NADPH-induced chemiluminescence and lipid peroxidation in kidney microsomes

NADPH-induced chemiluminescence and lipid peroxidation in kidney microsomes. Lipid peroxidation and reactive oxygen species have been shown to affect diverse biological processes potentially important in renal disease. We therefore examined NADPH-induced chemiluminescence (CL) and lipid peroxidation (LP) by renal cortical and, in some experiments, medullary microsomes. We further examined the role of reactive oxygen species in these processes by the use of enzymatic and chemical scavengers. Cortical microsomes gave a marked NADPH-induced CL accompanied by LP. The time course of LP closely paralleled the CL response. Cortical microsomal CL and LP increased with increasing concentrations of protein (0.3 to 1.8 mg) and NADPH (0.1 to 3.0mM); NADH could not substitute for NADPH. Using similar amounts of protein and NADPH concentrations, cortical CL was significantly higher than medullary CL at all time points examined (peak cortical CL: 490 ± 25 × 103 cpm/mg protein, N = 4; peak medullary CL: 226 ± 61 × 103 cpm/mg protein, N = 4). Cortical LP was similarly higher at all time points, values corresponding to peak CL being 44.7 ± 3 nmoles/mg protein for cortex and 29.9 ± 0.8 nmoles/mg protein for medulla. Para-chloromercuribenzoate (PCMB), an inhibitor of NADPH-cytochrome P450 reductase, caused a marked inhibition of the microsomal CL and LP whereas SKF 525A, an inhibitor of cytochrome P450, had a relatively minor effect. Marked inhibition of NADPH induced CL and LP was observed with chelators EDTA and 1,10-phenanthroline. The addition of NADPH to microsomes prepared with sucrose-EDTA and washed in a Chelex-treated buffer gave a negligible CL and LP response; the responses were restored by the addition of iron. Scavengers of superoxide anion (superoxide dismutase), hydrogen peroxide (catalase), and the hydroxyl radical (sodium benzoate, tryptophan) had a relatively minor effect on CL and LP. Singlet oxygen quenchers sodium azide and 1,4-diazabicyclo (2.2.2) octane (DABCO) caused an incomplete inhibition of CL and LP responses and then only after the first 30min. Taken together, these data suggest that other free radical mechanisms are likely to be important in the CL and LP responses. These results which demonstrate the production of excited states and LP by renal microsomes suggest that their role in renal disease deserves further study.Chemiluminescence induite par le NADPH et peroxydation des lipides dans les microsomes de rein. Il a été montré que la peroxydation des lipides et le type d'oxygène réactif modifient diversement les processus biologiques potentiellement importants dans les maladies rénales. C'est pourquoi nous avons examiné la chemiluminescence (CL) induite par le NADPH, et la peroxydation (LP) des lipides par des microsomes corticaux et dans quelques expériences, médullaires rénaux. Nous avons ensuite examiné le rôle du type d'oxygène réactif dans ces processus en utilisant des agents métabolisants enzymatiques et chimiques. Les microsomes corticaux donnaient une CL marquée induite par le NADPH accompagnée par une LP. Dans le temps, la LP était étroitement parallèle à la réponse CL. La CL et la LP microsomiales corticales s'élevaient avec l'accroissement des concentrations de protéines (0, 1 à 1,8 mg) et de NADPH (0,1 à 3,0mM); le NADH ne pouvait so substituer au NADPH. En utilisant des quantités identiques de protéines et de NADPH, la CL corticale était significativement plus élevée que la CL médullaire à tous les temps examinés (pic de CL corticale: 490 ± 25 × 103 cpm/mg protéine, N = 4, pic de CL médullaire: 226 ± 61 × 103 cpm/mg protéine, N = 4). De même la LP corticale était plus élevée à tous les temps, les valeurs correspondant au pic de CL étant de 44,7 ± 3 nmoles/mg protéine pour le cortex et de 29,9 ± 0,8 nmoles/mg protéine pour la médullaire. Le parachloromercuribenzoate (PCMB), un inhibiteur de la réductase NADPH-cytochrome P450a entraîné une inhibition marquée de la CL et de la LP microsomiales tandis que le SKF 525 A, un inhibiteur du cytochrome P450, avait un effet relativement minime. Une inhibition marquée de la CL induite par le NADPH et de la LP a été observée avec des chélateurs tels l'EDTA et le 1,10-phénanthroline. L'addition de NADPH à des microsomes préparés dans du sucrose-EDTA et lavés dans un tampon traité au Chelex entraînait une réponse CL et LP négligeable; les réponses étaient restaurées par l'addition de fer. Les agents métabolisants l'anion superoxide (dismutase superoxide), le peroxide d'hydrogène (catalase), et le radical hydroxylé (benzoate de sodium, tryptophane) avaient un effet relativement minime sur CL et LP. Les capteurs d'oxygène singulet comme l'azide de sodium et le 1,4-diazabicyclo (2.2.2) octane (DABCO) entraînaient une inhibition incomplète des réponses CL et LP et cela seulement après les 30 premières min. Prises dans leur ensemble, ces données suggèrent que d'autres mécanismes par radicaux libres sont probablement importants dans les réponses CL et LP. Ces résultats, qui démontrent la production d'états excités et de LP par des microsomes rénaux, suggèrent que leur rôle dans les maladies rénales nécessite d'autres études

Characterization of mammary neoplasia by electrical impedance spectroscopy: canine model

