Toll-like receptor 2 selectively modulates Ras isoforms expression in Leishmania major infection.

Leishmania infection of macrophages results in altered Ras isoforms expression and Toll-like receptor-2 (TLR2) expression and functions. Therefore, we examined whether TLR2 would selectively alter Ras isoforms' expression in macrophages. We observed that TLR2 ligands- Pam3CSK4, peptidoglycan (PGN), and FSL- selectively modulated the expression of Ras isoforms in BALB/c-derived elicited macrophages. Lentivirally-expressed TLR1-shRNA significantly reversed this Ras isoforms expression profile. TLR2-deficient L. major-infected macrophages and the lymph node cells from the L. major-infected mice showed similarly reversed Ras isoforms expression. Transfection of the macrophages with the siRNAs for the adaptors- Myeloid Differentiation factor 88 (MyD88) and Toll-Interleukin-1 Receptor (TIR) domain-containing adaptor protein (TIRAP)- or Interleukin-1 Receptor-Associated Kinases (IRAKs)- IRAK1 and IRAK4- significantly inhibited the L. major-induced down-regulation of K-Ras, and up-regulation of N-Ras and H-Ras, expression. The TLR1/TLR2-ligand Pam3CSK4 increased IL-10 and TGF-ß expression in macrophages. Pam3CSK4 upregulated N-Ras and H-Ras, but down-regulated K-Ras, expression in C57BL/6 wild-type, but not in IL-10-deficient, macrophages. IL-10 or TGF-ß signaling inhibition selectively regulated Ras isoforms expression. These observations indicate the specificity of the TLR2 regulation of Ras isoforms and their selective modulation by MyD88, TIRAP, and IRAKs, but not IL-10 or TGF-ß, signaling.

Low protein diet during lactation programs hepatic metabolism in adult male and female rats.

The liver is an essential regulator of energy metabolism, and its function can be disrupted by nutritional alterations. Since liver development continues during breastfeeding nutritional challenges during this period predispose patients to diseases throughout life. A maternal protein-restricted (PR) diet during lactation promotes reductions in the body weight, adiposity, and plasma glucose and insulin, leptin resistance and an increase in corticosterone and catecholamines in adult male rat offspring. Here, we investigated hepatic metabolism in the offspring (both sexes) of PR (8% protein diet during lactation) and control (23% protein diet) dams. Both male and female offspring were evaluated at 6 months of age. PR males had no liver steatosis and manifested a reduction in lipids in hepatocytes adjacent to the vasculature. These animals had lower levels of esterified cholesterol in hepatocytes, suggesting higher biliary excretion, unchanged glycolysis and gluconeogenesis, and lower contents of the markers of mitochondrial redox balance and endoplasmic reticulum (ER) stress response and estrogen receptor alpha. PR females showed normal hepatic morphology associated with higher uptake of cholesterol esters, normal glycolysis and gluconeogenesis, and lower ER stress parameters without changes in the key markers of the redox balance. Additionally, these animals had lower content of estrogen receptor alpha and higher content of androgen receptor. The maternal PR diet during lactation did not program hepatic lipid accumulation in the adult progeny. However, several repair homeostasis pathways were altered in males and females, possibly compromising maintenance of normal liver function.

Effect of Sublethal Prenatal Endotoxaemia on Murine Placental Transport Systems and Lipid Homeostasis.

