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  • 1
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract: A single human tyrosine hydroxylase (HTH) gene has been shown previously to generate four species of mRNA by alternative splicing. The four different HTH mRNAs were independently synthesized in vitro, using the SP6 transcription system. Each of these mRNA species was able to direct the synthesis of an active form of TH following injection into Xenopus oocytes. Quantitation of synthesized HTH polypeptides allowed the determination of the relative specific activity of each individual HTH form. A significant difference in specific activity was found between each form, suggesting that alternative splicing may play a role in regulating HTH activity in vivo.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract: To test for the relative contributions of the dopaminergicand serotoninergic systems in the striatum to the effects ofd-fenfluramine, an indirect serotonin receptor agonist, we assessedthe expression of Fos/Jun proteins induced by d-fenfluramine givenalone or in the presence of dopaminergic or serotoninergic agents. Todetermine the neuronal targets of d-fenfluramine in the striatum, weidentified the phenotypes of striatal neurons in which d-fenfluramineinduced Fos expression. Our results demonstrated that d-fenfluramineevokes nuclear expression of Fos/Jun B proteins in the striatum, and that theFos expression was dose-dependent and accompanied by transient induction ofc-fos mRNA. Fos expression was blocked byp-chloroamphetamine, a serotoninergic neurotoxin. Pretreatment withSCH 23390, a D1-dopamine receptor antagonist, led to a markeddecrease in Fos/Jun B expression in the caudoputamen, but not in the cortex,whereas pretreatment with methiothepin, a nonselective serotonin5-HT1 receptor antagonist, blocked Fos expression completely in thecortex and only partially in the caudoputamen. The expression of Fos/Jun B inthe striatum occurred mainly in dynorphin-containing neurons and in asubpopulation of striatal interneurons that exhibited NADPH-diaphoraseactivity. Most of the enkephalin-containing neurons of the striatum did notshow Fos/Jun B staining. These results suggest that the mechanism by whichd-fenfluramine induces c-fos and jun B expression in the rat caudoputamen depends at least in part on activation of the dopaminergic system by serotonin.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    FEBS Letters 205 (1986), S. 6-10 
    ISSN: 0014-5793
    Keywords: (Xenopus laevis) ; SP6 polymerase ; Translation ; Tyrosine hydroxylase
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-1106
    Keywords: In vivo receptor study ; Benzodiazepine receptors, CL 218,872 ; Epilepsy ; Positron emission tomography ; Baboon Papio papio
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In vivo benzodiazepine receptor occupancy by increasing doses of CL 218,872 has been evaluated in the baboon Papio papio, using (11C) RO 15-1788 as specific radioligand and positron emission tomography as external detection system. Although BZR heterogeneity has been previously demonstrated in the brain of the living baboon using PET, we did not observe in our studies that CL 218,872 interacts preferentially with one of the BZR subtypes. The monophasic pattern of the dose dependent CL 218,872 displacement curve and the corresponding “in vivo Hill coefficient” near unity suggest that CL 218,872 binds in cerebral baboon cortex with a similar affinity with BZ1 as well as BZ2 subtypes. The anticon-vulsant properties of CL 218,872 against bicuculline and allylglycine-induced seizures were correlated with benzodiazepine receptor occupancy by assessment of electroencephalographic activity during positron emission tomography studies. Our data confirmed in vivo the hypothesis of a partial agonist anticonvulsant activity of CL 218,872. At the same time, the use of a GABAantagonist (bicuculline) or an inhibitor of the GABA synthesis (allylglycine) suggested the existence of an allosteric interaction between benzodiazepine receptors and GABA receptors.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-1106
    Keywords: Noradrenergic hyperactivity ; NE ; ACh ; Fornix section ; DSP4 ; Spatial memory ; Alzheimer's disease ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Rats with unilateral or bilateral partial section of the fornix were impaired on an eight arm radial maze task. Neurochemical analysis of hippocampal tissue four weeks after the lesions revealed a 50% reduction of choline acetyltransferase (ChAT) activity. The cholinergic marker was correlated negatively with the number of errors in the maze; the lower the ChAT activity, the higher the error score. The fornix lesion also induced a 50% reduction in norepinephrine (NE), but no change in the noradrenergic metabolite methylhydroxyphenylglycol (MHPG), suggesting a net increase in turnover of NE in these animals. Additional lesion of the noradrenergic system with the neurotoxin DSP4 reduced both MHPG and NE levels by more than 90%, compared to nonlesioned controls, and reversed the behavioral deficit. This treatment had no further effect on cholinergic markers. There was a significant negative correlation between ChAT activity and the index of NE turnover, suggesting that hyperactivity in the noradrenergic system after fornix section inhibits the spared cholinergic function and thus exacerbates the cognitive deficit. The pattern of neurochemical results bear a striking resemblance to those seen in some Alzheimer's patients and suggest that an equilibrium among neurotransmitters is important to cognitive function.
    Type of Medium: Electronic Resource
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