13种樟科植物叶油细胞和粘液细胞的分布和结构的比较研究

利用组织透明法、石蜡制片法和薄切片法比较研究了樟科５属１３种植物叶片中油细胞和粘液细胞的分布和结构．结果表明：５属１１种植物叶片中有油细胞分布,其形状多为圆形,体积较小且大小基本一致,ｄ３０～４５μｍ;４属８种植物叶片中有粘液细胞分布,其形状多为椭圆形,体积较大,ｄ６０～１００μｍ．根据透明叶片观察,不同植物油细胞的分布密度不同;从叶片横切面观察,有些种油细胞分布于整个叶肉中,有的分布于栅栏组织与海绵组织之间及海绵组织中,有的仅分布于栅栏组织内．粘液细胞有些种分布于整个叶肉,而有的仅分布于栅栏组织中．因此,叶片内油细胞的分布密度、油细胞和粘液细胞的分布位置及其大小在种与种之间存在明显的差异,此种结构特征具有分类学上的意义     

2,3,7,8-四氯二苯并对二噁英对大鼠卵巢颗粒细胞雌二醇和孕酮分泌的影响

为研究2,3,7,8-四氯二苯并对二噁英(TCDD)对体外原代培养大鼠卵巢颗粒细胞活力和雌二醇(Estradiol,E2)、孕酮(Progestone,P)分泌的影响,探索TCDD对卵巢颗粒细胞的毒性作用阈值和程度,对未成熟SD大鼠卵巢颗粒细胞进行了原代培养,并设2组体外染毒实验:终浓度分别为0.1、1、10、100nmol·L-1TCDD染毒24h和10nmol·L-1TCDD染毒1、3、6、18、24h.染毒结束后采用MTT法检测细胞活力,RIA法检测收集培养液中的E2和P含量.结果表明,1、10、100nmol·L-1TCDD可显著抑制大鼠卵巢颗粒细胞活力和E2、P的分泌,与阴性对照、0.1%DMSO组、0.1nmol·L-1TCDD组比较差异均有显著性(p<0.05);10nmol·L-1TCDD染毒6、18、24h可明显抑制细胞活力和E2、P的分泌,与对照组和短期染毒组(1h、3h)差异均有显著性(p<0.05).痕量的TCDD可显著降低大鼠卵巢颗粒细胞活力并抑制细胞E2和P分泌,对大鼠卵巢颗粒细胞的毒性作用阈值可能为1nmol·L-1或更低.TCDD的生殖毒性作用可能与直接对卵巢颗粒细胞的毒性作用和抑制甾体激素的生物合成以及分泌有关.     

Eryxin通过抑制芳香化酶表达调控雌激素生物合成

雌激素水平与女性生理及心理健康密切相关,为探讨eryxin对雌激素生物合成的影响,采用Am-blue法检测eryxin对人卵巢颗粒细胞KGN细胞增殖的影响,磁微粒分离酶联免疫法检测雌二醇的合成,Western blotting检测KGN细胞芳香化酶蛋白表达水平,RT-qPCR检测KGN细胞芳香化酶基因及其启动子PromoterⅡ表达水平.结果显示,在1-150μg/mL范围内eryxin对细胞增殖没有影响,但是可以显著抑制KGN细胞中雌二醇的合成,且具有剂量依赖性;eryxin对芳香化酶过表达的HEK-293A细胞中雌二醇的合成没有影响;eryxin显著下调芳香化酶的mRNA和蛋白质表达水平,抑制芳香化酶启动子PromoterⅡ表达;降低eryxin中蛋白质含量可显著削弱其抑制雌激素合成的活性.本研究表明eryxin抑制人卵巢颗粒细胞雌激素的合成是通过其抑制芳香化酶mRNA及蛋白表达来实现的,结果可为进一步发现新型抗雌激素生物合成药物治疗相关相关疾病奠定基础.(图6表1参21)     

