A Novel’s Evidence of MSG-Induced Craniofacial Defects in Chick Embryo Models
DOI:
https://doi.org/10.48048/tis.2024.8718Keywords:
Monosodium glutamate, Craniofacial defect, Neural crest cells, Chick embryo, TeratogenAbstract
Monosodium glutamate (MSG), commonly used as an additive food enhancer, has been reported to have teratogenic effects on the embryo during development. The present study aimed to investigate the effect of MSG-induced teratogenicity, focusing on craniofacial formation in the chick embryo model. One hundred eighty fertilized eggs were divided into control and MSG groups. The chemicals were administered, and the results were investigated in 3-day-old embryos (ED-3), ED-6, and ED-10. The morphology and histology of craniofacial structures were studied using a stereomicroscope and light microscopy. The neural crest cells (NCCs) were investigated by the immunostaining technique. The results showed that a dose of 3 mg of MSG induced anterior neuropore opening and eye malformation in ED-3, and this was clearly demonstrated in ED-6. MSG also caused craniofacial bone malformation and delayed calcification in ED-10. Moreover, MSG induced apoptosis of NCCs and reduced the proliferation of NCCs in the craniofacial structures. These findings are the 1st report to demonstrate the teratogenicity of high doses of MSG-induced craniofacial defects in chick embryos during organogenesis.
HIGHLIGHTS
- Monosodium glutamate exposure causes craniofacial defects in chick embryos.
- The functions of the neural crest cells were abrogated due to monosodium glutamate-induced teratogenesis, which led to birth defects.
- The experimental protocols benefit teratogenicity studies, and the results can be applied to future studies to elucidate the causes of birth defects during organogenesis.
GRAPHICAL ABSTRACT
Downloads
References
S Rinkoff and RE Adlard. Embryology, craniofacial growth and development. StatPearls Publishing, Treasure Island, Florida, 2022.
AP Murillo-Rincón and M Kaucka. Insights into the complexity of craniofacial development from a cellular perspective. Front. Cell Dev. Biol. 2020; 8, 620735.
DM Roth, F Bayona, P Baddam and D Graf. Craniofacial development: Neural crest in molecular embryology. Head Neck Pathol. 2021; 15, 1-15.
Y Chai and RE Maxson Jr. Recent advances in craniofacial morphogenesis. Dev. Dynam. 2006; 235, 2353-75.
HN Shah, RE Jones, MR Borrelli, K Robertson, A Salhotra, DC Wan and MT Longaker. Craniofacial and long bone development in the context of distraction osteogenesis. Plast. Reconstr. Surg. 2021; 147, 54e-65e.
R Tevlin, A McArdle, D Atashroo, GG Walmsley, K Senarath-Yapa, ER Zielins, KJ Paik, MT Longaker and DC Wan. Biomaterials for craniofacial bone engineering. J. Dent. Res. 2014; 93, 1187-95.
SRF Twigg and AOM Wilkie. New insights into craniofacial malformations. Hum. Mol. Genet. 2015; 24, R50-R59.
ER Tamm. The development of the aqueous humor outflow pathway. In: DA Dartt (Ed.). Encyclopedia of the eye. Academic Press, Massachusetts, 2010, p. 16-21.
M Helwany, TC Arbor and P Tadi. Embryology, ear. StatPearls Publishing, Treasure Island, Florida, 2020.
TM Farhan, BA Al-Abdely, AN Abdullateef and AS Jubair. Craniofacial anomaly association with the internal malformations in the pediatric age group in Al-Fallujah City-Iraq. Biomed. Res. Int. 2020; 2020, 4725141.
W Shaw. Global strategies to reduce the health care burden of craniofacial anomalies: Report of WHO meetings on international collaborative research on craniofacial anomalies. Cleft Palate Craniofac. J. 2004; 41, 238-43.
S Liu, R Narumi, N Ikeda, O Morita and J Tasaki. Chemical‐induced craniofacial anomalies caused by disruption of neural crest cell development in a zebrafish model. Dev. Dyn. 2020; 249, 794-815.
W Huang, T Wu, WW Au and K Wu. Impact of environmental chemicals on craniofacial skeletal development: Insights from investigations using zebrafish embryos. Environ. Pollut. 2021; 286, 117541.
