Organoselenium Chemistry. Preparation of Allyl and Homoallyl Amines by Aminomethylation of Phenylseleno-Substituted Allyl Tin Reagents

Metalation of methallyl phenyl selenide, allyl phenyl selenide, and methallyl phenyl sulfide followed by tri-n-butylstannylation gave exclusively the γ-stannylated sulfide or selenide (e.g., 1-phenylseleno-2-methyl-3-tri-n-butylstannyl-1-propene ( 5 )). Compound 5 reacts with a series of immonium electrophiles to give products of aminomethylation α- to selenium. Electrophiles have included N-(bromomethyl)phthalimide/ZnBr₂, Eschenmoser salt (dimethylmethyleneammonium iodide), and Mannich reagents generated in situ from diethylamine, piperidine, isopropyl sarcosinate and benzylmethylamine. The selenide from the last of these amines (N, 3-dimethyl-N-benzyl-2-phenylseleno-3-butenamine, 10 ) has been subjected to further transformations as follows: (1) treatment of 10 with trimethylstannyllithium results in replacement of phenylseleno by stannyl; this allyltin ( 11 ) can then again be aminomethylated giving compound 12 or 13 ; (2) oxidation of 10 gives amino alcohol 14 by [2, 3] sigmatropic rearrangement of the allyl selenoxide; (3) photolysis of 10 results in 1,3-rearrangement of the phenylseleno group; oxidative rearrangement of this allyl selenide gives amino alcohol 16 . The phthalimidomethylation product ( 6 ) is converted to a precursor for the side chain of the cytokinin zeatin by oxidation and [2, 3] sigmatropic rearrangement.     

Reversibly Redox‐Switchable Anionic Surfactant Contains Two Selenium Atoms

To better control the interfacial activities of selenium‐containing surfactants, a redox‐switchable anionic surfactant containing 2 selenium atoms, namely sodium 3‐((3‐(benzylselanyl)propyl)selanyl)propyl sulfate (SBSe₂S), has been designed and synthesized. Upon oxidation by H₂O₂, the 2 divalent selenide groups in the hydrophobic tail of SBSe₂S are converted into the corresponding selenoxides. The initial hydrophobic tail of SBSe₂S gets separated into 3 segments by 2 hydrophilic selenoxide groups, destroying the bola‐type structure. The interfacial activities of SBSe₂S in aqueous solution could thereby be switched off to a greater degree than in the case of its counterparts containing only a single selenium atom. After reduction with Na₂SO₃, the 2 selenoxide groups in SBSe₂S‐Ox are restored to the initial selenide. Consequently, the interfacial activities of SBSe₂S could be reversibly switched by alternate addition of H₂O₂ and Na₂SO₃, without obvious deterioration over 5 cycles.     

Synthesis and Characterization of Cadmium Selenide (CdSe) Nanoparticles Using Trigonal Selenium (t-Se) Nanorods as Selenium Source

Cadmium selenide (CdSe) nanoparticles were synthesized through colloidal method in aqueous medium using the reaction intermediates selenium nanorods as selenium source. Trigonal selenium nanorods (t-Se) were synthesized in water by the reduction method in the presence of sodium borohydride at 60?°C using sodium selenite (Na₂SeO₃) as selenium source. These selenium nanorods were further utilized to synthesis cadmium selenide nanoparticles at 100?°C in water. The synthesized nanorods and nanoparticles were characterized using XRD, SEM, TEM and XPS analysis. X-ray diffraction (XRD) analysis shown that the nanorods possess trigonal phase while the nanoparticles possess a cubic zinc blende structure. Scanning electron microscope (SEM) analysis of the prepared hexagonal shaped nanorods reveals the diameter of the nanorods are about 150 nm. Transmission electron microscopy (TEM) analysis shows the size of the synthesized CdSe nanoparticles are about 4–8 nm. X-ray photoelectron spectroscopy (XPS) analysis illustrates the presence of respective elements Cd, Se with its corresponding oxidation states. The activity of nano selenium rods in aqueous solution during the conversion of cadmium selenide nanoparticles was discussed.     

