-
Je něco špatně v tomto záznamu ?
Plazmatické hladiny troponinu T u králíků po podání nových a anineoplastických látek (Oracinu a Dimefluronu) s daunorubicinem [Plasma levels of troponin T in rabbits after administration of new antineoplastic agents (Oracin and Dimefluron) and daunorubicin]
M. Adamcová, J. Machácková, V. Gersl, R. Hrdina, Y. Mazurová, M. Mĕlka, M. Nobilis,
Jazyk čeština Země Česko
Typ dokumentu anglický abstrakt, časopisecké články, práce podpořená grantem
- MeSH
- biologické markery krev MeSH
- daunomycin aplikace a dávkování toxicita MeSH
- ethanolaminy aplikace a dávkování toxicita MeSH
- fluoreny aplikace a dávkování toxicita MeSH
- isochinoliny aplikace a dávkování toxicita MeSH
- kardiomyopatie chemicky indukované diagnóza MeSH
- králíci MeSH
- protinádorová antibiotika aplikace a dávkování toxicita MeSH
- protokoly protinádorové kombinované chemoterapie toxicita MeSH
- troponin T krev MeSH
- zvířata MeSH
- Check Tag
- králíci MeSH
- zvířata MeSH
- Publikační typ
- anglický abstrakt MeSH
- časopisecké články MeSH
- práce podpořená grantem MeSH
Recently, cardiac troponin T (cTnT) has been shown to be a sensitive marker of anthracycline-induced cardiomyopathy. In our study, the cardiotoxicity of repeated i.v. administration (once a week, 10 administrations) of daunorubicin combined with new antineoplastic drugs (with mild side-effects) were followed in two groups of rabbits: 1) Dimefluron (3,9-dimethoxybenfluron hydrochloride-12 mg/kg) + daunorubicin (3 mg/kg), 2) Oracin (6-[2-(2-hydroxyethyl)aminoethyl]-5,11-dioxo-5,6-dihydro-11H- indeno[1,2c]isoquinoline hydrochloride--10 mg/kg) + daunorubicin (3 mg/kg) and compared with the control group (saline--1 ml/kg) and the group with experimentally induced cardiomyopathy (daunorubicin--3 mg/kg). The concentration of cTnT in heparinized plasma samples was measured using commercial kit (Roche). In the control group, plasma levels of cTnT were always within the physiological range (i.e. lower than 0.1 microgram/l) during the experiment. During the development of daunorubicin-induced cardiomyopathy, after the eighth administration of drug, cTnT was significantly higher (0.31 +/- 0.11 microgram/l) in animals with premature deaths compared with the rest of the group (0.04 +/- 0.03 microgram/l). The animals with pathological values of cTnT were at higher risk of premature deaths (P = 0.0006). The combination of daunorubicin either with Oracin or with Dimefluron caused neither significant changes of cTnT levels nor significant deterioration of other followed-up parameters (especially, functional and toxicological parameters). Similarly to the daunorubicin group, the animals with pathological levels of cTnT after the eighth administration of antineoplastic drugs were at higher risk of premature death (P = 0.025). Our results show that the plasma concentration of cardiac troponin T could be a suitable predictive marker of cardiotoxicity of antineoplastic drugs.
