少精、弱精不育症患者精液中微量元素含量的测定分析

用ICPOES法检测了54例男性少精、弱精不育者精液中Ca、Cd、Cu、Fe、Mg、Mn、Ni、Zn元素的含量,并对相关含量进行数据分析。结果表明,精液中微量元素含量的改变是影响精液质量的重要原因之一。     

正常与不育男性精浆锌和铜的研究

测定了正常男性３３例与不育男性１４４例糖浆微量元素锌和铜的含量（μｇ／ｍＬ）：正常组锌２０２．５９±５２．９，铜０．２５±０．０１９，不育组锌１１７±５７．５，铜０．４８±０．３８．所得结果表明：不育组精浆锌明显低于正常组，差别有极显著意义．不育组精浆铜明显高于正常组，差别有显著意义．     

冠心病与微量元素锌铜硒

以临床典型冠心病案为例，探讨了中医中药传统和微量元素关系，重点讨论了微量元素锌、铜、硒与冠心病的病因病理和治疗的关系。     

肾病综合征与锌铜铁

以临床典型肾病综合征病案为例，地中医中药传统理论和微量元素研究关系，重点了微量元素锌、铜、铁与肾病综合征的病因病机和治疗关系。     

微量元素与中药功效关系的探讨

中药中含有丰富的微量元素，其种类和含量与中药功效有着密切的关系。从微量元素与中药的滋补作用，解热作用．抗菌消炎作用和止血作用等四方面，论述了微量元素与中药功效的关系。     

中医药抗衰老与微量元素的相关性

重点讨论了各类抗衰老中药和微量元素的相关性，探讨了中医中药衰老和现代微量元素的关系，为人类健康防病抗衰、益寿延年做出新的贡献。     

肾炎的中医药论治与微量元素

以临床典型肾病病案为例，探讨了中医中药传统理论和微量元素研究的关系，重点讨论微量元素锌，铁，铜与肾病的病因，病机和治疗关系。     

帕金森氏病与头发中微量元素关系的研究

以人发为材料，探讨了帕金森氏病与微量元素的关系。采集了６０例患者头发和５０例健康人头发，用电感耦合高频等离子体发射光谱仪进行测定，结果发现，患者组头发铜、锌、铁、锰明显低于对照组，患者组轻、中、重分型病人的头发微量元素变化有一定的规律，上述结果提示微量元素与帕金森氏病有重要关系。     

中医补肾壮骨理论与微量元素

探讨了中医理论与微量元素的关系，重点介绍了补肾药和肾主骨主生长发育的理论与微量元素的关系。为中医随证配伍选药提供了理论基础。     

中药微量元素研究中若干热点课题

评进了当前中药徽量元素研究中的若干热点课题；1．微量元素与中药品种、产地的关系；2．微量元素与中药性味、归经，功效的关系；3．中药微量元素的存在状态；4．中药内有机成分与微量元素的相互关系；5．微量元素对中西药配伍的影响；6．微量元素的毒副作用．共引用文献29篇．     

Study on the Interaction between Gatifloxacin Mesylate and Salmon Sperm DNA by Fluorescence Method

The interaction between gatifloxacin mesylate (GM) and salmon sperm DNA was studied by fluorescence spectrometry and ultra‐violet (UV) spectrometry. Additions of salmon sperm DNA to GM solution resulted in its strong fluorescence quenching and UV absorbance decrease due to the strong interaction between GM and salmon sperm DNA. Both the maximum fluorescence emission wavelength and the maximum UV absorbance wavelength of GM did not change with the increasing concentration of salmon sperm DNA, indicating no intercalative binding existed between them. The Stern‐Volmer plot indicated that the fluorescence‐quenching constant at different temperatures or different salmon sperm DNA concentration ranges was different. Effects of ionic strength and I^? on the fluorescence quenching of GM by salmon sperm DNA indicated that electrostatic interaction and groove binding coexisted between them.     

