Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Selenium Compounds”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 1,441 records · Page 80Linked to original sources

Chemical forms of selenium in the metal-resistant bacterium Ralstonia metallidurans CH34 exposed to selenite and selenate.

Ralstonia metallidurans CH34, a soil bacterium resistant to a variety of metals, is known to reduce selenite to intracellular granules of elemental selenium (Se(0)). We have studied the kinetics of selenite (Se(IV)) and selenate (Se(VI)) accumulation and used X-ray absorption spectroscopy to identify the accumulated form of selenate, as well as possible chemical intermediates during the transformation of these two oxyanions. When introduced during the lag phase, the presence of selenite increased the duration of this phase, as previously observed. Selenite introduction was followed by a period of slow uptake, during which the bacteria contained Se(0) and alkyl selenide in equivalent proportions. This suggests that two reactions with similar kinetics take place: an assimilatory pathway leading to alkyl selenide and a slow detoxification pathway leading to Se(0). Subsequently, selenite uptake strongly increased (up to 340 mg Se per g of proteins) and Se(0) was the predominant transformation product, suggesting an activation of selenite transport and reduction systems after several hours of contact. Exposure to selenate did not induce an increase in the lag phase duration, and the bacteria accumulated approximately 25-fold less Se than when exposed to selenite. Se(IV) was detected as a transient species in the first 12 h after selenate introduction, Se(0) also occurred as a minor species, and the major accumulated form was alkyl selenide. Thus, in the present experimental conditions, selenate mostly follows an assimilatory pathway and the reduction pathway is not activated upon selenate exposure. These results show that R. metallidurans CH34 may be suitable for the remediation of selenite-, but not selenate-, contaminated environments.

Biodegradation, Environmental↗

The terminal reductases for selenate and nitrate respiration in Thauera selenatis are two distinct enzymes.

A number of approaches have been used to show that a recently isolated selenate-respiring bacterium, Thauera selenatis, is able to synthesize both a selenate reductase (SR) and a nitrate reductase (NR). (i) The pH optimum of the SR was found to be 6.0; that of the NR was 7.0. (ii) The presence of nitrate did not inhibit selenate reduction in selenate-grown cells. (iii) In cell extracts, the highest SR or NR activity was observed in cells grown with the respective electron acceptor. (iv) Mutants that were unable to grow with nitrate as the terminal electron acceptor and lacked NR activity were isolated; these mutants grew normally with selenate and synthesized SR. (v) The SR was found in the periplasmic space of the cell, whereas the NR was present in the cytoplasmic membrane. A hypothetical electron transport system involving the SR is described.

Bacteria, Anaerobic↗

Involvement of superoxide dismutases in the response of Escherichia coli to selenium oxides.

Selenium can provoke contrasting effects on living organisms. It is an essential trace element, and low concentrations have beneficial effects, such as the reduction of the incidence of cancer. However, higher concentrations of selenium salts can be toxic and mutagenic. The bases for both toxicity and protection are not clearly understood. To provide insights into these mechanisms, we analyzed the proteomic response of Escherichia coli cells to selenate and selenite treatment under aerobic conditions. We identified 23 proteins induced by both oxides and ca. 20 proteins specifically induced by each oxide. A striking result was the selenite induction of 8 enzymes with antioxidant properties, particularly the manganese and iron superoxide dismutases (SodA and SodB). The selenium inductions of sodA and sodB were controlled by the transcriptional regulators SoxRS and Fur, respectively. Strains with decreased superoxide dismutase activities were severely impaired in selenium oxide tolerance. Pretreatment with a sublethal selenite concentration triggered an adaptive response dependent upon SoxRS, conferring increased selenite tolerance. Altogether, our data indicate that superoxide dismutase activity is essential for the cellular defense against selenium salts, suggesting that superoxide production is a major mechanism of selenium toxicity under aerobic conditions.

Aerobiosis↗

Selenium is mobilized in vivo from free selenocysteine and is incorporated specifically into formate dehydrogenase H and tRNA nucleosides.

