Dexamethasone inhibits regeneration and causes ventricular aneurysm in the neonatal porcine heart after myocardial infarction. (July 2020)
- Record Type:
- Journal Article
- Title:
- Dexamethasone inhibits regeneration and causes ventricular aneurysm in the neonatal porcine heart after myocardial infarction. (July 2020)
- Main Title:
- Dexamethasone inhibits regeneration and causes ventricular aneurysm in the neonatal porcine heart after myocardial infarction
- Authors:
- Tao, Zhonghao
Loo, Szejie
Su, Liping
Abdurrachim, Desiree
Lalic, Janise
Lee, Teck Hock
Chen, Xin
Tan, Ru-San
Zhang, Jianyi
Ye, Lei - Abstract:
- Abstract: Aims: Recently, we demonstrated that the hearts of neonatal pigs (2-day old) have regenerative capacity, likely driven by cardiac myocyte division, but this potential is lost immediately after postnatal day 3. However, it is unknown if corticosteroid, a broad anti-inflammatory agent, will abrogate the regenerative capacity in the hearts of neonatal pigs. The aim of the current study is to evaluate the effect Dexamethasone (Dex), a broad anti-inflammatory agent, on heart regeneration, structure, and function of the neonatal pigs' post-myocardial infarction (MI). Methods and results: Dex (0.2 mg/kg/day) was injected intramuscularly into the neonatal pig (age: 2 days postnatal) during the first week post-MI. Myocardial scar and left ventricular function were determined by cardiac magnetic resonance (CMR) imaging. Bromodeoxyuridine (BrdU) pulse-chase labeling, histology, immunohistochemistry, and flow cytometry were performed to determine inflammatory cell infiltration, CM cytokinesis, and myocardial fibrosis. Dex injection during the first-week suppressed acute inflammation post-MI in the pig hearts. It inhibited BrdU incorporation to pig CMs and CM cytokinesis via inhibiting aurora-B protein expression which was associated with mature scar formation and thinned walls at the infarct site. CMR imaging showed Dex caused left ventricular aneurysm and poor ejection fraction. Conclusions: Dex inhibited CM cytokinesis and functional recovery and caused ventricular aneurysmAbstract: Aims: Recently, we demonstrated that the hearts of neonatal pigs (2-day old) have regenerative capacity, likely driven by cardiac myocyte division, but this potential is lost immediately after postnatal day 3. However, it is unknown if corticosteroid, a broad anti-inflammatory agent, will abrogate the regenerative capacity in the hearts of neonatal pigs. The aim of the current study is to evaluate the effect Dexamethasone (Dex), a broad anti-inflammatory agent, on heart regeneration, structure, and function of the neonatal pigs' post-myocardial infarction (MI). Methods and results: Dex (0.2 mg/kg/day) was injected intramuscularly into the neonatal pig (age: 2 days postnatal) during the first week post-MI. Myocardial scar and left ventricular function were determined by cardiac magnetic resonance (CMR) imaging. Bromodeoxyuridine (BrdU) pulse-chase labeling, histology, immunohistochemistry, and flow cytometry were performed to determine inflammatory cell infiltration, CM cytokinesis, and myocardial fibrosis. Dex injection during the first-week suppressed acute inflammation post-MI in the pig hearts. It inhibited BrdU incorporation to pig CMs and CM cytokinesis via inhibiting aurora-B protein expression which was associated with mature scar formation and thinned walls at the infarct site. CMR imaging showed Dex caused left ventricular aneurysm and poor ejection fraction. Conclusions: Dex inhibited CM cytokinesis and functional recovery and caused ventricular aneurysm in the hearts of 2-day old pigs post-MI. Graphical abstract: Unlabelled Image Highlights: Dexamethasone inhibits heart regeneration in the hearts of 2-day old pigs after acute myocardial infarction (AMI). Dexamethasone causes ventricular aneurysm in the hearts of 2-day old pigs after AMI. Dexamethasone inhibits cardiac macrophage expansion in the hearts of 2-day old pigs after AMI. Dexamethasone inhibits myocyte cytokinesis in the hearts of 2-day old pigs after AMI. … (more)
- Is Part Of:
- Journal of molecular and cellular cardiology. Volume 144(2020)
- Journal:
- Journal of molecular and cellular cardiology
- Issue:
- Volume 144(2020)
- Issue Display:
- Volume 144, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 144
- Issue:
- 2020
- Issue Sort Value:
- 2020-0144-2020-0000
- Page Start:
- 15
- Page End:
- 23
- Publication Date:
- 2020-07
- Subjects:
- Heart -- Regeneration -- Inflammation -- Corticosteroid
α-SA α-sarcomere actin -- BrdU Bromodeoxyuridine -- CMR Cardiac magnetic resonance -- CM Cardiomyocyte -- DBZ distal border zone -- Dex Dexamethasone -- EF ejection fraction -- GAPDH Glyceraldehyde phosphate dehydrogenase -- LGE late gadolinium enhancement -- LV Left ventricular -- MI Myocardial infarction -- PBZ proximal border zone -- SD Standard deviation
Cardiology -- Periodicals
Heart Diseases -- Periodicals
Molecular Biology -- Periodicals
Cardiologie -- Périodiques
Cardiology
Electronic journals
Periodicals
616.12 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00222828 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/00222828 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/00222828 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.yjmcc.2020.04.033 ↗
- Languages:
- English
- ISSNs:
- 0022-2828
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5020.690000
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- 13921.xml