ABSTRACT
BACKGROUND: Cryolipolysis is a non-invasive method capable of reducing the thickness of the fat layer. OBJECTIVE: To evaluate the effects of cryolipolysis with the use of plate applicators in the treatment of abdominal fat in women. MATERIALS AND METHODS: The sample was composed of 15 participants, who were evaluated before and at the end of the intervention. Three applications of cryolipolysis were performed in the infraumbilical portion of the abdominal region. The volunteers were divided into three groups G-1 (temperature of -2°C), G-2 (temperature of -3°C) and G3 (temperature of -4°C). RESULTS: There was a reduction in plicometry measurements in groups G2 and G3, in the comparison between the initial and final moments (p <0.05), and a reduction in perimetry and ultrasound (p < 0.05) in all groups. It was found that the G3 group was subject to higher risk of first degree burns and redness when compared to the other groups. CONCLUSION: It is suggested that plate cryolipolysis is a possibly effective resource for reducing adiposity, as shown in the evaluation of perimetry, plicometry, and ultrasound results, and in the photographic analysis.
Subject(s)
Abdominal Fat , Adiposity , Cryotherapy , Lipolysis , Female , Humans , Overweight/therapy , Treatment Outcome , UltrasonographyABSTRACT
Physical exercise is useful in people who underwent bariatric surgery. However, the right dosage is still a topic for discussion. The aim of this article is to consolidate the prescription criteria for physical activity and exercise in bariatric patients. A panel of experts to whom the topics were previously assigned for review, met to reach a consensus. Each topic was presented and subjected to discussion and voting by the participants and attendants who were exercise professionals from different obesity treatment centers. We report the conclusions reached for aerobic exercise, strength training, protein supplementation and physical activity for weight maintenance in bariatric patients.
Subject(s)
Humans , Adult , Obesity, Morbid/surgery , Exercise Tolerance , Bariatric Surgery/rehabilitation , Exercise Therapy , Body Mass Index , Guidelines as Topic , Consensus , Resistance TrainingABSTRACT
Physical exercise is useful in people who underwent bariatric surgery. However, the right dosage is still a topic for discussion. The aim of this article is to consolidate the prescription criteria for physical activity and exercise in bariatric patients. A panel of experts to whom the topics were previously assigned for review, met to reach a consensus. Each topic was presented and subjected to discussion and voting by the participants and attendants who were exercise professionals from different obesity treatment centers. We report the conclusions reached for aerobic exercise, strength training, protein supplementation and physical activity for weight maintenance in bariatric patients.
Subject(s)
Bariatric Surgery/rehabilitation , Exercise Therapy , Exercise Tolerance , Obesity, Morbid/surgery , Adult , Body Mass Index , Consensus , Guidelines as Topic , Humans , Resistance TrainingABSTRACT
Fenton systems (H2O2/Fe(II) or H2O2/Cu(II)) inhibited Trypanosoma cruzi and Crithidia fasciculata topoisomerase I activity. About 61-71% inactivation was produced by 25 mM Fe(II) or Cu(II) with 3 mM H2O2. Thiol compounds and free radicals scavengers prevented the Fenton systems effects, depending on the topoisomerase assayed. With the T. cruzi enzyme, reduced glutathione, DL-dithiothreitol, cysteine and N-acetyl-L-cysteine entirely prevented the effect of the H2O2/Fe(II) system, mannitol protected 37%, whereas histidine and ethanol were ineffective. With C. fasciculata topoisomerase, reduced glutathione, DL-dithiothreitol and N-acetyl-L-cysteine protected 100%, cysteine, histidine and mannitol protected 28, 34 and 48% respectively, whereas ethanol was ineffective. With the H2O2/Cu(II) system and T. cruzi topoisomerase, DL-dithiothreitol and histidine protected 100% and 60%, respectively but the other assayed protectors were less effective. Similar results were obtained with the C. fasciculata enzyme. Topoisomerase inactivation by H2O2/Fe(II) or H2O2/Cu(II) systems was irreversible since they were not reverted by the more effective enzyme protectors. It is suggested that topoisomerases could act either as scavengers of "reactive oxygen species" (ROS) generated by Fenton systems or bind the corresponding metal ions, whose redox cycling would generate reactive oxygen species "in situ".
