-
Je něco špatně v tomto záznamu ?
Differential remodeling of carotid artery in spontaneously hypertensive and hereditary hypertriglyceridemic rats
M. Cebová, F. Kristek, J. Kunes
Jazyk angličtina Země Česko
Typ dokumentu časopisecké články, práce podpořená grantem
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
- arteriae carotides patologie MeSH
- hypertenze patologie patofyziologie MeSH
- hypertriglyceridemie patologie patofyziologie MeSH
- krysa rodu rattus MeSH
- potkani inbrední SHR MeSH
- potkani Wistar MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
High blood pressure, increased level of cholesterol, diabetes, hypertriglyceridemia and obesity are risk factors accompanied metabolic syndrome. The aim of the study was to compare geometry of carotid artery (AC) of 3-week-old (3w) and 52-week-old (52w) hereditary hypertriglyceridemic rats (hHTG) and spontaneously hypertensive rats (SHR) which represent a genetic model of human essential hypertension with age-matched Wistar rats. After sacrificing the rats were perfused with a glutaraldehyde fixative under the pressure 90 mm Hg (3w) and 120 mm Hg (52w) for 10 min via cannula placed into left ventricle. Middle part of AC was excised and processed according to standard electron microscopy procedure. Geometry of AC was evaluated in light microscopy. SHR vs. Wistar rats: BP of 3w did not differ, in 52w it was increased; cardiac hypertrophy was found in both ages; wall thickness (WT) and cross sectional area (CSA) in 3w did not differ, in 52w both were increased; inner diameter (ID) in 3w and 52w was decreased; WT/ID was increased in both ages. Hereditary HTG vs. Wistar rats: BP was increased in both periods; cardiac hypertrophy was observed in 3w; WT in 3w was decreased, in 52w it was increased; CSA and ID were decreased in both ages; WT/ID was increased only in 52w. Discrepancies between development of BP, cardiac hypertrophy in SHR and hHTG rats were observed. Alterations of BP were not in harmony with alterations in geometry of carotid arteries in both SHR and hHTG rats. We suggest that BP is not the main stimuli evoked hemodynamic and structural alterations of cardiovascular system in ontogenic development of SHR and hHTG rats.
- 000
- 00000naa a2200000 a 4500
- 001
- bmc13034173
- 003
- CZ-PrNML
- 005
- 20151006114831.0
- 007
- ta
- 008
- 131021s2006 xr d f 000 0|eng||
- 009
- AR
- 035 __
- $a (PubMed)17177629
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Cebová, Martina $u Institute of Normal and Pathological Physiology, Slovak Academy of Sciences, Bratislava, Slovak Republic martina.cebova@savba.sk $7 _AN038417
- 245 10
- $a Differential remodeling of carotid artery in spontaneously hypertensive and hereditary hypertriglyceridemic rats / $c M. Cebová, F. Kristek, J. Kunes
- 520 9_
- $a High blood pressure, increased level of cholesterol, diabetes, hypertriglyceridemia and obesity are risk factors accompanied metabolic syndrome. The aim of the study was to compare geometry of carotid artery (AC) of 3-week-old (3w) and 52-week-old (52w) hereditary hypertriglyceridemic rats (hHTG) and spontaneously hypertensive rats (SHR) which represent a genetic model of human essential hypertension with age-matched Wistar rats. After sacrificing the rats were perfused with a glutaraldehyde fixative under the pressure 90 mm Hg (3w) and 120 mm Hg (52w) for 10 min via cannula placed into left ventricle. Middle part of AC was excised and processed according to standard electron microscopy procedure. Geometry of AC was evaluated in light microscopy. SHR vs. Wistar rats: BP of 3w did not differ, in 52w it was increased; cardiac hypertrophy was found in both ages; wall thickness (WT) and cross sectional area (CSA) in 3w did not differ, in 52w both were increased; inner diameter (ID) in 3w and 52w was decreased; WT/ID was increased in both ages. Hereditary HTG vs. Wistar rats: BP was increased in both periods; cardiac hypertrophy was observed in 3w; WT in 3w was decreased, in 52w it was increased; CSA and ID were decreased in both ages; WT/ID was increased only in 52w. Discrepancies between development of BP, cardiac hypertrophy in SHR and hHTG rats were observed. Alterations of BP were not in harmony with alterations in geometry of carotid arteries in both SHR and hHTG rats. We suggest that BP is not the main stimuli evoked hemodynamic and structural alterations of cardiovascular system in ontogenic development of SHR and hHTG rats.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a arteriae carotides $x patologie $7 D002339
- 650 _2
- $a hypertenze $x patologie $x patofyziologie $7 D006973
- 650 _2
- $a hypertriglyceridemie $x patologie $x patofyziologie $7 D015228
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a potkani inbrední SHR $7 D011918
- 650 _2
- $a potkani Wistar $7 D017208
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Kristek, František $u Institute of Normal and Pathological Physiology, Slovak Academy of Sciences, Bratislava, Slovak Republic $7 xx0259762
- 700 1_
- $a Kuneš, Jaroslav, $u Institute of Normal and Pathological Physiology, Slovak Academy of Sciences, Bratislava, Slovak Republic; CRC and Institute of Physiology AS CR, Prague, Czech Republic $d 1948- $7 nlk19990073450
- 773 0_
- $w MED00003824 $t Physiological research $x 0862-8408 $g Roč. 55,Suppl 1 (2006), s. S81-S87
- 773 0_
- $t Institute of Normal and Pathological Physiology, Slovak Academy of Sciences $x 0862-8408 $g Roč. 55,Suppl 1 (2006), s. S81-S87 $w MED00158875
- 856 41
- $u https://www.biomed.cas.cz/physiolres/pdf/55%20Suppl%201/55_S81.pdf $y plný text volně přístupný
- 910 __
- $a ABA008 $b A 4120 $c 266 $y 4 $z 0
- 990 __
- $a 20131021 $b ABA008
- 991 __
- $a 20151006115016 $b ABA008
- 999 __
- $a ok $b bmc $g 999295 $s 832643
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2006 $b 55 $c Suppl 1 $d S81-S87 $i 0862-8408 $m Physiological research $n Physiol. Res. (Print) $x MED00003824
- BMC __
- $a 2006 $b 55 $c Suppl 1 $d S81-S87 $i 0862-8408 $m Institute of Normal and Pathological Physiology, Slovak Academy of Sciences $n $x MED00158875
- LZP __
- $b NLK111 $a Pubmed-20131021