Rao M S, Subbarao V
Department of Pathology, Veterans Affairs Lakeside Medical Center, Chicago, IL, USA.
Cell Prolif. 1997 Jan;30(1):1-5. doi: 10.1046/j.1365-2184.1997.00063.x.
In a previous study we have shown that dehydroepiandrosterone (DHEA) inhibits hepatocyte DNA synthesis after short-term administration and induces hepatocellular carcinomas after long-term administration in the rat. It is not known whether DHEA is also capable of inhibiting replicative and mitogen-induced DNA synthesis. In the present study, we have evaluated the effect of DHEA on DNA synthesis in the rat liver after partial hepatectomy and mitogen administration. After partial hepatectomy, DHEA significantly inhibited DNA synthesis at 20, 26, 32 and 38 h. Similarly, combined administration of ciprofibrate, a peroxisome proliferator and mitogen, and DHEA also resulted in significant hepatocyte DNA synthesis. However, DHEA did not affect liver enlargement caused by ciprofibrate. This experimental system will serve as useful tool to evaluate the role of cell proliferation in carcinogenesis.
在之前的一项研究中,我们已经表明,脱氢表雄酮(DHEA)在大鼠短期给药后会抑制肝细胞DNA合成,而长期给药后会诱发肝细胞癌。目前尚不清楚DHEA是否也能够抑制复制性和有丝分裂原诱导的DNA合成。在本研究中,我们评估了DHEA对大鼠部分肝切除术后及给予有丝分裂原后肝脏DNA合成的影响。部分肝切除术后,DHEA在20、26、32和38小时显著抑制DNA合成。同样,过氧化物酶体增殖物及有丝分裂原环丙贝特与DHEA联合给药也导致肝细胞DNA合成显著减少。然而,DHEA并不影响环丙贝特引起的肝脏肿大。该实验系统将作为评估细胞增殖在致癌过程中作用的有用工具。