LAUSR.org creates dashboard-style pages of related content for over 1.5 million academic articles. Sign Up to like articles & get recommendations!

The roles of bone morphogenetic protein 2 in perfluorooctanoic acid induced developmental cardiotoxicity and L‐carnitine mediated protection

Photo by heytowner from unsplash

&NA; Perfluorooctanoic acid (PFOA), a wide spread environmental pollutant, was associated with developmental cardiotoxicity in chicken embryo, while the underlying molecular mechanism had not been fully elucidated. In the current… Click to show full abstract

&NA; Perfluorooctanoic acid (PFOA), a wide spread environmental pollutant, was associated with developmental cardiotoxicity in chicken embryo, while the underlying molecular mechanism had not been fully elucidated. In the current study, 2 mg/kg (egg weight) PFOA and/or 100 mg/kg (egg weight) L‐carnitine were exposed to embryonic day zero (ED0) chicken embryo via air cell injection, and then bone morphogenic protein 2 (BMP2) silencing lentivirus or BMP2 recombinant protein were introduced into ED2 embryo. Electrocardiography and histological methods were utilized to assess the cardiac function and morphology in hatchling chickens, respectively. Consistent with previous results, 2 mg/kg PFOA exposure at ED0 significantly elevated heart rate and thinned right ventricular wall in hatchling chickens, while L‐carnitine co‐treatment reverted such changes. BMP2 silencing induced very similar changes in hatchling chicken hearts as PFOA exposure, while co‐exposure of recombinant BMP2 protein alleviated PFOA‐induced changes. L‐carnitine exposure alleviated the BMP2‐silencing induced changes as well. Western blotting revealed that PFOA exposure enhanced BMP2 expression and suppressed pSMAD1 expression in ED15 chicken embryo hearts, while both changes were reverted by L‐carnitine co‐exposure. Furthermore, silencing of BMP2 significantly increased the expression level of PPAR alpha in ED15 chicken embryo hearts, while silencing of PPAR alpha did not have significant impact on BMP2 expression. In conclusion, BMP2/pSMAD1 signaling participates in the PFOA‐induced developmental cardiotoxicity in chicken embryo, which is likely located upstream of PPAR alpha for this particular endpoint. Protection of BMP2 signaling might contribute to L‐carnitine mediated protection against PFOA‐induced developmental cardiotoxicity. Highlightsin ovo BMP2 silencing mimics PFOA‐induced developmental cardiotoxicity.Supplement of recombinant BMP2 alleviates PFOA‐induced developmental cardiotoxicity.BMP2 silencing upregulates PPAR alpha in ED15 chicken embryo hearts.

Keywords: developmental cardiotoxicity; induced developmental; chicken embryo; bmp2; cardiotoxicity; carnitine

Journal Title: Toxicology and Applied Pharmacology
Year Published: 2018

Link to full text (if available)


Share on Social Media:                               Sign Up to like & get
recommendations!

Related content

More Information              News              Social Media              Video              Recommended



                Click one of the above tabs to view related content.