Infection alters the expression of transporters that mediate the placental exchange of xenobiotics, lipids and cytokines. We hypothesized that lipopolysaccharide (LPS) modifies the expression of placental transport systems and lipid homeostasis. LPS (150 µg/kg; i.p.) treatments were administered for 4 h or 24 h, animals were euthanized at gestational days (GD) 15.5 or 18.5, and maternal blood, fetuses and placentae were collected. Increased rates of fetal demise were observed at GD15.5 following LPS treatment, whereas at GD18.5, high rates of early labour occurred and were associated with distinct proinflammatory responses. Lipopolysaccharide did not alter ATP-binding cassette (ABC) transporter mRNA expression but decreased fatty acid binding protein associated with plasma membrane (Fabppm) at GD15.5 (LPS-4 h) and increased fatty acid translocase (Fat/Cd36) mRNA at GD18.5 (LPS-4 h). At the protein level, breast cancer-related protein (Bcrp) and ABC sub-family G member 1 (Abcg1) levels were decreased in the placental labyrinth zone (Lz) at GD15.5, whereas P-glycoprotein (P-gp) and Bcrp Lz-immunostaining was decreased at GD18.5. In the placental junctional zone (Jz), P-gp, Bcrp and Abcg1 levels were higher at GD18.5. Specific maternal plasma and placental changes in triacylglycerol, free fatty acid, cholesterol, cholesterol ester and monoacylglycerol levels were detected in a gestational age-dependent manner. In conclusion, LPS-increased risk of fetal death and early labour were associated with altered placental ABC and lipid transporter expression and deranged maternal plasma and placental lipid homeostasis. These changes may potentially modify fetal xenobiotic exposure and placental lipid exchange in cases of bacterial infection.

The Absence of HIF-1α Increases Susceptibility to Leishmania donovani Infection via Activation of BNIP3/mTOR/SREBP-1c Axis.

Hypoxia-inducible factor-1 alpha (HIF-1α) is considered a global regulator of cellular metabolism and innate immune cell functions. Intracellular pathogens such as Leishmania have been reported to manipulate host cell metabolism. Herein, we demonstrate that myeloid cells from myeloid-restricted HIF-1α-deficient mice and individuals with loss-of-function HIF1A gene polymorphisms are more susceptible to L. donovani infection through increased lipogenesis. Absence of HIF-1α leads to a defect in BNIP3 expression, resulting in the activation of mTOR and nuclear translocation of SREBP-1c. We observed the induction of lipogenic gene transcripts, such as FASN, and lipid accumulation in infected HIF-1α-/- macrophages. L. donovani-infected HIF-1α-deficient mice develop hypertriglyceridemia and lipid accumulation in splenic and hepatic myeloid cells. Most importantly, our data demonstrate that manipulating FASN or SREBP-1c using pharmacological inhibitors significantly reduced parasite burden. As such, genetic deficiency of HIF-1α is associated with increased lipid accumulation, which results in impaired host-protective anti-leishmanial functions of myeloid cells.

Programming of hepatic lipid metabolism in a rat model of postnatal nicotine exposure - Sex-related differences.

Maternal nicotine exposure during lactation induces liver damage in adult male rats. However, the mechanism in males is unknown and females have not been tested. Here, we determined the liver lipid composition and lipogenic enzymes in male and female offspring at two ages in a model of postnatal nicotine exposure. Osmotic minipumps were implanted in lactating Wistar rat dams at postnatal day (PND) 2 to release 6 mg/kg/day of nicotine (NIC group) or saline (CON group) for 14 days. Offspring received a standard diet from weaning until euthanasia at PND120 (1 pup/litter/sex) or PND180 (2 pups/litter/sex). At PND120, NIC males showed lower plasma triglycerides (TG), steatosis degree 1, higher hepatic cholesterol (CHOL) ester, free fatty acids, monoacylglycerol content as well as acetyl-coa carboxylase-1 (ACC-1) and fatty acid synthase (FAS) protein expression in the liver compared to CON males. At this age, NIC females had preserved hepatocytes architecture, higher plasma CHOL, higher CHOL ester and lower total CHOL content in the liver compared to CON females. At PND180, NIC males showed steatosis degrees 1 and 2, higher TG, lower free fatty acids and total CHOL content in the liver and an increase in ACC-1 hepatic protein expression. NIC females had higher plasma TG and CHOL levels, no change in hepatic morphology, lower CHOL ester and free fatty acids in the liver, which also showed higher total ACC-1 and FAS protein expression. Maternal nicotine exposure induces long-term liver dysfunction, with an alteration in hepatic cytoarchitecture that was aggravated with age in males. Concerning females, despite unchanged hepatic cytoarchitecture, lipid metabolism was compromised, which deserves further attention.

