Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 10 de 10
Filtrar
Mais filtros

Base de dados
Tipo de documento
Intervalo de ano de publicação
1.
Adv Drug Deliv Rev ; 188: 114396, 2022 09.
Artigo em Inglês | MEDLINE | ID: mdl-35798129

RESUMO

The propensity of the hepatic macrophages (Kupffer cells) to rapidly intercept particulate materials from the blood has been frustrating in redirecting intravenously injected nanomedicines to pathological sites in sufficient quantities to exert appropriate pharmacological effect. The development of long circulating nanoparticles has offered unprecedented opportunities for controlled drug release within vasculature and for drug delivery to sites other than Kupffer cells. These developments were based on mechanistic understanding of complex and integrated body's defences against intruders as well as translation of protective strategies developed by the body's own cells and virulent pathogens against immune attack. Thanks to interdisciplinary and integrated approaches, numerous organic and inorganic nanoparticles with long circulating properties have become available. By long circulation we mean particles that remain in the blood for periods of hours rather than minutes, but blood longevity must be tuned in accordance with therapeutic needs. Here, we provide a brief history of these efforts and highlight important lessons learned in camouflaging nanoparticles with strategies that avoid rapid interception by Kupffer cells.


Assuntos
Nanopartículas , Sistemas de Liberação de Medicamentos , Humanos , Células de Kupffer , Nanomedicina
2.
Science ; 278(5335): 114-7, 1997 Oct 03.
Artigo em Inglês | MEDLINE | ID: mdl-9311914

RESUMO

Apoptosis of mouse neocortical neurons induced by serum deprivation or by staurosporine was associated with an early enhancement of delayed rectifier (IK) current and loss of total intracellular K+. This IK augmentation was not seen in neurons undergoing excitotoxic necrosis or in older neurons resistant to staurosporine-induced apoptosis. Attenuating outward K+ current with tetraethylammonium or elevated extracellular K+, but not blockers of Ca2+, Cl-, or other K+ channels, reduced apoptosis, even if associated increases in intracellular Ca2+ concentration were prevented. Furthermore, exposure to the K+ ionophore valinomycin or the K+-channel opener cromakalim induced apoptosis. Enhanced K+ efflux may mediate certain forms of neuronal apoptosis.


Assuntos
Apoptose , Neurônios/citologia , Canais de Potássio/metabolismo , Potássio/metabolismo , Clorometilcetonas de Aminoácidos/farmacologia , Animais , Apoptose/efeitos dos fármacos , Benzopiranos/farmacologia , Cálcio/metabolismo , Córtex Cerebral/citologia , Cromakalim , Cicloeximida/farmacologia , Inibidores de Cisteína Proteinase/farmacologia , Gadolínio/farmacologia , Camundongos , N-Metilaspartato/farmacologia , Neurônios/metabolismo , Fármacos Neuroprotetores/farmacologia , Nifedipino/farmacologia , Técnicas de Patch-Clamp , Canais de Potássio/efeitos dos fármacos , Pirróis/farmacologia , Estaurosporina/farmacologia , Tetraetilamônio , Compostos de Tetraetilamônio/farmacologia , Veratridina/farmacologia
3.
J Clin Invest ; 98(1): 207-15, 1996 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-8690795

RESUMO

Aceruloplasminemia is an autosomal recessive disorder resulting in neurodegeneration of the retina and basal ganglia in association with iron accumulation in these tissues. To begin to define the mechanisms of central nervous system iron accumulation and neuronal loss in this disease, cDNA clones encoding murine ceruloplasmin were isolated and characterized. RNA blot analysis using these clones detected a 3.7-kb ceruloplasmin-specific transcript in multiple murine tissues including the eye and several regions of the brain. In situ hybridization of systemic tissues revealed cell-specific ceruloplasmin gene expression in hepatocytes, the splenic reticuloendothelial system and the bronchiolar epithelium of the lung. In the central nervous system, abundant ceruloplasmin gene expression was detected in specific populations of astrocytes within the retina and the brain as well as the epithelium of the choroid plexus. Analysis of primary cell cultures confirmed that astrocytes expressed ceruloplasmin mRNA and biosynthetic studies revealed synthesis and secretion of ceruloplasmin by these cells. Taken together these results demonstrate abundant cell-specific ceruloplasmin expression within the central nervous system which may account for the unique clinical and pathologic findings observed in patients with aceruloplasminemia.


