Physiological endpoints for potential SSRI interactions in fish

被引:110
作者
Kreke, N. [1 ]
Dietrich, D. R. [1 ]
机构
[1] Univ Konstanz, Dept Biol, POB X-918, D-78457 Constance, Germany
关键词
antidepressants; environmental risk; fish serotonergic system; HPG axis; HPI axis; 5-hydroxytryptamine; immune system; SSRIs;
D O I
10.1080/10408440801891057
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Selective serotonin reuptake inhibitors (SSRIs) are among the pharmaceutical compounds frequently detected in sewage treatment plant effluents and surface waters, albeit at very low concentrations, and have therefore become a focus of interest as environmental pollutants. These neuroactive drugs are primarily used in the treatment of depression but have also found broader use as medication for other neurological dysfunctions, consequently resulting in a steady increase of prescriptions worldwide. SSRIs, via inhibition of the serotonin (5-hydroxytryptamine, 5-HT) reuptake mechanism, induce an increase in extracellular 5-HT concentration within the central nervous system of mammals. The phylogenetically ancient and highly conserved neurotransmitter and neurohormone 5-HT has been found in invertebrates and vertebrates, although its specific physiological role and mode of action is unknown for many species. Consequently, it is difficult to assess the impact of chronic SSRI exposure in the environment, especially in the aquatic ecosystem. In view of this, the current knowledge of the functions of 5-HT in fish physiology is reviewed and, via comparison to the physiological role and function of 5-HT in mammals, a characterization of the potential impact of chronic SSRI exposure on fish is provided. Moreover, the insight on the physiological function of 5-HT strongly suggests that the experimental approaches currently used are inadequate if not entirely improper for routine environmental risk assessment of pharmaceuticals (e.g., SSRIs), as relevant endpoints are not assessed or impossible to determine.
引用
收藏
页码:215 / 247
页数:33
相关论文
共 222 条
[121]   Serotonin, but not melatonin, plays a role in shaping dorninant-subordinate relationships and aggression in rainbow trout [J].
Lepage, O ;
Larson, ET ;
Mayer, I ;
Winberg, S .
HORMONES AND BEHAVIOR, 2005, 48 (02) :233-242
[122]  
Lesch KP, 1997, HANDB EXP PHARM, V129, P671
[123]   Left-right asymmetry in embryonic development: a comprehensive review [J].
Levin, M .
MECHANISMS OF DEVELOPMENT, 2005, 122 (01) :3-25
[124]  
Levin Michael, 2006, Birth Defects Research, V78, P191, DOI 10.1002/bdrc.20078
[125]   Screening method for ecotoxicological hazard assessment of 42 pharmaceuticals considering human metabolism and excretory routes [J].
Lienert, Judit ;
Gudel, Karin ;
Escher, Beate I. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2007, 41 (12) :4471-4478
[126]  
LIMA L, 1994, J NEUROCHEM, V62, P528
[127]   PHORBOL ESTER CALCIUM IONOPHORE ACTIVATE FISH LEUKOCYTES AND INDUCE LONG-TERM CULTURES [J].
LIN, GL ;
ELLSAESSER, CF ;
CLEM, LW ;
MILLER, NW .
DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY, 1992, 16 (2-3) :153-163
[128]   SYNAPTIC INTERACTION OF SEROTONERGIC AXONS AND CORTICOTROPIN RELEASING-FACTOR (CRF) SYNTHESIZING NEURONS IN THE HYPOTHALAMIC PARAVENTRICULAR NUCLEUS OF THE RAT - A LIGHT AND ELECTRON-MICROSCOPIC IMMUNOCYTOCHEMICAL STUDY [J].
LIPOSITS, Z ;
PHELIX, C ;
PAULL, WK .
HISTOCHEMISTRY, 1987, 86 (06) :541-549
[129]   Fluoxetine metabolism and pharmacological interactions: The role of cytochrome P450 [J].
Mandrioli, R ;
Forti, GC ;
Raggi, MA .
CURRENT DRUG METABOLISM, 2006, 7 (02) :127-133
[130]   Phylogenetic analysis of the cytochrome P450 3 (CYP3) gene family [J].
McArthur, AG ;
Hegelund, T ;
Cox, RL ;
Stegeman, JJ ;
Liljenberg, M ;
Olsson, U ;
Sundberg, P ;
Celander, MC .
JOURNAL OF MOLECULAR EVOLUTION, 2003, 57 (02) :200-211