药品与个人护理品在鱼体中的累积及代谢研究进展

药品与个人护理品(pharmaceuticals and personal care products,PPCPs)作为一类广泛使用和具有特殊物理化学特性的新型环境污染物,能够在水环境中持续低浓度的存在,对水生生态系统具有潜在风险,已经引起了广泛的关注。鱼体内PPCPs的累积与代谢过程研究在PPCPs的生态风险评价中占据极其重要的地位。概述了PPCPs在鱼体内的分布,分析了影响PPCPs在鱼体内累积的因素如PPCPs的性质、组织差异、鱼的种类、不同的描述方法等,讨论了PPCPs的代谢机制,重点介绍了PPCPs在胆汁内的解毒机制和代谢产物,强调了胆汁应用的重要意义。最后,展望了PPCPs在鱼体内的累积和代谢这一研究领域的发展方向。     

抗氧化系统在蜈蚣草细胞砷解毒机制中的作用

砷超富集植物——蜈蚣草体内可以富集高浓度的砷且不表现出受害症状,暗示蜈蚣草细胞具有较强的砷解毒机制.为探讨抗氧化系统在蜈蚣草砷解毒机制中的作用,测定了0、0.5、1和2mmol/L的砷酸盐[As(Ⅴ)]、亚砷酸盐[As(Ⅲ)]和二甲基胂酸盐(DMA)处理下蜈蚣草愈伤组织的丙二醛(Malonyldiadehyde,MDA)含量、非酶类抗氧化物质含量和酶类抗氧化物质的活性.结果表明,0.5mmol/L As(Ⅴ)和DMA就可以诱导氧化胁迫的产生,浓度越高胁迫程度也越严重.而1mmol/L的As(III)仍未使蜈蚣草愈伤组织产生氧化胁迫.在As(Ⅲ)处理下,酸溶性巯基含量增加,叶绿素和类胡萝卜素含量不变,过氧化氢酶(Catalase,CAT)和过氧化物酶(Peroxidase,POD)活性增加.在As(Ⅴ)处理下,酸溶性巯基含量减少,叶绿素和类胡萝卜素含量略有上升;CAT和POD活性先增加后减少.在DMA处理下,酸溶性巯基含量减少,叶绿素含量降低而类胡萝卜素含量增加,CAT和POD活性先增加后减少.与As(Ⅴ)和DMA相比,As(Ⅲ)处理下高酸溶性巯基含量、高氧化酶活性和低MDA含量暗示As(Ⅲ)对蜈蚣草的毒性可能比As(Ⅴ)和DMA要小.这些结果表明,酸溶性巯基和酶类抗氧化物质(CAT和POD)在蜈蚣草细胞砷解毒机制中发挥着重要作用.图4参22     

集胞藻(Synechocystis sp. PCC6803)对砷吸收转化特性的初步研究

砷是一种广泛存在于环境中的有毒物质.集胞藻属于单细胞藻类,广泛分布在淡水生态环境中.采用营养液培养的方法探讨了集胞藻(Synechocystis sp.PCC6803)对砷的累积和转化特性.当集胞藻分别暴露于2和100 μM的无机As(Ⅲ)和As(Ⅴ)14 d后,体内的砷形态均以As(Ⅴ)为主,并且在100 μM浓度处...     

Antioxidant enzymes and compounds complement each other during arsenic detoxification in shoots of Isatis cappadocica Desv.

Isatis cappadocica has been reported to be an arsenic (As) hyperaccumulator. Antioxidant enzymes and compounds have been proposed to play an important role in the detoxification and tolerance of As. In the present study, As-induced oxidative stress and antioxidant responses were investigated on I. cappadocica grown hydroponically in response to application of arsenate (0–1200?μmol). As accumulation increased with an increase in arsenate concentration in the medium. Along with a significant increase in arsenate concentration, a build up in hydrogen peroxide, indicators of oxidative stress, was observed. The activity of superoxide dismutase and peroxidase was induced after arsenate treatment, reached a maximal value at 800?μmol arsenate and then declined at the highest arsenate treatment. Glutathione reductase activity and contents of non-enzymatic antioxidants (carotenoids, flavonoids and anthocyanins) increased significantly as arsenate concentration augmented. These results indicated that high efficient antioxidant system may play significant roles in As detoxification and improve I. cappadocica tolerance against As toxicity.     

