Anti-ischemic effects of multivalent dendrimeric A3 adenosine receptor agonists in cultured cardiomyocytes and in the isolated rat heart

被引：17

作者：

Chanyshev, Bella ^{[2
]}

Shainberg, Asher ^{[2
]}

Isak, Ahuva ^{[2
]}

Litinsky, Alexandra ^{[2
]}

Chepurko, Yelena ^{[3
]}

Tosh, Dilip K. ^{[1
]}

Khai Phan ^{[1
]}

Gao, Zhan-Guo ^{[1
]}

Hochhauser, Edith ^{[3
]}

Jacobson, Kenneth A. ^{[1
]}

机构：

[1] NIDDK, Mol Recognit Sect, LBC, NIH, Bethesda, MD 20892 USA

[2] Bar Ilan Univ, Mina & Everard Goodman Fac Life Sci, Ramat Gan, Israel

[3] Tel Aviv Univ, Dept Cardiothorac Surg, Rabin Med Ctr, Felsenstein Med Res Ctr,Cardiac Res Lab, Petah Tiqwa, Israel

来源：

PHARMACOLOGICAL RESEARCH | 2012年 / 65卷 / 03期

关键词：

Dendrimer; Cardiomyocyte; Adenosine receptor; Ischemia; Isolated heart; Rat; ISCHEMIA/REPERFUSION INJURY; CLICK CHEMISTRY; INFARCT SIZE; PROTECTS; A(1); ACTIVATION; RESPONSES; TARGET; A(2A);

D O I：

10.1016/j.phrs.2011.11.013

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

Adenosine released during myocardial ischemia mediates cardioprotective preconditioning. Multivalent drugs covalently bound to nanocarriers may differ greatly in chemical and biological properties from the corresponding monomeric agents. Here, we conjugated chemically functionalized nucleosides to poly(amidoamine) (PAMAM) dendrimeric polymers and investigated their effects in rat primary cardiac cell cultures and in the isolated heart. Three conjugates of A(3) adenosine receptor (AR) agonists, chain-functionalized at the C2 or N-6 position, were cardioprotective, with greater potency than monomeric agonist Cl-IB-MECA. Multivalent amide-linked MRS5216 was selective for A(1) and A(3)ARs, and triazole-linked MR55246 and MRS5539 (optionally containing fluorescent label) were A(3)AR-selective. The conjugates protected ischemic rat cardiomyocytes, an effect blocked by an A(3)AR antagonist MRS1523, and isolated hearts with significantly improved infarct size, rate of pressure product, and rate of contraction and relaxation. Thus, strategically derivatized nucleosides tethered to biocompatible polymeric carriers display enhanced cardioprotective potency via activation of A(3)AR on the cardiomyocyte surface. Published by Elsevier Ltd.

引用

页码：338 / 346

页数：9

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