亚致死剂量阿维菌素对家蚕血细胞的影响(Effects of Sublethal Concentration of Abamectin on the Hemocytes of Silkworm, Bombyx mori)

阿维菌素作为一种生物农药被广泛使用,是我国取代高毒有机磷农药的主要品种之一.为探讨阿维菌素对家蚕的生理影响,采用阿维菌素亚致死剂量LC0.(10.001mg·L-1)和LC(50.0045mg·L-1)处理的桑叶饲喂5龄家蚕,通过取血、染片和显微镜观察以及琼脂糖凝胶电泳,对血细胞数量、形态和DNA损伤进行了研究.结果表明,低剂量LC0.1处理的家蚕血球细胞数量明显高于对照,而LC5处理的家蚕其血细胞数量整体低于对照.试验所用的亚致死剂量阿维菌素未对家蚕血细胞DNA产生损伤,但血细胞出现了空泡、肿胀等病态变化,且随着用药浓度增高细胞异型数量和程度有加大趋势.     

固定化甲烷八叠球菌提高甲烷化作用研究

用聚乙烯醇（ Ｐ Ｖ Ａ） 为包埋剂对甲烷八叠球菌（ Ｍｅｔｈａｎｏｓａｒｃｉｎａ ） 的富集培养物进行固定化, 并以甲醇为唯一碳源对其产气特性进行了研究．结果表明：以甲醇为唯一碳源时,固定化甲烷八叠球菌与非固定化甲烷八叠球菌的总产气量相似,但两者的产气特性有明显不同．固定化甲烷八叠球菌产气迟于非固定化甲烷八叠球菌,固定化甲烷八叠球菌的产气集中,在产气高峰两天中的产气量占总产气量的６６ ．０ ％ ．非固定化甲烷八叠球菌产气平稳, 平均日产甲烷量为８ ．９１ ｍ Ｌ／ｄ．固定化甲烷八叠球的电子显微镜观察结果表明, 细胞在固定介质中多呈较大包囊存在,包囊直径３０ ～５０ μｍ ．固定化甲烷八叠球处理豆制品废水的结果表明,在低有机物负荷下,固定化甲烷八叠球菌发挥着很大作用,有较低的出水 Ｃ Ｏ Ｄ 和较高的甲烷含量．在较高有机物负荷下,与对照无明显差别．其原因是在高有机物负荷和短水滞留期运转条件下,固定化甲烷八叠球菌受到抑制而失去活性所致     

川牛膝多糖硫酸酯的体外抗单纯疱疹病毒2型活性

从传统的川产道地中药材川牛膝中提取多糖RCP，用氯磺酸-吡啶法制备了它的硫酸酯衍生物s—RCP,产物经红外鉴定，证实RCP硫酸酯化后羟基部分被硫酸基取代，在1250cm^-1和810cm^-1处显示了硫酸基的特征吸收峰值,ω(S)=8．27％，取代度Ds=0．569．体外实验研究了RCP和S—RCP对非洲绿猴肾细胞(Vero cell line)的细胞毒性和抗单纯疱疹病毒2型(HSV-2)的活性．细胞病变效应法(CPE)和MTT法结果表明RCP在6．0mg／mL以下，S-RCP在4．0mg／mL以下均无细胞毒性，RCP本身无抗病毒活性，经硫酸酯衍生后的S—RCP获得抗病毒活性，0．25—4．0mg／，mL的S—RCP能很好地抑制HSV-2引起的细胞病变,以0．5mg／mL的无环鸟苷(ACV)作为阳性对照，结果显示当S-RCP浓度为2．0mg／mL和4．0mg／mL时有显著的抗病毒作用，效果与阳性ACV相当．图1表8参20     