Korean Red Ginseng Improves Astrocytic Mitochondrial Function by Upregulating HO-1-Mediated AMPKα–PGC-1α–ERRα Circuit after Traumatic Brain Injury

Heme oxygenase-1 (HO-1) exerts beneficial effects, including angiogenesis and energy metabolism via the peroxisome proliferator-activating receptor-γ coactivator-1α (PGC-1α)–estrogen-related receptor α (ERRα) pathway in astrocytes. However, the role of Korean red ginseng extract (KRGE) in HO-1-mediated mitochondrial function in traumatic brain injury (TBI) is not well-elucidated. We found that HO-1 was upregulated in astrocytes located in peri-injured brain regions after a TBI, following exposure to KRGE. Experiments with pharmacological inhibitors and target-specific siRNAs revealed that HO-1 levels highly correlated with increased AMP-activated protein kinase α (AMPKα) activation, which led to the PGC-1α-ERRα axis-induced increases in mitochondrial functions (detected based on expression of cytochrome c oxidase subunit 2 (MTCO2) and cytochrome c as well as O₂ consumption and ATP production). Knockdown of ERRα significantly reduced the p-AMPKα/AMPKα ratio and PGC-1α expression, leading to AMPKα–PGC-1α–ERRα circuit formation. Inactivation of HO by injecting the HO inhibitor Sn(IV) protoporphyrin IX dichloride diminished the expression of p-AMPKα, PGC-1α, ERRα, MTCO2, and cytochrome c in the KRGE-administered peri-injured region of a brain subjected to TBI. These data suggest that KRGE enhanced astrocytic mitochondrial function via a HO-1-mediated AMPKα–PGC-1α–ERRα circuit and consequent oxidative phosphorylation, O₂ consumption, and ATP production. This circuit may play an important role in repairing neurovascular function after TBI in the peri-injured region by stimulating astrocytic mitochondrial biogenesis.     

Necroptosis Inhibition by Hydrogen Sulfide Alleviated Hypoxia-Induced Cardiac Fibroblasts Proliferation via Sirtuin 3

Myocardial ischemia or hypoxia can induce myocardial fibroblast proliferation and myocardial fibrosis. Hydrogen sulfide (H₂S) is a gasotransmitter with multiple physiological functions. In our present study, primary cardiac fibroblasts were incubated with H₂S donor sodium hydrosulfide (NaHS, 50 μM) for 4 h followed by hypoxia stimulation (containing 5% CO₂ and 1% O₂) for 4 h. Then, the preventive effects on cardiac fibroblast proliferation and the possible mechanisms were investigated. Our results showed that NaHS reduced the cardiac fibroblast number, decreased the hydroxyproline content; inhibited the EdU positive ratio; and down-regulated the expressions of α-smooth muscle actin (α-SMA), the antigen identified by monoclonal antibody Ki67 (Ki67), proliferating cell nuclear antigen (PCNA), collagen I, and collagen III, suggesting that hypoxia-induced cardiac fibroblasts proliferation was suppressed by NaHS. NaHS improved the mitochondrial membrane potential and attenuated oxidative stress, and inhibited dynamin-related protein 1 (DRP1), but enhanced optic atrophy protein 1 (OPA1) expression. NaHS down-regulated receptor interacting protein kinase 1 (RIPK1) and RIPK3 expression, suggesting that necroptosis was alleviated. NaHS increased the sirtuin 3 (SIRT3) expressions in hypoxia-induced cardiac fibroblasts. Moreover, after SIRT3 siRNA transfection, the inhibitory effects on cardiac fibroblast proliferation, oxidative stress, and necroptosis were weakened. In summary, necroptosis inhibition by exogenous H₂S alleviated hypoxia-induced cardiac fibroblast proliferation via SIRT3.     

