and the seminiferous tubular lumen occupied approximately
12-14% of the testicular volume for controls and the NaF-treated
groups. The interstitial space occupied approximately
9-11% of the total testis volume, the Leydig cells occupied
3-4%, blood vessels occupied 3%, macrophages occupied
0.40-0.60% for the controls and the 25 ppm, 100 ppm, 175
ppm and 250 pp m NaF treatment groups. No
statistically significant differences were observed between
the controls and NaF-treated groups for the above parameters."
•
"Statistically significant
differences were not observed in the mean numbers
of Sertoli cell nucleoli counted per cross-sectional seminiferous
tubles, the seminiferous tubule diameters or the height
of the seminiferous epithelium between
the control and NaF-treated group."
•
"Statistically significant
differences were not observed in the mean absolute
seminiferous tuble lengths or mean absolute surface areas
between the control and the sodium
fluoride treated groups."
•
"The number of Sertoli cell nucleoli was not
statistically different when the control and NaF-treated
rats were compared..."
•
"The mean diameters of the seminiferous tubules from
the treatment groups were not significantly
different from the control groups... "
•
"The numbers of homogenization resistant spermatids
per testis from the F1 generation NaF-treated male rats
used in the present study were
not statistically different from their F1 generation controls."
Statistificantly
significant effects the authors reported in their 1998 paper:
•
"... there was a significant
reduction in the absolute volume of the testicular capsule
in the 100 ppm NaF treatment group compared to the controls.
This finding was not considered
a treatment-related effect because no dose-response relationship
was observed and it is probably
a result of sampling error for this parameter..."
•
"A statistically significant
difference in body weight between the controls
and the NaF-treated rats in the 100 ppm, 175 ppm and a
borderline statistically significant effect was observed
in the 250 ppm NaF treatment groups: however, this
decrease in body weight was not dose related."
•
"A statistically significant
decrease in the absolute volume and volume
percent of the lymphatic endothelium was observed
in the 175 and 250 ppm
NaF-treated groups and in the testicular capsule in the
100 ppm NaF-treated
groups. The significance of this
finding is unknown at the present time..."
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Table
3. 1997 Study.
Effects: Control versus NaF treated groups.
Testing the potential of sodium fluoride to affect spermatogenesis
in the rat.
Sprando RL, Collins TFX, Black TN, Rorie J, Ames MJ, O'Donnell
M.
Food and Chemical Toxicology 35 (1997) 881-890. |
Again,
in this study the authors cite the lack of statistical signficance
for several parameters for NaF-treated groups compared to
the control. The public have no way to determine the lack
of significance without the blood and organ fluoride levels
in the control and treated groups.
Body
weight: "The mean body weights of the P and F1 generation
rats (Table 1) from all sodium fluoride treatment groups
were not statistically different
than their respective controls..."
Testis
weight: "Dose-related effects were not observed.
No statistically significant differences were observed
in mean testes weights (Table 2) between P and F1 controls
and their respective treatment groups."
Epididymal
weight: "Mean epididymal weights of treated and control
rats are presented in Table 3. Statistically
significant differences in mean epididymal weights were
not observed between control and treatment groups of the
P generation however; within the F1 generation
the right epididymal weight of the 175 ppm group was
significantly lower than the F1 control. No dose-related
effects were observed...."
Prostate/seminal
vesicle weight: "No statistically
significant difference in prostate/seminal vesicle weights
was observed between treated and control rats in either
the P or F1 generation. No significant differences
in prostate/seminal vesicle weights were observed between
generations when similar treatment groups were compared."
Spermatid
numbers: "Mean spermatid counts per testis, per gram
of testis, and per gram of testis per day of P and F1
generation male rats are shown in Table 5.
No statistically significant differences in spermatid
numbers between controls and sodium fluoride treatment
groups in either generation were observed. Similarly,
no statistically significant differences were observed
when the same treatment groups were compared between generations."
Serum
testosterone, LH and FSH: "Mean serum testosterone
concentrations, serum LH and serum FSH concentrations
of treated and control rats from the P and F1 generations
are shown in Table 5. No statistically
significant differences were observed between the treated
and control groups in either the P or F1 generation.
P v. F1: No significant differences were observed in mean
testosterone, LH or FSH values between generations when
the same dose levels were compared."