Uptake of arsenate, trimethylarsine oxide, and arsenobetaine by the shrimp Crangon crangon

Common shrimp, Crangon crangon (L.), were exposed to inorganic arsenic (arsenate), trimethylarsine oxide, or arsenobetaine in sea water (100 μg As l⁻¹) or in food (1 mg As g⁻¹ wet wt) for up to 24 d, followed by 16 d depuration in clean sea water with undosed food, in order to determine the efficiency of uptake and retention of the compounds. Accumulation of arsenic in the tail muscle, gills, midgut gland, exoskeleton, and remaining tissues was found to depend on the chemical form of the arsenic and the route of exposure. No arsenic was accumulated by C. crangon exposed to arsenate or trimethylarsine oxide in sea water. Shrimps exposed to waterborne arsenobetaine initially accumulated a small amount of arsenic in their tail muscle and gills. After 16 d, C. crangon fed arsenate, trimethylarsine oxide, or arsenobetaine had accumulated arsenic in their tail muscle to levels ∼2-, 2-, or 40-times, respectively, that of the control group. A roughly linear rate of accumulation was shown by shrimps fed trimethylarsine oxide or arsenobetaine, but C. crangon fed arsenate accumulated arsenic for 16 d, then lost arsenic such that their concentration on Day 24 was not significantly different from that of the control group. Patterns of arsenic accumulation in the gills of shrimps fed the compounds were similar to those seen in the tail muscle. On a whole animal basis, C. crangon retained ∼1.2% of the arsenate, 1.6% of the trimethylarsine oxide, and 42% of the arsenobetaine consumed over the first 16 d of exposure, with roughly half present in the tail muscle in each case. Data obtained support the view that the direct uptake of arsenobetaine from sea water does not make a significant contribution to the relatively high concentrations of this compound in marine crustaceans, and that food is the primary source. Naturally occurring arsenic compounds in C. crangon and possible transformations of the administered arsenic compounds were examined by high performance liquid chromatography using an inductively coupled plasma mass spectrometer as the arsenic-specific detector. Control C. crangon contained arsenobetaine as the major arsenic compound (>95% of total arsenic); tetramethylarsonium ion (0.7%) and an unknown arsenic compound (1.7%) were also present as minor constituents. Shrimp ingesting arsenobetaine accumulated it unchanged. Shrimp ingesting arsenate did not form methylated arsenic compounds; they appeared to contain their accumulated arsenic as unchanged arsenate only, although the possibility that some of the arsenic was reduced to arsenite could not be excluded. C. crangon ingesting trimethylarsine oxide biotransformed the compound predominantly to dimethylarsinate. Received: 9 October 1997 / Accepted: 11 February 1998     

毒死蜱对我国南方稻区水域中12种淡水鱼的毒性

毒死蜱作为稻田常用农药,普遍存在于稻区沟渠、池塘和河流中,从而对生活在其中的鱼类具有潜在风险。通过短期暴露试验,比较了毒死蜱在纯水、水-沉积物体系中对淡水鱼的毒性效应,进一步研究了毒死蜱在不同鱼体内的生物富集作用,以及对鱼脑Ach E活性的影响。试验结果表明:毒死蜱对12种淡水鱼均表现为高毒或剧毒,最敏感的是太阳鱼,但体系中沉积物的存在会通过吸附作用降低农药对鱼类的毒性;毒死蜱在鱼体内表现为中等或高富集性,其中斑马鱼的富集系数最大;毒死蜱对鱼脑Ach E酶活性有明显抑制作用,其中以虹鳟最敏感。研究结果为稻田常用农药对水生态环境中鱼类安全的风险性评价提供了科学依据。     

Non-carcinogenic effects of inorganic arsenic

This review will focus primarily on ohe effects of the inorganic arsenicals (arsenate and arsenite forms) that are present in drinking water. They are acutely toxic to both humans and animals, an effect that may be related to their bioavailibility. In humans, arsenicals have been reported to cause dermatitis and mucous membrane irritation upon exposure. They have also been reported to cause skin lesions and peripheral neurotoxicity in smelter workers and in patients treated with Fowler's Solution. When humans are exposed to arsenic in drinking water, effects such as hyperkeratosis, electromyographic abnormalities and vascular effects have been reported. In experimental animals, arsenic has been demonstrated to affect the liver and kidneys. In mice, arsenic has also been reported to decrease the animal's resistance to certain viral infections. The arsenite (+3) and arsenate (+5) forms have different modes of action. Arsenite binds to sulphhydryl groups and has been reported to inhibit over 100 different enzymes, while the arsenate can substitute for phosphate in various high energy intermediates, resulting in arsenolysis. In addition, when arsenate is reduced to arsenite in the body, it can also cause toxicity as that species.     

