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Prenatal Arsenite Exposure Alters Maternal Cardiac Remodeling During Late Pregnancy. | LitMetric

AI Article Synopsis

  • Inorganic arsenic exposure from drinking water is linked to chronic diseases, including cardiovascular issues, but its impact on maternal heart health during pregnancy has not been thoroughly researched.
  • A study with C57BL/6J mice exposed to sodium arsenite during pregnancy revealed that high levels (1000 µg/L) disrupted normal heart growth and reduced key hormone receptors, indicating potential risks to maternal cardiovascular health.
  • Findings suggest that arsenic exposure during pregnancy may impair maternal cardiac remodeling and contribute to future cardiovascular disease, emphasizing the need to minimize such exposure for maternal and fetal health.

Article Abstract

Exposure to inorganic arsenic through drinking water is widespread and has been linked to many chronic diseases, including cardiovascular disease. Arsenic exposure has been shown to alter hypertrophic signaling in the adult heart, as well as in-utero offspring development. However, the effect of arsenic on maternal cardiac remodeling during pregnancy has not been studied. As such, there is a need to understand how environmental exposure contributes to adverse pregnancy-related cardiovascular events. This study seeks to understand the impact of trivalent inorganic arsenic exposure during gestation on maternal cardiac remodeling in late pregnancy, as well as offspring outcomes. C57BL/6J mice were exposed to 0 (control), 100 or 1000 µg/L sodium arsenite (NaAsO ) beginning at embryonic day (E) 2.5 and continuing through E17.5. Maternal heart function and size were assessed via transthoracic echocardiography, gravimetric measurement, and histology. Transcript levels of hypertrophic markers were probed via qRT-PCR and confirmed by western blot. Offspring outcomes were assessed through echocardiography and gravimetric measurement. We found that exposure to 1000 µg/L iAs abrogated normal physiologic growth of the maternal heart during late pregnancy and reduced transcript levels of estrogen receptor alpha (ERα), progesterone receptor membrane component 1 (Pgrmc1) and progesterone receptor membrane component 2 (Pgrmc2). Both 100 and 1000 µg/L iAs also reduced transcription of protein kinase B (Akt) and atrial natriuretic peptide (ANP). Akt protein expression was also significantly reduced after 1000 µg/L iAs exposure in the maternal heart with no change in activating phosphorylation. This significant abrogation of maternal cardiac hypertrophy suggests that arsenic exposure during pregnancy can potentially contribute to cardiovascular disease. Taken together, our findings further underscore the importance of reducing arsenic exposure during pregnancy and indicate that more research is needed to assess the impact of arsenic and other environmental exposures on the maternal heart and adverse pregnancy events.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10557683PMC
http://dx.doi.org/10.1101/2023.09.28.559986DOI Listing

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