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  1. Article ; Online: Amantadine and/or transcranial magnetic stimulation for fatigue associated with multiple sclerosis (FETEM): study protocol for a phase 3 randomised, double-blind, cross-over, controlled clinical trial.

    Matias-Guiu, Jordi A / González-Rosa, Javier / Hernández, Miguel Ángel / Martínez-Ginés, Maria Luisa / Portolés, Antonio / Pérez-Macías, Natalia / Benito-León, Julián / Padrón, Iván / Prieto, Julio / Matias-Guiu, Jorge

    BMJ open

    2024  Volume 14, Issue 1, Page(s) e078661

    Abstract: Introduction: Fatigue is one of the most disabling symptoms of multiple sclerosis (MS), and effective treatments are lacking. Amantadine is one of the most used treatments, although its efficacy is under debate. Transcranial magnetic stimulation (TMS) ... ...

    Abstract Introduction: Fatigue is one of the most disabling symptoms of multiple sclerosis (MS), and effective treatments are lacking. Amantadine is one of the most used treatments, although its efficacy is under debate. Transcranial magnetic stimulation (TMS) is a promising intervention that has shown positive effects in some preliminary investigations. We aim to investigate the effect of 6 weeks of amantadine and/or TMS in fatigue due to MS.
    Methods and analysis: The study is a national, multicentre, phase 3, randomised, double-blind, cross-over, placebo-controlled and sham-controlled clinical trial. Adult patients with relapsing-remitting MS, Expanded Disability Status Scale score of 1.5-4.5 and Fatigue Severity Score>4 are eligible for the trial. Participants will be randomised to one of the sequences of the study. Each sequence consists of four periods of 6 weeks of treatment and three washout periods of 12-18 weeks. All patients will receive all the combinations of therapies. The primary outcome is the Modified Fatigue Impact Scale. The secondary outcomes are the Symbol Digit Modalities Test (cognition), Beck Depression Inventory-II (depressive symptoms) and Short-Survey 12 (quality of life). Safety and cost-effectiveness will also be evaluated. An exploratory substudy including MRI and blood biomarkers will be conducted.
    Ethics and dissemination: The study is approved by the Ethics Committee of the Hospital Clinico San Carlos and the Spanish Agency of Medications and Medical Devices. All study findings will be published in scientific peer-reviewed journals and presented at relevant scientific conferences.
    Trial registration number: EudraCT 2021-004868-95; NCT05809414.
    MeSH term(s) Adult ; Humans ; Multiple Sclerosis/complications ; Multiple Sclerosis/drug therapy ; Transcranial Magnetic Stimulation ; Quality of Life ; Amantadine/therapeutic use ; Double-Blind Method ; Fatigue/therapy ; Fatigue/chemically induced ; Treatment Outcome ; Randomized Controlled Trials as Topic ; Multicenter Studies as Topic ; Clinical Trials, Phase III as Topic
    Chemical Substances Amantadine (BF4C9Z1J53)
    Language English
    Publishing date 2024-01-04
    Publishing country England
    Document type Clinical Trial Protocol ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2599832-8
    ISSN 2044-6055 ; 2044-6055
    ISSN (online) 2044-6055
    ISSN 2044-6055
    DOI 10.1136/bmjopen-2023-078661
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Coronary angiography in patients without ST-segment elevation following out-of-hospital cardiac arrest. COUPE clinical trial.

    Viana-Tejedor, Ana / Andrea-Riba, Rut / Scardino, Claudia / Ariza-Solé, Albert / Bañeras, Jordi / García-García, Cosme / Jiménez Mena, Manuel / Vila, Monserrat / Martínez-Sellés, Manuel / Pastor, Gemma / García Acuña, José María / Loma-Osorio, Pablo / García Rubira, Juan Carlos / Jorge Pérez, Pablo / Pastor, Pablo / Ferrera, Carlos / Noriega, Francisco J / Pérez Macías, Natalia / Fernández-Ortiz, Antonio /
    Pérez-Villacastín, Julián

    Revista espanola de cardiologia (English ed.)

