Fast determination of minoxidil by photometric flow titration

A photometric flow titration based on the redox reaction between KMnO4 and minoxidil is described. The best titration results were observed at 3.20 x 10-4 mol L-1 KMnO4 and 1.00 x 10-3 mol L-1 minoxidil, using the minoxidil solutions as titrant. The flow rate was fixed at 17 mL min-1 and the titrant was added to the system in aliquots of 500 µL, the color changes were monitored at 550 nm. The method was applied to commercial samples and compared with the results from a chromatographic procedure. Recoveries from 97.6 to 102.8 % were observed depending on the sample. Comparison with the chromatographic procedure reveled relative errors of 3.5 - 4.0 %.

Liqum-järjestelmän optimointi eräällä paperikoneella

Tämän työn tarkoituksena oli jalkauttaa Liqum Oy:n kehittämä Chemistry Navi-gator (Chena) kunnossapidon ja tuotannon päivittäiseksi työkaluksi prosessin märän pään kemian seurantaan. Chena – analysaattorin mittausteknologia perustuu hapetus – pelkistysreaktioiden mittaamiseen. Analysaattori mittaa paperimassassa olevien ionien ja ionikombinaatioiden konsentraatioita ja aktiivisuuksia kuudella anturilla, joiden toiminta perustuu sähkökemiallisiin muutoksiin mitattavassa näytteessä. Diplomityön tarkoituksena oli erityisesti Chena – järjestelmän toimintakuntoon saattaminen sekä tutkia minkälaisia muutoksia märkäosan kemian tilassa analysaattorilla voidaan havaita. Työn kirjallisuusosassa esitellään yleisesti paperikoneen märkäosan kemiallisia ilmiöitä ja kemian tilan muuttujia. Lisäksi esitellään yleisimpiä prosessiin annosteltavia paperin laatuun sekä prosessin toimivuuteen vaikuttavia kemikaaleja. Kokeellisessa osassa optimoitiin järjestelmässä olevien ajoparametrien raja-arvoja vastaamaan nykypäivän ajo-olosuhteita sekä tutkittiin miten Chenan signaalit reagoivat eri massasuhteilla ja kemikaaliannoksilla. Kokeellisen osassa suoritettujen askelvastekokeiden tulosten perusteella havait-tiin, että peroksidi ja ditioniitti antoivat voimakkaimmat vasteet Chenan signaaleihin varsinkin suuremmilla pitoisuuksilla. Myös retentio- ja vaahdonestoaineen osalta oli havaittavissa selviä vasteita Chenan signaaleissa. Massasuhteiden osalta merkittävimmät vasteet Chenan signaaleihin PK4:n puolella aiheuttivat täysin hylytön massaseos sekä puolet kokonaistilavuudesta päällystämätöntä hylkyä sisältänyt massaseos. PK7:n puolella voimakkaimmat vasteet aiheutuivat alhaisen hylkypitoisuuden massoista. Chena avulla saadaan uutta

Potentiometric determination of Minoxidil in topical use pharmaceutical samples

A potentiometric titration method for the determination of minoxidil based on its redox reaction with K2Cr2O7 is described. The best results were observed using 1.00 x 10-3 mol L-1 K2Cr2O7 and 1.00 x 10-2 mol L-1 minoxidil solutions, and the minoxidil as titrant in 2.00 mol L-1 H2SO4 medium. The method was applied to commercial samples and compared with the results from a chromatographic procedure. Recoveries from 97.4 to 98.7 % were observed depending on the sample. Comparison with the chromatographic procedure reveled agreement within 90% confidence level.

Determinação de minoxidil em formulações farmacêuticas usando permanganometria

Um método clássico para a determinação de minoxidil em formulações farmacêuticas é proposto baseado na reação redox entre KMnO4 e o minoxidil. Os melhores resultados na permanganometria foram obtidos usando concentrações de 1,00 x 10-2 mol L-1 para o permanganato. O minoxidil foi usado como titulante na concentração de 2,00 x 10-2 mol L-1 diluído em solução de H2SO4 2,00 mol L-1. As recuperações para método proposto foram da ordem de 94,5 a 95,2 % dependendo da amostra comercial. O método proposto foi aplicado à amostras comerciais contendo minoxidil e comparado com resultados obtidos a partir de procedimentos cromatográficos com erros relativos da ordem de -1 a -5,26%. O procedimento se mostrou simples, rápido e pode ser uma alternativa para a determinação de minoxidil em amostras farmacêuticas, nas quais a concentração do fármaco é relativamente elevada.

