ABSTRACT
Accidental envenomation caused by Tityus serrulatus scorpions is very common in Brazil and may result in serious cardiorespiratory alterations that are frequently fatal to children. In the present study, the effects of T. serrulatus venom on the cardiorespiratory system of recently weaned male Wistar rats were evaluated. Fifteen animals were distributed into three groups (n = 5). The control group A received 400 miuL ultrapure water by subcutaneous injection, while the experimental groups B and C were injected with scorpion venom (100 and 450 miug, respectively, in 400 miuL water). Electrocardiogram (ECG) traces were obtained prior to the experiment, at five-minute intervals up to 30 minutes after treatment. At 40 minutes after envenomation, the animals had severe acute symptoms and were subsequently anesthetized for blood collection by means of intracardiac puncture. Biochemical profiles for the cardiac muscle were established by colorimetric analysis of creatine kinase (CK) and CK-MB isoenzyme. Semiquantitative analysis of troponin was performed using the immunochromatographic assay. Following euthanasia, the lungs and hearts were removed and subjected to histopathological examination. All experimental animals had ECG alterations compatible with electrolytic imbalance, myocarditis and alterations of the cardiac conduction system. Envenomed animals had accentuated bradycardia at 25 and 30 minutes after venom inoculation. All experimental animals had myocardial lesions, which were confirmed by increased serum levels of CK and CK-MB, although there were no alterations in the serum concentration of troponin. Pulmonary hemorrhage was detected in whole lungs and microscopically confirmed by the presence of congested capillaries and erythrocytes in the alveolar parenchyma. In conclusion, T. serrulatus venom caused great cardiorespiratory damage to weaned rats.
Subject(s)
Animals , Female , Rats , Creatine Kinase , Creatine Kinase, MB Form , Rats, Wistar , Scorpion Venoms , TroponinABSTRACT
Estudou-se o perfil eletrocardiográfico e ecodopplercardiográfico de ovinos intoxicados experimentalmente pela Mascagnia rigida Griseb (Malpighiaceae). Quinze ovinos machos da raça Santa Inês, com sete meses de idade e pesando, em média, 27kg, foram distribuídos em três grupos (G) com cinco animais cada: No G1 (controle), os animais receberam apenas água; nos G2, receberam 20g/kg de M. rigida durante três dias; e no G3, 20g/kg de M. rigida, durante sete dias. As folhas de M. rigida foram trituradas com água e administradas na forma de suspensão, por via oral, por meio de sonda. M. rigida promoveu aumento da FC em repouso e, principalmente, durante o esforço físico e diminuiu a fração de ejeção e o percentual de encurtamento sistólico do ventrículo esquerdo.
The electrocardiographical and echocardiographical alterations produced by intraruminal administration of Mascagnia rigida griseb. (Malpighiaceae) in sheep were studied. Fifteen male Santa Inês sheep were randomly allotted to three groups: G1 - animals only received water (control); G2 - animals were treated with M. rigida, 20g/kg/day, for three days; and G3 - animals were treated with M. rigida, 20g/kg/day, for seven days. All treatments were administered by an orogastric tube. M. rigida administration produced increase in heart rate during rest and exercise, and decreased in fractional ejection, and fractional shortening.
ABSTRACT
Estudou-se o perfil eletrocardiográfico e ecodopplercardiográfico de ovinos intoxicados experimentalmente pela Mascagnia rigida Griseb (Malpighiaceae). Quinze ovinos machos da raça Santa Inês, com sete meses de idade e pesando, em média, 27kg, foram distribuídos em três grupos (G) com cinco animais cada: No G1 (controle), os animais receberam apenas água; nos G2, receberam 20g/kg de M. rigida durante três dias; e no G3, 20g/kg de M. rigida, durante sete dias. As folhas de M. rigida foram trituradas com água e administradas na forma de suspensão, por via oral, por meio de sonda. M. rigida promoveu aumento da FC em repouso e, principalmente, durante o esforço físico e diminuiu a fração de ejeção e o percentual de encurtamento sistólico do ventrículo esquerdo.