Plasma levels of troponin T in rabbits after administration of new antineoplastic agents (Oracin and Dimefluron) and daunorubicin
- 000
- 00000naa a2200000 a 4500
- 001
- bmc15011977
- 003
- CZ-PrNML
- 005
- 20150903093324.0
- 007
- ta
- 008
- 150401s2001 xr f 000 0|cze||
- 009
- AR
- 035 __
- $a (PubMed)11892362
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a cze
- 044 __
- $a xr
- 100 1_
- $a Adamcová, Michaela, $u Univerzita Karlova v Praze, Lékarská fakulta v Hradci Králové. adamcova@lfhk.cuni.cz $d 1964- $7 xx0064762
- 245 10
- $a Plazmatické hladiny troponinu T u králíků po podání nových a anineoplastických látek (Oracinu a Dimefluronu) s daunorubicinem / $c M. Adamcová, J. Machácková, V. Gersl, R. Hrdina, Y. Mazurová, M. Mĕlka, M. Nobilis,
- 246 31
- $a Plasma levels of troponin T in rabbits after administration of new antineoplastic agents (Oracin and Dimefluron) and daunorubicin
- 520 9_
- $a Recently, cardiac troponin T (cTnT) has been shown to be a sensitive marker of anthracycline-induced cardiomyopathy. In our study, the cardiotoxicity of repeated i.v. administration (once a week, 10 administrations) of daunorubicin combined with new antineoplastic drugs (with mild side-effects) were followed in two groups of rabbits: 1) Dimefluron (3,9-dimethoxybenfluron hydrochloride-12 mg/kg) + daunorubicin (3 mg/kg), 2) Oracin (6-[2-(2-hydroxyethyl)aminoethyl]-5,11-dioxo-5,6-dihydro-11H- indeno[1,2c]isoquinoline hydrochloride--10 mg/kg) + daunorubicin (3 mg/kg) and compared with the control group (saline--1 ml/kg) and the group with experimentally induced cardiomyopathy (daunorubicin--3 mg/kg). The concentration of cTnT in heparinized plasma samples was measured using commercial kit (Roche). In the control group, plasma levels of cTnT were always within the physiological range (i.e. lower than 0.1 microgram/l) during the experiment. During the development of daunorubicin-induced cardiomyopathy, after the eighth administration of drug, cTnT was significantly higher (0.31 +/- 0.11 microgram/l) in animals with premature deaths compared with the rest of the group (0.04 +/- 0.03 microgram/l). The animals with pathological values of cTnT were at higher risk of premature deaths (P = 0.0006). The combination of daunorubicin either with Oracin or with Dimefluron caused neither significant changes of cTnT levels nor significant deterioration of other followed-up parameters (especially, functional and toxicological parameters). Similarly to the daunorubicin group, the animals with pathological levels of cTnT after the eighth administration of antineoplastic drugs were at higher risk of premature death (P = 0.025). Our results show that the plasma concentration of cardiac troponin T could be a suitable predictive marker of cardiotoxicity of antineoplastic drugs.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a protinádorová antibiotika $x aplikace a dávkování $x toxicita $7 D000903
- 650 _2
- $a protokoly protinádorové kombinované chemoterapie $x toxicita $7 D000971
- 650 _2
- $a biologické markery $x krev $7 D015415
- 650 _2
- $a kardiomyopatie $x chemicky indukované $x diagnóza $7 D009202
- 650 _2
- $a daunomycin $x aplikace a dávkování $x toxicita $7 D003630
- 650 _2
- $a ethanolaminy $x aplikace a dávkování $x toxicita $7 D004983
- 650 _2
- $a fluoreny $x aplikace a dávkování $x toxicita $7 D005449
- 650 _2
- $a isochinoliny $x aplikace a dávkování $x toxicita $7 D007546
- 650 _2
- $a králíci $7 D011817
- 650 _2
- $a troponin T $x krev $7 D020107
- 655 _2
- $a anglický abstrakt $7 D004740
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Macháčková, Jarmila $7 xx0139265
- 700 1_
- $a Geršl, Vladimír, $d 1946-2015 $7 nlk19990073168
- 700 1_
- $a Hrdina, Radomír $7 xx0077249
- 700 1_
- $a Mazurová, Yvona, $d 1951- $7 xx0054511
- 700 1_
- $a Mělka, Milan, $d 1937-2011 $7 jk01081159
- 700 1_
- $a Nobilis, Milan $7 xx0079581
- 773 0_
- $w MED00011344 $t Acta medica (Hradec Králové). Supplementum $x 1211-247X $g Roč. 44, č. 1 (2001), s. 3-8
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/11892362 $y Pubmed
- 910 __
- $a ABA008 $b A 3077 $c sign $y 4 $z 0
- 990 __
- $a 20150401 $b ABA008
- 991 __
- $a 20150903093445 $b ABA008
- 999 __
- $a ok $b bmc $g 1069513 $s 894823
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2001 $b 44 $c 1 $d 3-8 $i 1211-247X $m Acta medica. Supplementum $n Acta med., Suppl. $x MED00011344
- LZP __
- $a Pubmed-20150401