Plasmodium Infection Induces Dyslipidemia and a Hepatic Lipogenic State in the Host through the Inhibition of the AMPK-ACC Pathway.

Malaria is a major parasitic disease of humans and is a health public problem that affects more than 100 countries. In 2017, it caused nearly half a million deaths out of 219 million infections. Malaria is caused by the protozoan parasites of the genus Plasmodium and is transmitted by female mosquitoes of the genus Anopheles. Once in the bloodstream, Plasmodium merozoites invade erythrocytes and proliferate until the cells lyses and release new parasites that invade other erythrocytes. Remarkably, they can manipulate the vertebrate host's lipid metabolism pathways, since they cannot synthesize lipid classes that are essential for their development and replication. In this study, we show that mice infected with Plasmodium chabaudi present a completely different plasma profile from control mice, with marked hyperproteinemia, hypertriglyceridemia, hypoglycemia, and hypocholesterolemia. In addition, white adipose and hepatic tissue and analyses from infected animals revealed the accumulation of triacylglycerol in both tissues and free fatty acids and free cholesterol in the liver. Hepatic mRNA and protein expression of key enzymes and transcription factors involved in lipid metabolism were also altered by P. chabaudi infection, leading to a lipogenic state. The enzyme 5' AMP-activated protein kinase (AMPK), a master regulator of cell energetic metabolism, was also modulated by the parasite, which reduced AMPK phosphorylation levels upon infection. Pretreatment with metformin for 21 days followed by infection with P. chabaudi was effective in preventing infection of mice and also lowered the hepatic accumulation of lipids while activating AMPK. Together, these results provide new and important information on the specific molecular mechanisms induced by the malaria parasite to regulate hepatic lipid metabolism in order to facilitate its development, proliferation, and lifespan in its vertebrate host.

Bioactive lipids regulate Trypanosoma cruzi development.

Trypanosoma cruzi is the etiological agent of Chagas disease. These parasites undergo dramatic morphological and physiological changes during their life cycle. The human-infective metacyclic trypomastigotes differentiate from epimastigotes inside the midgut of the Triatominae insect vector. Our group has shown that the saliva and feces of Rhodnius prolixus contains a lysophospholipid, lysophosphatidylcholine (LPC), which modulates several aspects of T. cruzi infection in macrophages. LPC hydrolysis by a specific lysophospholipase D, autotaxin (ATX), generates lysophosphatidic acid (LPA). These bioactive lysophospholipids are multisignaling molecules and are found in human plasma ingested by the insect during blood feeding. Here, we show the role of LPC and LPA in T. cruzi proliferation and differentiation. Both lysophospholipids are able to induce parasite proliferation. We observed an increase in parasite growth with different fatty acyl chains, such as C18:0, C16:0, or C18:1 LPC. The dynamics of LPC and LPA effect on parasite proliferation was evaluated in vivo through a time- and space-dependent strategy in the vector gut. LPC but not LPA was also able to affect parasite metacyclogenesis. Finally, we determined LPA and LPC distribution in the parasite itself. Such bioactive lipids are associated with reservosomes of T. cruzi. To the best of our knowledge, this is the first study to suggest the role of surrounding bioactive lipids ingested during blood feeding in the control of parasite transmission.

Genetic polymorphisms in Plasmodium falciparum chloroquine resistance genes, pfcrt and pfmdr1, in North Sulawesi, Indonesia.

