-
Je něco špatně v tomto záznamu ?
Modulation of cardiac connexin-43 by omega-3 fatty acid ethyl-ester supplementation demonstrated in spontaneously diabetic rats
J. Radosinska, L. H. Kurahara, K. Hiraishi, C. Viczenczova, T. Egan Benova, B. Szeiffova Bacova, V. Dosenko, J. Navarova, B. Obsitnik, I. Imanaga, T. Soukup, N. Tribulova
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
- experimentální diabetes mellitus metabolismus patologie prevence a kontrola MeSH
- fixní kombinace léků MeSH
- konexin 43 metabolismus MeSH
- krysa rodu rattus MeSH
- kyselina eikosapentaenová farmakologie terapeutické užití MeSH
- kyseliny dokosahexaenové farmakologie terapeutické užití MeSH
- myokard metabolismus ultrastruktura MeSH
- potravní doplňky MeSH
- preklinické hodnocení léčiv MeSH
- proteinkinasa C-delta metabolismus MeSH
- proteinkinasa C-epsilon metabolismus MeSH
- srdce účinky léků MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
Previous data suggest that type 1 diabetes mellitus leads to the deterioration of myocardial intercellular communication mediated by connexin-43 (Cx43) channels. We therefore aimed to explore Cx43, PKC signaling and ultrastructure in non-treated and omega-3 fatty acid (omega-3) treated spontaneously diabetic Goto-Kakizaki (GK) rats considered as type 2 diabetes model. Four-week-old GK and non-diabetic Wistar-Clea rats were fed omega-3 (200 mg/kg/day) for 2 months and compared with untreated rats. Real-time PCR and immunoblotting were performed to determine Cx43, PKC-epsilon and PKC-delta expression. In situ Cx43 was examined by immunohistochemistry and subcellular alterations by electron microscopy. Omega-3 intake reduced blood glucose, triglycerides, and cholesterol in diabetic rats and this was associated with improved integrity of cardiomyocytes and capillaries in the heart. Myocardial Cx43 mRNA and protein levels were higher in diabetic versus non-diabetic rats and were further enhanced by omega-3. The ratio of phosphorylated (functional) to non-phosphorylated Cx43 was lower in diabetic compared to non-diabetic rats but was increased by omega-3, in part due to up-regulation of PKC-epsilon. In addition, pro-apoptotic PKC-delta expression was decreased. In conclusion, spontaneously diabetic rats at an early stage of disease benefit from omega-3 intake due to its hypoglycemic effect, upregulation of myocardial Cx43, and preservation of cardiovascular ultrastructure. These findings indicates that supplementation of omega-3 may be beneficial also in the management of diabetes in humans.
Bogomoletz Institute of Physiology Kyiv Ukraine
Department of Physiology Fukuoka University Medical School Fukuoka Japan
Institute for Heart Research Slovak Academy of Sciences Bratislava Slovakia
Institute of Experimental Pharmacology and Toxicology Slovak Academy of Sciences Bratislava Slovakia
Institute of Physiology Czech Academy of Sciences Prague Czech Republic
Institute of Physiology Faculty of Medicine Comenius University Bratislava Slovakia
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc16031109
- 003
- CZ-PrNML
- 005
- 20181119072918.0
- 007
- ta
- 008
- 161101s2015 xr ad f 000 0|ENG||
- 009
- AR
- 024 7_
- $a 10.33549/physiolres.932981 $2 doi
- 035 __
- $a (PubMed)26447526
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a ENG
- 044 __
- $a xr
- 100 1_
- $a Radošínská, Jana $u Institute of Physiology, Faculty of Medicine, Comenius University, Bratislava, Slovakia,; Institute for Heart Research, Slovak Academy of Sciences, Bratislava, Slovakia $7 _AN048690
- 245 10
- $a Modulation of cardiac connexin-43 by omega-3 fatty acid ethyl-ester supplementation demonstrated in spontaneously diabetic rats / $c J. Radosinska, L. H. Kurahara, K. Hiraishi, C. Viczenczova, T. Egan Benova, B. Szeiffova Bacova, V. Dosenko, J. Navarova, B. Obsitnik, I. Imanaga, T. Soukup, N. Tribulova
- 520 9_
