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1Academic Journal
المؤلفون: Olaya, María del Pilar, Vergel, Nadezdha Esperanza, López, Jose Luis, Viña, Dolores, Guerrero, Mario Francisco
المصدر: Brazilian Journal of Pharmaceutical Sciences. January 2020 56
مصطلحات موضوعية: Parkinson’s disease, Monoamine oxidase B, Coumarin, Mice, Reserpine, Levodopa, Carbidopa
وصف الملف: text/html
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2Academic Journal
المصدر: Revista Colombiana de Ciencias Químico-Farmacéuticas; Vol. 38 Núm. 1 (2009) ; Revista Colombiana de Ciencias Químico-Farmacéuticas; v. 38 n. 1 (2009) ; Revista Colombiana de Ciencias Químico-Farmacéuticas; Vol. 38 No. 1 (2009) ; 1909-6356 ; 0034-7418
مصطلحات موضوعية: Hot Plate, Acetic acid induced writhing, Formalin Test, Physalis peruviana, Critoniella acuminata, Salvia rubescens, Placa caliente, formalina, contorsiones abdominales
وصف الملف: application/pdf; text/html
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3Academic Journal
المؤلفون: Rodriguez, Marisol, Vergel, Nadezdha, Ospina, Luis, Calle, Jairo, Pizón, Roberto
المصدر: Revista Colombiana de Ciencias Químico-Farmacéuticas; Vol. 34 Núm. 1 (2005) ; Revista Colombiana de Ciencias Químico-Farmacéuticas; v. 34 n. 1 (2005) ; Revista Colombiana de Ciencias Químico-Farmacéuticas; Vol. 34 No. 1 (2005) ; 1909-6356 ; 0034-7418
مصطلحات موضوعية: Elastase – myeloperoxidase - amarisolide – arbutin – ayapin - Critoniella acuminata -Physalis peruviana - Salvia rubescens, Elastasa – mieloperoxidasa - amarisolide – arbutina – ayapín - Critoniella acuminata - Physalis peruviana - Salvia rubescens
وصف الملف: application/pdf
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4Academic Journal
المؤلفون: Rodriguez, Marisol, Vergel, Nadezdha, Ospina, Luis, Calle, Jairo, Pizón, Roberto
وصف الملف: application/pdf
Relation: http://revistas.unal.edu.co/index.php/rccquifa/article/view/1614; Universidad Nacional de Colombia Revistas electrónicas UN Revista Colombiana de Ciencias Químico Farmacéuticas; Revista Colombiana de Ciencias Químico Farmacéuticas; Revista Colombiana de Ciencias Químico Farmacéuticas; Vol. 34, núm. 1 (2005) 0034-7418 1909-6356; Rodriguez, Marisol and Vergel, Nadezdha and Ospina, Luis and Calle, Jairo and Pizón, Roberto (2005) Evaluación de actividades enzimáticas elastasa y mieloperoxidasa como marcadores de desgranulación leucocitaria en modelos de inflamación aguda. Revista Colombiana de Ciencias Químico Farmacéuticas; Vol. 34, núm. 1 (2005) 0034-7418 1909-6356 .; https://repositorio.unal.edu.co/handle/unal/22884; http://bdigital.unal.edu.co/13919/
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5Electronic Resource
المؤلفون: Universidade de Santiago de Compostela. Centro de Investigación en Medicina Molecular e Enfermidades Crónicas, Universidade de Santiago de Compostela. Departamento de Farmacoloxía, Farmacia e Tecnoloxía Farmacéutica, Pilar Olaya, María del, Vergel, Nadezdha Esperanza, López, Jose Luis, Viña Castelao, María Dolores
مصطلحات الفهرس: Parkinson’s disease, Monoamine oxidase B, Coumarin, Mice, Reserpine, Levodopa, Carbidopa, journal article
