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REPORT TO MONSANTO COMPANY MUTAGENIC STUDY WITH
AROCLOR 1260 IN ALBINO MICE JANUARY 13, 1972
IBT NO. E62 3
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Dear Mr. Wheeler:
R: 1ST No. 623 - Mutagenic Study with Aroclor 1260 in Albino Mica
We are submitting herewith our laboratory report dated
January 13, 1972, prepared la connection with the above study.
Very truly yours,
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J. C. Calandra President
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REPORT TO MONSANTO COMPANY MUTAGENIC STUDY WITH
AROCLOR 1260 IN ALBINO MICE JANUARY 13, 1972
IBT NO. E623
I. Introduction A mutation it a change in tha character of a gone euch that morpho*
logic, physiologic, and/or biochemical alterations are produced. If this change in gene character occurs in the germinal cell, the alteration can be transmitted to succeeding generations. Changes of this nature can be artificially induced (irradiation, chemical exposure, etc.) or they may be spontaneous. A dominant lethal mutation, occurring in the male germinal cell, may lead to the inability of the affected cell to fertilise an egg or. once having fertilised, to the failure of development beyond the blastocyst stage (implantation). Male mice, treated with the test compound, are mated with untreated femalea. The numbers of pre-implantation losses and early resorptions in female mice, dissected at mid-gestation, are used to calcu late the mutation rate based on the induction of dominant lethal mutations.
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II. Summary
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A dominant lethal mutagenic study was conducted using albino mice-.
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Males were treated with a single intraperitoneal injection of Aroclor 1260 at
levels of either S00 (T-I) or 1,000 (T-1I) mg /kg of body weight. Another
group of males received methyl methanesulfonate (MMS) at 100 mg/Vg and
was used as a positive control.
Mating indices for Aroclor 1260 treated animals were unaffected. Two
positive control males and 1 T-I male died during the course of the study.
Data for treated animals regarding implantation sites, resorption
sites, and embryos did not differ from the control data. Mutation rates
were not unusual for the Aroclor treated animals.
MMS treated animals showed a positive response for the first 2 weeks
following treatment.
Therefore, treating male mice with Aroclor 1260 via an intraperitoneal
injection of 500 or 1,000 mg/kg did not cause a dominant lethal response*'
Respectfully submitted.
Report prepared by:
INDUSTRIAL BIO-TEST LABORATORIES, INC.
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Dennis Arnold, B.S.
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Croup Leader
Mutagenic Studies
Report approved by:
Gerald Kennedy, Hb. S. Senior Group Leader Metabolic and Mutagenic Studies
January 13, 1972 -
Manager, Toxicology
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.. m. Procedure
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A. Outline of Experiment
The test materiel was Aroclor 1260. Methyl methanesulfonate wme
used as a positive control. Charles River strain albino mice were received
at this liboratory at 60 to 70 days of age for use in the study. The organi
zation of groups is presented in Table I.
Grouo C PC T-[ T-U
TABLE 1 TEST MATERIAL: Aroclor 1260
Mutagenic Study Albino Mice ~ Organization of Groups
Do.e Level* (mg/kg) 100 $00 1. 000
Number of Melee Tre.ted 12
12
12 12
* Aroclor 1260 was administered as a 10 percent solution in corn oil* Control males received th vehicle in amounts equivalent to those received by the T-ll males. Positive control males received methyl methane sulfonate in a 1 percent corn oil solution.
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B, Dosage Levels
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The treatment levels were selected by intraperitoneal admtnis(ration o/ single graded doses of the test material to male mice. The
*
maximum tolerated dose was determined and dose levels employed in the
main study were based on these findings. The test material was adminis
tered intraperitoneally in a corn oil solution to male mice. Control
animals received the vehicle in volumes equivalent to those giver the high test
group and positive control males received methyl methane sulfonate.
C. Mating Schedule Each group consisted of 12 male mice, each of which was placed
in a cage with 3 untreated virgin females immediately sfter dose adminis
tration. At the end of 1 week, the females were removed from the cage
and replaced by another group of 3 females* This procedure continued
for 6 consecutive weeks, a period of time required for maturation of the
male mouse germ cells from the spermatocyte to the mature spermatozoon.
Experiments at this laboratory have shown that the reference mutagenic
compound* affects germinal cells in the meiotic and post-meiotic stages
prior to or during the spermatid stage. Recovery from the effects of MMS
is generally seen 3 weeks post-treatment. Following the sixth week of mating,
all males were sacrificed,
D. Female Sacrifice
The females were sacrificed approximately 1 week after re
moval from the breeding cage, at which time most females that had
.