Selenophosphate synthetase (SPS), the selD gene product from Escherichia coli, catalyzes the biosynthesis of monoselenophosphate, AMP, and orthophosphate in a 1:1:1 ratio from selenide and ATP. It was recently demonstrated that selenium delivered from selenocysteine by an E. coli NifS-like protein could replace free selenide in the in vitro SPS assay for selenophosphate formation (G. M. Lacourciere, H. Mihara, T. Kurihara, N. Esaki, and T. C. Stadtman, J. Biol. Chem. 275:23769-23773, 2000). During growth of E. coli in the presence of 0.1 microM (75)SeO(3)(2-) and increasing amounts of L-selenocysteine, a concomitant decrease in (75)Se incorporation into formate dehydrogenase H and nucleosides of bulk tRNA was observed. This is consistent with the mobilization of selenium from L-selenocysteine in vivo and its use in selenophosphate formation. The ability of E. coli to utilize selenocysteine as a selenium source for selenophosphate biosynthesis in vivo supports the participation of the NifS-like proteins in selenium metabolism.

Biological Transport↗

Effects of selenium and copper supplementation on the growth of beef steers.

During the grazing seasons of 1978 and 1979, 126 Hereford cross Friesian and 25 Charolais cross Friesian steers were used in controlled trials of the effects of injecting them with copper and, or, selenium. In both seasons the unsupplemented steers had low blood concentrations of copper, selenium and glutathione peroxidase, whereas the supplemented steers maintained their serum copper concentrations within the normal range and had significantly higher whole blood concentrations of selenium and glutathione peroxidase than the unsupplemented animals. Supplementing the steers with 400 mg copper during 1978 increased their growth rate by 0.032 kg/day and supplementing them with 200 mg copper during 1979 increased it by 0.080 kg/day. Supplementing the steers in each year with two doses of selenium, each of 0.15 mg selenium/kg bodyweight, increased their growth rate by 0.041 kg/day in 1978 and by 0.060 kg/day in 1979. There was no interaction between the selenium and copper treatments and the total increases in liveweight gains due to both supplements were around 11 kg in 1978 and 16 kg in 1979.

Animals↗

Assimilation of selenate and selenite by Salmonella typhimurium.

A comparative study of selenate and selenite assimilation by Salmonella typhimurium revealed that selenite was not transported by the sulphate permease. Selenite uptake could be detected both in wild-type cells repressed for sulphate transport and in mutants that lacked a functional sulphate permease. In contrast, selenate was assimilated by the same process as was sulphate; selenate transport was repressed under the same conditions which repressed sulphate uptake and was absent in permeaseless mutants. Selenite transport was absent if cells were glucose starved or treated with either azide or p-chloromercuribenzoate. The pH optimum was between pH 6 and pH 7; transport was most rapid at 36 degrees C. The double reciprocal plot for selenite transport at different substrate concentrations was biphasic: between 10 and 50 microM SeO32(-) the apparent Km was 37.8 microM, and at higher concentrations, 2.87 mM. The transport rate for 0.1 mM SeO32(-) was significantly stimulated by sulphite concentrations up to 5.0 mM, with a maximum at 3.0 mM SO32-. The results establish a selenite transport process, in S. typhimurium, as the initial step of an assimilatory pathway selective for selenium.

Azides↗

Structural determinants of substrate specificity of the erythrocyte anion transporter.

The human erythrocyte anion transport protein (AE1) mediates the rapid, tightly coupled, electroneutral transmembrane exchange of bicarbonate for chloride. AE1 transports a wide range of oxyanions, such as phosphate, sulfate and the physiological substrate bicarbonate. In this study, the transport characteristics of the selenium based oxyanions selenite (SeO3(2-)) and selenate (SeO4(2-)) were determined. The pH dependence of selenate influx was consistent with a titratable carrier having a extracellular pK value of 5.67 +2- 0.09. In contrast, the pH dependence of selenite influx had a maximum near pH 7.0, consistent with a hypothesis proposed by Labotka and Omachi (J. Biol. Chem. 263: 1166-1173, 1988) that the pH maximum of the transport of titratable anions is located at the midpoint between the pK of the carrier (5.7) and the pK of the titratable anion (8.3). Analysis of the transport rates and structures of these as well as a variety of other oxyanions reported in the literature suggested that oxyanions bind in a three-oxygen atom binding site, and that the formation of the transition state necessary for transport is sterically restrained by oxyanions that protrude in a direction perpendicular to the three-oxygen binding plane. This hypothesis can be used to predict the relationship between the transport rates of many oxyanions reported in the literature and should prove useful in helping to understand the molecular mechanism of AE1 mediated transport.

