Search results for "TUBULE"

showing 10 items of 308 documents

Androglobin, a chimeric mammalian globin, is required for male fertility

2022

AbstractSpermatogenesis is a highly specialised process, involving multiple dedicated pathways and regulatory check-points. Defects ultimately lead to male sub-fertility or sterility, and numerous aspects of mammalian sperm formation remain unknown. The predominant expression of the latest globin family member, androglobin (Adgb) in mammalian testis tissue prompted us to assess its physiological function in spermatogenesis. Adgb knockout mice display male infertility, reduced testis weight, impaired maturation of elongating spermatids, abnormal sperm shape and ultrastructural defects in microtubule and mitochondrial organisation. Epididymal sperm from Adgb knockout animals display multiple …

Malecalmodulin610 Medicine & healthGenetics and Molecular BiologyFlagellumBiologySeptinMale infertility10052 Institute of PhysiologyMicedevelopmental biologySemenMicrotubuleTestiscell biologymedicineAnimalsGlobinhemeSperm annulusBiologyInfertility Malemouse[SDV.BDD.GAM]Life Sciences [q-bio]/Development Biology/GametogenesisMammalsMice Knockout[SDV.BDD.GAM] Life Sciences [q-bio]/Development Biology/GametogenesisGeneral Immunology and MicrobiologyGeneral NeuroscienceglobinGeneral Medicinemedicine.diseaseSpermatidsSpermatozoaSpermspermatogenesisGlobinsCell biologyFertilitySperm TailGeneral Biochemistry570 Life sciences; biologyHuman medicineinfertilityoxygenSpermatogenesis
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Ultrastructural changes of the intercellular relationship in impaired human spermatogenesis

1980

In seven hypo- or aspermic patients, electron microscopic investigations of the intercellular connections of the seminiferous tubule were performed. The analysis of cell junctions of Sertoli cells and germ cells revealed irregularities of the Sertoli-cell junctions, hypoplasias of occluding junctions, hypo- and hyperplasias of the Sertoli-spermatid cell junctions and abnormal formation of Sertoli cell junctions with early spermatids, spermatocytes, and spermatogonia. Gap junction-like cell membrane specializations were very rare. Intercellular cytoplasmic bridges of germ cells were always present together with these cells. One hypoplastic bridge connecting two spermatogonia was found. The r…

Maleendocrine systemBiologyCell junctionCell membraneGeneticsmedicineHumansSpermatogenesisCytoskeletonInfertility MaleGenetics (clinical)Blood–testis barrierSertoli CellsTight junctionurogenital systemDesmosomesSeminiferous TubulesSertoli cellSpermatidsSpermatozoaCell biologyMicroscopy ElectronIntercellular Junctionsmedicine.anatomical_structureSeminiferous tubuleSpermatogenesisGerm cellHuman Genetics
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Short-term ischemia usually used for ischemic preconditioning causes loss of dendritic integrity after long-term survival in the gerbil hippocampus

2006

Ischemic preconditioning has been established as a powerful experimental neuroprotective strategy, both after global and focal cerebral ischemia. Little is known, however, about the structural and functional long-term outcome. Therefore, our present study was designed to check for potential subtle alterations in the hippocampus after long-term survival. Gerbils were subjected either to short-term ischemia of 2.5 min duration usually used for ischemic preconditioning (n=8) or to sham operation (n=6) and allowed to survive for 6 weeks. Hippocampi with neuronal densities comparable to those of sham-operated control animals were analyzed for dendritic marker proteins MAP2, MAP1B and synaptopodi…

Malemedicine.medical_specialtyIschemiaCell CountHippocampal formationBiologyGerbilHippocampusNeuroprotectionInternal medicinemedicineAnimalsHippocampus (mythology)Ischemic PreconditioningMolecular BiologyNeurologic ExaminationGeneral NeuroscienceMicrofilament ProteinsLong-term potentiationDendritesmedicine.diseaseImmunohistochemistryEndocrinologynervous systemIschemic Attack TransientIschemic preconditioningSynaptopodinNeurology (clinical)GerbillinaeMicrotubule-Associated ProteinsNeuroscienceDevelopmental BiologyBrain Research
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Pigment variant of neuronal ceroid-lipofuscinosis

1995

A 6-year-old girl had progressive ataxia, and visual disturbances resulting in blindness. She died in her sleep at age 22 years. She shared with her sister and paternal relatives bilateral pes cavus deformities and impaired deep-tendon reflexes which suggested Charcot-Marie-Tooth disease. Her sister, who also had both polyneuropathy and a progressive central nervous system (CNS) disease, did not have pigmentary retinopathy. At autopsy, the patient was found to have neuronal ceroid-lipofuscinosis (NCL) marked by intraneuronal accumulation of autofluorescent granular lipopigments in ballooned perikarya and conspicuous extraneuronal pigmentation of subcortical grey matter, but without axonal s…