The electrocardiographical and echocardiographical alterations produced by intraruminal administration of Mascagnia rigida griseb. (Malpighiaceae) in sheep were studied. Fifteen male Santa Inês sheep were randomly allotted to three groups: G1 - animals only received water (control); G2 - animals were treated with M. rigida, 20g/kg/day, for three days; and G3 - animals were treated with M. rigida, 20g/kg/day, for seven days. All treatments were administered by an orogastric tube. M. rigida administration produced increase in heart rate during rest and exercise, and decreased in fractional ejection, and fractional shortening.
Subject(s)
Male , Animals , Echocardiography, Doppler/methods , Echocardiography, Doppler/veterinary , Electrocardiography/methods , Electrocardiography/veterinary , Plant Poisoning/veterinary , Malpighiaceae/toxicity , SheepABSTRACT
Avaliaram-se o índice de performance do miocárdio (IPM) e outros índices ecoDopplercardiográficos de função ventricular em cães de duas raças de diferentes biotipos. Foram utilizados 24 cães da raça Schnauzer Miniatura, com média de peso de 8,4±1,6kg, e 24 cães da raça Boxer, com média de peso de 25,1±2,6kg. O IPM na raça Schnauzer Miniatura foi 0,32 e na raça Boxer 0,48. Os valores do IPM, dos índices de fase de ejeção, do período de pré-ejeção, da relação período de pré-ejeção/período de ejeção e do tempo de desaceleração da onda E do fluxo mitral diferiram entre as duas raças. Observou-se correlação entre o peso corporal e esses índices, e o peso corporal foi considerado a principal característica racial responsável pelas diferenças observadas. O tempo de ejeção (r=-0,51), o período de pré-ejeção (r=-0,44) e o tempo de relaxamento isovolumétrico (r=-0,38) foram os únicos parâmetros a apresentar correlação com a freqüência cardíaca (FC). O uso da relação período de pré-ejeção/tempo de ejeção e do tempo de ejeção corrigido pela freqüência cardíaca diminui o efeito da FC sobre esses parâmetros.
The index of myocardial performance (IMP) and others ecoDopplercardiographic indexes of ventricular function were evaluated in dogs of two different breeds and somatotypes. Twenty-four Miniature Schnauzer dogs averaging 8.4±1.6kg and 24 Boxer dogs averaging 25.1±2.6kg were used. IPM, ejection phase indexes, pre-ejection period, pre-ejection period/ejection time relation, and E wave deceleration time of mitral inflow showed correlation to body weight with significant differences between the breeds. Body weight was considered the main breed characteristic responsible for the observed differences. Ejection time (r=-0.51), pre-ejection time (r=-0.44), and isovolumetric relaxation time (r=-0.38) presented correlation with heart rate. The use of pre-ejection period/ejection time relation and ejection time correct by heart rate diminishes the influence of heart rate on the parameters.
Subject(s)
Animals , Dogs , Echocardiography, Doppler , Epidemiology , Heart Ventricles , UltrasonographyABSTRACT
Dopamine receptor type 3 (DRD3) expressed in the limbic system sites involved in the regulation of GnRH seems to play a role in neuroendocrine control. We hypothesized that women with chronic anovulation should show exacerbated secretion of prolactin (PRL) after thyrotropin-releasing hormone (TRH) stimulation test, having more chances for dopamine inhibitory dysfunction due to alterations in the structure of DRD3. The DRD3-coding region was evaluated in 60 women with chronic anovulation (35 without and 25 with hyperresponse of PRL after TRH stimulation), and in 34 controls. Statistically similar frequencies of homozygous AGC polymorphism (43.4 and 33.4%) and heterozygous polymorphism (33.4 and 47.9%) at position 9 were found in controls and patients, respectively. Homozygous GCG polymorphism at position 17 was identified in 3.4% Type 3 dopaminergic receptor in chronic anovulationof the patients, while heterozygosis occurred in 20.8% of the patients and in 6.6% of the controls. The novel 41563_41567delTAAGT polymorphismof DRD3 was identified in 14.7% of the controls and 8.6% of the women with chronic anovulation displaying hyperresponse of PRL after TRH stimulation. Alteration 41563_41567delTAAGT of DRD3 was not found in patients who did not show hyperresponse of PRL after TRH stimulation. Normal baseline and peak levels of PRL and thyroid-stimulating hormone were similar for women with and without 41563_41567delTAAGT in the DRD3 gene. It is concluded that the novel polymorphism in DRD3 identified in this study is not associated with the response of PRL to TRH stimulation in women with chronic anovulation.
