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1.
Eur Rev Med Pharmacol Sci ; 24(12): 7063-7076, 2020 06.
Article in English | MEDLINE | ID: mdl-32633401

ABSTRACT

OBJECTIVE: Malaria parasites invade, grow and multiply inside erythrocytes and obtain nourishment from haemoglobin. Then, the released haem group is oxidized to haematin and inert dimeric haemozoin bio-crystals form, which provides the parasite a unique way to avoid the toxicity associated with the haem group. Therefore, antimalarial drugs are designed to inhibit dimer formation; however, recent electrochemical studies indicate that an inert dimer also promotes a toxic oxidizing environment. Therefore, this work explores drug reactivity in the presence of monomers and dimers to evaluate their contribution to redox activity. MATERIALS AND METHODS: Three medicines mixed with haemozoin or ß-haemozoin in carbon paste electrodes were tested using cyclic voltammetry. RESULTS: The data indicated again that the substances modify the natural redox state of haemozoin and ß-haemozoin. This effect could be attributed to the natural oxidation potential of the drugs. In addition, it was found that the oxidation potential decreased through quinine, lumefantrine and artemether with the same tendency in the presence of haemozoin but with less current density. Additionally, it was observed that the oxidation response between the monomer haemozoin and antimalarial drugs is carried out at more negative potentials. CONCLUSIONS: Together, the total results indicate that antimalarials per se can contribute to oxidation processes and that in combination with monomeric or dimeric haemozoin can increase or decrease the oxidizing power of the haemozoin forms. The various oxidizing environments suggest that the cell membranes can also be damaged by the unique presence of the antimalarial.


Subject(s)
Antimalarials/chemistry , Artemether/chemistry , Hemoglobins/chemistry , Lumefantrine/chemistry , Quinine/chemistry , Animals , Electrodes , Hemiptera/chemistry , Humans , Oxidation-Reduction , Particle Size , Surface Properties
2.
Eur J Clin Nutr ; 71(9): 1068-1073, 2017 09.
Article in English | MEDLINE | ID: mdl-28378850

ABSTRACT

BACKGROUND/OBJECTIVE: Few studies in Latin American paediatric populations have differentiated fat deposits in specific areas, such as intra-abdominal fat (IAF) and subcutaneous abdominal fat (SAF). Research in diverse populations is needed, as patterns of fat accumulation vary by ethnicity. The aim of this study was to determine whether IAF and/or SAF are related to cardiometabolic risk factors, independent of total body fat (TBF), in a group of Mexican schoolchildren. SUBJECTS/METHODS: A cross-sectional study was conducted in Mexico City with 94 children aged between 5 and 11 years. IAF and SAF were assessed by magnetic resonance using two different estimation methods: (a) at the midpoint of lumbar vertebras 4 and 5 (L4-L5) and (b) the sum of the areas of four slices (L1-L2, L2-L3, L3-L4 and L4-L5, which will be referred to as 'total' IAF and SAF). TBF was measured by dual-energy X-ray absorptiometry. The following cardiometabolic risk factors were assessed: total cholesterol, low-density lipoprotein-cholesterol, triglycerides, glucose, insulin, high-density lipoprotein-cholesterol, blood pressure, insulin resistance, number of risk factors and metabolic syndrome score. RESULTS: After adjusting for sex, age and TBF, total SAF was related to the number of cardiometabolic risk factors and metabolic syndrome score. Although IAF at L4-L5 was also related to the number of cardiometabolic risk factors, there was evidence of collinearity with TBF. CONCLUSIONS: In this sample of Mexican schoolchildren, TBF and SAF, but not IAF, were associated with higher cardiometabolic risk.


Subject(s)
Body Composition , Intra-Abdominal Fat/physiopathology , Metabolic Syndrome/physiopathology , Pediatric Obesity/physiopathology , Subcutaneous Fat, Abdominal/physiopathology , Child , Child Health Services , Female , Humans , Male , Metabolic Syndrome/blood , Metabolic Syndrome/etiology , Mexico , Pediatric Obesity/blood , Pediatric Obesity/complications , Predictive Value of Tests , Risk Factors , School Health Services , Sex Factors
4.
Pediatr. aten. prim ; 16(64): e155-e160, oct.-dic. 2014. ilus
Article in Spanish | IBECS | ID: ibc-131218

ABSTRACT

Los quistes aracnoideos son lesiones benignas, de origen congénito, formadas por una membrana aracnoidea, que contienen líquido cefalorraquídeo en su interior. Presentamos el caso de un niño de cinco años con una asimetría craneal con abombamiento frontoparietotemporal derecho. Refería vómitos ocasionales de un año de evolución y cefalea que no le despertaba por la noche desde hacía dos años, acompañada algunas veces de sonofobia y fotofobia. En las pruebas de imagen se visualizaba un gran quiste aracnoideo en la fosa craneal media derecha con desplazamiento de la línea media y colapso de las astas ventriculares adyacentes. Dado el tamaño del quiste y la clínica, se decidió tratamiento con cistocisternostomía endoscópica comunicando el quiste aracnoideo con las cisternas basales (AU)


Arachnoid cysts are benign, congenital malformations formed by an arachnoid membrane containing cerebrospinal fluid inside. We report the case of a 5 year old child with cranial asymmetry with right fronto-parieto-temporal bulging. Occasional vomiting a year of evolution and sometimes headache are refered, which did not wake him at night, accompanied by sonophobia and photophobia for two years. The imaging displays large arachnoid cyst in right middle cranial fossa with midline shift and collapse of adjacent ventricular horns. Because of the size of the cyst and the clinic, endoscopic treatment was selected, communicating arachnoid cyst and basal cisterns (AU)


