Search results for "pathogen"

showing 10 items of 1657 documents

Blood Brain Barrier Compromise with Endothelial Inflammation may Lead to Autoimmune Loss of Myelin during Multiple Sclerosis

2009

Multiple sclerosis is an autoimmune disease characterized by multifocal areas of inflammation and demyelination within the central nervous system. The mechanism that triggers the disease remains elusive. However, recent findings may indicate that multiple sclerosis, at its source, could be a hemodynamic disorder. It has been found that multiple sclerosis patients exhibit significant stenoses in extracranial veins draining the central nervous system (in azygous and internal jugular veins), which are associated with significant pressure gradients measured across strictures. Such anatomic venous abnormalities were not found in the control group of healthy subjects. In this review, it is hypoth…

Pathologymedicine.medical_specialtyCentral nervous systemInflammationBlood–brain barriermultiple sclerosisProinflammatory cytokinePathogenesisCellular and Molecular NeuroscienceMyelinDevelopmental Neurosciencevenous insufficiencyMedicineAnimalsHumansEndotheliumMyelin SheathAutoimmune diseaseInflammationbusiness.industryMultiple sclerosisblood-brain barriermedicine.diseasemedicine.anatomical_structureNeurologyImmunologymedicine.symptombusinessAdhesion moleculesCurrent Neurovascular Research
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Chronic cerebrospinal venous insufficiency is unlikely to be a direct trigger of multiple sclerosis

2013

Abstract Background Chronic cerebrospinal venous insufficiency, a vascular pathology affecting the veins draining the central nervous system can accompany multiple sclerosis and is suspected to be involved in its pathogenesis. Objective This study was aimed at exploring a potential role for chronic cerebrospinal venous insufficiency in triggering multiple sclerosis. If it were venous abnormalities responsible for neurological pathology, one should expect negative correlation, i.e. more severe vascular lesions in the patients with early onset of multiple sclerosis. Methods Localization and degree of venous blockages in 350 multiple sclerosis patients were assessed using catheter venography. …

Pathologymedicine.medical_specialtyCentral nervous systemVenographyDiseaseAzygous veinPathogenesisMultiple sclerosisVenous malformationInternal medicinemedicinePathologicalJugular veinsmedicine.diagnostic_testbusiness.industryMultiple sclerosisGeneral MedicinePhlebographymedicine.diseaseVenous insufficiencyChronic cerebrospinal venous insufficiencymedicine.anatomical_structureNeurologyCardiologyNeurology (clinical)businessVenous malformationMultiple Sclerosis and Related Disorders
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Contrasting responses of Kupffer cells and inflammatory mononuclear phagocytes to biliary obstruction in a mouse model of cholestatic liver injury.

2012

Background Biliary obstruction and cholestasis are serious complications of many liver diseases. Although resident hepatic macrophages (Kupffer cells) are frequently implicated in disease progression, most studies fail to differentiate the contribution of Kupffer cells and inflammatory mononuclear phagocytes (iMNPs) that infiltrate the liver subsequent to obstruction. Aim This study was undertaken to examine the roles and potential interactions of these two disparate mononuclear phagocyte populations in hepatic injury attending cholestasis. Methods Female, C57Bl/6 mice were injected with magnetic beads on day 3 prior to sham operation or bile duct ligation (BDL) to facilitate subsequent Kup…

Pathologymedicine.medical_specialtyChemokineLiver cytologyKupffer Cellsmedicine.medical_treatmentInflammationCholestasis IntrahepaticBiologyReal-Time Polymerase Chain Reactiondigestive systemMiceCholestasismedicineAnimalsMononuclear Phagocyte SystemLiver injuryHepatologyKupffer cellMononuclear phagocyte systemmedicine.diseaseFlow CytometrySpecific Pathogen-Free OrganismsMice Inbred C57BLmedicine.anatomical_structureCytokineImmunologybiology.proteinFemalemedicine.symptomLiver international : official journal of the International Association for the Study of the Liver
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Assessment of Tumor Development and Wound Healing Using Endoscopic Techniques in Mice

