The Impact of Biotechnology on Reproductive Medicine

D. Meldrum
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This remarkable study was published decades before stem cells (now induced pluripotent cells from the recipient to avoid rejection) became a clinical tool for repopulating the bone marrows of cancer patients following lethal doses of chemotherapy and or radiation. In 1992, Lou Ignarro, who later shared a Nobel Prize for the discovery of nitric oxide (NO), showed using human penile tissue that the effect of neural NO release was enhanced by an inhibitor of cyclic GMP degradation (2), leading to the development of highly effective treatments for erectile dysfunction (ED) (3). Further elucidation of the factors influencing NO production and degradation has led to important insights into lifestyle and nutritional factors influencing erectile health (4, 5). In the mid-1990’s, as the result of work carried out by the research group under Antonio Pellicer in Valencia, Spain and others, the etiology of increased vascular permeability and consequent extreme fluid shifts characteristic of ovarian hyperstimulation syndrome (OHSS) were shown to be due to increased expression of vascular endothelial growth factor (VEGF) and VEGF receptor2 (VEGFR2) (6). The incidence of OHSS was reduced by 50% by identifying and clinically utilizing the role of dopamine agonists to inhibit phosphorylation of VEGFR-2. That discovery, together with understanding and thereby avoidance of clinical factors stimulating VEGF, has now made morbid and potentially fatal OHSS a rare occurrence. Again in the 1990’s David Gardner, along with others, defined the reproductive tract nutrients available during in vivo embryo development and the specific stagespecific requirements of embryos developing to the blastocyst stage. 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Abstract

Reproductive Medicine has been at the forefront of the biotechnology revolution. Over the last three decades, a very significant proportion of abstracts at our major meetings and papers in our journals have employed molecular techniques to elucidate basic gene expression and cellular metabolic pathways in the study of reproductive processes. The resulting insights have yielded new understanding of the basic mechanisms of reproductive diseases and innovative therapeutic modalities. Specific examples will be used to illustrate this remarkable progress. In 1988, Hollands reported the rescue of lethally irradiated rats by infusion of haemopoietic stem cells from mouse blastocysts grown in vitro (1). This remarkable study was published decades before stem cells (now induced pluripotent cells from the recipient to avoid rejection) became a clinical tool for repopulating the bone marrows of cancer patients following lethal doses of chemotherapy and or radiation. In 1992, Lou Ignarro, who later shared a Nobel Prize for the discovery of nitric oxide (NO), showed using human penile tissue that the effect of neural NO release was enhanced by an inhibitor of cyclic GMP degradation (2), leading to the development of highly effective treatments for erectile dysfunction (ED) (3). Further elucidation of the factors influencing NO production and degradation has led to important insights into lifestyle and nutritional factors influencing erectile health (4, 5). In the mid-1990’s, as the result of work carried out by the research group under Antonio Pellicer in Valencia, Spain and others, the etiology of increased vascular permeability and consequent extreme fluid shifts characteristic of ovarian hyperstimulation syndrome (OHSS) were shown to be due to increased expression of vascular endothelial growth factor (VEGF) and VEGF receptor2 (VEGFR2) (6). The incidence of OHSS was reduced by 50% by