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  1. Article ; Online: Stress Resilience is Associated with Hippocampal Synaptoprotection in the Female Rat Learned Helplessness Paradigm.

    Huzian, Orsolya / Baka, Judith / Csakvari, Eszter / Dobos, Nikoletta / Leranth, Csaba / Siklos, Laszlo / Duman, Ronald S / Farkas, Tamas / Hajszan, Tibor

    Neuroscience

    2021  Volume 459, Page(s) 85–103

    Abstract: The synaptogenic hypothesis of major depressive disorder implies that preventing the onset of depressive-like behavior also prevents the loss of hippocampal spine synapses. By applying the psychoactive drugs, diazepam and fluoxetine, we investigated ... ...

    Abstract The synaptogenic hypothesis of major depressive disorder implies that preventing the onset of depressive-like behavior also prevents the loss of hippocampal spine synapses. By applying the psychoactive drugs, diazepam and fluoxetine, we investigated whether blocking the development of helpless behavior by promoting stress resilience in the rat learned helplessness paradigm is associated with a synaptoprotective action in the hippocampus. Adult ovariectomized and intact female Sprague-Dawley rats (n = 297) were treated with either diazepam, fluoxetine, or vehicle, exposed to inescapable footshocks or sham stress, and tested in an active escape task to assess helpless behavior. Escape-evoked corticosterone secretion, as well as remodeling of hippocampal spine synapses at a timepoint representing the onset of escape testing were also analyzed. In ovariectomized females, treatment with diazepam prior to stress exposure prevented helpless behavior, blocked the loss of hippocampal spine synapses, and muted the corticosterone surge evoked by escape testing. Although fluoxetine stimulated escape performance and hippocampal synaptogenesis under non-stressed conditions, almost all responses to fluoxetine were abolished following exposure to inescapable stress. Only a much higher dose of fluoxetine was capable of partly reproducing the strong protective actions of diazepam. Importantly, these protective actions were retained in the presence of ovarian hormones. Our findings indicate that stress resilience is associated with the preservation of spine synapses in the hippocampus, raising the possibility that, besides synaptogenesis, hippocampal synaptoprotection is also implicated in antidepressant therapy.
    MeSH term(s) Animals ; Depressive Disorder, Major ; Disease Models, Animal ; Female ; Fluoxetine/pharmacology ; Helplessness, Learned ; Hippocampus ; Rats ; Rats, Sprague-Dawley
    Chemical Substances Fluoxetine (01K63SUP8D)
    Language English
    Publishing date 2021-01-30
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 196739-3
    ISSN 1873-7544 ; 0306-4522
    ISSN (online) 1873-7544
    ISSN 0306-4522
    DOI 10.1016/j.neuroscience.2021.01.029
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Enantioselective Synthesis of 8-Hydroxyquinoline Derivative, Q134 as a Hypoxic Adaptation Inducing Agent.

    Hackler, László / Gyuris, Márió / Huzián, Orsolya / Alföldi, Róbert / Szebeni, Gábor J / Madácsi, Ramóna / Knapp, Levente / Kanizsai, Iván / Puskás, László G

    Molecules (Basel, Switzerland)

    2019  Volume 24, Issue 23

    Abstract: Hypoxia is a common feature of neurodegenerative diseases, including Alzheimer's disease that may be responsible for disease pathogenesis and progression. Therefore, the hypoxia-inducible factor (HIF)1 system, responsible for hypoxic adaptation, is a ... ...