Subject(s)
Humans , Male , Child , Brain Neoplasms/surgery , Brain Neoplasms , Medulloblastoma/complications , Medulloblastoma/surgery , Medulloblastoma , Diagnosis, Differential , Tomography, Emission-Computed/methods , Neurosurgery/methods , Neurosurgery/trends , Endoscopy/methods , Endoscopy
9.
Pediatr. aten. prim ; 12(48): 621-626, oct.-dic. 2010. ilus
Article in Spanish | IBECS | ID: ibc-84735

ABSTRACT

El hematocolpos constituye una patología poco prevalente en nuestro medio, secundaria a alteraciones en la génesis del aparato genitourinario femenino, entre las cuales el himen imperforado es la malformación congénita más frecuente. La sintomatología suele ser variable e inespecífica, y el dolor abdominal es la forma de presentación clínica más frecuente. En este artículo se exponen dos casos clínicos de adolescentes afectas de esta patología. Ambas presentaron abdominalgia y síntomas miccionales. La realización de una historia clínica detallada junto con la inspección de los genitales, así como la visualización en la ecografía abdominal de una colección sanguínea localizada en la vagina, fueron fundamentales para llegar al diagnóstico. En este artículo se pretende destacar la importancia de la anamnesis y la exploración genital ante una sintomatología tan inespecífica como son el dolor abdominal y la clínica miccional, ya que puede orientarnos al diagnóstico de forma sencilla, evitando pruebas innecesarias, medidas terapéuticas erróneas y aparición de complicaciones (AU)


Hematocolpos constitutes an unusual pathology in our environment, secondary to alterations in the genesis of female genitourinary tract, being the imperforate hymen the most common congenital malformation. The symptomatology is usually variable and nonspecific with abdominal pain as the most frequent clinical presentation. In this paper we present the description of two cases of teenagers affected by this disease. Both presented abdominal pain and urinary symptoms. Besides a detailed medical history along with the inspection of the genitalia as well as the visualization in the abdominal echography of a blood collection located in the vagina, were fundamental in order to make a diagnosis. Throughout this article we intend to emphasize the relevance of the medical history and genital examination before symptoms as nonspecific as abdominal pain and urinary symptoms because of it can help us to guide the diagnosis in an easy way avoiding unnecessary tests, erroneous therapeutic measures and appearance of complications (AU)


Subject(s)
Humans , Female , Child , Hematocolpos/complications , Hematocolpos/diagnosis , Hematocolpos/surgery , Hymen/abnormalities , Hymen/surgery , Abdominal Pain/complications , Urinary Retention/complications , Urogenital Abnormalities/diagnosis , Abdominal Pain/etiology , Urogenital Abnormalities/complications , Urogenital Abnormalities/surgery , Hymen
12.
Am J Trop Med Hyg ; 58(6): 715-20, 1998 Jun.
Article in English | MEDLINE | ID: mdl-9660451

ABSTRACT

We report here the evaluation of chagasic patients for the presence and/or severity of the disease, antibody to Trypanosoma cruzi, and nitric oxide (NO) serum levels. Serum samples tested by ELISA with autochthonous and commercial antigen revealed that 10% and 7.5% of the individuals were anti-T. cruzi antibody-positive, respectively. Ten of 21 seropositive individuals had no clinical signs, the other 11 cases presented cardiomyopathy and/or mega-gastrointestinal syndromes, and three patients presented a combined form. A statistical difference (P < 0.001) in antibody titer between asymptomatic and symptomatic patients with autochthonous antigen was detected, and serum NO levels was found to be three times higher in cases than in controls. These results suggest that it is recommended to use a sole source of antigen (autochthonous) for the serodiagnosis of Chagas' disease, and that the pathogenic role of NO in this disease should be evaluated.


Subject(s)
Antibodies, Protozoan/biosynthesis , Antigens, Protozoan/immunology , Chagas Disease/immunology , Nitric Oxide/blood , Trypanosoma cruzi/immunology , Adult , Aged , Aged, 80 and over , Animals , Antibodies, Protozoan/blood , Chagas Disease/blood , Enzyme-Linked Immunosorbent Assay , Female , Fluorescent Antibody Technique, Indirect , Hemagglutination Inhibition Tests , Humans , Male , Middle Aged
13.
Rev Enferm ; 20(221): 11-7, 1997 Jan.
Article in Spanish | MEDLINE | ID: mdl-9096048

ABSTRACT

Knowing the grave health consequences of adult obesity and the fact that a high percentage of these adults were obese as children we propose, using a transverse epidemiological study that includes anthropometric measurements and dietary surveys, to learn how this phenomena impacts our area of health care. The prevalence of juvenile obesity (from 6 to 13 years of age) in our community was analyzed, along with factors that are related to its development. The results of our study allow us to draw the following conclusions: The prevalence of juvenile obesity in our community (26%) is considerably higher than the national average (6-15% as of 1991). The factors that significantly influence the development of juvenile obesity are: degree of physical activity, genetic and environmental influences, and conditional behaviors of eating.


Subject(s)
Child Nutritional Physiological Phenomena , Child Welfare , Feeding Behavior , Obesity/etiology , Adolescent , Child , Female , Humans , Male , Obesity/genetics , Obesity/psychology , Physical Fitness
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