    2022  Volume 76, Issue 2, Page(s) 94–102

    Abstract: Introduction and objectives: The role of emergency coronary angiography (CAG) and percutaneous coronary intervention (PCI) following out-of-hospital cardiac arrest (OHCA) in patients without ST-segment elevation myocardial infarction (STEMI) remains ... ...

    Abstract Introduction and objectives: The role of emergency coronary angiography (CAG) and percutaneous coronary intervention (PCI) following out-of-hospital cardiac arrest (OHCA) in patients without ST-segment elevation myocardial infarction (STEMI) remains unclear. We aimed to assess whether emergency CAG and PCI would improve survival with good neurological outcome in this population.
    Methods: In this multicenter, randomized, open-label, investigator-initiated clinical trial, we randomly assigned 69 survivors of OHCA without STEMI to undergo immediate CAG or deferred CAG. The primary efficacy endpoint was a composite of in-hospital survival free of severe dependence. The safety endpoint was a composite of major adverse cardiac events including death, reinfarction, bleeding, and ventricular arrhythmias.
    Results: A total of 66 patients were included in the primary analysis (95.7%). In-hospital survival was 62.5% in the immediate CAG group and 58.8% in the delayed CAG group (HR, 0.96; 95%CI, 0.45-2.09; P=.93). In-hospital survival free of severe dependence was 59.4% in the immediate CAG group and 52.9% in the delayed CAG group (HR, 1.29; 95%CI, 0.60-2.73; P=.4986). No differences were found in the secondary endpoints except for the incidence of acute kidney failure, which was more frequent in the immediate CAG group (15.6% vs 0%, P=.002) and infections, which were higher in the delayed CAG group (46.9% vs 73.5%, P=.003).
    Conclusions: In this underpowered randomized trial involving patients resuscitated after OHCA without STEMI, immediate CAG provided no benefit in terms of survival without neurological impairment compared with delayed CAG.
    Clinicaltrials: gov Identifier: NCT02641626.
    MeSH term(s) Humans ; ST Elevation Myocardial Infarction/diagnosis ; ST Elevation Myocardial Infarction/surgery ; ST Elevation Myocardial Infarction/complications ; Coronary Angiography/adverse effects ; Out-of-Hospital Cardiac Arrest/therapy ; Percutaneous Coronary Intervention/adverse effects ; Arrhythmias, Cardiac/complications ; Treatment Outcome
    Language Spanish
    Publishing date 2022-06-22
    Publishing country Spain
    Document type Randomized Controlled Trial ; Multicenter Study ; Journal Article
    ZDB-ID 2592481-3
    ISSN 1885-5857 ; 1885-5857
    ISSN (online) 1885-5857
    ISSN 1885-5857
    DOI 10.1016/j.rec.2022.05.013
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Indazolylketones as new multitarget cannabinoid drugs.

    González-Naranjo, Pedro / Pérez-Macias, Natalia / Pérez, Concepción / Roca, Carlos / Vaca, Gabriela / Girón, Rocio / Sánchez-Robles, Eva / Martín-Fontelles, María Isabel / de Ceballos, María L / Martin-Requero, Angeles / Campillo, Nuria E / Páez, Juan A

    European journal of medicinal chemistry

    2019  Volume 166, Page(s) 90–107

    Abstract: Multitarget cannabinoids could be a promising therapeutic strategic to fight against Alzheimer's disease. In this sense, our group has developed a new family of indazolylketones with multitarget profile including cannabinoids, cholinesterase and BACE-1 ... ...