Dual Activities of Oxidation and Oxidative Decarboxylation by Flavoenzymes

Specific flavoenzyme oxidases catalyze oxidative decarboxylation in addition to their classical oxidation reactions in the same active sites. The mechanisms underlying oxidative decarboxylation by these enzymes and how they control their two activities are not clearly known. This article reviews the current state of knowledge of four enzymes from the l -amino acid oxidase and l -hydroxy acid oxidase families, including l -tryptophan 2-monooxygenase, l -phenylalanine 2-oxidase and l -lysine oxidase/monooxygenase and lactate monooxygenase which catalyze substrate oxidation and oxidative decarboxylation. Apart from specific interactions to allow substrate oxidation by the flavin cofactor, specific binding of oxidized product in the active sites appears to be important for enabling subsequent decarboxylation by these enzymes. Based on recent findings of l -lysine oxidase/monooxygenase, we propose that nucleophilic attack of H₂O₂ on the imino acid product is the mechanism enabling oxidative decarboxylation.     

Impact of Hydrogen Sulfide on Mitochondrial and Bacterial Bioenergetics

This review focuses on the effects of hydrogen sulfide (H₂S) on the unique bioenergetic molecular machines in mitochondria and bacteria—the protein complexes of electron transport chains and associated enzymes. H₂S, along with nitric oxide and carbon monoxide, belongs to the class of endogenous gaseous signaling molecules. This compound plays critical roles in physiology and pathophysiology. Enzymes implicated in H₂S metabolism and physiological actions are promising targets for novel pharmaceutical agents. The biological effects of H₂S are biphasic, changing from cytoprotection to cytotoxicity through increasing the compound concentration. In mammals, H₂S enhances the activity of F_oF₁-ATP (adenosine triphosphate) synthase and lactate dehydrogenase via their S-sulfhydration, thereby stimulating mitochondrial electron transport. H₂S serves as an electron donor for the mitochondrial respiratory chain via sulfide quinone oxidoreductase and cytochrome c oxidase at low H₂S levels. The latter enzyme is inhibited by high H₂S concentrations, resulting in the reversible inhibition of electron transport and ATP production in mitochondria. In the branched respiratory chain of Escherichia coli, H₂S inhibits the bo₃ terminal oxidase but does not affect the alternative bd-type oxidases. Thus, in E. coli and presumably other bacteria, cytochrome bd permits respiration and cell growth in H₂S-rich environments. A complete picture of the impact of H₂S on bioenergetics is lacking, but this field is fast-moving, and active ongoing research on this topic will likely shed light on additional, yet unknown biological effects.     

Selective oxidation of H<Subscript>2</Subscript>S to ammonium thiosulfate and elemental sulfur using mixtures of V-Bi-O and Sb<Subscript>2</Subscript>O<Subscript>4</Subscript>

The selective oxidation of hydrogen sulfide in the presence of excess water and ammonia was investigated by using vanadium-bismuth based mixed oxide catalysts. Synergistic effect on catalytic activity was observed for the mechanical mixtures of V-Bi-O and Sb₂O₄. Temperature programmed oxidation (TPO), X-ray photoelectron spectroscopy (XPS), and two separated bed reactivity test results supported the role of Sb₂O₄ for reoxidizing the reduced V-Bi-O during the reaction. This paper is dedicated to Professor Hyun-Ku Rhee on the occasion of his retirement from Seoul National University.     

Insulin-Dependent H2O2 Production Is Higher in Muscle Fibers of Mice Fed with a High-Fat Diet

Insulin resistance is defined as a reduced ability of insulin to stimulate glucose utilization. C57BL/6 mice fed with a high-fat diet (HFD) are a model of insulin resistance. In skeletal muscle, hydrogen peroxide (H₂O₂) produced by NADPH oxidase 2 (NOX2) is involved in signaling pathways triggered by insulin. We evaluated oxidative status in skeletal muscle fibers from insulin-resistant and control mice by determining H₂O₂ generation (HyPer probe), reduced-to-oxidized glutathione ratio and NOX2 expression. After eight weeks of HFD, insulin-dependent glucose uptake was impaired in skeletal muscle fibers when compared with control muscle fibers. Insulin-resistant mice showed increased insulin-stimulated H₂O₂ release and decreased reduced-to-oxidized glutathione ratio (GSH/GSSG). In addition, p47^phox and gp91^phox (NOX2 subunits) mRNA levels were also high (~3-fold in HFD mice compared to controls), while protein levels were 6.8- and 1.6-fold higher, respectively. Using apocynin (NOX2 inhibitor) during the HFD feeding period, the oxidative intracellular environment was diminished and skeletal muscle insulin-dependent glucose uptake restored. Our results indicate that insulin-resistant mice have increased H₂O₂ release upon insulin stimulation when compared with control animals, which appears to be mediated by an increase in NOX2 expression.     