铜、镉、敌敌畏和甲胺磷对南美白对虾的亚急性毒性作用

在恒温和充气条件下,研究了重金属(铜、镉)和有机磷农药(敌敌畏、甲胺磷)对南美白对虾的亚急性毒性作用及对虾体胆碱酯酶的影响.结果表明:南美白对虾幼虾在各浓度重金属(铜、镉)和有机磷农药(敌敌畏、甲胺磷)试液中经过60d的亚急性中毒试验,除铜在低浓度促进生长外,其他各组体长、体重及蜕皮次数均小于对照组,且随毒物浓度的增加而逐渐降低;有机磷农药对南美白对虾体内胆碱酯酶具有显著影响,虾体内胆碱酯酶含量随水体中有机磷农药浓度的升高而显著降低;重金属对胆碱酯酶也有一定影响,胆碱酯酶随重金属离子浓度升高也有逐渐降低的趋势,但重金属对胆碱酯酶的影响效果没有有机磷农药显著.     

定义

<正>生物体内积累:与环境中化学品的浓度相比,生物体内的化学品浓度随时间推移不断增加.化合物被吸收后,当其存储速度快于分解(新陈代     

菲和芘对蚯蚓(Eisenia fetida)细胞色素P450和抗氧化酶系的影响

研究了菲和芘在单一低剂量污染胁迫下对蚯蚓(Eisenia fetida)体内细胞色素P450酶系和抗氧化酶系的影响.通过滤纸接触染毒法,检测蚯蚓细胞色素P450含量以及超氧化物歧化酶(SOD)、过氧化物酶(POD)和过氧化氢酶(CAT)的活性.结果表明,在供试浓度范围内,蚯蚓体内细胞色素P450含量和三种抗氧化酶活性均对毒物产生了不同程度的响应.菲和芘在蚯蚓体内的代谢诱发了细胞色素P450总含量的增加,且在此过程中有活性氧自由基产生.不同酶对毒性效应响应的域值不同,其敏感性大小为:P450＞SOD(POD) ＞CAT.根据四个指标对污染物浓度响应的域值不同,可将四者联合应用互为补充作为一套生物标记物体系,以满足污染物不同暴露浓度下土壤的毒理诊断,增强指示的敏感性和有效性.     

变形虫Naegleria sp.TH8的分离鉴定及食藻特性

从太湖水样品中筛选分离到一株能吞噬水华鱼腥藻的原生动物TH8,经形态学及ITS rRNA序列分析鉴定为纳氏属变形虫(Naegleria sp.).显微观察显示变形虫TH8呈蛞蝓状,用透明半球形单伪足爆破前进,有运动滋养体、包囊和鞭毛体3个形态.变形虫TH8能在10~30℃生长并具有食藻活性,但在37℃或灭菌后的水华鱼腥藻中均不能生长.在新鲜水华鱼腥藻中25℃下指数期生长速率达到1.68 cell d-1.食藻特性研究表明,该变形虫在水华鱼腥藻生长的对数初期、对数后期和稳定期的吞食效果优于对数中期.水华鱼腥藻Chl a下降程度与变形虫初始浓度有关.     

柠檬酸对3种常见水产病原菌的抑菌作用

选用嗜水气单胞菌、副溶血弧菌、荧光假单胞菌3种常见水产病原菌,用于测定柠檬酸的抑菌效果及最小抑菌浓度,并研究了柠檬酸抑菌作用的持续性。3种菌均为革兰氏阴性菌。试验结果表明,柠檬酸对3种菌都有不同程度的抑菌作用,并得到最小抑菌浓度,依次是:0.0011g/mL,0.0008g/mL,0.00125g/mL;在最小浓度下抑菌作用可达6d之久,柠檬酸抑菌效果有较好的持续性。     

Antibacterial effects of Anodonta cygnea fluids on Escherichia coli and enterococci multi-drug-resistant strains: environmental implications

The persistence of bacteria in Anodonta cygnea largely depends on the hemolymph bactericidal activity against aquatic micro-organisms.