Non-reproductive
organ weights: "Mean organ weights of treated and
control rats from the P and F1 generation are presented
in Table 7... F1 generation:
Liver weight in the 100 and 250 ppm treatment groups were
significantly lower than controls. This was considered
a random occurrence and not biologically
significant because no dose-related effects
were observed. Otherwise, organ
weights in the F1 generation treatement groups were not
significantly different than F1 control values.
P v F1: There were no significant
differences observed in heart, liver, kidney or
spleen weights between generations for
any dose groups."
•
At injection site ... Occasionally, free germ cells (spermatocytes
or round spermatids) were found in the tubular lumen;
their presence was probably due
to mechanical trauma to the testis (handling or
cutting the testis; not shown)...
Significant
effects the authors reported in their 1997 paper:
"The
right testis weight and the paired testis weights from
the F1 generation controls were significantly
higher than the P generation controls. The left
testis weight of the F1 generation males was significantly
lower than that of the P males in the 25 ppm treatment
group. The right testis weight of the F1 generation males
was significantly higher than
that of the P generation males in the 100 ppm treatment
group."
Epididymal
weight: "... within the F1
generation the right epididymal weight of the 175 ppm
group was significantly lower
than the F1 control. No
dose-related effects were observed. P v F1: The
weight of the right epididymis from the F1 generation
was significantly lower than
that of the P group when epididymal weights for the 175
ppm treatment groups were compared. No other
differences in epididymal weight were observed between
generations."
Non-reproductive
organ weights: "Mean organ weights of treated and
control rats from the P and F1 generation are presented
in Table 7. P generation: Liver weight
in the 250 ppm treatment group was significantly
lower than the control group. Spleen weights in
the 175 and 250 ppm treatment groups were significantly
higher than the control group. These
events were considered random and not biologically significant
because dose-related toxic effects were not observed.
F1 generation: Liver weight in the 100
and 250 ppm treatment groups were significantly
lower than controls. This
was considered a random occurrence and not biologically
significant because no dose-related effects were observed.
Otherwise, organ weights in the F1 generation treatement
groups were not significantly different than F1 control
values. P v F1: When similar dose levels
were compared between generations, adrenal weights in
the F1 generation were significantly
lower than adrenal weights obtained from P generation
animals at all dose levels. No dose-related
toxic effects were observed and the differences observed
could be caused by technical differences in removing the
glands from the animals. There
were no significant differences observed in heart, liver,
kidney or spleen weights between generations for any dose
groups."
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Table
4. 1995 Study.
Effects: Control versus NaF treated groups.
Developmental toxicity of sodium fluroide in rats.
Collins TFX, Sprando RL, Shackelford ME, Black TN, Ames MJ,
Welsh JJ, Balmer MF, Olejnik N, Ruggles DI.
Food and Chemical Toxicology (1995) 33:11 951-960 |
"This
study was conducted to determine the effects of sodium
fluoride (NaF) on foetal development..." - page 951
|
Treated
groups with sodium fluoride levels in drinking water of:
10 ppm, 25 ppm, 100 ppm, 175 ppm, and 250 ppm (1.4, 3.9,
15.6, 24.7 or 25.1 mg/kg body weight)
Rats:
Caesarean-derived, viral antibody-free (CD-CRL: CD-BR, VAF+)
rats (Charles River Laboratories, Inc., Wilmington, MA,
USA) were used. On receipt, the males weighed 351-375 g,
and the females weighed 175-200 g. The males were used as
sires onlly, and were not treated.
Rat
Chow: Female rats were fed low-fluoride NIH-07 diet (7.95
ppm fluroide).
Animals
were mated. Caesarean sections were performed on gestation
day 20.
Analysis
of incidence of soft-tissue variations
in foetuses of rats treated with sodium fluoride
(Table 9). 6 of the 6 parameters:
•
Foetuses with 1+ variations: Control
group had higher number of effects compared to all treated
groups
•
Litters with foetuses with 1+ variations:
Control group had higher number
of effects compared to all treated groups
•
Foetuses with 2+ variations:
Control group had higher number of effects compared to
all treated groups
•
Litters with foetuses with 2+ variations:
Control group had higher number
of effects compared to all treated groups
•
Foetuses with 3+ variations: Control
group had higher number of effects compared to all treated
groups
•
Litters with foetuses with 3+ variations:
Control group had higher number
of effects compared to all treated groups
Incidence
of specific sternebral variations in foetuses
of rats treated with sodium fluoride (Table
4).