Subject(s)
Humans , Female , Anovulation/genetics , Polymorphism, Genetic , /genetics , Anovulation/etiology , Case-Control Studies , Chronic Disease , Gene Frequency , Genotype , Prolactin , Thyrotropin/pharmacologyABSTRACT
Primary chemotherapy is a useful strategy for the treatment of locally advanced breast cancer and therefore allows in vivo evaluation of the action of cytotoxic drugs and the possibility of accomplishing conservative breast surgeries, as well as the early treatment of metastasis. Mechanisms of resistance to the drugs include the action of protein associated with the efflux of drugs from the intracellular environment hindering their activity; one of the most studied proteins is P-glycoprotein codified by the MDR-1 gene. The presence of polymorphisms can determine different physiological actions of these proteins, intervening with the response of the drugs action. We evaluated the presence of single nucleotide polymorphism (SNP) C3435T of the MDR-1 gene and its correlation with the response to primary chemotherapy using the RECIST criteria. Forty-one Brazilian women with stages II and III breast cancer using the PCR-RFLP analysis were evaluated. Thirty-three patients with the SNP genotype (TT and CT) and eight patients with the wild genotype (CC) were found; there was no statistically significant correlation between the diverse genotypes and the clinical and pathological responses according to the Cramer correlation coefficient (V = 0.14). The parameters: nuclear and histological degree, and estrogens, progesterone and c-erb B2 receptors did not demonstrate a statistical correlation with the SNP C3435T. Patients with complete pathological response (12.5%) showed only the polymorphic genotype and not the wild genotype. The characteristics of miscegenation in our population could explain the absence of the characterization of a sub-group of individuals where the presence of the polymorphic genotype influenced the response to the primary chemotherapy.
Subject(s)
Humans , Female , Genes, MDR , ATP Binding Cassette Transporter, Subfamily B, Member 1/genetics , Breast Neoplasms/genetics , Breast Neoplasms/pathology , Polymorphism, Single Nucleotide , Case-Control Studies , DNA Mutational Analysis , Genotype , Breast Neoplasms/drug therapy , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Remission Induction , Treatment OutcomeABSTRACT
Thirty-seven 45 X Turner syndrome patients with confirmed peripheral blood lymphocyte karyotype were initially selected to determine the origin of the retained X chromosome and to correlate it with their parents stature. Blood samples were available in 25 families. The parental origin of the X chromosome was determined in 24 informativefamilies through the analysis of the exon 1 - CAG repeat variation of the androgen receptor gene. In 70.8% of the cases, the retained X chromosome was maternal in origin and 29.2% was paternal. When we classified the patients according to maternal (Xm) or paternal (Xp) X chromosome, there was a positive correlation between patients and maternal heights only in the Xm group. There was no correlation with paternal height in either group, and a significant correlation with target height was only observed in the Xm group. In conclusion, maternal height is the best variable correlating with the height of 45 X Turner syndrome patients who retain the maternal X chromosome, suggesting a strong influence of genes located on the maternal X chromosome on stature.