    Abstract Multitarget cannabinoids could be a promising therapeutic strategic to fight against Alzheimer's disease. In this sense, our group has developed a new family of indazolylketones with multitarget profile including cannabinoids, cholinesterase and BACE-1 activity. A medicinal chemistry program that includes computational design, synthesis and in vitro and cellular evaluation has allowed to us to achieve lead compounds. In this work, the synthesis and evaluation of a new class of indazolylketones have been performed. Pharmacological evaluation includes functional activity for cannabinoid receptors on isolated tissue. In addition, in vitro inhibitory assays in AChE/BuChE enzymes and BACE-1 have been carried out. Furthermore, studies of neuroprotective effects in human neuroblastoma SH-SY5Y cells and studies of the mechanisms of survival/death in lymphoblasts of patients with Alzheimer's disease have been achieved. The results of pharmacological tests have revealed that some of these derivatives (5, 6) behave as CB2 cannabinoid agonists and simultaneously show BuChE and/or BACE-1 inhibition.
    MeSH term(s) Aspartic Acid Endopeptidases/antagonists & inhibitors ; Butyrylcholinesterase/metabolism ; Cannabinoids/chemical synthesis ; Cannabinoids/chemistry ; Cannabinoids/pharmacology ; Cell Line, Tumor ; Cell Proliferation/drug effects ; Chemistry Techniques, Synthetic ; Cholinesterase Inhibitors/chemical synthesis ; Cholinesterase Inhibitors/chemistry ; Cholinesterase Inhibitors/pharmacology ; Drug Design ; Humans ; Indazoles/chemistry ; Ketones/chemical synthesis ; Ketones/chemistry ; Ketones/pharmacology ; Neurons/cytology ; Neurons/drug effects ; Receptor, Cannabinoid, CB2/antagonists & inhibitors
    Chemical Substances Cannabinoids ; Cholinesterase Inhibitors ; Indazoles ; Ketones ; Receptor, Cannabinoid, CB2 ; Butyrylcholinesterase (EC 3.1.1.8) ; Aspartic Acid Endopeptidases (EC 3.4.23.-)
    Language English
    Publishing date 2019-01-17
    Publishing country France
    Document type Journal Article
    ZDB-ID 188597-2
    ISSN 1768-3254 ; 0009-4374 ; 0223-5234
    ISSN (online) 1768-3254
    ISSN 0009-4374 ; 0223-5234
    DOI 10.1016/j.ejmech.2019.01.030
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Practical preparation of challenging amides from non-nucleophilic amines and esters under flow conditions

    Vrijdag, Johannes L / Delgado, Francisca / Alonso, Nerea / De Borggraeve, Wim M / Pérez-Macias, Natalia / Alcázar, Jesus

    Chemical communications. 2014 Nov. 4, v. 50, no. 95

    2014  

    Abstract: A fast and efficient protocol for the formation of amides from low nucleophilic amines and esters in flow is described. Products were obtained in good to excellent yields and with the advantage of simultaneous mixing of all reagents at once, avoiding ... ...

    Abstract A fast and efficient protocol for the formation of amides from low nucleophilic amines and esters in flow is described. Products were obtained in good to excellent yields and with the advantage of simultaneous mixing of all reagents at once, avoiding steps for intermediate formation. The protocol is also suitable to be combined with ester synthesis, resulting in the preparation of amides in-line from haloarenes.
    Keywords Lewis bases ; amides ; amines ; chemical reactions ; esters ; mixing
    Language English
    Dates of publication 2014-1104
    Size p. 15094-15097.
    Publishing place The Royal Society of Chemistry
    Document type Article
    ZDB-ID 1472881-3
    ISSN 1364-548X ; 1359-7345 ; 0009-241X
    ISSN (online) 1364-548X
    ISSN 1359-7345 ; 0009-241X
    DOI 10.1039/c4cc07129h
    Database NAL-Catalogue (AGRICOLA)

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  5. Article ; Online: Practical preparation of challenging amides from non-nucleophilic amines and esters under flow conditions.