Malemedicine.medical_specialtyPathologyPostmortem studiesNeurologyCentral nervous systemAutopsyBiologyGrey matterEpitheliumNuclear FamilyDiagnosis DifferentialCharcot-Marie-Tooth DiseaseNeuronal Ceroid-LipofuscinosesmedicineNeuropilHumansChildGenetics (clinical)Cerebral CortexNeuronsPigmentationPigments BiologicalAnatomymedicine.diseaseMicroscopy ElectronKidney Tubulesmedicine.anatomical_structureSpinal CordFemaleNeuronal ceroid lipofuscinosisPolyneuropathyAmerican Journal of Medical Genetics
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D-Glucose and fluid reabsorption in proximal surface tubule of the rat kidney

1972

Hexose reabsorption in the kidney was investigated by microperfusion of proximal cortical rat nephrons with Ringer's solution containingD-glucose (2.5, 5.0 and 18.0 mM/l), 3-O-methylD-glucose (4.5 mM/l) orD-fructose (18.0 mM/l) at perfusion rates of 20 or 40×10−6 ml/min. Inulin was used as a reference for fluid reabsorption. 1. The fraction of fluid reabsorbed was independent of the glucose concentration but it decreased when the perfusion rate increased from 20–40×10−6 ml/min. 2. At 18.0 mM/l the % glucose reabsorption was equal to the % fluid reabsorption. This equality was independent of the perfusion rate, (20 or 40×10−6 ml/min), indicating 1:1 coupling with net isotonic fluid reabsorpt…

Malemedicine.medical_specialtyPhysiologyClinical BiochemistryInulinBiological Transport ActiveFructoseAbsorptionchemistry.chemical_compoundD-GlucosePhysiology (medical)Internal medicinemedicineAnimalsHexosechemistry.chemical_classificationKidneyReabsorptionInulinWaterRatsRenal glucose reabsorptionGlucoseKidney TubulesEndocrinologymedicine.anatomical_structureTubulechemistryPerfusionPflügers Archiv European Journal of Physiology
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Time course of development of transtubular sodium concentration differences in proximal surface tubules of the rat kidney. Micropuncture experiments …

1969

Int the proximal and distal surface tubules isotonic Na reabsorption (Φ Naout) is impaired by adrenalectomy. In the present experiments the time course of development of transtubular Na concentration differences (Na)P−(Na)TF was studied in the proximal convolution. 1. Na concentration was measured in free flow mannitol diuresis. Endproximal (Na)P−(Na)TF averaged 23.0±0.5 meq/l after 8.5±0.6 sec (controls) and 15.2±1.7 meq/l after 13.6±0.5 sec (adrenalectomized rats). 2. In modified stopped flow experiments tubular fluid, aspirated at the beginning of the proximal convolution in mannitol diuresis, was injected between two oil columnes and reaspirated after 28–36 sec of contact time. (Na)P−(N…

Malemedicine.medical_specialtyPhysiologymedicine.medical_treatmentPotassiumSodiumClinical BiochemistryTubular fluidDiuresischemistry.chemical_elementPuncturesKidneyPermeabilityTimeKidney Concentrating AbilityPhysiology (medical)Internal medicineAdrenal GlandsmedicineAnimalsRenal sodium reabsorptionChemistryReabsorptionAdrenalectomySodiumInulinAdrenalectomyRatsEndocrinologyKidney TubulesPotassiumMannitolmedicine.drugGlomerular Filtration RatePflugers Archiv : European journal of physiology
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Different postischemic protein expression of the GABA_{A} receptor α2 subunit and the plasticity-associated protein MAP1B after treatment with BDNF v…

2009

Purpose Recent data indicate that both brain-derived neurotrophic factor (BDNF) and granulocyte-colony stimulating factor (G-CSF) exert substantial neuroregenerative effects and improve functional outcome after ischemic stroke. In the present study, we checked for potential differences in the postischemic modulation of various excitatory and inhibitory neurotransmitter receptors as well as various marker molecules for structural plasticity by BDNF versus G-CSF. Methods Adult male Wistar rats were subjected to photothrombotic ischemia and subsequently treated with NaCl, BDNF or G-CSF, respectively. After 6 weeks, postischemic protein expression of the NR1, GluR1 and alpha2 subunit of the NMD…

Malemedicine.medical_specialtyProtein subunitSynaptophysinHippocampusAMPA receptorFunctional LateralityRandom AllocationDevelopmental NeuroscienceNeurotrophic factorsInternal medicineGranulocyte Colony-Stimulating FactormedicineAnimalsRats WistarReceptorAnalysis of VariancebiologyChemistryGABAA receptorBrain-Derived Neurotrophic FactorBrainReceptors GABA-ARatsStrokeDisease Models AnimalEndocrinologyGene Expression Regulationnervous systemNeurologySynaptophysinbiology.proteinNMDA receptorNeurology (clinical)Intracranial ThrombosisMicrotubule-Associated ProteinsRestorative Neurology and Neuroscience
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A comparison of the effects of bilateral efferent duct ligation and of partial epididymectomy on the testes of rats.