4 of the 6 parameters:
•
Incomplete ossification: Control group
had higher number of effects compared to 10 ppm, 25 ppm,
and 175 ppm treated groups.
•
Non-ossified: Control group had higher
number of effects compared to 10 ppm, 100 ppm, and 175
ppm treated groups.
•
Malaligned: Control grouphad higher number
of effects compared to 10 ppm, 25 ppm, 100 ppm, and 175
ppm treated groups.
•
Misshapen: Control
group had higher number of effects compared to all treated
groups.
Analysis
of incidence of sternebral variations in
foetuses of rats treated with sodium fluroide (Table
5).
3 of the 4 parameters:
•
Foetuses with 1 + variations: Control
group had higher number of effects compared to 10 ppm,
25 ppm, and 175 ppm treated groups.
•
Litters with foetuses with 1 + variations:
Control group had higher number of effects compared to
10 ppm, 25 ppm, and 175 ppm treated groups.
•
Foetuses with 2 + variations: Control
group had higher number of effects compared to 10 ppm
ad 25 ppm treated groups.
Incidence
of specific skeletal variations in foetuses
of rats treated with sodium fluroide
(Table 6). 22 of the 38 parameters:
•
Ribs, wavy: Control group had higher
number of effects compared to 10 ppm, 25 ppm, and 175
ppm treated groups.
•
14th rib (C7): Control group had higher
number of effects compared to 10 ppm, 25 ppm, and 100
ppm treated groups. Control group had same number of effects
as the 250 ppm treated group. (No effects in 10 ppm and
100 ppm treated groups.)
•
14th rib bud (L1): Control
group had higher number of effects compared to all treated
groups.
•
Ossified bud off L4: Control group had
same number of effects as 250 ppm group. (No effects in
10 ppm, 25 ppm, and 175 ppm treated groups).
•
Rib missing: Control group had same number
of effects as 25 ppm and 175 ppm treated groups. (No effects
in 10 ppm, 100 ppm, and 250 ppm treated groups.)
•
Centra. red. oss.: Control
group had higher number of effects compared to all treated
groups.
•
Centra. misshapen: Control group had
higher number of effects compared to 25 ppm and 175 ppm
treated groups.
•
Centra. bipartite: Control group had
higher number of effects compared to 10 ppm, 25 ppm, 100
ppm and 250 ppm treated groups. Control group had same
number of effects as the 175 ppm treated group.
•
Centra. not ossified: Control group had
same number of effects as the 250 ppm treated group.
•
Dorsal arches. red. oss: Control group
had higher number of effects than 10 ppm, 175 ppm and
250 ppm treated groups. (Note: these treated groups had
no effects listed).
•
Parietal red. oss: Control group had
same number of effects as the 175 ppm and 250 ppm treated
groups. (No effects listed for 10 ppm and 25 ppm treated
groups.)
•
Frontal. red. oss: Control group had
same number of effects as 100 ppm treated group. (All
other treated groups had no effect listed.)
•
Nasal. red. oss: Control group had same
number of effects as 175 ppm treated group. (No effect
listed for 10 ppm treated group.)
•
Supraoccipital. red. oss: Control group
had higher number of effects than 10 ppm treated group.
•
Hyoid. red. oss: Control group had higher
number of effects than 10 ppm and 175 ppm treated groups.
•
Zygomatic. red. oss: Control group had
same number of effects as 10 ppm treated group.
•
Ischicm. red. oss: Control group had
same number of effects as 25 ppm treated group. (No effects
listed for 10 ppm and 175 ppm treated groups.)
•
Pubis. red. oss: Control group had higher
number of effects compared to 10 ppm and 175 ppm treated
groups (these treated groups had no effects listed).
•
Metacarpals red. oss: Control group had
same number of effects as 100 ppm treated group. (No effects
listed for 10 ppm and 175 ppm treated groups.)
•
Metatarsals. red. oss: Control group
had higher number of effects compared to 10 ppm treated
group. (No effects listed for 175 ppm treated group.)
•
Basisphenoid. red. oss: Control
group is only group listed with effects.
•
Centrium. unilateral oss: Control group
and 175 ppm treated group had same number of effects.
(All other treated groups had no effects listed.)
