This study analyzed repeated methylphenidate (MPH) administration and its effects on brain-derived neurotrophic factor (BDNF) in the dorsal striatum and nucleus accumbens of male and female adolescent rats. In Experiment 1, rats were administered intraperitoneal (ip) saline, 1, 3, or 5 mg/kg dose of MPH every second day from postnatal day (P)33–P49. Locomotor activity was analyzed for 10 min after each administration. Results revealed that the 1 mg/kg dose of MPH produced locomotor suppression, however, the 5 mg/kg dose of MPH produced locomotor sensitization and robust behavioral activation in females as compared to males. In Experiment 2, animals were administered ip saline or the 5 mg/kg dose of MPH using an identical regimen but a 30 min behavioral test was employed. Dorsal striatum and nucleus accumbens tissue was assayed for BDNF at P50. Females demonstrated sensitization to MPH and increased locomotor activation compared to males. Interestingly, females given MPH demonstrated a significant 42% decrease of striatal BDNF whereas males administered MPH demonstrated a significant 50.4% increase of striatal BDNF compared to controls. There were no effects on accumbal BDNF. This report demonstrates robust sex differences in the behavioral response, but sex-dependent changes in striatal BDNF in response to MPH in adolescence.

Testing an integrated information system that relies on data from multiple sources can be a challenge, particularly when the data is confidential. This thesis describes a novel test data extraction approach, called semantic-based test data extraction for integrated systems (iSTDE) that solves many of the problems associated with creating realistic test data for integrated information systems containing confidential data. iSTDE reads a consistent cross-section of data from the production databases, manipulates that data to obscure individual identities while still preserving overall semantic data characteristics that are critical to thorough system testing, and then moves that test data to an external test environment. This thesis also presents a theoretical study that compares test-data extraction with a competing technique, named test-data generation. Specifically, this thesis a) describes a comparison method that includes a comprehensive list of characteristics essential for testing the database applications organized into seven different areas, b) presents an analysis of the relative strengths and weaknesses of the different test-data creation techniques, and c) reports a number of specific conclusions that will help testers make appropriate choices.

Multiple interactions between dopamine (DA), glutamate, and nitric oxide (NO) in mesolimbic and corticostriatal circuits suggest that NO may play a critical role in cocaine-induced behavioral and neural plasticity. Clinical and preclinical studies have revealed that females and adolescents display unique vulnerabilities to the behavioral and neurochemical effects of cocaine as a result of sex-dependent and ontogeny-dependent differences in dopaminergic systems. Thus, my research objectives were to investigate the contributions of the neuronal nitric oxide synthase (nNOS) gene, ontogeny, and gender on the rewarding and sensitizing effects of cocaine. I found that nNOS significantly influences the rewarding aspects of cocaine in adolescent mice and adult male mice (i.e., major deficits in several phases of cocaine conditioned place preference (CPP) were detected in nNOS knockout (KO) adolescent mice and nNOS KO adult male mice). However, the contribution of nNOS was sex-dependent as CPP phases were normal in KO adult females. In contrast to CPP, I found a major ontogeny-dependent contribution of nNOS to the sensitizing effects of cocaine. Namely, while nNOS is essential for the development of behavioral sensitization in adult males, this type of behavioral plasticity develops independently of nNOS during adolescence. The contribution of nNOS was once again sex-dependent as behavioral sensitization was normal in adult KO females. Together, this line of investigation has revealed that the NO-signaling pathway has a) a sex-dependent role in the neuroplasticity underlying cocaine CPP and b) a sex-dependent and ontogeny-dependent influence on cocaine-induced behavioral sensitization. Stereological and western blot analysis revealed that a sensitizing regimen of cocaine resulted in an increase in nNOS and tyrosine hydroxylase (TH) immunoreactivity in the dorsal striatum (dST) of adult, but not adolescent, wild-type (WT) male mice. In the absence of nNOS, dopaminergic neurons in the ventral tegmental area (VTA) were severely reduced and cocaine caused a downregulation of dST TH suggesting that nitrergic levels modulate TH. Thus, the finding that nNOS is essential for the development of sensitization in adulthood, but not adolescence, together with the fact that cocaine upregulated nNOS and TH in the dST in adult, but not adolescent mice, strongly suggest that the nitrergic system underlies behavioral sensitization through modulation of the dopaminergic system in adulthood. These findings suggest different approaches in the clinical treatment of drug craving and drug-seeking behavior in adolescent and adult patients.