2010

Mouse models of intestinal inflammation and colon cancer are valuable tools to gain insights into the pathogenesis of the corresponding human diseases. Recently, in vivo mouse endoscopy has been developed, allowing not only the high-resolution monitoring and scoring of experimental disease development, but also enables the investigator to perform manipulations, including local injection of reagents or the taking of biopsies for molecular and histopathologic analyses. Chromoendoscopic staining with methylene blue enables visualization of the crypt structure and allows discrimination between inflammatory and neoplastic changes. The development of endoscopic techniques in live mice opened new …

Pathologymedicine.medical_specialtyColorectal cancerBiopsyDiseasePathogenesisMiceMicromanipulation03 medical and health sciences0302 clinical medicineIn vivoIntestinal inflammationmedicineAnimalsHumans030304 developmental biologyWound Healing0303 health sciencesMiniaturizationHepatologymedicine.diagnostic_testbusiness.industryDisease mechanismsGastroenterologyEndoscopyColitismedicine.disease3. Good healthEndoscopyEndoscopes GastrointestinalDisease Models AnimalColonic Neoplasms030211 gastroenterology & hepatologybusinessWound healingGastroenterology
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Solitary polypoid laryngeal xanthoma.

2013

We report the case of a 51-year-old male smoker with diabetes mellitus and hyperlipidaemia and a long history of human immunodeficiency virus (HIV)/hepatitis C virus (HCV) infection treated with various antiretroviral regimes, who was referred to the otolaryngology department with progressive dysphonia. Fibre-optic laryngoscopy showed a solitary, yellowish-white pedunculated polyp on the anterior third of the left cord, with no other abnormality. Pathological analysis revealed a polypoid laryngeal xanthoma that was immunoreactive against CD68, perilipin, and adipophilin. This unusual laryngeal lesion in the clinical context of our patient suggests a possible role of antiretroviral treatment…

Pathologymedicine.medical_specialtyCordmedicine.diagnostic_testbusiness.industryHepatitis C virusLaryngoscopyContext (language use)Case ReportGeneral MedicineXanthomamedicine.diseasemedicine.disease_causelcsh:Otorhinolaryngologylcsh:RF1-547PathogenesisDiabetes mellitusMedicinebusinessPathologicalCase reports in otolaryngology
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From clinical description, to in vitro and animal studies, and backward to patients: Oxidative stress and mitochondrial dysfunction in Fanconi anemia

2013

Fanconi anemia (FA) is a rare genetic disease associated with deficiencies in DNA repair pathways. A body of literature points to a pro-oxidant state in FA patients, along with evidence for oxidative stress (OS) in the FA phenotype reported by in vitro, molecular, and animal studies. A highlight arises from the detection of mitochondrial dysfunction (MDF) in FA cell lines of complementation groups A, C, D2, and G. As yet lacking, in vivo studies should focus on FA-associated MDF, which may help in the understanding of the mitochondrial basis of OS detected in cells and body fluids from FA patients. Beyond the in vitro and animal databases, the available analytical devices may prompt the dir…

Pathologymedicine.medical_specialtyDNA RepairFree RadicalsDNA repairmitochondrial nutrientsCell Cycle ProteinsFree radicalsDiseaseBiologymedicine.disease_causeBioinformaticsBiochemistryChemopreventionPathogenesis03 medical and health sciencesMice0302 clinical medicineIn vivoFanconi anemiaPhysiology (medical)medicineAnimalsHumans030304 developmental biology0303 health sciencesMitochondrial nutrientNuclear ProteinsFanconi anemia Mitochondrial dysfunction Mitochondrial nutrients Chemoprevention Free radicalsmedicine.diseasePhenotype3. Good healthMitochondriaOxidative StressFanconi Anemia030220 oncology & carcinogenesisFanconi anemiaAnimal studiesReactive Oxygen SpeciesMitochondrial dysfunctionOxidative stress
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Altered elemental profile as indicator of homeostatic imbalance in pathogenesis of oral submucous fibrosis

2002

Oral submucous fibrosis (OSF) is a potential precancerous condition of the oral cavity and oropharynx. The etiopathogenesis of this complex precancerous condition is still obscure. In addition to deleterious oral habits, malnutrition, and possible genetic predisposition, altered bioelemental status is also likely to play an important role in its pathogenesis. The present study analyzed 68 elements by inductively coupled plasma-mass spectroscopy in oral mucosa of normal and OSF individuals and some interesting alterations in elemental profile in the diseased tissue have been noted, indicating a homeostatic imbalance. These bioelemental alterations leading to homeostatic imbalance might be co…