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6Academic Journal
المؤلفون: Olaya, María del Pilar, Vergel, Nadezdha Esperanza, López, José Luis, Viña, María Dolores, Guerrero, Mario Francisco
المصدر: Biomedica; Vol. 39 No. 3 (2019); 491-501 ; Biomédica; Vol. 39 Núm. 3 (2019); 491-501 ; 2590-7379 ; 0120-4157
مصطلحات موضوعية: Parkinson’s disease, monoamine oxidase, coumarins, models, animal, reserpine, levodopa, haloperidol, antioxidants, enfermedad de Parkinson, monoaminooxidasa, cumarinas, modelos animales, reserpina, antioxidantes
وصف الملف: application/pdf; text/xml
Relation: https://revistabiomedica.org/index.php/biomedica/article/view/4299/4139; https://revistabiomedica.org/index.php/biomedica/article/view/4299/4413; Elbaz A, Carcaillon L, Kab S, Moisan F. Epidemiology of Parkinson’s disease. Rev Neurol (Paris). 2016;172:14-26. https://doi.org/10.1016/j.neurol.2015.09.012; Dorsey ER, Constantinescu R, Thompson JP, Biglan KM, Holloway RG, Kieburtz K, et al. Projected number of people with Parkinson disease in the most populous nations, 2005 through 2030. Neurology. 2007;68:384-6. https://doi.org/10.1212/01.wnl.0000247740.47667.03; Connolly BS, Lang AE. Pharmacological treatment of Parkinson disease: A review. JAMA. 2014; 311:1670-83. https://doi.org/10.1001/jama.2014.3654; Alexi T, Borlongan C, Faull R, Williams C, Clark R, Gluckman P, et al. Neuroprotective strategies for basal ganglia degeneration: Parkinson’s and Huntington’s diseases. Prog Neurobiol. 2000;60:409-70. https://doi.org/10.1016/S0301-0082(99)00032-5; Emborg M. Evaluation of animal models of Parkinson’s disease for neuroprotective strategies. J Neurosci Methods. 2004;139:121-43. https://doi.org/10.1016/j.jneumeth.2004.08.004; Gershanik OS. Improving L-dopa therapy: The development of enzyme inhibitors. Mov Disord. 2015;30:103-13. https://doi.org/10.1002/mds.26050; Finberg J. Update on the pharmacology of selective inhibitors of MAO-A and MAO-B; focus on modulation of CNS monoamine neurotransmitter release. Pharmacol Ther. 2014;143:133-52. https://doi.org/10.1016/j.pharmthera.2014.02.010; Ariza S, Rueda D, Rincón J, Linares E, Guerrero M. Efectos farmacológicos sobre el sistema nervioso central inducidos por cumarina aislada de Hygrophila tyttha Leonard. Vitae. 2007;14:51-8.; Vergel N, López J, Orallo F, Viña D, Buitrago D, Olmo E, et al. Antidepressant-like profile and MAO-A inhibitory activity of 4-propyl-2H-benzo[h]- chromen-2-one. Life Sci. 2010;86:819-24. https://doi.org/10.1016/j.lfs.2010.04.001; Matos M, Viña D, Picciau C, Orallo F, Santana L, Uriarte E. Synthesis and evaluation of 6-methyl-3-phenylcoumarins as potent and selective MAO-B inhibitors. Bioorg Med Chem Lett. 2009;19:5053-5. https://doi.org/10.1016/j.bmcl.2009.07.039; Matos M, Viña D, Quezada E, Picciau C, Delogu G, Orallo F, et al. A new series of 3-phenylcoumarins as potent and selective MAO-B inhibitors. Bioorg Med Chem Lett. 2009;19:3268-70. https://doi.org/10.1016/j.bmcl.2009.04.085; Matos M, Viña D, Janeiro P, Borges F, Santana L, Uriarte E. New halogenated 3-phenylcoumarins as potent and selective MAO-B inhibitors. Bioorg