    Abstract Hypoxia is a common feature of neurodegenerative diseases, including Alzheimer's disease that may be responsible for disease pathogenesis and progression. Therefore, the hypoxia-inducible factor (HIF)1 system, responsible for hypoxic adaptation, is a potential therapeutic target to combat these diseases by activators of cytoprotective protein induction. We have selected a candidate molecule from our cytoprotective hydroxyquinoline library and developed a novel enantioselective synthesis for the production of its enantiomers. The use of quinidine or quinine as a catalyst enabled the preparation of enantiomer-pure products. We have utilized in vitro assays to evaluate cytoprotective activity, a fluorescence-activated cell sorting (FACS) based assay measuring mitochondrial membrane potential changes, and gene and protein expression analysis. Our data showed that the enantiomers of Q134 showed potent and similar activity in all tested assays. We have concluded that the enantiomers exert their cytoprotective activity via the HIF1 system through HIF1A protein stabilization.
    MeSH term(s) Cell Line, Tumor ; Flow Cytometry ; Gene Expression Profiling ; Gene Expression Regulation/drug effects ; Humans ; Hydroxyquinolines/chemical synthesis ; Hydroxyquinolines/chemistry ; Hydroxyquinolines/pharmacology ; Hypoxia-Inducible Factor 1, alpha Subunit/chemistry ; Hypoxia-Inducible Factor 1, alpha Subunit/metabolism ; Membrane Potential, Mitochondrial/drug effects ; Oxidative Stress/drug effects ; Oxyquinoline/analogs & derivatives ; Protein Stability/drug effects ; Quinidine/chemistry ; Quinine/chemistry ; Stereoisomerism
    Chemical Substances HIF1A protein, human ; Hydroxyquinolines ; Hypoxia-Inducible Factor 1, alpha Subunit ; Oxyquinoline (5UTX5635HP) ; Quinine (A7V27PHC7A) ; Quinidine (ITX08688JL)
    Language English
    Publishing date 2019-11-23
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 1413402-0
    ISSN 1420-3049 ; 1431-5165 ; 1420-3049
    ISSN (online) 1420-3049
    ISSN 1431-5165 ; 1420-3049
    DOI 10.3390/molecules24234269
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Synthesis and Cytoprotective Characterization of 8-Hydroxyquinoline Betti Products.

    Kanizsai, Iván / Madácsi, Ramóna / Hackler, László / Gyuris, Márió / Szebeni, Gábor J / Huzián, Orsolya / Puskás, László G

    Molecules (Basel, Switzerland)

    2018  Volume 23, Issue 8

    Abstract: The 8-hydroxyquinoline pharmacophore scaffold has been shown to possess a range of activities as metal chelation, enzyme inhibition, cytotoxicity, and cytoprotection. Based on our previous findings we set out to optimize the scaffold for cytoprotective ... ...

    Abstract The 8-hydroxyquinoline pharmacophore scaffold has been shown to possess a range of activities as metal chelation, enzyme inhibition, cytotoxicity, and cytoprotection. Based on our previous findings we set out to optimize the scaffold for cytoprotective activity for its potential application in central nervous system related diseases. A 48-membered Betti-library was constructed by the utilization of formic acid mediated industrial-compatible coupling with sets of aromatic primary amines such as anilines, oxazoles, pyridines, and pyrimidines, with (hetero)aromatic aldehydes and 8-hydroxiquinoline derivatives. After column chromatography and re-crystallization, the corresponding analogues were obtained in yields of 13⁻90%. The synthesized analogs were optimized with the utilization of a cytoprotection assay with chemically induced oxidative stress, and the most active compounds were further tested in orthogonal assays, a real time cell viability method, a fluorescence-activated cell sorting (FACS)-based assay measuring mitochondrial membrane potential changes, and gene expression analysis. The best candidates showed potent, nanomolar activity in all test systems and support the need for future studies in animal models of central nervous system (CNS) disorders.
    MeSH term(s) Aldehydes/chemistry ; Aniline Compounds/chemistry ; Cell Death/drug effects ; Cell Line ; Cell Survival/drug effects ; Cytoprotection/drug effects ; Gene Expression Regulation/drug effects ; Humans ; Hypoxia/genetics ; Inhibitory Concentration 50 ; Membrane Potential, Mitochondrial/drug effects ; Oxidative Stress/drug effects ; Oxyquinoline/chemical synthesis ; Oxyquinoline/chemistry ; Oxyquinoline/pharmacology ; Structure-Activity Relationship
    Chemical Substances Aldehydes ; Aniline Compounds ; Oxyquinoline (5UTX5635HP) ; aniline (SIR7XX2F1K)
    Language English
    Publishing date 2018-08-02
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 1413402-0
    ISSN 1420-3049 ; 1431-5165 ; 1420-3049
    ISSN (online) 1420-3049
    ISSN 1431-5165 ; 1420-3049
    DOI 10.3390/molecules23081934
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Q134R: Small chemical compound with NFAT inhibitory properties improves behavioral performance and synapse function in mouse models of amyloid pathology.

