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  1. Article ; Online: A proof of concept phase II study with the PDE-4 inhibitor roflumilast in patients with mild cognitive impairment or mild Alzheimer's disease dementia (ROMEMA): study protocol of a double-blind, randomized, placebo-controlled, between-subjects trial.

    Possemis, Nina / Verhey, Frans / Prickaerts, Jos / Blokland, Arjan / Ramakers, Inez

    Trials

    2024  Volume 25, Issue 1, Page(s) 162

    Abstract: Background: Research into the neurobiological underpinnings of learning and memory has demonstrated the cognitive-enhancing effects associated with diverse classes of phosphodiesterase (PDE) inhibitors. Specific PDE inhibitors have been identified to ... ...

    Abstract Background: Research into the neurobiological underpinnings of learning and memory has demonstrated the cognitive-enhancing effects associated with diverse classes of phosphodiesterase (PDE) inhibitors. Specific PDE inhibitors have been identified to improve neuronal communication through selective inhibition of PDE activity. Roflumilast, a PDE4 inhibitor, has demonstrated efficacy in enhancing episodic memory in healthy adults and elderly participants with pronounced memory impairment, indicative of amnestic mild cognitive impairment (aMCI). In alignment with these findings, the present protocol aims to provide a proof of concept phase II of the potential of roflumilast to aid patients diagnosed with (a)MCI or mild Alzheimer's disease (AD) dementia.
    Methods: The study will be conducted according to a double-blind, randomized placebo-controlled, between-subjects design. Participants with (a)MCI and mild AD dementia will be recruited through the Memory Clinic at the Maastricht University Medical Centre + (MUMC +) in Maastricht, the Netherlands, alongside outreach through regional hospitals, and social media. The study will have three arms: placebo, 50 μg roflumilast, and 100 μg roflumilast, with a treatment duration of 24 weeks. The primary outcome measure will focus on the assessment of episodic memory, as evaluated through participants' performance on the 15-word Verbal Learning Task (VLT). Our secondary objectives are multifaceted, including an exploration of various cognitive domains. In addition, insights into the well-being and daily functioning of participants will be investigated through interviews with both the participants and their (informal) caregivers, we are interested in the well-being and daily functioning of the participants.
    Discussion: The outcomes of the present study aim to elucidate the significance of the PDE4 inhibition mechanism as a prospective therapeutic target for enhancing cognitive function in individuals with (a)MCI and mild AD dementia. Identifying positive effects within these patient cohorts could extend the relevance of this treatment to encompass a broader spectrum of neurological disorders.
    Trial registration: The Medical Ethics Committee of MUMC + granted ethics approval for the 4th version of the protocol on September 10th, 2020. The trial was registered at the European Drug Regulatory Affairs Clinical Trials (EudraCT) registered on the 19th of December 2019 ( https://www.clinicaltrialsregister.eu/ctr-search/trial/2019-004959-36/NL ) and ClinicalTrial.gov (NCT04658654, https://clinicaltrials.gov/study/NCT04658654?intr=roflumilast&cond=mci&rank=1 ) on the 8th of December 2020. The Central Committee on Research Involving Human Subjects (CCMO) granted approval on the 30th of September 2020.
    MeSH term(s) Adult ; Aged ; Humans ; Alzheimer Disease/diagnosis ; Alzheimer Disease/drug therapy ; Phosphodiesterase 4 Inhibitors/adverse effects ; Dementia ; Cognitive Dysfunction/diagnosis ; Cognitive Dysfunction/drug therapy ; Randomized Controlled Trials as Topic ; Clinical Trials, Phase II as Topic ; Aminopyridines ; Benzamides ; Cyclopropanes
    Chemical Substances Phosphodiesterase 4 Inhibitors ; Roflumilast (0P6C6ZOP5U) ; Aminopyridines ; Benzamides ; Cyclopropanes
    Language English
    Publishing date 2024-03-04
    Publishing country England
    Document type Clinical Trial Protocol ; Journal Article
    ZDB-ID 2040523-6
    ISSN 1745-6215 ; 1468-6694 ; 1745-6215
    ISSN (online) 1745-6215
    ISSN 1468-6694 ; 1745-6215
    DOI 10.1186/s13063-024-08001-3
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Phosphodiesterase 4 inhibition after retrieval switches the memory fate favoring extinction instead of reconsolidation.