Leaf-Targeted Ferredoxin-NADP+-Oxidoreductase (FNR): Electron Transfer Properties and Thylakoid Association in Arabidopsis thaliana

Photosynthetic reactions are divided in two parts: light-driven electron transfer reactions and carbon fixation reactions. Electron transfer reactions capture solar energy and split water molecules to form reducing energy (NADPH) and energy-carrying molecules (ATP). These end-products are used for fixation of inorganic carbon dioxide into organic sugar molecules. Ferredoxin-NADP⁺ oxidoreductase (FNR) is an enzyme that acts at the branch point between the electron transfer reactions and reductive metabolism by catalyzing reduction of NADP+ at the last step of the electron transfer chain. In this thesis, two isoforms of FNR from A rabidopsis thaliana, FNR1 and FNR2, were characterized using the reverse genetics approach. The fnr1 and fnr2 mutant plants resembled each other in many respects. Downregulation of photosynthesis protected the single fnr mutant plants from excess formation of reactive oxygen species (ROS), even without significant upregulation of antioxidative mechanisms. Adverse growth conditions, however, resulted in phenotypic differences between fnr1 and fnr2. While fnr2 plants showed downregulation of photosynthetic complexes and upregulation of antioxidative mechanisms under low-temperature growth conditions, fnr1 plants had the wild-type phenotype, indicating that FNR2 may have a specific role in redistribution of electrons under unfavorable conditions. The heterozygotic double mutant (fnr1xfnr2) was severely devoid of chloroplastic FNR, which clearly restricted photosynthesis. The fnr1xfnr2 plants used several photoprotective mechanisms to avoid oxidative stress. In wild-type chloroplasts, both FNR isoforms were found from the stroma, the thylakoid membrane, and the inner envelope membrane. In the absence of the FNR1 isoform, FNR2 was found only in the stroma, suggesting that FNR1 and FNR2 form a dimer, by which FNR1 anchors FNR2 to the thylakoid membrane. Structural modeling predicted formation of an FNR dimer in complex with ferredoxin. In this thesis work, Tic62 was found to be the main protein that binds FNR to the thylakoid membrane, where Tic62 and FNR formed high molecular weight complexes. The formation of such complexes was shown to be regulated by the redox state of the chloroplast. The accumulation of Tic62-FNR complexes in darkness and dissociation of complexes from the membranes in light provide evidence that the complexes may have roles unrelated to photosynthesis. This and the high viability of fnr1 mutant plants lacking thylakoid-bound FNR indicate that the stromal pool of FNR is photosynthetically active.

Eletrodo de pasta de carbono em minicavidade de contato sólido

Este trabalho descreve a preparação de eletrodo de pasta de carbono (EPC) em minicavidade de contato sólido e sua avaliação quando a pasta de carbono contém ou não partículas sub-micormétricas de SiO2(Eu3+ 2%) e SiO2(Eu3+ 2%)-lisina. Nestes estudos, medidas de voltametria cíclica e impedância eletroquímica foram realizadas em PBS (0,1 mol L-1 pH 7,4) contendo as espécies redox Fe(CN)6-3/-4. Os resultados de impedância foram interpretados baseados na reação de transferência de carga envolvendo as espécies Fe(CN)6-3/-4 e/ou oxigênio em frequências mais altas e, difusão das espécies eletroativas e características da pasta de carbono a baixas frequências. EPC-minicavidade é apropriado para eletroanálises usando pasta de carbono modificada.