Arsenic metabolism in marine bacteria and yeast

Arsenic metabolism was studied for two marine microorganisms, a facultative anaerobic bacterium, Serratia marinorubra, and an obligately aerobic yeast, Rhodotorula rubra. Both were cultivated in media with (⁷⁴As) arsenate (As V), and the products of arsenate metabolism were determined qualitatively. Both the bacterium and the yeast produced arsenite (AS III) and methylarsonic acid [CH₃AsO(OH)₂]. In addition to the foregoing, only the yeast produced dimethylarsinic acid (CH₃)₂AsO(OH) and volatile alkylarsines. In contrast, the bacterium growing anaerobically with cobalamine as a cofactor did not synthesize gaseous forms of arsenic such as methylarsines. Neither organism synthesized arsoniumphospholipids such as those produced by marine phytoplankton or terrestrial fungi. The yeast did not accumulate arsenite, but instead transported some of it into the culture medium and methylated the remainder first to methylarsonic acid and then to dimethylarsinic acid. Finally, the latter compound was methylated further and volatile alkylarsines were formed. In contrast, the bacterium retained all products of arsenate metabolism intracellularly. Both the bacterium and the yeast, therefore, converted relatively toxic arsenate, the most abundant arsenic compound in seawater, to products that were presumably less toxic.     

Interaction effects of lead on bioavailability and pharmacokinetics of arsenic in the rat

Arsenic (As) and lead (Pb) are common contaminants found in mine waste materials. For an evidence-based risk assessment, it is important to better understand the potential interaction of mixed contaminants; and this interaction study was investigated in an in vivo rat model. Following co-administration of a fixed dose of As^V as in sodium arsenate and different doses of Pb as lead acetate to Sprague–Dawley rats, blood arsenic concentration and bioavailability decreased. A decrease in As blood concentration when lead was co-administered was observed with increasing lead doses. Pharmacokinetic parameters for As in the blood showed faster absorption and elimination of this metalloid in the presence of Pb. The elimination half-life of As decreased from 67 days in As solo group to 27–30 with doses of Pb. Bioavailability of As was also decreased by 30–43 % in the presence of Pb. Decreased urinary excretion of Pb and tissue accumulation were also observed. It indicates lower absorption of As when co-administered with Pb. A probable explanation for these findings is that As co-administration with Pb could have resulted in the formation of less soluble lead arsenate. However, such an interaction between As and Pb could only explain about one-third of the variation when real mine waste materials containing both of these elements were administered to rats. This suggests that other effects from physical and chemical parameters could contribute to the bioavailability of arsenic in complex real environmental samples.     

大同盆地富砷地下水的水化学与地球化学研究

为弄清大同盆地地下水中影响砷的迁移、富集的主要地球化学与生物地球化学过程,为区域供水安全提供指导作用,针对高砷地下水系统开展了水文地球化学与含水层沉积物全岩地球化学研究;并在此基础上探讨了研究区高砷地下水成因。结果表明,研究区高砷地下水为偏碱性、强还原环境,砷含量为0.31～452μg·L-1,主要以砷酸盐形式存在,地下水中砷与三价铁的浓度有显著的相关性。高砷含水层沉积物中有机质、铁与砷含量表现出显著相关性。以上结果说明,碱性还原环境有利于地下水中砷的富集;微生物参与下,沉积物相有机质的氧化和Fe氧化物/氢氧化物的还原过程是本区高砷地下水形成的主控因素。     

Incidence of organochlorine pesticide and PCB residues in an aquatic ecosystem of river duero in castile and Leon (Spain)

The occurrence of organochlorine pesticides and polychlorinated biphenyls (PCBs) in an aquatic ecosystem of River Duero was checked by means of a bioindicator organism: the grey heron (Ardea cinerea). Analyses of water, sediments, fish fat tissues and heron viscera revealed a marked bioaccumulation of organochlorine compounds, particularly hexa‐ and heptachlorinated biphenyls of industrial origin, which may account for the gradual decline in the number of individuals that make up the heron colonies studied.     

