Effects of PCB on reproductive success in Sprague-Dawley rats exposed to Aroclor 1254[R] for one year (1).
Donahue, Douglas A. ; Bowen, Christa L. ; Provost, Terri L. 等
ABSTRACT. Polychlorinated biphenyls (PCB) are environmental
contaminants that have been a problem since the 1960s. PCB are a serious
concern because they are widespread, lipophilic, and bioaccumulate
through food webs concentrating in adipose tissue. PCB are a threat to
both wildlife and humans because they elicit metabolic and endocrine
disruptions with some problems including hypothyroxinemia, spatial
learning and memory deficits, neurochemical and neurobehavioral
alterations, and reproductive alterations. Sprague-Dawley rats were
obtained that had been exposed to Aroclor 1254[R] in the diet at 1.25
ppm or 25.0 ppm dosage for one year before being mated. Males and
females were placed together in a cage and females were tested each day
for a sperm-positive vaginal smear. After a sperm positive vaginal
smear, females were housed separately, maintained on their respective
diets, and weighed daily until weight gain reversal or miscarriage. AH
animals in the present study that were fed PCB had weight gain reversal
or miscarriage, whereas controls of a similar age all carried pregnancy
to term. The results of the present study indicate that continuous
ingestion of Aroclor 1254[R] at low doses has a depressive effect on
reproductive success.
OHIO J SCI 102 (5):102-105, 2002
INTRODUCTION
Polychlorinated biphenyls (PCB) are environmental contaminants that
have been a recognized problem since the 1960s (Jacobsen and Jacobsen
1997). PCB are a serious concem because they are widespread, lipophilic,
and bioaccumulate through food webs by concentrating in adipose tissue.
These contaminants are a threat to both wildlife and humans because they
cause metabolic and endocrine disruption (Aronson and others 2000;
Gerstenberger and others 2000). Some of the problems associated with PCB
include hypothyroxinemia, spatial learning and memory deficits,
neurochemical and neurobehavioral alterations, and reproductive
alterations (Schantz and others 1997). Accidental ingestion by humans,
which occurred in Japan in 1968 and Taiwan in 1979, has caused many
long-term effects including hyperpigmentation, inflamed conjunctival glands, and intellectual impairment (Kuratsune and others 1972). As a
result of human exposure, PCB have been detected in human serum, adipose tissues, breast tissues, and brain tissues (Aronson and others 2000).
Previous studies done in our lab using large amounts of the PCB
mixture Aroclor 1254[R] (62.5, 125, or 250 ppm) in the maternal diet
have reported a decrease in body weight, spatial learning problems, and
subnormal thyroid status in young rats (Juarez de Ku 1992; Pritts 1996).
Using smaller amounts of Aroclor 1254[R] (1.25, 12.5, or 25.0 ppm)
resulted in alterations in pup thyroid status, depressed body weight,
and problems in spatial learning in the Morris Water Maze (Pritts 1996;
Provost and others 1999). The present study was designed to examine the
long-term reproductive effects of Aroclor 1254[R] on animals exposed to
a diet containing small amounts of PCB (1.25 and 25.0 ppm) and on the
second generation of offspring from animals exposed for one year.
MATERIALS AND METHODS
Sprague-Dawley rats were obtained from the Bowling Green State
University Animal Research Facility. Animals received food and water ad
libitum in a temperature-monitored environment of 20[degrees]C and
20-50% humidity. Parents of the animals used in the present study were
female rats weighing 225-275 g that were mated to males of the same
strain. Once females were determined to be pregnant, confirmed by a
sperm-positive vaginal smear, they were caged separately. Rats were fed
a diet consisting of standard rat chow (Mowlan Teklad, Madison, WI) with
Aroclor 1254[R] (AccuStandard, Inc., New Haven, CT) added at 1.25 or
25.0 ppm (w/w). Control animals were continued on standard diet after
conception. On the third day following birth, litters were culled to
eight pups consisting of four females and four males, where possible.
The pups remained in the maternal cage until thirty days of age, at
which time two rats were removed for use in another study. The remaining
six rats were housed three females and three males per cage, where
possible.
Ten of the rats for the present study were maintained on the
control diet of standard rat chow. Six of the rats for the present study
were born to mothers fed PCB, and were given a control diet (consisting
of standard rat chow with no PCB) at thirty days of age. The remaining
thirty rats were left on the PCB-containing diet that their mothers were
fed from the first day of pregnancy (standard rats chow containing
Aroclor 1254[R] at 1.25 or 25.0 ppm). At approximately one year of age
these female rats were mated to males of the same strain with varying
degrees of exposure to PCB. The mating protocol resulted in the
generation of a total of five groups. Controls consisted of mating pairs
of female and male rats that had never been exposed to PCB. Treatment
group one consisted of PCB-control males (males exposed to Aroclor
1254[R] during gestation and for thirty days after birth, then given a
control diet) mated to 1.25 ppm Aroclor 1254[R] females. Treatment group
2 consisted of PCB-control males mated to 25.0 ppm Aroclor 1254[R]
females. The 3rd treatment group consisted of males and females both
continuously exposed to 1.25 ppm Aroclor 1254[R] from gestation. The 4th
treatment group consisted of males and females continuously exposed to
25.0 ppm Aroclor 1254[R] from gestation. Females pregnant from these
matings were caged separately and weighed daily until birth of pups or
miscarriage. Statistical analysis was performed using StatView (SAS
Institute, Cary, NC). Statistical significance was ascribed to p
<0.05 with ANOVA and Fisher's PLSO was used to detect
statistical differences between groups.