- $a Previous data suggest that type 1 diabetes mellitus leads to the deterioration of myocardial intercellular communication mediated by connexin-43 (Cx43) channels. We therefore aimed to explore Cx43, PKC signaling and ultrastructure in non-treated and omega-3 fatty acid (omega-3) treated spontaneously diabetic Goto-Kakizaki (GK) rats considered as type 2 diabetes model. Four-week-old GK and non-diabetic Wistar-Clea rats were fed omega-3 (200 mg/kg/day) for 2 months and compared with untreated rats. Real-time PCR and immunoblotting were performed to determine Cx43, PKC-epsilon and PKC-delta expression. In situ Cx43 was examined by immunohistochemistry and subcellular alterations by electron microscopy. Omega-3 intake reduced blood glucose, triglycerides, and cholesterol in diabetic rats and this was associated with improved integrity of cardiomyocytes and capillaries in the heart. Myocardial Cx43 mRNA and protein levels were higher in diabetic versus non-diabetic rats and were further enhanced by omega-3. The ratio of phosphorylated (functional) to non-phosphorylated Cx43 was lower in diabetic compared to non-diabetic rats but was increased by omega-3, in part due to up-regulation of PKC-epsilon. In addition, pro-apoptotic PKC-delta expression was decreased. In conclusion, spontaneously diabetic rats at an early stage of disease benefit from omega-3 intake due to its hypoglycemic effect, upregulation of myocardial Cx43, and preservation of cardiovascular ultrastructure. These findings indicates that supplementation of omega-3 may be beneficial also in the management of diabetes in humans.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a konexin 43 $x metabolismus $7 D018031
- 650 _2
- $a experimentální diabetes mellitus $x metabolismus $x patologie $x prevence a kontrola $7 D003921
- 650 _2
- $a potravní doplňky $7 D019587
- 650 _2
- $a kyseliny dokosahexaenové $x farmakologie $x terapeutické užití $7 D004281
- 650 _2
- $a fixní kombinace léků $7 D004338
- 650 _2
- $a preklinické hodnocení léčiv $7 D004353
- 650 _2
- $a kyselina eikosapentaenová $x farmakologie $x terapeutické užití $7 D015118
- 650 _2
- $a srdce $x účinky léků $7 D006321
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a myokard $x metabolismus $x ultrastruktura $7 D009206
- 650 _2
- $a proteinkinasa C-delta $x metabolismus $7 D051745
- 650 _2
- $a proteinkinasa C-epsilon $x metabolismus $7 D051744
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Kurahara, L. H. $u Department of Physiology, Fukuoka University Medical School, Fukuoka, Japan
- 700 1_
- $a Hiraishi, K. $u Department of Physiology, Fukuoka University Medical School, Fukuoka, Japan
- 700 1_
- $a Viczenczova, C $u Institute for Heart Research, Slovak Academy of Sciences, Bratislava, Slovakia
- 700 1_
- $a Egan Benová, Tamara, $d 1985- $7 xx0229479 $u Institute for Heart Research, Slovak Academy of Sciences, Bratislava, Slovakia
- 700 1_
- $a Szeiffova Bacova, B. $u Institute for Heart Research, Slovak Academy of Sciences, Bratislava, Slovakia
- 700 1_
- $a Szeiffová Bačová, B $7 xx0307206
- 700 1_
- $a Dosenko, V. $u Bogomoletz Institute of Physiology, Kyiv, Ukraine
- 700 1_
- $a Navarová, Jana $7 xx0078893 $u Institute of Experimental Pharmacology and Toxicology, Slovak Academy of Sciences, Bratislava, Slovakia
- 700 1_
- $a Obsitnik, B. $u St Elisabeth Institute of Oncology, Bratislava, Slovakia
- 700 1_
- $a Imanaga, I. $u Department of Physiology, Fukuoka University Medical School, Fukuoka, Japan
- 700 1_
- $a Soukup, Tomáš $7 xx0140789 $u Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic
- 700 1_
- $a Tribulová, Narcisa, $d 1946- $7 xx0104473 $u Institute for Heart Research, Slovak Academy of Sciences, Bratislava, Slovakia
- 773 0_
- $w MED00003824 $t Physiological research $x 1802-9973 $g Roč. 64, č. 6 (2015), s. 795-806
- 856 41
- $u http://www.biomed.cas.cz/physiolres/ $y domovská stránka časopisu
- 910 __
- $a ABA008 $b A 4120 $c 266 $y 4 $z 0
- 990 __
- $a 20161101 $b ABA008
- 991 __
- $a 20181119073011 $b ABA008
- 999 __
- $a ok $b bmc $g 1172196 $s 955767
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2015 $b 64 $c 6 $d 795-806 $e 2015Oct08 $i 1802-9973 $m Physiological research $n Physiol. Res. (Print) $x MED00003824
- LZP __
- $b NLK118 $a Pubmed-20161101