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  1. Article ; Online: Human-relevant exposure to di-n-butyl phthalate tampers with the ovarian insulin-like growth factor 1 system and disrupts folliculogenesis in young adult mice.

    Jauregui, Estela J / McSwain, Maile / Liu, Xiaosong / Miller, Kara / Burns, Kimberlie / Craig, Zelieann R

    Toxicological sciences : an official journal of the Society of Toxicology

    2023  Volume 195, Issue 1, Page(s) 42–52

    Abstract: Phthalates are compounds used in consumer and medical products worldwide. Phthalate exposure in women has been demonstrated by detection of phthalate metabolites in their urine and ovarian follicular fluid. High urinary phthalate burden has been ... ...

    Abstract Phthalates are compounds used in consumer and medical products worldwide. Phthalate exposure in women has been demonstrated by detection of phthalate metabolites in their urine and ovarian follicular fluid. High urinary phthalate burden has been associated with reduced ovarian reserve and oocyte retrieval in women undergoing assisted reproduction. Unfortunately, no mechanistic explanation for these associations is available. In short term in vivo and in vitro animal studies modeling human-relevant exposures to di-n-butyl phthalate (DBP), we have identified ovarian folliculogenesis as a target for phthalate exposures. In the present study, we investigated whether DBP exposure negatively influences insulin-like growth factor 1 (IGF1) signaling in the ovary and disrupts ovarian folliculogenesis. CD-1 female mice were exposed to corn oil (vehicle) or DBP (10 µg/kg/day, 100 µg/kg/day, or 1000 mg/kg/day) for 20-32 days. Ovaries were collected as animals reached the proestrus stage to achieve estrous cycle synchronization. Levels of mRNAs encoding IGF1 and 2 (Igf1 and Igf2), IGF1 receptor (Igf1r), and IGF-binding proteins 1-6 (Ifgbp1-6) were measured in whole ovary homogenates. Ovarian follicle counts and immunostaining for phosphorylated IGF1R protein (pIGF1R) were used to evaluate folliculogenesis and IGF1R activation, respectively. DBP exposure, at a realistic dose that some women may experience (100 µg/kg/day for 20-32 days), reduced ovarian Igf1 and Igf1r mRNA expression and reduced small ovarian follicle numbers and primary follicle pIGF1R positivity in DBP-treated mice. These findings reveal that DBP tampers with the ovarian IGF1 system and provide molecular insight into how phthalates could influence the ovarian reserve in females.
    MeSH term(s) Humans ; Female ; Mice ; Animals ; Ovary ; Dibutyl Phthalate/toxicity ; Insulin-Like Growth Factor I/genetics ; Phthalic Acids
    Chemical Substances Dibutyl Phthalate (2286E5R2KE) ; phthalic acid (6O7F7IX66E) ; Insulin-Like Growth Factor I (67763-96-6) ; Phthalic Acids
    Language English
    Publishing date 2023-07-13
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 1420885-4
    ISSN 1096-0929 ; 1096-6080
    ISSN (online) 1096-0929
    ISSN 1096-6080
    DOI 10.1093/toxsci/kfad064
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Human relevant exposure to di-n-butyl phthalate tampers with the ovarian insulin-like growth factor 1 system and disrupts folliculogenesis in young adult mice.

    Jauregui, Estela J / McSwain, Maile / Liu, Xiaosong / Miller, Kara / Burns, Kimberlie / Craig, Zelieann R

    bioRxiv : the preprint server for biology

    2023  

    Abstract: Phthalates are compounds used in consumer and medical products worldwide. Phthalate exposure in women has been demonstrated by detection of phthalate metabolites in their urine and ovarian follicular fluid. High urinary phthalate burden has been ... ...