-
in 14 of the 38 parameters: the 100 ppm treated group
had no effects listed
- in 15 of the 38 parameters: the Control group had no
effects listed
- in 15 of the 38 parameters: the 25 ppm treated group
had no effects listed
- in 15 of the 38 parameters: the 250 ppm treated group
had no effects listed
- in 20 of the 38 parameters: the 175 ppm treated group
had no effects listed
- in 26 of the 38 parameters: the 10 ppm treated group
had no effects listed
-
175 ppm treated group: the Control group had higher number
of effects: 14 vs. 8
- 10 ppm treated group: the Control group had higher number
of effects: 20 vs. 4
-
250 ppm treated group: in 8 parameters the Control group
had higher number of effects:
- 100 ppm treated group: in 7 parameters the Control had
higher number of effects
- 25 ppm treated group: in 11 parameters the Control group
had higher number of effects.
- 10 ppm treated group: in 1 parameter the Control had
same number of effects.
- 25 ppm treated group: in 2 parameters the Control group
had same number of effects.
- 100 ppm treated group: in 1 parameter the Control group
had same number of effects
- 175 ppm treated group: in 5 parameters the Control group
had same number of effects
- 250 ppm treated group: in 4 parameters the Control had
same number of effects
Analysis
of incidence of skeletal variations in
foetses of rats treated with sodium fluoride (Table
7) . 5 of the 6 parameters:
*
Foetuses with 1+ variations: Control
group had higher number of effects compared to 10 ppm,
and 175 ppm treated groups. Control group and 250 ppm
treated group had same number of effects.
•
Litters with foetuses with 1+ variations:
Control group had higher number
of effects compared to all treated groups.
•
Foetuses with 2+ variations: Control
group had higher number of effects compared to 10 ppm
treated group.
•
Litters with foetuses with 2+ variations:
Control group had higher number of effects compared to
10 ppm and 175 ppm treated groups.
•
Litters with foetuses with 3+ variations:
Control group had higher number of effects compared to
10 ppm treated group.
Incidence
of specific soft-tissue variations in foetuses
of rats treated with sodium fluroide (Table
8).
6 of 11 parameters:
•
Haemorrhages, internal: Control group
had higher number of effects compared to 175 ppm and 250
ppm treated groups. Control group had same number of effects
as the 100 ppm treated groups.
•
Hydroureter severe: Control group had
higher number of effects compared to 10 ppm, 25 ppm, 175
ppm, and 250 ppm treated groups.
•
Hydroureter moderate: Control
group had higher number of effects compared to all treated
groups.
•
Enlarged renal pelvis - moderate: Control
group had higher number of effects compared to 10 ppm,
25 ppm, 175 ppm, and 250 ppm treated groups. (Note: 25
ppm and 250 ppm treated groups had no effects listed.)
•
Enlarged uretal kidney - severe: Control
group had the same number of effects as the 25 ppm, 175
ppm, and 250 ppm treated groups.
•
Enlarged uretal kidney - moderate: Control
group had higher number of effects compared to all treated
groups.
-
in 5 of the 11 parameters: Control group had no effects
listed
- in 5 of the 11 parameters: 250 ppm treated group had
no effects listed
- in 4 of the 11 parameters: 10 ppm treated group had
no effects listed
- in 4 of the 11 parameters: 100 ppm treated group had
no effects listed
- in 4 of the 11 parameters: 175 ppm treaed group had
no effects listed
- in 3 of the 11 parameters: 25 ppm treated group had
no effects listed
Some
comments by the authors:
•
The data from our study can be compared with the data
available from other studies only to a limited degree,
owing to the differences in procedures, or species, or
both.
•
In the control group, one foetus had a cleft palate.
•
The control group showed the highest occurrence of in
utero deaths per litter (Table 3), and there was no
statistically significant difference between the control
and treated groups.
•
The average number of foetuses with at least one, at least
two and at least three sof-tissue variations
was less in all treated groups.
•
The average number of litters with foetuses with one or
more and two or more soft-tissue variations was
less in the treated groups than in the control group,
with no indication of dose relationship.
•
The average number of litters containing foetuses with
three or more soft-tissue variations was similar
in the control and treated groups.
•
Significant decreases in body weight gain were seen in
the females of the 250-ppm group on days 0-3 and 6-9 and
overall on days 0-20; these decreases are probably
related to decreased feed consumption.