Med Chem Lett. 2010;20:5157-60. https://doi.org/10.1016/j.bmcl.2010.07.013; Matos M, Viña D, Vázquez-Rodríguez S, Uriarte E, Santana L. Focusing on new monoamine oxidase inhibitors: Differently substituted coumarins as an interesting scaffold. Curr Top Med Chem. 2012;12:2210-39. https://doi.org/10.2174/1568026611212200008; Matos M, Vilar S, González-Franco R, Uriarte E, Santana L, Friedman C, et al. Novel (coumarin-3-yl) carbamates as selective MAO-B inhibitors: Synthesis, in vitro and in vivo assays, theoretical evaluation of ADME properties and docking study. Eur J Med Chem. 2013;63:151-61. https://doi.org/10.1016/j.ejmech.2013.02.009; Pisani L, Farina R, Nicolotti O, Gadaleta D, Soto-Otero R, Catto M, et al. In silico design of novel 2H-chromen-2-one derivatives as potent and selective MAO-B inhibitors. Eur J Med Chem. 2015;89:98-105. https://doi.org/10.1016/j.ejmech.2014.10.029; Epifano F, Molinaro G, Genovese S, Ngomba R, Nicoletti F, Curini M. Neuroprotective effect of prenyloxycoumarins from edible vegetables. Neurosci Lett. 2008;443:57-60. https://doi.org/10.1016/j.neulet.2008.07.062; Liu WB, Zhou J, Qu Y, Li X, Lu CT, Xie KL, et al. Neuroprotective effect of osthole on MPP+-induced cytotoxicity in PC12 cells via inhibition of mitochondrial dysfunction and ROS production. Neurochem Int. 2010;57:203-15. https://doi.org/10.1016/j.neuint.2010.05.011; Philippens I. Non-human primate models for Parkinson’s disease. Drug Discov Today Dis Models. 2008;5:105-11. https://doi.org/10.1016/j.ddmod.2008.06.004; Matos M, Rodríguez F, Borges F, Santana L, Uriarte E, Estrada M, et al. 3-Amidocoumarins as potential multifunctional agents against neurodegenerative diseases. Chem Med Chem. 2015;10:2071-9. https://doi.org/10.1002/cmdc.201500408; Aguirre P, García O, Tapia V, Muñoz Y, Cassels BK, Núñez MT. Neuroprotective effect of a new 7,8-dihydroxycoumarin-based Fe2+/Cu2+ chelator in cell and animal models of Parkinson’s disease. ACS Chem Neurosci. 2017;8:178-85. https://doi.org/10.1021/acschemneuro.6b00309; Reglodi D, Renaud J, Tamas A, Tizabi Y, Socías SB, Del-Bel E, et al. Novel tactics for neuroprotection in Parkinson’s disease: Role of antibiotics, polyphenols and neuropeptides. Prog Neurobiol. 2017;155:120-48. https://doi.org/10.1016/j.pneurobio.2015.10.004; Garazd M, Garazd Y, Ogorodniichuk A, Khilya V. Modified coumarins. Synthesis of substituted 5-(4-methoxyphenyl)-7H-furo [3,2-g] chromen-7-ones. Chem Nat Compd. 2002;38:539-48. https://doi.org/10.1023/A:1022626402415; National Center for Biotechnology Information. PubChem Open Chemistry Database Compound Summary for CID 608273. Accessed on: January 20, 2018. Available at: https://pubchem.ncbi.nlm.nih.gov/compound/608273; Tadaiesky M, Andreatini R, Vital M. Different effects of 7-nitroindazole in reserpine-induced hypolocomotion in two strains of mice. Eur J Pharmacol. 