Developmental Toxicology - Re - Lated Studies with Zebrafish Embryos

نویسندگان

  • Hiroki Teraoka
  • Wu Dong
  • Takeo Hiraga
چکیده

lt is widely believed that embryos and infants during devetopment are highly sensitiye to chemicals that cause serious damage to growth. However, knowledge on the mechanisms of developmenta1 toxicity is scarce. One reason for this is limited convenient model system other than organ cultures using rodents to study the various aspects of developmentat toxicology. Cuttured cells are not always adequate for this purpose, since events in morphogenesis are processed through interactions with other tissues. We focused on zebrafish embryo (Danio rerio), one of the most important organisms in deyelopmental biology. Saturation mutagenesis, applied to drosophila and nematode to define the functions of genes, has been carried out in zebrafish but almost no other vertebrate, and seyeral thousand lines are available due to the rapid growth and transparent body of this embryo. Enhanced databases for the geneme and ESTs are ayailable at websites with abundant genetic and biologica) background. By targeted gene knock-down with morpholinomodified antisense oligonucleotieds Received April 3, 2003; revised and accepted May IS, 2003. mechanism of congenital anomaly, which arises from genetic mutation.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Investigation of Toxicological Effects of di-2-ethylhexyl with Fish Embryo Test (FET) in Zebrafish (Danio rerio)

Di(2-ethylhexyl)phthalate (DEHP) is a plasticizer in a variety of consumer products. Given the adverse toxicity effects of DEHP on living organisms, its high consumption and dispersal has been caused a serious concern. . Nowedays, the Fish Embryo Test (FET) method is widely used among the conventional methods of toxicology .The aim of the this study was to determine the acute toxicity of Di(2-e...

متن کامل

Development of a screening assay to identify teratogenic and embryotoxic chemicals using the zebrafish embryo.

We developed and optimized a screening procedure, in which zebrafish embryos were explored as a model for the evaluation of the specific embryotoxic and teratogenic potential of chemicals. A selection of known positive (retinoic acid, valproic acid, caffeine, lithium chloride) and negative (glucose, saccharin) compounds for developmental toxicity were used to evaluate this method. We exposed em...

متن کامل

ARNT2 is not required for TCDD developmental toxicity in zebrafish.

ZfAHR2 has been identified as the receptor that is essential for mediating the developmental toxicity caused by 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in zebrafish. One form of zfARNT2, zfARNT2b, forms a functional heterodimer with zfAHR2 that specifically recognizes XREs in gel shift experiments and induces XRE-driven transcription in COS-7 cells treated with TCDD. However, it has not been...

متن کامل

Oxygen requirements of zebrafish (Danio rerio) embryos in embryo toxicity tests with environmental samples.

The zebrafish embryo test is a widely used bioassay for the testing of chemicals, effluents and other types of environmental samples. Oxygen depletion in the testing of sediments and effluents is especially important and may be a confounding factor in the interpretation of apparent toxicity. In order to identify oxygen levels critical to early developmental stages of zebrafish, oxygen consumpti...

متن کامل

P-121: Which Developmental Stage is Suitable for Re-vitrification? Compact Stage Re-vitrification or Early Blastocyst Stage Re-vitrification

Background: The aim of this study was evaluation of developmental rate and Bax, Bcl-2 and ErbB4 genes expression following re-vitrification in compact and early blastocysts stages. Materials and Methods: 5-8 cell embryos were collected from female mature mice, 60-62 hours post hCG injection. The embryos were divided to five groups including: fresh, vitrified at 5-8 cells, vitrified at blastocys...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2017