The aim of this study was to assess the in vitro bactericidal activity of whole hemolymph against multi-drug-resistant Escherichia coli and enterococci strains. Four mussels were injected with multi-resistant strains of E. coli in order to determine their in vivo bactericidal reactivity. In vitro experiments showed that the hemocytes viability decreased almost 70% in 4 h, the same happened in the control hemolymph. Enterococci tested in in vitro experiments were more susceptible than E. coli to whole hemolymph and hemocytes fractions. None of the enterococci bacteria was detected in the hemolymph fractions from 24 to 72 h, while E. coli was still detectable 72 h after inoculation both in the control and respective plasma fractions. The microbial inhibition on both hemolymph and cell pellets suggest that hemocytes may be the main responsibles for that process.

In vivo experiments showed that hemolymph inhibited the E. coli load injected and it was correlated with a high tendency for the increase in hemocytes counts, after 72 h. High adherence of E. coli and an intense pseudopods manifestation, mainly to the granulocytes, suggest a clear phagocytosis process.     

Effects of induced paralysis on hemocytes and tissues of the giant lions-paw scallop by paralyzing shellfish poison

In general, bivalves are not affected by exposure to toxic dinoflagellates that produce paralyzing shellfish poisons (PSP). After injection with PSP extracted from the Gymnodinium catenatum, Nodipecten subnodosus is paralyzed, indicating that PSP provokes effects similar to what is observed in vertebrates, including paralysis and metabolic stress. To investigate the processes involved in poisoning by PSP, lions-paw scallops were injected with gonyautoxin (GTX) 2/3 epimers in the adductor muscle. Mild doses provoked adductor muscle contractions and paralysis, mantle retraction, and incapacity of shell closure, but scallops gradually recovered in a clear, dose-time recovery pattern. With high doses of GTX 2/3, scallops were permanently paralyzed, and hemocytes in hemolymph were reduced. Surprisingly, under these conditions, scallops continued normal feeding and did not show any microscopic defect in intestine or gills, but hemocytes infiltrated the adductor muscle and abnormal vitellogenesis and mantle melanization occurred. Paralysis stress was accompanied by negative scallop responses, based on visible effects, generation of nitric oxide, lipid peroxidation, and changes in antioxidant and hydrolytic enzymes in hemocytes and tissues. These data can be used to understand potential side effects of PSP in bivalves.     

Involvement of quinones and phenoloxidase in the allorejection reaction in a colonial ascidian, Botrylloides simodensis: histochemical and immunohistochemical study

When incompatible colonies of Botrylloides simodensis were brought into contact at their artificially cut surfaces, allorejection occurred and a black line was formed along the contact border. Morula cells (MCs), a type of hemocytes, are the major effector in the allorejection reaction and are known to possess phenoloxidase (PO) that generates quinones. In this rejection reaction, MCs infiltrate the tunic and break down, discharging their vacuolar contents. Ascorbic acid (antioxidant) and benzamidine (protease inhibitor) showed inhibitory effects on MC breakdown, black line formation and new tunic cuticle formation, whereas tropolone (metal chelator) and sodium benzoate (substrate analog) did not. MCs probably store some amount of quinones, as well as PO; oxidants derived from the quinones appear to disintegrate the tissue to form a black line and promote MC breakdown. Histochemical and immunohistochemical studies revealed that MCs contain eosinophilic materials, PO and quinones. Quinones that are stored in MCs and produced by PO probably have a destructive function, forming rejection lesions.     

Starvation-induced barotolerance as a survival mechanism of a psychrophilic marine vibrio in the waters of the Antarctic convergence

Ant-300, a psychrophilic marine vibrio isolated from the Antarctic convergence, was tested for survival under conditions simulating those expected in situ for this organism. In particular, the organism's response to increased hydrostatic pressure was examined. Under a hydrostatic pressure of 250 atm, the viability of Ant-300 was reduced over 755 in growth media and under starvation conditions after 3 and 2 days, respectively. However, if the cells were starved for 1 week prior to pressurization of the starving suspension, 100% viability was maintained for over 6 weeks at the same pressure. After 10 weeks, the viability of a population of cells suspended for 1 week in natural or artificial seawater at a density of 10³ cells ml^–1 prior to pressurization of the suspension was 2 to 3 times greater than 1 atm controls. The data indicate that starvation conditions are a contributory if not the primary factor for the barotolerance of this organism in Antarctic waters. The data also indicate that under certain conditions, not unlike those expected in situ, hydrostatic pressure actually increases the survival of this organism under low nutrient conditions.Technical Paper No. 4907, Oregon Agricultural Experiment Station.     

