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. 2013 Nov;28(6):391–403. doi: 10.1152/physiol.00029.2013

Table 3.

Effects of intracardiac-injected substances on myocardial structure and function after injury

Substance Injected Effects
ECM-derived Hep I Promotes cell attachment, migration, and proliferation; induces Erk1/2 activation; promotes angiogenesis and arteriogenesis
ECM-derived Hep III Promotes cell attachment, migration, and proliferation; induces Erk1/2 activation; promotes angiogenesis and arteriogenesis; prevents worsening of LV function; interacts with other Hep III peptides and ECM proteins; forms polymer-like matrix
ECM-derived RDG Promotes cell attachment, migration, and proliferation; induces Erk1/2 activation; promotes angiogenesis and arteriogenesis
ECM-derived FC/HV Adherent cells noticeable within 24 h; induces Erk1/2 activation
Injection of decellularized matrix Thickens the LV infarcted wall; prevents LV systolic dysfunction; improves EF
Fibrin Preserves infarcted wall thickness and cardiac function
Tannic acid Prevents collagen degradation via cross-linking; inhibits MMP-9 activity

Effects of intracardiac-injected substances on myocardial structure and function after injury (14, 60).