BACKGROUND: Malaria still poses one of the major threats to human health. Development of effective antimalarial drugs has decreased this threat; however, the emergence of drug-resistant Plasmodium falciparum, a cause of Malaria, is disconcerting. The antimalarial drug chloroquine has been effectively used, but resistant parasites have spread worldwide. Interestingly, the withdrawal of the drug reportedly leads to an increased population of susceptible parasites in some cases. We examined the prevalence of genomic polymorphisms in a malaria parasite P. falciparum, associated with resistance to an antimalarial drug chloroquine, after the withdrawal of the drug from Indonesia. RESULTS: Blood samples were collected from 95 malaria patients in North Sulawesi, Indonesia, in 2010. Parasite DNA was extracted and analyzed by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) for pfcrt and pfmdr1. In parallel, multiplex amplicon sequencing for the same genes was carried out with Illumina MiSeq. Of the 59 cases diagnosed as P. falciparum infection by microscopy, PCR-RFLP analysis clearly identified the genotype 76T in pfcrt in 44 cases. Sequencing analysis validated the identified genotypes in the 44 cases and demonstrated that the haplotype in the surrounding genomic region was exclusively SVMNT. Results of pfmdr1 were successfully obtained for 51 samples, where the genotyping results obtained by the two methods were completely consistent. In pfmdr1, the 86Y mutant genotype was observed in 45 cases (88.2%). CONCLUSIONS: Our results suggest that the prevalence of the mutated genotypes remained dominant even 6 years after the withdrawal of chloroquine from this region. Diversified haplotype of the resistance-related locus, potentially involved in fitness costs, unauthorized usage of chloroquine, and/or a short post-withdrawal period may account for the observed high persistence of prevalence.

Sodium selenite supplementation during pregnancy and lactation promotes anxiolysis and improves mnemonic performance in wistar rats' offspring.

Selenium is a micronutrient which is part of selenoprotein molecules and participates in a vast number of physiological roles and, among them,we have fetal and neonatal development. Therefore, the aimof this studywas to evaluate possible behavioral changes in offspring of female rats supplemented during pregnancy and lactation with sodium selenite. To address that, we treated two groups of female rats by saline or sodium selenite at a dose of 1mg/kg through oral route and performed neurochemical and behavioral tests. In the offspring, the thyroid profile and hippocampal neurochemistrywere evaluated. Behavioral testswere performed in pups both during childhood and adulthood. We found out that selenium (Se) supplementation increased serum levels of triiodothyronine (25%, p b 0.001) and thyroxine (18%, p b 0.05) and promoted a tryptophan hydroxylase 2 (TPH 2) expression decrease (17%, p b 0.01) and tyrosine hydroxylase (TH) expression increase (202%, p b 0.01) in the hippocampus. The cholinesterase activity was decreased (28%, p b 0.01) in Se supplemented rats, suggesting a neurochemical modulation in the hippocampal activity. During childhood, the Sesupplemented offspring had a reduction in anxiety-like behavior both in elevated plus maze test and in light­dark box test. In adulthood, Se-treated pups had an increase in the locomotor activity (36%, p b 0.05) and in rearing episodes (77%, p b 0.001) in the open field test, while in the elevated plus maze test they also exhibited an increase in the time spent in the open arms (243%, p b 0.01). For the object recognition test, Se-treated offspring showed increase in the absolute (230.16%, p b 0.05) and relative index discrimination (234%, p b 0.05). These results demonstrate that maternal supplementation by sodium selenite promoted psychobiological changes both during childhood and adulthood. Therefore, the behavioral profile observed possibly can be explained by neurochemical changes induced by thyroid hormones during the critical period of the central nervous system ontogeny.

Perimicrovillar membrane assembly: the fate of phospholipids synthesised by the midgut of Rhodnius prolixus.