•
A significant decrease in the mean number of corpora lutea
per female was seen in the dams of the 250-ppm group.
Because the number of corpora lutea is determined at birth,
this decrease is considered to be
random.
•
The mean number of viable male foetuses per litter was
significantly decreased in the 175-ppmn group when compared
with the control group, but this decrease was not dose-related
and is considered to be random.
•
Vertebral ossification, also considered a measure of fetal
ossification, showed no-dose-related
effects. In the control group,
8.2 vertebrae were ossified, and 8.6 [25 ppm] ,
8.3 [100 ppm], 8.2 [175 ppm], and 8.2 [250 ppm] ossified
vertebrae, respectively, were seen per fetus in the treated
groups.
•
the
foetuses were taken just before parturition: hence there
were no teeth to observe.
•
In the 2001 study the average number of fetuses per litter
with three or more skeletal variations in the 250 ppm
group was double that of the control
group (1.0 vs 0.5 per litter) but this
increase was insufficient to make the value statistically
significant.
|
Table
5. 1996 Study.
Effects: Control versus NaF treated groups.
Effect
of intratesticular injection of sodium fluoride on spermatogenesis
Sprando and Black et al.
Food and Chemical Toxicology (1996) 34:377-384
|
The
left testis of each rat was injected with either vehicle
(0.9% sodium chloride; vehicle-injected testis) or 50 ul
sodium fluoride (99% pure;p sodium fluoride-injected testis)
in vehicle at the following concentrations: 50, 175 and
250 ppm. The contralateral (right) testis of each rat was
not injected and served as an intact control (non-injected
control). Testicular tissues were collected at 24 hr and
1, 2 and 3 wk post injection and processed.
Discussion
(excerpt, page 383):
...
The only significant finding
in the present study was a local infilitraiton of leucocytes
and free germ cells into the inertubular space at the
injection site in both the vehicle-
and fluoride-injected testes. Leucocyte
infilitration in these groups was not considered a treatment-related
effect. Leucocyte infilitration is not an uncommon occurrence
when it injections are used (R.L. Sprando, unpublished
observation, 1990). A slight increase
in the amount of leucocyte infilitration was observed
in the 175 ppm fluoride treatment groups (25% of sections
observed) compared with that in the vehicle-injected
control group, the non-injected control group (13% and
0% of sections observed, respectively) and the other fluroide
treatment groups (18% and 17% of the sections observed
for the 50 and 250 ppm treatment groups, respectively).
At present it is not known why this
increase was observed; however, it
may have been a result of the tissue sampling procedure.
The appearance of both germ and Sertoli cells in
the interstitial space among the leucocytes was most likely
caused by trauma to the seminferous tubules at the time
of injection, since free germ cells were not observed
in the intertubular space distal to the site of injection
or in non-injected controls.
|
| Table
6. June 2001 Study. Control
versus NaF treated groups.
Multigenerational
evaluation of sodium fluoride in rats.
Collins
and Sprando et al.
Food
Chem Toxicol. 2001 Jun;39(6):601-13. |
"This
study evaluated the effects of sodium fluoride exposure
on reproductive function in three generations of rats."
- pae 611
|
•
The treated groups were exposed to NaF in drinking water
at levels of
25 ppm, 100 ppm, 175 ppm, and 250 ppm.
• No Fluoride levels in blood, bone and tissue are
presented
• Incidence of specific soft -tissue variations are
not identified by sex
•
Spontaneous disease lesions and incidental findings not
defined
•
Overall mean feed consumption of F1
females showed a significant
negative linear regression for days 0-70, although
none of the values was significantly
less than the control value (Table 1). During the
same period, F1 males in
the treated groups consumed less
feed than did the control group, but the decreases were
neither dose-related nor significant.
(page 606)
•
Thymus, heart, liver, spleen, kidney, adrenal and brain
weights were measured in adult females (150 days old)
and males (129 days old), as well as reproductive organs
(ovary wiehgt in females, and testis, epididymis, seminal
vesicle and prostate weights in males). No
significant differences were observed between control
and treated groups. (page 609)
•
Thymus, heart, liver, spleen, kidney, adrenal and brain
weights were also measured in weanling females and males
(25-27 days old), as well as reproductive organs (ovary
weight in females, and testis, epididymis, seminal vesicle
and prostate weights in males).
No significant differences were observed between control
and treated groups. (page 609-610).