    Machado Batista Sohn, Jeferson / Cardoso, Nathalie Carla / Raymundi, Ana Maria / Prickaerts, Jos / Stern, Cristina Aparecida Jark

    Scientific reports

    2023  Volume 13, Issue 1, Page(s) 20384

    Abstract: Phosphodiesterase 4 (PDE4), an enzyme expressed in the dorsal hippocampus (DH), hydrolyzes the cAMP, limiting the PKA-induced CREB phosphorylation (pCREB) and BDNF expression. Depending on the brain region, PKA and pCREB mediate reconsolidation or ... ...

    Abstract Phosphodiesterase 4 (PDE4), an enzyme expressed in the dorsal hippocampus (DH), hydrolyzes the cAMP, limiting the PKA-induced CREB phosphorylation (pCREB) and BDNF expression. Depending on the brain region, PKA and pCREB mediate reconsolidation or extinction, whereas BDNF is mainly related to extinction facilitation. The mechanisms underpinning the switch between reconsolidation and extinction are relatively unknown. Here, we tested the hypothesis that PDE4 might control these processes. We showed in Wistar rats submitted to contextual fear conditioning that PDE4 inhibition with roflumilast (ROF) within the DH, after a short retrieval, did not change freezing behavior after one day (TestA
    MeSH term(s) Rats ; Animals ; Memory/physiology ; Cyclic Nucleotide Phosphodiesterases, Type 4/metabolism ; Rats, Wistar ; Brain-Derived Neurotrophic Factor/metabolism ; Extinction, Psychological/physiology ; Hippocampus/metabolism
    Chemical Substances Cyclic Nucleotide Phosphodiesterases, Type 4 (EC 3.1.4.17) ; Brain-Derived Neurotrophic Factor
    Language English
    Publishing date 2023-11-21
    Publishing country England
    Document type Journal Article
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-023-47717-1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Treatment with the selective PDE4B inhibitor A-33 or PDE4D inhibitor zatolmilast prevents sleep deprivation-induced deficits in spatial pattern separation.

    Zhao, Hongyu / Blokland, Arjan / Prickaerts, Jos / Havekes, Robbert / Heckman, Pim R A

    Behavioural brain research

    2023  Volume 459, Page(s) 114798

    Abstract: Sleep deprivation (SD) disrupts hippocampus-dependent memory, particularly in the dentate gyrus (DG) region, an area crucial for pattern separation. Previous research showed that non-selective phosphodiesterase type 4 (PDE4) inhibitors like roflumilast ... ...

    Abstract Sleep deprivation (SD) disrupts hippocampus-dependent memory, particularly in the dentate gyrus (DG) region, an area crucial for pattern separation. Previous research showed that non-selective phosphodiesterase type 4 (PDE4) inhibitors like roflumilast can alleviate these deficits. However, it remains unclear whether these outcomes are specific to a particular subfamily of PDE4. Hence, this study examined the specific impact of PDE4B inhibitor (A-33) and PDE4D inhibitor (zatolmilast) on spatial pattern separation in sleep deprived mice. Results demonstrated that SD impairs pattern separation, but both zatolmilast and A-33 alleviate these effects. However, A-33 impaired pattern separation in non-sleep deprived animals. The cognitive benefits of these inhibitors after SD may arise from alterations in relevant signaling pathways in the DG. This study provides initial evidence that inhibiting PDE4B or PDE4D holds promise for mitigating memory deficits due to SD.
    MeSH term(s) Animals ; Mice ; Cyclic Nucleotide Phosphodiesterases, Type 4/metabolism ; Hippocampus/metabolism ; Phosphodiesterase 4 Inhibitors/therapeutic use ; Sleep Deprivation/complications ; Sleep Deprivation/metabolism ; Memory Disorders/etiology ; Memory Disorders/prevention & control ; Pyrimidines/therapeutic use
    Chemical Substances Cyclic Nucleotide Phosphodiesterases, Type 4 (EC 3.1.4.17) ; Phosphodiesterase 4 Inhibitors ; PDE4B inhibitor A33 ; Pyrimidines
    Language English
    Publishing date 2023-12-04
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 449927-x
    ISSN 1872-7549 ; 0166-4328
    ISSN (online) 1872-7549
    ISSN 0166-4328
    DOI 10.1016/j.bbr.2023.114798
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Role of cyclic nucleotides and their downstream signaling cascades in memory function: Being at the right time at the right spot.

