Detail
Článek
Článek online
FT
Medvik - BMČ
  • Je něco špatně v tomto záznamu ?

Age, genetic characteristics and number of cycles are critical factors to consider for successful protection of the murine heart with postconditioning

S. J. Somers, L. Lacerda, L. Opie, S. Lecour

. 2011 ; 60 (6) : 971-974.

Jazyk angličtina Země Česko

Typ dokumentu práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc12006380

Postconditioning (PostC) is a recently discovered phenomenon whereby brief repetitive cycles of ischaemia with intermittent reperfusion following prolonged ischaemia elicit cardioprotection. This study investigated whether the age, genetic characteristics or number of repetitive cycles influenced the protective effect of PostC in mice. C57BL/6 floxed or non-floxed STAT-3 mice aged between 14-16 weeks (young) or 18-20 weeks (older) were perfused on a Langendorff apparatus and subjected to 35 min global ischaemia and 45 min reperfusion. PostC was elicited by either 3 (PostC-3) or 6 cycles (PostC-6) of 10s ischaemia and 10 s reperfusion. PostC-3 and PostC-6 in both young and older non-floxed mice reduced the myocardial infarct size. In contrast, only PostC-3 reduced myocardial infarct size in young floxed mice. Neither PostC-3 nor PostC-6 reduced the infarct in older floxed mice. Our data reveal that genetic characteristics, a minute difference in age or the number of postconditioning cycles are critical factors to be considered for the successful effect of ischaemic postconditioning in a murine model. Moreover, these factors should be taken into consideration for future experimental research or clinical applications of this protective phenomenon.

Citace poskytuje Crossref.org

Bibliografie atd.

Literatura

000      
00000naa a2200000 a 4500
001      
bmc12006380
003      
CZ-PrNML
005      
20120910114047.0
007      
ta
008      
120229s2011 xr d f 000 0eng||
009      
AR
024    7_
$a 10.33549/physiolres.932129 $2 doi
040    __
$a ABA008 $d ABA008 $e AACR2 $b cze
041    0_
$a eng
044    __
$a xr
100    1_
$a Somers, S. J. $u Hatter Cardiovascular Research Institute, Department of Medicine, University of Cape Town, Cape Town, South Africa
245    10
$a Age, genetic characteristics and number of cycles are critical factors to consider for successful protection of the murine heart with postconditioning / $c S. J. Somers, L. Lacerda, L. Opie, S. Lecour
504    __
$a Literatura $b 13
520    9_
$a Postconditioning (PostC) is a recently discovered phenomenon whereby brief repetitive cycles of ischaemia with intermittent reperfusion following prolonged ischaemia elicit cardioprotection. This study investigated whether the age, genetic characteristics or number of repetitive cycles influenced the protective effect of PostC in mice. C57BL/6 floxed or non-floxed STAT-3 mice aged between 14-16 weeks (young) or 18-20 weeks (older) were perfused on a Langendorff apparatus and subjected to 35 min global ischaemia and 45 min reperfusion. PostC was elicited by either 3 (PostC-3) or 6 cycles (PostC-6) of 10s ischaemia and 10 s reperfusion. PostC-3 and PostC-6 in both young and older non-floxed mice reduced the myocardial infarct size. In contrast, only PostC-3 reduced myocardial infarct size in young floxed mice. Neither PostC-3 nor PostC-6 reduced the infarct in older floxed mice. Our data reveal that genetic characteristics, a minute difference in age or the number of postconditioning cycles are critical factors to be considered for the successful effect of ischaemic postconditioning in a murine model. Moreover, these factors should be taken into consideration for future experimental research or clinical applications of this protective phenomenon.
650    02
$a zvířata $7 D000818
650    02
$a ischemický postconditioning $7 D057775
650    02
$a mužské pohlaví $7 D008297
650    02
$a myši $7 D051379
650    02
$a myši inbrední C57BL $7 D008810
650    02
$a infarkt myokardu $x genetika $x patologie $x prevence a kontrola $7 D009203
650    02
$a ischemická choroba srdeční $x genetika $x patologie $x prevence a kontrola $7 D017202
650    02
$a myokard $x patologie $7 D009206
650    02
$a transkripční faktor STAT3 $x metabolismus $7 D050796
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Lacerda, L. $u Hatter Cardiovascular Research Institute, Department of Medicine, University of Cape Town, Cape Town, South Africa
700    1_
$a Opie, L. $u Hatter Cardiovascular Research Institute, Department of Medicine, University of Cape Town, Cape Town, South Africa
700    1_
$a Lecour, S. $u Hatter Cardiovascular Research Institute, Department of Medicine, University of Cape Town, Cape Town, South Africa
773    0_
$t Physiological research $x 0862-8408 $g Roč. 60, č. 6 (2011), s. 971-974 $w MED00003824
910    __
$a ABA008 $b A 4120 $c 266 $y 2
990    __
$a 20120229072848 $b ABA008
991    __
$a 20120910114221 $b ABA008
999    __
$a ok $b bmc $g 899433 $s 763209
BAS    __
$a 3
BMC    __
$a 2011 $b 60 $c 6 $d 971-974 $i 0862-8408 $m Physiological research $n Physiol. Res. (Print) $x MED00003824
LZP    __
$a 2012-12/ipme

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...