Ensino de imunologia na educação médica: lições de Akira Kurosawa

O ensino e a investigação no campo da Imunologia se inscrevem, prevalentemente, num paradigma marcial - ou belicoso -, segundo o qual as interações hospedeiro-microrganismo são vistas de acordo com uma concepção de processos de ataque-defesa. Uma vez que este saber é tradicionalmente abordado nos cursos de graduação da área de saúde, tal perspectiva tem evidente influência na formação destes profissionais, incluídos os médicos. No presente artigo, reflete-se sobre as questões pedagógicas relativas ao modelo ataque-defesa. Realizou-se uma pesquisa teórica, utilizando-se o seguinte método: (1) revisão crítica da literatura, com textos obtidos nos livros e nos capítulos de livros de Imunologia; (2) leitura crítica dos textos; (3) elaboração de síntese reflexiva sobre o tema. Identificou-se que o modelo marcial da Imunologia se apresentou hegemônico nos livros-texto consultados, estando inscrito em idêntica concepção teórica inerente à medicina ocidental, ajudando a compor a visão dos estudantes dos cursos de graduação e pós-graduação e dos trabalhadores da área de saúde. É possível buscar alternativas, inclusive possibilidades para pensar a Imunologia em termos de novos modelos, em termos de homeostase e interdependência (ambos delimitando um paradigma ecológico), talvez mais propícios à abordagem das questões que ora se impõem nos seus horizontes, com inquestionáveis efeitos na educação.

NADPH-Dependent Thioredoxin System In Regulation of Chloroplast Functions

Photosynthesis, the process in which carbon dioxide is converted into sugars using the energy of sunlight, is vital for heterotrophic life on Earth. In plants, photosynthesis takes place in specific organelles called chloroplasts. During chloroplast biogenesis, light is a prerequisite for the development of functional photosynthetic structures. In addition to photosynthesis, a number of other metabolic processes such as nitrogen assimilation, the biosynthesis of fatty acids, amino acids, vitamins, and hormones are localized to plant chloroplasts. The biosynthetic pathways in chloroplasts are tightly regulated, and especially the reduction/oxidation (redox) signals play important roles in controlling many developmental and metabolic processes in chloroplasts. Thioredoxins are universal regulatory proteins that mediate redox signals in chloroplasts. They are able to modify the structure and function of their target proteins by reduction of disulfide bonds. Oxidized thioredoxins are restored via the action of thioredoxin reductases. Two thioredoxin reductase systems exist in plant chloroplasts, the NADPHdependent thioredoxin reductase C (NTRC) and ferredoxin-thioredoxin reductase (FTR). The ferredoxin-thioredoxin system that is linked to photosynthetic light reactions is involved in light-activation of chloroplast proteins. NADPH can be produced via both the photosynthetic electron transfer reactions in light, and in darkness via the pentose phosphate pathway. These different pathways of NADPH production enable the regulation of diverse metabolic pathways in chloroplasts by the NADPH-dependent thioredoxin system. In this thesis, the role of NADPH-dependent thioredoxin system in the redox-control of chloroplast development and metabolism was studied by characterization of Arabidopsis thaliana T-DNA insertion lines of NTRC gene (ntrc) and by identification of chloroplast proteins regulated by NTRC. The ntrc plants showed the strongest visible phenotypes when grown under short 8-h photoperiod. This indicates that i) chloroplast NADPH-dependent thioredoxin system is non-redundant to ferredoxinthioredoxin system and that ii) NTRC particularly controls the chloroplast processes that are easily imbalanced in daily light/dark rhythms with short day and long night. I identified four processes and the redox-regulated proteins therein that are potentially regulated by NTRC; i) chloroplast development, ii) starch biosynthesis, iii) aromatic amino acid biosynthesis and iv) detoxification of H₂O₂. Such regulation can be achieved directly by modulating the redox state of intramolecular or intermolecular disulfide bridges of enzymes, or by protecting enzymes from oxidation in conjunction with 2-cysteine peroxiredoxins. This thesis work also demonstrated that the enzymatic antioxidant systems in chloroplasts, ascorbate peroxidases, superoxide dismutase and NTRC-dependent 2-cysteine peroxiredoxins are tightly linked up to prevent the detrimental accumulation of reactive oxygen species in plants.

Recovery and refining of manganese as by-product from hydrometallurgical processes