The aim of this thesis was to identify risk factors for the onset of adult asthma. Other objectives were to study determinants of smoking habits and the association between sensitization and outcome of asthma. In 1990, a questionnaire was distributed to 12,732 individuals from three age groups (16, 30-39 and 60-69 years) in two counties of Sweden. In a second phase, 2538 subjects who had reported respiratory symptoms and 600 controls were invited to clinical investigations, 81% participated. At the follow-up in 2003 subjects of the remaining cohort (11,282) were re-invited. Analyses are based on the 67% (n=7563) who responded to both questionnaires 1990 and 2003. In 2003, 17.2% of the young adults, 11.4% of the middle-aged and 10.3% of the elderly reported having, or having had, asthma. A total of 791 subjects reported onset of asthma during the 13-year study period. Lifestyle factors such as smoking, obesity, hard physical training and a low consumption of fruit and fish were constant risk factors for onset of asthma after adjusting for socioeconomic group. A smoker’s risk of asthma onset was increased by 37%. The impact of risk factors differed between the age-groups. BMI had a significantly higher impact in the middle-aged and elderly. In subjects participating in the clinical investigations in 1990, sensitization to pets, were determinants of both persistent asthma and onset of asthma in 2003. The risk for persistent asthma was threefold. The risk for onset of asthma was more than doubled. Smoking at baseline in 1990 was the strongest determinant of being a smoker in 2003. Allergic sensitization and clinically verified asthma were not associated with smoking habits in 2003. No differences in changing smoking habits could be identified between smokers with or without asthma. In conclusion, modifiable lifestyle factors are important risk factors for adult onset asthma. The co-occurrence and interplay between asthma and cigarette smoking is still puzzling.

The correct development and function of CNS is critical for brain health of the organism. Early or chronic stress causes prominent alterations in brain function, and affects the expression of neurotrophic factors in limbic brain regions involved in the regulation of mood and cognition. Recent evidences have opened the idea that in complex organisms, an altered expression of certain neurotrophins by stress could be involved in the onset and pathophysiology of most psychiatric disorders, such as depression, squizophrenia or anxiety disorders. It is hypothesized that altered levels of neurotrophic factors could contribute to the atrophy and cell death of these regions, including the hippocampus and prefrontal cortex, which would produce a malfunction in limbic-related areas, and as a consequence, a precipitation or worsening of psychiatric illnesses. We were interested in panic disorder pathophysiology, which is a stress-related disorder and is characterized by an altered cognitive processing of emotional information. Although little evidence has been found supporting a neurotrophic role in PD, recent data has revealed that NT-3/TrkC signaling might play a key role in limbic system morphology and function. Therefore, we suggest that NT-3/TrkC system is involved in PD pathogenesis. The main objective in the work of this doctoral thesis lie to determine the role of NTRK3 gene, that codifies for TrKC, in emotional cognition and stress response processes that underlies PD. To this end, we used a genetically modified mouse model of NTRK3 overexpression, which was validated as a model of PD. Here, it is characterized the effects produced by the increase of NTRK3 expression in the CNS, focusing in neural alterations that might influence changes in cognitive processes involved in coping strategies. Moreover, it is studied the mechanisms that underlie in these processes by different approaches, 1/physiologically, measuring the HPA axis response, 2/brain activation, analyzing the activation pattern to a stress stimulus, 3/cellular and gene expression profiling, characterizing key brain regions in cognitive processes, and 4/pharmacologically, studying neurotransmitters function.

No description available.

