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一氧化氮的生物学效应 总被引:1,自引:0,他引:1
一氧化氮是新近发现的一种重要的细胞内信使和神经介质,它在免疫系统、心血管系统、神经系统等的调节中起着重要的作用。NO功能的研究为生物学的许多领域提供新的认识。 相似文献
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为了揭示当前我国土壤环境中污染严重的代表性重金属铜和有机磷农药毒死蜱联合作用的毒性效应及风险,本研究以赤子爱胜蚓为模式生物,分别应用人工土壤法和滤纸法探讨铜、毒死蜱单一及复合暴露对蚯蚓生长及抗氧化防御系统的影响.结果表明: 随着铜、毒死蜱单一暴露浓度的增大,人工土壤法蚯蚓体质量增长率趋于降低;二者复合暴露组蚯蚓体质量变化则相对平缓.采用概率相加法求得不同浓度组合铜、毒死蜱对蚯蚓体质量联合作用的q值均小于0.55,表明二者的联合作用类型为显著拮抗作用.滤纸法铜、毒死蜱对蚯蚓过氧化氢酶、超氧化物歧化酶活性的联合作用类型主要为拮抗作用;而对还原型谷胱甘肽和丙二醛含量的影响表现为低浓度协同而高浓度拮抗的作用类型. 相似文献
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生长激素生物学效应的研究进展 总被引:1,自引:0,他引:1
人类生长激素(growthhormone,GH)最先作为替代疗法用于治疗儿童GH缺乏性侏儒症,后来的研究表明,它具有明显的节氮效应,因而广泛用于烧伤、感染及严重创伤,并取得了良好疗效.此后,进一步研究表明GH能促进胰岛素样生长因子(IGF)的形成进而促进骨折愈合,使其应用范围进一步扩大.本文就生长激素生物学效应进行综述. 相似文献
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激光的生物学效应研究 总被引:4,自引:0,他引:4
本文通过分析多种激光(十五种激光器,波长从266nm—447.2×l03nm)对生物体(九十多种生物,如果把品种计算在内,则大约200多种)的生物学效应研究发现:①不同波长激光都能对生物体产生作用;②激光对动物、植物、微生物均能产生生物学效应;③低剂量辐照对生物体主要是刺激作用,随着剂量增加则产生抑制、损伤,以及诱变和致死作用;④激光对60Co—γ射线的辐射损伤有一定的修复作用;⑤低功率激光对生物体的作用主要在于其电效应和电磁场效应(关于这个方面,将另文详细讨论)。 相似文献
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激光生物学效应的研究 总被引:1,自引:5,他引:1
本文较系统地报道了CO_2激光,He-Ne激光的生物学作用,证明激光确能导致生物体内生理生化的变化,确能诱发染色体畸变和基因突变。作者认为激光作为育种上一种新的诱变因素是有根据的。 相似文献
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环境胁迫与生物防御反应 总被引:2,自引:0,他引:2
生物的生存总是逃避不了周围各种环境胁迫因素的影响。非生物因素如温度、水分、湿度、光照、营养、环境污染、物理干扰和土壤坚实度等;生物因素如有害生物的袭击等。兴衰存亡的关键,除了取决于胁迫的种类、强度 相似文献
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Genetically altered mice are an important tool for biomedical research. Several transgenic mice have been created in which activation of the transgene results in production of β-galactosidase that can be detected by histological means. While preservation and subsequent visualization of enzyme activity in soft tissues can be complicated, it is particularly difficult in bone specimens, especially those that have been decalcified. For these studies, we examined the bones of parathyroid hormone-related peptide (PTHrP) knock-in mice in which expression of PTHrP resulted in β-galactosidase production. During the past decade, several studies have demonstrated the importance of PTHrP in bone. Thus, it is important to preserve and detect β-galactosidase enzymatic activity in bone for these studies. We demonstrate here that β-galactosidase was visualized better in slides with bone sections taken from PTHrP knock-in mice when bones were frozen and sectioned compared to bones that were embedded in plastic and sectioned using a microtome. Importantly, we were able to visualize β-galactosidase in plastic embedded bones when specimens were fixed, stained (X-gal), embedded in plastic, and then sectioned rather than being fixed, embedded in plastic, sectioned, then stained. 相似文献
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细胞珠蛋白的结构及其生物学效应 总被引:1,自引:0,他引:1
细胞珠蛋白(cytoglobin,Cygb)是最近发现的脊椎动物珠蛋白超家族的一员,在体内分布广泛。人Cygb基因定位于染色体17q25,含有4个外显子和3个内含子,编码190个氨基酸残基(分子量20.9kD)。Cygb拥有经典的“three-over-three”α螺旋三明治折叠结构,同神经珠蛋白(Ngb)一样,Cygb血红素在缺乏外源性配体时呈“六配位”结构。Cygb的确切功能尚不十分清楚,目前主要有携氧与储氧、氧感受器、活性氧基团和NO的清道夫、NADH氧化酶或过氧化氢酶样作用和参与胶原形成等假说。 相似文献
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Effects of Soil pH on the Biodegradation of Chlorpyrifos and Isolation of a Chlorpyrifos-Degrading Bacterium 总被引:7,自引:1,他引:7 下载免费PDF全文
Brajesh K. Singh Allan Walker J. Alun W. Morgan Denis J. Wright 《Applied microbiology》2003,69(9):5198-5206
We examined the role of microorganisms in the degradation of the organophosphate insecticide chlorpyrifos in soils from the United Kingdom and Australia. The kinetics of degradation in five United Kingdom soils varying in pH from 4.7 to 8.4 suggested that dissipation of chlorpyrifos was mediated by the cometabolic activities of the soil microorganisms. Repeated application of chlorpyrifos to these soils did not result in the development of a microbial population with an enhanced ability to degrade the pesticide. A robust bacterial population that utilized chlorpyrifos as a source of carbon was detected in an Australian soil. The enhanced ability to degrade chlorpyrifos in the Australian soil was successfully transferred to the five United Kingdom soils. Only soils with a pH of ≥6.7 were able to maintain this degrading ability 90 days after inoculation. Transfer and proliferation of degrading microorganisms from the Australian soil to the United Kingdom soils was monitored by molecular fingerprinting of bacterial 16S rRNA genes by PCR-denaturing gradient gel electrophoresis (DGGE). Two bands were found to be associated with enhanced degradation of chlorpyrifos. Band 1 had sequence similarity to enterics and their relatives, while band 2 had sequence similarity to strains of Pseudomonas. Liquid enrichment culture using the Australian soil as the source of the inoculum led to the isolation of a chlorpyrifos-degrading bacterium. This strain had a 16S rRNA gene with a sequence identical to that of band 1 in the DGGE profile of the Australian soil. DNA probing indicated that genes similar to known organophosphate-degrading (opd) genes were present in the United Kingdom soils. However, no DNA hybridization signal was detected for the Australian soil or the isolated degrader. This indicates that unrelated genes were present in both the Australian soil and the chlorpyrifos-degrading isolate. These results are consistent with our observations that degradation of chlorpyrifos in these systems was unusual, as it was growth linked and involved complete mineralization. As the 16S rRNA gene of the isolate matched a visible DGGE band from the Australian soil, the isolate is likely to be both prominent and involved in the degradation of chlorpyrifos in this soil. 相似文献