Animal assisted intervention for oncology and palliative care patients: A systematic review.

INTRODUCTION: Animal assisted interventions (AAI) have been used in different contexts including oncology/palliative care and can improve mood, quality of life and wellness. The goal of this review was to evaluate studies about AAI and its effects on oncological/palliative care patients. METHODS: The search was conducted on PubMed, Scopus and Lilacs databases. The inclusion criteria were original articles that measured quantitatively the health-related outcomes of an AAI on oncological/palliative care patients. RESULTS: Ten studies fulfilled the inclusion criteria. Benefits related to the AAI were described. Mood, pain perception and quality of life seemed to be the variables that had improvement with the intervention. Due to the small sample sizes/heterogeneous methodologies, additional analyses could not be performed. CONCLUSIONS: AAI can be an important tool for improving psychosocial/physiological parameters in cancer/palliative care patients. Further well designed studies are needed to provide a better knowledge of the AAI benefits in this setting.

Rational selection of immunodominant and preserved epitope Sm043300e from Schistosoma mansoni and design of a chimeric molecule for biotechnological purposes.

Human schistosomiasis is a neglected tropical disease of great importance in public health. A large number of people are infected with schistosomiasis, making vaccine development and effective diagnosis important control strategies. A rational epitope prediction workflow using Schistosoma mansoni hypothetical proteins was previously presented by our group, and an improvement to that approach is presented here. Briefly, immunodominant epitopes from parasite membrane proteins were predicted by reverse vaccinology strategy with additional in silico analysis. Furthermore, epitope recognition was evaluated using sera of individuals infected with S. mansoni. The epitope that stood out in both in silico and in vitro assays was used to compose a rational chimeric molecule to improve immune response activation. Out of 2185 transmembrane proteins, four epitopes with high binding affinities for human and mouse MHCII molecules were selected through computational screening. These epitopes were synthesized to evaluate their ability to induce TCD4+ lymphocyte proliferation in mice. Sm204830e and Sm043300e induced significant TCD4+ proliferation. Both epitopes were submitted to enzyme-linked immunosorbent assay to evaluate their recognition by IgG antibodies from the sera of infected individuals, and epitope Sm043300 was significantly recognized in most sera samples. Epitope Sm043300 also showed good affinity for human MHCII molecules in molecular docking, and its sequence is curiously highly conserved in four S. mansoni proteins, all of which are described as G-protein-coupled receptors. In addition, we have demonstrated the feasibility of incorporating this epitope, which showed low similarity to human sequences, into a chimeric molecule. The stability of the molecule was evaluated by molecular modeling aimed at future molecule production for use in diagnosis and vaccination trials.

Chemical and toxicological effects of medicinal Baccharis trimera extract from coal burning area.

The entire process of power generation, extraction, processing and use of coal strongly impact water resources, soil, air quality and biota leads to changes in the fauna and flora. Pollutants generated by coal burning have been contaminating plants that grow in area impacted by airborne pollution with high metal contents. Baccharis trimera is popularly consumed as tea, and is widely developed in Candiota (Brazil), one of the most important coal burning regions of the Brazil. This study aims to investigate the phytochemical profile, in vivo genotoxic and mutagenic potential of extracts of B. trimera collected from an exposed region to pollutants generated by coal burning (Candiota City) and other unexposed region (Bagé City), using the Comet assay and micronucleus test in mice and the Salmonella/microsome short-term assay. The HPLC analyses indicated higher levels of flavonoids and phenolic acids for B. trimera aqueous extract from Bagé and absence of polycyclic aromatic hydrocarbons for both extracts. The presence of toxic elements such as cobalt, nickel and manganese was statistically superior in the extract from Candiota. For the Comet assay and micronucleus test, the mice were treated with Candiota and Bagé B. trimera aqueous extracts (500-2000 mg/kg). Significant genotoxicity was observed at higher doses treated with B. trimera aqueous extract from Candiota in liver and peripheral blood cells. Micronuclei were not observed but the results of the Salmonella/microsome short-term assay showed a significant increase in TA98 revertants for B. trimera aqueous extract from Candiota. The extract of B. trimera from Candiota bioacumulated higher levels of trace elements which were associated with the genotoxic effects detected in liver and peripheral blood cells.