2006;535:199-207. https://doi.org/10.1016/j.ejphar.2006.02.004; Schmidt W, Mayerhofer A, Meyer A, Kovar K. Ecstasy counteracts catalepsy in rats, an antiparkinsonian effect? Neurosci Lett. 2002;330:251-4.; Wei L, Chen L. Effects of 5-HT in globus pallidus on haloperidol-induced catalepsy in rats. Neurosci Lett. 2009;454:49-52. https://doi.org/10.1016/j.neulet.2009.02.053; Hijova E, Nistiar F, Sipulova A. Changes in ascorbic acid and malondialdehyde in rats after exposure to mercury. Bratis Lek Listy. 2005;106:248-51.; Levine R, Garland D, Oliver C, Amici A, Climent I, Lenz A, et al. Determination of carbonyl content in oxidatively modified proteins. Methods Enzymol. 1990;186:464-78. https://doi.org/10.1016/0076-6879(90)86141-H; Baltacioglu E, Akalin FA, Alver A, Deger O, Karabulut E. Protein carbonyl levels in serum and gingival crevicular fluid in patients with chronic periodontitis. Arch Oral Biol. 2008;53:716-22. https://doi.org/10.1016/j.archoralbio.2008.02.002; Yáñez M, Fraiz N, Cano E, Orallo F. Inhibitory effects of cis- and trans-resveratrol on noradrenaline and 5-hydroxytryptamine uptake and on monoamine oxidase activity. Biochem Biophys Res Commun. 2006;344:688-95. https://doi.org/10.1016/j.bbrc.2006.03.190; Colpaert F. Pharmacological characteristics of tremor, rigidity and hypokinesia induced by reserpine in rats. Neuropharmacology. 1987;26:1431-40.; Kaur S, Starr M. Antiparkinsonian action of dextramethorphan in the reserpine-treated mouse. Eur J Pharmacol. 1995;280:159-66.; Menzaghi F, Whelan K, Risbrough V, Rao T, Lloyd G. Interactions between a novel cholinergic ion channel agonist, SIB-1765F and L-DOPA in the reserpine model of Parkinson’s disease in rats. J. Pharmacol Exp Ther. 1997;280:393-401.; Foley P, Gerlach M, Youdim M, Riederer P. MAO-B inhibitors: Multiple roles in the therapy of neurodegenerative disorders? Parkinsonism Relat Disord. 2000;6;25-47. https://doi.org/10.1016/S1353-8020(99)00043-7; Fernández H, Chen J. Monoamine oxidase-B inhibition in the treatment of Parkinson’s disease. Pharmacotherapy. 2007;27:174S-85S. https://doi.org/10.1592/phco.27.12part2.174S; Fisher A, Biggs C, Eradiri O, Starr M. Dual effects of L-3,4-dihydroxyphenylalanine on aromatic L-amino acid decarboxylase, dopamine release and motor stimulation in the reserpine-treated rat: Evidence that behavior is dopamine independent. Neuroscience. 2000;95:97-111. https://doi.org/10.1016/S0306-4522(99)00406-6; Haleem DJ, Inam QU, Haleem MA. Effects of clinically relevant doses of methyphenidate on spatial memory, behavioral sensitization and open field habituation: A time related study. Behav Brain Res. 2015;281:208-14. https://doi.org/10.1016/j.bbr.2014.12.031; Deacon RM, Koros E, Bornemann KD, Rawlins JN. Aged Tg2576 mice are impaired on social memory and open field habituation tests. Behav Brain Res. 2009;197:466-8. https://doi.org/10.1016/j.bbr.2008.09.042; Wang X, Han C, Xu Y, Wu K, Chen S, Hu M, et al. Synthesis and evaluation of phenylxanthine derivatives as potential dual A2AR antagonists/MAO-B inhibitors for Parkinson’s disease. Molecules. 2017;22:1-13. https://doi.org/10.3390/molecules22061010; Duty S, Jenner P. Animal models of Parkinson´s disease: A source of novel treatments and clues to the cause of the disease. Br J Pharmacol. 