A Caged,Destabilized, Free Radical Intermediate in the Q‐Cycle

The Rieske/cytochrome b complexes, also known as cytochrome bc complexes, catalyze a unique oxidant‐induced reduction reaction at their quinol oxidase (Q_o) sites, in which substrate hydroquinone reduces two distinct electron transfer chains, one through a series of high‐potential electron carriers, the second through low‐potential cytochrome b. This reaction is a critical step in energy storage by the Q‐cycle. The semiquinone intermediate in this reaction can reduce O₂ to produce deleterious superoxide. It is yet unknown how the enzyme controls this reaction, though numerous models have been proposed. In previous work, we trapped a Q‐cycle semiquinone anion intermediate, termed SQ_o, in bacterial cytochrome bc₁ by rapid freeze‐quenching. In this work, we apply pulsed‐EPR techniques to determine the location and properties of SQ_o in the mitochondrial complex. In contrast to semiquinone intermediates in other enzymes, SQ_o is not thermodynamically stabilized, and can even be destabilized with respect to solution. It is trapped in Q_o at a site that is distinct from previously described inhibitor‐binding sites, yet sufficiently close to cytochrome b_L to allow rapid electron transfer. The binding site and EPR analyses show that SQ_o is not stabilized by hydrogen bonds to proteins. The formation of SQ_o involves “stripping” of both substrate ‐OH protons during the initial oxidation step, as well as conformational changes of the semiquinone and Q_o proteins. The resulting charged radical is kinetically trapped, rather than thermodynamically stabilized (as in most enzymatic semiquinone species), conserving redox energy to drive electron transfer to cytochrome b_L while minimizing certain Q‐cycle bypass reactions, including oxidation of prereduced cytochrome b and reduction of O₂.     

Human Genetic Disorders Resulting in Systemic Selenoprotein Deficiency

Selenium, a trace element fundamental to human health, is incorporated as the amino acid selenocysteine (Sec) into more than 25 proteins, referred to as selenoproteins. Human mutations in SECISBP2, SEPSECS and TRU-TCA1-1, three genes essential in the selenocysteine incorporation pathway, affect the expression of most if not all selenoproteins. Systemic selenoprotein deficiency results in a complex, multifactorial disorder, reflecting loss of selenoprotein function in specific tissues and/or long-term impaired selenoenzyme-mediated defence against oxidative and endoplasmic reticulum stress. SEPSECS mutations are associated with a predominantly neurological phenotype with progressive cerebello-cerebral atrophy. Selenoprotein deficiency due to SECISBP2 and TRU-TCA1-1 defects are characterized by abnormal circulating thyroid hormones due to lack of Sec-containing deiodinases, low serum selenium levels (low SELENOP, GPX3), with additional features (myopathy due to low SELENON; photosensitivity, hearing loss, increased adipose mass and function due to reduced antioxidant and endoplasmic reticulum stress defence) in SECISBP2 cases. Antioxidant therapy ameliorates oxidative damage in cells and tissues of patients, but its longer term benefits remain undefined. Ongoing surveillance of patients enables ascertainment of additional phenotypes which may provide further insights into the role of selenoproteins in human biological processes.     

