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Persistent improvement in synaptic and cognitive functions in an Alzheimer mouse model after rolipram treatment
Open accessAbstract
Evidence suggests that Alzheimer disease (AD) begins as a disorder of synaptic function, caused in part by increased levels of amyloid beta-peptide 1-42 (Abeta42). Both synaptic and cognitive deficits are reproduced in mice double transgenic for amyloid precursor protein (AA substitution K670N,M671L) and presenilin-1 (AA substitution M146V). Here we demonstrate that brief treatment with the phosphodiesterase 4 inhibitor rolipram ameliorates deficits in both long-term potentiation (LTP) and contextual learning in the double-transgenic mice. Most importantly, this beneficial effect can be extended beyond the duration of the administration. One course of long-term systemic treatment with rolipram improves LTP and basal synaptic transmission as well as working, reference, and associative memory deficits for at least 2 months after the end of the treatment. This protective effect is possibly due to stabilization of synaptic circuitry via alterations in gene expression by activation of the cAMP-dependent protein kinase (PKA)/cAMP regulatory element-binding protein (CREB) signaling pathway that make the synapses more resistant to the insult inflicted by Abeta. Thus, agents that enhance the cAMP/PKA/CREB pathway have potential for the treatment of AD and other diseases associated with elevated Abeta42 levels.
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“Tg-mouse AD models manifest a spontaneous age-onset impairment of LTP (Gong et al., 2004) that presumably is linked to impaired performance in memory tests (Arendash et al., 2001).”
From The Aβ oligomer hypothesis for synapse failure and memory loss in Alzheimer’s disease (2011) · cites this paper as Gong et al., 2004
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ResultKubota, K., Fukue, H., Sato, H., Hashimoto, K., Fujikane, A., Moriyama, H., Watanabe, T., Katsurabayashi, S., Kainuma, M., & Iwasaki, K. (2017) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00850 · Cited by 25
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BackgroundStrategies for Treatment of Disease-Associated Dementia Beyond Alzheimer's Disease: An Update
Khan, S. S., Khatik, G. L., & Datusalia, A. K. (2022) · Current Neuropharmacology · doi:10.2174/1570159x20666220411083922 · Cited by 25
“Phosphodiesterase type-4 inhibitor enhances LTP formation by increasing the level of c-AMP and enhancing the cAMP/PKA/CREB pathway [83].”
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Methylxanthine reversal of opioid-evoked inspiratory depression via phosphodiesterase-4 blockade
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Armstrong, P., Güngör, H., Anongjanya, P., Tweedy, C., Parkin, E. T., Johnston, J., Carr, I., Dawson, N., & Clapcote, S. J. (2024) · Neuropsychopharmacology · doi:10.1038/s41386-024-01852-z · Cited by 25
“Rolipram had no effect on A β peptide levels or plaque load in the PS/APP and Tg2576 strains [20, 21], although treatment over 24 days was shown to decrease A β peptide levels in brain tissue from 11-month-old 3xTg-AD mice [22].”
BackgroundMethodInfluentialKhorshidahmad, T., Tabrizian, K., Vakilzadeh, G., Nikbin, P., Moradi, S., Hosseini-Sharifabad, A., Roghani, A., Naghdi, N., & Sharifzadeh, M. S. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.12.028 · Cited by 24
Rezvanfar, M. A., Rezvanfar, M. A., Ranjbar, A., Baeeri, M., Mohammadirad, A., & Abdollahi, M. R. (2010) · Pesticide Biochemistry and Physiology · doi:10.1016/j.pestbp.2010.06.001 · Cited by 24
“been described in several models of neurological disorders, both acute and chronic [73–76].”
BackgroundWang, Z., Liang, Y., Zhang, L., Zhang, N., Liu, Q., & Wang, Z. (2018) · Aging · doi:10.18632/aging.101559 · Cited by 24
“Although much has been learned about the potential benefits of PDE4 inhibitors in the treatment of agingrelated diseases such as Alzheimer's disease [7, 8, 19], relatively little is known about their effects on adipose deposition and metabolic disorders during aging.”