Assuntos
Encéfalo/metabolismo , Ceruloplasmina/biossíntese , Ceruloplasmina/genética , Olho/metabolismo , Sequência de Aminoácidos , Animais , Ceruloplasmina/deficiência , Clonagem Molecular , DNA Complementar , Expressão Gênica , Genes Recessivos , Hibridização In Situ , Erros Inatos do Metabolismo/etiologia , Camundongos , Dados de Sequência Molecular , Neuroglia/citologia , Neuroglia/metabolismo , Neurônios/citologia , Neurônios/metabolismo , Homologia de Sequência de Aminoácidos , Distribuição Tecidual
4.
Neuroreport ; 8(5): 1127-30, 1997 Mar 24.
Artigo em Inglês | MEDLINE | ID: mdl-9175098

RESUMO

A hallmark of Alzheimer's disease (AD) is the extracellular deposition and accumulation of a 39-43 amino peptide, known as the amyloid beta (A beta) protein, within the brain. It has been postulated that A beta may in some way contribute directly to AD pathogenesis. The epsilon 4 allele of apolipoprotein E (apoE) is a major AD risk factor. Since both apoE and A beta are components of lipoproteins in plasma and cerebrospinal fluid, we asked whether lipoproteins and apoE isoforms would modify the toxicity of A beta (1-42) in cortical cell cultures. We show that high density lipoprotein with or without apoE reduces A beta toxicity and that apoE in the absence of lipoproteins does not affect A beta toxicity. These results suggest that interactions between A beta and lipoproteins in the brain could influence AD pathogenesis.


Assuntos
Peptídeos beta-Amiloides/toxicidade , Apolipoproteínas E/farmacologia , Córtex Cerebral/efeitos dos fármacos , Lipoproteínas HDL/farmacologia , Alelos , Doença de Alzheimer/genética , Doença de Alzheimer/metabolismo , Peptídeos beta-Amiloides/antagonistas & inibidores , Animais , Apolipoproteínas E/análise , Células Cultivadas , Córtex Cerebral/citologia , Lipoproteínas HDL/química , Camundongos , Fatores de Risco
5.
J Innate Immun ; 4(5-6): 509-28, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22722900

RESUMO

Particulate systems in the form of liposomes, polymeric micelles, polymeric nano- and microparticles, and many others offer a rational approach for selective delivery of therapeutic agents to the macrophage from different physiological portals of entry. Particulate targeting of macrophages and intracellular drug release processes can be optimized through modifications of the drug carrier physicochemical properties, which include hydrodynamic size, shape, composition and surface characteristics. Through such modifications together with understanding of macrophage cell biology, targeting may be aimed at a particular subset of macrophages. Advances in basic and therapeutic concepts of particulate targeting of macrophages and related nanotechnology approaches for immune cell modifications are discussed.


Assuntos
Portadores de Fármacos/química , Sistemas de Liberação de Medicamentos/métodos , Macrófagos/efeitos dos fármacos , Nanopartículas/administração & dosagem , Animais , Portadores de Fármacos/administração & dosagem , Humanos , Camundongos , Nanotecnologia , Fagocitose/efeitos dos fármacos , Fagocitose/fisiologia , Coelhos , Ratos
6.
Biochemistry ; 34(46): 14970-4, 1995 Nov 21.
Artigo em Inglês | MEDLINE | ID: mdl-7578110

RESUMO

Horseradish peroxidase (HRP) was oxidized by IrCl6(2-) to a mixture of compounds I and II, the rate of oxidation and the ratio of the mixture being greatly affected by pH (Hayashi & Yamazaki, 1979). Oxidation of HRP by IrCl6(2-) in the presence of fluoride was significantly accelerated. This resulted in the formation of a new compound which is a ferric fluoride complex containing a porphyrin pi-cation radical. The spectrum of the new compound showed a decreased absorption band in the Soret region and a broad band at 570 nm; which was converted to that of the original ferric fluoride complex by addition of ascorbate or hydroquinone. Addition of cyanide slowed down the oxidation of HRP by IrCl6(2-), and the oxidation product was the same as that obtained in the absence of cyanide. Compound I was formed when H2O2 was added to HRP in the presence of fluoride or cyanide. The one-electron reduction potential (Eo') of the oxidized HRP-fluoride complex was measured at several pH values, the Eo' value at pH 7 being 861 +/- 4 mV. The ratio of delta Eo' to delta pH was 49 mV/pH unit.


