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1.
Molecules ; 22(8)2017 Aug 18.
Artigo em Inglês | MEDLINE | ID: mdl-28820487

RESUMO

The efficient and mild copper-catalyzed synthesis of unsymmetrical diorganyl chalcogenides under ligand- and solvent-free conditions is described. The cross-coupling reaction was performed using aryl boric acids and 0.5 equiv. of diorganyl dichalcogenides (Te/Se/S) in the presence of 3 mol % of CuI and 3 equiv. of DMSO, under microwave irradiation. This new protocol allowed the preparation of several unsymmetrical diorganyl chalcogenides in good to excellent yields.


Assuntos
Ácidos Borônicos/química , Calcogênios/química , Cobre/química , Estrutura Molecular , Catálise , Ligantes , Solventes/química
2.
Mol Neurobiol ; 54(2): 1513-1530, 2017 03.
Artigo em Inglês | MEDLINE | ID: mdl-26852411

RESUMO

Parkinson's disease (PD) is a neurodegenerative disorder characterized by non-motor and motor disabilities. This study investigated whether succinobucol (SUC) could mitigate nigrostriatal injury caused by intranasal 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) administration in mice. Moreover, the effects of SUC against MPTP-induced behavioral impairments and neurochemical changes were also evaluated. The quantification of tyrosine hydroxylase-positive (TH+) cells was also performed in primary mesencephalic cultures to evaluate the effects of SUC against 1-methyl-4-phenylpyridinium (MPP+) toxicity in vitro. C57BL/6 mice were treated with SUC (10 mg/kg/day, intragastric (i.g.)) for 30 days, and thereafter, animals received MPTP infusion (1 mg/nostril) and SUC treatment continued for additional 15 days. MPTP-infused animals displayed significant non-motor symptoms including olfactory and short-term memory deficits evaluated in the olfactory discrimination, social recognition, and water maze tasks. These behavioral impairments were accompanied by inhibition of mitochondrial NADH dehydrogenase activity (complex I), as well as significant decrease of TH and dopamine transporter (DAT) immunoreactivity in the substantia nigra pars compacta and striatum. Although SUC treatment did not rescue NADH dehydrogenase activity inhibition, it was able to blunt MPTP-induced behavioral impairments and prevented the decrease in TH and DAT immunoreactivities in substantia nigra (SN) and striatum. SUC also suppressed striatal astroglial activation and increased interleukin-6 levels in MPTP-intoxicated mice. Furthermore, SUC significantly prevented the loss of TH+ neurons induced by MPP+ in primary mesencephalic cultures. These results provide new evidence that SUC treatment counteracts early non-motor symptoms and neurodegeneration/neuroinflammation in the nigrostriatal pathway induced by intranasal MPTP administration in mice by modulating events downstream to the mitochondrial NADH dehydrogenase inhibition.


Assuntos
Anticolesterolemiantes/uso terapêutico , Corpo Estriado/efeitos dos fármacos , Transtornos Parkinsonianos/tratamento farmacológico , Probucol/análogos & derivados , Substância Negra/efeitos dos fármacos , Animais , Anticolesterolemiantes/farmacologia , Corpo Estriado/metabolismo , Corpo Estriado/patologia , Feminino , Masculino , Transtornos da Memória/tratamento farmacológico , Transtornos da Memória/metabolismo , Transtornos da Memória/patologia , Camundongos , Camundongos Endogâmicos C57BL , Doenças Neurodegenerativas/tratamento farmacológico , Doenças Neurodegenerativas/metabolismo , Doenças Neurodegenerativas/patologia , Transtornos Parkinsonianos/metabolismo , Transtornos Parkinsonianos/patologia , Gravidez , Probucol/farmacologia , Probucol/uso terapêutico , Distribuição Aleatória , Ratos , Ratos Sprague-Dawley , Olfato/efeitos dos fármacos , Olfato/fisiologia , Substância Negra/metabolismo , Substância Negra/patologia
3.
Behav Brain Res ; 305: 30-6, 2016 May 15.
Artigo em Inglês | MEDLINE | ID: mdl-26921691