The response patterns of human stretch receptors in the finger extensor muscles of the forearm were studied using the microneurography technique. Single-unit recordings were obtained from one-hundred and twenty-four afferents. A procedure was developed to classify the units in muscle spindle primary afferents, secondary afferents, and Golgi tendong organ afferents. The procedure allows an objective and reproducible classification on the basis of the afferents’ responses to a series of tests which individually are non-conclusive. It was demonstrated that maximal twitch contractions can be elicited in the finger extensor muscles of the forearm, without causing undue discomfort to the subjects, or hazarding the single-unit recording. The response of the units to this test allowed, in most cases but not always, a separation in muscle spindle and tendon organ afferents. Thus the test was not adequate for an unequivocal classification. Three discrete response parameters were extracted from ramp-and-hold stretches, viz. the presence or absence of an initial burst and a deceleration response, and prompt silencing at slow muscle shortening. The distributions of the parameters were significantly different among the three unit types. These parameters which were pair-wise independent constituted a set of considerable discriminative power. It was shown that human muscle spindles have about the same static position sensitivity to fractional muscle stretch as previously found in animals. Stretch sensitization was demonstrated by rapid, repeated stretches of the muscle which enhanced the réponse to subsequent slow stretches of muscle spindles. Sensitization was different with primary and secondary muscle spindle afferents whereas Golgi tendon organ afferents never displayed stretch sensitization. One-to-one driving with small-amplitude sinusoidal stretches superimposed on ramp-and- hold stretches was almost exclusively seen with primary muscle spindle afferents, whereas secondaries seldom and tendon organ afferents never displayed driving. The afferent responses during slowly increasing isometric contractions and rapid relaxations were analysed. An increased discharge rate on relaxation was common among spindle afferents whereas it was never seen in tendon organs afferents. Two separate groups of spindles afferents were found with regard to fusimotor recruitment. The largest group was recruited at rather low and variable contractile forces whereas the smaller group was not recruited at all. The proportions of the three unit types, spindle primary, spindle secondary, and Golgi tendon organ afferents were estimated from a preliminary classification and the distribution of the eight response features were analyzed for each class of afferents. On the basis of these estimates and the response pattern of the individual unit Bayes’ theorem was used to calculate the probabilities that the unit was a spindle primary, a spindle secondary, or a tendon organ afferent. Estimates indicate that about 19 out of 20 muscle afferents are correctly classified when all eight features are analyzed. / <p>Diss. (sammanfattning) Umeå : Umeå universitet, 1988, härtill 6 uppsatser.</p> / digitalisering@umu

Chemical intolerance (CI) is a term that refers to the surprisingly common phenomenon of persons getting ill from everyday chemicals. Although seemingly similar to asthma and allergies, CI sufferers do not react to exposures with increased histamine release. CI neither conforms to toxicological dose-response relationships as sufferers react to very low concentrations of chemicals assumed to be harmless. In addition, no particular chemical can be tied to any particular set of symptoms as in the case of other kinds of toxic injuries. The two overreaching goals of this thesis were to empirically investigate important hypotheses regarding CI, and to develop a theoretical framework that integrates previous theories of CI into a coherent whole.There are four empirical studies in this thesis. Utilizing event-related potentials (ERPs), magnitude estimations of perceived intensity, detection tests and functional magnetic resonance imaging (fMRI), the studies provided support for the following hypotheses: (1) persons with self-reported CI sensitize to olfactory and chemosomatosensory stimuli, whereas non-intolerant individuals