1990

Testis weight as a percentage of body weight did not change following bilateral ligation of the efferent ducts (EDL) close to the epididymis, whereas following removal of part of the epididymis between the site of ligation and a point close to the junction between the caput and corpus (PCE), testis weight first rose linearly until Day 4 and then showed an exponential decrease between Days 4 and 28. After EDL, the perimeter of the seminiferous tubules rose for the first 7 days and then remained elevated, whereas after PCE, there was a linear decrease between Days 4 and 28. Following EDL, the percentage of altered and degenerated tubular cross-sections rose to about 30% and 10%, respectively,…

Malemedicine.medical_specialtyReproductive technologyBiologyEndocrinologyInternal medicineLactationTestisGeneticsmedicineEndocrine systemAnimalsMolecular BiologyLigationEpididymisBody WeightEfferent ductsRats Inbred StrainsOrgan SizeSeminiferous TubulesEpididymisRatsEndocrinologymedicine.anatomical_structureReproductive MedicineAnimal Science and ZoologyFolliculogenesisLigationSpermatogenesisDevelopmental BiologyBiotechnologyReproduction, fertility, and development
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Transient oligemia is associated with long-term changes in binding densities of cortical inhibitory GABAA receptors in the rat brain

2009

Recently, we could demonstrate in rats that a short transient oligemic period of only 20-minute duration, induced by systemic hypotension, resulted in a transient decline of spatial memory capacities without any histological damage over a subsequent period of 6 months. In our present study, we checked for more subtle alterations within the highly vulnerable hippocampal CA1 subfield using quantification of neuronal cell density and semi-quantitative analysis of the ischemia-sensitive protein MAP2. Since hippocampal excitatory and inhibitory neurotransmitter receptors are crucially involved in spatial memory processes, quantitative in vitro receptor autoradiography was performed using [(3)H]M…

Malemedicine.medical_specialtyTime FactorsDown-RegulationAMPA receptorHippocampal formationTritiumInhibitory postsynaptic potentialBinding CompetitiveHippocampusReceptors N-Methyl-D-AspartateTimeRadioligand Assaychemistry.chemical_compoundParietal LobeInternal medicinemedicineAnimalsReceptors AMPARats WistarReceptorGABA AgonistsMolecular Biologygamma-Aminobutyric AcidCerebral CortexMemory DisordersMuscimolChemistryGABAA receptorGeneral NeuroscienceReceptors GABA-ARatsDisease Models AnimalEndocrinologynervous systemMuscimolHypoxia-Ischemia BrainExcitatory postsynaptic potentialNMDA receptorNeurology (clinical)Microtubule-Associated ProteinsDevelopmental BiologyBrain Research
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Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations

2004

Contains fulltext : 48815.pdf (Publisher’s version ) (Closed access) Opitz syndrome (OS; MIM 145410 and MIM 300000) is a congenital midline malformation syndrome characterized by hypertelorism, hypospadias, cleft lip/palate, laryngotracheoesophageal (LTE) abnormalities, imperforate anus, developmental delay, and cardiac defects. The X-linked form (XLOS) is caused by mutations in the MID1 gene, which encodes a microtubule-associated RBCC protein. In this study, phenotypic manifestations of patients with and without MID1 mutations were compared to determine genotype-phenotype correlations. We detected 10 novel mutations, 5 in familial cases, 2 in sporadic cases, and 3 in families for whom it …

Malemedicine.medical_specialtyUbiquitin-Protein LigasesBiologymedicine.disease_causeGastroenterologyG/BBB SYNDROMEFAMILIESGenomic disorders and inherited multi-system disorders [IGMD 3]Genotype-phenotype distinctionInternal medicineGeneticsmedicineHumansHypertelorismGeneGenetics (clinical)GeneticsFamily HealthX-linked Opitz syndromeMutationMID1Nuclear ProteinsGenetic Diseases X-LinkedExonsOpitz G/BBB Syndromemedicine.diseasePhenotypeGENEPedigreeSmith-Lemli-Opitz SyndromePhenotypeGenetic defects of metabolism [UMCN 5.1]HypospadiasMutationMicrotubule ProteinsFemalephenotypic variabilityXP22medicine.symptomImperforate anusFunctional Neurogenomics [DCN 2]BBBTranscription FactorsAmerican Journal of Medical Genetics. Part A
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