BackgroundPKA-CREB Signaling Suppresses Tau Transcription
Liu, H., Jin, X., Yin, X., Jin, N., Liu, F., & Qian, W. (2015) · Journal of Alzheimer s Disease · doi:10.3233/jad-142610 · Cited by 25
Amyloid β: Walking on the dark side of the moon
Fedele, E., Rivera, D., Marengo, B., Pronzato, M. A., & Ricciarelli, R. (2015) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2015.09.001 · Cited by 23
“The impairment of PKA/CREB activity has been observed in the brain of AD patients and AD animal models (Gong et al., 2004; Liang et al., 2007; Yamamoto-Sasaki et al., 1999), thus leading to the hypothesis that cAMP-enhancing strategies may be ben ficial for the treatment of memory loss in AD and…”
BackgroundVitale, P., Pereira, A. R. S., Lupaşcu, C. A., Willem, M., Migliore, R., Migliore, M., & Marie, H. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.668948 · Cited by 26
Accumulation of carboxy-terminal fragments of APP increases phosphodiesterase 8B.
Kametani, F., & Haga, S. (2015) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2014.09.029 · Cited by 23
“The effectiveness of repeated administration of PDE3 inhibitor (cilostazol), PDE4 inhibitor (rolipram or GEBR-7b), PDE5 inhibitor (sildenafil or tadalafil), PDE7 inhibitor (S14), and PDE9A inhibitor (BAY 73e6691) has been demonstrated in several model animals of AD (Bruno et al., 2011; Cheng et al., 2010; García-Barro…”
BackgroundSabouri, M., Kordi, M. R., Shabkhiz, F., Taghibeikzadehbadr, P., & Geramian, Z. S. (2020) · Experimental Gerontology · doi:10.1016/j.exger.2020.111056 · Cited by 22
Chiu, Y., Lin, T., Chen, C., Lin, C., Teng, Y.-S., Lin, C., Sun, Y., Hsieh‐Li, H. M., Su, M., Lee‐Chen, G., et al. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/3058861 · Cited by 22
“The cognitive function of presenilin 1 (PS1)/APP transgenic mice is significantly improved by increasing CREB phosphorylation with phosphodiesterase inhibitors [18, 19].”
BackgroundBate, C., & Williams, A. (2015) · Biology · doi:10.3390/biology4030591 · Cited by 22
Jin, G., Zhu, L., Liu, P., Xu, Q., Qi, Y. A., Zhou, X., Xu, J., Ji, X., Chi, T., & Zou, L. (2019) · The Journal of Physiological Sciences · doi:10.1007/s12576-019-00664-x · Cited by 22
Bonato, J. M., Meyer, E., de Mendonça, P. S. B., Milani, H., Prickaerts, J., & de Oliveira, R. M. W. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.15089 · Cited by 22
“The pharmacological effects of PDE4 inhibitors in the central nervous system have been demonstrated to be dependent on molecular mechanisms underlying synaptic plasticity (Gong et al., 2004; Soares et al., 2016; Wiescholleck & Manahan-Vaughan, 2012).”
BackgroundRahim, M. A., Nakajima, A., Misawa, N., Shindo, K., Adachi, K., Shizuri, Y., Ohizumi, Y., & Yamakuni, T. (2008) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2008.09.046 · Cited by 21
The Role of Protein Kinase A in Anxiety Behaviors
Keil, M. F., Briassoulis, G. C., & Stratakis, C. A. (2016) · Neuroendocrinology · doi:10.1159/000444880 · Cited by 21
Akar, F., Mutlu, O., Celikyurt, I. K., Ulak, G., Erden, F., Bektaş, E., & Tanyerı, P. (2014) · Medical science monitor basic research/Medical science monitor. Basic research · doi:10.12659/msmbr.891149 · Cited by 20
Hotte, M., Dauphin, F., Fréret, T., Boulouard, M., & Levallet, G. (2012) · PLoS ONE · doi:10.1371/journal.pone.0032244 · Cited by 22
“In fact, several studies have already reported a positive effect of PDE4 inhibition on spatial memory [3,5,33–37], inhibitory avoidance learning [5,33,38], contextual fear conditioning [4,39], and object recognition [40–42].”