    Vrijdag, Johannes L / Delgado, Francisca / Alonso, Nerea / De Borggraeve, Wim M / Pérez-Macias, Natalia / Alcázar, Jesus

    Chemical communications (Cambridge, England)

    2014  Volume 50, Issue 95, Page(s) 15094–15097

    Abstract: A fast and efficient protocol for the formation of amides from low nucleophilic amines and esters in flow is described. Products were obtained in good to excellent yields and with the advantage of simultaneous mixing of all reagents at once, avoiding ... ...

    Abstract A fast and efficient protocol for the formation of amides from low nucleophilic amines and esters in flow is described. Products were obtained in good to excellent yields and with the advantage of simultaneous mixing of all reagents at once, avoiding steps for intermediate formation. The protocol is also suitable to be combined with ester synthesis, resulting in the preparation of amides in-line from haloarenes.
    MeSH term(s) 4-Aminopyridine/chemistry ; Amides/chemical synthesis ; Amides/chemistry ; Esters
    Chemical Substances Amides ; Esters ; 4-Aminopyridine (BH3B64OKL9)
    Language English
    Publishing date 2014-12-11
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1472881-3
    ISSN 1364-548X ; 1359-7345 ; 0009-241X
    ISSN (online) 1364-548X
    ISSN 1359-7345 ; 0009-241X
    DOI 10.1039/c4cc07129h
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Cannabinoid agonists showing BuChE inhibition as potential therapeutic agents for Alzheimer's disease.

    González-Naranjo, Pedro / Pérez-Macias, Natalia / Campillo, Nuria E / Pérez, Concepción / Arán, Vicente J / Girón, Rocio / Sánchez-Robles, Eva / Martín, María Isabel / Gómez-Cañas, María / García-Arencibia, Moisés / Fernández-Ruiz, Javier / Páez, Juan A

    European journal of medicinal chemistry

    2014  Volume 73, Page(s) 56–72

    Abstract: Designing drugs with a specific multi-target profile is a promising approach against multifactorial illnesses as Alzheimer's disease. In this work, new indazole ethers that possess dual activity as both cannabinoid agonists CB2 and inhibitors of BuChE ... ...

    Abstract Designing drugs with a specific multi-target profile is a promising approach against multifactorial illnesses as Alzheimer's disease. In this work, new indazole ethers that possess dual activity as both cannabinoid agonists CB2 and inhibitors of BuChE have been designed by computational methods. On the basis of this knowledge, the synthesis, pharmacological evaluation and docking studies of a new class of indazoles has been performed. Pharmacological evaluation includes radioligand binding assays with [(3)H]-CP55940 for CB1R and CB2R and functional activity for cannabinoid receptors on isolated tissue. Additionally, in vitro inhibitory assays of AChE/BuChE and the corresponding competition studies have been carried out. The results of pharmacological tests have revealed that three of these derivatives behave as CB2 cannabinoid agonists and simultaneously show BuChE inhibition. In particular, compounds 3 and 24 have emerged as promising candidates as novel cannabinoids that inhibit BuChE by a non-competitive or mixed mechanism, respectively. On the other hand, both molecules show antioxidant properties.
    MeSH term(s) Alzheimer Disease/drug therapy ; Animals ; Butyrylcholinesterase/metabolism ; Cannabinoid Receptor Agonists/chemical synthesis ; Cannabinoid Receptor Agonists/chemistry ; Cannabinoid Receptor Agonists/pharmacology ; Cannabinoid Receptor Agonists/therapeutic use ; Cholinesterase Inhibitors/chemical synthesis ; Cholinesterase Inhibitors/chemistry ; Cholinesterase Inhibitors/pharmacology ; Cholinesterase Inhibitors/therapeutic use ; Computational Biology ; Drug Design ; Horses ; Humans ; Indazoles/chemical synthesis ; Indazoles/chemistry ; Indazoles/pharmacology ; Indazoles/therapeutic use ; Ligands ; Molecular Docking Simulation ; Molecular Structure ; Radioligand Assay ; Receptor, Cannabinoid, CB1/agonists ; Receptor, Cannabinoid, CB2/agonists
    Chemical Substances Cannabinoid Receptor Agonists ; Cholinesterase Inhibitors ; Indazoles ; Ligands ; Receptor, Cannabinoid, CB1 ; Receptor, Cannabinoid, CB2 ; Butyrylcholinesterase (EC 3.1.1.8)
    Language English
    Publishing date 2014-02-12
    Publishing country France
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 188597-2
    ISSN 1768-3254 ; 0009-4374 ; 0223-5234
    ISSN (online) 1768-3254
    ISSN 0009-4374 ; 0223-5234
    DOI 10.1016/j.ejmech.2013.11.026
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Encoded library technology as a source of hits for the discovery and lead optimization of a potent and selective class of bactericidal direct inhibitors of Mycobacterium tuberculosis InhA.