Deleterious effects of a nonPST bioactive compound(s) from <Emphasis Type="Italic">Alexandrium tamarense</Emphasis> on bivalve hemocytes

The known negative effects of shellfish toxin-producing dinoflagellates on feeding, burrowing and survival of some bivalve mollusks has prompted questions concerning whether they might also impair the internal defense system of affected bivalves and make them more susceptible to disease agents. The primary components of the cellular defense system are hemocytes. Many toxic dinoflagellates are too large to be ingested whole by hemocytes and would most likely be exposed to intracellular toxins only after the algae are consumed, broken down, and the water-soluble toxins, released. Therefore, we conducted a series of experiments in which hemocytes from two suspension-feeding bivalves—the Manila clam, Ruditapes philippinarum, and the softshell clam, Mya arenaria—were exposed in vitro to filtered extracts of one highly toxic paralytic shellfish toxin (PST)-producing and one nonPST-producing strain of Alexandrium tamarense (isolates PR18b, 76 ± 6 STXeq cell⁻¹ and CCMP115, with undetectable PST, respectively). We measured adherence and phagocytosis, two hemocyte attributes known to be inhibited by bacterial pathogens and other stressors. We found no measurable effect of a cell-free extract from a highly concentrated suspension of the PST-producing strain on hemocytes of either bivalve species. Instead, extract from the nonPST-producing strain had a consistent negative effect on both clams, resulting in significantly lower adherence and phagocytosis compared to strain PR18b and filtered seawater controls. The bioactive compound produced by strain CCMP115, which has yet to be characterized, may be similar to the PST-independent allelopathic compounds described for Alexandrium spp., which act on other plankters. These compounds and those produced by other harmful algae are known to cause immobilization, cellular deformation and lysis of co-occurring target organisms. Thus, nonPST producing Alexandrium spp., which do not cause paralysis and burrowing incapacitation of clams, may still produce a compound(s) that has negative effects not only on hemocytes, but on other molluscan cell types and their functions, as well.     

碳纳米管导致小鼠肺部急性氧化损伤作用的研究

为了检测未经处理的碳纳米管作为送药载体对肺组织是否会产生毒性作用,将35只雄性昆明小鼠随机分成7组,用腹腔注射进行一次性染尘,6组分别注入0.1、0.2、0.4mg·mL-1的多壁碳纳米管(粒径20￣40nm)或标准碳黑颗粒(粒径<5μm)颗粒悬液1mL,对照组注入等体积生理盐水.染尘7天后对肺组织匀浆中丙二醛(MDA)和谷胱甘肽(GSH)含量进行测定,从而比较二者对肺组织的急性氧化损伤作用.结果表明,不同浓度的碳纳米管染尘组小鼠与对照组小鼠比较,肺组织MDA水平均有显著性升高(p<0.01);但所有标准碳黑组的升高却无统计学意义(p>0.05);0.2、0.4mg·mL-1碳纳米管染尘组与同浓度的标准碳黑染尘组比较,肺组织MDA水平显著升高(p<0.01),0.1mg·mL-1无显著变化.碳纳米管染尘组小鼠肺部GSH含量较对照组均有不同程度的降低,且均有统计学意义(0.1mg·mL-1组p<0.05,0.2mg·mL-1组p<0.01,0.4mg·mL-1组p<0.01).碳黑染尘组也有所降低,但仅0.2mg·mL-1和0.4mg·mL-1组有统计学意义(p<0.05).碳纳米管染尘组小鼠肺部GSH含量与同浓度的标准碳黑组比较,仅0.4mg·mL-1浓度组GSH含量显著降低(p<0.01),其他浓度组无显著变化.结果提示未经处理的碳纳米管作为送药载体对肺将产生一定程度毒性作用,且毒性大于相同浓度的标准碳黑.     