Subject(s)
Humans , Male , Female , Body Height/genetics , Chromosomes, Human, X/genetics , Parents , Turner Syndrome/genetics , Exons , Phenotype , Polymerase Chain Reaction , Receptors, Androgen/genetics , Trinucleotide RepeatsABSTRACT
Adrenal hypoplasia congenita (AHC) is a rare disease that can be caused by many abnormalities, including an X-linked form. Mutations in the DAX1 gene have been assigned as the genetic cause of AHC. We describe here three siblings with AHC, clinically presented at different ages, two in the neonatal period and one oligosymptomatic during infancy. Molecular analysis was able to detect a novel mutation in exon 1 of the DAX1 gene, consisting of a transition of C to T at position 359, determining a stop codon at position 359 (Q359X). The mutated gene encodes a truncated protein missing a large portion of the ligand-binding domain (C-terminal domain). The recognition of the disease in the index case suggested the diagnosis in the other siblings. Interestingly, the same mutation is presented with different phenotypes, suggesting that first-degree family members of patients with DAX1 mutations should be carefully evaluated routinely.
Subject(s)
Humans , Male , Female , Infant , Child, Preschool , Child , Codon, Nonsense , Adrenal Insufficiency/genetics , Point Mutation , Repressor Proteins/genetics , DNA-Binding Proteins/genetics , Receptors, Retinoic Acid/genetics , Family , Phenotype , Siblings , Pedigree , ExonsABSTRACT
Dopplerfluxometry of renal arteries has been used to estimate renal perfusion in humans. The aim of this study was to use Dopplerfluxometry technique to calculate the resistive index of main renal arteries in dogs, measuring their systolic and diastolic blood flow velocities. Twenty (10 males, 10 females), adult mongrel dogs, were used in this study. The dogs were submitted to Doppler sonographic evaluation of left and right main renal arteries. The systolic and diastolic blood flow velocities, expressed (in centimeters per second) as mean and standard deviation were 79.96± 8.82 and 28.86± 5.11 in the right main renal artery and 80.22± 6.99 and 29.62± 4.14 in the left main renal artery. The value of resistive index expressed as mean ± standard deviation was 0.64± 0.04 for the right main renal artery and 0.63± 0.028 in the left main renal artery.
Subject(s)
Animals , Male , Female , Renal Artery/metabolism , Dogs , Laser-Doppler Flowmetry/methods , Kidney Diseases/diagnosis , Kidney Diseases/epidemiology , Kidney Diseases/prevention & control , Kidney Diseases/veterinaryABSTRACT
Point mutations and small insertions or deletions in the human alpha-globin genes may produce alpha-chain structural variants and alpha-thalassemia. Mutations can be detected either by direct DNA sequencing or by screening methods, which select the mutated exon for sequencing. Although small (about 1 kb, 3 exons and 2 introns), the alpha-globin genes are duplicate (alpha2 and alpha1) and highy G-C rich, which makes them difficult to denature, reducing sequencing efficiency and causing frequent artifacts. We modified some conditions for PCR and electrophoresis in order to detect mutations in these genes employing nonradioactive single-strand conformation polymorphism (SSCP). Primers previously described by other authors for radioactive SSCP and phast-SSCP plus denaturing gradient gel electrophoresis were here combined and the resultant fragments (6 new besides 6 original per alpha-gene) submitted to silver staining SSCP. Nine structural and one thalassemic mutations were tested, under different conditions including two electrophoretic apparatus (PhastSystemÖ and GenePhorÖ, Amersham Biosciences), different polyacrylamide gel concentrations, run temperatures and denaturing agents, and entire and restriction enzyme cut fragments. One hundred percent of sensitivity was achieved with four of the new fragments formed, using the PhastSystemÖ and 20 percent gels at 15ºC, without the need of restriction enzymes. This nonradioactive PCR-SSCP approach showed to be simple, rapid and sensitive, reducing the costs involved in frequent sequencing repetitions and increasing the reliability of the results. It can be especially useful for laboratories which do not have an automated sequencer.