◀ Back to NPPA
NPPA — PGF
Text-mined interactions from Literome
Jiang et al., Sheng Li Xue Bao 2005
(Hypertrophy, Right Ventricular) :
In vitro experiments showed that 0.1 micromol/L
PGF ( 2alpha ) significantly increased the cardiomyocyte diameter and protein content, and
promoted ANP and CaN mRNA expressions, which was blocked by cyclosporin A, a CaN inhibitor
Jiang et al., Acta Pharmacol Sin 2007
(Cardiomegaly) :
PGF2alpha ( 100 nmol/L ) significantly increased the cardiomyocyte diameter, protein content and [Ca2+ ] i, and
promoted ANP , CaN mRNA, and CaN/NFAT3/GATA4 protein expressions, which were inhibited by either Rb1 in a concentration dependent manner ( 50, 100, and 200 microg/mL ) or L-arginine ( 1 mmol/L )
Bai et al., Peptides 2009
(Hypertension, Renal) :
PGF2alpha and PGD2
caused dose dependent increases in
ANP release and intra-atrial pressure ... The potency for the
stimulation of
ANP secretion by
PGF2alpha was higher than that by PGD2 ... The increases in intra-atrial pressure and
ANP secretion
induced by
PGF2alpha and PGD2 were significantly attenuated by the pretreatment with an inhibitor of PGF2alpha receptor ... By the pretreatment with an inhibitor for phospholipase C (PLC), inositol 3-phosphate ( IP3 ) receptor, protein kinase C ( PKC ), or myosin light chain kinase (MLCK),
PGF2alpha mediated
increase in
ANP secretion and positive inotropy were attenuated ... In hypertrophied rat atria,
PGF2alpha induced positive inotropy and
ANP secretion were markedly attenuated whereas COX-2 inhibitor stimulated ANP secretion ... These results suggest that
PGF2alpha increased the
ANP secretion and positive inotropy through PLC-IP3-PKC-MLCK pathway, and the modulation of ANP secretion by COX-2 inhibitor and PGF2alpha may partly relate to the development of renal hypertension