•
Mating indices of F1 females were also over 90%, indicating
lack of compound-related effects. The fertility indices
of the females in the 25 and 250 ppm groups were slightly
less than the control animals, but the differences
were not statistically significant (Table 4) and are probably
due to random variation.
•
Spontaneous disease lesions and incidental findings in
other organs and tissues were of the usual
number and type commonly observed in Sprague-Dawley
rats at each age. These lesions
and findings occurred at
similar incidence rates in control and treated rats.
| Significant
Effects:
•
Body weights ... Weight
gain of F0 females and males during days 0-70 showed
a significant negative linerar regression. Only
the individual weight gain
of F0 males in the 250 ppm
was statistically less than the control.
In the F1 generation, weight gain of females and
males were similar. No significant
dose-related effects
•
... During development, the teeh of F1
adult females and males (34-35 animals per
group) were examined for color variations. No stained
or mottled teeth were observed in either sex of
any group. Mild whitening
of the teeth was observed in both females
and males at 100, 175 and
250 ppm NaF. Although
the effect was mild, the number of affected females
and males was increased
in a dose-related, statistically
signficant manner. (page 610-611)
... Rats
normally have orange-brown pigments in their teeth.
Loss of this pigment and the appearance of whitened
teeth is a known response to fluoride consumption
in rats. In the study reported here, adult
F1 females and males (34-35 per group) were
observed for tooth color. No dark discrete discolorations
(i.e. mottling) were observed in any of the animals
in our study at any time. The incidence of whitened
teeth was increased in a dose-related manner in
females and males from the groups given 100,
175 and 250 ppm sodium fluoride. The
effect was mild and of a cosmetic nature.
(page 612) |
|
Table
7. Rat chow used in the 6 Sprando and Collins et al. studies
Note
on "low fluoride diet"
Messer et al. (1973) state: "The diet used for all
experimental groups was the low
fluoride diet of Taylor et al. ... The fluoride
content varied from 0.1 to 0.3 ppm
fluoride, on a dry weight basis. Growth rates of
mice and rats fed this diet were found to be at least
equal to those of animals fed a standard laboratory ration."
- (page 1320)
Unlike
Sprando and Collins et. al, the Messer et al. 1973 study
published the fluoride levels in the humeri for 2 generations.
The authors state, "The concentration of fluoride
in the humeri of mice fed the low fluoride diet was 70
to 80 times lower than in animals receiving 50 pppm fluoride
in their drinking water." - (page 1325)
References:
Messer et al. (1973). Influence of fluoride intake on
reproduction in mice. Journal
of Nutrition 103:1319-1327
Taylor et al. (1961). Toxic effects of fluoride on the
rat kidney. Toxicol. Appl.
Pharmacol. 3, 290.
|
| Year
study published |
Title |
Authors
comments on Rat Chow used in study |
| 1995 |
Developmental
toxicity of sodium fluroide in rats.
Collins and Sprando et al.
Food and Chemical Toxicology 33:11 951-960 |
The males
were used as sires only, and were not treated. Female rats
were fed low-fluoride NIH-07 diet (7.95
ppm fluoride) to minimize interference with fluoride
in drinking water. The diet was prepared by Ziegler
Bros. Inc. (Gardiners, PA, USA),
the company that provided the diet for the fluoride studies
conducted by the NTP (NTP, 1990). |
| 1996 |
Effect
of intratesticular injection of sodium fluoride on spermatogenesis
Sprando and Black et al.
Food and Chemical Toxicology 34:377-384 |
No
mention of rat chow in this study. |
| 1997 |
Testing
the potential of sodium fluoride to affect spermatogenesis
in the rat.
Sprando and Collins et al.
Food and Chemical Toxicology 35: 881-890. |
During
the course of this study... fed a low
fluoride NIH-07 diet (7.95 ppm fluoride) to
minimize interference with fluoride in the drinking water.
The diet was prepared by Ziegler Bros.,
Inc. (Gardiners, PA, USA) and is the same
formulation as that used in the NTP chronic study (NTP,
1990). |
| 1998 |
Testing
the potential of sodium fluoride to affect spermatogenesis:
a morphometric study.
Sprando and Collins et al.
Food and Chemical Toxicology 36: 1117-1124 |
| June
2001 |
Multigenerational
evaluation of sodium fluoride in rats.
Collins
and Sprando et al.
