Inhibition of Fumonisin B1 Cytotoxicity by Nanosilicate Platelets during Mouse Embryo Development

• Published in: PloS one Vol. 9; no. 11; p. e112290
• Main Authors: Liao, Yu-Jing, Yang, Jenn-Rong, Chen, Shuen-Ei, Wu, Sing-Jhou, Huang, San-Yuan, Lin, Jiang-Jen, Chen, Lih-Ren, Tang, Pin-Chi
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 10.11.2014; Public Library of Science (PLoS)
• Subjects: Abnormalities; Adsorbents; Adsorption; Agricultural biotechnology; Agriculture; Animal sciences; Animals; Biocompatibility; Biology and Life Sciences; Biomedical materials; Blastocyst - drug effects; Clay; Councils; Cytotoxicity; Cytotoxins - antagonists & inhibitors; Cytotoxins - chemistry; Cytotoxins - toxicity; Defects; Ecology and Environmental Sciences; Embryonic Development - drug effects; Embryos; Engineering and Technology; Feed additives; Feeds; Female; Females; Fetuses; Fumonisin B1; Fumonisins - antagonists & inhibitors; Fumonisins - chemistry; Fumonisins - toxicity; Galliformes; Gene expression; Genomics; Genotoxicity; Homology; Implantation; Lipid metabolism; Liver; Livestock; Male; Metabolism; Mice; Montmorillonite; Mycotoxins; Nanoparticles; Nanostructures; Phosphates; Physical Sciences; Physiology; Placenta; Platelets; Pregnancy; Proteins; Rodents; Salmonella; Signal transduction; Silicates - chemistry; Silicates - pharmacology; Sphingosine 1-phosphate; Sphingosine 1-phosphate phosphatase; Sphingosine kinase; Surgical implants; Teratogenesis; Toxicity; Uterus; Vitamin B; Weight reduction; Zoology
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0112290

Nanosilicate platelets (NSP), the form of natural silicate clay that was exfoliated from montmorillonite (MMT), is widely used as a feed additive for its high non-specific binding capacity with mycotoxins such as fumonisin B1 (FB1), and has been evaluated its safety for biomedical use including cytotoxicity, genotoxicity, and lethal dosage (LD). In the study, we further examined its toxicity on the development of CD1 mouse embryos and its capacity to prevent teratogenesis-induced by FB1. In vitro cultures, NSP did not disturb the development and the quality of intact pre-implantation mouse embryos. Further, newborn mice from females consumed with NSP showed no abnormalities. NSP had an unexpected high adsorption capacity in vitro. In contrast to female mice consumed with FB1 only, a very low residual level of FB1 in the circulation, reduced incidence of neutral tube defects and significantly increased fetal weight were observed in the females consumed with FB1 and NSP, suggesting a high alleviation effect of NSP on FB1 in vivo. Furthermore, FB1 treatment disturbed the gene expression of sphingolipid metabolism enzymes (longevity assurance homolog 5, LASS 5; sphingosine kinase 1, Sphk1; sphingosine kinase 2, Sphk2; sphingosine 1- phosphate lyase, Sgpl1; sphingosine 1-phosphate phosphatase, Sgpp1) in the maternal liver, uterus, fetus, and placenta, but NSP administration reversed the perturbations. Based on these findings, we conclude that NSP is a feasible and effective agent for supplementary use in reducing the toxicity of FB1 to animals.