The consumption of manganese is increasing, but huge amounts of manganese still end up in waste in hydrometallurgical processes. The recovery of manganese from multi-metal solutions at low concentrations may not be economical. In addition, poor iron control typically prevents the production of high purity manganese. Separation of iron from manganese can be done with chemical precipitation or solvent extraction methods. Combined carbonate precipitation with air oxidation is a feasible method to separate iron and manganese due to the fast kinetics, good controllability and economical reagents. In addition the leaching of manganese carbonate is easier and less acid consuming than that of hydroxide or sulfide precipitates. Selective iron removal with great efficiency from MnSO4 solution is achieved by combined oxygen or air oxidation and CaCO3 precipitation at pH > 5.8 and at a redox potential of > 200 mV. In order to avoid gypsum formation, soda ash should be used instead of limestone. In such case, however, extra attention needs to be paid on the reagents mole ratios in order to avoid manganese coprecipitation. After iron removal, pure MnSO4 solution was obtained by solvent extraction using organophosphorus reagents, di-(2-ethylhexyl)phosphoric acid (D2EHPA) and bis(2,4,4- trimethylpentyl)phosphinic acid (CYANEX 272). The Mn/Ca and Mn/Mg selectivities can be increased by decreasing the temperature from the commonly used temperatures (40 –60oC) to 5oC. The extraction order of D2EHPA (Ca before Mn) at low temperature remains unchanged but the lowering of temperature causes an increase in viscosity and slower phase separation. Of these regents, CYANEX 272 is selective for Mn over Ca and, therefore, it would be the better choice if there is Ca present in solution. A three-stage Mn extraction followed by a two-stage scrubbing and two-stage sulfuric acid stripping is an effective method of producing a very pure MnSO4 intermediate solution for further processing. From the intermediate MnSO4 some special Mn- products for ion exchange applications were synthesized and studied. Three types of octahedrally coordinated manganese oxide materials as an alternative final product for manganese were chosen for synthesis: layer structured Nabirnessite, tunnel structured Mg-todorokite and K-kryptomelane. As an alternative source of pure MnSO4 intermediate, kryptomelane was synthesized by using a synthetic hydrometallurgical tailings. The results show that the studied OMS materials adsorb selectively Cu, Ni, Cd and K in the presence of Ca and Mg. It was also found that the exchange rates were reasonably high due to the small particle dimensions. Materials are stable in the studied conditions and their maximum Cu uptake capacity was 1.3 mmol/g. Competitive uptake of metals and acid was studied using equilibrium, batch kinetic and fixed-bed measurements. The experimental data was correlated with a dynamic model, which also accounts for the dissolution of the framework manganese. Manganese oxide micro-crystals were also bound onto silica to prepare a composite material having a particle size large enough to be used in column separation experiments. The MnOx/SiO2 ratio was found to affect significantly the properties of the composite. The higher the ratio, the lower is the specific surface area, the pore volume and the pore size. On the other hand, higher amount of silica binder gives composites better mechanical properties. Birnesite and todorokite can be aggregated successfully with colloidal silica at pH 4 and with MnO2/SiO2 weight ratio of 0.7. The best gelation and drying temperature was 110oC and sufficiently strong composites were obtained by additional heat-treatment at 250oC for 2 h. The results show that silica–supported MnO2 materials can be utilized to separate copper from nickel and cadmium. The behavior of the composites can be explained reasonably well with the presented model and the parameters estimated from the data of the unsupported oxides. The metal uptake capacities of the prepared materials were quite small. For example, the final copper loading was 0.14 mmol/gMnO2. According to the results the special MnO2 materials are potential for a specific environmental application to uptake harmful metal ions.

High-Throughput Screening for Novel Prostate Cancer Drug Targets –Getting Personal

Prostate cancers form a heterogeneous group of diseases and there is a need for novel biomarkers, and for more efficient and targeted methods of treatment. In this thesis, the potential of microarray data, RNA interference (RNAi) and compound screens were utilized in order to identify novel biomarkers, drug targets and drugs for future personalized prostate cancer therapeutics. First, a bioinformatic mRNA expression analysis covering 9873 human tissue and cell samples, including 349 prostate cancer and 147 normal prostate samples, was used to distinguish in silico prevalidated putative prostate cancer biomarkers and drug targets. Second, RNAi based high-throughput (HT) functional profiling of 295 prostate and prostate cancer tissue specific genes was performed in cultured prostate cancer cells. Third, a HT compound screen approach using a library of 4910 drugs and drug-like molecules was exploited to identify potential drugs inhibiting prostate cancer cell growth. Nine candidate drug targets, with biomarker potential, and one cancer selective compound were validated in vitro and in vivo. In addition to androgen receptor (AR) signaling, endoplasmic reticulum (ER) function, arachidonic acid (AA) pathway, redox homeostasis and mitosis were identified as vital processes in prostate cancer cells. ERG oncogene positive cancer cells exhibited sensitivity to induction of oxidative and ER stress, whereas advanced and castrate-resistant prostate cancer (CRPC) could be potentially targeted through AR signaling and mitosis. In conclusion, this thesis illustrates the power of systems biological data analysis in the discovery of potential vulnerabilities present in prostate cancer cells, as well as novel options for personalized cancer management.

