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1.
Int Arch Otorhinolaryngol ; 18(1): 16-20, 2014 Jan.
Article in English | MEDLINE | ID: mdl-25992057

ABSTRACT

Introduction The research in long latency auditory evokes potentials (LLAEP) in newborns is recent because of the cortical structure maturation, but studies note that these potentials may be evidenced at this age and could be considered as indicators of cognitive development. Purpose To research the exogenous potentials in term and premature infants during their first month of life. Materials and Methods The sample consisted of 25 newborns, 15 term and 10 premature infants. The infants with gestational age under 37 weeks were considered premature. To evaluate the cortical potentials, the infants remained in natural sleep. The LLAEPs were researched binaurally, through insertion earphones, with frequent /ba/ and rare /ga/ speech stimuli in the intensity of 80 dB HL (decibel hearing level). The frequent stimuli presented a total of 80% of the presentations, and the rare, 20%. The data were statistically analyzed. Results The average gestational age of the term infants was 38.9 weeks (± 1.3) and for the premature group, 33.9 weeks (± 1.6). It was possible to observe only the potentials P1 and N1 in both groups, but there was no statistically significant difference for the latencies of the components P1 and N1 (p > 0.05) between the groups. Conclusion It was possible to observe the exogenous components P1 and N1 of the cortical potentials in both term and preterm newborns of no more than 1 month of age. However, there was no difference between the groups.

2.
Mutat Res Genet Toxicol Environ Mutagen ; 757(2): 99-103, 2013 Oct 09.
Article in English | MEDLINE | ID: mdl-23994570

ABSTRACT

Spinocerebellar ataxia type 3, also called Machado-Joseph disease (MJD), is an hereditary autosomal dominant neurodegenerative disease that affects the cerebellum and its afferent and efferent connections. Since the mechanism by which mutant ataxin-3 eventually leads to neuronal death is poorly understood, additional investigations to clarify the biological alterations related to Machado-Joseph disease are necessary. Recent investigations suggest that oxidative stress may contribute significantly to Machado-Joseph disease. We compared markers of oxidative stress between Machado-Joseph disease and healthy control subjects. The results showed that Machado-Joseph patients have higher catalase levels and lower thiol protein levels compared to control subjects. The peripheral blood lymphocyes of MJD patients also showed higher levels of DNA damage by the comet assay than control subjects. Our results corroborate the hypothesis that the oxidative stress is associated with MJD patients. However, whether strategies to increase cellular antioxidative capacity may be effective therapies for the treatment of Machado-Joseph disease is an open question.


Subject(s)
Catalase/blood , Lymphocytes/enzymology , Machado-Joseph Disease/blood , Oxidative Stress , Adult , Biomarkers/blood , Case-Control Studies , Female , Humans , Lymphocytes/pathology , Machado-Joseph Disease/genetics , Machado-Joseph Disease/pathology , Male , Middle Aged
3.
Eur J Pharmacol ; 661(1-3): 92-101, 2011 Jul 01.
Article in English | MEDLINE | ID: mdl-21549114

ABSTRACT

Acetaminophen (APAP) hepatotoxicity has been related with several cases of cirrhosis, hepatitis and suicides attempts. Notably, oxidative stress plays a central role in the hepatic damage caused by APAP and antioxidants have been tested as alternative treatment against APAP toxicity. In the present study, we observed the hepatoprotector activity of the diethyl-2-phenyl-2-tellurophenyl vinylphosphonate (DPTVP), an organotellurium compound with low toxicity and high antioxidant potential. When the dose of 200 mg/kg of APAP was used, we observed that all used doses of DPTVP were able to restore the -SH levels that were depleted by APAP. Furthermore, the increase in thiobarbituric acid reactive substances levels and in the seric alanine aminotransferase (ALT) activity and the histopathological alterations caused by APAP were restored to control levels by DPTVP (30, 50 and 100 µmol/kg). On the other hand, when the 300 mg/kg dose of APAP was used, DPTVP restored the non-proteic -SH levels and repaired the normal liver morphology of the intoxicated mice only at 50 µmol/kg. Our in vitro results point out to a scavenging activity of DPTVP against several reactive species, action that is attributed to its chemical structure. Taken together, our results demonstrate that the pharmacological action of DPTVP as a hepatoprotector is probably due to its scavenging activity related to its chemical structure.