Subject(s)
Crithidia fasciculata/enzymology , Enzyme Inhibitors/pharmacology , Hydrogen Peroxide/pharmacology , Iron/pharmacology , Protozoan Proteins/antagonists & inhibitors , Topoisomerase I Inhibitors , Trypanosoma cruzi/enzymology , Animals , Chelating Agents/pharmacology , Crithidia fasciculata/drug effects , Hydrogen Peroxide/antagonists & inhibitors , Iron/antagonists & inhibitors , Oxidation-Reduction , Reactive Oxygen Species/metabolism , Species Specificity , Sulfhydryl Reagents/pharmacology , Trypanosoma cruzi/drug effectsABSTRACT
Los sistemas Fenton (H2O2/Fe o H2O2/Cu) fueron capaces de inhibir la actividad topoisomerasa I de extractos crudos de Trypanosoma cruzi y Crithidia fasciculata. El agregado de compuestos de tioles o complejantes de metales, modificó la inhibición y dicho efecto dependió del metal y del origen de la enzima. El glutation reducido, DL-ditiotreitol, y N-aceti-L-cisteína 1 mM fueron efectivos protectores frente a la inhibición, inducida por el sistema H2O2/Fe, de la actividad presente en T.cruzi, el manitol protegió 37 por ciento, mientras que la histidina y etanol fueron inefectivos. Con la topoisomerasa de C.fasciculata, glutatión reducido, DL-ditiotreitol y N-acetil L-cisteína protegieron 100 por ciento a la enzima de la acción deletérea del sistema Fenton (Fe), los compuestos manitol, histidina y cisteína 1 mM protegieron 48, 34 y 28 por ciento, respectivamente, mientras que el etanol 4 mM fue inefectivo. Con el sistema H2O2/Cu y la enzima de T.cruzi, el DL-ditiotreitol y la histidina 1mM protegieron 100 y 60 por ciento, respectivamente, los otros protectores ensayados fueron menos efectivos. Resultados semejantes se obtuvieron con la topoisomerasa de C.fasciculata. La disminución por sistemas Fenton de la actividad topoisomerasa I de los extractos resultó no ser revertida por posterior incubación con los compuestos que tuvieron efecto protector. Se sugiere que la estructura molecular de la proteína podría actuar como secuestrante de radicales libres generados por los sismtemas Fenton o mediante la unión de metales como el Cu o Fe, facilitando la generación de los mismos in situ. Ambos mecanismos conducirían a la inactivación de la misma. (AU)
Subject(s)
Trypanosoma cruzi , Crithidia fasciculata , ArgentinaABSTRACT
Los sistemas Fenton (H2O2/Fe o H2O2/Cu) fueron capaces de inhibir la actividad topoisomerasa I de extractos crudos de Trypanosoma cruzi y Crithidia fasciculata. El agregado de compuestos de tioles o complejantes de metales, modificó la inhibición y dicho efecto dependió del metal y del origen de la enzima. El glutation reducido, DL-ditiotreitol, y N-aceti-L-cisteína 1 mM fueron efectivos protectores frente a la inhibición, inducida por el sistema H2O2/Fe, de la actividad presente en T.cruzi, el manitol protegió 37 por ciento, mientras que la histidina y etanol fueron inefectivos. Con la topoisomerasa de C.fasciculata, glutatión reducido, DL-ditiotreitol y N-acetil L-cisteína protegieron 100 por ciento a la enzima de la acción deletérea del sistema Fenton (Fe), los compuestos manitol, histidina y cisteína 1 mM protegieron 48, 34 y 28 por ciento, respectivamente, mientras que el etanol 4 mM fue inefectivo. Con el sistema H2O2/Cu y la enzima de T.cruzi, el DL-ditiotreitol y la histidina 1mM protegieron 100 y 60 por ciento, respectivamente, los otros protectores ensayados fueron menos efectivos. Resultados semejantes se obtuvieron con la topoisomerasa de C.fasciculata. La disminución por sistemas Fenton de la actividad topoisomerasa I de los extractos resultó no ser revertida por posterior incubación con los compuestos que tuvieron efecto protector. Se sugiere que la estructura molecular de la proteína podría actuar como secuestrante de radicales libres generados por los sismtemas Fenton o mediante la unión de metales como el Cu o Fe, facilitando la generación de los mismos in situ. Ambos mecanismos conducirían a la inactivación de la misma.
Subject(s)
Crithidia fasciculata , DNA Topoisomerases, Type I , Trypanosoma cruzi , ArgentinaABSTRACT
Fenton systems (H2O2/Fe(II) or H2O2/Cu(II)) inhibited Trypanosoma cruzi and Crithidia fasciculata topoisomerase I activity. About 61-71
inactivation was produced by 25 mM Fe(II) or Cu(II) with 3 mM H2O2. Thiol compounds and free radicals scavengers prevented the Fenton systems effects, depending on the topoisomerase assayed. With the T. cruzi enzyme, reduced glutathione, DL-dithiothreitol, cysteine and N-acetyl-L-cysteine entirely prevented the effect of the H2O2/Fe(II) system, mannitol protected 37
, whereas histidine and ethanol were ineffective. With C. fasciculata topoisomerase, reduced glutathione, DL-dithiothreitol and N-acetyl-L-cysteine protected 100
, cysteine, histidine and mannitol protected 28, 34 and 48
respectively, whereas ethanol was ineffective. With the H2O2/Cu(II) system and T. cruzi topoisomerase, DL-dithiothreitol and histidine protected 100
and 60
, respectively but the other assayed protectors were less effective. Similar results were obtained with the C. fasciculata enzyme. Topoisomerase inactivation by H2O2/Fe(II) or H2O2/Cu(II) systems was irreversible since they were not reverted by the more effective enzyme protectors. It is suggested that topoisomerases could act either as scavengers of [quot ]reactive oxygen species[quot ] (ROS) generated by Fenton systems or bind the corresponding metal ions, whose redox cycling would generate reactive oxygen species [quot ]in situ[quot ].
ABSTRACT
Crithidia fasciculata poly(ADP-ribose)polymerase (PARP) has been isolated and partially purified. This is the first PARP isolated from trypanosomatids; it requires DNA and histone for activity, using NAD(+) as substrate. Thiol compounds specially dithiothreitol essentially contributed to PARP stability during purification and to PARP activity during assays. Nicotinamide, 3-aminobenzamide, theophylline, histamine, histidine, N-ethylmaleimide, p-chloromercuribenzoic acid, p-chloromercuriphenylsulfonic acid and o-iodosobenzoate inhibited PARP, thus confirming enzyme identity. PARP was also inhibited by the Fe(II)/H(2)O(2) Fenton system. beta-Lapachone inhibited PARP, apparently by direct interaction with the enzyme.