In this study, we describe the fate of fatty acids that are incorporated from the lumen by the posterior midgut epithelium of Rhodnius prolixus and the biosynthesis of lipids. We also demonstrate that neutral lipids (NL) are transferred to the haemolymphatic lipophorin (Lp) and that phospholipids remain in the tissue in which they are organised into perimicrovillar membranes (PMMs). 3H-palmitic acid added at the luminal side of isolated midguts of R. prolixus females was readily absorbed and was used to synthesise phospholipids (80%) and NL (20%). The highest incorporation of 3H-palmitic acid was on the first day after a blood meal. The amounts of diacylglycerol (DG) and triacylglycerol synthesised by the tissue decreased in the presence of Lp in the incubation medium. The metabolic fates of 3H-lipids synthesised by the posterior midgut were followed and it was observed that DG was the major lipid released to Lp particles. However, the majority of phospholipids were not transferred to Lp, but remained in the tissue. The phospholipids that were synthesised and accumulated in the posterior midgut were found to be associated with Rhodnius luminal contents as structural components of PMMs.

Perimicrovillar membrane assembly: the fate of phospholipids synthesised by the midgut of Rhodnius prolixus

In this study, we describe the fate of fatty acids that are incorporated from the lumen by the posterior midgut epithelium of Rhodnius prolixus and the biosynthesis of lipids. We also demonstrate that neutral lipids (NL) are transferred to the haemolymphatic lipophorin (Lp) and that phospholipids remain in the tissue in which they are organised into perimicrovillar membranes (PMMs). 3H-palmitic acid added at the luminal side of isolated midguts of R. prolixus females was readily absorbed and was used to synthesise phospholipids (80%) and NL (20%). The highest incorporation of 3H-palmitic acid was on the first day after a blood meal. The amounts of diacylglycerol (DG) and triacylglycerol synthesised by the tissue decreased in the presence of Lp in the incubation medium. The metabolic fates of 3H-lipids synthesised by the posterior midgut were followed and it was observed that DG was the major lipid released to Lp particles. However, the majority of phospholipids were not transferred to Lp, but remained in the tissue. The phospholipids that were synthesised and accumulated in the posterior midgut were found to be associated with Rhodnius luminal contents as structural components of PMMs.

Electrokinetic properties of wavellite and its floatability with cationic and anionic collectors.

The reverse apatite flotation with fatty acids has been widely used for the reduction of phosphorus content of magmatic origin iron ores. However, the occurrence of phosphorus intensely disseminated as secondary minerals such as wavellite renders the anionic reverse flotation a challenge. Zeta potential measurements and microflotation tests of wavellite with the use of anionic and cationic collectors were carried out in this work. The wavellite's IEP value was achieved at pH 4.5. Below the IEP value, the surface positively charged sites are made up of aluminum ions. The species H(+), Al(OH)(2)(+), Al(OH)(2+), Al(3+), OH(-), H(2)PO(4)(-), HPO(4)(2-), and PO(4)(3-) play a role in the protonation and deprotonation reactions that will determine the wavellite-solution interface properties. The highest values of wavellite's floatability under basic pH conditions were achieved in the presence of cationic collectors (1 × 10(-4) mol L(-1)). The formation of surface complexes and the precipitation of insoluble salt of aluminum onto wavellite surface seems to be the most likely hypothesis for the chemical nature interactions between amines and wavellite. The surface formation of aluminum oleate on the wavellite's surface seems to be the most probable hypothesis for the adsorption mechanism and the resultant high floatability of wavellite between pH 7.5 and pH 10.0 in the presence of sodium oleate (1 × 10(-4) mol L(-1)). The results showed that the cationic reverse flotation of secondary phosphates is a promising route to reduce the phosphorus content of iron ores from deposits that underwent a supergene enrichment process, since wavellite floatability in the alkaline pH range, using amine as collector, was not significantly affected by the presence of corn starch.