2011;164:1357-91. https://doi.org/10.1111/j.1476-5381.2011.01426.x; Bishnoi M, Chopra K, Kulkarni S. Involvement of adenosinergic receptor system in an animal model of tardive dyskinesia and associated behavioural, biochemical and neurochemical changes. Eur J Pharmacol. 2006;552:55-66. https://doi.org/10.1016/j.ejphar.2006.09.010; Bishnoi M, Chopra K, Kulkarni S. Possible anti-oxidant and neuroprotective mechanisms of zolpidem in attenuating typical anti-psychotic-induced orofacial dyskinesia -A biochemical and neurochemical study. Prog Neuropsychopharmacol Biol Psychiatry. 2007;31:1130-8. https://doi.org/10.1016/j.pnpbp.2007.04.007; Martins M, Petronilho F, Gomes K, Dai-Pizzol F, Streck E, Quevedo J. Antipsychotic induced oxidative stress in rat brain. Neurotox Res. 2008;13:63-9. https://doi.org/10.1007/BF03033368; Naidu P, Singh A, Kulkarni S. Quercetin, a bioflavonoid attenuated haloperidol induced orofacial dyskinesia. Neuropharmacology. 2003;44:1100-6. https://doi.org/10.1016/S0028-3908(03)00101-1; Singh A, Naidu P, Kulkarni S. Possible antioxidant and neuroprotective mechanisms of FK506 in attenuating haloperidol-induced orofacial dyskinesia. Eur J Pharmacol. 2003;477:87-94. https://doi.org/10.1016/S0014-2999(03)02124-1; Pavshintsev VV, Podshivalova LS, Frolova OY, Belopolskaya OA, Averina OA, Kushnir EA, et al. Effects of mitochondrial antioxidant SkQ1 on biochemical and behavioural parameters in a Parkinsonism model in mice. Biochemistry (Mosc). 2003;82:1513-20. https://doi.org/10.1134/S0006297917120100; Molina-Jiménez M F, Sánchez-Reus M I, Benedi J. Effect of fraxetin and myricetin on rotenone-induced cytotoxicity in SH-SY5Y cells: Comparison with N-acetylcysteine. Eur J Pharmacol. 2003;472:81-7. https://doi.org/10.1016/S0014-2999(03)01902-2; Kong LD, Tan RX, Woo AY, Cheng CH. Inhibition of rat brain monoamine oxidase activities by psoralen and isopsoralen: Implications for the treatment of affective disorders. Pharmacol Toxicol. 2001;88:75-80.; https://revistabiomedica.org/index.php/biomedica/article/view/4299
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7Electronic Resource
Additional Titles: El análogo de cumarina 3-metil-7H-furo[3,2-g]cromen-7-ona, un posible agente antiparkinsoniano
المؤلفون: Olaya, María del Pilar, Vergel, Nadezdha Esperanza, López, José Luis, Viña, María Dolores, Guerrero, Mario Francisco
المصدر: Biomedica; Vol. 39 No. 3 (2019); 491-501; Biomédica; Vol. 39 Núm. 3 (2019); 491-501; 2590-7379; 0120-4157
مصطلحات الفهرس: Parkinson’s disease, monoamine oxidase, coumarins, models, animal, reserpine, levodopa, haloperidol, antioxidants, enfermedad de Parkinson, monoaminooxidasa, cumarinas, modelos animales, reserpina, antioxidantes, info:eu-repo/semantics/article, info:eu-repo/semantics/publishedVersion
URL:
https://revistabiomedica.org/index.php/biomedica/article/view/4299 https://revistabiomedica.org/index.php/biomedica/article/view/4299/4139 https://revistabiomedica.org/index.php/biomedica/article/view/4299/4413 https://revistabiomedica.org/index.php/biomedica/article/view/4299/4139 https://revistabiomedica.org/index.php/biomedica/article/view/4299/4413