habituate; (2) sensitization in CI is similar in terms of brain activation patterns to both non-clinical sensitization and other unexplained illnesses such as fibromyalgia; (3) persons with CI have an attention bias to chemical exposures, reflected by problems with withdrawing attention from such stimuli; (4) measures of peripheral hyperreactivity are correlated with chemosensory ERP measures; but failed to corroborate (5) the reactions of women resemble those found in persons with CI to a greater degree than the case in men.Three major theories of CI are also discussed. The neural sensitization theory describes CI as pathological and non-immunological increases in neural responsiveness. The conditioning theory describes CI as the result of basic associative learning mechanisms. The neurogenic inflammation theory describes CI as proliferation of sensory c-fibers and inflammatory responses carried to several parts of the body through axon reflexes and release of inflammatory mediators. The main point of the theoretical synthesis is that the theories offer different and complementary perspectives on CI, rather than presenting conflicting ontologies. With an integrated perspective, infected debates whether CI is a psychological or organic illness can hopefully be avoided.Finally, the unexplained characteristics of CI, the empirical findings and the theoretical accounts are described within the theoretical framework of signal detection theory. Several features of CI, e.g. sensitization and peripheral hyperreactivity, are described in terms of applying a low criterion (ß). / Kemisk intolerans, det vill säga att få symtom av vardagliga lukter, är ett förvånansvärt vanligt problem. Trots att åkomman i många avseenden liknar astma och allergi, reagerar de drabbade inte med exempelvis ökad histaminfrisättning. Kemisk intolerans överensstämmer inte heller med toxikologiska dos-responsförhållanden, eftersom de drabbade blir sjuka av väldigt låga koncentrationer av luktämnen. Enskilda kemikalier kan inte kopplas till en karaktäristisk symtombild, vilket är vanligt vid andra typer av toxikologiska skador. I denna avhandling har jag två mål. För det första undersöker jag viktiga hypoteser om kemisk intolerans. För det andra erbjuder jag ett teoretiskt ramverk där jag integrerar tidigare teorier om kemisk intolerans till en sammanhängande helhet.Den empiriska delen av avhandlingen består av fyra forskningsstudier. Baserat på händelserelaterade hjärnpotentialer (ERPs), magnitudestimationer av upplevd styrka, detektionstest samt funktionell magnetresonansavbildning (fMRI) stöder studierna följande hypoteser: (1) personer med självrapporterad kemisk intolerans sensitiserar till olfaktoriska och kemosomatosensoriska stimuli, medan icke-intoleranta individer habituerar; (2) med avseende på hjärnaktiveringsmönster liknar sensitisering hos kemiskt intoleranta det mönster man finner både i icke-klinisk sensitisering och i exempelvis fibromyalgi; (3) personer med kemisk intolerans har en benägenhet att uppmärksamma kemisk exponering, vilket reflekteras i en oförmåga att ignorera sådana stimuli; (4) mått på perifer hyperreaktivitet korrelerar med kemosensoriska ERP-mått. Hypotesen att (5) kvinnors reaktioner på kemosensoriska stimuli liknar de man kan finna hos de kemiskt intoleranta i större utsträckning än vad fallet är för män, stöds däremot inte.Tre teorier om kemisk intolerans diskuteras. Den neurala sensitiseringsteorin beskriver intoleransen som en patologisk ökning av neural aktivitet. Betingningsteorin beskriver kemisk intolerans som ett resultat av grundläggande associativa inlägningsmekanismer. Slutligen beskriver teorin om neurogen inflammation intoleransen som en förhöjd aktivering av c-fiberaktivitet och ökade inflammatoriska processer. Huvudargumentet i den teoretiska sammanfattningen är att dessa teorier erbjuder komplementära perspektiv på kemisk intolerans. Med ett integrerat perspektiv kan förhoppningsvis infekterade debatter om huruvida kemisk intolerans är en psykologisk eller organisk åkomma undvikas.De oförklarade egenskaperna av kemisk intolerans, de empiriska fynden, samt de teoretiska förklaringarna beskrivs slutligen inom ett teoretiskt ramverk som utgår från signaldetektionsteorin. Flera egenskaper hos kemisk intolerans beskrivs i termer av ett förändrat eller lågt satt kriterium (ß).

