Several studies indicate that in-utero and peri-natal exposure to polychlorinated biphenyls (PCBs) induces adverse reproductive effects but it remains unclear whether such effects may be transmitted to subsequent generations. We therefore investigated the association between maternal exposure to PCBs and reproductive health in male and female offspring over three generations.Mouse dams were fed 0, 1, 10, 100 μg/kg/day of a PCB mixture (101+118) during pregnancy and lactation. PCB levels were measured in the tissues of both dams and offspring.PCB concentrations at all doses investigated were greater in the offspring than in the dams (P≤0.0001) confirming that the progeny were exposed as a result of maternal exposure. In F1 offspring, exposure to PCBs resulted in reductions in: i) testis weight (P≤0.05) and seminiferous tubule diameter (P≤0.05); ii) sperm viability (P≤0.0001) and developmental capacity (P≤0.05); iii) ovary weight (P≤0.05); iv) oocyte developmental capacity (P≤0.05), and in v) increased follicular atresia (P≤0.0001).In females, adverse effects were observed only in the F1 animals. In contrast, male offspring exhibited reduced sperm viability and altered seminiferous tubule distribution up to the third generation, showing intergenerational transmission.In summary, our data indicate that exposure to PCBs at the time of gonadal sex determination perturbed, significantly, the reproductive physiology of male and female offspring in adulthood. Furthermore, male reproductive deficiencies may be observed in at least two further generations. These findings have significant implications for reproductive health and fertility of animals and humans.

Effects of polychlorinated biphenyls in Cd-1 mice : reproductive toxicity and intergenerational transmission / P. Pocar, N. Fiandanese, C. Secchi, A. Berrini, B. Fischer, J.S. Schmidt, K. Schaedlich, S.M. Rhind, Z. Zhang, V. Borromeo. - In: TOXICOLOGICAL SCIENCES. - ISSN 1096-6080. - 126:1(2012 Mar), pp. 213-226.

Effects of polychlorinated biphenyls in Cd-1 mice : reproductive toxicity and intergenerational transmission

P. Pocar
Primo
;
N. Fiandanese
Secondo
;
C. Secchi;A. Berrini;V. Borromeo
Ultimo
2012

Abstract

Several studies indicate that in-utero and peri-natal exposure to polychlorinated biphenyls (PCBs) induces adverse reproductive effects but it remains unclear whether such effects may be transmitted to subsequent generations. We therefore investigated the association between maternal exposure to PCBs and reproductive health in male and female offspring over three generations.Mouse dams were fed 0, 1, 10, 100 μg/kg/day of a PCB mixture (101+118) during pregnancy and lactation. PCB levels were measured in the tissues of both dams and offspring.PCB concentrations at all doses investigated were greater in the offspring than in the dams (P≤0.0001) confirming that the progeny were exposed as a result of maternal exposure. In F1 offspring, exposure to PCBs resulted in reductions in: i) testis weight (P≤0.05) and seminiferous tubule diameter (P≤0.05); ii) sperm viability (P≤0.0001) and developmental capacity (P≤0.05); iii) ovary weight (P≤0.05); iv) oocyte developmental capacity (P≤0.05), and in v) increased follicular atresia (P≤0.0001).In females, adverse effects were observed only in the F1 animals. In contrast, male offspring exhibited reduced sperm viability and altered seminiferous tubule distribution up to the third generation, showing intergenerational transmission.In summary, our data indicate that exposure to PCBs at the time of gonadal sex determination perturbed, significantly, the reproductive physiology of male and female offspring in adulthood. Furthermore, male reproductive deficiencies may be observed in at least two further generations. These findings have significant implications for reproductive health and fertility of animals and humans.
Intergenerational transmission; Maternal exposure; Mouse; PCBs; Reproductive toxicity
Settore VET/01 - Anatomia degli Animali Domestici
Settore BIO/12 - Biochimica Clinica e Biologia Molecolare Clinica
Settore BIO/10 - Biochimica
mar-2012
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/168004
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