Key result
GW0742 pretreatment ameliorated Angiotensin II-induced cardiomyocyte hypertrophy and inhibited the expression of inflammatory cytokines MMP9, MMP2, and IL-1beta in vitro.
Why the study?
Does GW0742 prevent Angiotensin II-induced cardiac hypertrophy in neonatal rat cardiomyocytes?
Does GW0742 prevent Angiotensin II-induced cardiac hypertrophy in neonatal rat cardiomyocytes?
GW0742, a PPARbeta/delta agonist, exerts a beneficial effect on Angiotensin II-induced cardiac hypertrophy and related inflammatory responses in vitro.
Answers are grounded in this paper and cite their sources.
Supports PPARβ/δ agonism in rat cardiomyocyte hypertrophy; hypothesis-generating, requires in vivo and human validation before any clinical consideration.
Agonists of the peroxisome proliferator-activated receptor alpha (PPARalpha) and gamma (gamma) exert anti-proliferative and anti-inflammatory effects that led to the testing of these drugs in experimental cardiac hypertrophy. However, the effect of PPAR beta/delta (beta/delta) agonists in hypertrophy is not yet known. In this paper, an experiment was conducted to explore whether PPARbeta/delta activation has an effect on cardiac hypertrophy. An in vitro cardiomyocyte hypertrophy from neonatal rats was induced with Angiotensin II (Ang II1micromol x L(-1)) stimulation. For the examination of PPAR beta/delta effect, the cultured rat cardiac myocytes were pretreated with GW0742 (10 micromol.L(-1)), an agonist of PPARbeta/delta, for 48h before Ang II stimulation. The following parameters in the cultured cells were determined: surface areas of myocytes were measured by the NIH Image Software; (3)H-leucine incorporation into myocytes was counted by liquid scintillometer; mRNA expression of PPARbeta/delta, ANP, BNP, MMP9, MMP2, and IL-1beta was detected by RT-PCR; PPARbeta/delta protein expression was evaluated with immunofluorescence staining; GW0742 could ameliorate Ang II-induced cardiomyocyte hypertrophy, as indicated by its inhibitory effects on the surface area of myocytes, and ANP and BNP mRNA expressions in myocytes and (3)H-leucine incorporation into myocytes. Meanwhile, GW0742 pretreatment exerted inhibition on mRNA expression augmentation of such cytokines as MMP9, MMP2, and IL-1beta in hypertrophic myocytes. In addition, the down-regulated expression of PPARbeta/delta mRNA and protein in hypertrophic myocytes was also significantly reversed by GW0742. We demonstrate for the first time that GW0742 exerts a beneficial effect on Ang II-induced cardiac hypertrophy and the relation to inflammation response.
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Sheng et al. (2008) studied Angiotensin II-induced cardiac hypertrophy. GW0742 vs. Angiotensin II stimulation alone was evaluated on Cardiomyocyte hypertrophy (surface area, ANP/BNP mRNA, 3H-leucine incorporation). GW0742 pretreatment ameliorated Angiotensin II-induced cardiomyocyte hypertrophy and inhibited the expression of inflammatory cytokines MMP9, MMP2, and IL-1beta in vitro.
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