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  4. Antiandrogenic and Estrogenic Activity Evaluation of Oxygenated and Nitrated Polycyclic Aromatic Hydrocarbons Using Chemically Activated Luciferase Expression Assays
 
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Antiandrogenic and Estrogenic Activity Evaluation of Oxygenated and Nitrated Polycyclic Aromatic Hydrocarbons Using Chemically Activated Luciferase Expression Assays

ISSN
16604601
16617827
Năm xuất bản
2023
Tác giả
K., Misaki, Kentaro
Center for Marine Environmental Studies, Ehime University, Matsuyama, Japan
N.M., Tue, Nguyen Minh  
University of Shizuoka, Shizuoka, Japan
T., Takamura-Enya, Takeji
Vietnam National University, Hanoi, Hanoi, Viet Nam
H., Takigami, Hidetaka
Kanagawa Institute of Technology, Atsugi, Japan
G., Suzuki, Go
National Institute for Environmental Studies of Japan, Tsukuba, Japan
L.H., Tuyen, Le Huu  
Ehime University, Matsuyama, Japan
S., Takahashi, Shin
S., Tanabe, Shinsuke
DOI
10.3390/ijerph20010080
Tóm tắt
To establish the risk of the endocrine disrupting activity of polycyclic aromatic compounds, especially oxygenated and nitrated polycyclic aromatic hydrocarbons (oxy-PAHs and nitro-PAHs, respectively), antiandrogenic and estrogenic activities were determined using chemically activated luciferase expression (CALUX) assays with human osteoblast sarcoma cells. A total of 27 compounds including 9 oxy-PAHs (polycyclic aromatic ketones and quinones) and 8 nitro-PAHs was studied. The oxy-PAHs of 7H-benz[de]anthracen-7-one (BAO), 11H-benzo[a]fluoren-11-one (B[a]FO), 11H-benzo[b]fluoren-11-one (B[b]FO), and phenanthrenequinone (PhQ) exhibited significantly the potent inhibition of AR activation. All nitro-PAHs exhibited high antiandrogenic activities (especially high for 3-nitrofluoranthene (3-NFA) and 3-nitro-7H-benz[de]anthracen-7-one (3-NBAO)), and the AR inhibition was confirmed as noncompetitive for 3-NFA, 3-NBAO, and 1,3-dinitropyrene (1,3-DNPy). Antiandrogenic activity of 3-NFA demonstrated characteristically a U-shaped dose–response curve
however, the absence of fluorescence effect on the activity was confirmed. The prominent estrogenic activity dependent on dose–response curve was confirmed for 2 oxy-PAHs (i.e., B[a]FO and B[b]FO). Elucidating the role of AR and ER on the effects of polycyclic aromatic compounds (e.g., oxy- and nitro-PAHs) to endocrine dysfunctions in mammals and aquatic organisms remains a challenge. © 2023 Elsevier B.V., All rights reserved.
Chủ đề

Antiandrogenic Activi...

Chemically Activated ...

Estrogenic Activity

Nitrated Polycyclic A...

Polycyclic Aromatic K...

Polycyclic Aromatic Q...

1 Nitropyrene

Androstanolone

Benz[a]anthracene

Chrysene

Estradiol

Glyceryl Trinitrate

Phenanthrene

Phenanthrenequinone

Testosterone

Luciferases

Nitrates

Polycyclic Aromatic H...

Polycyclic Compounds

Quinones

1 Nitropyrene

3 Nitrofluoranthene

Androgen Receptor

Androstanolone

Benz[a]anthracene

Chrysene

Estradiol

Glyceryl Trinitrate

Ketone

Luciferase

Phenanthrene

Phenanthrenequinone

Polycyclic Aromatic H...

Quinone Derivative

Testosterone

Unclassified Drug

Nitric Acid Derivativ...

Polycyclic Hydrocarbo...

Androgen

Dose-response Relatio...

Endocrine Disruptor

Estrogenic Compound

Gene Expression

Inhibition

Nitrate

Pah

Reaction Kinetics

Risk Assessment

Animal Cell

Article

Binding Affinity

Chemical Structure

Cognition

Cytotoxicity

Environmental Factor

Estrogen Activity

Genetic Transcription...

Human

Hydrogen Bond

Mouse

Mutagenicity

Nonhuman

Obesity

Oocyte Maturation

Oxidative Stress

Reproductive Health

Sexual Function

Spermatogenesis

Spermatozoon Density

Animal

Chemistry

Mammal

Animals

Humans

Luciferases

Mammals

Nitrates

Polycyclic Aromatic H...

Polycyclic Compounds

Quinones

Duyệt theo
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