RESUMO
Background: Major abdominal oncology surgery is associated with substantial postoperative loss of functional capacity, and exercise may be an effective intervention to improve outcomes. The aim of this study was to assess efficacy, feasibility and safety of a supervised postoperative exercise programme. Methods: We performed a single-blind, parallel-arm, randomized trial in patients who underwent major abdominal oncology surgery in a tertiary university hospital. Patients were randomized to an early mobilization postoperative programme based on supervised aerobic exercise, resistance and flexibility training or to standard rehabilitation care. The primary outcome was inability to walk without human assistance at postoperative day 5 or hospital discharge. Results: A total of 108 patients were enrolled, 54 into the early mobilization programme group and 54 into the standard rehabilitation care group. The incidence of the primary outcome was nine (16.7%) and 21 (38.9%), respectively (P=0.01), with an absolute risk reduction of 22.2% [95% confidence interval (CI) 5.9-38.6] and a number needed to treat of 5 (95% CI 3-17). All patients in the intervention group were able to follow at least partially the exercise programme, although the performance among them was rather heterogeneous. There were no differences between groups regarding clinical outcomes or complications related to the exercises. Conclusions: An early postoperative mobilization programme based on supervised exercises seems to be safe and feasible and improves functional capacity in patients undergoing major elective abdominal oncology surgery. However, its impact on clinical outcomes is still unclear. Clinical trial registration: NCT01693172.
Assuntos
Neoplasias Abdominais/reabilitação , Neoplasias Abdominais/cirurgia , Terapia por Exercício/métodos , Tolerância ao Exercício , Avaliação de Programas e Projetos de Saúde/métodos , Idoso , Estudos de Viabilidade , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Método Simples-Cego , Resultado do TratamentoRESUMO
This study was aimed to reveal the principal colloidal properties of the aqueous dispersion of extremely small primary single-crystalline diamond particles in water. Together with the non-diamond layer, the size of the colloidal species is 2.8 ± 0.6 nm as found via DLS of the initial 5.00 wt/vol% hydrosol. Anionic dyes are readily adsorbed on the colloidal species. This is in line with the positive zeta-potential. The critical coagulation concentrations of the 0.19 wt/vol% nanodiamond hydrosol were determined with a set of inorganic electrolytes and anionic surfactants. The data are in line with the Schulze-Hardy rule for "positive" sols. The fulfillment of the lyotropic (Hofmeister) series was also observed for single-charged anions. The abnormal influence of alkali gives evidence of the acidic nature of the positive charge of the nanodiamond species. Application of acid-base indicators allows estimating the value of the interfacial electrical potential of the nanodiamond particles. Upon dilution from 5.00% to 0.01%, the colloidal system under study exhibits unusual changes. The average size increases ca. ten-fold as determined by DLS. The TEM images support this observation. At the same time, the viscosity drops. This phenomenon was explained in terms of the so-called periodic colloidal structures (colloidal crystals) in concentrated solutions.
RESUMO
The relative importance of the liver and kidney for glycine conjugation of ortho-substituted benzoic acids was investigated. Glycine conjugation of ortho-substituted benzoic acids was investigated in mouse liver and kidney mitochondria. The extent of glycine conjugation of benzoic acids with the halogen group decreased in the order F > Cl > Br > I. The conjugation of salicylic acid with glycine took place in only the kidney. 2-Methoxybenzoic acid exhibited no activity in the liver and kidney. The difference in glycine conjugation of ortho-substituted benzoic acids was observed between liver and kidney. The kidney was more active in glycine conjugation of ortho-substituted acids than the liver. In addition, the relationship between glycine conjugation and the chemical structure of ortho-substituted acids was examined in the liver and kidney. The size of the substituent had a far greater influence over glycine conjugation in the liver and kidney. Glycine conjugation was also dependent on the substituent electronegativity. It may be important that the substrates undergoing glycine conjugation contain a flat region coplanar to the carboxylate group.