Les lymphomes diffus à grandes cellules B (DLBCL) sont la forme de lymphomes non–Hodgkiniens agressifs la plus fréquente chez l’adulte, et sont très hétérogènes à la fois sur le plan biologique et clinique. Bien que plus de la moitié des patients peuvent être guéris avec le traitement standard R-CHOP (combinant la polychimiothérapie CHOP aux anti-CD20 comme le rituximab) 30 à 40 % des patients échappent ou sont réfractaires au traitement, déterminant des morbidités et mortalités importantes liées au nombre limité d’alternatives thérapeutiques. L’objectif des travaux de cette thèse était centré sur les mécanismes de résistance thérapeutique dans ces lymphomes, et plus particulièrement les résistances au rituximab. Dans une première partie de la thèse, nous avons étudié le rôle de facteurs endogènes neuropeptidiques, les neurotrophines (NTs), et l’implication de leur signalisation dans la survie des cellules tumorales et leur sensibilité à l’apoptose induite par le rituximab. Nous avons montré dans un premier temps que les cellules B tumorales des patients présentaient des taux parfois élevés de neurotrophines (NGF, BDNF) et de leurs récepteurs de haute (Trk) et de basse affinité p75NTR. Puis les résultats obtenus in vitro sur des lignées cellulaires humaines de DLBCL et in vivo (xénogreffes tumorales) ont mis en évidence l’existence d’un axe de survie BDNF/TrkB/p75NTR pouvant interférer avec l’efficacité de l’immunothérapie. Cet axe contribue à la survie des cellules tumorales et pourrait aussi participer à la résistance thérapeutique aux anti-CD20 en modulant l’expression du CD20 à la surface des exosomes. En effet ces microvésicules, sécrétées en grande quantité par les cellules B tumorales, expriment le CD20 à leur surface et seraient à ce titre impliquées dans l’échappement thérapeutique en réalisant des « récepteurs –leurres » vis-à-vis des anticorps thérapeutiques. Dans une 2e partie de cette thèse, nous avons évalué dans les DLBCL le rôle potentiel de nouvelles cibles émergentes en oncologie, les prohibitines (PHBs) et le facteur d’initiation de la traduction eIF4A. Pour cela, nous avons utilisé un ligand de ces acteurs cellulaires de la famille des flavaglines, le FL3. Nous avons montré que le FL3 présente un effet apoptotique très important in vitro sur les lignées cellulaires de DLBCL et in vivo sur les tumeurs induites chez la souris. Nos travaux ont permis d’en préciser les mécanismes moléculaires, mettant en évidence le rôle des PHBs en lien notamment avec l’activation d’Erk1/2, et la formation et l’activité du complexe eIF4F dans la survie des cellules de DLBCL. Les données préliminaires obtenues à partir des biopsies de patients montrent, de plus, que la forte expression de PHB1 pourrait avoir une valeur pronostique dans ces lymphomes. L’ensemble de nos travaux ont permis de mettre en évidence de nouvelles voies de survie et d’échappement thérapeutique dans les DLBCL, qui pourraient permettre d’identifier aussi de nouveaux marqueurs biologiques à valeur diagnostique et/ou pronostique pour le choix de thérapies ciblées. / Diffuse large B cell Lymphomas (DLBCL) are the most aggressive and heterogeneous biological and clinical form of non-Hodgkin lymphomas in adults. Although more than 50% of patients can be cured with standard therapy R-CHOP (combining the CHOP chemotherapy to the anti-CD20 as rituximab) 30 to 40% of patients exhibit primary refractory disease or relapse after initial response to therapy, determining morbidities and significant mortality related to the limited number of treatment options. The aim of this thesis was focussed on therapeutic resistances of these lymphomas, notably those of rituximab. In the first part of this thesis, we have evaluated the role of endogenous factor signaling, the neurotrophins (NTs), in DLBCL cell survival and sensitivity to the cytotoxicity of rituximab. We showed first that a high expression of neurotrophines (NGF, BDNF) and their high (Trk) and low (p75NTR) affinity receptors was often found in tumor B cells of DLBCL patients. Results obtained in vitro, on human cell lines of DLBCL, but also in vivo (xenografts) showed evidence of a survival BDNF/TrkB/p75NTR axis that can interfere with the efficacy of immunotherapy. This axis promotes survival of tumor cells and may also participate in rituximab resistance in regulating CD20 expression at the surface of exosomes. Indeed, these microvesicles, secreted in large amounts by the tumoral B cells, express the CD20 and would be involved in the therapeutic escape acting as decoy receptors upon rituximab exposure. In the second part of the thesis, we evaluated in DLBCL the potential role of new oncogenic targets, PHBs proteins and the initiation factor of translation eIF4A. To this end, we used one of their ligands, a synthetic flavagline named FL3. We showed that FL3 determines a strong apoptosis in vitro on DLBCL cell lines and in vivo on tumors induced in mice (xenografts). Our works have clarified the molecular mechanisms, demonstrating involvement of PHBs, in correlation with ERK1/2 activation, and eIF4F complex formation and activity. Preliminary data obtained in patient biopsies showed a high expression of PHB1 in tumor B cells that may be decisive for cell survival and patient outcome lymphomas.Overall, present results show evidence of new survival and rituximab escape mechanisms in DLBCL, that should allow to identify new diagnostic and prognostic biomarkers for alternative therapeutic options.

