Eto Y, Nitta K, Uchida K, Tsutsui T, Natori K, Kawashima A, Yumura W, Nihei H
Department of Medicine, Tokyo Women's Medical College, Japan.
Life Sci. 1997;60(11):PL193-9. doi: 10.1016/s0024-3205(97)00018-0.
We investigated the effects of the new 5-HT2A receptor antagonist, sarpogrelate, on DNA synthesis in renal mesangial cells stimulated with 5-HT in the presence and absence of platelet-derived growth factor (PDGF)-BB. Both 5-HT and PDGF-BB demonstrated a mitogenic effect on these cells. When mesangial cells were incubated in the absence of PDGF-BB, sarpogrelate inhibited DNA synthesis in these cells in a dose-dependent manner. In the presence of PDGF-BB, sarpogrelate had a weaker anti-mitogenic effect in mesangial cells stimulated with 5-HT. Sarpogrelate was cytotoxic at concentrations over 10(-5) M according to the results of LDH release assays, and it reduced the S1 phase in mesangial cells stimulated with 5-HT by a flow cytometry. These findings suggest that sarpogrelate may be effective in the treatment of some glomerulonephritis associated with mesangial cell proliferation.
我们研究了新型5-羟色胺2A(5-HT2A)受体拮抗剂沙格雷酯在有无血小板衍生生长因子(PDGF)-BB的情况下,对5-羟色胺刺激的肾系膜细胞中DNA合成的影响。5-羟色胺和PDGF-BB均对这些细胞表现出促有丝分裂作用。当系膜细胞在无PDGF-BB的情况下孵育时,沙格雷酯以剂量依赖的方式抑制这些细胞中的DNA合成。在有PDGF-BB存在的情况下,沙格雷酯在5-羟色胺刺激的系膜细胞中具有较弱的抗有丝分裂作用。根据乳酸脱氢酶(LDH)释放试验结果,沙格雷酯在浓度超过10^(-5) M时具有细胞毒性,并且通过流式细胞术减少了5-羟色胺刺激的系膜细胞中的S1期。这些发现表明,沙格雷酯可能对治疗某些与系膜细胞增殖相关的肾小球肾炎有效。