Shiverick K T, Salafia C
Department of Pharmacology and Therapeutics, College of Medicine, University of Florida, Gainesville 32610-0267, USA.
Placenta. 1999 May;20(4):265-72. doi: 10.1053/plac.1998.0377.
This review examines the major observations and principal controversies relating to the effects of smoking and the constituents of tobacco on ovarian, uterine and placental tissues. Maternal exposure is assessed relative to specific tobacco-related chemicals and the feto-placental impact of mutagenic products, in addition to nicotine replacement as a pharmacological intervention for smoking cessation. Important new information is being learned from clinical in vitro fertilization and assisted reproduction technologies regarding the effects of smoking on fertility. Present evidence supports an adverse effect of smoking on ovarian function which is prolonged and dose-dependent, whereas there appear to be more reversible effects on implantation and ongoing pregnancy. The anti-oestrogenic effect of smoking is reviewed in terms of direct effects of nicotine, cadmium and polyaromatic hydrocarbons on oestrogen synthesis and metabolism, oocytes and granulosa-luteal function. Innovative new models provide evidence that smoking may alter fertility through effects on uterine-fallopian tube functions which mediate gamete and conceptus transport. It is of interest that smoking is associated with a decreased incidence of uterine fibroids, endometriosis and uterine cancer, which may reflect inhibitory effects of smoke constituents on uterine cell proliferation and extracellular matrix interactions. The increased miscarriage rate among mothers who smoke may be related to direct adverse effects of nicotine, cadmium and polyaromatic hydrocarbons on trophoblast invasion and proliferation. In this respect, alterations in trophoblast differentiation along invasive or proliferative pathways may explain the changes in endocrine function and vascular morphology that are observed in smokers. In summary, significant advances are being made in the understanding of cellular and molecular mechanisms which underlie the differential effects of cigarette smoking on reproductive tissues.
本综述探讨了与吸烟及烟草成分对卵巢、子宫和胎盘组织的影响相关的主要观察结果和主要争议。除了将尼古丁替代作为戒烟的药物干预措施外,还评估了母体暴露于特定烟草相关化学物质的情况以及诱变产物对胎儿-胎盘的影响。从临床体外受精和辅助生殖技术中正在了解到关于吸烟对生育能力影响的重要新信息。目前的证据支持吸烟对卵巢功能有不良影响,这种影响是长期且剂量依赖性的,而对着床和持续妊娠的影响似乎更具可逆性。从尼古丁、镉和多环芳烃对雌激素合成与代谢、卵母细胞和颗粒黄体功能的直接影响方面综述了吸烟的抗雌激素作用。创新的新模型提供了证据,表明吸烟可能通过影响子宫-输卵管功能来改变生育能力,而子宫-输卵管功能介导配子和孕体的运输。有趣的是,吸烟与子宫肌瘤、子宫内膜异位症和子宫癌的发病率降低有关,这可能反映了烟雾成分对子宫细胞增殖和细胞外基质相互作用的抑制作用。吸烟母亲流产率增加可能与尼古丁、镉和多环芳烃对滋养层细胞侵袭和增殖的直接不良影响有关。在这方面,滋养层细胞沿侵袭或增殖途径的分化改变可能解释了吸烟者中观察到的内分泌功能和血管形态变化。总之,在理解吸烟对生殖组织的不同影响所基于的细胞和分子机制方面正在取得重大进展。