Jee In Kim
Kyungpook National University School of Medicine, South Korea
Title: A pan-histone deacetylase inhibitor valproic acid prevented high fat diet-induced hypertension in mice
Biography
Biography: Jee In Kim
Abstract
Obesity is an epidemic increasing its number worldwide due to westernized high fat diet and one of the major risk factors of hypertension. Histone deacetylases (HDAC) involve in gene expression through regulating histone protein deacetylation. HDAC inhibitors are known to exert anti-cancer, anti-inflammatory effect and play protective role in cardiovascular diseases. In the present study, we applied high fat diet (HFD) mice model to mimic human obesity and observed increased body weight and higher blood pressure of HFD-fed mice compared with normal diet (ND)-fed mice. Then hypothesized that valproic acid (VPA), a FDA-approved HDAC inhibitor, might prevent HFD-induced hypertension. When HFD group reached to pre-hypertensive phase (130-140 mmHg systolic blood pressure), VPA was administered for 6 days (300mg·kg-1/day). To evaluate the effect of VPA on developing HFD-induced hypertension, the expression of renin-angiotensin system (RAS) components and HDAC1, and acetylation of histone proteins were analyzed. VPA administration attenuated the progression of hypertension and altered RAS activation. In addition, increased HDAC1 in HFD-fed mice was reduced responding to VPA administration and lowered histone acetylation level was restored by VPA. The regulatory effect of HDAC1 on angiotensinogen expression was elucidated in MDCK cells using siRNA-mediated gene silencing system. In conclusion, VPA prevented HFD-induced hypertension through downregulation of RAS activity following reduced HDAC1.