    Encinas, Lourdes / O'Keefe, Heather / Neu, Margarete / Remuiñán, Modesto J / Patel, Amish M / Guardia, Ana / Davie, Christopher P / Pérez-Macías, Natalia / Yang, Hongfang / Convery, Maire A / Messer, Jeff A / Pérez-Herrán, Esther / Centrella, Paolo A / Alvarez-Gómez, Daniel / Clark, Matthew A / Huss, Sophie / O'Donovan, Gary K / Ortega-Muro, Fátima / McDowell, William /
    Castañeda, Pablo / Arico-Muendel, Christopher C / Pajk, Stane / Rullás, Joaquín / Angulo-Barturen, Iñigo / Alvarez-Ruíz, Emilio / Mendoza-Losana, Alfonso / Ballell Pages, Lluís / Castro-Pichel, Julia / Evindar, Ghotas

    Journal of medicinal chemistry

    2014  Volume 57, Issue 4, Page(s) 1276–1288

    Abstract: Tuberculosis (TB) is one of the world's oldest and deadliest diseases, killing a person every 20 s. InhA, the enoyl-ACP reductase from Mycobacterium tuberculosis, is the target of the frontline antitubercular drug isoniazid (INH). Compounds that directly ...

    Abstract Tuberculosis (TB) is one of the world's oldest and deadliest diseases, killing a person every 20 s. InhA, the enoyl-ACP reductase from Mycobacterium tuberculosis, is the target of the frontline antitubercular drug isoniazid (INH). Compounds that directly target InhA and do not require activation by mycobacterial catalase peroxidase KatG are promising candidates for treating infections caused by INH resistant strains. The application of the encoded library technology (ELT) to the discovery of direct InhA inhibitors yielded compound 7 endowed with good enzymatic potency but with low antitubercular potency. This work reports the hit identification, the selected strategy for potency optimization, the structure-activity relationships of a hundred analogues synthesized, and the results of the in vivo efficacy studies performed with the lead compound 65.
    MeSH term(s) Antitubercular Agents/pharmacology ; Bacterial Proteins/antagonists & inhibitors ; Drug Discovery ; Magnetic Resonance Spectroscopy ; Microbial Sensitivity Tests ; Mycobacterium tuberculosis/drug effects ; Mycobacterium tuberculosis/metabolism ; Oxidoreductases/antagonists & inhibitors ; Spectrometry, Mass, Electrospray Ionization
    Chemical Substances Antitubercular Agents ; Bacterial Proteins ; Oxidoreductases (EC 1.-) ; InhA protein, Mycobacterium (EC 1.3.1.9)
    Language English
    Publishing date 2014-02-27
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 218133-2
    ISSN 1520-4804 ; 0022-2623
    ISSN (online) 1520-4804
    ISSN 0022-2623
    DOI 10.1021/jm401326j
    Database MEDical Literature Analysis and Retrieval System OnLINE

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