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  1. Article ; Online: Improved synthesis of [18F] fallypride and characterization of a Huntington’s disease mouse model, zQ175DN KI, using longitudinal PET imaging of D2/D3 receptors

    Tuulia Huhtala / Pekka Poutiainen / Jussi Rytkönen / Kimmo Lehtimäki / Teija Parkkari / Iiris Kasanen / Anu J. Airaksinen / Teija Koivula / Patrick Sweeney / Outi Kontkanen / John Wityak / Celia Dominiquez / Larry C. Park

    EJNMMI Radiopharmacy and Chemistry, Vol 4, Iss 1, Pp 1-

    2019  Volume 10

    Abstract: Abstract Purpose Dopamine receptors are involved in pathophysiology of neuropsychiatric diseases, including Huntington’s disease (HD). PET imaging of dopamine D2 receptors (D2R) in HD patients has demonstrated 40% decrease in D2R binding in striatum, and ...

    Abstract Abstract Purpose Dopamine receptors are involved in pathophysiology of neuropsychiatric diseases, including Huntington’s disease (HD). PET imaging of dopamine D2 receptors (D2R) in HD patients has demonstrated 40% decrease in D2R binding in striatum, and D2R could be a reliable quantitative target to monitor disease progression. A D2/3R antagonist, [18F] fallypride, is a high-affinity radioligand that has been clinically used to study receptor density and occupancy in neuropsychiatric disorders. Here we report an improved synthesis method for [18F]fallypride. In addition, high molar activity of the ligand has allowed us to apply PET imaging to characterize D2/D3 receptor density in striatum of the recently developed zQ175DN knock-in (KI) mouse model of HD. Methods We longitudinally characterized in vivo [18F] fallypride -PET imaging of D2/D3 receptor densities in striatum of 9 and 12 month old wild type (WT) and heterozygous (HET) zQ175DN KI mouse. Furthermore, we verified the D2/D3 receptor density in striatum with [3H] fallypride autoradiography at 12 months of age. Results We implemented an improved synthesis method for [18F] fallypride to yield high molar activity (MA, 298–360 GBq/μmol) and good reproducibility. In the HET zQ175DN KI mice, we observed a significant longitudinal decrease in binding potential (BPND) (30.2%, p < 0.001, 9 months of age and 51.6%, p < 0.001, 12 months of age) compared to WT littermates. No mass effect was observed when the MA of [18F] fallypride was > 100 GBq/μmol at the time of injection. Furthermore, the decrease of D2/D3 receptor density in striatum in HET zQ175DN KI was consistent using [3H] fallypride autoradiography. Conclusions We observed a significant decrease in D2/D3R receptor densities in the striatum of HET zQ175DN KI mice compared to WT mice at 9 and 12 months of age. These results are in line with clinical findings in HD patients, suggesting [18F] fallypride PET imaging has potential as a quantitative translational approach to monitor disease progression ...
    Keywords Huntington’s disease ; [18F] fallypride ; PET ; Autoradiography ; Translational imaging ; Medical physics. Medical radiology. Nuclear medicine ; R895-920 ; Therapeutics. Pharmacology ; RM1-950
    Subject code 616
    Language English
    Publishing date 2019-08-01T00:00:00Z
    Publisher SpringerOpen
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  2. Article ; Online: Synthesis of novel bisphosphonate polyamine conjugates and their affinity to hydroxyapatite

    Elina Sankala / Janne M. Weisell / Tuulia Huhtala / Ale T.O. Närvänen / Jouko J. Vepsäläinen

    ARKIVOC, Vol 2012, Iss 4, Pp 233-

    2012  Volume 241

    Keywords Organic chemistry ; QD241-441
    Language English
    Publishing date 2012-02-01T00:00:00Z
    Publisher Arkat USA, Inc.
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Online: Native and Complexed IGF-1

    Raili Riikonen / Ale Närvänen / Jarno Salonen / Martti Kaasalainen / Anu Jalanko / Jussi Rytkönen / Tuulia Huhtala

