The role of xenobiotic-metabolizing enzymes in the placenta: a growing research field

被引:17
作者
Blanco-Castaneda, Ricardo [1 ]
Galaviz-Hernandez, Carlos [1 ]
Souto, Paula C. S. [2 ]
Lima, Victor Vitorino [2 ]
Giachini, Fernanda R. [2 ]
Escudero, Carlos [3 ]
Damiano, Alicia E. [4 ,5 ]
Barragan-Zuniga, L. Jazel [1 ]
Martinez-Aguilar, Gerardo [6 ]
Sosa-Macias, Martha [1 ]
机构
[1] Inst Politecn Nacl CIIDIR Durango, Acad Genom, Sigma 119,Fracc 20 Noviembre 2, Durango 34220, Mexico
[2] Univ Fed Mato Grosso, Inst Hlth Sci & Hlth, Lab Vasc Biol, Barra Do Garcas, Brazil
[3] Univ Bio Bio, Grp Res & Innovat Vasc Hlth GRIVAS Hlth, Grp Invest Tumor Angiogenesis GIANT, Basic Sci Dept,Fac Sci,Vasc Physiol Lab, Chillan, Chile
[4] UBA, IFIBIO Houssay, CONICET, Lab Biol Reprod, Buenos Aires, DF, Argentina
[5] UBA, Fac Farm & Bioquim, Dept Ciencias Biol, Buenos Aires, DF, Argentina
[6] Inst Mexicano Seguro Social IMSS Durango, Unidad Invest Biomed, Durango, Mexico
关键词
CYP450; enzyme; drug; gene expression; placenta; placental metabolism; pregnancy; transport protein; ARYL-HYDROCARBON RECEPTOR; HUMAN TERM PLACENTA; POLYCYCLIC AROMATIC-HYDROCARBONS; CYTOCHROME-P450 3A ENZYMES; MESSENGER-RNA EXPRESSION; OXIDIZING SYSTEM MEOS; BISPHENOL-A BPA; PAH-DNA ADDUCTS; TRANSPLACENTAL TRANSFER; GLUCOCORTICOID-RECEPTOR;
D O I
10.1080/17512433.2020.1733412
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: The placenta is a temporary and unique organ that allows for the physical connection between a mother and fetus; this organ regulates the transport of gases and nutrients mediating the elimination of waste products contained in the fetal circulation. The placenta performs metabolic and excretion functions, on the basis of multiple enzymatic systems responsible for the oxidation, reduction, hydrolysis, and conjugation of xenobiotics. These mechanisms give the placenta a protective role that limits the fetal exposure to harmful compounds. During pregnancy, some diseases require uninterrupted treatment even if it is detrimental to the fetus. Drugs and other xenobiotics alter gene expression in the placenta with repercussions for the fetus and mother's well-being. Areas covered: This review provides a brief description of the human placental structure and function, the main drug and xenobiotic transporters and metabolizing enzymes, placenta-metabolized substrates, and alterations in gene expression that the exposure to xenobiotics may cause. Expert opinion: Research should be focused on the identification and validation of biological markers for the assessment of the harmful effects of some drugs in pregnancy, including the evaluation of polymorphisms and methylation patterns in chorionic villous samples and/or amniotic fluid.
引用
收藏
页码:247 / 263
页数:17
相关论文
共 50 条
  • [31] Nonviral gene transfer as a tool for studying transcription regulation of xenobiotic metabolizing enzymes
    Bonamassa, Barbara
    Liu, Dexi
    ADVANCED DRUG DELIVERY REVIEWS, 2010, 62 (13) : 1250 - 1256
  • [32] Developmental expression of drug metabolizing enzymes and transporter proteins in human placenta and fetal tissues
    Myllynen, Paivi
    Immonen, Elina
    Kummu, Maria
    Vahakangas, Kirsi
    EXPERT OPINION ON DRUG METABOLISM & TOXICOLOGY, 2009, 5 (12) : 1483 - 1499
  • [33] Potential of Cytochrome P450, a Family of Xenobiotic Metabolizing Enzymes, in Cancer Therapy
    Singh, Ragini D. D.
    Avadhesh, Avadhesh
    Sharma, Gaurav
    Dholariya, Sagar
    Shah, Rima B. B.
    Goyal, Bela
    Gupta, Subash Chandra
    ANTIOXIDANTS & REDOX SIGNALING, 2023, 38 (10-12) : 853 - 876
  • [34] Maternal drug abuse and human term placental xenobiotic and steroid metabolizing enzymes in vitro
    Paakki, P
    Stockmann, H
    Kantola, M
    Wagner, P
    Lauper, U
    Huch, R
    Elovaara, E
    Kirkinen, P
    Pasanen, M
    ENVIRONMENTAL HEALTH PERSPECTIVES, 2000, 108 (02) : 141 - 145
  • [35] Differentiation-associated urothelial cytochrome P450 oxidoreductase predicates the xenobiotic-metabolizing activity of "luminal" muscle-invasive bladder cancers
    Baker, Simon C.
    Arlt, Volker M.
    Indra, Radek
    Joel, Madeleine
    Stiborova, Marie
    Eardley, Ian
    Ahmad, Niaz
    Otto, Wolfgang
    Burger, Maximilian
    Rubenwolf, Peter
    Phillips, David H.
    Southgate, Jennifer
    MOLECULAR CARCINOGENESIS, 2018, 57 (05) : 606 - 618
  • [36] Alteration of xenobiotic metabolizing enzymes by resveratrol in liver and lung of CD1 mice
    Canistro, D.
    Bonamassa, B.
    Pozzetti, L.
    Sapone, A.
    Abdel-Rahman, S. Z.
    Biagi, G. L.
    Paolini, M.
    FOOD AND CHEMICAL TOXICOLOGY, 2009, 47 (02) : 454 - 461
  • [37] Phase I to II cross-induction of xenobiotic metabolizing enzymes: A feedforward control mechanism for potential hormetic responses
    Zhang, Qiang
    Pi, Jingbo
    Woods, Courtney G.
    Andersen, Melvin E.
    TOXICOLOGY AND APPLIED PHARMACOLOGY, 2009, 237 (03) : 345 - 356
  • [38] Characterization of xenobiotic metabolizing enzymes of a reconstructed human epidermal model from adult hair follicles
    Bacqueville, Daniel
    Jacques, Carine
    Duprat, Laure
    Jamin, Emilien L.
    Guiraud, Beatrice
    Perdu, Elisabeth
    Bessou-Touya, Sandrine
    Zalko, Daniel
    Duplan, Helene
    TOXICOLOGY AND APPLIED PHARMACOLOGY, 2017, 329 : 190 - 201
  • [39] Effects of cypermethrin on monoamine transporters, xenobiotic metabolizing enzymes and lipid peroxidation in the rat nigrostriatal system
    Tiwari, Manindra Nath
    Singh, Anand Kumar
    Ahmad, Israr
    Upadhyay, Ghanshyam
    Singh, Dhirendra
    Patel, Devendra Kumar
    Singh, Chetna
    Prakash, Om
    Singh, Mahendra Pratap
    FREE RADICAL RESEARCH, 2010, 44 (12) : 1416 - 1424
  • [40] Comparative liver accumulation of dioxin-like compounds in sheep and cattle: Possible role of AhR-mediated xenobiotic metabolizing enzymes
    Girolami, F.
    Spalenza, V.
    Benedetto, A.
    Manzini, L.
    Badino, P.
    Abete, M. C.
    Nebbia, C.
    SCIENCE OF THE TOTAL ENVIRONMENT, 2016, 571 : 1222 - 1229