* The reference mutagen in methyl methanesulfonate (MhlSV*
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mated were at mid-pregnancy. AH animals were sacrificed by carbon . dioxide asphyxiation. The numbers of Implantation sites, resorption rites, and embryos were recorded. Females were Judged to be pregnant if corpora lutea were present in the ovaries.
Resorption sites were divided into 2 groups, early deaths (dec!duomata) and late deaths. Lnte deaths refer to embryos which develop to a relatively advanced stage prior to death, so that the placenta and fetal membranes or remnants thereof are visible. The frequency of late deaths is apparently unaffected by mutagens and. therefore, would appear to be non-genetic in this test system. Deciduomata occur at the sites of implanted blastocysts which fail to develop following implantation. The mutagenicity of the chemical can bo measured by the proportions of all implantations which are deciduomata.
Mutagenicity can also be measured by comparing the mean num ber of viable embryos in the test group to the number obtained In the con trol group. Calculation of the mutation rate using this criterion assumes that pre-implantation losses among non-affected test animals will be es sentially the same ae losses observed among control animals.
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IV. Results
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A. Treatment Levels
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Doses were administered to groups of 4 male mice each to .
determine the levels for the main study. Exposures of 30, 100, 300, or .
1, 000 mg of Aroclor 1260 per kg of body weight failed to elicit any abnormal
reactions and no deaths were recorded during the 14-day observation period
following treatment.
B. Mortality and Reaction#
Two positive control males (weeks 1 and 3) and 1 T-I male
(week 3) died during the study. No other deaths occurred.
C. Mating Performance
Mating indices, defined as the number of ammalt pregnant
divided by the number of females mated times 100, and the number of
surviving males for each poet-treatment week are shown in Table IT.
All mating indices for the Aroclor 1260 treated animals seen in the
experiment are considered to bo normal for the mouse strain employed.
Positive control animals had a low mating index for the first week post
treatment.
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Mating Performance
To it Number of
Week Surviving
Crouo Number
Melee
Number of Animals Precnant Number of Females Mated
Meting Index (Percent!
C1 2 3 4 5 &
12 12 12 12 12 12
25/36 26/36 31/36 29/36 26/36 29/36
69.4 77.8 86. 1 80.6 77.8 80.6
PC i 2 3_ 4 5 6
11 11 tl 10 10 10
14/33 19/33 23/33 26/30 23/30 24/30
42.4 57.6 69.7 86.7 76. 7 80.0
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TABLE II continued
TEST MATERIAL: Aroclor 1260
Mutagenic Study - Albino Mice
Mating Performance
Teat Number of
Week Surviving
Group Number
Males
Number of Animals Pregnant Number of Females Mated
Mating Index (Percent)
T-I i 2
3 4 5 6
12 12 12 11 11 11
31/36 31/36 26/36 28/33 29/33 32/33
86. 1 86. 1 72.2 84.8 87.9 97.0
T-II
1 2 J 4 3 6
12 12 12 12 . 12 12
30/36 30/36 23/36 31/36 27/36 28/36
83.3 83.3 69.4 86. 1 75.0 77.8
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Group
Test Week Number
CI 2
3 4 S 6
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6
TABLE III
TEST MATERIAL: Aroclor 1260
Mutagenic Study - Albino Mice
Pregnant Animals Examined
25 28 31* 29 28 29
14 19 23 26 23 24
Summary of Sacrifice Data
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Calculated
Implantation
Corpora Lutea
Sites
Resorption Sites
Early
Late
338 378 417
392 378 392
293 (11.7) 355 (12.7) 342 (11.0) 357 (12. 3) 341 (12.2) 349 (U.0)
5 (0.2) 9 (0.3) 14 (0.4) 15 (0.5) 13 (0. 5) 12 (0.4)
1 (0. 1) 0 (0. 0) 5 (0.2) 5 (0.2) 3 (0. 1) 3 (0. 1)
189 256 3 10 351 310 324
134 (9.6) 178 ( 9.4) 294 (12.8) 334 (12.8) 291(12.6) 292 (12.2)
41 (2.9) 47 (2.5) 13 (0.6) 16 (0.6) 14 (0.6) 17 (0.7)
2 (0. 1) 0 (0.0) 3 (0. 1) 4 (0.2) 5 (0.2) 2 (0. 1)
Embryos
287 (11.5) 346 (12.4| 323 (10.4) 337 (It.6) 325 (11.6) 334 (11.5)
91 ( 6.51 131 ( 6.9) 278 (12. 1) 314 (12. 1) 272 (11.8) 273 (11.4)
Note: Numbers in parentheses are the means per female. * Includes 1 pseudo-pregnant female (corpora lutea only).
