-
Je něco špatně v tomto záznamu ?
Cardiac morphofunctional characteristics of transgenic rats with overexpression of the bradykinin B1 receptor in the endothelium
R. F. Levy, A. J. Serra, E. L. Antonio, L. Dos Santos, D. S. Bocalini, J. B. Pesquero, M. Bader, V. F. Merino, H. A. de Oliveira, E. C. de Arruda Veiga, J. A. Silva, P. J. Tucci
Jazyk angličtina Země Česko
Typ dokumentu časopisecké články
NLK
Directory of Open Access Journals
od 1991
Free Medical Journals
od 1998
ProQuest Central
od 2005-01-01
Medline Complete (EBSCOhost)
od 2006-01-01
Nursing & Allied Health Database (ProQuest)
od 2005-01-01
Health & Medicine (ProQuest)
od 2005-01-01
ROAD: Directory of Open Access Scholarly Resources
od 1998
- MeSH
- dysfunkce levé srdeční komory genetika metabolismus patofyziologie MeSH
- endoteliální buňky metabolismus MeSH
- fenotyp MeSH
- funkce levé komory srdeční * MeSH
- genetická predispozice k nemoci MeSH
- kontrakce myokardu * MeSH
- papilární svaly metabolismus patofyziologie MeSH
- potkani Sprague-Dawley MeSH
- potkani transgenní MeSH
- receptor bradykininu B1 genetika metabolismus MeSH
- remodelace komor MeSH
- upregulace MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
Our aim was to evaluate whether endothelial overexpressing of the bradykinin B1 receptor could be associated with altered left ventricular and myocardial performance. Echocardiography and hemodynamic were employed to assess left ventricular morphology and function in Sprague Dawley transgenic rats overexpressing the endothelial bradykinin B1 receptor (Tie2B1 rats). The myocardial inotropism was evaluated on papillary muscles contracting in vitro. In Tie2B1 animals, an enlarged left ventricular cavity and lower fractional shortening coupled with a lower rate of pressure change values indicated depressed left ventricular performance. Papillary muscle mechanics revealed that both Tie2B1 and wild-type rat groups had the same contractile capacities under basal conditions; however, in transgenic animals, there was accentuated inotropism due to post-pause potentiation. Following treatment with the Arg(9)-BK agonist, Tie2B1 papillary muscles displayed a reduction in myocardial inotropism. Endothelial B1 receptor overexpression has expanded the LV cavity and worsened its function. There was an exacerbated response of papillary muscle in vitro to a prolonged resting pause, and the use of a B1 receptor agonist impairs myocardial inotropism.
Johns Hopkins University School of Medicine Baltimore USA
Max Delbrück Center for Molecular Medicine Berlin Buch Germany
Universidade Federal da Paraíba João Pessoa Paraíba Brazil
Universidade Federal de São Paulo São Paulo SP Brazil
Universidade Federal do Espírito Santo Vitória Espírito Santo Brazil
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc18027502
- 003
- CZ-PrNML
- 005
- 20180815074339.0
- 007
- ta
- 008
- 180807s2017 xr d f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.33549/physiolres.933596 $2 doi
- 035 __
- $a (PubMed)28937259
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Levy, R. F. $u Universidade Federal da Paraíba, João Pessoa, Paraíba, Brazil
- 245 10
- $a Cardiac morphofunctional characteristics of transgenic rats with overexpression of the bradykinin B1 receptor in the endothelium / $c R. F. Levy, A. J. Serra, E. L. Antonio, L. Dos Santos, D. S. Bocalini, J. B. Pesquero, M. Bader, V. F. Merino, H. A. de Oliveira, E. C. de Arruda Veiga, J. A. Silva, P. J. Tucci
- 520 9_