Amigdalites / Tonsillitis

As doenças infecciosas são um dos motivos mais comuns de consulta ao médico. Destas, 70% correspondem a infecções do trato respiratório, em especial as faringotonsilites. As infecções virais são as mais frequentes. Dentre as infecções bacterianas, o Streptococcus Pyogenes beta-hemolítico do grupo A é o agente mais prevalente e o que merece especial atenção devido ao risco de complicações. O padrão-ouro para diagnóstico etiológico desta patologia é a cultura de secreção nasofaríngea. O tratamento de escolha continua sendo a penicilina e seus derivados. O objetivo deste artigo é revisar os tipos mais comuns de faringotonsilites, a dificuldade encontrada para estabelecer o diagnóstico diferencial e etiológico desta patologia e o seu tratamento.

LUDOPATIA: Características de la población que asiste a salas de juego en Tegucigalpa / Compulsive gambling: characterization of people that visit gambling casinos in Tegucigalpa

La ludopatía consiste en una alteración progresiva del comportamiento por la que un individuo siente una incontrolable necesidad de jugar, menospreciando cualquier consecuencia negativa. Objetivo: Caracterizar la población que asiste a lugares de juego de azar en Tegucigalpa M.D.C., diciembre de 2006. Metodologí­a: Tipo de estudio. Descriptivo transversal. El universo de estudio fue de 50,000 personas que asistían a lugares de juegos de azar. El tamaño de muestra fue de 384 personas. El método de muestreo fue estratificado, conformado por: 40 billares y 8 casinos. La unidad de análisis fue seleccionada aleatoriamente. Procedimiento: previo consentimiento informado de las personas que asist­an a los lugares de juego, se solicitó permiso a los gerentes de los establecimientos.Se utilizarón dos instrumentos de recolección de datos: un cuestionario de carácter general con preguntas abiertas y cerradas que recogía datos personales; el segundo instrumento utilizado fue el SOGS(South Oaks ambling Scrren). El Grpo de investigadores se capacitó para el levantamiento de datos y aclarar dudas en aquellos casos que el entrevistado desaba llenar los instrumentos. Resultados: la población de estudio fur clasificada en: Jugador social 143(37%), con problemas 86(22%) y jugador patológico 155(40%). La edad de la población predominó en el grupo de 20-29 años 184(48%) y mayores de 50 años con 38(10%); el sexo mayoritario fue masculino co 301(78%), la edad de inicio en el juego fue de 15-19 años 204(53%), el motivo de inicio fue por entretenimiento 184(48%) e influencia de amiastades 93(24%); La escolaridad era universidad incompleta 109(28%), secundaria completa 93(24%) y universidad completa (22%), la actividad laboral fue: estudiantes 113(29%), comerciante 82(21%) con ingreso económico en el rango 2,501-5,000 Lempiras. Los jugadores juegan, los días sábado 152(40%) y viernes 128(33%), el tiempo de permanencia...(AU)

Can oculomotricity be altered in patients with tinnitus only? A preliminary study.

The study of oculomotricity is performed by evaluating three systems: saccadic ocular movements (SOMs), optokinetic nystagmus (OKN), and smooth pursuit eye movements (SPEMs). Our aim was to study oculomotricity in patients with a complaint of only tinnitus and to compare it with the value of our control group. We studied the SOMs, OKN, and SPEMs in 25 patients complaining only about tinnitus and in 35 normal adults and compared the results. The data analysis showed a significant difference in the value of the SOMs and SPEMs between the two groups. Sensorineural tinnitus can originate in the organ of Corti, in the cochlear nerve, or in the auditory pathways of the central nervous system. The auditory cortex connects with visual areas and with the superior colliculus. The latter structure is involved in the origin of SOMs and OKN. In our study, we found an increased delay in saccadic tests. In the SPEMs, we observed an increase in the degree of distortion, and a reduction in the gain. This outcome is in accordance with the literature. However, we detected a few alterations in the OKN, and this finding is in partial agreement with the studies analyzed. Alterations in oculomotricity can indicate involvement of the central nervous system in patients with a complaint of only tinnitus.

