Alpha 7 Nicotinic Acetylcholine Receptor Agonist PHA 568487 Reduces Acute Inflammation but Does Not Affect Cardiac Function or Myocardial Infarct Size in the Permanent Occlusion Model

التفاصيل البيبلوغرافية
العنوان: Alpha 7 Nicotinic Acetylcholine Receptor Agonist PHA 568487 Reduces Acute Inflammation but Does Not Affect Cardiac Function or Myocardial Infarct Size in the Permanent Occlusion Model
المؤلفون: Mjörnstedt, Filip, Miljanovic, Azra, 1979, Wilhelmsson, Rebecka, Levin, Malin, 1973, Johansson, Maria E I, 1961
المصدر: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 25(8)
مصطلحات موضوعية: Cardiac and Cardiovascular Systems, Kardiologi, alpha 7 nicotinic acetylcholine receptor (alpha 7nAChR), myocardial infarction, inflammation, alpha 7nAChR agonist
الوصف: Stimulation of the alpha 7 nicotinic acetylcholine receptor (alpha 7nAChR) has shown beneficial effects in several acute inflammatory disease models. This study aims to examine whether treatment with the selective alpha 7nAChR agonist PHA 568487 can dampen inflammation and thereby improve cardiac function after myocardial infarction in mice. The possible anti-inflammatory properties of alpha 7nAChR agonist PHA 568487 were tested in vivo using the air pouch model and in a permanent occlusion model of acute myocardial infarction in mice. Hematologic parameters and cytokine levels were determined. Infarct size and cardiac function were assessed via echocardiography 24 h and one week after the infarction. Treatment with alpha 7nAChR agonist PHA 568487 decreased 12 (CCL27, CXCL5, IL6, CXCL10, CXCL11, CXCL1, CCL2, MIP1a, MIP2, CXCL16, CXCL12 and CCL25) out of 33 cytokines in the air pouch model of acute inflammation. However, alpha 7nAChR agonist PHA 568487 did not alter infarct size, ejection fraction, cardiac output or stroke volume at 24 h or at 7 days after the myocardial infarction compared with control mice. In conclusion, despite promising immunomodulatory effects in the acute inflammatory air pouch model, alpha 7nAChR agonist PHA 568487 did not affect infarct size or cardiac function after a permanent occlusion model of acute myocardial infarction in mice. Consequently, this study does not strengthen the hypothesis that stimulation of the alpha 7nAChR is a future treatment strategy for acute myocardial infarction when reperfusion is lacking. However, whether other agonists of the alpha 7nAChR can have different effects remains to be investigated.
URL الوصول: https://gup.ub.gu.se/publication/339082
قاعدة البيانات: SwePub
الوصف
تدمد:16616596
14220067
DOI:10.3390/ijms25084414