ME Bronner and NM LeDouarin. Development and evolution of the neural crest: An overview. Dev. Biol. 2012; 366, 2-9.
BK Hall. The neural crest and neural crest cells in vertebrate development and evolution. Springer, New York, 2008, p. 400.
J Casale and AO Giwa. Embryology, branchial arches. StatPearls Publishing, Treasure Island, Florida, 2021.
R Hunt and PN Hunt. The role of cell mixing in branchial arch development. Mech. Dev 2003; 120, 769-90.
P Noisa and T Raivio. Neural crest cells: From developmental biology to clinical interventions. Birth Defects Res. Part C Embryo Today 2014; 102, 263-74.
TL Creazzo, RE Godt, L Leatherbury, SJ Conway and ML Kirby. Role of cardiac neural crest cells in cardiovascular development. Annu. Rev. Physiol. 1998; 60, 267-86.
MN Vergara and MV Canto-Soler. Rediscovering the chick embryo as a model to study retinal development. Neural Dev. 2012; 7, 22.
MR Passos‐Bueno, CC Ornelas and RD Fanganiello. Syndromes of the first and second pharyngeal arches: A review. Am. J. Med. Genet. Part A 2009; 149, 1853-9.
JM Johnson, G Moonis, GE Green, R Carmody and HN Burbank. Syndromes of the first and second branchial arches, part 1: Embryology and characteristic defects. Am. J. Neuroradiol. 2011; 32, 14-9.
SA Green, M Simoes-Costa and ME Bronner. Evolution of vertebrates as viewed from the crest. Nature 2015; 520, 474-82.
MED Bellard, Y Rao and M Bronner-Fraser. Dual function of Slit2 in repulsion and enhanced migration of trunk, but not vagal, neural crest cells. Int. J. Cell Biol. 2003; 162, 269-79.
Y Shi, J Li, C Chen, M Gong, Y Chen, Y Liu, Jie Chen, Tingyu Li and W Song. 5-Mehtyltetrahydrofolate rescues alcohol-induced neural crest cell migration abnormalities. Mol. Brain 2014; 7, 67.
S Cerrizuela, GA Vega‐Lopez and MJ Aybar. The role of teratogens in neural crest development. Birth Defects Res. 2020; 112, 584-632.
KM Appaiah. Monosodium glutamate in foods and its biological effects. In: CE Boisrobertm, A Stjepanovic, S Oh and HLM Lelieveld (Eds.). Ensuring global food safety: Exploring Global Harmonization. Elsevier, Amsterdam, Netherlands, 2010, p. 217-26.
K Beyreuther, HK Biesalski, JD Fernstrom, P Grimm, WP Hammes, U Heinemann, O Kempski, P Stehle, H Steinhart and R Walker. Consensus meeting: Monosodium glutamate - an update. Eur. J. Clin. Nutr. 2007; 61, 304-13.
Z Kazmi, I Fatima, S Perveen and SS Malik. Monosodium glutamate: Review on clinical reports. Int. J. Food Prop. 2017; 20, 1807-15.
K Niaz, E Zaplatic and J Spoor. Extensive use of monosodium glutamate: A threat to public health? EXCLI J. 2018; 17, 273-8.
J Roongruangchai, Y Viravud, V Plakornkul, K Sripaoraya, W Boonmark and K Roongruangchai. The teratogenic effects of monosodium glutamate (MSG) on the development of chick embryos. Siriraj Med. J. 2018; 70, 514-22.
F Al-Qudsi and A Al-Jahdali. Effect of monosodium glutamate on chick embryo development. J. Am. Sci. 2012; 8, 499-509.
A Zanfirescu, A Ungurianu, AM Tsatsakis, GM Nițulescu, D Kouretas, A Veskoukis, D Tsoukalas, AB Engin, M Aschner and D Margină. A review of the alleged health hazards of monosodium glutamate. Compr. Rev. Food Sci. Food Saf. 2019; 18, 1111-34.