    Abstract Phthalates are compounds used in consumer and medical products worldwide. Phthalate exposure in women has been demonstrated by detection of phthalate metabolites in their urine and ovarian follicular fluid. High urinary phthalate burden has been associated with reduced ovarian reserve and oocyte retrieval in women undergoing assisted reproduction. Unfortunately, no mechanistic explanation for these associations is available. In short term in vivo and in vitro animal studies modeling human relevant exposures to di-n-butyl phthalate (DBP), we have identified ovarian folliculogenesis as a target for phthalate exposures. In the present study, we investigated whether DBP exposure negatively influences insulin-like growth factor 1 (IGF) signaling in the ovary and disrupts ovarian folliculogenesis. CD-1 female mice were exposed to corn oil (vehicle) or DBP (10 or 100 μg/kg/day) for 20-32 days. Ovaries were collected as animals reached the proestrus stage to achieve estrous cycle synchronization. Levels of mRNAs encoding IGF1 and 2 (
    Language English
    Publishing date 2023-03-16
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2023.03.15.532792
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Mono-n-Butyl Phthalate Distributes to the Mouse Ovary and Liver and Alters the Expression of Phthalate-Metabolizing Enzymes in Both Tissues.

    Jauregui, Estela J / Lock, Jasmine / Rasmussen, Lindsay / Craig, Zelieann R

    Toxicological sciences : an official journal of the Society of Toxicology

    2021  Volume 183, Issue 1, Page(s) 117–127

    Abstract: Humans are exposed to phthalates daily via items such as personal care products and medications. Reproductive toxicity has been documented in mice exposed to di-n-butyl phthalate (DBP); however, quantitative evidence of its metabolite, mono-n-butyl ... ...

    Abstract Humans are exposed to phthalates daily via items such as personal care products and medications. Reproductive toxicity has been documented in mice exposed to di-n-butyl phthalate (DBP); however, quantitative evidence of its metabolite, mono-n-butyl phthalate (MBP), reaching the mouse ovary and its effects on hepatic and ovarian biotransformation enzymes in treated mice is still lacking. Liquid chromatography/tandem mass spectrometry (LC-MS/MS) was employed to quantify MBP levels in liver, serum, and ovary from mice treated with a single or repeated exposure to the parent compound, DBP. Adult CD-1 females were pipet fed once or for 10 days with vehicle (tocopherol-stripped corn oil) or DBP at 1, 10, and 1000 mg/kg/day. Tissues and serum were collected at 2, 6, 12, and 24 h after the single or final dose and subjected to LC-MS/MS. Ovaries and livers were processed for qPCR analysis of selected phthalate-associated biotransformation enzymes. Regardless of duration of exposure (single vs repeated), MBP was detected in the tissues of DBP-treated mice. In single dose mice, MBP levels peaked at ≤6 h and fell close to background levels by 24 h post-exposure. Following the last repeated dose, MBP levels peaked at ≤2 h and fell to background levels by 12 h. Hepatic and ovarian expression of Lpl, Aldh1a1, Adh1, Ugt1a6a, and Cyp1b1 were altered in DBP-treated mice in a time- and dose-specific manner. These findings confirm that MBP reaches the mouse liver and ovary after oral exposure to DBP and influences the expression of hepatic and ovarian phthalate-associated biotransformation enzymes.
    MeSH term(s) Animals ; Chromatography, Liquid ; Dibutyl Phthalate/toxicity ; Female ; Liver ; Mice ; Ovary ; Phthalic Acids/toxicity ; Tandem Mass Spectrometry
    Chemical Substances Phthalic Acids ; Dibutyl Phthalate (2286E5R2KE) ; phthalic acid (6O7F7IX66E) ; monobutyl phthalate (ZI46LWZ45G)
    Language English
    Publishing date 2021-06-28
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 1420885-4
    ISSN 1096-0929 ; 1096-6080
    ISSN (online) 1096-0929
    ISSN 1096-6080
    DOI 10.1093/toxsci/kfab085
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Retinoic acid receptor signaling is necessary in steroidogenic cells for normal spermatogenesis and epididymal function.

    Jauregui, Estela J / Mitchell, Debra / Topping, Traci / Hogarth, Cathryn A / Griswold, Michael D

    Development (Cambridge, England)

    2018  Volume 145, Issue 13

    Abstract: Spermatogenesis in mammals is a very complex, highly organized process, regulated in part by testosterone and retinoic acid (RA). Much is known about how RA and testosterone signaling pathways independently regulate this process, but there is almost no ... ...