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Group
Tt W.k Number
T-l 1 2 3 4 5 6
T-II
1 2 3 4 5 6
TABLE III continued
TEST MATERIAL: Aroclor 1260
Mutagenic Study - Albino Mice
Summary of Sacrifice Data
Pregnant Animals Examined
31 31 26* 28 29 32
30 30 25 31 27 28
Calculated
Implantation
Corpora Lutea
Sites
418
418
349 378 392 432
339 (10.9) 384 (12.4) 314 (12.1) 335 (12.0) 381 (13. 1) 398 (12.4)
405 342 (11.4) 405 371 (12.4) 338 312 (12. 5) 418 376 (12. 1) 364 330 (12.2) 378 349 (12.5)
Resorption Sites
Early
Late
13 (0.4)
7 (0. 2) 7 (0.3) 11 (0.4) 14 (0.5) 14 (0.4)
1 (0. 1)
7 (0. 1) 2 (0. 1) 5 (0. 2)
1 (0. 1) 4 (0. 1)
13 (0.4) IS (0. 5) 15 (0.6) 16 (0.5) 18 (0. 7) 13 (0. 5)
1 (0. 1) 2 (0. 1) 4 (0.2) 3 (0. 1)
1 (0. 1) 1 (0. 1)
Embryos
325 (10.5) 375 (12. 1) 305 (11. 7) 319 (11.4) 366 (12.6) 380 (11.9)
328 (10. 9) 354 (11.8) 293 (11. 7) 357 (11.5) 311 (11.5) 335 (12.0)
Notes Numbers In parentheses are the means per female. * Includes 1 pseudo-pregnant female (corpora lutea only).
E. Mutagenic Data
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A summary of results for the mutagenic study is presented
in Table IV.
PreImplantatinn Loss is defined ast
Number of Corpora Lutes Number of Implantation Sites K jqq Number of Corpora Lutea
The mutation rate may be calculated by comparing the number
of early resorptions (deciduomata) to the total number of implantations for each group.
Numbor of Early Resorption Sites x jqq ^ Number of Implantation Sites
table)
Another way of expressing the mutation rate, which takes into
account prs-implantation losses, is by comparing the mean number of
normal embryos in each test group to the mean number of embryos in
the control group.
inn / Embryos Test Croup/Female * ' Embryos Control Group/Female x
' (B in table)
Values prtsented were obtained by comparing each group to the contem*
porary control group (a) and to cumulative control data (b). Values with a
minus () sign indicate that the mean number of embryoa for that group and
week was greater than that of controls. The deviation from aero should not
txeeed 25 percent in the positive direction.
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TABLE IV
TEST MATERIAL* Aroclor 1260
Mutagenic Study - Albino Mice
Summary of Mutagenic Data
Tet Wek Number
1 2 3 4 5 6
1 2 3 4 5 6
Pre-Implantation Loaa and Mutation Rate a
Mutation Ratee
Pre-Implantation Loaa
B
(Percent) 13. 3
Aa
b
.1.7 - 0.9
6. 1 78.0 .
.2.5 -10.7
4. 1 10.4
8.9 4.2 - 0,9
9.8 3.8
0.9
11.0
3.4 - 1.7
29. 1 10.5
5.2 4.8 6. 1 9.9
30.6 26.4
4.4 4. 8 4.8 5.8
43.5 44.4 .16.3 -4.3
- 1.7 0.9
43.0 38.4 .4.3 .5.2 0.8
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TABLE IV continued
TEST MATERIAL: ArocJor 1260
Mutagenic Study - Albino Mice
Summary of Mutagenic Data
Teet Week Number
Pre-Implantation Ijoas and Mutation Rates
Pre-Implantation Loaa (Percent)
A
Mutation Rate* B
ab
1
18.9
3.8 8.7 7.9
2 8. 1 1.8 2.4 8.0
3
10.0
2.2 -12.5 -0.9
4
11.4
3.3 1.7 0.9
5 2.8 3.7 - 8.6 -7.7
6 7.9 3.5 - 3.5 -1.7
1
15. 6
3.8 5.2 4.4
2 8.4 4, 0 4.8 -5.4
3 7.7 4. 8 -11.5 -0.9
4
10.0
4.2 0.9 0.0
5 9.3 5.4 0.9 1.7
6 7.7 3.7 - 4.3 -2.5
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