Wu Dongmei, Doods Henri, Stassen Jean Marie
Department of Research, Mount Sinai Medical Center, Miami Beach, FL 33140, USA.
J Cardiovasc Pharmacol. 2006 Aug;48(2):34-40. doi: 10.1097/01.fjc.0000239691.69346.6a.
Abnormal growth of vascular smooth muscle cells is seen in various pathological conditions such as hypertension, atherosclerosis, and restenosis. Na/H exchanger (NHE) activation appears to play a permissive role in vascular smooth muscle cell proliferation and vascular remodeling. The present study investigated the effect of a new specific NHE-1 inhibitor, sabiporide, on human pulmonary artery smooth muscle cell proliferation and migration. Concentrations of sabiporide as low as 20 micromol/L in the culture medium containing growth factors inhibited cell proliferation, as measured by cell counting, and also inhibited the rate of DNA synthesis, as examined by measuring BrdU incorporation into DNA. Cell growth inhibition was not caused by cell death, as demonstrated by the measurement of intracellular lactate dehydrogenase release and by the reversibility of inhibition upon washing. By fluorescent-activated cell sorting analysis, we are the first to demonstrate that NHE-1 inhibition arrests the cell cycle progression at G0/G1 phase, suggesting that NHE activation plays a permissive role in entrance of cells into the cell cycle. Sabiporide also concentration-dependently inhibited human pulmonary artery smooth muscle cell migration. The present study showed that sabiporide inhibits vascular smooth muscle cell proliferation and migration by blocking the cell cycle progression at G0/G1 phase.
在诸如高血压、动脉粥样硬化和再狭窄等各种病理状况下,均可观察到血管平滑肌细胞的异常生长。钠/氢交换体(NHE)激活似乎在血管平滑肌细胞增殖和血管重塑过程中发挥着允许作用。本研究调查了一种新型特异性NHE-1抑制剂沙比普利德对人肺动脉平滑肌细胞增殖和迁移的影响。在含有生长因子的培养基中,低至20微摩尔/升的沙比普利德浓度即可抑制细胞增殖(通过细胞计数测定),还可抑制DNA合成速率(通过测量BrdU掺入DNA来检测)。细胞内乳酸脱氢酶释放量的测定以及洗涤后抑制作用的可逆性表明,细胞生长抑制并非由细胞死亡所致。通过荧光激活细胞分选分析,我们首次证明NHE-1抑制使细胞周期进程停滞在G0/G1期,这表明NHE激活在细胞进入细胞周期过程中发挥着允许作用。沙比普利德还浓度依赖性地抑制人肺动脉平滑肌细胞迁移。本研究表明,沙比普利德通过在G0/G1期阻断细胞周期进程来抑制血管平滑肌细胞增殖和迁移。