Developmental Toxicity of Doxorubicin Hydrochloride in Embryo-larval Stages of Zebrafish

被引:23
作者
Chang, Can [1 ]
Wu, Shao Ling [1 ]
Zhao, Xin Dong [1 ]
Zhao, Chun Ting [1 ]
Li, Yan Hui [2 ]
机构
[1] Qingdao Univ, Affiliated Hosp, Coll Med, Dept Hematol, Qingdao 266003, Shandong, Peoples R China
[2] Qingdao Univ, Growing Base State Key Lab, Qingdao 266071, Shandong, Peoples R China
关键词
Doxorubicin hydrochloride; developmental toxicity; zebrafish; embryotoxicity; INDUCED CARDIOTOXICITY; SOLVENTS; DRUG;
D O I
10.3233/BME-130885
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Doxorubicin hydrochloride is widely used to treat various types of cancers. Its therapeutic and side effects are well documented. However, the developmental toxicity of doxorubicin has not been previously described. Lethal and sublethal effects on embryo-larval stages of zebrafish in a study of the developmental toxicity of doxorubicin were observed. Zebrafish embryos were exposed to different concentrations (0-100 mg/L) of doxorubicin between 4 and 120 h post fertilization, and zebrafish larvae were exposed to different concentrations (0-200 mg/L) of doxorubicin for 96 h. The markers about the development toxicity of doxorubicin in zebrafish were observed under a stereomicroscope. Higher doxorubicin concentrations mainly caused acute lethal effects, and lower doxorubicin concentrations mainly caused sublethal effects, such as multiple malformations in embryos and larvae. Moreover, with the increase of doxorubicin concentration, the malformation rate increased. The heart rate of embryos was accelerated at lower concentrations of doxorubicin (<= 10 mg/L) and decelerated at higher concentrations (>= 25 mg/L). The hatching rate and body length were inhibited at higher concentrations of doxorubicin (>= 25 mg/L). In conclusion, doxorubicin has serious developmental toxicity and this raises a concern for developmental effects of doxorubicin in clinical practice.
引用
收藏
页码:909 / 916
页数:8
相关论文
共 22 条
  • [1] ADRIAMYCIN - NEW ANTICANCER DRUG WITH SIGNIFICANT CLINICAL ACTIVITY
    BLUM, RH
    CARTER, SK
    [J]. ANNALS OF INTERNAL MEDICINE, 1974, 80 (02) : 249 - 259
  • [2] Brand M., 2002, ZEBRAFISH PRACTICAL
  • [3] Inorganics and hormesis
    Calabrese, EJ
    Baldwin, LA
    [J]. CRITICAL REVIEWS IN TOXICOLOGY, 2003, 33 (3-4) : 215 - 304
  • [4] Protection against doxorubicin-induced cardiotoxicity in weanling rats by dexrazoxane
    Della Torre, P
    Mazué, G
    Podestà, A
    Moneta, D
    Sammartini, U
    Imondi, AR
    [J]. CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1999, 43 (02) : 151 - 156
  • [5] Systolic and diastolic ventricular function in zebrafish embryos: Influence of norepenephrine, MS-222 and temperature
    Denvir, Martin A.
    Tucker, Carl S.
    Mullins, John J.
    [J]. BMC BIOTECHNOLOGY, 2008, 8 (1)
  • [6] Developmental toxicity evaluation of three hexabromocyclododecane diastereoisomers on zebrafish embryos
    Du, Miaomiao
    Zhang, Dandan
    Yan, Changzhou
    Zhang, Xian
    [J]. AQUATIC TOXICOLOGY, 2012, 112 : 1 - 10
  • [7] Catechin and proanthocyanidin B4 from grape seeds prevent doxorubicin-induced toxicity in cardiomyocytes
    Du, Yu
    Lou, Hongxiang
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 2008, 591 (1-3) : 96 - 101
  • [8] Comparative embryotoxicity and proteotoxicity of three carrier solvents to zebrafish (Danio rerio) embryos
    Hallare, A
    Nagel, K
    Köhler, HR
    Triebskorn, R
    [J]. ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY, 2006, 63 (03) : 378 - 388
  • [9] Development toxicity and stress protein responses in zebrafish embryos after exposure to diclofenac and its solvents, DMSO
    Hallare, AV
    Köhler, HR
    Triebskorn, R
    [J]. CHEMOSPHERE, 2004, 56 (07) : 659 - 666
  • [10] He J.H., 2012, J PHARMACOL TOX MET, V67, P1