Plantas medicinais e óleos essenciais representam um importante papel na terapêutica, tanto na cura como também na prevenção de diferentes enfermidades, sendo esta prática medicinal uma das mais antigas formas de tratamento. Devido à utilização dos óleos essenciais na terapêutica e a importância do conhecimento do pontencial de toxicidade destes, objetivou-se: (i) identificar os principais componentes químicos dos óleos essenciais de Origanum vulgare (orégano), Origanum majorana (manjerona) e Rosmarinus officinalis (alecrim); (ii) avaliar a atividade antifúngica in vitro destes óleos essenciais frente a leveduras isoladas de animais hígidos e casos clínicos; (iii) avaliar a irritação/corrosão cutânea e ocular aguda dos três óleos essenciais e (iv) avaliar a sensibilização cutânea do óleo essencial de orégano. O material vegetal foi adquirido de distribuidor comercial e encaminhado para extração do óleo essencial por hidrodestilação em Clevenger e, para análise cromatográfica através da cromatografia gasosa. Para realização dos testes in vitro foi utilizado o método de microdiluição em caldo, documento M27A3 do Clinical and Laboratory Standards Institute (CLSI) com adaptações para fitofármacos e Malassezia pachydermatis. Os óleos essenciais de orégano, manjerona e alecrim foram testados nas concentrações de 28 a 0,87mg/mL, 60 a 1,87mg/mL e 112,8 a 3,52mg/mL, respectivamente. Os testes de toxicidade in vivo foram realizados conforme a Organisation for Economic Co-operation and Development (OECD). Para os testes de irritação/corrosão cutânea (OECD 404, 2002) e ocular aguda (OECD 405, 2002) foram utilizados 24 coelhos albinos (Oryctolagus cuniculus), Nova Zelândia, machos, adultos e hígidos. Na sensibilização cutânea (OECD 406, 1992) utilizaram-se 33 cobaios (Cavia porcellus), fêmeas, adultas e hígidas. Os compostos majoritários do orégano foram timol, -terpineno e 4-terpineol; da manjerona timol, 4-terpineol e p-cimeno e; do alecrim α-pineno e 1,8 cineol. A Concentração Inibitória Mínima (CIM) e Concentração Fungicida Mínima (CFM) do óleo essencial de orégano para M. pachydermatis variaram de ≤0,87 a 7mg/mL. Para manjerona a CIM e a CFM foram de ≤1,87 a 30mg/mL e de ≤3,52 a 112,8mg/mL para o alecrim nos isolados de M. pachydermatis, Candida spp e T. asahii. Nas avaliações da irritação/corrosão cutânea do óleo essencial de orégano 3% somente um animal apresentou eritema leve nas 24h com regressão aos sete dias e, edema leve nas 72h com regressão aos sete dias. Na irritação/corrosão ocular, apenas um animal apresentou reação inflamatória nas avaliações de 24 e 48h, regredindo nas 72h. Na sensibilização cutânea, os animais responderam à indução, mas nenhum respondeu ao desafio. Nos animais tratados com óleo essencial de manjerona 6% nas 24, 48 e 72h apresentaram eritema leve, regredindo em até sete dias. Dois animais apresentaram edema leve nas 24 e 48h com remissão nas 72h e um animal permaneceu sem alterações Em dois animais do grupo alecrim 24% as lesões de eritema/escara regrediram em 21 dias. Quanto ao edema, as lesões foram consideradas reversíveis aos sete dias. Conclui-se que M. pachydermatis é sensível ao óleo essencial de orégano; que os óleos essenciais de manjerona e alecrim possuem atividade antifúngica in vitro frente a isolados de animais; o óleo essencial de orégano 3% causa irritação cutânea e ocular aguda leve e, não causa sensibilização cutânea na concentração testada. O óleo essencial