    Sompol, Pradoldej / Gollihue, Jenna L / Kraner, Susan D / Artiushin, Irina A / Cloyd, Ryan A / Chishti, Emad A / Koren, Shon A / Nation, Grant K / Abisambra, Jose F / Huzian, Orsolya / Nagy, Lajos I / Santha, Miklos / Hackler, Laszlo / Puskas, Laszlo G / Norris, Christopher M

    Aging cell

    2021  Volume 20, Issue 7, Page(s) e13416

    Abstract: Inhibition of the protein phosphatase calcineurin (CN) ameliorates pathophysiologic and cognitive changes in aging rodents and mice with aging-related Alzheimer's disease (AD)-like pathology. However, concerns over adverse effects have slowed the ... ...

    Abstract Inhibition of the protein phosphatase calcineurin (CN) ameliorates pathophysiologic and cognitive changes in aging rodents and mice with aging-related Alzheimer's disease (AD)-like pathology. However, concerns over adverse effects have slowed the transition of common CN-inhibiting drugs to the clinic for the treatment of AD and AD-related disorders. Targeting substrates of CN, like the nuclear factor of activated T cells (NFATs), has been suggested as an alternative, safer approach to CN inhibitors. However, small chemical inhibitors of NFATs have only rarely been described. Here, we investigate a newly developed neuroprotective hydroxyquinoline derivative (Q134R) that suppresses NFAT signaling, without inhibiting CN activity. Q134R partially inhibited NFAT activity in primary rat astrocytes, but did not prevent CN-mediated dephosphorylation of a non-NFAT target, either in vivo, or in vitro. Acute (≤1 week) oral delivery of Q134R to APP/PS1 (12 months old) or wild-type mice (3-4 months old) infused with oligomeric Aβ peptides led to improved Y maze performance. Chronic (≥3 months) oral delivery of Q134R appeared to be safe, and, in fact, promoted survival in wild-type (WT) mice when given for many months beyond middle age. Finally, chronic delivery of Q134R to APP/PS1 mice during the early stages of amyloid pathology (i.e., between 6 and 9 months) tended to reduce signs of glial reactivity, prevented the upregulation of astrocytic NFAT4, and ameliorated deficits in synaptic strength and plasticity, without noticeably altering parenchymal Aβ plaque pathology. The results suggest that Q134R is a promising drug for treating AD and aging-related disorders.
    MeSH term(s) Alzheimer Disease/genetics ; Animals ; Disease Models, Animal ; Mice ; NFATC Transcription Factors/antagonists & inhibitors ; Plaque, Amyloid/physiopathology
    Chemical Substances NFATC Transcription Factors
    Language English
    Publishing date 2021-06-12
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2113083-8
    ISSN 1474-9726 ; 1474-9718
    ISSN (online) 1474-9726
    ISSN 1474-9718
    DOI 10.1111/acel.13416
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Stress induces equivalent remodeling of hippocampal spine synapses in a simulated postpartum environment and in a female rat model of major depression.

    Baka, Judith / Csakvari, Eszter / Huzian, Orsolya / Dobos, Nikoletta / Siklos, Laszlo / Leranth, Csaba / MacLusky, Neil J / Duman, Ronald S / Hajszan, Tibor

    Neuroscience

    2016  Volume 343, Page(s) 384–397

    Abstract: Stress and withdrawal of female reproductive hormones are known risk factors of postpartum depression. Although both of these factors are capable of powerfully modulating neuronal plasticity, there is no direct electron microscopic evidence of ... ...

