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1.
Pest Manag Sci ; 74(11): 2608-2617, 2018 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-29700928

RESUMO

BACKGROUND: Studies show that insects can adapt to the toxins of Bacillus thuringiensis under field and laboratory conditions through the development of resistance to the bacterium and its formulations. This has been demonstrated in the failure to control Tuta absoluta populations in Brazil. This study evaluated membrane receptors using peroxidase-labeled lectins and the midgut histochemistry of T. absoluta populations to assess susceptibility to the insecticides Bt fomulations. The histochemistry analysis used Periodic Acid-Schiff for glycogen and Ponceau Xylidine for total proteins. The presence of glucose/mannose and N-acetylgalactosamine (GalNAc) was analyzed using specific lectins. One susceptible and one tolerant population were used in the study; insects were exposed to the insecticide concentrations recommended by the manufacturers. The midgut was collected after an interval of 20 min and analyzed using optical microscopy. RESULTS: Bt fomulation interferes with the glycogen content, whereas XenTari® interferes with the protein content, irrespective of the level of susceptibility. High expression of GalNAc residues was observed using soybean lectin labeling, indicating a direct relationship between the glycosylation pattern and susceptibility to Bt fomulation in the Pelotas population. CONCLUSION: The use of Bt fomulation caused greater alterations in the larval intestinal histophysiology compared to the use of XenTari® . © 2018 Society of Chemical Industry.


Assuntos
Bacillus thuringiensis/química , Metabolismo dos Carboidratos , Resistência a Inseticidas , Inseticidas/farmacologia , Lectinas/química , Mariposas/fisiologia , Acetilgalactosamina/metabolismo , Animais , Sistema Digestório/anatomia & histologia , Fenômenos Fisiológicos do Sistema Digestório , Glucose/metabolismo , Larva/crescimento & desenvolvimento , Larva/metabolismo , Larva/fisiologia , Manose/metabolismo , Mariposas/crescimento & desenvolvimento , Mariposas/microbiologia
2.
Clin Exp Pharmacol Physiol ; 44(2): 275-284, 2017 02.
Artigo em Inglês | MEDLINE | ID: mdl-27864828

RESUMO

The Na+ -ATPase, a secondary pump in the proximal tubule, is only weakly responsive to angiotensin II in adult offspring exposed perinatally to high Na+ intake. We have investigated whether the offspring from mothers given 0.3 mol/L NaCl show an ineffective angiotensin II action to increase in blood pressure. It was hypothesized that functional alterations at adult life are associated with the number of angiotensin II-positive cells in the developing kidney, with increased oxidative stress in maternal/foetal organs, or with morphometrical changes in placentas. Wistar female rats were maintained on 0.3 mol/L NaCl in their drinking water from 20 days before conception until weaning. After weaning, some of the male offspring were treated with enalapril for 21 days. Glomerular filtration rate was recorded up to 210 days of age, when mean arterial pressure was measured after infusion of angiotensin II. To investigate the placenta and foetal kidneys, mothers on tap water or NaCl were also treated with alpha-tocopherol, pregnancy being interrupted on the 20th day. There were no changes in the number of cells positive for angiotensin II in the foetal kidney and unchanged lipid peroxidation in the placenta of offspring exposed to NaCl, but the intermediate trophoblast area in the junctional zone was increased, possibly reducing maternal-foetal exchange. Glomerular filtration rate was reduced and there was an attenuated effect of angiotensin II on elevation of blood pressure, which could be mediated by an elevated angiotensin II during early life, once these disturbances had been prevented by early and short-term treatment with enalapril.


Assuntos
Inibidores da Enzima Conversora de Angiotensina/uso terapêutico , Rim/efeitos dos fármacos , Efeitos Tardios da Exposição Pré-Natal/prevenção & controle , Insuficiência Renal/prevenção & controle , Cloreto de Sódio na Dieta/efeitos adversos , Inibidores da Enzima Conversora de Angiotensina/administração & dosagem , Animais , Pressão Sanguínea/efeitos dos fármacos , Relação Dose-Resposta a Droga , Feminino , Taxa de Filtração Glomerular/efeitos dos fármacos , Rim/embriologia , Rim/crescimento & desenvolvimento , Rim/fisiopatologia , Tamanho do Órgão/efeitos dos fármacos , Estresse Oxidativo/efeitos dos fármacos , Placenta/efeitos dos fármacos , Placenta/patologia , Gravidez , Efeitos Tardios da Exposição Pré-Natal/sangue , Efeitos Tardios da Exposição Pré-Natal/etiologia , Ratos Wistar , Insuficiência Renal/sangue , Insuficiência Renal/embriologia , Insuficiência Renal/etiologia
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