• Something wrong with this record ?

Effects of the lipid regulator drug gemfibrozil: A toxicological and behavioral perspective

JF. Henriques, AR. Almeida, T. Andrade, O. Koba, O. Golovko, AM. Soares, M. Oliveira, I. Domingues,

. 2016 ; 170 (-) : 355-64. [pub] 20151003

Language English Country Netherlands

Document type Journal Article, Research Support, Non-U.S. Gov't

Pharmaceuticals are emerging contaminants as their worldwide consumption increases. Fibrates such as gemfibrozil (GEM) are used in human medicine to reduce blood concentrations of cholesterol and triacylglycerol and also are some of the most frequently reported pharmaceuticals in waste waters and surface waters. Despite some studies have already demonstrated the negative impact in physiological and/or reproductive endpoints in adult fish, data on survival and behavioral effects in fish larvae are lacking. This study aimed to assess the effects of GEM on zebrafish eleutheroembryo development and locomotor behavior. A fish embryo toxicity (FET) test was undertaken to evaluate GEM acute toxicity by exposing embryos to 0, 6.58, 9.87, 14.81, 22.22, 33.33 and 50mg/L. Developmental endpoints such as hatching success, edemas and malformations were recorded. A second test was undertaken by exposing embryos to 0, 1.5, 3 and 6mg/L in order to evaluate the effects of GEM on 120 and 144h post fertilization (hpf) larvae locomotor activity by video tracking, using a Zebrabox(®) (Viewpoint, France) device. From the data recorded, several parameters such as total swimming distance (TSD) and total swimming time (TST) in each 120s integration time were calculated. Data showed that this compound has a moderate toxic effect on fish embryo development, affecting both survival and hatching success with a calculated 96h LC50 of 11.01mg/L and no effects at the developmental level at 6mg/L. GEM seems to impair locomotor activity, even at concentrations where developmental abnormalities were unperceived, at concentrations as low as 1.5mg/L. Both TSD and TST were sensitive to GEM exposure. These effects do not seem to be independent of the developmental stage as 120hpf larvae seem to present a development bias with repercussions in locomotor behavior. This study highlights the need to include behavioral endpoints in ecotoxicological assays as this seems to be a more sensitive endpoint often disregarded.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc16028069
003      
CZ-PrNML
005      
20161018121606.0
007      
ta
008      
161005s2016 ne f 000 0|eng||
009      
AR
024    7_
$a 10.1016/j.aquatox.2015.09.017 $2 doi
024    7_
$a 10.1016/j.aquatox.2015.09.017 $2 doi
035    __
$a (PubMed)26482382
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a ne
100    1_
$a Henriques, Jorge F $u Department of Biology & CESAM, University of Aveiro, Campus Universitário de Santiago, 3810-193 Aveiro, Portugal. Electronic address: jfhenriques@ua.pt.
245    10
$a Effects of the lipid regulator drug gemfibrozil: A toxicological and behavioral perspective / $c JF. Henriques, AR. Almeida, T. Andrade, O. Koba, O. Golovko, AM. Soares, M. Oliveira, I. Domingues,
520    9_
$a Pharmaceuticals are emerging contaminants as their worldwide consumption increases. Fibrates such as gemfibrozil (GEM) are used in human medicine to reduce blood concentrations of cholesterol and triacylglycerol and also are some of the most frequently reported pharmaceuticals in waste waters and surface waters. Despite some studies have already demonstrated the negative impact in physiological and/or reproductive endpoints in adult fish, data on survival and behavioral effects in fish larvae are lacking. This study aimed to assess the effects of GEM on zebrafish eleutheroembryo development and locomotor behavior. A fish embryo toxicity (FET) test was undertaken to evaluate GEM acute toxicity by exposing embryos to 0, 6.58, 9.87, 14.81, 22.22, 33.33 and 50mg/L. Developmental endpoints such as hatching success, edemas and malformations were recorded. A second test was undertaken by exposing embryos to 0, 1.5, 3 and 6mg/L in order to evaluate the effects of GEM on 120 and 144h post fertilization (hpf) larvae locomotor activity by video tracking, using a Zebrabox(®) (Viewpoint, France) device. From the data recorded, several parameters such as total swimming distance (TSD) and total swimming time (TST) in each 120s integration time were calculated. Data showed that this compound has a moderate toxic effect on fish embryo development, affecting both survival and hatching success with a calculated 96h LC50 of 11.01mg/L and no effects at the developmental level at 6mg/L. GEM seems to impair locomotor activity, even at concentrations where developmental abnormalities were unperceived, at concentrations as low as 1.5mg/L. Both TSD and TST were sensitive to GEM exposure. These effects do not seem to be independent of the developmental stage as 120hpf larvae seem to present a development bias with repercussions in locomotor behavior. This study highlights the need to include behavioral endpoints in ecotoxicological assays as this seems to be a more sensitive endpoint often disregarded.
650    _2
$a zvířata $7 D000818
650    _2
$a embryonální vývoj $x účinky léků $7 D047108
650    _2
$a gemfibrozil $x toxicita $7 D015248
650    _2
$a larva $x účinky léků $7 D007814
650    _2
$a pohybová aktivita $x účinky léků $7 D009043
650    _2
$a plavání $7 D013550
650    _2
$a testy akutní toxicity $7 D023382
650    _2
$a chemické látky znečišťující vodu $x toxicita $7 D014874
650    _2
$a dánio pruhované $x růst a vývoj $x fyziologie $7 D015027
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Almeida, Ana Rita $u Department of Biology & CESAM, University of Aveiro, Campus Universitário de Santiago, 3810-193 Aveiro, Portugal. $7 gn_A_00004618
700    1_
$a Andrade, Thayres $u Department of Biology & CESAM, University of Aveiro, Campus Universitário de Santiago, 3810-193 Aveiro, Portugal. $7 gn_A_00006290
700    1_
$a Koba, Olga $u University of South Bohemia in Ceske Budejovice, Faculty of Fisheries and Protection of Waters, South Bohemian Research Center of Aquaculture and Biodiversity of Hydrocenoses, Zatisi 728/II, Vodnany, 389 25, Czech Republic.
700    1_
$a Golovko, Oksana $u University of South Bohemia in Ceske Budejovice, Faculty of Fisheries and Protection of Waters, South Bohemian Research Center of Aquaculture and Biodiversity of Hydrocenoses, Zatisi 728/II, Vodnany, 389 25, Czech Republic.
700    1_
$a Soares, Amadeu M V M $u Department of Biology & CESAM, University of Aveiro, Campus Universitário de Santiago, 3810-193 Aveiro, Portugal.
700    1_
$a Oliveira, Miguel $u Department of Biology & CESAM, University of Aveiro, Campus Universitário de Santiago, 3810-193 Aveiro, Portugal.
700    1_
$a Domingues, Inês $u Department of Biology & CESAM, University of Aveiro, Campus Universitário de Santiago, 3810-193 Aveiro, Portugal.
773    0_
$w MED00008569 $t Aquatic toxicology (Amsterdam, Netherlands) $x 1879-1514 $g Roč. 170, č. - (2016), s. 355-64
856    41
$u https://pubmed.ncbi.nlm.nih.gov/26482382 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20161005 $b ABA008
991    __
$a 20161018122010 $b ABA008
999    __
$a ok $b bmc $g 1166383 $s 952699
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2016 $b 170 $c - $d 355-64 $e 20151003 $i 1879-1514 $m Aquatic toxicology $n Aquat Toxicol $x MED00008569
LZP    __
$a Pubmed-20161005

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...