甲基百里酚蓝-钐(III)配合物与鲱鱼精DNA的相互作用

在pH＝7.25的Tris-HCl缓冲溶液中, 以中性红(NR)作为光谱探针, 采用UV光谱、FS光谱、粘度等方法研究了甲基百里酚蓝(MTB)与稀土金属离子钐[Sm(III)]形成的配合物Sm(III)(MTB)₂与鲱鱼精DNA的作用机制. 确定了Sm(III)(MTB)₂与鲱鱼精DNA之间有嵌插作用方式存在, 说明Sm(III)(MTB)₂金属配合物能使鲱鱼精DNA的功能产生一定影响.     

Study on in vitro sperm capacitation and egg-penetration of giant panda

A preliminary report on in vitro sperm capacitation and egg-penetration of giant panda is briefly presented. The panda spermatozoon consists of head, neck and tail, just like the spermatozoa of other animals. Before capacitation sperm heads clustered together and dispersed after capacitation. They were then able to swim straight forward. During the time of in vitro capacitation the plasma membrane of the sperm head was first expanded to various degrees, then disintegrated, and finally became detached. The electro-dense material in the acrosome appeared in small clumps with high density. Extensive vesiculation occurred between the bi-layered acrosome membranes and thus led to disintegration. Vesiculation in panda sperm differs from that reported in hamsters. When the capacitated panda spermatozoa came into contact with the hamster eggs, the region between the acrosome collar and postacrosome cap first fused with the egg membrane followed by the penetration of the nucleus into the cortex of the egg. Some of the penetrating sperm nuclei became decondensed and some did not. The success of in vitro sperm capacitation and egg-penetration of giant panda is of great significance, suggesting that it is possible to carry out in vitro fertilization and embryo transplantation in this endangered species.     

Thin Layer Chromatography of Phospholipid Composition in Mouse and Rabbit Spermatozoa

Abstract

The time course of the loss of different components of the phospholipids of rabbit and mouse epididymal spermatozoa during spontaneous lipid peroxidation was determined, using thin layer chromatography with a specific situ hydrolysis method to differentiate the acyl and alkenyl (plasmalogen) moieties. The components followed were phosphatidylethanolamine (PE), phosphatidylcholine (PC), the PE and PC phasmalogens, sphingomyelin (SP), cardiolipin (CL), and phosphatidyl-glycerol (PG). In both mouse and rabbit sperm, the PE component was found to be more than 90% diplasmalogen: 1,2-di(0-1′-alkenyl) glycerophosphoethanolamine. This component was lost rapidly during peroxidation. All PE has disappeared from rabbit sperm after 4 h aerobic incubation, at which point the other phospholipids had been little affected. In both mouse and rabbit sperm, the PC component was found to be 50% monoplasmalogen. The decrease in PC plasmalogen of rabbit sperm amounted to 74% after 20 h, compared to 42% loss of total PC. Similar observations were made with mouse sperm, except that rates of loss of all components were approximately twice those in rabbit. Distribution of the phospholipid components between sperm heads and tails was also determined: PE diplasmalogen was almost entirely found in the tail fraction, in both mouse and rabbit sperm. This mode of analysis allows the differentiation of sensitivities towards spontaneous peroxidation of the different types of phospholipid present in sperm membranes.     

Magnetic Micromotors for Multiple Motile Sperm Cells Capture,Transport, and Enzymatic Release

An integrated system combining a magnetically-driven micromotor and a synthetized protein-based hyaluronic acid (HA) microflake is presented for the in situ selection and transport of multiple motile sperm cells (ca. 50). The system appeals for targeted sperm delivery in the reproductive system to assist fertilization or to deliver drugs. The binding mechanism between the HA microflake and sperm relies on the interactions between HA and the corresponding sperm HA receptors. Once sperm are captured within the HA microflake, the assembly is trapped and transported by a magnetically-driven helical microcarrier. The trapping of the sperm-microflake occurs by a local vortex induced by the microcarrier during rotation-translation under a rotating magnetic field. After transport, the microflake is enzymatically hydrolyzed by local proteases, allowing sperm to escape and finally reach the target location. This cargo-delivery system represents a new concept to transport not only multiple motile sperm but also other actively moving biological cargoes.     

