-
Je něco špatně v tomto záznamu ?
Altered neural and vascular mechanisms in hypertension
M. Pintérová, J. Kuneš, J. Zicha
Jazyk angličtina Země Česko
Typ dokumentu přehledy, 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
- adrenergní receptory fyziologie MeSH
- cévní endotel patofyziologie MeSH
- guanosinmonofosfát cyklický metabolismus MeSH
- hypertenze metabolismus patofyziologie MeSH
- krevní tlak fyziologie MeSH
- lidé MeSH
- membránové potenciály MeSH
- svaly hladké cévní fyziologie MeSH
- sympatický nervový systém patofyziologie MeSH
- vápník metabolismus MeSH
- vápníkové kanály - typ L metabolismus MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- práce podpořená grantem MeSH
- přehledy MeSH
Essential hypertension is a multifactorial disorder which belongs to the main risk factors responsible for renal and cardiovascular complications. This review is focused on the experimental research of neural and vascular mechanisms involved in the high blood pressure control. The attention is paid to the abnormalities in the regulation of sympathetic nervous system activity and adrenoceptor alterations as well as the changes of membrane and intracellular processes in the vascular smooth muscle cells of spontaneously hypertensive rats. These abnormalities lead to increased vascular tone arising from altered regulation of calcium influx through L-VDCC channels, which has a crucial role for excitation-contraction coupling, as well as for so-called "calcium sensitization" mediated by the RhoA/Rho-kinase pathway. Regulation of both pathways is dependent on the complex interplay of various vasodilator and vasoconstrictor stimuli. Two major antagonistic players in the regulation of blood pressure, i.e. sympathetic nervous system (by stimulation of adrenoceptors coupled to stimulatory and inhibitory G proteins) and nitric oxide (by cGMP signaling pathway), elicit their actions via the control of calcium influx through L-VDCC. However, L-type calcium current can also be regulated by the changes in membrane potential elicited by the activation of potassium channels, the impaired function of which was detected in hypertensive animals. The dominant role of enhanced calcium influx in the pathogenesis of high blood pressure of genetically hypertensive animals is confirmed not only by therapeutic efficacy of calcium antagonists but especially by the absence of hypertension in animals in which L-type calcium current was diminished by pertussis toxin-induced inactivation of inhibitory G proteins. Although there is considerable information on the complex neural and vascular alterations in rats with established hypertension, the detailed description of their appearance during the induction of hypertension is still missing.
Citace poskytuje Crossref.org
Lit.: 141
- 000
- 00000naa 2200000 a 4500
- 001
- bmc11031996
- 003
- CZ-PrNML
- 005
- 20130131145830.0
- 008
- 110912s2011 xr e eng||
- 009
- AR
- 024 7_
- $a 10.33549/physiolres.932189 $2 doi
- 040 __
- $a ABA008 $b cze $c ABA008 $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Pintérová, Mária $7 xx0102050
- 245 10
- $a Altered neural and vascular mechanisms in hypertension / $c M. Pintérová, J. Kuneš, J. Zicha
- 314 __
- $a Institute of Physiology, Academy of Sciences of the Czech Republic, Prague, Czech Republic. majapinter@yahoo.com.
- 504 __
- $a Lit.: 141
- 520 9_
- $a Essential hypertension is a multifactorial disorder which belongs to the main risk factors responsible for renal and cardiovascular complications. This review is focused on the experimental research of neural and vascular mechanisms involved in the high blood pressure control. The attention is paid to the abnormalities in the regulation of sympathetic nervous system activity and adrenoceptor alterations as well as the changes of membrane and intracellular processes in the vascular smooth muscle cells of spontaneously hypertensive rats. These abnormalities lead to increased vascular tone arising from altered regulation of calcium influx through L-VDCC channels, which has a crucial role for excitation-contraction coupling, as well as for so-called "calcium sensitization" mediated by the RhoA/Rho-kinase pathway. Regulation of both pathways is dependent on the complex interplay of various vasodilator and vasoconstrictor stimuli. Two major antagonistic players in the regulation of blood pressure, i.e. sympathetic nervous system (by stimulation of adrenoceptors coupled to stimulatory and inhibitory G proteins) and nitric oxide (by cGMP signaling pathway), elicit their actions via the control of calcium influx through L-VDCC. However, L-type calcium current can also be regulated by the changes in membrane potential elicited by the activation of potassium channels, the impaired function of which was detected in hypertensive animals. The dominant role of enhanced calcium influx in the pathogenesis of high blood pressure of genetically hypertensive animals is confirmed not only by therapeutic efficacy of calcium antagonists but especially by the absence of hypertension in animals in which L-type calcium current was diminished by pertussis toxin-induced inactivation of inhibitory G proteins. Although there is considerable information on the complex neural and vascular alterations in rats with established hypertension, the detailed description of their appearance during the induction of hypertension is still missing.
- 650 02
- $a zvířata $7 D000818
- 650 02
- $a krevní tlak $x fyziologie $7 D001794
- 650 02
- $a vápník $x metabolismus $7 D002118
- 650 02
- $a vápníkové kanály - typ L $x metabolismus $7 D020746
- 650 02
- $a guanosinmonofosfát cyklický $x metabolismus $7 D006152
- 650 02
- $a cévní endotel $x patofyziologie $7 D004730
- 650 02
- $a lidé $7 D006801
- 650 02
- $a hypertenze $x metabolismus $x patofyziologie $7 D006973
- 650 02
- $a membránové potenciály $7 D008564
- 650 02
- $a svaly hladké cévní $x fyziologie $7 D009131
- 650 02
- $a adrenergní receptory $x fyziologie $7 D011941
- 650 02
- $a sympatický nervový systém $x patofyziologie $7 D013564
- 655 _2
- $a přehledy $7 D016454
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Kuneš, Jaroslav, $d 1948- $7 nlk19990073450
- 700 1_
- $a Zicha, Josef, $d 1950- $7 jk01152609
- 773 0_
- $w MED00003824 $t Physiological research $g Roč. 60, č. 3 (2011), s. 381-402 $x 0862-8408
- 856 41
- $u http://www.biomed.cas.cz/physiolres/pdf/60/60_381.pdf $y plný text volně přístupný
- 910 __
- $a ABA008 $b A 4120 $c 266 $y 2
- 990 __
- $a 20110912095705 $b ABA008
- 991 __
- $a 20130131145957 $b ABA008
- 999 __
- $a ok $b bmc $g 877076 $s 742072
- BAS __
- $a 3
- BMC __
- $a 2011 $b 60 $c 3 $d 381-402 $m Physiological research $x MED00003824
- LZP __
- $a 2011-16/mkme