Food
Chem Toxicol. Jun;39(6):601-13. |
Throughout
the study, males and females were fed
low-fluoride NIH-07 diet (7.95 pm fluoride)
to mimize interference with fluoride in drinking water.
The diet was prepared by Ziegler Bros.
Inc. (Gardiners, PA, USA), the company that provided
the low fluoride diet for the National Toxicology Program
(1990) studies, and the diet was the
same formulation as that used in the NTP studies. |
| Aug 2001 |
Developmental
toxicity of sodium fluoride measured during multiple generations.
Collins and Sprando et al.
Food Chem Toxicol. Aug;39(8):867-76. |
| Table
8. Rats used in the 6 Sprando and Collins et al. studies |
| Year
study published |
Title |
Authors
comments on Rats used in study |
Comments
|
| 1995 |
Developmental
toxicity of sodium fluroide in rats.
Collins and Sprando et al.
Food and Chemical Toxicology (1995) 33:11 951-960 |
Caesarean-derived,
viral antibody-free (CD-CRL:CD-BR, VAF + ) rats (Charles
River Laboratories, Inc., Wilmington, MA, USA) were
used. On receipt, the males weighed 351-375 g, and the females
weighted 175-200 g. |
The assumption
is that these rats were obtained directly from Charles River
Laboratories. |
| 1996 |
Effect
of intratesticular injection of sodium fluoride on spermatogenesis
Sprando and Black et al.
Food and Chemical Toxicology (1996) 34:377-384 |
96 adult
male Sprague-Dawley rats weighing 225-460 g were used. |
Authors
do not state where rats came from.
|
| 1997 |
Testing
the potential of sodium fluoride to affect spermatogenesis
in the rat.
Sprando and Collins et al.
Food and Chemical Toxicology 35 (1997) 881-890. |
The
124 male rats (P generation: n = 64 rats; F1 generation: n
= 60 rats) utilized in this study were obtained from a larger
two generation reproduction study. |
| 1998 |
Testing
the potential of sodium fluoride to affect spermatogenesis:
a morphometric study.
Sprando and Collins et al.
Food and Chemical Toxicology 36 (1998) 1117-1124 |
The
25 male rats utilized in this study were obtained from a
larger two-generation reproduction study (see Sprando et
al, 1997). |
| June
2001 |
Multigenerational
evaluation of sodium fluoride in rats.
Collins
and Sprando et al.
Food
Chem Toxicol. 2001 Jun;39(6):601-13. |
Caesarean-derived
(CD CRL:CD-BR). viral anti-body-free (240 males and 240 females)
were obtained from Charles River Laboratories
Inc. (Wilmington, MA, USA). The males and females weighed
51-75 g at the time of receipt. |
| Aug 2001 |
Developmental
toxicity of sodium fluoride measured during multiple generations.
Collins and Sprando et al.
Food Chem Toxicol. 2001 Aug;39(8):867-76. |
Caesarean-derived
(CD CRL-CD-BR). viral anti-body-free rats were obtained
from Charles River Laboratories, Inc. (Wilmington,
MA, USA). the males and females weighed 51-75 g at the time
of receipt. |
Attachments to FAN's September
13, 2005, Submission
to US EPA. Docket OPP-2005-0174.
Links for Tables will soon be added
Table 1. Sulfuryl fluoride:
Some of the Effects on Brain
Table 2. Sulfuryl Fluoriode Effects: Thyroid, Adrenal Cortex,
Heart, Kidney, Lung.
Table 3. Studies reporting effects on Brain from Fluoride
Table 4. Fluoride studies: IQ and Behavioral Effects.
Table 5. A few studies on G-Proteins and Fluoride
Table 6. Studies reporting effects on the Male Reproductive System
from Fluoride
Appendix
A. March 23, 2004. Objections and Request for Hearing
in the matter of Sulfuryl fluoride; Pesticide Tolerance. Final
Rule. Docket control number OPP-204-0373. Submitted to U.S EPA
by Fluoride Action Network and Beyond Pesticides. Online at http://www.fluorideaction.org/epa-sf.pdf
Appendix
C. March 30, 2005. Submission to the National Research
Council Committee: Toxicologic Risk of Fluoride in Drinking Water;
BEST-K-02-05-A. From Fluoride Action Network. Online at http://www.fluoridealert.org/fan-nrc.final.pdf
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