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. 2024 Feb 1;13(1):tfae014.
doi: 10.1093/toxres/tfae014. eCollection 2024 Feb.

Effects of acrylamide exposure during pregnancy and lactation on the development of myelin sheath of corpus callosum in offspring rats

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Effects of acrylamide exposure during pregnancy and lactation on the development of myelin sheath of corpus callosum in offspring rats

Shuping Liu et al. Toxicol Res (Camb). .

Abstract

Acrylamide is an alkene known to induce neurotoxicity in humans and experimental animals. However, the effects of acrylamide on the development of myelin sheath are unclear. The present study was to explore the effects of acrylamide exposure during pregnancy and lactation on the development of myelin sheath in offspring rats. Four groups of thirty-two pregnant Sprague-Dawley rats were exposed to 0, 4.5, 9 and 18 mg/kg BW acrylamide by gavage from gestational day 15 to postnatal day 13. The corpus callosum of nine offspring rats per group were dissected in postpartum day 14. Structural changes and lipid contents in myelin sheaths were examined by transmission electron microscopy(TEM) and Luxol Fast Blue staining(LFB). The expression of MBP and PLP was evaluated by immunohistochemistry and Western blotting. TEM showed that the myelin sheaths in the 18 mg/kg group were disordered compared with control group. Luxol Fast Blue staining gradually decreased with increasing acrylamide maternal exposure. The immunohistochemistry and Western Blotting results showed that maternal exposure to acrylamide caused a decreasing trend in MBP and PLP in the corpus callosum of rats at postnatal day 14. Furthermore, these reduced protein levels may be neurodevelopmental toxicity's mechanism in response to maternal exposure to acrylamide.

Keywords: Corpus callosum; acrylamide; myelin basic protein (MBP); myelin proteolipid protein (PLP); offspring rats.

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References

    1. Taeymans D, Wood J, Ashby P, Blank I, Studer A, Stadler RH, Gondé P, Eijck P, Lalljie S, Lingnert H, et al. . A review of acrylamide: an industry perspective on research, analysis, formation, and control. Crit Rev Food Sci Nutr. 2004:44(5):323–347. - PubMed
    1. Koszucka A, Nowak A, Nowak I, Motyl I. Acrylamide in human diet, its metabolism, toxicity, inactivation and the associated European Union legal regulations in food industry. Crit Rev Food Sci Nutr. 2020:60(10):1677–1692. - PubMed
    1. Wu R, Wang Q, Wang G. Immobilized enzyme on pulp fiber through layer-by-layer technique using cationic polyacrylamide for whitewater treatment from papermaking. Bioprocess Biosyst Eng. 2019:42(10):1583–1589. - PubMed
    1. Zhao M, Zhang B, Deng L. The mechanism of acrylamide-induced neurotoxicity: current status and future perspectives. Front Nutr. 2022:9:859189. - PMC - PubMed
    1. Huang M, Jiao J, Wang J, Xia Z, Zhang Y. Exposure to acrylamide induces cardiac developmental toxicity in zebrafish during cardiogenesis. Environ Pollut. 2018:234:656–666. - PubMed

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