Ion-exchange resins modified with metal-porphyrin as a catalysis for oxidation of epinephrine (adrenaline)

To develop a solid catalyst which can be a model of catechol oxidase and/or catecholamine monoamine oxidase, the ion-exchange resins modified with metal-tetrakis(4-sulfophenyl)porphine (M-TSPP wherein M is Mn³⁺, Co³⁺, Fe³⁺ or Cu²⁺) were examined for a catalytic activity in the oxidative reaction of epinephrine (adrenaline, Ad). Among M-TSPP-modified resins (M-TSPP_rs), Mn-TSPP_r exhibited the strongest catalytic activity in the oxidation of Ad with O₂ in the air to adrenochrome and adrenolutin. Mn-TSPP had little catalytic activity in an aqueous solution of Ad. The optimum conditions for the oxidation reaction catalyzed by Mn-TSPP_r were determined. Oxidation of catecholamines and related compounds thereof were conducted under the optimum conditions thus determined, which revealed that Mn-TSPP_r only catalyzes oxidation of catecholamines.     

Mori Ramulus Suppresses Hydrogen Peroxide-Induced Oxidative Damage in Murine Myoblast C2C12 Cells through Activation of AMPK

Mori Ramulus, the dried twigs of Morus alba L., has been attracting attention for its potent antioxidant activity, but its role in muscle cells has not yet been elucidated. The purpose of this study was to evaluate the protective effect of aqueous extracts of Mori Ramulus (AEMR) against oxidative stress caused by hydrogen peroxide (H₂O₂) in C2C12 mouse myoblasts, and in dexamethasone (DEX)-induced muscle atrophied models. Our results showed that AEMR rescued H₂O₂-induced cell viability loss and the collapse of the mitochondria membrane potential. AEMR was also able to activate AMP-activated protein kinase (AMPK) in H₂O₂-treated C2C12 cells, whereas compound C, a pharmacological inhibitor of AMPK, blocked the protective effects of AEMR. In addition, H₂O₂-triggered DNA damage was markedly attenuated in the presence of AEMR, which was associated with the inhibition of reactive oxygen species (ROS) generation. Further studies showed that AEMR inhibited cytochrome c release from mitochondria into the cytoplasm, and Bcl-2 suppression and Bax activation induced by H₂O₂. Furthermore, AEMR diminished H₂O₂-induced activation of caspase-3, which was associated with the ability of AEMR to block the degradation of poly (ADP-ribose) polymerase, thereby attenuating H₂O₂-induced apoptosis. However, compound C greatly abolished the protective effect of AEMR against H₂O₂-induced C2C12 cell apoptosis, including the restoration of mitochondrial dysfunction. Taken together, these results demonstrate that AEMR could protect C2C12 myoblasts from oxidative damage by maintaining mitochondrial function while eliminating ROS, at least with activation of the AMPK signaling pathway. In addition, oral administration of AEMR alleviated gastrocnemius and soleus muscle loss in DEX-induced muscle atrophied rats. Our findings support that AEMR might be a promising therapeutic candidate for treating oxidative stress-mediated myoblast injury and muscle atrophy.     

Sustainable Process for Production of Azelaic Acid Through Oxidative Cleavage of Oleic Acid

This work describes two sustainable methods for production and purification of azelaic acid (AA) to replace the current process of ozonolysis of oleic acid (OA). The first proceeds in two steps, coupling smooth oxidation of OA to 9,10‐dihydroxystearic acid (DSA) with subsequent oxidative cleavage by sodium hypochlorite. An alternative methodology is also proposed, using a chemocatalytic system consisting of H₂O₂/H₂WO₄ for direct oxidative cleavage of the double bond of OA at 373 K. A convenient technique for separation and purification of azelaic acid is also proposed.     

Electrochemical oxidation of sulfide ion at a Ti/IrO<Subscript>2</Subscript>–Ta<Subscript>2</Subscript>O<Subscript>5</Subscript> anode in the presence and absence of naphthenic acids

Electrochemical oxidation of sulfide ion at a Ti/IrO₂–Ta₂O₅ anode followed partial order kinetics (between current and mass transport control) in the absence and presence of chloride ion and of naphthenic acids, at sulfide concentrations typical of sour brines. The desired outcome was to promote the 2-electron oxidation of sulfide to elemental sulfide rather than the 8-electron oxidation to sulfate. Although elemental sulfur accumulated to some extent at low conversion of sulfide, sulfate ion became the principal product as the reaction progressed. At high conversion, the overall current efficiencies were typically higher than 50%, with material balance about 90%. However, this anode material was gradually poisoned by sulfide in long term use.     