~(35)S-杀虫双在模拟水生生态系统中的生物吸收和消失

本文应用模拟生态实验装置和同位素示踪技术研究了~(35)S-杀虫双农药在模拟水生生态系统中的生物吸收和消失。在水—芜萍(Wolffia arrhiza wimm)—草鱼(Ctenopharyngodon idellus)—螺生态系统中,为期20d的蓄积试验表明,芜萍生物积聚率达24.65≥螺(肉1.67)>鱼(肉0.52);鱼体内脏因含未排出的芜萍而其积聚率(4.01)>鳃(1.66)>骨(0.95)>肉(0.52);转入洁水后,鱼体内的~(35)S-杀虫双可因排泄、代谢等原因而消失,残留消失半减期约10d,无生物浓缩。     

微生物砷还原机制的研究进展

砷是一种剧毒物质,环境中的砷对人体健康存在潜在威胁,因此长期以来备受关注.微生物的各种代谢过程对砷在环境中的归趋起着重要作用,其中砷还原微生物能将吸附于固体矿物中的As(Ⅴ)还原为可溶性强的As(Ⅲ),使砷进入液相,从而加剧了地下水等饮用水源的砷污染.论文主要介绍了两种微生物砷还原机制(异化砷还原和细胞质砷还原)在作用...     

Aufnahmepfade von POPs in Biota

POPs (persistent organic pollutants) associated with aquatic sediments can pose a risk to aquatic food chains, since they can be re-introduced to the food web. One major pathway is the bioaccumulation of POPs by endobenthic, sedimentingesting invertebrates (especially tubificid oligochaetes). These worms serve as food for benthivorous fish, which thereby ingest the sediment-borne chemicals and may accumulate contaminant concentrations far higher than from water exposure alone, and consequently transfer them to organisms of higher trophic levels. In order to evaluate such a potential biomagnification, a laboratory test was developed. It consisted of a two-step food chain including the sediment dwelling freshwater oligochaete Tubifex tubifex (Müller) and the three-spined stickleback (Gasterosteus aculeatus, Linné), a small teleost fish which often feeds primarily on benthic invertebrates. Artificial sediment and reconstituted water were used. To examine the influence of benthic prey on the bioaccumulation of a POP in the predator, fish were exposed to ¹⁴C-labelled hexachlorobenzene via spiked water, spiked sediment, pre-contaminated prey organisms, and to combinations of these exposure routes. Summarising the results of these experiments, it could be shown that the exposure to HCB via different routes resulted in a significantly higher accumulation in fish than an exposure to single pathways. It was concluded that the major uptake routes for fish were the overlying water and the food, whereas the contribution of spiked sediment itself was relatively small. HCB was biomagnified in the rested laboratory food chain. Therefore, concerning secondary poisoning, the environmental risk assessment of POPs like HCB should not be based on existing bioaccumulation tests alone, since they focus only on exposure via the water pathway. Instead, the influence of food and sediment as exposure routes should be considered as well, using comprehensive food chain modelling and/or laboratory studies.     

不同磷浓度下水稻短根突变体与野生型对五价砷吸收和转运的差异

为研究水稻根形态及磷营养状况对水稻吸收和转运五价砷的调控作用,采用水培的方法,研究了在不同外部磷浓度(0、10、50、150、300μM KH2PO4)下水稻(Oryza sativa L.)短根突变体与野生型短期内对五价砷(10μM Na3AsO4)吸收和转运的差异.结果表明,水稻根形态(短根突变体与野生型)和磷营养状况均能对水稻吸收和转运五价砷产生显著影响:1)磷能竞争性抑制水稻对五价砷的吸收,随营养液中磷浓度的增加,水稻地上部和地下部五价砷含量、单位根干重砷吸收量(根系砷吸收能力)均显著降低;2)水稻短根突变体对五价砷的吸收能力低于野生型,但转运能力高于野生型.     

三氯生对水生生物的毒性效应研究进展

三氯生(TCS)作为一种广谱抗菌剂,在个人护理品中的广泛应用,将使其不可避免地释放到水环境中.随着在河流、湖泊、河口系统等水环境以及水生生物体内检测到TCS,TCS对于水生生物的生态毒理效应引起了学者们的广泛关注.本文概述了TCS在水环境及水生生物体内的赋存状况,归纳总结了TCS对水生生物的急性毒性、亚急性毒性、酶及基因毒性、内分泌干扰性及其降解产物毒性,最后展望了TCS对水生生物的生态毒理效应这一研究领域的发展方向.     

Health importance of arsenic in drinking water and food

Arsenic is a toxic metalloid of global concern. It usually originates geogenically but can be intensified by human activities such as applications of pesticides and wood preservatives, mining and smelting operations, and coal combustion. Arsenic-contaminated food is a widespread problem worldwide. Data derived from population-based studies, clinical case series, and case reports relating to ingestion of inorganic arsenic in drinking water, medications, or contaminated food or beverages show the capacity of arsenate and arsenite to adversely affect multiple organ systems. Chronic arsenic poisoning can cause serious health effects including cancers, melanosis (hyperpigmentation or dark spots, and hypopigmentation or white spots), hyperkeratosis (hardened skin), restrictive lung disease, peripheral vascular disease (blackfoot disease), gangrene, diabetes mellitus, hypertension, and ischemic heart disease.     

