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| Yazarlar | Çömelekoğlu, Ülkü Sucu, Nehir Yalın, Ali Erdinç Yılmaz, Şakir Necat Yalın, Serap Söğüt, Fatma Kibar, Kezban Akkapulu, Merih |
| Kurum Dışı Yazarlar | Vezir, Özden Yaman, Selma Koç, Meryem İlkay Seçer, Didem |
| Tek Biçim Adres (URI) | https://hdl.handle.net/20.500.14114/9542 |
| Yayın Türü | Makale |
| Yayın Yılı | 2017 |
| DOI Adresi | 10.1016/j.pharep.2017.03.019 |
| Yayıncı | Elsevier |
| Dergi Adı | Pharmacological Reports |
| Konu Başlıkları | Potasyum kanalları N-acetyl cysteine |
| İndekslenen Platformlar | Web of Science Scopus |
Background
In this study, we aimed to investigate the role of ATP-sensitive potassium (KATP) channel, Na+/K+-ATPase activity, and intracellular calcium levels on the vasodilatory effect of N-acetylcysteine (NAC) in thoracic aorta by using electrophysiological and molecular techniques.
Methods
Rat thoracic aorta ring preparations and cultured thoracic aorta cells were divided into four groups as control, 2 mM NAC, 5 mM NAC, and 10 mM NAC. Thoracic aorta rings were isolated from rats for measurements of relaxation responses and Na+/K+-ATPase activity. In the cultured thoracic aorta cells, we measured the currents of KATP channel, the concentration of intracellular calcium and mRNA expression level of KATP channel subunits (KCNJ8, KCNJ11, ABCC8 and ABCC9).
Results
The relaxation rate significantly increased in all NAC groups compared to control. Similarly, Na+/K+- ATPase activity also significantly decreased in NAC groups. Outward KATP channel current significantly increased in all NAC groups compared to the control group. Intracellular calcium concentration decreased significantly in all groups with compared control. mRNA expression level of ABCC8 subunit significantly increased in all NAC groups compared to the control group. Pearson correlation analysis showed that relaxation rate was significantly associated with KATP current, intracellular calcium concentration, Na+/K+-ATPase activity and mRNA expression level of ABCC8 subunit.
Conclusion
Our findings suggest that NAC relaxes vascular smooth muscle cells through a direct effect on KATP channels, by increasing outward K+ flux, partly by increasing mRNA expression of KATP subunit ABCC8, by decreasing in intracellular calcium and by decreasing in Na+/K+-ATPase activity.
- Fakülteler
- Tıp Fakültesi
- Temel Tıp Bilimleri Bölümü
- Biyofizik Anabilim Dalı
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Eser Adı dc.title |
N -Acetylcysteine-induced vasodilatation is modulated by K ATP channels, Na /K -ATPase activity and intracellular calcium concentration: An in vitro study |
|---|---|
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Yazarlar dc.contributor.author |
Çömelekoğlu, Ülkü |
|
Yazarlar dc.contributor.author |
Sucu, Nehir |
|
Yazarlar dc.contributor.author |
Yalın, Ali Erdinç |
|
Yazarlar dc.contributor.author |
Yılmaz, Şakir Necat |
|
Yazarlar dc.contributor.author |
Yalın, Serap |
|
Yazarlar dc.contributor.author |
Söğüt, Fatma |
|
Yazarlar dc.contributor.author |
Kibar, Kezban |
|
Yazarlar dc.contributor.author |
Akkapulu, Merih |
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Kurum Dışı Yazarlar dc.contributor.other |
Vezir, Özden |
|
Kurum Dışı Yazarlar dc.contributor.other |
Yaman, Selma |
|
Kurum Dışı Yazarlar dc.contributor.other |
Koç, Meryem İlkay |
|
Kurum Dışı Yazarlar dc.contributor.other |
Seçer, Didem |
|
Yayıncı dc.publisher |
Elsevier |
|
Yayın Türü dc.type |
Makale |
|
Özet dc.description.abstract |
Background In this study, we aimed to investigate the role of ATP-sensitive potassium (KATP) channel, Na+/K+-ATPase activity, and intracellular calcium levels on the vasodilatory effect of N-acetylcysteine (NAC) in thoracic aorta by using electrophysiological and molecular techniques. Methods Rat thoracic aorta ring preparations and cultured thoracic aorta cells were divided into four groups as control, 2 mM NAC, 5 mM NAC, and 10 mM NAC. Thoracic aorta rings were isolated from rats for measurements of relaxation responses and Na+/K+-ATPase activity. In the cultured thoracic aorta cells, we measured the currents of KATP channel, the concentration of intracellular calcium and mRNA expression level of KATP channel subunits (KCNJ8, KCNJ11, ABCC8 and ABCC9). Results The relaxation rate significantly increased in all NAC groups compared to control. Similarly, Na+/K+- ATPase activity also significantly decreased in NAC groups. Outward KATP channel current significantly increased in all NAC groups compared to the control group. Intracellular calcium concentration decreased significantly in all groups with compared control. mRNA expression level of ABCC8 subunit significantly increased in all NAC groups compared to the control group. Pearson correlation analysis showed that relaxation rate was significantly associated with KATP current, intracellular calcium concentration, Na+/K+-ATPase activity and mRNA expression level of ABCC8 subunit. Conclusion Our findings suggest that NAC relaxes vascular smooth muscle cells through a direct effect on KATP channels, by increasing outward K+ flux, partly by increasing mRNA expression of KATP subunit ABCC8, by decreasing in intracellular calcium and by decreasing in Na+/K+-ATPase activity. |
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Kayıt Giriş Tarihi dc.date.accessioned |
2017-03-29 |
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Yayın Yılı dc.date.issued |
2017 |
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Açık Erișim Tarihi dc.date.available |
2026-01-28 |
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Dil dc.language.iso |
eng |
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Konu Başlıkları dc.subject |
Potasyum kanalları |
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Konu Başlıkları dc.subject |
N-acetyl cysteine |
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Atıf İçin Künye dc.identifier.citation |
Vezir, Ö., Çömelekoğlu, Ü., Sucu, N., Yalın, A. E., Yılmaz, Ş. N., Yalın, S., Söğüt, F., Yaman, S., Kibar, K., Akkapulu, M., Koç, M. İ., & Seçer, D. (2017). N-Acetylcysteine-induced vasodilatation is modulated by KATP channels, Na+/K+-ATPase activity and intracellular calcium concentration: An in vitro study. Pharmacological reports : PR, 69(4), 738–745. https://doi.org/10.1016/j.pharep.2017.03.019 |
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Haklar dc.rights |
Elsevier Ltd |
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ISSN dc.identifier.issn |
17341140 |
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İlk Sayfa dc.identifier.startpage |
738 |
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Son Sayfa dc.identifier.endpage |
745 |
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Dergi Adı dc.relation.journal |
Pharmacological Reports |
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Dergi Sayısı dc.identifier.issue |
4 |
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Dergi Cilt dc.identifier.volume |
69 |
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Tek Biçim Adres (URI) dc.identifier.uri |
https://hdl.handle.net/20.500.14114/9542 |
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DOI Numarası dc.identifier.doi |
10.1016/j.pharep.2017.03.019 |
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İndekslenen Platformlar dc.source.database |
Web of Science |
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İndekslenen Platformlar dc.source.database |
Scopus |