Insulin and GSK3β-inhibition abrogates the infarct sparing-effect of ischemic postconditioning in ex vivo rat hearts. (4th May 2017)
- Record Type:
- Journal Article
- Title:
- Insulin and GSK3β-inhibition abrogates the infarct sparing-effect of ischemic postconditioning in ex vivo rat hearts. (4th May 2017)
- Main Title:
- Insulin and GSK3β-inhibition abrogates the infarct sparing-effect of ischemic postconditioning in ex vivo rat hearts
- Authors:
- Helgeland, Erik
Wergeland, Anita
Sandøy, Rune M.
Askeland, Maren
Aspevik, Anne
Breivik, Lars
Jonassen, Anne K. - Abstract:
- Abstract: Objectives. Pharmacological treatment of reperfusion injury using insulin and GSK3β inhibition has been shown to be cardioprotective, however, their interaction with the endogenous cardioprotective strategy, ischemic postconditioning, is not known. Design. Langendorff perfused ex vivo rat hearts were subjected to 30 min of regional ischemia and 120 min of reperfusion. For the first 15 min of reperfusion hearts received either vehicle (Ctr), insulin (Ins) or a GSK3β inhibitor (SB415286; SB41), with or without interruption of ischemic postconditioning (IPost; 3 × 30 s of global ischemia). In addition, the combination of insulin and SB41 for 15 min was assessed. Results. Insulin, SB41 or IPost significantly reduced infarct size versus vehicle treated controls (IPost 33.5 ± 3.3%, Ins 33.5 ± 3.4%, SB41 30.5 ± 3.0% vs. Ctr 54.7 ± 6.8%, p < 0.01). Combining insulin and SB415286 did not confer additional cardioprotection compared to the treatments given alone (SB41 + Ins 26.7 ± 3.5%, ns). Conversely, combining either of the pharmacological reperfusion treatments with IPost completely abrogated the cardioprotection afforded by the treatments separately (Ins + IPost 59.5 ± 3.4% vs. Ins 33.5 ± 3.4% and SB41 + IPost 50.2 ± 6.6% vs. SB41 30.5 ± 3.0%, both p < 0.01), and was associated with blunted Akt, GSK3β and STAT3 phosphorylation. Conclusion. Pharmacological reperfusion treatment with insulin and SB41 interferes with the cardioprotection afforded by ischemicAbstract: Objectives. Pharmacological treatment of reperfusion injury using insulin and GSK3β inhibition has been shown to be cardioprotective, however, their interaction with the endogenous cardioprotective strategy, ischemic postconditioning, is not known. Design. Langendorff perfused ex vivo rat hearts were subjected to 30 min of regional ischemia and 120 min of reperfusion. For the first 15 min of reperfusion hearts received either vehicle (Ctr), insulin (Ins) or a GSK3β inhibitor (SB415286; SB41), with or without interruption of ischemic postconditioning (IPost; 3 × 30 s of global ischemia). In addition, the combination of insulin and SB41 for 15 min was assessed. Results. Insulin, SB41 or IPost significantly reduced infarct size versus vehicle treated controls (IPost 33.5 ± 3.3%, Ins 33.5 ± 3.4%, SB41 30.5 ± 3.0% vs. Ctr 54.7 ± 6.8%, p < 0.01). Combining insulin and SB415286 did not confer additional cardioprotection compared to the treatments given alone (SB41 + Ins 26.7 ± 3.5%, ns). Conversely, combining either of the pharmacological reperfusion treatments with IPost completely abrogated the cardioprotection afforded by the treatments separately (Ins + IPost 59.5 ± 3.4% vs. Ins 33.5 ± 3.4% and SB41 + IPost 50.2 ± 6.6% vs. SB41 30.5 ± 3.0%, both p < 0.01), and was associated with blunted Akt, GSK3β and STAT3 phosphorylation. Conclusion. Pharmacological reperfusion treatment with insulin and SB41 interferes with the cardioprotection afforded by ischemic postconditioning. … (more)
- Is Part Of:
- Scandinavian cardiovascular journal. Volume 51:Number 3(2017:Jun.)
- Journal:
- Scandinavian cardiovascular journal
- Issue:
- Volume 51:Number 3(2017:Jun.)
- Issue Display:
- Volume 51, Issue 3 (2017)
- Year:
- 2017
- Volume:
- 51
- Issue:
- 3
- Issue Sort Value:
- 2017-0051-0003-0000
- Page Start:
- 159
- Page End:
- 166
- Publication Date:
- 2017-05-04
- Subjects:
- Heart -- insulin -- ischemia reperfusion injury -- ischemic postconditioning -- reperfusion -- Akt -- GSK3β -- STAT3 -- GSK3β inhibition
Cardiovascular system -- Diseases -- Periodicals
617.41 - Journal URLs:
- http://informahealthcare.com/loi/cdv ↗
http://informahealthcare.com ↗ - DOI:
- 10.1080/14017431.2017.1288920 ↗
- Languages:
- English
- ISSNs:
- 1401-7431
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8087.472600
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 97.xml