de manjerona 6% causa irritação cutânea e ocular aguda leve e, o óleo essencial de alecrim 24% causa irritação cutânea e ocular aguda moderada. / Medicinal plants and essential oils represent an important therapeutic role in the cure and diseases different prevention both, this medical practice is one the oldest treatment forms. Thus, the aim was: (i) identify the main chemical components of essential oils from Origanum vulgare (oregano), Origanum majorana (marjoram) and Rosmarinus officinalis (rosemary), (ii) evaluate the in vitro antifungal activity of essential oils against yeasts isolated from healthy animals and clinical cases, (iii) evaluate the irritation/skin corrosion and acute eye of the three essential oils and (iv) assess the skin sensitization of the oregano essential oil. The plant material was purchased from commercial distributor and referred for essential oil extraction and gas chromatography. We used the method of microdilution M27-A3 with adaptations for phytochemicals and Malassezia pachydermatis. The oregano essential oils, marjoram and rosemary were tested at concentrations from 28 to 0.87 mg/mL, 60 to 1.87 mg/mL and 112.8 to 3.52 mg/mL, respectively. The in vivo toxicity tests were performed according to the Organization for Economic Co-operation and Development (OECD). The twenty-four males, adults and healthy rabbits (Oryctolagus cuniculus) were used for irritation/corrosion skin (OECD 404, 2002) and eye acute (OECD 405, 2002) tests. The thirty-three adults, females and healthy guinea pigs (Cavia porcellus) were used for sensitization skin test (OECD 406, 1992). The major compounds in oregano were thymol, α-terpinene and 4-terpineol, in marjoram were thymol, 4-terpineol, and p-cymene and in rosemary were α-pinene and 1,8 cineole. The Minimum Inhibitory Concentration (MIC) and Minimum Fungicidal Concentration (MFC) of the oregano essential oil against to M. pachydermatis were ≤ 0.87 to 7mg/mL, while the MIC and MFC of the marjoram were ≤ 1.87 to 30mg/mL. The MIC and CFM of the rosemary were ≤ 3.52 to 112.8 mg/mL against to M. pachydermatis, Candida spp and T. asahii. In the irritation/skin corrosion test, only one animal at 24h had slight erythema with regression at 7 days and slight edema at 72 h with regression to 7 days against to oregano essential oil at 3%. In the eye irritation/corrosion test, only one animal showed inflammatory reaction signs at 24 and 48h evaluates, but the assessments 72h had regressed. In the skin sensitization test, the animals responded, but anyone responded to the challenge. The treated with marjoram essential oils at 6%, the animals showed slight erythema at 24, 48 and 72h evaluate, with regression to 7 days. About to edema presentation, two animals showed moderate at 24 and 48h, with regression at 72h, only one animal without signs. The group rosemary at 24%, the erythema/eschar lesions in two animals were regression at 21 days. About the edema, the lesions were reversible for seven days. The conclusion was the sensibility of M. pachydermatis against to oregano essential oil, antifungal activity in vitro of marjoram and rosemary essential oils against animals isolates, the oregano essential oil at 3% induces skin and eye irritation slight acute and doesn’t induce skin sensitization. The marjoram essential oil at 6% induces skin and eye irritation slight acute, the rosemary essential oil at 24% induces skin and eye irritation moderate acute.