BackgroundBrullo, C., Massa, M., Villa, C., Ricciarelli, R., Rivera, D., Pronzato, M. A., Fedele, E., Barocelli, E., Bertoni, S., Flammini, L., et al. (2015) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2015.04.027 · Cited by 20
Brullo, C., Massa, M., Rocca, M., Rotolo, C., Guariento, S., Rivera, D., Ricciarelli, R., Fedele, E., Fossa, P., & Bruno, O. (2014) · Journal of Medicinal Chemistry · doi:10.1021/jm500855w · Cited by 20
Phosphodiesterase Inhibition to Target the Synaptic Dysfunction in Alzheimer’s Disease
Bales, K. R., Plath, N., Svenstrup, N., & Menniti, F. S. (2010) · Topics in medicinal chemistry · doi:10.1007/7355_2010_8 · Cited by 22
“LTP deficits are also observed in slices prepared from transgenic mice that overexpress Ab [90].”
BackgroundHajjHussein, H., Suvarna, N. U., Gremillion, C., Chandler, L. J., & O’Donnell, J. M. (2007) · Brain Research · doi:10.1016/j.brainres.2007.02.090 · Cited by 20
“…PDE4, and PDE2 have been implicated in hippocampal-LTP and memory performance (Bevilaqua et al., 2005; Boess, 2004; Chien et al., 2003; 2005; Gong et al., 2004; Liauw et al., 2005; Lu et al., 1999; Nicoll and Malenka, 1999; Roberson and Sweatt, 1996; Vianna et al., 2000; Wong et al., 1999;…”
BackgroundMehan, S., Kaur, G., Dudi, R., Rajput, M., & Kalra, S. (2017) · Open Journal of Parkinson s Disease and Treatment · doi:10.17352/ojpdt.000001 · Cited by 19
“Moreover, increase level of cAMP involved in the inhibition of apoptotic and necrotic cell death leads to improvement in cognitive functioning [52-61].”
BackgroundCasares, N., Alfaro, M., Cuadrado‐Tejedor, M., Lasarte-Cía, A., Navarro, F. C., Vivas, I., Espelosin, M., Cartas‐Cejudo, P., Fernández‐Irigoyen, J., Santamaría, E., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1130044 · Cited by 20
Phosphodiesterase 10A inhibitors as a novel therapeutic approach for schizophrenia
Siuciak, J. A., & Strick, C. A. (2007) · Expert Opinion on Drug Discovery · doi:10.1517/17460441.2.7.1001 · Cited by 19
Phosphodiesterase-4 inhibition restored hippocampal long term potentiation after primary blast
Vogel, E. W., Morales, F. N., Meaney, D. F., Bass, C. R., & Morrison, B. (2017) · Experimental Neurology · doi:10.1016/j.expneurol.2017.03.025 · Cited by 23
“…was effective in improving outcome in someexperimentalmodels of TBI and also reduced cognitive impairments associated with Alzhemer's disease, schizophrenia and aging (Gong et al., 2004; Maxwell et al., 2004; Smith et al., 2009; Titus et al., 2014; Wiescholleck and Manahan-Vaughan, 2012).”
