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Summary We conducted a survey of the presence, prevalence and diversity of gastrointestinal helminths in faecal samples and stomach
contents of three turtle species, — Erymnochelys madagascariensis (Chelonia: Podocnemididae), Pelomedusa subrufa and Pelusios castanoides (Chelonia: Pelomedusidae), — from several localities in Madagascar. Four nematode species were detected: Atractis chabaudi, Camallanus chelonius, Falcaustra pelusios, and Spiroxys sp. E. madagascariensis, with all four species, had the greatest helminth diversity. A. chabaudi was the community’s core species, whereas Spiroxys sp. was a satellite species. Only two species (A. chabaudi and Spiroxys sp.) were found in P. subrufa and only one, Spiroxys sp., in P. castanoides. These are the first helminthological data on E. madagascariensis, one of the most threatened freshwater turtles in the world. 相似文献
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Borras Merce; Valdivielso Jose M.; Egido Ramon; Vicente de Vera Pilar; Bordalba Josep Ramon; Fernandez Elvira 《Nephrology, dialysis, transplantation》2006,21(3):789-791
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Juan J. Muoz Cristina Roca Jos L. Santos Miguel Arroyo Rafael E. de Salamanca 《Basic & clinical pharmacology & toxicology》1993,73(4):189-191
Two alternatives for the treatment of lead intoxication, administration of zinc or a thiol donor, S-adenosyl-L-methionine (SAM), were analysed. Rats were exposed to lead (Pb)-acetate (60 mg/1) in drinking water during 90 days; one group also received SO4Zn in water (40 mg/l), while another received both Pb and SAM (5 mg/24 hr intraperitoneally. Erythrocytic δ-aminolaevulinic dehydratase (ALA-D) activity was significantly reduced (P<0.001) both in rats receiving Pb alone and in rats receiving Pb and each of the other two treatments. The high erythrocytic uroporphyrinogen synthetase (URO-S) activity noticed in Pb administered rats, was significantly (P< 0.001) reduced in animals treated either with zinc or with SAM. Hepatic ALA-D activity tended to decrease while renal enzyme activity was not modified by the low level Pb exposure used in this work. Interestingly, SAM treated rats in both tissues exhibited significantly (P<0.01) higher activities of the enzyme. It is argued that SAM treatment causes a surplus of thiols that allows the full expression of ALA-D catalytic activity. 相似文献
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The aim of this work is to evaluate citrate in a group of patients with calcium oxalate urolithiasis and in a control group
for detecting possible differences between the two groups. The mean urinary concentration in the stone-formers was found significantly
lower than in the controls. Particularly interesting was the correlation study between citrate and calcium. It was found that
patients with hypocitraturia have hypercalciuria. Thus, it is particularly interesting to point out the importance of citrate
in preventing the risk of lithiasis in the group of stone-formers studied by us. 相似文献
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Jordi Llorens Cristina Su ol Josep M. Tusell Eduard Rodrí guez-Farr 《Neurotoxicology and teratology》1990,12(6):607-610
The inhibition of [35S]t-butylbicyclophosphorothionate ([35S]TBPS) binding to the GABAA receptor by the insecticide γ-hexachlorocyclohexane, lindane, was studied in several brain regions and using different membrane preparation methods, both in vitro and after dosing the animals with the chemical. In the latter studies, the amount of lindane remaining in the membrane suspensions used for binding assays was determined. In vitro data showed values of IC50 from 150 to 1675 nM, varying in function of the membrane preparation method used. This may account for the discrepancies in IC50 values found in the literature. IC50 values within the range of 150–250 nM were determined using extensively washed membranes from several brain regions, so no evidence arose for brain regional differences in the affinity of lindane for the TBPS binding site. After different schedules of acute treatment with lindane, we found a manifest relationship between the extent of the observable inhibition of [35S]TBPS binding and the lindane amount remaining in the membrane suspensions used for binding assays. This relationship was in good agreement with the in vitro data, so no support for an in vivo acute regulation of the binding site was obtained. 相似文献