    Journal of Drug Delivery , Vol

    Biodistribution and Pharmacokinetics in Infantile Neuronal Ceroid Lipofuscinosis

    2012  Volume 2012

    Keywords Pharmacy and materia medica ; RS1-441 ; Medicine ; R ; DOAJ:Pharmacy and materia medica ; DOAJ:Medicine (General) ; DOAJ:Health Sciences
    Language English
    Publishing date 2012-01-01T00:00:00Z
    Publisher Hindawi Publishing Corporation
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  4. Article ; Online: Inaugural Charles River World Congress on Animal Models in Drug Discovery and Development

    Jay A. Berzofsky / Lauren Gerard Koch / Steven L. Britton / Shaochen Chen / Wei Zhu / Xuanyi Ma / Anthony G. Comuzzie / Laetitia Devy-Dimanche / Ryan Feaver / Jan Grimm / Christoph Hock / Roger M. Nitsch / James B. Hoying / Aldons J. Lusis / Francesco Marincola / Josue Samayoa / Tolga Turan / David A. Pearce / Antti Nurmi /
    Tuulia Huhtala / Artem Shatillo / Jukka Puoliväli / Taneli Heikkinen / Timo Bragge / Kimmo Lehtimäki / Arun J. Sanyal / Kevin Strange / D. Lansing Taylor / Mark Miedel / Shanhang Jia / Alex Soto-Guterriez / Andrew Stern / Albert Gough

    Journal of Translational Medicine, Vol 15, Iss S3, Pp 1-

    2017  Volume 7

    Keywords Medicine ; R
    Language English
    Publishing date 2017-09-01T00:00:00Z
    Publisher BMC
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  5. Article: Preclinical pharmacology of FL442, a novel nonsteroidal androgen receptor modulator

    Poutiainen, Pekka K / Ale Närvänen / Aleksanteri Petsalo / Hannu Raunio / Jenni Küblbeck / Jorma J. Palvimo / Juha T. Pulkkinen / Mikael Peräkylä / Paavo Honkakoski / Reino Laatikainen / Risto O. Juvonen / Sanna Kaikkonen / Tiina Jääskeläinen / Tuulia Huhtala

    Molecular and Cellular Endocrinology. 2014 Apr. 25, v. 387

    2014  

    Abstract: The preclinical profiles of two most potent compounds of our recently published cycloalkane[d]isoxazole pharmacophore-based androgen receptor (AR) modulators, FL442 (4-(3a,4,5,6,7,7a-hexahydro-benzo[d]isoxazol-3-yl)-2-(trifluoromethyl)benzonitrile) and ... ...

    Abstract The preclinical profiles of two most potent compounds of our recently published cycloalkane[d]isoxazole pharmacophore-based androgen receptor (AR) modulators, FL442 (4-(3a,4,5,6,7,7a-hexahydro-benzo[d]isoxazol-3-yl)-2-(trifluoromethyl)benzonitrile) and its nitro analog FL425 (3-(4-nitro-3-(trifluoromethyl)phenyl)-3a,4,5,6,7,7a-hexahydrobenzo[d]isoxazole), were explored to evaluate their druggability for the treatment of AR dependent prostate cancer. The studies revealed that both compounds are selective to AR over other closely related steroid hormone receptors and that FL442 exhibits equal inhibition efficiency towards the androgen-responsive LNCaP prostate cancer cell line as the most widely used antiandrogen bicalutamide and the more recently discovered enzalutamide. Notably, FL442 maintains antiandrogenic activity with enzalutamide-activated AR mutant F876L. In contrast to bicalutamide, FL442 does not stimulate the VCaP prostate cancer cells which express elevated levels of the AR. Distribution analyses showed that [14CN]FL442 accumulates strongly in the mouse prostate. In spite of its low plasma concentration obtained by intraperitoneal administration, FL442 significantly inhibited LNCaP xenograft tumor growth. These findings provide a preclinical proof for FL442 as a promising AR targeted candidate for a further optimization.
    Keywords androgen receptors ; intraperitoneal injection ; mice ; mutants ; neoplasm cells ; pharmacology ; prostatic neoplasms
    Language English
    Dates of publication 2014-0425
    Size p. 8-18.
    Publishing place Elsevier Ireland Ltd
    Document type Article
    ZDB-ID 187438-x
    ISSN 1872-8057 ; 0303-7207
    ISSN (online) 1872-8057
    ISSN 0303-7207
    DOI 10.1016/j.mce.2014.02.008
    Database NAL-Catalogue (AGRICOLA)

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