Toxic dinoflagellates (Alexandrium fundyense and A. catenella) have minimal apparent effects on oyster hemocytes

The possible effect of Alexandrium spp. containing paralytic shellfish poisoning (PSP) toxins on the hemocytes of oysters was tested experimentally. In one trial, eastern oysters, Crassostrea virginica Gmelin, were exposed to bloom concentrations of the sympatric dinoflagellate, Alexandrium fundyense Balech, alone and in a mixture with a non-toxic diatom, Thalassiosira weissflogii (Grun) Fryxell et Hasle. Subsequently, another experiment exposed Pacific oysters, Crassostrea gigas Thunberg, to a mixed suspension of the sympatric, toxic species Alexandrium catenella (Whedon et Kofoid) Balech, with T. weissflogii. Measurements of numbers of oyster hemocytes, percentages of different cell types, and functions (phagocytosis, reactive oxygen species (ROS) production, and mortality) were made using flow-cytometry. During and after exposure, almost no significant effects of Alexandrium spp. upon hemocyte numbers, morphology, or functions were detected, despite observations of adductor-muscle paralysis in C. virginica and measured toxin accumulation in C. gigas. The only significant correlation found was between toxin accumulation at one temperature and higher numbers of circulating live and dead hemocytes in C. gigas. The PSP toxins are known to interfere specifically with sodium-channel function; therefore, the finding that the toxins had no effect on measured hemocyte functions suggests that sodium-channel physiology is not important in these hemocyte functions. Finally, because oysters were exposed to the living algae, not purified toxins, there was no evidence of bioactive compounds other than PSP toxins affecting hemocytes in the two species of Alexandrium studied.     

Response of bioaerosol cells to photocatalytic inactivation with ZnO and TiO2 impregnated onto Perlite and Poraver carriers

•ZnO/Perlite inactivated 72% of bioaerosols in continuous gas phase. •TiO₂ triggered the highest level of cytotoxicity with 95% dead cells onto Poraver. •Inactivation mechanism occurred by membrane damage, morphological changes and lysis. •ZnO/Poraver showed null inactivation of bioaerosols. •Catalysts losses at the outlet of the photoreactor for all systems were negligible. Bioaerosols are airborne microorganisms that cause infectious sickness, respiratory and chronic health issues. They have become a latent threat, particularly in indoor environment. Photocatalysis is a promising process to inactivate completely bioaerosols from air. However, in systems treating a continuous air flow, catalysts can be partially lost in the gaseous effluent. To avoid such phenomenon, supporting materials can be used to fix catalysts. In the present work, four photocatalytic systems using Perlite or Poraver glass beads impregnated with ZnO or TiO₂ were tested. The inactivation mechanism of bioaerosols and the cytotoxic effect of the catalysts to bioaerosols were studied. The plug flow photocatalytic reactor treated a bioaerosol flow of 460×1 0⁶ cells/m³_air with a residence time of 5.7 s. Flow Cytometry (FC) was used to quantify and characterize bioaerosols in terms of dead, injured and live cells. The most efficient system was ZnO/Perlite with 72% inactivation of bioaerosols, maintaining such inactivation during 7.5 h due to the higher water retention capacity of Perlite (2.8 mL/g_Perlite) in comparison with Poraver (1.5 mL/g_Perlite). However, a global balance showed that TiO₂/Poraver system triggered the highest level of cytotoxicity to bioaerosols retained on the support after 96 h with 95% of dead cells. SEM and FC analyses showed that the mechanism of inactivation with ZnO was based on membrane damage, morphological cell changes and cell lysis; whereas only membrane damage and cell lysis were involved with TiO₂. Overall, results highlighted that photocatalytic technologies can completely inactivate bioaerosols in indoor environments.