DPS-Like Peroxide Resistance Protein: Structural and Functional Studies on a Versatile Nanocontainer

Oxidative stress is a constant threat to almost all organisms. It damages a number of biomolecules and leads to the disruption of many crucial cellular functions. It is caused by reactive oxygen species (ROS), such as hydrogen peroxide (H2O₂), superoxide (•O₂ -), and hydroxyl radical (•OH). The most harmful of these compounds is •OH, which is only formed in cells in the presence of redox-cycling transition metals, such as iron and copper. Bacteria have developed a number of mechanisms to cope with ROS. One of the most widespread means employed by bacteria is the DNA-binding proteins from starved cells (Dps). Dps proteins protect the cells by binding and oxidizing Fe2+, thus greatly reducing the production of •OH. The oxidized iron is stored inside the protein as an iron core. In addition, Dps proteins bind directly to DNA forming a protective coating that shields DNA from harmful agents. Moreover, Dps proteins have been found to elicit other protective functions in cells and to participate in bacterial virulence. Dps proteins are of special importance to Streptococci owing to the lack of catalase in this genus of bacteria.This study was focused on structural and functional characterization of streptococcal Dpslike peroxide resistance (Dpr) proteins. Initially, crystal structures of Streptococcus pyogenes Dpr were determined. The data confirmed the presence of a di-metal ferroxidase center (FOC) in Dpr proteins and revealed the presence of a novel N-terminal helix as well as a surface metal-binding site. The crystal structures of Streptococcus suis Dpr complexed with transition metals demonstrated the metal specificity of the FOC. Solution binding studies also indicated the presence of a di-metal FOC. These results suggested a possible role for Dpr in the detoxification of various metals. Iron was found to mineralize inside the protein as ferrihydrite based on X-ray absorption spectroscopy data. The iron core was found to exhibit clear superparamagnetic behaviour using magnetic and Mössbauer measurements. The results from this study are expected to further increase our understanding on the binding, oxidation, and mineralization of iron and other metals in Dpr proteins. In particular, the structural and magnetic properties of the iron core can form a basis for potential new applications in nanotechnology. From the streptococcal viewpoint, the results would help in understanding better the complicated picture of bacterial pathogenesis. Dpr proteins may also provide a novel target for drug design due to their tight involvement in bacterial virulence.

Uso da termografia infravermelha na análise da termorregulação de cavalo em treinamento

O estresse térmico em equinos aciona mecanismos termorregulatórios, como mudanças no fluxo sanguíneo periférico, para a manutenção da homeostase corporal. A termografia infravermelha permite detectar estas alterações, sendo uma ferramenta útil para avaliar o estresse em animais. Assim, o objetivo deste estudo foi avaliar o uso da termografia infravermelha na termorregulação de equino em condição de treinamento. Foi utilizado um cavalo anglo-árabe, exercitado uma vez ao dia. Foram captadas imagens termográficas da axila, garupa, peito e virilha do cavalo e registrados os parâmetros fisiológicos antes e após exercício e 0; 5 e 10 minutos após o banho, durante 8 dias. A temperatura, a umidade relativa e a velocidade do ar foram monitoradas. A temperatura de superfície da garupa e do peito não diferiu entre os tratamentos, indicando baixa participação destas partes na termorregulação. Em contrapartida, a temperatura superficial da axila e da virilha aumentou após o exercício e diminuiu após o banho, sugerindo evidência dos mecanismos vasomotores para a troca térmica do cavalo. Comportamento semelhante foi observado para as variáveis fisiológicas, o que demonstra tentativas orgânicas do organismo para sair das condições de estresse térmico. Concluiu-se que a termografia infravermelha permitiu determinar com precisão a temperatura de superfície corporal do cavalo, sendo possível inferir sobre a termorregulação.