Antineoplásicos y riesgos laborales para los enfermeros: una revisión integral / Antineoplásicos e os riscos ocupacionais para os enfermeiros: uma revisão integrativa Antineoplastic and occupational risks for nurses: an integrative review

Introducción: Son muchos los riesgos laborales a los que están expuestos los trabajadores de salud que manipulan quimioterápicos. Objetivos: Identificar y describir los daños a corto, medio y largo plazo, causados en el organismo de los enfermeros y otros profesionales de la salud, que están expuestos a los fármacos antineoplásicos en el lugar de trabajo. Metodología: Estudio de revisión integradora de la literatura, con la recogida de datos en la Biblioteca Virtual en Salud, en los meses de septiembre a octubre de 2013, en las bases de datos de biblioteca electrónica Scientific Electronic Library Online y en las bases de datos de la Literatura Latino Americana y Caribeña Ciencias de la Salud, la Base de Datos de Enfermería y el Análisis de la Literatura Médica y Recuperación del Sistema en Línea, con las palabras: 'Antineoplasicos and Risco Ocupacional and Enfermagem', 'Antineoplastic and Occupational Risk' y 'Antineoplastic and Nursing'. Resultados: Daño en el material genético, aumento de la frecuencia de micronúcleos en linfocitos, aumento de intercambio de cromátidas hermanas, un mayor nivel de la excreción urinaria antineoplásica, aumento de casos de cáncer, mayor incidencia de anomalías congénitas en la descendencia y aborto en el primer trimestre del embarazo son algunos de los resultados encontrados en este estudio. Conclusión: El daño más frecuente ocurre al ácido desoxirribonucleico, el predominio a medio y largo plazo, siendo el tiempo de exposición fundamental para aumentar el daño. A corto y largo plazo predominaron daños relacionado con el embarazo y el desarrollo fetal, con aumento de anomalías congénitas y aborto. Acompañamiento genético, así como equipos de protección individual son esenciales para minimizar los daños (AU)

Introdução: são inúmeros os riscos ocupacionais aos quais os trabalhadores de saúde que manipulam quimioterápicos são expostos. Objetivos: identificar e descrever os danos em curto, médio e longo prazo, causados ao organismo dos enfermeiros, e demais profissionais da saúde, que são expostos à antineoplásicos no ambiente de trabalho. Metodologia: estudo de revisão integrativa da literatura, com coleta de dados na Biblioteca Virtual da Saúde, nos meses de setembro a outubro de 2013, nas bases de dados da biblioteca eletrônica Scientific Electronic Library Online e nas bases de dados da Literatura Latino-Americana e do Caribe em Ciências da Saúde, da Base de Dados de Enfermagem e da Medical Literature Analysis and Retrieval System Online, tendo como descritores: "Antineoplasicos and Risco Ocupacional and Enfermagem", "Antineoplastic and Occupational Risk" e "Antineoplastic and Nursing". Resultados: danos ao material genético, aumento da frequência de micronúcleos em linfócitos, aumento da troca das cromátides irmãs, aumento do nível de antineoplásicos na excreção urinária, aumento dos casos de câncer, aumento da incidência de anomalias congênitas na prole e aborto no primeiro trimestre da gravidez são alguns dos resultados encontrados por este estudo. Conclusão: o dano mais frequente ocorreu ao ácido desoxirribonucleico, e predominou em médio e longo prazo, com o tempo de exposição sendo decisivo ao aumento dos prejuízos. Em curto e longo prazo predominaram danos ligados à gestação e ao desenvolvimento do feto, com aumento das anomalias congênitas e aborto. Acompanhamento genético, bem como Equipamentos de Proteção Individual são fundamentais para minimizar os danos

