-
Je něco špatně v tomto záznamu ?
The cardiovascular effects of central hydrogen sulfide are related to KATP channels activation
W.Q. Liu, C. Chai, X.Y. Li, W.J. Yuan, W.Z. Wang, Y. Lu
Jazyk angličtina Země Česko
Typ dokumentu 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
- bradykardie chemicky indukované patofyziologie MeSH
- gating iontového kanálu účinky léků MeSH
- hypotenze chemicky indukované patofyziologie MeSH
- KATP kanály účinky léků MeSH
- krevní tlak účinky léků MeSH
- krysa rodu rattus MeSH
- mozek patofyziologie účinky léků MeSH
- potkani Sprague-Dawley MeSH
- srdce patofyziologie účinky léků MeSH
- srdeční frekvence účinky léků MeSH
- sulfan aplikace a dávkování metabolismus MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- práce podpořená grantem MeSH
Hydrogen sulfide (H2S), an endogenous “gasotransmitter”, exists in the central nervous system. However, the central cardiovascular effects of endogenous H2S are not fully determined. The present study was designed to investigate the central cardiovascular effects and its possible mechanism in anesthetized rats. Intracerebroventricular (icv) injection of NaHS (0.17~17 μg) produced a significant and dose-dependent decrease in blood pressure (BP) and heart rate (HR) (P<0.05) compared to control. The higher dose of NaHS (17 μg, n=6) decreased BP and HR quickly of rats and 2 of them died of respiratory paralyse. Icv injection of the cystathionine betasynthetase (CBS) activator s-adenosyl-L-methionine (SAM, 26 μg) also produced a significant hypotension and bradycardia, which were similar to the results of icv injection of NaHS. Furthermore, the hypotension and bradycardia induced by icv NaHS were effectively attenuated by pretreatment with the KATP channel blocker glibenclamide but not with the CBS inhibitor hydroxylamine. The present study suggests that icv injection of NaHS produces hypotension and bradycardia, which is dependent on the KATP channel activation.
Department of Clinical Laboratory San Ai Tang Hospital Lanzhou China
Department of General Surgery 1st Hospital of Lanzhou University Lanzhou China
Department of Physiology 2nd Military Medical University Shanghai China
Department of Physiology Ningxia Medical University YinChuan China
Citace poskytuje Crossref.org
Literatura
- 000
- 00000naa a2200000 a 4500
- 001
- bmc12006458
- 003
- CZ-PrNML
- 005
- 20120420110222.0
- 007
- ta
- 008
- 120301s2011 xr d f 000 0eng||
- 009
- AR
- 024 7_
- $a 10.33549/physiolres.932092 $2 doi
- 040 __
- $a ABA008 $d ABA008 $e AACR2 $b cze
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Liu, W. Q. $u Department of Clinical Laboratory, San Ai Tang Hospital, Lanzhou, China; Department of Anus and Intestine Surgery, Daxing Hospital Affiliated to Capital Medical University, Beijing, China
- 245 14
- $a The cardiovascular effects of central hydrogen sulfide are related to KATP channels activation / $c W.Q. Liu, C. Chai, X.Y. Li, W.J. Yuan, W.Z. Wang, Y. Lu
- 504 __
- $a Literatura $b 47
- 520 9_
- $a Hydrogen sulfide (H2S), an endogenous “gasotransmitter”, exists in the central nervous system. However, the central cardiovascular effects of endogenous H2S are not fully determined. The present study was designed to investigate the central cardiovascular effects and its possible mechanism in anesthetized rats. Intracerebroventricular (icv) injection of NaHS (0.17~17 μg) produced a significant and dose-dependent decrease in blood pressure (BP) and heart rate (HR) (P<0.05) compared to control. The higher dose of NaHS (17 μg, n=6) decreased BP and HR quickly of rats and 2 of them died of respiratory paralyse. Icv injection of the cystathionine betasynthetase (CBS) activator s-adenosyl-L-methionine (SAM, 26 μg) also produced a significant hypotension and bradycardia, which were similar to the results of icv injection of NaHS. Furthermore, the hypotension and bradycardia induced by icv NaHS were effectively attenuated by pretreatment with the KATP channel blocker glibenclamide but not with the CBS inhibitor hydroxylamine. The present study suggests that icv injection of NaHS produces hypotension and bradycardia, which is dependent on the KATP channel activation.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a krevní tlak $x účinky léků $7 D001794
- 650 _2
- $a bradykardie $x chemicky indukované $x patofyziologie $7 D001919
- 650 _2
- $a mozek $x patofyziologie $x účinky léků $7 D001921
- 650 _2
- $a srdce $x patofyziologie $x účinky léků $7 D006321
- 650 _2
- $a srdeční frekvence $x účinky léků $7 D006339
- 650 _2
- $a sulfan $x aplikace a dávkování $x metabolismus $7 D006862
- 650 _2
- $a hypotenze $x chemicky indukované $x patofyziologie $7 D007022
- 650 _2
- $a gating iontového kanálu $x účinky léků $7 D015640
- 650 _2
- $a KATP kanály $x účinky léků $7 D054086
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a potkani Sprague-Dawley $7 D017207
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Chai, C. $u Department of General Surgery, First Hospital of Lanzhou University, Lanzhou, China
- 700 1_
- $a Li, X. Y. $u Department of Clinical Laboratory, San Ai Tang Hospital, Lanzhou, China
- 700 1_
- $a Yuan, W. J. $u Department of Physiology, Second Military Medical University, Shanghai, China; Department of Physiology, Ningxia Medical University, YinChuan, China
- 700 1_
- $a Wang, W. Z. $u Department of Physiology, Second Military Medical University, Shanghai, China
- 700 1_
- $a Lu, Y. $u Department of Clinical Laboratory, San Ai Tang Hospital, Lanzhou, China
- 773 0_
- $t Physiological research $x 0862-8408 $g Roč. 60, č. 5 (2011), s. 729-738 $w MED00003824
- 910 __
- $a ABA008 $b A 4120 $c 266 $y 2
- 990 __
- $a 20120229072848 $b ABA008
- 991 __
- $a 20120420110159 $b ABA008
- 999 __
- $a ok $b bmc $g 899516 $s 763289
- BAS __
- $a 3
- BMC __
- $a 2011 $b 60 $c 5 $d 729-738 $i 0862-8408 $m Physiological research $n Physiol. Res. (Print) $x MED00003824
- LZP __
- $a 2012-12/ipme