Anion Transport Proteins↗

Selenium regulates cyclooxygenase-2 and extracellular signal-regulated kinase signaling pathways by activating AMP-activated protein kinase in colon cancer cells.

Epidemiologic and experimental evidences indicate that selenium, an essential trace element, can reduce the risk of a variety of cancers. Protection against certain types of cancers, particularly colorectal cancers, is closely associated with pathways involving cyclooxygenase-2 (COX-2). We found that AMP-activated protein kinase (AMPK), which functions as a cellular energy sensor, mediates critical anticancer effects of selenium via a COX-2/prostaglandin E(2) signaling pathway. Selenium activated AMPK in tumor xenografts as well as in colon cancer cell lines, and this activation seemed to be essential to the decrease in COX-2 expressions. Transduction with dominant-negative AMPK into colon cancer cells or application of cox-2(-/-)-negative cells supported the evidence that AMPK is an upstream signal of COX-2 and inhibits cell proliferation. In HT-29 colon cancer cells, carcinogenic agent 12-O-tetradecanoylphorbol-13-acetate (TPA) activated extracellular signal-regulated kinase (ERK) that led to COX-2 expression and selenium blocked the TPA-induced ERK and COX-2 activation via AMPK. We also showed the role of a reactive oxygen species as an AMPK activation signal in selenium-treated cells. We propose that AMPK is a novel and critical regulatory component in selenium-induced cancer cell death, further implying AMPK as a prime target of tumorigenesis.

AMP-Activated Protein Kinases↗

Inhibition of androgen receptor signaling by selenite and methylseleninic acid in prostate cancer cells: two distinct mechanisms of action.

The development of prostate cancer and its progression to a hormone-refractory state is highly dependent on androgen receptor (AR) expression. Recent studies have shown that the selenium-based compound methylseleninic acid (MSeA) can disrupt AR signaling in prostate cancer cells. We have found that selenite can inhibit AR expression and activity in LAPC-4 and LNCaP prostate cancer cells as well but through a different mechanism. On entering the cell, selenite consumes reduced glutathione (GSH) and generates superoxide radicals. Pretreatment with N-acetylcysteine, a GSH precursor, blocked the down-regulation of AR mRNA and protein expression by selenite and restored AR ligand binding and prostate-specific antigen expression to control levels. MSeA reacts with reduced GSH within the cell; however, N-acetylcysteine did not effect MSeA-induced down-regulation of AR and prostate-specific antigen. The superoxide dismutase mimetic MnTMPyP was also found to prevent the decrease in AR expression caused by selenite but not by MSeA. A Sp1-binding site in the AR promoter is a key regulatory component for its expression. Selenite decreased Sp1 expression and activity, whereas MSeA did not. The inhibition of Sp1 by selenite was reversed in the presence of N-acetylcysteine. In conclusion, we have found that selenite and MSeA disrupt AR signaling by distinct mechanisms. The inhibition of AR expression and activity by selenite occurs via a redox mechanism involving GSH, superoxide, and Sp1.

Acetylcysteine↗

Comparative effect of selenate and selenite on serum selenium concentration and glutathione peroxidase activity in selenium-depleted rats.

The biological effect of selenate and selenite was compared in selenium-depleted rats by using both serum selenium concentration and glutathione peroxidase activity as an indicator of body selenium status. A single oral dose of selenium (125 micrograms/kg body weight) as sodium selenate or sodium selenite increased serum selenium concentration and glutathione peroxidase activity significantly (p less than 0.001). The effect of selenate and selenite on serum selenium and glutathione peroxidase activity was similar. Serum selenium concentration correlated positively with serum glutathione peroxidase activity both before (r = 0.815; p less than 0.001) and after (r = 0.800; p less than 0.001) treatment. These results indicate that the biological availability of selenate and selenite is similar.

Administration, Oral↗

Rapid response of transient acantholytic dermatosis to selenium sulfide treatment for pityriasis versicolor.

