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作 者:王晓玲[1] 刘平[2] 李伯勤[3] 应馨萍[3]
机构地区:[1]上海中医药大学生物教研室,上海201203 [2]上海中医药大学肝病研究所,上海201203 [3]上海中医药大学教学实验中心,上海201203
出 处:《上海中医药大学学报》2006年第2期35-36,共2页Academic Journal of Shanghai University of Traditional Chinese Medicine
基 金:国家自然科学基金青年基金资助项目(30000230)
摘 要:目的:探讨丹酚酸B(SAB)对血小板生长因子(PDGF)和丙二醛(MDA)刺激的大鼠原代肝星状细胞(HSC)增殖的影响。方法:采用原位灌注法消化大鼠肝脏,108g/LNycodenz密度梯度离心,分离HSC,以MTT法观察细胞的增殖能力,免疫组化法检测血小板生长因子受体(PDGFR)含量。结果:MDA组与正常组相比可明显增加MTT吸光度(P<0.05),PDGF组亦较正常组明显增加MTT吸光度(P<0.01);1μmol/LSAB和10μmol/LSAB不仅可显著抑制MDA刺激的HSC吸光度增加(P均<0.01),也可抑制PDGF-BB刺激的HSC吸光度增加(P均<0.01)。PDGF及MDA作用后细胞PDGFR的表达均明显增加,而10μmol/LSAB则可抑制PDGFR的表达。结论:SAB可通过抑制PDGFR的表达而抑制体外培养HSC的增殖,这种抑制作用与SAB的抗氧化作用有一定的关系。Objective: To research the effects of salvianolic acid B (SAB) on proliferation of PDGF and MDA-stimulated rat primary cultured hepatic stellate cells, Methods: Hepatic stellate cells were derived from normal rats by in situ perfusion, digestion and density gradient centrifugation with 108 g/L Nycodenz. The cells were stimulated by various concentrations of PDGF or MDA, and then treated with SAB. The proliferation of cells was assayed by MTF incorporation; PDGF receptor was analyzed by immunohistology. Results: MDA and PDGF obviously promoted MTI" incorporation compared with that of the normal cells (P〈0.05,P〈0.01); 1 μmol/L (P〈0,01) and 10 μmol/L SAB (P〈0.01) both markedly inhibited MDA-stimulated HSC from MTF incorporation, and both 1 μ mol/L (P 〈 0.01 ) and 10 μ mol/L SAB (P 〈 0.01 ) markedly suppressed MTT incorporation of PDGF-stimulated HSC. Either PDGF or MDA induced the expression of PDGF receptor, which was decreased by 10 μmol/L SAB. Conclusion: SAB can inhibit the proliferation of rat primary cultured hepatic stellate cells by suppressing the expression of PDGF receptor, which is associated with the antioxidant effect of SAB.
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