Tissue uptake of cadmium in brook trout during chronic sublethal exposure.
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Biomedical subjects
Publications and source records attributed to H C Freeman.
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An in vitro study on the effects of the contaminants polychlorinated biphenyl (Aroclor 1254) (PCB), methyl mercury (MeHg), arsenic (As), cadmium (Cd), and selenium (Se) on the biosynthesis of steroid hormones in the gray seal (Halichoerus grypus) indicated altered steroid biosynthesis. Biotransformed delta4-androstene-3, 17-dione (delta 4A), dehydroepiandrosterone, 11-ketotestosterone (11-KT), and testosterone (T) were detected in all seal testicular incubates. Yields of 11-KT were greatly increased in the presence of Aroclor 1254. All contaminants except As and Se stimulated the in vitro biosyntheses of T, with the greatest increase in production of T being in the Cd-treated tissue. Cortisol (F), corticosterone (B), aldosterone (ALDO) but no cortisone (E), were biosynthesized by the seal adrenal tissue. Corticosterone (B) was the principal transformation product in all incubations with less B produced by the treated adrenals than by the control. The lowest yeild of B was achieved by the Se-treated adrenal. The yeild of ALDO was also lower in all contaminant treated incubations, with Se and Cd giving the greatest inhibition. More F was biosynthesized by all the treated adrenals than by the control. The greatest increase of production of F(6-fold) from progesterone was by the As-treated adrenal.
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Hematological and blood chemistry values were examined in harp seals (Pagophilus groenlandicus) exposed to daily oral dosages of methylmercuric chloride (MMC). Two seals, exposed to 0.25 mg MMC/kg body weight/day for 60 and 90 days, respectively, did not show abnormal blood values. Two other seals exposed to 25.0 mg MMC/kg body weight/day died on day 20 and 26 of exposure. Blood parameters indicated toxic hepatitis, uremia and renal failure. Total mercury and methylmercury values in the tissues of the experimental animals indicated that harp seals can tolerate high levels of mercury in the brain and that the observed renal and hepatic dysfunction were related to the high accumulation of mercury in these tissues. Tests of renal function are useful in cases of severe methylmercury poisoning.
A method is described for determining selenium in fish tissues, meat, cereals, milk powder, and other materials by flameless atomic absorption spectrophotometry. Samples are solubilized in HNO3 and atomized in a graphite furnace in the presence of nickel nitrate. Recoveries of 0.500 and 1.000 microgram selenium added to several fish samples averaged 99.0 and 98.3%, respectively, with standard deviations of 5.3 and 4.0. Results agreed with those obtained for samples previously analyzed by fluorometry, and with results for NBS Standard Reference Material. The detection limit was 3 ng/ml solution and 50 ng/g sample.
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1. The proton NMR spectra of oxidised and reduced French bean plastocyanin have been recorded on a 270 MHz pulsed spctrometer. 2. The spectrum of a mixture containing the protein in the paramagnetic Cu(II) and diamagnetic Cu(I) states is a superposition of the separate spectra. When ferrirate spectra. 3. The results show that self-exchange between Cu(II)- and Cu(I)-plastocyanin is slow on the NMR time scale (kex less than 2-10(4) M-1-s-1 at 50 degrees C), and that electron transfer in the presence of ferricyanide is rapid (k greater than 1-10(5) M-1-s-1).
Arsenite ion, as arsenic trichloride was extracted into benzene from strongly acidified tissue homogenates. Following this, arsenite was extracted from the benzene into water, made up in 1N HCl and analyzed polarographically. Arsenate ion, left in the homogenate after arsenite extraction is isolated in exactly the same way following treatment of the homogenate with cuprous ion to reduce arsenate to arsenite ion. Treatment of the acidified homogenate with cuprous ion prior to extraction gives a homogenate which is readily analyzed for total "inorganic" arsenic. The method was efficient to a maximum level of about 20 mug inorganic arsenic since at higher levels lower recoveries were found. Analysis of a variety of marine biological specimens, with levels of total arsenic up to 40.5 ppm, indicated little of this arsenic was present in an inorganic form. Post mortem reduction of arsenate to arsenite was found to occur rapidly in fish tissue.
Livers from brook trout (Salvelinus fontinalis) held in water containing 3.8 p.p.m. (mg/l) Corexit and in water containing 3.8 p.p.m. Corexit + 0.2 p.p.m. polychlorinated biphenyl (PCB) were firmer in texture than livers taken from control trout held in fresh water. The testes from the PCB-treated trout were darker in color, smaller in size, contained less spermatic fluid, and appeared to be regressed when compared with testes from the control fish. Only 72% of the eggs from PCB-treated trout hatched compared to 92% for control eggs when eggs were incubated in fresh water. Fertilized eggs incubated in water containing 0.2 p.p.m. PCB + 3.8 p.p.m. Corexit resulted in less than 1% of the eggs from the untreated fish and none of the eggs from PCB-treated fish being hatched. The young fish from the control group lived only a few days in the water containing PCB. PCB greatly stimulated the in vitro 11beta-hydroxylation of testosterone by trout testicular tissue. There was no significant change in 11-ketotestosterone blood levels in maturing brook trout after treatment with 3.8 p.p.m. Corexit or 3.8 p.p.m. Corexit + 0.2 p.p.m. PCB for 21 days during the final stages of maturation. It is thought that sublethal levels of PCB can interfere with the reproduction process in this species.