Environmental effects of aluminium

Aluminium (Al), when present in high concentrations, has for long been recognised as a toxic agent to aquatic freshwater organisms,i.e. downstream industrial point sources of Al-rich process water. Today the environmental effects of aluminium are mainly a result of acidic precipitation; acidification of catchments leads to increased Al- concentrations in soil solution and freshwaters. Large parts of both the aquatic and terrestrial ecosystems are affected.In the aquatic environment, aluminium acts as a toxic agent on gill-breathing animals such as fish and invertebrates, by causing loss of plasma- and haemolymph ions leading to osmoregulatory failure. In fish, the inorganic (labile) monomeric species of aluminium reduce the activities of gill enzymes important in the active uptake of ions. Aluminium seems also to accumulate in freshwater invertebrates. Dietary organically complexed aluminium, maybe in synergistic effects with other contaminants, may easily be absorbed and interfere with important metabolic processes in mammals and birds.The mycorrhiza and fine root systems of terrestrial plants are adversely affected by high levels of inorganic monomeric aluminium. As in the animals, aluminium seems to have its primary effect on enzyme systems important for the uptake of nutrients. Aluminium can accumulate in plants. Aluminium contaminated invertebrates and plants might thus be a link for aluminium to enter into terrestrial food chains.     

A farewell to Dr Thomas Knacker (* 29.04.1951 – ? 30.10.2011): scientific contributions and personal memories

Background

The bioaccumulation potential of chemical substances is commonly determined in flow-through fish tests according to the Organization for Economic Cooperation and Development (OECD) technical guideline (TG) 305, aiming at the determination of bioconcentration factors (BCF). Investigations on aquatic organisms have shown a significant positive correlation between the accumulation of a chemical and the lipid content of organisms. Residue levels can thus differ between individuals, species, and size groups depending on their lipid content. BCF values can be normalized by lipid content; however, this requires the use of appropriate extraction techniques to ensure the complete extraction of total lipids from fish/tissue samples. The OECD TG 305 is currently under revision. A literature review was carried out to select preferred methods which shall be included in the updated OECD TG 305 along with a sampling schedule for lipid measurement in fish.

Results

An overview and appraisal of a broad range of lipid extraction methods is presented. Extraction procedures applied in bioaccumulation studies described in the literature and procedures currently used for such studies by governmental, academic, and industrial labs are surveyed. Possible impacts of unsuitable extraction techniques on lipid normalized BCF results were assessed. Default values for BCF normalization commonly used in bioaccumulation studies are described. The effect of differences in residue distribution over different organs and/or lipids on the normalization of BCF values is discussed.

Conclusions

A broad range of procedures for lipid extraction are available. However, only the use of suitable extraction techniques guarantees the complete extraction of total lipids from fish samples in bioaccumulation studies which is required to ensure the correct lipid normalization of BCF values. Preferred methods for inclusion in the updated OECD 305 test guideline as well as a standard schedule for lipid measurements are suggested.     

Aquatic and terrestrial organic matter in the diet of stream consumers: implications for mercury bioaccumulation

The relative contribution of aquatic vs. terrestrial organic matter to the diet of consumers in fluvial environments and its effects on bioaccumulation of contaminants such as mercury (Hg) remain poorly understood. We used stable isotopes of carbon and nitrogen in a gradient approach (consumer isotope ratio vs. periphyton isotope ratio) across temperate streams that range in their pH to assess consumer reliance on aquatic (periphyton) vs. terrestrial (riparian vegetation) organic matter, and whether Hg concentrations in fish and their prey were related to these energy sources. Taxa varied in their use of the two sources, with grazing mayflies (Heptageniidae), predatory stoneflies (Perlidae), one species of water strider (Metrobates hesperius), and the fish blacknose dace (Rhinichthys atratulus) showing strong connections to aquatic sources, while Aquarius remigis water striders and brook trout (Salvelinus fontinalis) showed a weak link to in-stream production. The aquatic food source for consumers, periphyton, had higher Hg concentrations in low-pH waters, and pH was a much better predictor of Hg in predatory invertebrates that relied mainly on this food source vs. those that used terrestrial C. These findings suggest that stream biota relying mainly on dietary inputs from the riparian zone will be partially insulated from the effects of water chemistry on Hg availability. This has implications for the development of a whole-system understanding of nutrient and material cycling in streams, the choice of taxa in contaminant monitoring studies, and in understanding the fate of Hg in stream food webs.