Introduction: There are countless occupational hazards to which health workers who handle chemotherapeutic substances are exposed. Objectives: To identify and describe the short-, medium- and long-term damages that are caused in the bodies of nurses and other health professionals who are exposed to antineoplastic drugs in the workplace. Methodology: To study an integrative literature review, with data collection in the Virtual Health Library in the months from September to October 2013, the database of the Scientific Electronic Library Online, and in the databases of the Latin American and Caribbean Health Sciences, the Database of Nursing and the Medical Literature Analysis and Retrieval System Online, with the keywords: 'Antineoplasicos and Risco Ocupacional and Enfermagem', 'Antineoplastic and Occupational Risk' and 'Antineoplastic and Nursing.' Results:, Damage to genetic material, increased frequency of micronuclei in lymphocytes, increased exchange of sister chromatids, increased levels of antineoplastic urinary excretion, increased cases of cancer, increased incidence of congenital anomalies in offspring and miscarriages in the first trimester of pregnancy are some of the results found in this study. Conclusion: The most frequent damage occurred in the deoxyribonucleic acid, and predominated in medium and long terms, with the exposure time being crucial to increasing damage. In short and long term predominated damage linked to pregnancy and the developing fetus, with increase in congenital abnormalities and abortion. Genetic monitoring as well as Personal Protective Equipment are essential to minimize damage (AU)

In vitro and in vivo antiparasitic activity of Physalis angulata L. concentrated ethanolic extract against Trypanosoma cruzi.

BACKGROUND: The current treatment of Chagas disease, endemic in Latin America and emerging in several countries, is limited by the frequent side effects and variable efficacy of benznidazole. Natural products are an important source for the search for new drugs. AIM/HYPOTHESIS: Considering the great potential of natural products as antiparasitic agents, we investigated the anti-Trypanosoma cruzi activity of a concentrated ethanolic extract of Physalis angulata (EEPA). METHODS: Cytotoxicity to mammalian cells was determined using mouse peritoneal macrophages. The antiparasitic activity was evaluated against axenic epimastigote and bloodstream trypomastigote forms of T. cruzi, and against amastigote forms using T. cruzi-infected macrophages. Cell death mechanism was determined in trypomastigotes by flow cytometry analysis after annexin V and propidium iodide staining. The efficacy of EEPA was examined in vivo in an acute model of infection by monitoring blood parasitaemia and survival rate 30 days after treatment. The effect against trypomastigotes of EEPA and benznidazole acting in combination was evaluated. RESULTS: EEPA effectively inhibits the epimastigote growth (IC50 2.9 ± 0.1 µM) and reduces bloodstream trypomastigote viability (EC50 1.7 ± 0.5 µM). It causes parasite cell death by necrosis. EEPA impairs parasite infectivity as well as amastigote development in concentrations noncytotoxic to mammalian cells. In mice acutely-infected with T. cruzi, EEPA reduced the blood parasitaemia in 72.7%. When combined with benznidazole, EEPA showed a synergistic anti-T. cruzi activity, displaying CI values of 0.8 ± 0.07 at EC50 and 0.83 ± 0.1 at EC90. CONCLUSION: EEPA has antiparasitic activity against T. cruzi, causing cell death by necrosis and showing synergistic activity with benznidazole. These findings were reinforced by the observed efficacy of EEPA in reducing parasite load in T. cruzi-mice. Therefore, this represents an important source of antiparasitic natural products.

Clove (Syzygium aromaticum): a precious spice.

Clove (Syzygium aromaticum) is one of the most valuable spices that has been used for centuries as food preservative and for many medicinal purposes. Clove is native of Indonesia but nowadays is cultured in several parts of the world including Brazil in the state of Bahia. This plant represents one of the richest source of phenolic compounds such as eugenol, eugenol acetate and gallic acid and posses great potential for pharmaceutical, cosmetic, food and agricultural applications. This review includes the main studies reporting the biological activities of clove and eugenol. The antioxidant and antimicrobial activity of clove is higher than many fruits, vegetables and other spices and should deserve special attention. A new application of clove as larvicidal agent is an interesting strategy to combat dengue which is a serious health problem in Brazil and other tropical countries. Pharmacokinetics and toxicological studies were also mentioned. The different studies reviewed in this work confirm the traditional use of clove as food preservative and medicinal plant standing out the importance of this plant for different applications.

A cDNA sequence coding for a glutamic acid-rich protein is differentially expressed in cassava storage roots.

We report the isolation and characterization of a cDNA sequence (Mec1) coding for a glutamic acid-rich protein (Pt2L4) from cassava storage roots. Comparative sequence analysis showed a high identity of Pt2L4 with cassava protein C54, which is expressed in vascular tissues of storage roots. Northern blot analysis showed that the Mec1 transcript expression pattern might be related to the maturation of the storage parenchyma cells.