Subject(s)
Acetaminophen/adverse effects , Cytoprotection/drug effects , Free Radical Scavengers/pharmacology , Liver/drug effects , Organometallic Compounds/pharmacology , Organophosphonates/pharmacology , Animals , Dose-Response Relationship, Drug , Free Radical Scavengers/metabolism , Free Radicals/metabolism , Liver/pathology , Male , Mice , Organometallic Compounds/metabolism , Organophosphonates/metabolism
4.
Rev Bras Anestesiol ; 60(6): 614-9, 341-3, 2010.
Article in English, Portuguese, Spanish | MEDLINE | ID: mdl-21146057

ABSTRACT

BACKGROUND AND OBJECTIVES: The brachial plexus represents an important network of nerves, commonly approached in nerve blocks prior to surgical procedures. Therefore, the knowledge of its anatomy is indispensable so those procedures can be carried out accordingly. The objective of the present study was to analyze the morphology of brachial plexus cords with special emphasis to its topographic relationships. METHODS: This study was undertaken by dissecting the cervical, axillary, and brachial regions of a human cadaver fixed in 10% phormol, from the Human Anatomy Laboratory of the Morphology Department of Universidade Federal de Santa Maria. Access to the cords was obtained by pushing back the pectoralis minor and pectoralis major muscles, clavicular section, and extraction of part of the subclavius muscle. RESULTS: Cords originated from the anterior and posterior divisions of the trunks (upper, middle, and lower) of the brachial plexus. The lateral fascicle originated from the anterior divisions of the upper and middle trunks; the posterior, from the posterior divisions of the trunks; and the middle fascicle consisted from the continuation of the anterior division of the lower trunk. The cords showed relationships with the axillary artery, and they were located posteriorly to the pectoralis minor muscle, close to its insertion on the coracoid process. CONCLUSIONS: The results were in concordance with the anatomical descriptions of classical authors. This study allowed the analysis of the morphology of the brachial plexus cords, demonstrating its main topographic relationships.


Subject(s)
Brachial Plexus/anatomy & histology , Cadaver , Humans
5.
Arq Bras Cardiol ; 88(5): 559-64, 2007 May.
Article in English, Portuguese | MEDLINE | ID: mdl-17589631

ABSTRACT

OBJECTIVE: To describe morphological features of the interatrial septum in normal fetuses, especially foramen ovale (FO) and septum primum (SP), in order to compare septum primum excursion with foramen ovale diameter. METHODS: Septum primum excursion (SPE) toward the left atrium (LA) and foramen ovale diameter (FOD) were measured in the hearts of ten formaldehyde-fixed human fetuses ranging from 28 to 36 weeks of gestation. Histological sections were obtained from the foramen ovale (FO), septum primum (SP), septum secundum (SS), left atrium (LA), and right atrium (RA). RESULTS: FOD and SPE measurements were the following: FOD 3.1-3.5 mm and SPE 2.8-3.1 mm in three fetuses with presumed gestational age (GA) of 28 weeks; FOD 3.3-3.5 mm, and SP excursion 4.0-5.0 mm in four fetuses with presumed GA of 34 weeks, plus FOD 3.3-4.5 mm and SPE 6.0-9.0 in three fetuses with presumed GA of 36 weeks. Cardiac muscular fibers were identified in both the septum primum and secundum. CONCLUSION: Based on its muscular components, it may be suggested that SP is active in character, influencing blood flow through the FO, SP mobility, and its excursion into the LA.


Subject(s)
Atrial Septum/anatomy & histology , Fetus/anatomy & histology , Foramen Ovale/anatomy & histology , Atrial Septum/embryology , Foramen Ovale/embryology , Humans
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