-
Je něco špatně v tomto záznamu ?
Ivabradine does not impair anxiety-like behavior and memory in both healthy and L-NAME-induced hypertensive rats
K. Krajcirovicova, S. Aziriova, T. Baka, K. Repova, M. Adamcova, L. Paulis, F. Simko
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
- hypertenze chemicky indukované farmakoterapie patofyziologie MeSH
- inhibitory enzymů farmakologie terapeutické užití MeSH
- ivabradin farmakologie terapeutické užití MeSH
- krevní tlak účinky léků fyziologie MeSH
- krysa rodu rattus MeSH
- NG-nitroargininmethylester toxicita MeSH
- paměť účinky léků fyziologie MeSH
- potkani Wistar MeSH
- srdeční frekvence účinky léků fyziologie MeSH
- úzkost * patofyziologie MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
Cardiovascular pathologies are frequently associated with anxiety and other behavioral disturbances. Ivabradine, an inhibitor of the hyperpolarization-activated cyclic nucleotide-gated channels in the sinoatrial node, decreases heart rate and provides cardiovascular protection. Although ivabradine is increasingly used in cardiovascular medicine, the data on its behavioral effects are lacking. The aim of this work was to show ivabradine's potential effect on behavior in healthy and hypertensive rats. After a four-week treatment period, systolic blood pressure was increased in the N(G)-nitro-L-arginine methyl ester (L-NAME)-group and ivabradine significantly reduced it. Furthermore, it reduced the heart rate in both the control and L-NAME-group. In the control group, ivabradine enhanced the time spent in and transition to the open arms of the elevated plus maze test (EPM). In the L-NAME-group, ivabradine does not show a significant effect on the time spent in the EPM open arms and the number of transitions into them. Furthermore, ivabradine has no impact on cognitive function in both control and L-NAME groups. We conclude that ivabradine showed no undesirable effects on anxiety, locomotion or learning; in fact, some of these parameters were even improved. For the first time it has been shown that ivabradine is a safe cardiovascular drug regarding its effect on psycho-behavioral manifestations.
Department of Physiology Faculty of Medicine Charles University Hradec Kralove Czech Republic
Institute of Pathophysiology Faculty of Medicine Comenius University Bratislava Slovak Republic
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc19005371
- 003
- CZ-PrNML
- 005
- 20230112094429.0
- 007
- ta
- 008
- 190204s2018 xr d f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.33549/physiolres.934048 $2 doi
- 035 __
- $a (PubMed)30607972
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Krajcirovicova, K. $u Institute of Pathophysiology, Faculty of Medicine, Comenius University, Bratislava, Slovak Republic
- 245 10
- $a Ivabradine does not impair anxiety-like behavior and memory in both healthy and L-NAME-induced hypertensive rats / $c K. Krajcirovicova, S. Aziriova, T. Baka, K. Repova, M. Adamcova, L. Paulis, F. Simko
- 520 9_
- $a Cardiovascular pathologies are frequently associated with anxiety and other behavioral disturbances. Ivabradine, an inhibitor of the hyperpolarization-activated cyclic nucleotide-gated channels in the sinoatrial node, decreases heart rate and provides cardiovascular protection. Although ivabradine is increasingly used in cardiovascular medicine, the data on its behavioral effects are lacking. The aim of this work was to show ivabradine's potential effect on behavior in healthy and hypertensive rats. After a four-week treatment period, systolic blood pressure was increased in the N(G)-nitro-L-arginine methyl ester (L-NAME)-group and ivabradine significantly reduced it. Furthermore, it reduced the heart rate in both the control and L-NAME-group. In the control group, ivabradine enhanced the time spent in and transition to the open arms of the elevated plus maze test (EPM). In the L-NAME-group, ivabradine does not show a significant effect on the time spent in the EPM open arms and the number of transitions into them. Furthermore, ivabradine has no impact on cognitive function in both control and L-NAME groups. We conclude that ivabradine showed no undesirable effects on anxiety, locomotion or learning; in fact, some of these parameters were even improved. For the first time it has been shown that ivabradine is a safe cardiovascular drug regarding its effect on psycho-behavioral manifestations.
- 650 _2
- $a zvířata $7 D000818
- 650 12
- $a úzkost $x patofyziologie $7 D001007
- 650 _2
- $a krevní tlak $x účinky léků $x fyziologie $7 D001794
- 650 _2
- $a inhibitory enzymů $x farmakologie $x terapeutické užití $7 D004791
- 650 _2
- $a srdeční frekvence $x účinky léků $x fyziologie $7 D006339
- 650 _2
- $a hypertenze $x chemicky indukované $x farmakoterapie $x patofyziologie $7 D006973
- 650 _2
- $a ivabradin $x farmakologie $x terapeutické užití $7 D000077550
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a paměť $x účinky léků $x fyziologie $7 D008568
- 650 _2
- $a NG-nitroargininmethylester $x toxicita $7 D019331
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a potkani Wistar $7 D017208
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Aziriová, Silvia. $7 xx0233145 $u Institute of Pathophysiology, Faculty of Medicine, Comenius University, Bratislava, Slovak Republic
- 700 1_
- $a Baka, Tomáš, $u Institute of Pathophysiology, Faculty of Medicine, Comenius University, Bratislava, Slovak Republic $d 1989- $7 xx0263984
- 700 1_
- $a Repová, Kristína, $u Institute of Pathophysiology, Faculty of Medicine, Comenius University, Bratislava, Slovak Republic $d 1984- $7 xx0264906
- 700 1_
- $a Adamcová, Michaela, $d 1964- $7 xx0064762 $u Department of Physiology, Faculty of Medicine, Charles University, Hradec Kralove, Czech Republic
- 700 1_
- $a Paulis, L. $u Institute of Pathophysiology, Faculty of Medicine, Comenius University, Bratislava, Slovak Republic; Institute of Normal and Pathological Physiology, Center for Experimental Medicine, Slovak Academy of Sciences, Bratislava, Slovak Republic
- 700 1_
- $a Šimko, Fedor $7 xx0097039 $u Institute of Pathophysiology, Faculty of Medicine, Comenius University, Bratislava, Slovak Republic; Third Department of Internal Medicine, Faculty of Medicine, Comenius University, Bratislava, Slovak Republic; Institute of Experimental Endocrinology, Biomedical Research Center, Slovak Academy of Sciences, Bratislava, Slovak Republic
- 773 0_
- $w MED00003824 $t Physiological research $x 1802-9973 $g Roč. 67, Suppl. 4 (2018), s. S655-S664
- 773 0_
- $t Proceedings of the ... Physiological days $x 1802-9973 $g Roč. 94, Suppl. 4 (2018), s. S655-S664 $w MED00183838
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/30607972 $y Pubmed
- 910 __
- $a ABA008 $b A 4120 $c 266 $y 4 $z 0
- 990 __
- $a 20190204 $b ABA008
- 991 __
- $a 20230112094422 $b ABA008
- 999 __
- $a ok $b bmc $g 1377944 $s 1043576
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2018 $b 67 $c Suppl. 4 $d S655-S664 $i 1802-9973 $m Physiological research $n Physiol. Res. (Print) $x MED00003824
- BMC __
- $a 2018 $b 94 $c Suppl. 4 $d S655-S664 $i 1802-9973 $m Proceedings of the ... Physiological days $n Physiol. Res. (Print) $x MED00183838
- LZP __
- $b NLK118 $a Pubmed-20190204