Abstract | BACKGROUND: PURPOSE: The present study was designed to investigate the effect of SP on MI-induced cardiac injury and elucidate its underlying molecular mechanisms. METHODS: To create an in vivo model of MI, we ligated the left coronary artery of Wistar rats. For our in vitro model of MI, we treated primary neonatal rat ventricular myocytes with hypoxia. Myocardial infarct size was measured by triphenyltetrazolium chloride (TTC) staining. Intracellular calcium concentration (Ca2+) was measured by confocal microscopy, and cardiomyocyte apoptosis was assessed by TUNEL assay. Western blot was applied to determine protein levels. RESULTS: Three days post-MI, SP significantly improved MI-induced impairment of cardiac function, as indicated by increased left ventricular systolic pressure (LVSP), maximum rate of left ventricular pressure rise and fall (± dp/dt max), and decreased left ventricular end-diastolic pressure (LVEDP). In addition, SP treatment markedly reduced the infarct size and serum lactate dehydrogenase (LDH) activity; inhibited cardiomyocyte apoptosis and Caspase-3 activation both in vivo and in vitro; and decreased intracellular calcium overload, Cav1.2, phosphorylated JNK (p-JNK), and p38 MAPK (p-p38 MAPK) levels in ischemic myocardium. CONCLUSION: SP alleviated cardiac ischemic injury and inhibited cardiomyocyte apoptosis by attenuating intracellular calcium overload, suppressing Caspase-3 activation, and downregulating protein expression of p-JNK and p-p38MAPK. These results suggest that SP may serve as a potential novel therapeutic drug for MI.
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Authors | Guanlin Yang, Dongyu Min, Junwei Yan, Ming Yang, Guijun Lin |
Journal | Phytomedicine : international journal of phytotherapy and phytopharmacology
(Phytomedicine)
Vol. 42
Pg. 18-24
(Mar 15 2018)
ISSN: 1618-095X [Electronic] Germany |
PMID | 29655684
(Publication Type: Journal Article)
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Copyright | Copyright © 2018. Published by Elsevier GmbH. |
Chemical References |
- Cardiotonic Agents
- Drugs, Chinese Herbal
- p38 Mitogen-Activated Protein Kinases
- Casp3 protein, rat
- Caspase 3
- Calcium
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Topics |
- Animals
- Apoptosis
(drug effects)
- Calcium
(metabolism)
- Cardiotonic Agents
(pharmacology)
- Caspase 3
(metabolism)
- Drugs, Chinese Herbal
(pharmacology)
- Male
- Myocardial Infarction
(metabolism, pathology, prevention & control)
- Myocytes, Cardiac
(drug effects)
- Phosphorylation
(drug effects)
- Rats, Sprague-Dawley
- Rats, Wistar
- Trichosanthes
(chemistry)
- p38 Mitogen-Activated Protein Kinases
(metabolism)
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