    Argyrousi, Elentina K / Heckman, Pim R A / Prickaerts, Jos

    Neuroscience and biobehavioral reviews

    2020  Volume 113, Page(s) 12–38

    Abstract: A plethora of studies indicate the important role of cAMP and cGMP cascades in neuronal plasticity and memory function. As a result, altered cyclic nucleotide signaling has been implicated in the pathophysiology of mnemonic dysfunction encountered in ... ...

    Abstract A plethora of studies indicate the important role of cAMP and cGMP cascades in neuronal plasticity and memory function. As a result, altered cyclic nucleotide signaling has been implicated in the pathophysiology of mnemonic dysfunction encountered in several diseases. In the present review we provide a wide overview of studies regarding the involvement of cyclic nucleotides, as well as their upstream and downstream molecules, in physiological and pathological mnemonic processes. Next, we discuss the regulation of the intracellular concentration of cyclic nucleotides via phosphodiesterases, the enzymes that degrade cAMP and/or cGMP, and via A-kinase-anchoring proteins that refine signal compartmentalization of cAMP signaling. We also provide an overview of the available data pointing to the existence of specific time windows in cyclic nucleotide signaling during neuroplasticity and memory formation and the significance to target these specific time phases for improving memory formation. Finally, we highlight the importance of emerging imaging tools like Förster resonance energy transfer imaging and optogenetics in detecting, measuring and manipulating the action of cyclic nucleotide signaling cascades.
    MeSH term(s) Cyclic AMP ; Cyclic GMP ; Humans ; Nucleotides, Cyclic ; Phosphoric Diester Hydrolases/metabolism ; Signal Transduction
    Chemical Substances Nucleotides, Cyclic ; Cyclic AMP (E0399OZS9N) ; Phosphoric Diester Hydrolases (EC 3.1.4.-) ; Cyclic GMP (H2D2X058MU)
    Language English
    Publishing date 2020-02-07
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 282464-4
    ISSN 1873-7528 ; 0149-7634
    ISSN (online) 1873-7528
    ISSN 0149-7634
    DOI 10.1016/j.neubiorev.2020.02.004
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  5. Article: A perspective on causality assessment in epigenetic research on neurodegenerative disorders.

    Koulousakis, Philippos / Tiane, Assia / Hellings, Niels / Prickaerts, Jos / van den Hove, Daniel / Vanmierlo, Tim

    Neural regeneration research

    2022  Volume 18, Issue 2, Page(s) 331–332

    Language English
    Publishing date 2022-08-24
    Publishing country India
    Document type Journal Article
    ZDB-ID 2388460-5
    ISSN 1876-7958 ; 1673-5374
    ISSN (online) 1876-7958
    ISSN 1673-5374
    DOI 10.4103/1673-5374.343898
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Computational investigation of the dynamic control of cAMP signaling by PDE4 isoform types.

    Paes, Dean / Hermans, Sammy / van den Hove, Daniel / Vanmierlo, Tim / Prickaerts, Jos / Carlier, Aurélie

    Biophysical journal

    2022  Volume 121, Issue 14, Page(s) 2693–2711

    Abstract: Cyclic adenosine monophosphate (cAMP) is a generic signaling molecule that, through precise control of its signaling dynamics, exerts distinct cellular effects. Consequently, aberrant cAMP signaling can have detrimental effects. Phosphodiesterase 4 (PDE4) ...