Assuntos
Fluoretos/metabolismo , Peroxidase do Rábano Silvestre/metabolismo , Porfirinas/metabolismo , Ácido Ascórbico/farmacologia , Radicais Livres , Peroxidase do Rábano Silvestre/química , Peróxido de Hidrogênio/farmacologia , Concentração de Íons de Hidrogênio , Hidroquinonas/farmacologia , Irídio/química , Oxirredução , Porfirinas/química , Cianeto de Potássio/farmacologia , Fluoreto de Sódio/farmacologia , Espectrofotometria
7.
Biochemistry ; 31(44): 10763-8, 1992 Nov 10.
Artigo em Inglês | MEDLINE | ID: mdl-1420193

RESUMO

Monochlorodimedone (MCD), commonly used as a halogen acceptor for haloperoxidase assays, was oxidized by hydrogen peroxide in the presence of lignin peroxidase isoenzymes H2 and H8. When oxidized, it produced a weak absorption band with an intensity that varied with pH. This absorbance was used as a simple method for the product analysis because it disappeared when MCD was brominated or chlorinated. We assessed the activity of the lignin peroxidases for oxidation of bromide by measuring the bromination of MCD, the formation of tribromide, the bromide-mediated oxidation of glutathione, and the bromide-mediated catalase-like activity. We analyzed the reaction products of MCD and the halide-mediated oxidation of glutathione when bromide was replaced by chloride. These enzymes demonstrated no significant activity for oxidation of chloride. Unlike other peroxidases, the lignin peroxidases exhibited similar pH-activity curves for the iodide and bromide oxidations. The optimum pH for activity was about 2.5. Surprisingly, this pH dependence of lignin peroxidase activity for the halides was nearly the same in the reactions with hydrogen donors, such as hydroquinone and guaiacol. The results suggested that protonation of the enzymes with pKa approximately 3.2 is necessary for the catalytic function of lignin peroxidases, irrespective of whether the substrates are electron or hydrogen donors. These unique reaction profiles of lignin peroxidases are compared to those of other peroxidases, such as lactoperoxidase, bromoperoxidase, chloroperoxidase, and horseradish peroxidase. Isozyme H2 was more active than isozyme H8, but isozyme H8 was more stable at very acidic pH.


Assuntos
Basidiomycota/enzimologia , Isoenzimas/metabolismo , Peroxidases/metabolismo , Brometos/metabolismo , Cloretos/metabolismo , Cicloexanonas/metabolismo , Glutationa/metabolismo , Peróxido de Hidrogênio/metabolismo , Concentração de Íons de Hidrogênio , Iodetos/metabolismo , Cinética , Oxirredução , Espectrofotometria
8.
Biochemistry ; 34(9): 2866-71, 1995 Mar 07.
Artigo em Inglês | MEDLINE | ID: mdl-7893700

RESUMO

The reduction potentials of the compound II/ferric and compound I/compound II couples have been studied, using potassium hexachloroiridate as a mediator titrant, by thin-layer spectroelectrochemistry. Compound I, which is 2 equiv more oxidized than the ferric (i.e., resting) form of the enzyme, was reversibly formed via a compound II intermediate; no evidence for a ferric porphyrin pi-cation radical intermediate was obtained. At 25 degrees C, E degrees' (compound I/compound II) = 897.9 +/- 3 mV (NHE) and E degrees'-(compound II/ferric) = 869.1 +/- 2 mV. Redox thermodynamic parameters, obtained from the temperature dependences of the reduction potentials of both couples, are reported. The reaction entropies (delta S degrees rc) for the compound II/ferric and compound I/compound II couples are 19.8 +/- 3.9 and 12.1 +/- 3.7 eu, respectively. This result indicates that the reorganization energy for the macrocycle-centered couple is lower than that for the metal-centered one. Together with our observation that E degrees' for the former is ca. 30 mV greater than that for the latter, these results suggest that compound I is more reactive toward outer-sphere reductants than compound II. In particular, the electron self-exchange rates for the compound I/compound II and compound II/ferric couples are estimated to be 4.4 x 10(-1) and 4.9 x 10(-4) M-1 s-1, respectively. Surprisingly, the formation of compound I from ferric HRP is accompanied by an almost zero standard entropy (delta S degrees') change.


