TY - JOUR
T1 - Evaluation of drug toxicity profiles based on the phenotypes of ascidian Ciona intestinalis
AU - Mizotani, Yuji
AU - Itoh, Shun
AU - Hotta, Kohji
AU - Tashiro, Etsu
AU - Oka, Kotaro
AU - Imoto, Masaya
N1 - Funding Information:
We thank the National Bio-Resource Project for providing the Ciona. This work was supported by Grant-in-Aid for Challenging Exploratory Research (JSPS KAKENHI Grant Number 25560419 ) to MI and ( 24657164 ) to KH.
Publisher Copyright:
© 2015 Elsevier Inc. All rights reserved.
Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2015/7/13
Y1 - 2015/7/13
N2 - In vivo toxicity evaluation using model organisms is an important step for the development of new drugs. Here, we report that Ciona intestinalis, a chordate invertebrate, is beneficial to drug toxicity evaluation for the following reasons: rapid embryonic and larval development, resemblance to vertebrates, ease of management, low cost, transparent body, and low risk of ethical issues. The dynamic phenotypic change of Ciona larvae during metamorphosis prompted us to examine the effect of cytotoxic drugs on its development by quantifying six toxicity endpoints: degenerated tail size, ampulla length, rotation of body axis, stomach size, heart rate, and body size. As a result, mitochondrial respiratory inhibitors, tubulin polymerization/depolymerization inhibitors, or DNA/RNA synthesis inhibitors showed distinct toxicity profiles against these six endpoints, but drugs with the same targets showed a similar toxicity profile in Ciona. Our results suggest Ciona is an effective animal model for profiling drug toxicity and exploring the mechanisms of drugs with unknown targets.
AB - In vivo toxicity evaluation using model organisms is an important step for the development of new drugs. Here, we report that Ciona intestinalis, a chordate invertebrate, is beneficial to drug toxicity evaluation for the following reasons: rapid embryonic and larval development, resemblance to vertebrates, ease of management, low cost, transparent body, and low risk of ethical issues. The dynamic phenotypic change of Ciona larvae during metamorphosis prompted us to examine the effect of cytotoxic drugs on its development by quantifying six toxicity endpoints: degenerated tail size, ampulla length, rotation of body axis, stomach size, heart rate, and body size. As a result, mitochondrial respiratory inhibitors, tubulin polymerization/depolymerization inhibitors, or DNA/RNA synthesis inhibitors showed distinct toxicity profiles against these six endpoints, but drugs with the same targets showed a similar toxicity profile in Ciona. Our results suggest Ciona is an effective animal model for profiling drug toxicity and exploring the mechanisms of drugs with unknown targets.
KW - Ciona intestinalis
KW - DNA/RNA synthesis inhibitor
KW - Mitochondria respiratory inhibitor
KW - Toxicity endpoint
KW - Toxicity profile
KW - Tubulin polymerization/depolymerization inhibitor
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U2 - 10.1016/j.bbrc.2015.05.119
DO - 10.1016/j.bbrc.2015.05.119
M3 - Article
C2 - 26043689
AN - SCOPUS:84936890091
SN - 0006-291X
VL - 463
SP - 656
EP - 660
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 4
ER -