*ref*/Elbaz A, Carcaillon L, Kab S, Moisan F. Epidemiology of Parkinson’s disease. Rev Neurol (Paris). 2016;172:14-26. https://doi.org/10.1016/j.neurol.2015.09.012
*ref*/Dorsey ER, Constantinescu R, Thompson JP, Biglan KM, Holloway RG, Kieburtz K, et al. Projected number of people with Parkinson disease in the most populous nations, 2005 through 2030. Neurology. 2007;68:384-6. https://doi.org/10.1212/01.wnl.0000247740.47667.03
*ref*/Connolly BS, Lang AE. Pharmacological treatment of Parkinson disease: A review. JAMA. 2014; 311:1670-83. https://doi.org/10.1001/jama.2014.3654
*ref*/Alexi T, Borlongan C, Faull R, Williams C, Clark R, Gluckman P, et al. Neuroprotective strategies for basal ganglia degeneration: Parkinson’s and Huntington’s diseases. Prog Neurobiol. 2000;60:409-70. https://doi.org/10.1016/S0301-0082(99)00032-5
*ref*/Emborg M. Evaluation of animal models of Parkinson’s disease for neuroprotective strategies. J Neurosci Methods. 2004;139:121-43. https://doi.org/10.1016/j.jneumeth.2004.08.004
*ref*/Gershanik OS. Improving L-dopa therapy: The development of enzyme inhibitors. Mov Disord. 2015;30:103-13. https://doi.org/10.1002/mds.26050
*ref*/Finberg J. Update on the pharmacology of selective inhibitors of MAO-A and MAO-B; focus on modulation of CNS monoamine neurotransmitter release. Pharmacol Ther. 2014;143:133-52. https://doi.org/10.1016/j.pharmthera.2014.02.010
*ref*/Ariza S, Rueda D, Rincón J, Linares E, Guerrero M. Efectos farmacológicos sobre el sistema nervioso central inducidos por cumarina aislada de Hygrophila tyttha Leonard. Vitae. 2007;14:51-8.
*ref*/Vergel N, López J, Orallo F, Viña D, Buitrago D, Olmo E, et al. Antidepressant-like profile and MAO-A inhibitory activity of 4-propyl-2H-benzo[h]- chromen-2-one. Life Sci. 2010;86:819-24. https://doi.org/10.1016/j.lfs.2010.04.001
*ref*/Matos M, Viña D, Picciau C, Orallo F, Santana L, Uriarte E. Synthesis and evaluation of 6-methyl-3-phenylcoumarins as potent and selective MAO-B inhibitors. Bioorg Med Chem Lett. 2009;19:5053-5. https://doi.org/10.1016/j.bmcl.2009.07.039
*ref*/Matos M, Viña D, Quezada E, Picciau C, Delogu G, Orallo F, et al. A new series of 3-phenylcoumarins as potent and selective MAO-B inhibitors. Bioorg Med Chem Lett. 2009;19:3268-70. https://doi.org/10.1016/j.bmcl.2009.04.085
*ref*/Matos M, Viña D, Janeiro P, Borges F, Santana L, Uriarte E. New halogenated 3-phenylcoumarins as potent and selective MAO-B inhibitors. Bioorg Med Chem Lett. 2010;20:5157-60. https://doi.org/10.1016/j.bmcl.2010.07.013
*ref*/Matos M, Viña D, Vázquez-Rodríguez S, Uriarte E, Santana L. Focusing on new monoamine oxidase inhibitors: Differently substituted coumarins as an interesting scaffold. Curr Top Med Chem. 2012;12:2210-39. https://doi.org/10.2174/1568026611212200008
*ref*/Matos M, Vilar S, González-Franco R, Uriarte E, Santana L, Friedman C, et al. Novel (coumarin-3-yl) carbamates as selective MAO-B inhibitors: Synthesis, in vitro and in vivo assays, theoretical evaluation of ADME properties and docking study. Eur J Med Chem. 2013;63:151-61. https://doi.org/10.1016/j.ejmech.2013.02.009