The observation of a 51-year-old male patient with transient acantholytic dermatosis (TAD) is briefly reported. The discrete eruption, composed of erythematous escoriated papules and papulovesicles, moderately itching, was located on the back and chest, more permanent during the summer season. The biopsy revealed suprabasal acantholysis and Darier-like elements. Lesions of pityriasis versicolor, confirmed by microscopic examination and fluorescence in Wood's light, were intermingled with TAD in the same patient. A topical treatment with selenium sulfide brought TAD lesions to the disappearance in 1 week. Comments are made in relation with the possibility of Malassezia furfur to induce acantholytic phenomena.

Acantholysis↗

Comparative clinical trial of bifonazole solution versus selenium sulphide shampoo in the treatment of pityriasis versicolor.

38 patients were entered into a controlled randomised trial, comparing two forms of topical treatment for pityriasis versicolor. Diagnosis was made on clinical criteria and confirmed by direct microscopic examination of Parker Quink/KOH preparations. 20 patients were treated with bifonazole solution daily for 2 weeks. 18 patients were treated with 2.5% selenium sulphide shampoo daily for one week and weekly for six weeks. Mycological examination showed that Malassezia furfur was present in all patients prior to treatment. At the end of the trial, 1 patient (5%) treated with bifonazole and 4 patients (22%) of those treated with selenium sulphide shampoo showed the presence of the fungus in the skin. This study demonstrates that bifonazole solution is an effective and well-tolerated form of treatment for pityriasis versicolor. A 2-week course of bifonazole solution was as effective as a 7-week course of selenium sulphide shampoo in eradicating the disease and had a lower relapse rate at 4 weeks.

Administration, Topical↗

On the influence of topically applied drugs on cell kinetics in the sebaceous gland. Investigations with the example of selenium disulfide in the Syrian hamster ear.

60 male Syrian hamsters were treated on one ear with 2.5% selenium disulfide in a surfactant base and on the other ear with the same surfactant base. After treatment 15 animals were investigated by 3H-thymidine autoradiography, 15 animals by the colcemid method and 15 animals by the in vivo double labelling technique with 3H- and 14C-thymidine. In 15 animals the porportion of labeled cells was determined which still had contact with the basal lamina in the sebaceous gland 6 days after 3H-thymidine injection. Besides an increase in sebaceous gland size and in cell proliferation, a shortening of the S phase and a reduction of the labeled sebaceous gland cells which still have contact with the basal lamina of the sebaceous gland 6 days after 3H - thymidine injection were determined.

Animals↗

Antioxidant activity in cells and organs.

Antioxidant activity in cells occurs at several levels. The present work focuses on some aspects of enzymatic antioxidant defense. In particular, the so-called ancillary enzymes and transport systems are presented. Recent aspects on the control of the levels of antioxidant enzymes include the oxyR regulon in microorganisms as well as the response to DNA hypomethylation in livers of mice. Ebselen is a novel selenoorganic compound with antioxidant activity capable of conferring protection against oxidative challenge. Its activity to catalyse the GSH-peroxidase reaction is thought to mediate the effect in intact cells. The nonenzymatic antioxidant defense (e.g., vitamins E and C and other natural or chemically synthesized compounds) form an important complementary part of cellular antioxidant defense.

Animals↗

Optical spectra of nanowires of Cu and Zn chalcogenides.

Nanowires of CuS, ZnS, CuSe, and ZnSe, with diameters in the 5-150-nm range and high aspect ratios, have been prepared with the use of surfactants and characterized by X-ray diffraction and electron microscopy. Electronic absorption spectra and photoluminescence spectra of chalcogenide nanowires have been studied. The spectra show blue-shifts compared with those of bulk samples.

Chalcogens↗

Photoluminescence decay dynamics and mechanism of energy transfer in undoped and Mn2+ doped ZnSe nanoparticles.

Energy transfer dynamics in Mn2+-doped ZnSe nanoparticles have been studied by monitoring the photoluminescence using time-integrated and time-resolved spectroscopic techniques. Upon Mn2+ doping, static photoluminescence (PL) spectra show that the bandedge excitonic state is quenched and the characteristic Mn2+ emission appears at 584 nm. Picosecond PL kinetics and femtosecond transient absorption studies have both found that the Mn2+ doping substantially shortens the average lifetimes of the bandedge excitonic state as well as shallow trap states. The energy transfer from ZnSe to Mn2+ likely follows two mechanisms, one mediated through trap states and another without.

Computer Simulation↗