Major correlates of mercury in small fish and common loons (Gavia immer) across four large study areas in Canada.

We investigated mercury (Hg) concentrations in small fish (mainly yellow perch, Perca flavescens; ∼60% of fish collected) and in blood of common loons (Gavia immer) that prey upon them during the breeding season on lakes in 4 large, widely separated study areas in Canada (>13 lakes per study area; total number of lakes = 93). Although surface sediments from lakes near a base metal smelter in Flin Flon, Manitoba had the highest Hg concentrations, perch and other small fish and blood of common loon chicks sampled from these same lakes had low Hg concentrations similar to those from uncontaminated reference lakes. Multiple regression modeling with AIC analysis indicated that lake pH was by far the most important single factor influencing perch Hg concentrations in lakes across the four study areas (R(2) = 0.29). The best model was a three-variable model (pH + alkalinity + sediment Se; Wi = 0.61, R(2) = 0.85). A single-variable model (fish Hg) best explained among-lake variability in loon chick blood Hg (Wi = 0.17; R(2) = 0.53). From a toxicological risk perspective, all lakes posing a potential Hg health risk for perch and possibly other small pelagic fish species (where mean fish muscle Hg concentrations exceeded 2.4 µg/g dry wt.), and for breeding common loons (where mean fish muscle Hg concentrations exceeded 0.8 µg/g dry wt., and loon chick blood Hg exceeded 1.4 µg/g dry wt.) had pH < 6.7 and were located in eastern Canada.

Relationships among mercury, selenium, and neurochemical parameters in common loons (Gavia immer) and bald eagles (Haliaeetus leucocephalus).

Fish-eating birds can be exposed to levels of dietary methylmercury (MeHg) known or suspected to adversely affect normal behavior and reproduction, but little is known regarding Hg's subtle effects on the avian brain. In the current study, we explored relationships among Hg, Se, and neurochemical receptors and enzymes in two fish-eating birds--common loons (Gavia immer) and bald eagles (Haliaeetus leucocephalus). In liver, both species demonstrated a wide range of total Hg (THg) concentrations, substantial demethylation of MeHg, and a co-accumulation of Hg and Se. In liver, there were molar excesses of Se over Hg up to about 50-60 microg/g THg, above which there was an approximate 1:1 molar ratio of Hg:Se in both species. However, in brain, bald eagles displayed a greater apparent ability to demethylate MeHg than common loons. There were molar excesses of Se over Hg in brains of bald eagles across the full range of THg concentrations, whereas common loons often had extreme molar excesses of Hg in their brains, with a higher proportion of THg remaining as MeHg compared with eagles. There were significant positive correlations between brain THg and muscarinic cholinergic receptor concentrations in both species studied; whereas significant negative correlations were observed between N-methyl-D-aspartic acid (NMDA) receptor levels and brain Hg concentration. There were no significant correlations between brain Se and neurochemical receptors or enzymes (cholinesterase and monoamine oxidase) in either species. Our findings suggest that there are significant differences between common loons and bald eagles with respect to cerebral metabolism and toxicodynamics of MeHg and Se. These interspecies differences may influence relative susceptibility to MeHg toxicity; however, neurochemical responses to Hg in both species were similar.

The R1 subunit of herpes simplex virus ribonucleotide reductase is a good substrate for host cell protein kinases but is not itself a protein kinase.

The N terminus of the R1 subunit of herpes simplex virus type 2 ribonucleotide reductase is believed to be a protein kinase domain mainly because the R1 protein was phosphorylated in a protein kinase assay on blot. Using Escherichia coli and adenovirus expression vectors to produce R1, we found that, whereas the reductase activity of both recombinant proteins was similar, efficient phosphorylation of R1 and casein in the presence of Mg2+ was obtained only with the R1 purified from eukaryotic cells. Phosphorylation of this R1, in solution or on blot, results mainly from the activity of casein kinase II (CKII), a co-purifying protein kinase. Labeling on blot occurs from CKII leakage off the membrane and its subsequent high affinity binding to in vivo CKII-phosphorylated R1. CKII target sites were mapped to an acidic serine-rich segment of the R1 N terminus. Improvement in purification of the R1 expressed in eukaryotic cells nearly completely abolished its phosphorylation potential. An extremely low level of phosphorylation observed in the presence of Mn2+ with the R1 produced in E. coli was probably due to an unidentified prokaryotic protein kinase. These results provide evidence that the herpes simplex virus type 2 R1 does not possess an intrinsic protein kinase activity.

