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      Effects of p-nonylphenol and resveratrol on body and organ weight and in vivo fertility of outbred CD-1 mice

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          Abstract

          The aim of this study was to analyse the multigenerational effects of para-nonylphenol (NP) and resveratrol (RES) on the body weight, organ weight and reproductive fitness of outbred CD-1 mice. The data indicate that in male mice, NP had an effect on the weight of selected reproductive organs and the kidneys in the parental (P) generation males. Effects on selected reproductive organs, the liver and kidneys in the F1-generation males were also seen. In females, effects of NP on body weight and kidney weight were seen in the P generation, but no effects on any measured parameter were seen in the F1 generation. RES had no effect on body weight but did have some effect on selected male and female reproductive organs in the P generation. RES altered the spleen and liver weights of P-generation males and the kidney weight of F1-generation males. Acrosomal integrity (using a monoclonal antibody against intra-acrosomal sperm proteins) was assessed for both generations of NP- and RES-treated mice. A significant reduction in acrosomal integrity was seen in both generations of NP-treated, but not in RES-treated, mice. Fewer offspring were observed in the second litter of the F2 generation of mice treated with NP; no similar effect was seen in RES-treated mice. The litter sex ratio was not different from controls. Unlike RES, NP had a negative effect on spermatogenesis and sperm quality with a resultant impact on in vivo fertility.

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          Most cited references23

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          Disruption of male reproductive tract development by administration of the xenoestrogen, nonylphenol, to male newborn rats.

          Louisa Lee (1998)
          Nonylphenol (NP) treatment of neonatal male rat pups decreased the size of their testes, epididymis, seminal vesicle, and ventral prostate, and increased the frequency of cryptorchidism (60.7%, n = 56 vs 0% in vehicle-treated control, n = 58) when examined at 31 d of age. NP effects are dose-dependent. These effects were only seen when NP was given at > or =20.8 mg/kg daily for 15 d. There is a critical period of vulnerability to NP during male reproductive development in the neonatal stage. Changes were found when NPs were given to male pups before 13 d of age, but not when given at > or =13 d of age. NP acts on the male reproductive tissues through the estrogen receptor (ER), since concomitant treatment with ICI 182,780, a specific ER antagonist, blocked NP's effects on the testis and male accessory organs. NP-treated males in the neonatal period had greatly reduced their subsequent capacity to impregnate young fertile females. Our results suggest that exposure of neonatal male rats to NP is potentially deleterious to their reproductive development and affects their reproductive performance.
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            Concentration of the phytoalexiin resveratrol in wine

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              Bioaccumulation of the lipophilic metabolites of nonionic surfactants in freshwater organisms.

              Nonylphenol (NP), nonlyphenol monoethoxylate (NP1EO) and nonylphenol diethoxylate (NP2EO) were determined in different freshwater organisms from the surface waters in the Glatt Valley, Switzerland. Rather high concentrations of the compounds investigated have been found to occur in macrophytic algae, particularly Cladophora glomerata (up to 38 mg kg(-1), 80 mg kg(-1), and 28 mg kg(-1) of NP, NP1EO and NP2EO, respectively), the bioconcentration factors of NP reaching up to 10,000. The concentrations in fish were much lower (NP: < 0.03-1.6 mg kg(-1), NP1EO: 0.06-7.0 mg kg(-1), and NP2EO: <0.03-3.1 mg kg(-1) indicating that biomagnification did not take place. Similar concentrations to those in the fish were determined in different tissues of a wild duck. The estimated bioconcentration factors in fish tissues ranged from 13 to 410 for NP, 3 to 300 for NP1EO and 3 to 330 for NP2EO.
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                Author and article information

                Journal
                Reprod Biol Endocrinol
                Reproductive biology and endocrinology : RB&E
                BioMed Central (London )
                1477-7827
                2003
                24 March 2003
                : 1
                : 30
                Affiliations
                [1 ]Department of Biology and Biochemistry of Fertilization, Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, Videnska 1083, 142 20 Prague 4, Czech Republic
                [2 ]Department of Toxicology, Institute of Experimental Medicine, Academy of Sciences of the Czech Republic, Videnska 1083, 142 20 Prague 4, Czech Republic
                [3 ]Department of Mammalian Gene Expression, Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, Videnska 1083, 142 20 Prague 4, Czech Republic
                Article
                1477-7827-1-30
                10.1186/1477-7827-1-30
                155686
                12749770
                41d4dc72-9484-4315-a76f-8f515cab488b
                Copyright © 2003 Kyselova et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
                History
                : 28 February 2003
                : 24 March 2003
                Categories
                Research

                Human biology
                Human biology

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