RESULTS
All PCB-fed animals demonstrated an increase in the time between
placement of males and females in the same cage and presence of a
sperm-positive vaginal smear (Fig. 1), as compared with controls (p
<0.001). Animals exposed to 25.0 ppm Aroclor 1254[R] required a
significantly greater time of cohabitation for copulation to occur than
either controls or 1.25 ppm animals (p <0.007) (Fig. 1).
[FIGURE 1 OMITTED]
All control females delivered normal, healthy young. None of the
PCB-exposed groups produced young, with pregnancy ending in miscarriage
(p <0.001) (Fig. 2). Miscarriages were detected by reversal of weight
gain demonstrated by all females after a sperm-positive vaginal smear
(Fig. 3). When an animal returned to its pre-pregnancy weight or less,
vaginal smears were performed in order to determine whether reproductive
cyclicity had been re-established, and return to cyclicity was taken as
evidence of miscarriage. All animals which were assumed to have
miscarried returned to reproductive cyclicity by what would have been
the middle of pregnancy (day 11) (Fig. 3).
[FIGURES 2-3 OMITTED]
DISCUSSION
The results of the present study indicate that Aroclor 1254[R] has
a depressive effect on reproductive success in animals exposed to this
PCB mixture for one year. The effect of Aroclor 1254[R] may be explained
if one examines more closely reported effects of PCB on reproduction.
Polychlorinated biphenyls have been shown to mimic estrogenic
affects (Ahmed 2000) by actively competing for estrogen receptors
(Krogenaes and others 1998) and by causing modifications similar to
those resulting from an overproduction of estrogen (Safe 1994).
Ovulation in rats occurs during estrus temporally coincident with
behavioral changes that allow copulation to occur (Hadley 2000). An
explanation for the increase in time to copulation for animals exposed
to Aroclor 1254[R] for one year may be based on occurrence of delays of
behavioral estrus of the animals. Jonsson and others (1976) exposed
animals to Aroclor 1242[R] in dosages of 3.7 and 7.5 mg/ kg/day
(equivalent to 111 ppm and 225 ppm) for 36 weeks and observed altered
estrous cycles, most often skipping estrus, with ovulation inhibited in
50% of treated animals. Brezner and others (1984) showed that in rats
exposed to 10.0 mg/kg/day (equivalent to 300 ppm) of Aroclor 1254[R] for
6 weeks, the animals developed prolonged estrous cycles. These previous
investigators used large doses of PCB to cause altered estrous cycles,
which would have increased time to copulation. Although cycle length was
not measured in the present study, demonstrated increased time to
copulation may be inferred that the estrous cycle was altered. Previous
studies have treated animals with PCB for 0-6 months, but never for
longer than 6 months. The present study treated the animals with PCB for
one year, and the possibility exists that bioaccumulation of the smaller
dosages of PCB used in the present study (1.25 or 25.0 ppm) may be equal
to the short duration of larger dosages of PCB.
Since all males in the present study were also exposed to PCB,
their input to unsuccessful pregnancy maintenance can also be
considered. Rats undergo fertilization by oogamy, where mobile sperm
swim to a stationary egg (Gilbert 2000). It has been found that in male
animals exposed to PCB, doses as small as 1.25 ppm have altered semen
quality (Guo and others 2000). The same study reported that humans
exposed to PCB have reduced daily sperm production and an increase in
the number of abnormal sperm. PCB have been reported to cause
alterations in sperm, including mutation in the genome and outward
phenotypic expression (Guo and others 2000). Sager and others (1987)
reported that early postnatal exposure to Aroclor 1254[R] did not affect
the production, morphology, or motility of sperm; however, the ability
of these sperm to fertilize eggs was severely impaired. If the sperm
were able to swim to the egg and successfully fertilize the egg, it is
possible that the zygote that resulted was abnormal, which might cause
the natural abortion of the young by our exposed animals.
Future studies should include breeding of unexposed males to
PCB-exposed females and also breeding unexposed females to PCB-exposed
males. This would help to determine whether the reproductive effects
seen in exposed animals in the present study were caused by the males,
females, or both sexes. Krajnak and others (2001) showed that, as an
animal ages, there is a delay in completion of the estrous cycle
extending the cycle beyond the normal 4-5 days. Since the animals in the
present study were one year of age, mating PCB-exposed rats at 6-12
months of age may allow for viable offspring. With such offspring, it
might be possible to investigate the specific mechanisms that come into
play to explain potential increased sperm abnormality and abnormal
reproductive cyclicity.
ACKNOWLEDGEMENTS. The authors thank Dr. Suzanne K. Miller for her
financial assistance; Denise Hook, KoriAnne Bagrowski, Brent Drouillard,
and the BGSU Animal Care Facility for their help in raising the animals;
Anne Collaco for her help with StatView and the endless questions
concerning the program; and Dr. Stan L. Smith for his comments on this
manuscript.
(1) Manuscript received 9 October 2001 and in revised form 20 March
2002 (#01-26).
(2) Present Address: Utica College of Syracuse University, 1600
Burrstone Road, Utica, NY 13502.
(3) To whom requests for reprints should be addressed.
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DOUGLAS A. DONAHUE, CHRISTA, L. BOWEN, TERRI L. PROVOST (2), AND
LEE A. MESERVE (3), Department of Biological Sciences, Bowling Green
State University, Bowling Green, OH 43403