    Abstract Stress and withdrawal of female reproductive hormones are known risk factors of postpartum depression. Although both of these factors are capable of powerfully modulating neuronal plasticity, there is no direct electron microscopic evidence of hippocampal spine synapse remodeling in postpartum depression. To address this issue, hormonal conditions of pregnancy and postpartum period were simulated in ovariectomized adult female Sprague-Dawley rats (n=76). The number of hippocampal spine synapses and the depressive behavior of rats in an active escape task were investigated in untreated control, hormone-withdrawn 'postpartum', simulated proestrus, and hormone-treated 'postpartum' animals. After 'postpartum' withdrawal of gonadal steroids, inescapable stress caused a loss of hippocampal spine synapses, which was related to poor escape performance in hormone-withdrawn 'postpartum' females. These responses were equivalent with the changes observed in untreated controls that is an established animal model of major depression. Maintaining proestrus levels of ovarian hormones during 'postpartum' stress exposure did not affect synaptic and behavioral responses to inescapable stress in simulated proestrus animals. By contrast, maintaining pregnancy levels of estradiol and progesterone during 'postpartum' stress exposure completely prevented the stress-induced loss of hippocampal spine synapses, which was associated with improved escape performance in hormone-treated 'postpartum' females. This protective effect appears to be mediated by a muted stress response as measured by serum corticosterone concentrations. In line with our emerging 'synaptogenic hypothesis' of depression, the loss of hippocampal spine synapses may be a novel perspective both in the pathomechanism and in the clinical management of postpartum affective illness.
    MeSH term(s) Animals ; Corticosterone/blood ; Depression, Postpartum/metabolism ; Depression, Postpartum/pathology ; Depressive Disorder, Major/metabolism ; Depressive Disorder, Major/pathology ; Disease Models, Animal ; Estradiol/administration & dosage ; Estradiol/metabolism ; Female ; Hippocampus/metabolism ; Hippocampus/pathology ; Neuronal Plasticity/physiology ; Ovariectomy ; Postpartum Period ; Proestrus/physiology ; Progesterone/administration & dosage ; Progesterone/metabolism ; Rats, Sprague-Dawley ; Synapses/metabolism ; Synapses/pathology
    Chemical Substances Progesterone (4G7DS2Q64Y) ; Estradiol (4TI98Z838E) ; Corticosterone (W980KJ009P)
    Language English
    Publishing date 2016-12-22
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 196739-3
    ISSN 1873-7544 ; 0306-4522
    ISSN (online) 1873-7544
    ISSN 0306-4522
    DOI 10.1016/j.neuroscience.2016.12.021
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: The small molecule AUTEN-99 (autophagy enhancer-99) prevents the progression of neurodegenerative symptoms.

    Kovács, Tibor / Billes, Viktor / Komlós, Marcell / Hotzi, Bernadette / Manzéger, Anna / Tarnóci, Anna / Papp, Diána / Szikszai, Fanni / Szinyákovics, Janka / Rácz, Ákos / Noszál, Béla / Veszelka, Szilvia / Walter, Fruzsina R / Deli, Mária A / Hackler, Laszlo / Alfoldi, Robert / Huzian, Orsolya / Puskas, Laszlo G / Liliom, Hanna /
    Tárnok, Krisztián / Schlett, Katalin / Borsy, Adrienn / Welker, Ervin / Kovács, Attila L / Pádár, Zsolt / Erdős, Attila / Legradi, Adam / Bjelik, Annamaria / Gulya, Károly / Gulyás, Balázs / Vellai, Tibor

    Scientific reports

    2017  Volume 7, Page(s) 42014

    Abstract: Autophagy functions as a main route for the degradation of superfluous and damaged constituents of the cytoplasm. Defects in autophagy are implicated in the development of various age-dependent degenerative disorders such as cancer, neurodegeneration and ...

    Abstract Autophagy functions as a main route for the degradation of superfluous and damaged constituents of the cytoplasm. Defects in autophagy are implicated in the development of various age-dependent degenerative disorders such as cancer, neurodegeneration and tissue atrophy, and in accelerated aging. To promote basal levels of the process in pathological settings, we previously screened a small molecule library for novel autophagy-enhancing factors that inhibit the myotubularin-related phosphatase MTMR14/Jumpy, a negative regulator of autophagic membrane formation. Here we identify AUTEN-99 (autophagy enhancer-99), which activates autophagy in cell cultures and animal models. AUTEN-99 appears to effectively penetrate through the blood-brain barrier, and impedes the progression of neurodegenerative symptoms in Drosophila models of Parkinson's and Huntington's diseases. Furthermore, the molecule increases the survival of isolated neurons under normal and oxidative stress-induced conditions. Thus, AUTEN-99 serves as a potent neuroprotective drug candidate for preventing and treating diverse neurodegenerative pathologies, and may promote healthy aging.
    MeSH term(s) Animals ; Autophagy/drug effects ; Cell Survival/drug effects ; Cells, Cultured ; Disease Models, Animal ; Drosophila ; Neurodegenerative Diseases/prevention & control ; Neurons/drug effects ; Neurons/physiology ; Neuroprotective Agents/administration & dosage ; Neuroprotective Agents/pharmacology
    Chemical Substances Neuroprotective Agents
    Language English
    Publishing date 2017-02-16
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/srep42014
    Database MEDical Literature Analysis and Retrieval System OnLINE

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