Search results for "substitut"

showing 10 items of 1337 documents

The photoperiod entrains the molecular clock of the rat pineal.

2005

The suprachiasmatic nucleus-pineal system acts as a neuroendocrine transducer of seasonal changes in the photoperiod by regulating melatonin formation. In the present study, we have investigated the extent to which the photoperiod entrains the nonself-cycling oscillator in the Sprague-Dawley rat pineal. For this purpose, the 24-h expression of nine clock genes (bmal1, clock, per1, per2, per3, cry1, cry2, dec1 and dec2) and the aa-nat gene was monitored under light-dark 8 : 16 and light-dark 16 : 8 in the rat pineal by using real-time RT-PCR. The 24-h pattern of the expression of only per1, dec2 and aa-nat genes was affected by photoperiod. In comparison with the short photoperiod, the durat…

Maleendocrine systemmedicine.medical_specialtyTime FactorsPhotoperiodCLOCK ProteinsClockworkBiologyPineal GlandRats Sprague-DawleyBiological ClocksInternal medicinemedicineAnimalsCircadian rhythmRNA MessengerphotoperiodismAnalysis of VarianceReverse Transcriptase Polymerase Chain ReactionGeneral NeuroscienceAdaptation PhysiologicalRatsPER2CLOCKDEC1PER3EndocrinologyGene Expression RegulationTrans-ActivatorsFemaleSuprachiasmatic Nucleussense organshormones hormone substitutes and hormone antagonistsPER1The European journal of neuroscience
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Influence of photoperiodic history on clock genes and the circadian pacemaker in the rat retina

2006

The influence of seasonal lighting conditions on expression of clock genes and the circadian pacemaker was investigated in the rat retina. For this purpose, the 24-h profiles of nine clock genes (bmal1, clock, per1, per2, per3, dec1, dec2, cry1 and cry 2) and the arylalkylamine N-acetyltransferase gene as an indicator of the circadian pacemaker output were compared between light-dark periods of 8 : 16 and 16 : 8 h. The photoperiod influenced the daily patterns of the amount of transcript for per1, per3, dec2 and arylalkylamine N-acetyltransferase. This indicates that photoperiodic information modulates clock gene expression in addition to the circadian pacemaker of the retina. Under constan…

Maleendocrine systemmedicine.medical_specialtyTime FactorsPhotoperiodGene ExpressionBiologyRetinaRats Sprague-DawleyInternal medicinemedicineAnimalsRNA MessengerEye ProteinsOscillating genephotoperiodismAnalysis of VarianceReverse Transcriptase Polymerase Chain ReactionGeneral NeuroscienceNuclear ProteinsCircadian RhythmRatsPER2CLOCKDEC1PER3EndocrinologyGene Expression RegulationArylalkylamineFemalesense organshormones hormone substitutes and hormone antagonistsPER1European Journal of Neuroscience
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The Effects of Chlorotrianisene (Tace) on Kinetics of 3H-testosterone Metabolism in Patients with Carcinoma of the Prostate

1982

Summary— Alterations in the metabolism of testosterone and plasma levels of testosterone, luteinising hormone (LH), follicle stimulating hormone (FSH), prolactin and oestradiol were studied in 6 patients with newly diagnosed prostatic carcinoma before and during treatment with chlorotrianisene at a daily dosage of 48 mg for 14 days. Parameters of plasma kinetics were determined according to the single injection technique and the 2-compartment model, and the plasma hormones by radioimmunoassay. Chlorotrianisene altered neither plasma levels of testosterone, gonadotrophins, prolactin and oestradiol, nor metabolic clearance rate, production rate and other kinetic parameters of testosterone. Th…

Maleendocrine systemmedicine.medical_specialtyUrologyFollicle-stimulating hormoneProstateInternal medicinemedicineCarcinomaHumansTestosteroneTestosteroneAgedEstradiolbusiness.industryProstatic NeoplasmsRadioimmunoassayLuteinizing HormoneMiddle Agedmedicine.diseaseProlactinProlactinKineticsEndocrinologymedicine.anatomical_structureChlorotrianiseneFollicle Stimulating Hormonebusinesshormones hormone substitutes and hormone antagonistsChlorotrianisenemedicine.drugHormoneBritish Journal of Urology
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The role of the hypothalamic paraventricular nuclei for the regulation of pineal melatonin synthesis: New aspects derived from the vasopressin-defici…

1990

Abstract There is evidence for an involvement of the hypothalamic paraventricular nuclei (PVN) in the regulation of pineal melatonin synthesis in rats. Since electrical stimulation of the PVN or the systemic administration of arginine-vasopressin (AVP) result in a depression of the nocturnal melatonin surge, this neuropeptide appears to be pivotal for the transduction of PVN-efferent, pinealopetal signals. We therefore used an AVP-deficient animal model, the Brattleboro rat, to further investigate the mechanisms responsible for pineal regulation. Anesthetized adult male animals received 2 min of bilateral electrical stimulation of the PVN either during the day or at night. Thirty min later,…