Assuntos
Benzoatos/metabolismo , Glicina/metabolismo , Rim/metabolismo , Fígado/metabolismo , Animais , Benzoatos/química , Cromatografia Líquida de Alta Pressão , Masculino , Camundongos , Mitocôndrias Hepáticas/metabolismo , Estrutura MolecularRESUMO
Preparative constant-current electrolysis of N,N-dimethylaniline(100 mM, DMA) was carried out in dry acetonitrile containing Et4NClO4 to give N,N,N',N'-tetra-methylbenzidine(TMB) and 4,4'-methylenebis(N,N-dimethylaniline) (MDMA). In the presence of HCl, DMA was quantitatively oxidized to TMB. Formation mechanism of MDMA was discussed using the results of semi-empirical calculations that were PM3 and AM1. The proposed mechanism by Hand and coworker was ruled out and an alternative one is suggested as follows. DMA undergoes one-electron oxidation at the anode and gives the corresponding N,N-dimethylaniline cation (A). Aydroxy ion, instead of DMA, abstracts a proton from A and gives H2O and methyl(phenyl)aminomethyl radical (B). B reacts with DMA to give a 1-dimethylamino-4-(N-methyl-N-phenylamino)methyl-2,5-cyclohexadienyl radical (I). The radical I decomposes to N-methylaniline and a 1-dimethylamino-4-methylene-2,5-cyclohexadienyl radical (J). The radical J reacts with DMA to give a 1-dimethylamino-4-(4-dimethylaminobenzyl)-2,5-cyclohexadienyl radical (K), which is oxidized to MDMA by the anode.
Assuntos
Compostos de Anilina/metabolismo , Compostos de Anilina/química , Cromatografia Líquida de Alta Pressão , OxirreduçãoRESUMO
Dichloromethane containing metalloporphyrins [meso-tetraphenylporphyrinatomanganese(III) chloride (1) or meso-tetraphenylporphyrinatoiron(III) chloride (2)] and Bu4NClO4 was treated with an aqueous solution of NaOH (5%), and subjected to controlled potential electrolysis at -1.0 V (vs. S.C.E. (saturated calomel electrode)) in a divided cell after addition of diphenyl sulfide (3). Diphenyl sulfoxide (4) and diphenyl sulfone (5) were found in an electrolyzed solution as the reaction products. Results obtained from cyclic voltammetry and visible spectrometry suggested that the treatment of dichloromethane containing metalloporphyrins with the aqueous solution of NaOH did not change the fifth ligand of metalloporphyrins from Cl to OH. On the electrode, dissolved dioxygen was reduced to hydrogen peroxide. Compounds 1 and 2 catalyze the oxidation of 3 by hydrogen peroxide without imidazole. Compound 2 showed higher selectivity than compound 1.
Assuntos
Sistema Enzimático do Citocromo P-450 , Sulfetos , Eletrólise , Metaloporfirinas , Modelos Químicos , Oxirredução , Hidróxido de Sódio , Soluções , ÁguaRESUMO
Bone morphogenetic proteins (BMPs) are well-studied regulators of cartilage and bone development that have been Food and Drug Administration (FDA)-approved for the promotion of bone formation in certain procedures. BMPs are seeing more use in oral and maxillofacial surgeries because of recent FDA approval of InFUSE(®) for sinus augmentation and localized alveolar ridge augmentation. However, the utility of BMPs in medical and dental applications is limited by the delivery method. Currently, BMPs are delivered to the surgical site by the implantation of bulky collagen sponges. Here we evaluate the potential of detonation nanodiamonds (NDs) as a delivery vehicle for BMP-2 and basic fibroblast growth factor (bFGF). Nanodiamonds are biocompatible, 4- to 5-nm carbon nanoparticles that have previously been used to deliver a wide variety of molecules, including proteins and peptides. We find that both BMP-2 and bFGF are readily loaded onto NDs by physisorption, forming a stable colloidal solution, and are triggered to release in slightly acidic conditions. Simultaneous delivery of BMP-2 and bFGF by ND induces differentiation and proliferation in osteoblast progenitor cells. Overall, we find that NDs provide an effective injectable alternative for the delivery of BMP-2 and bFGF to promote bone formation.