    Abstract Spermatogenesis in mammals is a very complex, highly organized process, regulated in part by testosterone and retinoic acid (RA). Much is known about how RA and testosterone signaling pathways independently regulate this process, but there is almost no information regarding whether these two signaling pathways directly interact and whether RA is crucial for steroidogenic cell function. This study uses a transgenic mouse line that expresses a dominant-negative form of RA receptor α (RAR-DN) and the steroidogenic cell-specific Cre mouse line,
    MeSH term(s) Animals ; Blood-Testis Barrier/cytology ; Blood-Testis Barrier/metabolism ; Fertility/physiology ; Male ; Mice ; Mice, Transgenic ; Retinoic Acid Receptor alpha/genetics ; Retinoic Acid Receptor alpha/metabolism ; Signal Transduction/physiology ; Spermatocytes/cytology ; Spermatocytes/metabolism ; Spermatogenesis/physiology ; Steroid 17-alpha-Hydroxylase/genetics ; Steroid 17-alpha-Hydroxylase/metabolism
    Chemical Substances Rara protein, mouse ; Retinoic Acid Receptor alpha ; Steroid 17-alpha-Hydroxylase (EC 1.14.14.19)
    Language English
    Publishing date 2018-07-09
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 90607-4
    ISSN 1477-9129 ; 0950-1991
    ISSN (online) 1477-9129
    ISSN 0950-1991
    DOI 10.1242/dev.160465
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Leydig cell genes change their expression and association with polysomes in a stage-specific manner in the adult mouse testis.

    Jauregui, Estela J / Mitchell, Debra / Garza, Savanna M / Topping, Traci / Hogarth, Cathryn A / Griswold, Michael D

    Biology of reproduction

    2018  Volume 98, Issue 5, Page(s) 722–738

    Abstract: Spermatogenesis in mammals occurs in a very highly organized manner within the seminiferous epithelium regulated by different cell types in the testis. Testosterone produced by Leydig cells regulates blood-testis barrier formation, meiosis, ... ...

    Abstract Spermatogenesis in mammals occurs in a very highly organized manner within the seminiferous epithelium regulated by different cell types in the testis. Testosterone produced by Leydig cells regulates blood-testis barrier formation, meiosis, spermiogenesis, and spermiation. However, it is unknown whether Leydig cell function changes with the different stages of the seminiferous epithelium. This study utilized the WIN 18,446 and retinoic acid (RA) treatment regime combined with the RiboTag mouse methodology to synchronize male germ cell development and allow for the in vivo mapping of the Leydig cell translatome across the different stages of one cycle of the seminiferous epithelium. Using microarrays analysis, we identified 11 Leydig cell-enriched genes that were expressed in stage-specific manner such as the glucocorticoid synthesis and transport genes, Cyp21a1 and Serpina6. In addition, there were nine Leydig cell transcripts that change their association with polysomes in correlation with the different stages of the spermatogenic cycle including Egr1. Interestingly, the signal intensity of EGR1 and CYP21 varied among Leydig cells in the adult asynchronous testis. However, testosterone levels across the different stages of germ cell development did not cycle. These data show, for the first time, that Leydig cell gene expression changes in a stage-specific manner during the cycle of the seminiferous epithelium and indicate that a heterogeneous Leydig cell population exists in the adult mouse testis.
    MeSH term(s) Animals ; Blood-Testis Barrier ; Gene Expression ; Leydig Cells/cytology ; Leydig Cells/metabolism ; Male ; Mice ; Polyribosomes/metabolism ; Seminiferous Epithelium/cytology ; Seminiferous Epithelium/metabolism ; Spermatogenesis/physiology ; Steroid 21-Hydroxylase/genetics ; Steroid 21-Hydroxylase/metabolism ; Testis/cytology ; Testis/metabolism ; Transcortin/genetics ; Transcortin/metabolism
    Chemical Substances Serpina6 protein, mouse ; Transcortin (9010-38-2) ; Cyp21a1 protein, mouse (EC 1.14.14.16) ; Steroid 21-Hydroxylase (EC 1.14.14.16)
    Language English
    Publishing date 2018-02-05
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 1118-6
    ISSN 1529-7268 ; 0006-3363
    ISSN (online) 1529-7268
    ISSN 0006-3363
    DOI 10.1093/biolre/ioy031
    Database MEDical Literature Analysis and Retrieval System OnLINE

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