Desempenho cardíaco e resposta hemodinâmica sob açäo do isoproterenol e D-isosorbitol em portadores de miocardiopatia dilatada / Cardiac performance and hemodynamic response under the effect of isoproterenol and D-isosorbitol in patients with dilated cardiomyopathy

Os autores estudaram o desempenho cardíaco de 36 pacientes com miocardiopatia dilatada (MD) através de cateterismo e cineventriculografia esquerda, estabelecendo relaçäo com grupo normal. Foi verificado que o VSF é mais sensível e melhor que a FE como indicador da presença e grau da disfunçäo sitólica. Foram utilizados isoproterenol (IP) (18 pacientes) e D-isosorbitol (IS) (18 pacientes) na avaliaçäo da resposta hemodinâmica da MD. Verificaram-se respostas equivalentes com as duas substâncias tais como: 1 - diminuiçäo do VSF e da Pd2; 2 - aumento do VSE e da FE. Os índices de contratilidade do VE, no entanto, apresentaram respostas diferentes com as duas substâncias: 1 - com o IP houve aumento do pico da dp/dt e da dp/dt PI 45 mmHg; 2 - com o IS näo houve variaçäo. Os autores concluem que: 1 - O Isoproterenol ou drogas similares podem ser utilizados na sala de cateterismo cardíaco para avaliar a reserva contrátil do miocárdio; 2 - o D-isosorbital pode ser utilizado no tratamento ambulatorial da MD por melhorar a funçäo ventricular através de uma tendência à normalizaçäo de relaçäo pressäo-volume intracardíaca

Miocardiopatia hipertrófica apical / Apical hypertrophic cardiomyopathy

Os autores fizeram a revisäo de 4591 pacientes submetidos ao cateterismo cardíaco com cineangiocoronariografia e encontraram 246 (5,3%) portadores de miocardiopatias em geral. Destes, 45 (0,98% do geral e 18,3% do grupo) apresentavam Cardiomiopatia Hipertrófica (CH), sendo que os últimos 34 pacientes foram estudados por apresentarem a cineventriculografia simultânea no VD-VE em OAE a 60 graus (CS VD-VE). Os autores encontraram 3 grupos de CH: 1 - CH clássica: 19 pacientes (55,9%). 2 - CH apical )MHA): 9 pacientes (26,5%) 3 - CH mista (grupo 1 + grupo 2): 6 pacientes (17,6%). Os autores estudaram particularmente a Miocardiopatia Hipertrófica Apical (grupo 2), que apresentou aspectos clínicos, radiológicos, eletrocardiográficos, ecocardiográficos, hemodinâmicos e cineangiocardiográficos especiais. Os autores concluíram que: 1 - A MHA é um tipo de CH näo obstrutiva que necessita ser devidamente procurada para se fazer o diagnóstico. 2 - O diagnóstico pode ser feito através do ecocardiograma e da CS VD-VE. 3 - Os nossos dados do E.C.G. na MHA näo apresentaram aspectos que pudessem ser imputados como características da doença

Desempenho da funçäo ventricular na pericardite crónica constritiva / Performance of ventricular function in chronic constrictive pericarditis

Os autores avaliaram a funçäo ventricular em 13 pacientes com PCC através dos registros pressóricos intracardíacos e da cineangiocardiografia dos ventrículos direito e esquerdo, e fizeram comparaçäo com umgrupo considerado normal. O estudo do ventrículo direito mostrou: 1 - Diminuiçäo do VDF, VSE, FE e CpE; 2 - Aumento da Pd2. No estudo do ventrículo esquerdo, encontraram: 1 - Diminuiçäo do VSE, FE e CpE; 2 - Aumento da Pd2 e do VDF. Todos os parâmetros acima apresentaram significaçäo estatistica (P < 0,001): näo foi observada variaçäo do VSF do ventrículo direito e do VDF do ventrículo esquerdo (P >0,05). Os autores concluem que, além das alteraçöes referentes à restriçäo diastólica ventricular, foram encontrados achados compatíveis com disfunçäo sistólica biventricular na maioria dos pacientes estudados