PCBs, dioxins and furans in Hooded Merganser (Lophodytes cucullatus), Common Merganser (Mergus merganser) and mink (Mustela vison) collected along the St. Maurice River near La Tuque, Quebec.

A pulp and paper mill located in La Tuque on the St. Maurice River, Quebec, and using the kraft bleaching process was historically the largest pulp and paper industry point source of chlorinated dibenzo-p-dioxins and dibenzofurans in Quebec. A study was undertaken to document the bioaccumulation of PCBs, dioxins and furans in piscivorous birds and mammals in this area. Hooded and Common Merganser eggs were collected in nest boxes along the St. Maurice River and Common Merganser fledglings were collected at two sites on the river. Wild minks were trapped along the St. Maurice River and in a control area upstream. Analysis of pooled merganser eggs showed contamination with dioxins, furans and PCBs. Liver samples of fledglings were contaminated with 2,3,7,8-tetrachlorodibenzofuran at the downstream site. Analysis of mink livers showed a significant higher contamination with dioxins and furans in some downstream samples compared with the upstream samples.

ß-carotene and retinoids in eggs of Great Blue Herons (Ardea herodias) in relation to St Lawrence River contamination.

: The potential use of retinoids and ß-carotene as biomarkers in the eggs of the Great Blue Heron was investigated. In the spring of 1991, 65 eggs were collected from nine heronries (seven along the St Lawrence River and two reference sites). A method was specifically developed for the extraction and analysis of ß-carotene and the retinoids in heron egg yolks by reversed-phase HPLC. When results were expressed either as the molar ratio of retinol: retinyl palmitate or as retinyl palmitate concentration, significant differences were found between colonies; however, retinyl palmitate concentration was deemed the better biomarker because it was not significantly influenced by embryonic stage of development. Retinyl palmitate concentrations in freshwater colonies were negatively related to PCB congeners Nos 105 and 118 as well as their TCDD-EQ values (p < 0.02, r (2)=0.78). Egg tetrachloro-mono-ortho biphenyl concentrations were also negatively related to retinyl palmitate (p < 0.005, r (2)=0.90). With the exception of the two mono-ortho co-planar congeners detected in the present study, the contamination levels found in heron eggs were well below those found for other bird species in the Great Lakes area and, so far, no detrimental effects have been reported in Great Blue Heron populations in Quebec. These results suggest that retinyl palmitate may be useful as a sensitive and non-invasive biomarker for monitoring organochlorine contaminant effects in the Great Blue Heron in freshwater sites.

[Continuous phentolamine perfusion in the treatment of severe arterial hypertension associated with neuroblastoma]. / Phentolamine en perfusion continue dans le traitement d'une hypertension arterielle sévère associée à un neuroblastome.

Treatment of severe arterial hypertension associated with neuroblastoma is not well discussed in the literature. A six-month-old boy was referred for evaluation of an abdominal mass which proved to be neuroblastoma stage IV. Arterial hypertension of 26/16 kPa (190/110 mmHg) was also found. Because of the degree of malignancy and the risk of intra-tumoral haemorrhage, urgent management of the hypertension was required before proceeding to surgery. Phentolamine, a short-acting alpha-blocking agent, was administered as a continuous infusion of a 0.01 per cent solution, at a rate of 1 to 4 microgram X kg-1 X min-1 titrated according to the arterial blood pressure (BP), central venous pressure and urinary output. BP was rapidly controlled and the child went to surgery within 48 hours. The operation was uneventful but only 80 per cent of the tumour could be resected. Phentolamine was discontinued intraoperatively but was reinstituted postoperatively when hypertension recurred. With the return of normal intestinal function five days after surgery, phenoxybenzamine was begun p.o. and phentolamine was tapered over 24 hours and discontinued. A continuous infusion of phentolamine provided satisfactory control pre- and post-operatively with no significant hypotension. We consider this technique to be potentially very useful in the management of severe arterial hypertension associated with neuroblastoma, as it permits early surgical intervention under optimal conditions.