Kim, Dongkyu Hong, Jueun Moon, Hyung-Ho Nam, Hye Yeong Mok, Hyejung Jeong, Ji Hoon Kim, Sung Wan Choi, Donghoon Kim, Sun Hwa 2024-01-20T12:03:59Z 2024-01-20T12:03:59Z 2021-09-04 2013-06-10 0168-3659 https://pubs.kist.re.kr/handle/201004/127970 The cardiomyocyte apoptosis plays a critical role in the development of myocardial injury after ischemia and reperfusion. Thus, alteration of the major apoptosis-regulatory factors during myocardial ischemia-reperfusion is expected to have favorable cardioprotective effects. Herein, we report ischemic-reperfused myocardial infarction (MI) repair with siRNA against Src homology region 2 domain-containing tyrosine phosphatase-1 (SHP-1), which is known as a key factor involved in regulating the progress of apoptosis in many cell types. A low molecular weight polyethyleneimine modified with deoxycholic acid (PEI1.8-DA)-based delivery strategy was suggested for the cardiac application of SHP-1 siRNA to overcome the poor gene delivery efficiency to myocardium due to the highly charged structures of the compact cardiac muscles. The PEI1.8-DA conjugates formed stable nanocomplexes with SHP-1 siRNA via electrostatic and hydrophobic interactions. The PEI1.8-DA/SHP-1 siRNA polyplexes effectively silenced SHP-1 gene expression in cardiomyocytes, leading to a significant inhibition of cardiomyocyte apoptosis under hypoxia. In comparison to conventional gene carriers, relatively large amounts of siRNA molecules remained after treatment with the PEI1.8-DA/SHP-1 siRNA polyplexes. Cardiac administration of the PEI1.8-DA/SHP-1 siRNA polyplexes resulted in substantial improvement in SHP-1 gene silencing, which can be explained by the enhancement of cardiac delivery efficiency of the PEI1.8-DA conjugates. In addition, in vivo treatment with the PEI1.8-DA/SHP-1 siRNA polyplexes induced a highly significant reduction in myocardial apoptosis and infarct size in rat MI models. These results demonstrate that the PEI1.8-DA/SHP-1 siRNA polyplex formulation is a useful system for efficient gene delivery into the compact myocardium that provides a fundamental advantage in treating ischemic-reperfused MI. (C) 2013 Elsevier B.V. All rights reserved. English ELSEVIER ATTENUATES MYOCARDIAL-INFARCTION SYSTEMIC DELIVERY BCL-2 PROTEIN CELL-DEATH EFFICIENT EXPRESSION MUSCLE SIZE RNA DNA Anti-apoptotic cardioprotective effects of SHP-1 gene silencing against ischemia-reperfusion injury: Use of deoxycholic acid-modified low molecular weight polyethyleneimine as a cardiac siRNA-carrier Article 10.1016/j.jconrel.2013.02.031 1 JOURNAL OF CONTROLLED RELEASE, v.168, no.2, pp.125 - 134 JOURNAL OF CONTROLLED RELEASE 168 2 125 134 scie scopus 000319499200003 2-s2.0-84876177910 Chemistry, Multidisciplinary Pharmacology & Pharmacy Chemistry Pharmacology & Pharmacy Article ATTENUATES MYOCARDIAL-INFARCTION SYSTEMIC DELIVERY BCL-2 PROTEIN CELL-DEATH EFFICIENT EXPRESSION MUSCLE SIZE RNA DNA SHP-1 siRNA Myocardial apoptosis Deoxycholic acid Low molecular weight PEI Myocardial ischemia-reperfusion injury