Abstract

The present study was designed to explore the effects of PGE2 on cardiac fibrosis and the involved mechanism. We used western blot analysis, real-time quantitative PCR and immunostaining etc. to testify the mechanism. Our data showed that in cultured adult rat cardiac fibroblasts (CFs), PGE2 effectively promoted the expression of α-smooth muscle actin (α-SMA), connective tissue growth factor (CTGF),fibronectin (FN), Collagen I and induced [Ca2+]i increase. Besides, calcium increase evoked by PGE2 is mediated by virtue of EP1 activation. Instead of EP3 or EP4, inhibition of EP1 attenuated PGE2-stimulated upregulation of α-SMA,CTGF, FN, collagen I and [Ca2+]i, as well as the nuclear factor of activated T cell cytoplasmic 4 protein (NFATc4) translocation. PGE2 may promote cardiac fibrosis via EP1receptor and calcium signal pathway.

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