Magnetic Micromotors for Multiple Motile Sperm Cells Capture,Transport, and Enzymatic Release

An integrated system combining a magnetically‐driven micromotor and a synthetized protein‐based hyaluronic acid (HA) microflake is presented for the in situ selection and transport of multiple motile sperm cells (ca. 50). The system appeals for targeted sperm delivery in the reproductive system to assist fertilization or to deliver drugs. The binding mechanism between the HA microflake and sperm relies on the interactions between HA and the corresponding sperm HA receptors. Once sperm are captured within the HA microflake, the assembly is trapped and transported by a magnetically‐driven helical microcarrier. The trapping of the sperm‐microflake occurs by a local vortex induced by the microcarrier during rotation‐translation under a rotating magnetic field. After transport, the microflake is enzymatically hydrolyzed by local proteases, allowing sperm to escape and finally reach the target location. This cargo‐delivery system represents a new concept to transport not only multiple motile sperm but also other actively moving biological cargoes.     

Effects of exposure to dibutyltin dichloride on sperm density,viability and morphology in male mice

Experiments on the effects of 0.025–0.40 µg of dibutyltin dichloride (DBTCl) per kilogram body weight (kg bw), on sperm density, viability and morphology in mature mice were conducted by daily intraperitoneal injection for 7 days at 22 ± 2 °C and 12 h light–dark cycle conditions. The results demonstrated that DBTCl exhibited strong toxicity on sperm quality. Dosed with ≥ 0.05 µg DBTCl/kg bw groups, the testes weight, sperm density and the rate of survival of sperm decreased, whereas the rate of sperm abnormalities increased significantly. In addition, treatment with 0.05 µg DBTCl/kg bw resulted in increasing rate of sperm head abnormalities, whereas administration at 0.20 and 0.40 µg DBTCl/kg bw significantly increased the rate of sperm tail abnormalities. In the group treated at ≥ 0.10 µg DBTCl/kg bw, the mice body weights decreased. It appeared there was a noticeable dose–response relationship between DBTCl and the parameters studied. ED₅₀ values (7 days) of DBTCl for survival rate of sperm and density were 0.17 µg/kg bw and 0.19 µg/kg bw respectively. The present study provides a possibility for early diagnostic indicators and methods for sperm quality induced by organotin compounds (DBTCl) in mammals. Copyright © 2001 John Wiley & Sons, Ltd.     

十六烷基三甲基溴化铵对DNA热稳定性的影响

研究十六烷基三甲基溴化铵(CTAB)对DNA分子热稳定性的影响对于认识阳离子表面活性剂与DNA二者之间的相互作用具有重要的意义。用差示扫描量热法和变温紫外光谱法研究了CTAB对鲑鱼精DNA及降解的鲱鱼精DNA热稳定性的影响,发现CTAB使鲑鱼精DNA的热稳定性降低,但降低程度随CTAB浓度的增大而先增大后减小;CTAB使鲱鱼精DNA发生了两阶段熔解行为。     

STUDY ON in vitro SPERM CAPACITATION AND EGG-PENETRATION OF GIANT PANDA

A preliminary report on in vitro sperm capacitation and egg-penetration of giant panda is briefly presented. The panda spermatozoon consists of head, neck and tail, just like the spermatozoa of other animals. Before capacitation sperm heads clusterd together and dispersed after capacitation. They were then able to swim straight forwared. During the time of in vitro capacitation the plasm membrane of the sperm head was first expanded tov arious degrees, then disintegrated, and finally became detached. The electro-dense material in the acrosome appeared in small clumps with high density. Extensive vesiculation occurred between the bi-layered acrosome membranes and thus led to disintegration. Vesiculation in panda sperm differs from that reported in hamsters. When the capacitated panda spermatozoa came into contact with the hamster eggs, the region between the acrosome collar and postacrosome cap first fused with the egg membrane followed by the penetration of the nucleus into the cortex of the egg. Some o