Biochemical Studies to Understand Teratogenicity and Lethality Outcomes in Modified-FETAX

Küçük Resim Yok

Tarih

2024

Dergi Başlığı

Dergi ISSN

Cilt Başlığı

Yayıncı

Humana Press Inc.

Erişim Hakkı

info:eu-repo/semantics/closedAccess

Özet

The frog embryo teratogenesis assay-Xenopus (FETAX) is a standardized test used to assess the toxic and teratogenic effects of xenobiotics. With this test, toxic and/or teratogenic concentrations of xenobiotic substances can be determined using morphological parameters such as lethality, length, and malformations in stage 8–11 Xenopus laevis embryos after 96 h exposure. These parameters enable the determination of the median lethal and effective concentrations (LC50 and EC50), minimum concentration to inhibit growth (MCIG), and teratogenic index of the tested chemical to reveal the short-term effects of relatively high concentrations. On the other hand, although FETAX provides quantitative and qualitative data on teratogenicity and toxicity, the biochemical and molecular mechanisms of these effects cannot be explained. Recent studies have tried to elucidate the mechanisms causing malformations and to explain the underlying causes of toxicity and teratogenicity by biochemical marker analysis. This chapter describes methods to analyze modified-FETAX and some detoxification and oxidative stress-related biomarkers during the early embryonic development of X. laevis. © The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature 2024.

Açıklama

Anahtar Kelimeler

Biochemical markers, FETAX, Teratogenicity, Toxicity, Xenopus laevis

Kaynak

Methods in Molecular Biology

WoS Q Değeri

Scopus Q Değeri

Q3

Cilt

2753

Sayı

Künye