identifying and clinically utilizing the role of dopamine agonists to inhibit phosphorylation of VEGFR-2. That discovery, together with understanding and thereby avoidance of clinical factors stimulating VEGF, has now made morbid and potentially fatal OHSS a rare occurrence. Again in the 1990’s David Gardner, along with others, defined the reproductive tract nutrients available during in vivo embryo development and the specific stagespecific requirements of embryos developing to the blastocyst stage. Those insights and clinical experience enabled the design of media specifically for embryos over the first 72 hours and the following 24 to 84 hours of culture (7), improving IVF efficiency and making accurate chromosome analysis a reality. Study of blastocyst metabolism that predicts a successful pregnancy has been progressing rapidly (8). In the late 1990’s techniques became available to assess DNA fragmentation of sperm, first by flow cytometry and later by techniques such as TUNEL and COMET. DNA fragmentation increases with age (9) and may contribute to the low success rates in women over age 40, although the effect of male age was observed to be less with younger female age (10). The effect on IVF outcome also appears to be less for women responding normally to ovarian stimulation compared to low responders (11). These observations have suggested that cytoplasm of the better quality oocyte may be able to correct DNA fragmentation. The observation that DNA fragmentation is correlated with semen oxidative stress (12) has validated successful treatment with antioxidants (13). Because DNA fragmentation increases during transit through the male collecting system, testicular extraction of sperm has been used successfully if frequent ejaculation and antioxidants are not sufficient (14). Decreased coital frequency with age, in part due to decreased erectile function, contributes to infertility in older couples (15). In the late 1990’s the importance of omega-3 fatty acids in the function of sperm membranes was being elucidated and correlated with indices of sperm quality and male infertility (16). Safarinejad reported a randomized trial showing highly significant benefits of omega-3 supplementation on sperm density, motility, and strict morphology (16). Semen concentrations of omega-3’s correlated with those improvements and also with semen endogenous antioxidants. Supplementation with omega-
生物技术对生殖医学的影响
生殖医学一直处于生物技术革命的前沿。在过去的三十年里,在我们的主要会议和期刊上的论文摘要中,有很大一部分使用分子技术来阐明生殖过程研究中的基本基因表达和细胞代谢途径。由此产生的见解使人们对生殖疾病的基本机制和创新的治疗方式有了新的认识。具体的例子将用来说明这一显著的进步。1988年,Hollands报道了通过输注从体外培养的小鼠囊胚中提取的造血干细胞来拯救受致命辐射的大鼠(1)。这项引人注目的研究发表于几十年前,干细胞(现在来自受体的诱导多能细胞以避免排斥反应)成为一种临床工具,用于在致命剂量的化疗和/或放疗后重新填充癌症患者的骨髓。1992年,后来因发现一氧化氮(NO)而获得诺贝尔奖的Lou Ignarro利用人体阴茎组织表明,一种环GMP降解抑制剂可以增强神经NO释放的效果(2),从而开发出治疗勃起功能障碍(ED)的高效方法(3)。进一步阐明影响NO产生和降解的因素,使人们对影响勃起健康的生活方式和营养因素有了重要的认识(4)。在20世纪90年代中期,在西班牙瓦伦西亚安东尼奥·佩利塞领导下的研究小组和其他人所进行的工作的结果,卵巢过度刺激综合征(OHSS)的血管通透性增加和随之而来的极端液体移位的病因被证明是由于血管内皮生长因子(VEGF)和VEGF受体2 (VEGFR2)的表达增加(6)。通过识别和临床利用多巴胺激动剂抑制VEGFR-2磷酸化的作用,OHSS的发病率降低了50%。这一发现,以及对刺激VEGF的临床因素的理解和避免,现在已经使病态和潜在致命的OHSS罕见发生。在20世纪90年代,David Gardner和其他人一起定义了体内胚胎发育过程中可用的生殖道营养物质以及胚胎发育到囊胚期的特定阶段的特定需求。这些见解和临床经验使我们能够在前72小时和随后的24至84小时培养中设计专门用于胚胎的培养基(7),从而提高了体外受精效率,并使准确的染色体分析成为现实。预测成功怀孕的囊胚代谢研究进展迅速(8)。在20世纪90年代后期,通过流式细胞术和后来的TUNEL和COMET等技术,可以评估精子的DNA片段。DNA片段随着年龄的增长而增加(9),这可能导致40岁以上女性的成功率较低,尽管观察到男性年龄对年轻女性的影响较小(10)。与低应答者相比,对卵巢刺激反应正常的女性对体外受精结果的影响似乎更小(11)。这些观察结果表明,质量较好的卵母细胞的细胞质可能能够纠正DNA断裂。观察到DNA断裂与精液氧化应激相关(12),证实了抗氧化剂的成功治疗(13)。由于DNA碎片在男性收集系统的运输过程中增加,如果频繁射精和抗氧化剂不足,睾丸提取精子已经成功使用(14)。随着年龄的增长,性交频率下降,部分原因是勃起功能下降,导致老年夫妇不孕(15)。在20世纪90年代末,omega-3脂肪酸在精子膜功能中的重要性被阐明,并与精子质量和男性不育的指标相关(16)。Safarinejad报告了一项随机试验,该试验显示omega-3补充剂对精子密度、活力和严格形态有显著的益处(16)。精液中omega-3脂肪酸的浓度与这些改善以及精液中内源性抗氧化剂的浓度有关。补充omega-
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