Maleendocrine systemmedicine.medical_specialtyVasopressinNeuropeptideStimulationBiologyPineal GlandRats Mutant StrainsMelatoninInternal medicinemedicineAnimalsCircadian rhythmMelatoninEpiphysis cerebriGeneral NeuroscienceRats Brattleborobiology.organism_classificationElectric StimulationBrattleboro ratCircadian RhythmRatsArginine VasopressinEndocrinologynervous systemHypothalamushormones hormone substitutes and hormone antagonistsParaventricular Hypothalamic Nucleusmedicine.drugNeuroscience Letters
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The role of arginine-vasopressin for pineal melatonin synthesis in the rat: involvement of vasopressinergic receptors.

1991

Abstract The endogenously synthesized nonapeptide arginine vasopressin (AVP) is thought to be involved in transduction of photic information to the pineal gland. The enhancement of circulating AVP leads to a suppression of the nocturnal melatonin surge the mechanisms of which are unknown so far. We therefore studied the effect of dDAVP, an AVP analog with antidiuretic but without vasopressor activity, on pineal melatonin synthesis in Sprague-Dawley and AVP-deficient Brattleboro rats. The nocturnal intra-arterial application of dDAVP mimicked the inhibitory effect of AVP on the activity of the rate-limiting enzyme for pineal melatonin synthesis, N-acetyltransferase (NAT), in both rat strains…

Maleendocrine systemmedicine.medical_specialtyVasopressinReceptors VasopressinArylamine N-AcetyltransferaseBlindnessPineal GlandMelatoninPineal glandInternal medicinemedicineAnimalsDeamino Arginine VasopressinCircadian rhythmReceptorMelatoninReceptors Angiotensinbiologyurogenital systemSuprachiasmatic nucleusGeneral NeuroscienceRats BrattleboroRats Inbred Strainsbiology.organism_classificationBrattleboro ratRatsArginine VasopressinEndocrinologymedicine.anatomical_structurenervous systemInjections Intra-Arterialhormones hormone substitutes and hormone antagonistsEndocrine glandmedicine.drugNeuroscience letters
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Comparative investigations on the actions of ACTH1-24, somatostatin, neurotensin, substance P and vasopressin on locus coeruleus neuronal activity in…

1987

A considerable number of neuropeptides have been localized immunohistochemically in the area of the locus coeruleus of the rat. The objective of this study was to assess the actions of some of these transmitter candidates on spontaneously active locus coeruleus neurons in vitro. The effects of bath-applied peptides on the discharge rate of individual locus coeruleus neurons were investigated. A midpontine slice preparation of the gerbil brain was used. Excitatory dose-dependent effects were found with four peptides with the following rank order of potency: Substance P, (Arg8)-vasopressin, neurotensin, ACTH1–24. Somatostatin hyperpolarized all neurons tested. Given the pronounced effects see…

Maleendocrine systemmedicine.medical_specialtyVasopressinVasopressinsNeuropeptideSubstance PIn Vitro TechniquesSubstance Pchemistry.chemical_compoundSlice preparationInternal medicinemedicinePremovement neuronal activityAnimalsNeurotensinPharmacologyNeuronsChemistryNeuropeptidesGeneral MedicineArginine VasopressinEndocrinologySomatostatinnervous systemLocus coeruleusCosyntropinLocus CoeruleusGerbillinaeSomatostatinhormones hormone substitutes and hormone antagonistsNeurotensinNaunyn-Schmiedeberg's archives of pharmacology
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The effects of sex hormones, prolactin, and chorionic gonadotropin on pineal electrical activity in guinea pigs.

1981

Microelectrophoretic application of sex hormones onto pineal cells in guinea pigs has shown different responses in pregnant females as compared to males. In pregnant females estrone caused excitation in 74% of the cells tested, while progesterone and testosterone, prolactin, and HCG were inhibitory in a majority of the cells tested, while progesterone and testosterone, prolactin, and HCG were inhibitory in a majority of the cells. In contrast, in males estrone caused excitation of only 19% but inhibition of 37%. A smaller percentage of cells was inhibited by progesterone, while the predominant response to testosterone was excitation. These results suggest that the pineal gland may be under …

Maleendocrine systemmedicine.medical_specialtymedicine.drug_classEstroneGuinea PigsEstroneBiologyInhibitory postsynaptic potentialChorionic GonadotropinPineal GlandCellular and Molecular Neurosciencechemistry.chemical_compoundPineal glandSex FactorsInternal medicinemedicineAnimalsTestosteroneCircadian rhythmTestosteroneProgesteroneCell BiologyGeneral MedicineProlactinProlactinEndocrinologymedicine.anatomical_structurechemistryFemaleGonadotropinhormones hormone substitutes and hormone antagonistsHormoneCellular and molecular neurobiology
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Testosterone metabolism in patients with advanced carcinoma of the prostate: a comparative in vivo study of the effects of oestrogen and antiprolacti…