Pathologymedicine.medical_specialtyEndocrinology Diabetes and MetabolismClinical BiochemistryPhysiologyOral Submucous FibrosisBiologyOral cavityBiochemistryMass SpectrometryInorganic ChemistryPathogenesismedicineGenetic predispositionHomeostasisHumansOral mucosaBiochemistry (medical)Oral habitsGeneral Medicinemedicine.diseaseTrace ElementsPrecancerous conditionstomatognathic diseasesmedicine.anatomical_structureOral submucous fibrosisHomeostasis
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Aggregated neutrophil extracellular traps occlude Meibomian glands during ocular surface inflammation

2021

Abstract Purpose Obstructive Meibomian gland dysfunction (MGD) is one of the leading causes of evaporative dry eye disease. Meibomian glands at the eyelid secrete lipids that prevent evaporation of the aqueous tear film. The pathogenesis of obstructive MGD is incompletely understood to date. Herein, we aim to investigate the pathogenesis of obstructive MGD using murine and human samples with various forms of ocular surface inflammation. Method The presence of Neutrophil extracellular Traps (NETs) was detected with immunofluorescence analysis of ocular surface discharge and biopsy samples from patients with blepharitis. Tear fluid from patients with MGD and blepharitis were evaluated for the…

Pathologymedicine.medical_specialtyEye diseaseMeibomian glandInflammationExtracellular TrapsPathogenesis03 medical and health sciencesMice0302 clinical medicineBiopsymedicineAnimalsHumansBlepharitis030304 developmental biologyInflammation0303 health sciencesmedicine.diagnostic_testbusiness.industryMeibomian GlandsNeutrophil extracellular trapsmedicine.diseaseeye diseases3. Good healthOphthalmologymedicine.anatomical_structureTears030221 ophthalmology & optometryEyelid DiseasesDry Eye Syndromessense organsEyelidmedicine.symptombusinessThe Ocular Surface
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Usefulness of DNA quantification in diagnosis of hypertrophic cardiomyopathies

2006

Hypertrophic cardiomyopathies (HCM) are a frequent cause of sudden death in both young people and adults. Different cardiomyopathies can be distinguished according to the etiological agent and, although there are morphological differences too, alterations in the quantity of DNA in the cardiomyocytes may play an important role in their pathogenesis and evolution. To understand the characteristics and the behaviour of the DNA index in hypertrophic cardiomyopathies, we have studied thirty cases (10 primaries or essential, 10 hypertensives and 10 toxic) and compared the results with those obtained for 10 macroscopically normal hearts. The results showed that the different cardiomyopathies were …

Pathologymedicine.medical_specialtyHeart diseasebusiness.industryHypertrophic cardiomyopathyCardiomyopathymedicine.diseaseSudden deathPathology and Forensic MedicineMuscle hypertrophyPathogenesismedicine.anatomical_structureVentriclemedicineDifferential diagnosisbusinessLawForensic Science International
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Evidence for developmental precursor lesions in epilepsy-associated glioneuronal tumors

1999

The etiology and pathogenesis of epilepsy-associated local lesions remain largely unknown. Histopathologically, the most frequent lesions comprise gangliogliomas and glioneuronal malformations, i.e., hamartias or hamartomas, with a preferred location in the temporal lobe of young patients. A characteristic histopathological admixture of glial and neuronal elements, the focal appearance and the benign clinical behaviour suggest a malformative nature. So far, no molecular genetic alterations specifically involved in the pathogenesis of these glioneuronal lesions have been identified. However, immunohistochemical analysis revealed distinct distribution patterns of oncofetal antigens. The embry…

Pathologymedicine.medical_specialtyHistologyBiologymedicine.diseaseStem cell markerGangliogliomaTemporal lobePathogenesisMedical Laboratory TechnologyEpilepsymedicineHamartomaImmunohistochemistryNeural cell adhesion moleculeAnatomyInstrumentationMicroscopy Research and Technique
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