RESUMO

Bradykinesia and hypokinesia represent well-known motor symptoms of Parkinson's disease (PD). While bradykinesia (slow execution of movements) is present in less affected PD patients and aggravates as the disease severity increases, hypokinesia (reduction of movement) seems to emerge prominently only in the more affected patients. Here we developed a model based on the central infusion of low dose (40µg) 6-hydroxydopamine (6-OHDA) in mice in an attempt to discriminate bradykinesia (accessed through forelimb inability) from hypokinesia (accessed through locomotor and exploratory activities). The potential beneficial effects of succinobucol against 6-OHDA-induced forelimb inability were also evaluated. One week after the beginning of treatment with succinobucol (i.p. injections, 10mg/kg/day), mice received a single i.c.v. infusion of 6-OHDA (40µg/site). One week after 6-OHDA infusion, general locomotor/exploratory activities (open field test), muscle strength (grid test), forelimb skill (single pellet task), as well as striatal biochemical parameters related to oxidative stress and cellular homeostasis (glutathione peroxidase, glutathione reductase and NADH dehydrogenases activities, lipid peroxidation and TH levels), were evaluated. 6-OHDA infusions did not change locomotor/exploratory activities and muscle strength, as well as the evaluated striatal biochemical parameters. However, 6-OHDA infusions caused significant reductions (50%) in the single pellet reaching task performance, which detects forelimb skill inability and can be used to experimentally identify bradykinesia. Succinobucol partially protected against 6-OHDA-induced forelimb inability. The decreased forelimb ability with no changes in locomotor/exploratory behavior indicates that our 6-OHDA-based protocol represents a useful tool to mechanistically study the dissociation of bradykinesia and hypokinesia in PD.


Assuntos
Adrenérgicos/administração & dosagem , Membro Anterior/fisiopatologia , Hipocinesia/induzido quimicamente , Hipocinesia/fisiopatologia , Oxidopamina/administração & dosagem , Animais , Relação Dose-Resposta a Droga , Comportamento Exploratório/efeitos dos fármacos , Comportamento Alimentar/efeitos dos fármacos , Glutationa Peroxidase/metabolismo , Glutationa Redutase/metabolismo , Antígenos de Histocompatibilidade Classe I/metabolismo , Hipocinesia/diagnóstico , Injeções Intraventriculares , Peroxidação de Lipídeos/efeitos dos fármacos , Masculino , Camundongos , Força Muscular/efeitos dos fármacos , Fragmentos de Peptídeos/metabolismo , Probucol/administração & dosagem , Probucol/análogos & derivados , Desempenho Psicomotor/efeitos dos fármacos , Substâncias Reativas com Ácido Tiobarbitúrico/metabolismo
4.
Mol Neurobiol ; 53(2): 1280-1295, 2016 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-25619973

RESUMO

Succinobucol (succinyl ester of probucol) is a lipid-lowering compound with anti-inflammatory and antioxidant properties. Recent experimental evidence has highlighted the potential neuroprotective effects of succinobucol. In the present study, cultured neuroblastoma (SH-SY5Y) cells were used to investigate mechanisms mediating the potential protective effect of succinobucol against mitochondrial metabolic impairment and oxidative stress induced by 3-nitropropionic acid (3-NP), a succinate dehydrogenase inhibitor that has been used in experimental models of the Huntington disease (HD). 3-NP decreased cellular viability after 24 h of incubation. This decline in cellular viability was preceded by (i) reduced mitochondrial complex II activity, (ii) increased reactive species generation, (iii) decreased mitochondrial membrane potential (ΔΨm), and (iv) diminished glutathione (GSH) levels. Succinobucol pretreatment (6 days) significantly prevented 3-NP-induced loss of cellular viability, generation of reactive oxygen species, and decrease of ΔΨm. However, succinobucol pretreatment did not protect against 3-NP-induced inhibition of mitochondrial complex II activity, pointing to the mitigation of secondary events resultant from mitochondrial complex II inhibition. Succinobucol pretreatment (6 days) significantly increased (50 %) the levels of GSH in SH-SY5Y cells, and this event was paralleled by significant increases in glutamate cysteine ligase messenger RNA (mRNA) expression and activity (GCL; the first enzyme in the GSH biosynthesis). The present findings are the first to show that succinobucol increases GSH levels via upregulation of GCL activity (possibly through the activation of the nuclear (erythroid-derived 2)-related factor (Nrf2)/antioxidant response element (ARE) pathway), displaying protective effects against mitochondrial dysfunction-derived oxidative stress.