    Abstract Cyclic adenosine monophosphate (cAMP) is a generic signaling molecule that, through precise control of its signaling dynamics, exerts distinct cellular effects. Consequently, aberrant cAMP signaling can have detrimental effects. Phosphodiesterase 4 (PDE4) enzymes profoundly control cAMP signaling and comprise different isoform types wherein enzymatic activity is modulated by differential feedback mechanisms. Because these feedback dynamics are non-linear and occur coincidentally, their effects are difficult to examine experimentally but can be well simulated computationally. Through understanding the role of PDE4 isoform types in regulating cAMP signaling, PDE4-targeted therapeutic strategies can be better specified. Here, we established a computational model to study how feedback mechanisms on different PDE4 isoform types lead to dynamic, isoform-specific control of cAMP signaling. Ordinary differential equations describing cAMP dynamics were implemented in the VirtualCell environment. Simulations indicated that long PDE4 isoforms exert the most profound control on oscillatory cAMP signaling, as opposed to the PDE4-mediated control of single cAMP input pulses. Moreover, elevating cAMP levels or decreasing PDE4 levels revealed different effects on downstream signaling. Together these results underline that cAMP signaling is distinctly regulated by different PDE4 isoform types and that this isoform specificity should be considered in both computational and experimental follow-up studies to better define PDE4 enzymes as therapeutic targets in diseases in which cAMP signaling is aberrant.
    MeSH term(s) 3',5'-Cyclic-AMP Phosphodiesterases/metabolism ; Cyclic AMP ; Cyclic Nucleotide Phosphodiesterases, Type 4/metabolism ; Protein Isoforms/metabolism ; Signal Transduction
    Chemical Substances Protein Isoforms ; Cyclic AMP (E0399OZS9N) ; 3',5'-Cyclic-AMP Phosphodiesterases (EC 3.1.4.17) ; Cyclic Nucleotide Phosphodiesterases, Type 4 (EC 3.1.4.17)
    Language English
    Publishing date 2022-06-18
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 218078-9
    ISSN 1542-0086 ; 0006-3495
    ISSN (online) 1542-0086
    ISSN 0006-3495
    DOI 10.1016/j.bpj.2022.06.019
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  7. Article ; Online: Soluble guanylyl cyclase: A novel target for the treatment of vascular cognitive impairment?

    Nelissen, Ellis / Schepers, Melissa / Ponsaerts, Laura / Foulquier, Sébastien / Bronckaers, Annelies / Vanmierlo, Tim / Sandner, Peter / Prickaerts, Jos

    Pharmacological research

    2023  Volume 197, Page(s) 106970

    Abstract: Vascular cognitive impairment (VCI) describes neurodegenerative disorders characterized by a vascular component. Pathologically, it involves decreased cerebral blood flow (CBF), white matter lesions, endothelial dysfunction, and blood-brain barrier (BBB) ...

    Abstract Vascular cognitive impairment (VCI) describes neurodegenerative disorders characterized by a vascular component. Pathologically, it involves decreased cerebral blood flow (CBF), white matter lesions, endothelial dysfunction, and blood-brain barrier (BBB) impairments. Molecularly, oxidative stress and inflammation are two of the major underlying mechanisms. Nitric oxide (NO) physiologically stimulates soluble guanylate cyclase (sGC) to induce cGMP production. However, under pathological conditions, NO seems to be at the basis of oxidative stress and inflammation, leading to a decrease in sGC activity and expression. The native form of sGC needs a ferrous heme group bound in order to be sensitive to NO (Fe(II)sGC). Oxidation of sGC leads to the conversion of ferrous to ferric heme (Fe(III)sGC) and even heme-loss (apo-sGC). Both Fe(III)sGC and apo-sGC are insensitive to NO, and the enzyme is therefore inactive. sGC activity can be enhanced either by targeting the NO-sensitive native sGC (Fe(II)sGC), or the inactive, oxidized sGC (Fe(III)sGC) and the heme-free apo-sGC. For this purpose, sGC stimulators acting on Fe(II)sGC and sGC activators acting on Fe(III)sGC/apo-sGC have been developed. These sGC agonists have shown their efficacy in cardiovascular diseases by restoring the physiological and protective functions of the NO-sGC-cGMP pathway, including the reduction of oxidative stress and inflammation, and improvement of vascular functioning. Yet, only very little research has been performed within the cerebrovascular system and VCI pathology when focusing on sGC modulation and its potential protective mechanisms on vascular and neural function. Therefore, within this review, the potential of sGC as a target for treating VCI is highlighted.
    MeSH term(s) Humans ; Soluble Guanylyl Cyclase ; Vascular Diseases ; Cognitive Dysfunction/drug therapy ; Cyclic GMP ; Heme ; Inflammation
    Chemical Substances Soluble Guanylyl Cyclase (EC 4.6.1.2) ; Cyclic GMP (H2D2X058MU) ; Heme (42VZT0U6YR)
    Language English
    Publishing date 2023-10-24
    Publishing country Netherlands
    Document type Journal Article ; Review
    ZDB-ID 1003347-6
    ISSN 1096-1186 ; 0031-6989 ; 1043-6618
    ISSN (online) 1096-1186
    ISSN 0031-6989 ; 1043-6618
    DOI 10.1016/j.phrs.2023.106970
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  8. Article ; Online: Phosphodiesterase (PDE) 4 inhibition boosts Schwann cell myelination in a 3D regeneration model.