1978

In the light of the high incidence of cardiovascular side effects with oestrogen therapy in patients with prostatic cancer, other medications altering androgen metabolism are under investigation. The influence of the anti-prolactin bromocriptine (CB154) on plasma kinetics of testosterone and on endogenous hormones was studied and compared with the effect of ethinyl oestradiol in 25 patients with prostatic carcinoma. Bromocriptine significantly suppressed both prolactin and testosterone, inhibited the transfer of androgen from the inner pool into the deep compartment and favoured its degradation. Ethinyl oestradiol decreased testosterone, LH and FSH, and prolonged the biological half-life of…

Maleendocrine systemmedicine.medical_specialtymedicine.drug_classUrologyProstateInternal medicinemedicineCarcinomaHumansTestosteroneTestosteroneBromocriptineDose-Response Relationship DrugEstradiolbusiness.industryCancerProstatic NeoplasmsLuteinizing HormoneAndrogenmedicine.diseaseProlactinBromocriptineProlactinmedicine.anatomical_structureEndocrinologyReceptors AndrogenFollicle Stimulating Hormonebusinesshormones hormone substitutes and hormone antagonistsmedicine.drugHormoneUrological research
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Evaluation of antidiuretic hormone before and after long-term treatment with desmopressin in a group of enuretic children

1998

Objective To determine the effect of long-term desmopressin therapy in enuretic patients on the levels of antidiuretic hormone (ADH) during and after the end of therapy. Patients and methods The study comprised 25 outpatients (18 boys and seven girls) aged 8–12 years at the start of therapy and 12–16 years at the end. The morning (08.00 hours) plasma ADH level was determined before treatment (T0) with desmopressin and 2 years after (T1) ending the therapy. Seven of the 25 patients evaluated had monosymptomatic (simple enuresis, SE) and 18 had other symptoms (complex enuresis, CE). Results In the patients with SE, the mean (SD) duration of therapy was 305 (183) days and they were re-evaluate…

Malemedicine.medical_specialtyAdolescentVasopressinsUrologyUrinary incontinenceRenal AgentsGastroenterologyCholinergic AntagonistsEnuresisInternal medicineHumansMedicineDeamino Arginine VasopressinChildOxybutyninDesmopressinMorningbusiness.industryEnuresisLong-Term CareEndocrinologyEl NiñoMandelic AcidsDrug Therapy CombinationFemalemedicine.symptombusinesshormones hormone substitutes and hormone antagonistsHormoneAntidiureticmedicine.drugBJU International
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Enuresis Subtypes Based on Nocturnal Hypercalciuria: A Multicenter Study

2003

Purpose: Desmopressin may not be effective for nocturnal enuresis associated with polyuria and hypercalciuria. Nighttime hypercalciuria in an enuretic population from 5 centers and its correlation with nighttime polyuria were verified. Materials and Methods: A total of 450 enuretic patients (278 males, 172 females, mean age 9.7 years) were evaluated with 72-hour micturition charts, urinalysis, serum creatinine and osmolarity, diurnal and nocturnal electrolytes with fractional Na+ and K+ urinary excretion, and nocturnal (4 a.m.) plasma vasopressin. Creatinine electrolytes and osmolarity were measured in daytime (8 a.m. to 8 p.m.) and nighttime (8 p.m. to 8 a.m.) urine volumes. Patients were …

Malemedicine.medical_specialtyAdolescentendocrine system diseasesUrinalysisVasopressinsUrologymedia_common.quotation_subjectPopulationUrinary incontinenceUrologyUrinary incontinenceurologic and male genital diseasesUrinationDiagnosis DifferentialElectrolytesAdrenocorticotropic HormonePolyuriaEnuresisElectrolyteInternal medicineEnuresimedicineHumansEnuresis; Polyuria; Urinary incontinence; Vasopressin; Adolescent; Adrenocorticotropic Hormone; Calcium; Child; Circadian Rhythm; Creatinine; Deamino Arginine Vasopressin; Diagnosis Differential; Electrolytes; Enuresis; Female; Humans; Male; Polyuria; Vasopressins; UrologyDeamino Arginine VasopressinHypercalciuriaChildDesmopressineducationmedia_commoneducation.field_of_studymedicine.diagnostic_testPolyuriabusiness.industryEnuresismedicine.diseasefemale genital diseases and pregnancy complicationsCircadian RhythmEndocrinologyCreatinineCalciumFemalemedicine.symptombusinessVasopressinhormones hormone substitutes and hormone antagonistsHumanmedicine.drugJournal of Urology
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