-
Je něco špatně v tomto záznamu ?
Acute Toxic Injuries of Rat's Visceral Tissues Induced by Different Oximes
V. Jaćević, E. Nepovimova, K. Kuča,
Jazyk angličtina Země Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Directory of Open Access Journals
od 2011
Free Medical Journals
od 2011
Nature Open Access
od 2011-12-01
PubMed Central
od 2011
Europe PubMed Central
od 2011
ProQuest Central
od 2011-01-01
Open Access Digital Library
od 2011-01-01
Open Access Digital Library
od 2011-01-01
Health & Medicine (ProQuest)
od 2011-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2011
Springer Nature OA/Free Journals
od 2011-12-01
- MeSH
- biopsie MeSH
- chemické bojové látky škodlivé účinky chemie toxicita MeSH
- histocytochemie MeSH
- krysa rodu rattus MeSH
- LD50 MeSH
- molekulární struktura MeSH
- orgánová specificita MeSH
- oximy aplikace a dávkování škodlivé účinky chemie toxicita MeSH
- plíce účinky léků metabolismus patologie MeSH
- vnitřnosti účinky léků patologie MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- žaludek účinky léků patologie MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Certain AChE reactivators, asoxime, obidoxime, K027, K048, and K075, when taken in overdoses and sometimes even when introduced within therapeutic ranges, may injure the different organs. As a continuation of previously published data, in this study, Wistar rats have sacrificed 24 hrs and 7 days after single im application of 0.1LD50, 0.5LD50 and 1.0LD50 of each reactivator, and examinated tissue samples were obtained for pathohistological and semiquantitative analysis. A severity of tissue alteration, expressed as different tissue damage scores were evaluated. Morphological structure of examinated tissues treated with of 0.1LD50 of all reactivators was comparable with the control group of rats. Moderate injuries were seen in visceral tissues treated with 0.5LD50 of asoxime, obidoxime and K027. Acute damages were enlarged after treatment with 0.5LD50 and 1.0LD50 of all reactivators during the next 7 days. The most prominent changes were seen in rats treated with 1.0LD50 of K048 and K075 (P < 0.001 vs. control and asoxime-treated group). All reactivators given by a single, high, unitary dose regimen, have an adverse effect not only on the main visceral tissue, but on the whole rat as well, but the exact mechanism of cellular injury remains to be confirmed in further investigation.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc20028755
- 003
- CZ-PrNML
- 005
- 20210114155008.0
- 007
- ta
- 008
- 210105s2019 xxk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1038/s41598-019-52768-4 $2 doi
- 035 __
- $a (PubMed)31712702
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxk
- 100 1_
- $a Jaćević, Vesna $u National Poison Control Centre, Military Medical Academy, Belgrade, Serbia. Faculty of Medicine of the Military Medical Academy, University of Defense, Belgrade, Serbia. Department of Chemistry, Faculty of Science, University of Hradec Kralove, Hradec Kralove, Czechia.
- 245 10
- $a Acute Toxic Injuries of Rat's Visceral Tissues Induced by Different Oximes / $c V. Jaćević, E. Nepovimova, K. Kuča,
- 520 9_
- $a Certain AChE reactivators, asoxime, obidoxime, K027, K048, and K075, when taken in overdoses and sometimes even when introduced within therapeutic ranges, may injure the different organs. As a continuation of previously published data, in this study, Wistar rats have sacrificed 24 hrs and 7 days after single im application of 0.1LD50, 0.5LD50 and 1.0LD50 of each reactivator, and examinated tissue samples were obtained for pathohistological and semiquantitative analysis. A severity of tissue alteration, expressed as different tissue damage scores were evaluated. Morphological structure of examinated tissues treated with of 0.1LD50 of all reactivators was comparable with the control group of rats. Moderate injuries were seen in visceral tissues treated with 0.5LD50 of asoxime, obidoxime and K027. Acute damages were enlarged after treatment with 0.5LD50 and 1.0LD50 of all reactivators during the next 7 days. The most prominent changes were seen in rats treated with 1.0LD50 of K048 and K075 (P < 0.001 vs. control and asoxime-treated group). All reactivators given by a single, high, unitary dose regimen, have an adverse effect not only on the main visceral tissue, but on the whole rat as well, but the exact mechanism of cellular injury remains to be confirmed in further investigation.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a biopsie $7 D001706
- 650 _2
- $a chemické bojové látky $x škodlivé účinky $x chemie $x toxicita $7 D002619
- 650 _2
- $a vztah mezi dávkou a účinkem léčiva $7 D004305
- 650 _2
- $a histocytochemie $7 D006651
- 650 _2
- $a LD50 $7 D007928
- 650 _2
- $a plíce $x účinky léků $x metabolismus $x patologie $7 D008168
- 650 _2
- $a molekulární struktura $7 D015394
- 650 _2
- $a orgánová specificita $7 D009928
- 650 _2
- $a oximy $x aplikace a dávkování $x škodlivé účinky $x chemie $x toxicita $7 D010091
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a žaludek $x účinky léků $x patologie $7 D013270
- 650 _2
- $a vnitřnosti $x účinky léků $x patologie $7 D014781
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Nepovimova, Eugenie $u Department of Chemistry, Faculty of Science, University of Hradec Kralove, Hradec Kralove, Czechia.
- 700 1_
- $a Kuča, Kamil $u Department of Chemistry, Faculty of Science, University of Hradec Kralove, Hradec Kralove, Czechia. kamil.kuca@uhk.cz.
- 773 0_
- $w MED00182195 $t Scientific reports $x 2045-2322 $g Roč. 9, č. 1 (2019), s. 16425
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/31712702 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20210105 $b ABA008
- 991 __
- $a 20210114155005 $b ABA008
- 999 __
- $a ok $b bmc $g 1609090 $s 1119935
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 9 $c 1 $d 16425 $e 20191111 $i 2045-2322 $m Scientific reports $n Sci Rep $x MED00182195
- LZP __
- $a Pubmed-20210105