Introducción: La espectroscopia de impedancia eléctrica (EIE) es una técnica fácil de usar y de bajo costo que se puede utilizar para analizar tejidos biológicos en condiciones normales o patológicas. El objetivo de este trabajo fue caracterizar neoplasias de glándula mamaria benignas y malignas aplicando la técnica EIE en muestras extraídas de 45 caninos hembras (Canis lupus familiaris). Métodos: Se utilizó un medidor de impedancia eléctrica, Hioki 3532-50, para determinar los parámetros bioeléctricos: resistencia de la matriz extracelular (R), resistencia de la matriz intracelular (S), frecuencia característica (Fc) y capacitancia de membrana (Cm) en un rango de frecuencias entre 42 Hz y 5 MHz y se analizaron estadísticamente mediante la prueba no paramétrica U de Mann-Whitney (Wilcoxon) de dos colas. La precisión diagnóstica de la EIE se efectuó a través de curvas características de operación del receptor (COR) y tablas de doble entrada, con la histopatología como referencia. Resultados: Se encontraron diferencias estadísticamente significativas entre el tejido mamario sano y las neoplasias benignas para los parámetros R, Fc y Cm, p-value < 0,05. Entre tejido mamario sano y neoplasias mamarias malignas se encontraron diferencias estadísticamente significativas para R y Fc con un p-value < 0,05. La comparación entre lesiones tumorales benignas y malignas no presentó diferencias estadísticamente significativas, p-value > 0,05, para ninguna de las variables incluidas en este estudio. Conclusiones: De los parámetros analizados por EIE, la resistencia de la matriz extracelular es la que mejor permite diferenciar entre tejidos mamarios normales y neoplásicos. La EIE es una herramienta diagnóstica potencial que puede ser utilizada en la detección de cáncer mamario, con una precisión diagnóstica cercana al 80%.Introduction: Electrical Impedance Spectroscopy (EIS) it is an easy to use and low-cost technique that can be used to analyze biological tissues in normal or pathological condition. The goal of this work was to characterize benign and malign mammary gland neoplasms applying the EIS technique in 45 female dogs (Canis lupus familiaris). Methods: An impedance meter Hioki 3532-50 was used to determine bioelectric parameters, extracellular matrix resistance (R), intracellular matrix resistance (S), characteristic frequency (Cf), and membrane capacitance (Mc), which were obtained in a 42 Hz and 5 MHz frequencies range. Were statistically analyzed with the non-parametric test of two-tailed MannWhitney (Wilcoxon). The diagnostic precision of the test was performed using receiver operating characteristics (ROC) and two-way tables using histopathology results as reference. Results: Significant differences between healthy mammary tissue and benign neoplasms were found for variables R, Cf and Mc (p < 0.05). There were statistically major differences between the healthy mammary tissue and malign mammary tumors groups for R and Cf (p < 0.05). The comparison between malign and benign tumor lesions did not show a statistically significant difference, p-value > 0.05, for any of the variables included in this study. Conclusion: Among all parameters analyzed for EIS, the extracellular matrix resistance R is the one that best allows differentiating between healthy and neoplastic mammary tissues. EIS is a diagnostic tool that can be used for breast cancer detection with a diagnostic precision close to 80%

Shell sclerochronology and stable isotopes of the bivalve Anomalocardia flexuosa (Linnaeus, 1767) from southern Brazil: : implications for environmental and archaeological studies

We conduct the first stable isotopic and sclerochronological calibration of the bivalve Anomalocardia flexuosa (Linnaeus, 1767) in relation to environmental variables in a subtropical coastal area of southern Brazil. We investigate incremental shell growth patterns and δ18O and δ13C values of modern specimens collected alive from the Laguna Lagoonal System (LLS). As shells of Anomalocardia flexuosa are also the main components of pre-Columbian archaeological shell mounds and middens distributed along the Brazilian coastline, late Holocene archaeological specimens from a local shell mound (Cabeçuda) were selected to compare their stable carbon and oxygen isotopes with those of modern specimens. Shell growth increments, δ18O and δ13C values respond to a complex of environmental conditions, involving, for example, the effects of temperature and salinity. The isotopic information extracted from archaeological specimens from Cabeçuda shell midden in the LLS indirectly indicates that environmental conditions during the late Holocene were different from present day. In particular, intra-shell δ18O and δ13C values of archaeological shells reveal a stronger marine influence at 3 ka cal BP, which is in contrast to the seasonal freshwater/seawater balance that currently prevails at the LLS

El Modelo de Crecimiento Económico de Robert Solow en el Perú 1950-2021

The objective of this research is to explain the Robert Solow Model, the Macroeconomic Per Capita production function with Cobb Technological neutrality. Douglas, Robert Solow's Labor Intensive Per Capita Macroeconomic Production Function. The fundamental Equation of Percapita Capital of Robert Solow in Peru is: AK= 0, 43 K0,57 - (0.0152 + 0,032 + 0,0007) Solution: K= 1, 29% (Stationary state) PBIR = 4, 72% Peru's economic growth rate in 2020  El objetivo de esta investigación es explicar el Modelo de Robert Solow, la función de producción Macroeconómica Per Cápita con neutralidad Tecnológica de Cobb. Douglas, función de produccion Macroeconómica Per Cápita intensiva de trabajo de Robert Solow. La Ecuación fundamental de Capital Percapita de Robert Solow en el Perú es: AK= 0, 43 K0,57 - (0.0152 + 0,032 + 0,0007) Solución: K= 1, 29% (Estado estacionario) PBIR = 4, 72%