    Schepers, Melissa / Malheiro, Afonso / Gamardo, Adrián Seijas / Hellings, Niels / Prickaerts, Jos / Moroni, Lorenzo / Vanmierlo, Tim / Wieringa, Paul

    European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences

    2023  Volume 185, Page(s) 106441

    Abstract: Phosphodiesterase 4 (PDE4) inhibitors have been extensively researched for their anti-inflammatory and neuroregenerative properties. Despite the known neuroplastic and myelin regenerative properties of nonselective PDE4 inhibitors on the central nervous ... ...

    Abstract Phosphodiesterase 4 (PDE4) inhibitors have been extensively researched for their anti-inflammatory and neuroregenerative properties. Despite the known neuroplastic and myelin regenerative properties of nonselective PDE4 inhibitors on the central nervous system, the direct impact on peripheral remyelination and subsequent neuroregeneration has not yet been investigated. Therefore, to examine the possible therapeutic effect of PDE4 inhibition on peripheral glia, we assessed the differentiation of primary rat Schwann cells exposed in vitro to the PDE4 inhibitor roflumilast. To further investigate the differentiation promoting effects of roflumilast, we developed a 3D model of rat Schwann cell myelination that closely resembles the in vivo situation. Using these in vitro models, we demonstrated that pan-PDE4 inhibition using roflumilast significantly promoted differentiation of Schwann cells towards a myelinating phenotype, as indicated by the upregulation of myelin proteins, including MBP and MAG. Additionally, we created a unique regenerative model comprised of a 3D co-culture of rat Schwann cells and human iPSC-derived neurons. Schwann cells treated with roflumilast enhanced axonal outgrowth of iPSC-derived nociceptive neurons, which was accompanied by an accelerated myelination speed, thereby showing not only phenotypic but also functional changes of roflumilast-treated Schwann cells. Taken together, the PDE4 inhibitor roflumilast possesses a therapeutic benefit to stimulate Schwann cell differentiation and, subsequently myelination, as demonstrated in the biologically relevant in vitro platform used in this study. These results can aid in the development of novel PDE4 inhibition-based therapies in the advancement of peripheral regenerative medicine.
    MeSH term(s) Rats ; Animals ; Humans ; Cyclic Nucleotide Phosphodiesterases, Type 4/metabolism ; Phosphodiesterase 4 Inhibitors/pharmacology ; Phosphodiesterase 4 Inhibitors/metabolism ; Schwann Cells/metabolism ; Myelin Sheath/genetics
    Chemical Substances Roflumilast (0P6C6ZOP5U) ; Cyclic Nucleotide Phosphodiesterases, Type 4 (EC 3.1.4.17) ; Phosphodiesterase 4 Inhibitors
    Language English
    Publishing date 2023-03-31
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 1154366-8
    ISSN 1879-0720 ; 0928-0987
    ISSN (online) 1879-0720
    ISSN 0928-0987
    DOI 10.1016/j.ejps.2023.106441
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  9. Article ; Online: Exogenous Oxytocin Administration Restores Memory in Female APP/PS1 Mice.

    Koulousakis, Philippos / Willems, Emily / Schepers, Melissa / Rombaut, Ben / Prickaerts, Jos / Vanmierlo, Tim / van den Hove, Daniel

    Journal of Alzheimer's disease : JAD

    2023  Volume 96, Issue 3, Page(s) 1207–1219

    Abstract: Background: Current treatment options for Alzheimer's disease (AD) are limited, inefficient, and often have serious side effects. Oxytocin is a neuropeptide implicated in a variety of central processes, such as social and reproductive behaviors. Among ... ...