Antitumor Effects of Selenium

Functions of selenium are diverse as antioxidant, anti-inflammation, increased immunity, reduced cancer incidence, blocking tumor invasion and metastasis, and further clinical application as treatment with radiation and chemotherapy. These functions of selenium are mostly related to oxidation and reduction mechanisms of selenium metabolites. Hydrogen selenide from selenite, and methylselenol (MSeH) from Se-methylselenocyteine (MSeC) and methylseleninicacid (MSeA) are the most reactive metabolites produced reactive oxygen species (ROS); furthermore, these metabolites may involve in oxidizing sulfhydryl groups, including glutathione. Selenite also reacted with glutathione and produces hydrogen selenide via selenodiglutathione (SeDG), which induces cytotoxicity as cell apoptosis, ROS production, DNA damage, and adenosine-methionine methylation in the cellular nucleus. However, a more pronounced effect was shown in the subsequent treatment of sodium selenite with chemotherapy and radiation therapy. High doses of sodium selenite were effective to increase radiation therapy and chemotherapy, and further to reduce radiation side effects and drug resistance. In our study, advanced cancer patients can tolerate until 5000 μg of sodium selenite in combination with radiation and chemotherapy since the half-life of sodium selenite may be relatively short, and, further, selenium may accumulates more in cancer cells than that of normal cells, which may be toxic to the cancer cells. Further clinical studies of high amount sodium selenite are required to treat advanced cancer patients.     

Phase cooperation of V<Subscript>2</Subscript>O<Subscript>5</Subscript> and Bi<Subscript>2</Subscript>O<Subscript>3</Subscript> in the selective oxidation of H<Subscript>2</Subscript>S containing ammonia and water

The selective oxidation of hydrogen sulfide containing excess water and ammonia was studied over vanadium oxide-based catalysts. The investigation was focused on the role of V₂O₅, and phase cooperation between V₂O₅ and Bi₂O₃ in this reaction. The conversion of H₂S continued to decrease since V₂O₅ was gradually reduced by treatment with H₂S. The activity of V₂O₅ was recovered by contact with oxygen. A strong synergistic phenomenon in catalytic activity was observed for the mechanically mixed catalysts of V₂O₅ and Bi₂O₃. Temperature-programmed reduction (TPR) and oxidation (TPO) and two bed reaction tests were performed to explain this synergistic effect by the reoxidation ability of Bi₂O₃. This paper is dedicated to Professor Wha Young Lee on the occasion of his retirement from Seoul National University.     

Impact of dissolved wastewater constituents on peroxidase‐catalyzed treatment of phenol

The impact of dissolved wastewater constituents on the treatment of synthetic phenol solutions using horseradish peroxidase (HRP) and hydrogen peroxide was investigated under a variety of reaction conditions. The constituents studied included various inorganic salts, organic compounds and heavy metals. Higher H₂O₂ doses were required to treat phenol in the presence of sodium sulfite, thiosulfate and sulfide; however, enhanced levels of phenol conversion were achieved once sufficient H₂O₂ was supplied. Sulfide and cyanide inhibited phenol transformation. The inhibition of sulfide was overcome by supplying sufficient H₂O₂ to oxidize the sulfide to sulfur. However, increasing the H₂O₂ dose was ineffective in attempting to overcome the strong inhibiting effect of cyanide. Among the heavy metal ions tested, only Mn(II) substantially inhibited phenol removal when it was present at a concentration of 1 mmol dm^?3. The presence of inorganic salts including NaCl, CaCl₂, MgCl₂, NH₄Cl and (NH₄)₂SO₄ reduced phenol conversion as compared with the treatment in distilled‐deionized water. This can be attributed to the increased ionic strength of the solution. © 2002 Society of Chemical Industry