Assuntos
Glutamato-Cisteína Ligase/metabolismo , Glutationa/metabolismo , Hipolipemiantes/farmacologia , Mitocôndrias/metabolismo , Estresse Oxidativo/efeitos dos fármacos , Probucol/análogos & derivados , Regulação para Cima/efeitos dos fármacos , Butionina Sulfoximina/farmacologia , Morte Celular/efeitos dos fármacos , Linhagem Celular Tumoral , Sobrevivência Celular/efeitos dos fármacos , Glutamato-Cisteína Ligase/genética , Glutationa Peroxidase/metabolismo , Humanos , Hidroquinonas/farmacologia , Mitocôndrias/efeitos dos fármacos , Nitrocompostos , Probucol/farmacologia , Propionatos , Substâncias Protetoras/farmacologia , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Fatores de Tempo
5.
J Org Chem ; 80(4): 2120-7, 2015 Feb 20.
Artigo em Inglês | MEDLINE | ID: mdl-25607341

RESUMO

Herein, we report a solvent- and metal-free methodology for the alkoxy-chalcogenylation of styrenes, using molecular iodine as a catalyst, DMSO as a stoichiometric oxidant, and different nucleophiles under microwave irradiation. This eco-friendly approach afforded the desired products in good to excellent yields in only 10 min. In addition, using the same protocol, we carried out the cyclization reaction of relevant molecules, such as lapachol derivatives.


Assuntos
Dimetil Sulfóxido/química , Éteres/síntese química , Iodo/química , Estirenos/química , Catálise , Ciclização , Éteres/química , Micro-Ondas , Estrutura Molecular , Oxidantes/química
6.
J Org Chem ; 79(9): 4125-30, 2014 May 02.
Artigo em Inglês | MEDLINE | ID: mdl-24712301

RESUMO

Herein, we describe a solvent- and metal-free method for the synthesis of 3-chalcogenyl-indoles from indoles and diorganyl dichalcogenides using an equivalent amount of DMSO as an oxidant, under catalysis by molecular iodine. This mild and eco-friendly approach allowed the preparation of a wide range of 3-selenyl- and 3-sulfenyl-indoles in good to excellent yields.


Assuntos
Dimetil Sulfóxido/química , Indóis/síntese química , Iodo/química , Catálise , Indóis/química , Estrutura Molecular , Oxirredução , Solventes/química
7.
Mitochondrion ; 13(2): 125-33, 2013 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-23333792

RESUMO

This study evaluated and compared the potential protective effects of probucol and succinobucol, two lipid-lowering compounds with anti-inflammatory and antioxidant properties, on oxidative stress and mitochondrial dysfunction induced by 3-nitropropionic acid (3-NP, a succinate dehydrogenase (SDH) inhibitor largely used as model of Huntington's disease) in rat brain mitochondria-enriched synaptosomes. 3-NP caused significant inhibition of mitochondrial complex II activity, induced mitochondrial dysfunction and oxidative stress. Probucol and succinobucol prevented oxidative stress, but only succinobucol was able to prevent the mitochondrial dysfunction induced by 3-NP. Succinobucol, which did not recover complex II inhibition, was able to protect against 3-NP-induced decreased of MTT reduction, indicating that SDH is not the only enzyme responsible for MTT reduction. The present findings suggest that succinobucol might be a novel strategy to slow or halt oxidative events in neurodegenerative conditions.


Assuntos
Antioxidantes/metabolismo , Encéfalo/efeitos dos fármacos , Mitocôndrias/efeitos dos fármacos , Nitrocompostos/toxicidade , Estresse Oxidativo , Probucol/análogos & derivados , Probucol/metabolismo , Propionatos/toxicidade , Animais , Complexo II de Transporte de Elétrons/metabolismo , Masculino , Ratos , Ratos Wistar
8.
Dalton Trans ; 40(43): 11347-55, 2011 Nov 21.
Artigo em Inglês | MEDLINE | ID: mdl-21904736

RESUMO

In recent years, there has been an increasing application of chiral selenium compounds as ligands in metal-catalyzed enantioselective transformations. One of the most important challenges in this field is the development of new chiral complexes (catalyst) generated from the reaction between a metal and appropriate chiral selenium-containing compounds (ligand). The vast majority of these ligands are easily synthesized in a few high-yielding synthetic steps, starting from readily available chiral amino alcohols. In this context, the advantages of using these compounds will be discussed, mainly with regard to their easy accessibility, modular nature and the formation of strong bonds with soft or, more rarely, hard metals. Important selective contributions within the field of chiral selenium complexes are examined, according to their applications. As final remarks, future developments and perspectives of the field are discussed.

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