RESUMO
PURPOSE: To evaluate the tissue response of the mucosa of the tympanic cavity of guinea pigs, when receiving biodegradable implant. METHODS: A total of 20 male guinea pigs were divided into 2 groups. After paracentesis in both ears, a biodegradable polymer of poly lactic-co-glycolic acid was implanted in only one middle ear. Histological analysis using neutrophil exudate and vascular neoformation (acute inflammation) and fibroblast proliferation and mononuclear inflammatory cells (chronic inflammation) as parameters was performed after 10 and 30 days of survival (groups 1 and 2, respectively). RESULTS: Four ears in group 1 and 7 in group 2 had an increase of neutrophil exudate. Vascular neoformation occurred in ears with or without the implant, in both groups. Fibroblast proliferation and mononuclear inflammatory cells (lymphocytes and macrophages) increased in ears with implant in group 2. CONCLUSION: The tissue response by histological analysis of the mucosa of the tympanic cavity of guinea pigs, when receiving biodegradable implant, showed no statistically significant difference between ears with or without the implant. .
Assuntos
Animais , Cobaias , Masculino , Implantes Absorvíveis , Orelha Média/efeitos dos fármacos , Lactatos/uso terapêutico , Polímeros/uso terapêutico , Ácido Tióctico/análogos & derivados , Biopolímeros/uso terapêutico , Exsudatos e Transudatos , Orelha Média/patologia , Fibroblastos/efeitos dos fármacos , Mucosa/efeitos dos fármacos , Mucosa/patologia , Neovascularização Patológica , Neutrófilos/efeitos dos fármacos , Distribuição Aleatória , Reprodutibilidade dos Testes , Fatores de Tempo , Ácido Tióctico/uso terapêuticoRESUMO
Dihydrolipoamide dehydrogenase (LADH) from Trypanosoma cruzi, the causative agent of Chagas' disease, was inactivated by treatment with myeloperoxidase (MPO)-dependent systems. LADH lipoamide reductase and diaphorase activities decreased as a function of incubation time and composition of the MPO/H2O2/halide system, a transient increase preceding the loss of diaphorase activity. Iodide, bromide, thiocyanide and chloride were effective components of MPO/H2O2 or MPO/NADH systems. Catalase prevented LADH inactivation by the MPO/NADH/halide systems in agreement with H2O2 production by NADH-supplemented LADH. Thiol compounds (L-cysteine, N-acetylcysteine, penicillamine, N-(2-mercaptopropionylglycine) and Captopril prevented LADH inactivation by the MPO/H2O2/NaCl system and by NaOCl, thus supporting HOCl as agent of the MPO/H2O2/NaCl system. MPO/H2O2/NaNO2 and MPO/NADH/NaNO2 inactivated LADH, the reaction being prevented by MPO inhibitors and thiol compounds. T. cruzi LADH was affected by MPO-dependent systems like myocardial LADH, allowance being made for the variation of the diaphorase activity and the greater sensitivity of the T. cruzi enzyme to MPO/H2O2/halide systems.
Assuntos
Animais , Humanos , Ácido Hipocloroso/farmacologia , Di-Hidrolipoamida Desidrogenase , Neutrófilos/fisiologia , Nitritos , Peroxidase , Proteínas de Protozoários/antagonistas & inibidores , Explosão Respiratória , Trypanosoma cruzi , Acetilcisteína/farmacologia , Ácido Tióctico/análogos & derivados , Ácido Tióctico/metabolismo , Brometos , Captopril , Catalase , Cisteína/farmacologia , Cloreto de Sódio/farmacologia , Compostos de Sódio/farmacologia , Citotoxicidade Imunológica , Espécies Reativas de Oxigênio/metabolismo , Glutationa , Glicina , Cinética , Miocárdio , NAD , Neutrófilos/enzimologia , Oxirredução , Penicilamina , Peróxido de Hidrogênio/farmacologia , Proteínas Recombinantes/antagonistas & inibidores , Compostos de Sulfidrila , Triptofano , TirosinaRESUMO
Comparative detoxification of scorpion venom by using different chemical agents was investigated. Detoxification by formalin showed the best optimum detoxifying agent. The formalin treatment resulted in 2.3% protein loss with 6-fold detoxification. This formal toxoid was immunogenic in rabbit giving high neutralizing antibodies as revealed from indirect haemagglutination test. Toxoid antiserum protected mice against the lethal action of venom. It also effectively antagonized the smooth muscle contractile response of venom, and venom-induced neuromuscular paralysis. This toxoid antiserum also protected the venom-induced cardiac arrest. The possibility of using this formal toxoid for antisera production and immunization for therapeutic use needs to be explored.