Application of electrokinetic Fenton process for the remediation of soil contaminated with HCB

Electrokinetic remediation coupled with Fenton oxidation, widely called as Electrokinetic Fenton process is a potential soil remediation technique used for low permeable soil. The applicability of the process has been proved with soil contaminated with a wide range of organic compounds from phenol to the most recalcitrant ones such as PAHs and POPs. This thesis summarizes the major findings observed during an Electrokinetic Fenton Process study conducted for the remediation of low permeable soil contaminated with HCB, a typical hydrophobic organic contaminant. Model low permeable soil, kaolin, was artificially contaminated with HCB and subjected to Electrokinetic Fenton treatments in a series of laboratory scale batch experiments. The use of cyclodextrins as an enhancement agent to mobilize the sorbed contaminant through the system was investigated. Major process hindrances such as the oxidant availability and treatment duration were also addressed. The HCB degradation along with other parameters like soil pH, redox and cumulative catholyte flow were analyzed and monitored. The results of the experiments strengthen the existing knowledge on electrokinetic Fenton process as a promising technology for the treatment of soil contaminated with hydrophobic organic compounds. It has been demonstrated that HCB sorbed to kaolin can be degraded by the use of high concentrations of hydrogen peroxide during such processes. The overall system performances were observed to be influenced by the point and mode of oxidant delivery. Furthermore, the study contributes to new knowledge in shortening the treatment duration by adopting an electrode polarity reversal during the process.

Apoptose, neutrófilos e o cirurgião

O estudo do processo de morte celular programada ganhou impulso a partir da demonstração da sua presença em células maduras não germinativas em 1971. A apoptose é um mecanismo vital normal, que acontece a todo o tempo nos organismos, permitindo a preservação da homeostase e renovação celular, possuindo características cito/histológicas próprias. Este trabalho faz uma revisão sumária de aspectos básicos da apoptose de interesse do cirurgião. São revistos dados da literatura referentes à apoptose no tocante às características cito/histológicas e sua importância na ontogênese, homeostasia, patogênese, inflamação sistêmica, sepse abdominal e trauma. Alterações no processo de apoptose no embrião podem levar a malformações congênitas. No adulto, algumas doenças expressam-se por aumento (ex. isquemia miocárdica, Alzheimer etc.) ou diminuição nas taxas de apoptose (ex. câncer, doenças auto-imunes etc.). De particular interesse para o cirurgião, a elevação numérica dos neutrófilos que ocorre durante processos de inflamação sistêmica e trauma, deve-se à inibição da apoptose. A morte celular programada nos neutrófilos pode ser alterada por uma série de processos celulares (ex: adesão, transmigração etc.), substâncias endógenas e exógenas (ex: citocinas e lipopolissacarídeo), produzindo diferentes taxas de apoptose de acordo com a interação dos fatores. O aprofundamento no estudo da morte celular programada, com a possibilidade de sua modulação, a coloca como potencialmente aliada na terapêutica.

Hipotensão controlada induzida por halotano em coelhos

OBJETIVO: Descrever e analisar um estudo experimental com o objetivo de pesquisar o uso do halotano em diferentes concentrações, visando à obtenção de hipotensão induzida ou controlada e à análise das repercussões hemodinâmicas decorrentes do método. MÉTODO: Foram utilizados vinte e nove coelhos (Oryctolagus cuniculus), do tipo Nova Zelândia subdivididos em quatro grupos, dentre os quais havia um controle composto por cinco animais, e outros três contendo oito coelhos cada um. Os grupos I,II e III (n=8 cada)) foram submetidos a um período de hipotensão induzida, utilizando-se o halotano em concentrações de 1,0%, 1,5% e 2,0%, respectivamente. Foram avaliadas as freqüências cardíaca (FC) e respiratória (FR), a pressão arterial média (PAM) e a temperatura corporal. No sangue arterial analisaram-se os valores do potencial hidrogeniônico (pH), da pressão parcial do oxigênio (PaO2), da pressão parcial do gás carbônico (PaCO2), do bicarbonato (-HCO3), do excesso de bases (BE), da saturação do oxigênio da hemoglobina (Sat.O2). Estes parâmetros foram obtidos em três momentos: antes (MAnH), durante (MDuH) e após (MApH) a hipotensão induzida. Acompanhou-se, periodicamente, os reflexos corneano e pupilar e, de forma contínua, o eletrocardiograma. RESULTADOS: A análise estatística dos resultados evidenciou hipotensão e redução de frequência cardíaca com o uso do halotano. O pH dos coelhos é mais alcalino que o do homem. Não obstante haver uma tendência à acidose metabólica, esta decorreu de uma condição transitória, sem comprometer a homeostase. CONCLUSÃO: O halotano é um anestésico seguro e eficaz para promover a hipotensão induzida ou controlada, em coelhos.