    Abstract Background: Current treatment options for Alzheimer's disease (AD) are limited, inefficient, and often have serious side effects. Oxytocin is a neuropeptide implicated in a variety of central processes, such as social and reproductive behaviors. Among others, it has garnered attention in various domains of psychiatric research, while its role in the development and course of neurodegenerative disorders like AD is rather unknown.
    Objective: This study aimed to investigate the role of exogenous oxytocin administration on memory, specifically in view of AD, as a potential novel treatment option.
    Methods: We describe a novel treatment approach by using a relatively low dose of long-term intranasal oxytocin treatment, to restore memory deficits in female APPswePS1dE9 mice.
    Results: Female APPswePS1dE9 mice treated with oxytocin showed increased spatial memory performance in the object location task and improved working memory in the Y-Maze, while indicating decreased sociability.
    Conclusions: These results indicate that oxytocin is able to reverse acquired cognitive deficits in female APPswePS1dE9 mice.
    MeSH term(s) Animals ; Female ; Mice ; Alzheimer Disease/drug therapy ; Alzheimer Disease/psychology ; Amyloid beta-Peptides ; Amyloid beta-Protein Precursor/genetics ; Disease Models, Animal ; Maze Learning ; Memory Disorders/drug therapy ; Memory Disorders/etiology ; Memory, Short-Term ; Mice, Transgenic ; Oxytocin/pharmacology ; Oxytocin/therapeutic use ; Presenilin-1
    Chemical Substances Amyloid beta-Peptides ; Amyloid beta-Protein Precursor ; Oxytocin (50-56-6) ; Presenilin-1
    Language English
    Publishing date 2023-11-05
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1440127-7
    ISSN 1875-8908 ; 1387-2877
    ISSN (online) 1875-8908
    ISSN 1387-2877
    DOI 10.3233/JAD-230657
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  10. Article ; Online: Blood-Brain Barrier Rescue by Roflumilast After Transient Global Cerebral Ischemia in Rats.

    Bonato, Jéssica Mendes / de Mattos, Bianca Andretto / Oliveira, Daniela Velasquez / Milani, Humberto / Prickaerts, Jos / de Oliveira, Rúbia Maria Weffort

    Neurotoxicity research

    2023  Volume 41, Issue 4, Page(s) 311–323

    Abstract: Phosphodiesterase 4 inhibitors (PDE4-I), which selectively increase cyclic adenosine monophosphate (cAMP) levels, have shown neuroprotective effects after several neurological injuries inducing blood-brain barrier (BBB) damage including local/focal ... ...

    Abstract Phosphodiesterase 4 inhibitors (PDE4-I), which selectively increase cyclic adenosine monophosphate (cAMP) levels, have shown neuroprotective effects after several neurological injuries inducing blood-brain barrier (BBB) damage including local/focal cerebral ischemia. The present investigated whether roflumilast confers BBB neuroprotection in the hippocampus after transient global cerebral ischemia (TGCI) in rats. TGCI resulted in whole BBB disruption as measured by the increase of Evans blue (EB) and IgG extravasation, neurodegeneration, and downregulation of claudin-5 and endothelial nitric oxide synthase (eNOS) levels in the CA1 hippocampal subfield of ischemic rats. Roflumilast attenuated BBB disruption and restored the levels of eNOS in the CA1 hippocampal area. Moreover, roflumilast increased the levels of B2 cell lymphoma (BcL-2) and neuron-glial antigen-2 (NG2) in the CA1 subfield after global ischemia in rats. The protective effects of roflumilast against TGCI-induced BBB breakdown might involve preservation of BBB integrity, vascularization and angiogenesis, and myelin repair.
    MeSH term(s) Rats ; Animals ; Blood-Brain Barrier/metabolism ; Ischemic Attack, Transient ; Brain Ischemia/metabolism ; Hippocampus/metabolism
    Chemical Substances Roflumilast (0P6C6ZOP5U)
    Language English
    Publishing date 2023-03-16
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2036826-4
    ISSN 1476-3524 ; 1029-8428
    ISSN (online) 1476-3524
    ISSN 1029-8428
    DOI 10.1007/s12640-023-00639-2
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