Assuntos
Proteína Morfogenética Óssea 2/administração & dosagem , Sistemas de Liberação de Medicamentos , Fator 2 de Crescimento de Fibroblastos/administração & dosagem , Nanodiamantes/química , Osteogênese/efeitos dos fármacos , Fosfatase Alcalina/análise , Materiais Biocompatíveis/química , Técnicas de Cultura de Células , Diferenciação Celular/efeitos dos fármacos , Proliferação de Células/efeitos dos fármacos , Coloides/química , Difusão , Humanos , Mioblastos/efeitos dos fármacos , Osteoblastos/efeitos dos fármacos , Osteoblastos/fisiologia , Tamanho da Partícula , Ligação Proteica , Espectroscopia de Infravermelho com Transformada de Fourier , Células-Tronco/efeitos dos fármacos , Células-Tronco/fisiologia , Propriedades de SuperfícieRESUMO
A semi-empirical calculation (PM3) was applied to elucidate the anodic oxidation mechanism of N,N-dimethylaniline (DMA) and the dimerization of a cation radical (A) derived from DMA was ruled out. The heat of reaction value of the dimerization of A was 42.43 kcal/mol. We propose the following. Cation radical A reacts with DMA to generate another cation radical (D). This reaction was exothermic and the heat of reaction value and the activation energy were -0.35 kcal/mol and 1.31 kcal/mol, respectively. Deprotonation of D by DMA gives neutral radical (E), which is oxidized to TMB by A. All these reactions were exothermic.
Assuntos
Compostos de Anilina/química , Fenômenos Químicos , Físico-Química , Ciclização , Eletrodos , Radicais Livres , OxirreduçãoRESUMO
Coptisine and 8-oxocoptisine were isolated as principles of the gastric-mucous membrane protection from Coptidis rhizoma. The two compounds showed stronger activity than cimetidine and sucralfate. We prepared several derivatives having a partial structure of coptisine from commercially available starting materials. The compounds obtained were tested for gastric-mucous membrane protective activity and a correlation between activity and structure was studied. Our results suggest that the partial charge of the catechol skeleton is related to activity.
Assuntos
Berberina/análogos & derivados , Berberina/farmacologia , Mucosa Gástrica/efeitos dos fármacos , Animais , Berberina/síntese química , Coptis chinensis , Medicamentos de Ervas Chinesas/síntese química , Medicamentos de Ervas Chinesas/farmacologia , Etanol/toxicidade , Mucosa Gástrica/patologia , Masculino , Raízes de Plantas/química , Ratos , Ratos Wistar , Relação Estrutura-AtividadeRESUMO
Conformational parameters of pheromonally active analogs (1 and 2) of periplanones, the sex pheromones of the American cockroach, were investigated by molecular mechanics calculations. They existed in several conformers with small energy differences. These results were supported by NMR analysis. The structural features of the conformers of the analogs were compared with X-ray structures of periplanones.
RESUMO
Conformational analysis using molecular mechanics (MM) was performed for a determination of the stereochemistry of serricornin, the sex pheromone of the cigarette beetle (Lasioderma serricorne F.). An exhaustive conformational analysis using MM2 calculations with algorithms for covering torsional energy surfaces of flexible molecules furnishes coordinates and steric energies of all local energy minimum conformers of serricornin, both acyclic and the corresponding cyclic forms. These coordinates gave angles required for the calculation of vicinal H/H coupling constants ((3) J HHs) of each energy minima by Altona's modified Karplus equation. The Boltzmann distributions of all local energy minima were calculated from their steric energies to furnish populations of each energy minimum conformer. Populationweighted averaged(3) J HHs of four enantiomeric pairs, (S (*),S (*),S (*))-, (S (*),S (*),R (*))-, (S (*),R (*),S (*))-, and (R (*),S (*),S (*))-serricornins were calculated from the data above. The observed(3) J HHs of the naturally occurring serricornin, both acyclic and cyclic forms, are fitted best to calcd.(3) J HHs of (4S (*), 6S (*), 7S (*))-acyclic and (3S (*), 5S (*), 6S (*))-cyclic serricornin, respectively, among those of four enantiomeric pairs of serricornin.