BackgroundBorreca, A., Latina, V., Corsetti, V., Middei, S., Piccinin, S., Valle, F. D., Bussani, R., Ammassari‐Teule, M., Nisticò, R., Calissano, P., et al. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-0974-3 · Cited by 18
Pharmacokinetics and pharmacodynamics of nitric oxide mimetic agents
Horton, A., & Schiefer, I. T. (2019) · Nitric Oxide · doi:10.1016/j.niox.2019.01.001 · Cited by 19
Virk, D., Kumar, A., Jaggi, A. S., & Singh, N. (2021) · Environmental Science and Pollution Research · doi:10.1007/s11356-021-15189-3 · Cited by 19
“Rolipram (0.03 and 0.06 mg/kg body weight) (Zhang and O’Donnell 2000; Gong et al. 2004; Akar et al. 2015) was administered intraperitoneally (i.p.) whereas sodium arsenite (SA) (5 mg/kg body weight) (El-Demerdash et al. 2009) and donepezil (0.5mg/kg body weight) (Gawel et al. 2014) were…”
BackgroundMethodInfluentialNovel Therapies for Parkinsonian Syndromes–Recent Progress and Future Perspectives
Przewodowska, D., Marzec, W. Z., & Madetko‐Alster, N. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.720220 · Cited by 20
X-linked mental retardation and epigenetics
Froyen, G., Bauters, M., Voet, T., & Marynen, P. (2006) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2006.tb00526.x · Cited by 19
“βΑ deposits impair phosphorylation of CREB [89] and this can be restored in vivo [90, 91].”
BackgroundBonardi, C., Pardon, M., & Armstrong, P. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.07.008 · Cited by 17
Selective inhibitors of phosphodiesterases: therapeutic promise for neurodegenerative disorders
Umar, T., & Hoda, N. (2015) · MedChemComm · doi:10.1039/c5md00419e · Cited by 18
Keskin, H., Keskin, F., Tavacı, T., Halıcı, H., Yüksel, T. N., Özkaraca, M., Bilen, A., & Halıcı, Z. (2021) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/1440-1681.13493 · Cited by 18
Mohammadi, M., Guan, J., Khodagholi, F., Yans, A., Khalaj, S., Gholami, M., Taghizadeh, G., Aliaghaei, A., Abdollahi, M. R., Ghahremani, M., et al. (2016) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-016-1222-x · Cited by 18
Targeting phosphodiesterase 4 as a therapeutic strategy for cognitive improvement
Wei, X., Yu, G., Shen, H., Luo, Y., Shang, T., Shen, R., Xi, M., & Sun, H. (2022) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2022.106278 · Cited by 17
Metadata
- Authors
- Gong, B., Vitolo, O. V., Trinchese, F., Liu, S., Shelanski, M., & Arancio, O.
- Affiliations
- Nathan Kline Institute for Psychiatric Research (US)
- Columbia University (US)
- Venue
- Journal of Clinical Investigation
- Published
- 2004-12-01
- Volume
- 114
- Issue
- 11
- Pages
- 1624-1634
- ISSN
- 0021-9738 (ISSN-L)
- PMC
- PMC529285
- OpenAlex
- W2034986487
- Cited by
- 442
- References
- 60
- Citations by year
- 2026: 12 · 2025: 14 · 2024: 16 · 2023: 15 · 2022: 11 · 2021: 13 · 2020: 21 · 2019: 20 · 2018: 17 · 2017: 33 · 2016: 17 · 2015: 20 · 2014: 28 · 2013: 23 · 2012: 23
- FWCI
- 12.13
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Clinical Investigation (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Alzheimer's Association
- University of Minnesota
- York University
- National Institutes of Health
- School of Medicine, New York University
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Keywords
- Alzheimer's disease, rolipram, amyloid-beta 42, synaptic plasticity, long-term potentiation, contextual learning, memory impairment, phosphodiesterase-4 inhibitors, cAMP/PKA/CREB signaling, synaptic transmission, APP/PS1 double transgenic mice
- MeSH terms
- Alzheimer Disease, Animals, Cognition, Disease Models, Animal, Hippocampus, Humans, Learning, Male, Membrane Proteins, Mice, Transgenic, Synaptic Transmission, Phosphodiesterase Inhibitors, Amyloid beta-Protein Precursor, Cyclic AMP Response Element-Binding Protein, Long-Term Potentiation, Rolipram, Mice, Presenilin-1, In Vitro Techniques
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