S Pintarasri, V Plakornkul, Y Viravud, W Payuhakrit and T Rungruang. Folic acid attenuates MSG-induced teratogenicity during A 2-month pregnancy by preventing neural crest cell destruction and malformation in chick embryo models. Trends Sci. 2023; 20, 6656-6.
E Fauzia, TK Barbhuyan, AK Shrivastava, M Kumar, P Garg, MA Khan, AAB Robertson and SS Raza. Chick embryo: A preclinical model for understanding ischemia-reperfusion mechanism. Front. Pharmacol. 2018; 9, 1034.
M Fisher and CG Schoenwolf. The use of early chick embryos in experimental embryology and teratology: Improvements in standard procedures. Teratology 1983; 27, 65-72.
J Männer, W Seidl, F Heinicke and H Hesse. Teratogenic effects of suramin on the chick embryo. Anat. Embryol. 2003; 206, 229-37.
GK Uggini, PV Patel and S Balakrishnan. Embryotoxic and teratogenic effects of pesticides in chick embryos: A comparative study using two commercial formulations. Environ. Toxicol. 2012; 27, 166-74.
H Butler and BH Juurlink. An atlas for staging mammalian and chick embryos. CRC Press, Florida, 2018, p. 232.
B Arnaout, KE Lantigua, EM MacKenzie, IW McKinnell and HC Maddin. Development of the chicken skull: A complement to the external staging table of Hamburger and Hamilton. Anat. Rec. 2021; 304, 2726-40.
FAM Al-Ghamdi. Pomegranate peel extracts effects to reduce monosodium glutamate toxic effects on chicken embryos: Morphological studies. Saudi J. Biol. Sci. 2022; 29, 975-83.
G Breeland, MA Sinkler and RG Menezes. Embryology, bone ossification. StatPearls Publishing, Treasure Island, Florida, 2023.
P Zhang, G Wang, Z Lin, Y Wu, J Zhang, M Liu, KKH Lee, M Chuai and X Yang. Alcohol exposure induces chick craniofacial bone defects by negatively affecting cranial neural crest development. Toxicol. Lett. 2017; 281, 53-64.
A Adams, K Mankad, C Offiah and L Childs. Branchial cleft anomalies: A pictorial review of embryological development and spectrum of imaging findings. Insights Imaging. 2016; 7, 69-76.
MS Demirtaş. The pathogenesis of congenital anomalies: Roles of teratogens and infections. In: RP Verma (Ed.). Congenital anomalies in newborn infants-clinical and etiopathological perspectives. IntechOpen, London, 2020, p. 226.
P Zhang, G Wang, Z Lin, Y Wu, J Zhang, M Liu, KKH Lee, M Chuai and X Yang. Alcohol exposure induces chick craniofacial bone defects by negatively affecting cranial neural crest development. Toxicol. Lett. 2017; 281, 53-64.
KN Thomas, N Srikanth, SS Bhadsavle, KR Thomas, KN Zimmel, A Basel, AN Roach, NA Mehta, YS Bedi and MC Golding. Preconception paternal ethanol exposures induce alcohol-related craniofacial growth deficiencies in fetal offspring. J. Clin. Invest. 2023; 133, e167624.
C Therapontos, L Erskine, ER Gardner, WD Figg and N Vargesson. Thalidomide induces limb defects by preventing angiogenic outgrowth during early limb formation. Proc. Natl. Acad. Sci. U. S. A. 2009; 106, 8573-8.
JH Kim and AR Scialli. Thalidomide: The tragedy of birth defects and the effective treatment of disease. Toxicol. Sci. 2011; 122, 1-6.
DA Ridenour, R McLennan, JM Teddy, CL Semerad, JS Haug and PM Kulesa. The neural crest cell cycle is related to phases of migration in the head. Development 2014; 141, 1095-103.
Y Yan, G Wang, J Huang, Y Zhang, X Cheng, M Chuai, B Brand-Saberi, G Chen, X Jiang and X Yang. Zinc oxide nanoparticles exposure-induced oxidative stress restricts cranial neural crest development during chicken embryogenesis. Ecotoxicol. Environ. Saf. 2020; 194, 110415.
Downloads
Published
Issue
Section
License
Copyright (c) 2024 Walailak University

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.