- $a Our aim was to evaluate whether endothelial overexpressing of the bradykinin B1 receptor could be associated with altered left ventricular and myocardial performance. Echocardiography and hemodynamic were employed to assess left ventricular morphology and function in Sprague Dawley transgenic rats overexpressing the endothelial bradykinin B1 receptor (Tie2B1 rats). The myocardial inotropism was evaluated on papillary muscles contracting in vitro. In Tie2B1 animals, an enlarged left ventricular cavity and lower fractional shortening coupled with a lower rate of pressure change values indicated depressed left ventricular performance. Papillary muscle mechanics revealed that both Tie2B1 and wild-type rat groups had the same contractile capacities under basal conditions; however, in transgenic animals, there was accentuated inotropism due to post-pause potentiation. Following treatment with the Arg(9)-BK agonist, Tie2B1 papillary muscles displayed a reduction in myocardial inotropism. Endothelial B1 receptor overexpression has expanded the LV cavity and worsened its function. There was an exacerbated response of papillary muscle in vitro to a prolonged resting pause, and the use of a B1 receptor agonist impairs myocardial inotropism.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a endoteliální buňky $x metabolismus $7 D042783
- 650 _2
- $a genetická predispozice k nemoci $7 D020022
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 12
- $a kontrakce myokardu $7 D009200
- 650 _2
- $a papilární svaly $x metabolismus $x patofyziologie $7 D010210
- 650 _2
- $a fenotyp $7 D010641
- 650 _2
- $a potkani Sprague-Dawley $7 D017207
- 650 _2
- $a potkani transgenní $7 D055647
- 650 _2
- $a receptor bradykininu B1 $x genetika $x metabolismus $7 D043783
- 650 _2
- $a upregulace $7 D015854
- 650 _2
- $a dysfunkce levé srdeční komory $x genetika $x metabolismus $x patofyziologie $7 D018487
- 650 12
- $a funkce levé komory srdeční $7 D016277
- 650 _2
- $a remodelace komor $7 D020257
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Serra, A. J. $u Universidade Nove de Julho, São Paulo, SP, Brazil
- 700 1_
- $a Antonio, E. L. $u Universidade Federal de São Paulo, São Paulo, SP, Brazil
- 700 1_
- $a Dos Santos, L. $u Universidade Federal do Espírito Santo, Vitória, Espírito Santo, Brazil
- 700 1_
- $a Bocalini, D. S. $u Universidade São Judas Tadeu, São Paulo, SP, Brazil
- 700 1_
- $a Pesquero, J. B. $u Universidade Federal de São Paulo, São Paulo, SP, Brazil
- 700 1_
- $a Bader, M. $u Max-Delbrück-Center for Molecular Medicine (MDC), Berlin-Buch, Germany
- 700 1_
- $a Merino, V. F. $u Johns Hopkins University School of Medicine, Baltimore, USA
- 700 1_
- $a Oliveira, H. A. de $u Universidade Nove de Julho, São Paulo, SP, Brazil
- 700 1_
- $a Arruda Veiga, E. C. de $u Universidade Federal de São Paulo, São Paulo, SP, Brazil
- 700 1_
- $a Silva, J. A. $u Universidade Nove de Julho, São Paulo, SP, Brazil
- 700 1_
- $a Tucci, P. Jf. $u Universidade Federal de São Paulo, São Paulo, SP, Brazil
- 773 0_
- $w MED00003824 $t Physiological research $x 1802-9973 $g Roč. 66, č. 6 (2017), s. 925-932
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/28937259 $y Pubmed
- 910 __
- $a ABA008 $b A 4120 $c 266 $y 4 $z 0
- 990 __
- $a 20180807 $b ABA008
- 991 __
- $a 20180810144722 $b ABA008
- 999 __
- $a ok $b bmc $g 1326206 $s 1024450
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2017 $b 66 $c 6 $d 925-932 $e 20170922 $i 1802-9973 $m Physiological research $n Physiol. Res. (Print) $x MED00003824
- LZP __
- $b NLK118 $a Pubmed-20180807