Elevated vascular γ‐butyrobetaine levels attenuate the development of high glucose‐induced endothelial dysfunction. (29th July 2013)
- Record Type:
- Journal Article
- Title:
- Elevated vascular γ‐butyrobetaine levels attenuate the development of high glucose‐induced endothelial dysfunction. (29th July 2013)
- Main Title:
- Elevated vascular γ‐butyrobetaine levels attenuate the development of high glucose‐induced endothelial dysfunction
- Authors:
- Vilskersts, Reinis
Zharkova‐Malkova, Olga
Mezhapuke, Rudolfs
Grinberga, Solveiga
Cirule, Helena
Dambrova, Maija - Abstract:
- <abstract abstract-type="main" id="cep12127-abs-0001"> <title>Summary</title> <p> <list id="cep12127-list-0001" list-type="order"> <list-item> <p>The aim of the present study was to investigate the effects of vascular tissue levels of <sc>l</sc>‐carnitine and its precursor, γ‐butyrobetaine (GBB), on the development of endothelial dysfunction induced by 5 μmol/L lysophosphatidylcholine (LPC), 10 mmol/L triglycerides (TG) or a high glucose concentration (44 mmol/L).</p> </list-item> <list-item> <p>Changes in vascular tissue levels of <sc>l</sc>‐carnitine and GBB were induced by administration of <sc>l</sc>‐carnitine (100 mg/kg), mildronate (100 mg/kg; an inhibitor of <sc>l</sc>‐carnitine synthesis) or their combination to male Wistar rats for 2 weeks.</p> </list-item> <list-item> <p>Treatment with <sc>l</sc>‐carnitine elevated vascular tissue levels of <sc>l</sc>‐carnitine, whereas administration of mildronate reduced <sc>l</sc>‐carnitine levels and increased GBB levels. Experimental animals that received the combination of both drugs showed elevated tissue levels of GBB.</p> </list-item> <list-item> <p>The results from organ bath experiments demonstrated that increased GBB levels with preserved <sc>l</sc>‐carnitine content in vascular tissues attenuated the development of endothelial dysfunction induced by high glucose. However, changes in vascular tissue <sc>l</sc>‐carnitine and GBB levels had no impact on endothelial dysfunction induced by TG or LPC.</p> </list-item><abstract abstract-type="main" id="cep12127-abs-0001"> <title>Summary</title> <p> <list id="cep12127-list-0001" list-type="order"> <list-item> <p>The aim of the present study was to investigate the effects of vascular tissue levels of <sc>l</sc>‐carnitine and its precursor, γ‐butyrobetaine (GBB), on the development of endothelial dysfunction induced by 5 μmol/L lysophosphatidylcholine (LPC), 10 mmol/L triglycerides (TG) or a high glucose concentration (44 mmol/L).</p> </list-item> <list-item> <p>Changes in vascular tissue levels of <sc>l</sc>‐carnitine and GBB were induced by administration of <sc>l</sc>‐carnitine (100 mg/kg), mildronate (100 mg/kg; an inhibitor of <sc>l</sc>‐carnitine synthesis) or their combination to male Wistar rats for 2 weeks.</p> </list-item> <list-item> <p>Treatment with <sc>l</sc>‐carnitine elevated vascular tissue levels of <sc>l</sc>‐carnitine, whereas administration of mildronate reduced <sc>l</sc>‐carnitine levels and increased GBB levels. Experimental animals that received the combination of both drugs showed elevated tissue levels of GBB.</p> </list-item> <list-item> <p>The results from organ bath experiments demonstrated that increased GBB levels with preserved <sc>l</sc>‐carnitine content in vascular tissues attenuated the development of endothelial dysfunction induced by high glucose. However, changes in vascular tissue <sc>l</sc>‐carnitine and GBB levels had no impact on endothelial dysfunction induced by TG or LPC.</p> </list-item> <list-item> <p>The results demonstrate that increased levels of GBB with preserved <sc>l</sc>‐carnitine content in vascular tissue attenuate the development of endothelial dysfunction induced by high glucose concentrations.</p> </list-item> </list> </p> </abstract> … (more)
- Is Part Of:
- Clinical and experimental pharmacology and physiology. Volume 40:Number 8(2013:Aug.)
- Journal:
- Clinical and experimental pharmacology and physiology
- Issue:
- Volume 40:Number 8(2013:Aug.)
- Issue Display:
- Volume 40, Issue 8 (2013)
- Year:
- 2013
- Volume:
- 40
- Issue:
- 8
- Issue Sort Value:
- 2013-0040-0008-0000
- Page Start:
- 518
- Page End:
- 524
- Publication Date:
- 2013-07-29
- Subjects:
- Clinical pharmacology -- Periodicals
Pharmacology, Experimental -- Periodicals
Physiology, Experimental -- Periodicals
Physiology, Pathological -- Periodicals
615.1 - Journal URLs:
- http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=cep ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/1440-1681.12127 ↗
- Languages:
- English
- ISSNs:
- 0305-1870
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.252000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3514.xml