Assuntos
Peroxidase do Rábano Silvestre/química , Eletroquímica , Isoenzimas/química , Oxirredução , Espectrofotometria , Temperatura , Termodinâmica
9.
Biochemistry ; 33(18): 5647-52, 1994 May 10.
Artigo em Inglês | MEDLINE | ID: mdl-8180190

RESUMO

At neutral pH, compound I of Arthromyces ramosus peroxidase (ARP) was stable and was reduced to ferric ARP without apparent formation of compound II upon titration with ascorbate or hydroquinone. In the titration experiments, compound II was seen as an intermediate only at alkaline pH. However, measuring a difference spectrum in the Soret region by a stopped-flow method, we found that compound II was formed during the catalytic oxidation of ascorbate even at neutral pH. Using an EPR spectrometer with a microflow system, we measured the steady-state concentration of benzosemiquinone formed in the ARP-catalyzed oxidation of hydroquinone. The results clearly showed that ARP catalyzes the oxidation of hydroquinone by a one-electron-transfer mechanism, as does horseradish peroxidase. These observations led to the conclusion that compound I is reduced to compound II through a one-electron reduction by ascorbate or hydroquinone. Therefore, we concluded that ARP compound II is unusually unstable and is rapidly reduced to ferric enzyme without accumulation in the titration experiment. The unusual instability of ARP compound II is explained in terms of the high reduction potential of compound II. The reduction potentials (E0') of compounds I and II were measured at several pH values from redox equilibria with potassium hexachloroiridate on the basis of E0' = 0.90 V for the IrCL6(2)-IrCl6(3)- couple. These values were determined to be 0.915 and 0.982 V at pH 7, respectively, and decreased with increasing pH. This pH dependence was markedly changed by the buffer concentration.(ABSTRACT TRUNCATED AT 250 WORDS)


Assuntos
Fungos Mitospóricos/enzimologia , Peroxidase/química , Ácido Ascórbico/farmacologia , Catálise , Espectroscopia de Ressonância de Spin Eletrônica , Estabilidade Enzimática , Concentração de Íons de Hidrogênio , Hidroquinonas/farmacologia , Oxirredução , Peroxidase/efeitos dos fármacos , Peroxidase/metabolismo
10.
Neurobiol Dis ; 5(2): 81-8, 1998 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-9746905

RESUMO

In light of recent evidence implicating the upregulation of outward K+ current in mediating several forms of neuronal apoptosis, we tested the hypothesis that such an upregulation might specifically contribute to the pathogenesis of beta-amyloid peptide (A beta)-induced neuronal death. Exposure to A beta fragment 25-35 (20 microM) or 1-42 (20 microM) enhanced the delayed rectifier K+ current IK, shifting its activation voltage relationship toward hyperpolarized levels and increasing maximal conductance, but did not affect the transient K+ current IA or charybdotoxin-sensitive BK current. Reducing IK by adding the channel blocker tetraethylammonium (TEA, 5 mM) or raising extracellular K+ to 25 mM attenuated A beta-induced neuronal death, even in the presence of nifedipine or gadolinium to block associated increases in Ca2+ influx. The IA blocker 4-aminopyridine (4-AP, 5 mM) and the CI- channel blocker anthracene-9-carboxylic acid (ACA, 500 microM) were not neuroprotective. These data raise the intriguing possibility that manipulations aimed at reducing outward K+ current may provide an approach to reducing neuronal degeneration in patients with Alzheimer's disease.


Assuntos
Peptídeos beta-Amiloides/farmacologia , Córtex Cerebral/fisiologia , Neurônios/fisiologia , Fragmentos de Peptídeos/farmacologia , Canais de Potássio de Abertura Dependente da Tensão da Membrana , Canais de Potássio/fisiologia , Animais , Morte Celular/efeitos dos fármacos , Células Cultivadas , Córtex Cerebral/citologia , Córtex Cerebral/efeitos dos fármacos , Técnicas de Cocultura , Canais de Potássio de Retificação Tardia , Feto , Camundongos , Neuroglia , Neurônios/efeitos dos fármacos , Potássio/fisiologia , Canais de Potássio/efeitos dos fármacos , Compostos de Amônio Quaternário/farmacologia
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA