Exposure to hexavalent chromium causes infertility by disrupting cytoskeletal machinery and mitochondrial function of the metaphase II oocytes in superovulated rats

• Published in: Toxicology reports Vol. 9; pp. 219 - 229
• Main Authors: Wuri, Liga, Arosh, Joe A., Wu, John Z., Banu, Sakhila K.
• Format: Journal Article
• Language: English
• Published: Ireland Elsevier B.V 01.01.2022; Elsevier
• Subjects: Chromium; Cortical granules; F-actin; Mitochondria; Oocyte; Regular; Superovulation; Chromium; Mitochondria; F-actin; Superovulation; Oocyte; Cortical granules
• ISSN: 2214-7500; 2214-7500
• DOI: 10.1016/j.toxrep.2022.02.002

•Cr(VI) negatively impacted oocyte quality and morphology.•Cr(VI) disrupted cortical granules distribution.•Cr(VI) increased F-actin and distorted it’s spatiotemporal distribution.•Cr(VI) delayed first polar body extrusion.•Cr(VI) diminished mitochondrial function in the metaphase II oocyte. Previous studies from our laboratory showed that prenatal exposure to hexavalent chromium, Cr(VI), caused premature ovarian failure and decreased pregnancy rates and litter size. Exposure to the endocrine disrupting chemicals (EDCs) can cause X-chromosome aneuploidy of the oocytes, increasing chromosome missegregation and risk of infertility, autoimmune diseases, cancers, and various genetic disorders. Cr(VI) is an EDC that is widely used in numerous industries. Environmental exposure to Cr(VI) caused detrimental reproductive effects in women and health effects in infants from California. Women with occupational Cr(VI) exposure experienced infertility, pregnancy loss, spontaneous abortion, and stillbirth. However, the adverse effects of Cr(VI) on oocyte development and quality have not been reported. Mitochondrial membrane potential and function are the critical determinants of oocyte quality in natural pregnancies and successful assisted reproductive techniques. The cytoskeletal machinery of the oocytes orchestrates the meiotic division of the oocytes, whereas cortical granules (CGs) prevent polyspermy. Therefore, the objective of the current study was to examine whether the mechanism by which Cr(VI) compromises oocyte quality and morphology is by altering cytoskeleton dynamics and mitochondrial function of the metaphase II (MII) oocytes. Rats were treated with environmentally relevant doses of Cr(VI) (1 and 5 ppm potassium dichromate) in drinking water from postnatal day (PND) 22–28, followed by superovulation and retrieval of MII oocytes. The data indicate that Cr(VI) exposure disrupted F-actin structure and distribution pattern, compromised mitochondrial function, altered CGs distribution, increased dysmorphic and degenerated oocytes, delayed first polar body extrusion, and caused infertility.