*ref*/Pisani L, Farina R, Nicolotti O, Gadaleta D, Soto-Otero R, Catto M, et al. In silico design of novel 2H-chromen-2-one derivatives as potent and selective MAO-B inhibitors. Eur J Med Chem. 2015;89:98-105. https://doi.org/10.1016/j.ejmech.2014.10.029
*ref*/Epifano F, Molinaro G, Genovese S, Ngomba R, Nicoletti F, Curini M. Neuroprotective effect of prenyloxycoumarins from edible vegetables. Neurosci Lett. 2008;443:57-60. https://doi.org/10.1016/j.neulet.2008.07.062
*ref*/Liu WB, Zhou J, Qu Y, Li X, Lu CT, Xie KL, et al. Neuroprotective effect of osthole on MPP+-induced cytotoxicity in PC12 cells via inhibition of mitochondrial dysfunction and ROS production. Neurochem Int. 2010;57:203-15. https://doi.org/10.1016/j.neuint.2010.05.011
*ref*/Philippens I. Non-human primate models for Parkinson’s disease. Drug Discov Today Dis Models. 2008;5:105-11. https://doi.org/10.1016/j.ddmod.2008.06.004
*ref*/Matos M, Rodríguez F, Borges F, Santana L, Uriarte E, Estrada M, et al. 3-Amidocoumarins as potential multifunctional agents against neurodegenerative diseases. Chem Med Chem. 2015;10:2071-9. https://doi.org/10.1002/cmdc.201500408
*ref*/Aguirre P, García O, Tapia V, Muñoz Y, Cassels BK, Núñez MT. Neuroprotective effect of a new 7,8-dihydroxycoumarin-based Fe2+/Cu2+ chelator in cell and animal models of Parkinson’s disease. ACS Chem Neurosci. 2017;8:178-85. https://doi.org/10.1021/acschemneuro.6b00309
*ref*/Reglodi D, Renaud J, Tamas A, Tizabi Y, Socías SB, Del-Bel E, et al. Novel tactics for neuroprotection in Parkinson’s disease: Role of antibiotics, polyphenols and neuropeptides. Prog Neurobiol. 2017;155:120-48. https://doi.org/10.1016/j.pneurobio.2015.10.004
*ref*/Garazd M, Garazd Y, Ogorodniichuk A, Khilya V. Modified coumarins. Synthesis of substituted 5-(4-methoxyphenyl)-7H-furo [3,2-g] chromen-7-ones. Chem Nat Compd. 2002;38:539-48. https://doi.org/10.1023/A:1022626402415
*ref*/National Center for Biotechnology Information. PubChem Open Chemistry Database Compound Summary for CID 608273. Accessed on: January 20, 2018. Available at: https://pubchem.ncbi.nlm.nih.gov/compound/608273
*ref*/Tadaiesky M, Andreatini R, Vital M. Different effects of 7-nitroindazole in reserpine-induced hypolocomotion in two strains of mice. Eur J Pharmacol. 2006;535:199-207. https://doi.org/10.1016/j.ejphar.2006.02.004
*ref*/Schmidt W, Mayerhofer A, Meyer A, Kovar K. Ecstasy counteracts catalepsy in rats, an antiparkinsonian effect? Neurosci Lett. 2002;330:251-4.
*ref*/Wei L, Chen L. Effects of 5-HT in globus pallidus on haloperidol-induced catalepsy in rats. Neurosci Lett. 2009;454:49-52. https://doi.org/10.1016/j.neulet.2009.02.053
*ref*/Hijova E, Nistiar F, Sipulova A. Changes in ascorbic acid and malondialdehyde in rats after exposure to mercury. Bratis Lek Listy. 2005;106:248-51.
*ref*/Levine R, Garland D, Oliver C, Amici A, Climent I, Lenz A, et al. Determination of carbonyl content in oxidatively modified proteins. Methods Enzymol. 1990;186:464-78. https://doi.org/10.1016/0076-6879(90)86141-H
*ref*/Baltacioglu E, Akalin FA, Alver A, Deger O, Karabulut E. Protein carbonyl levels in serum and gingival crevicular fluid in patients with chronic periodontitis. Arch Oral Biol. 2008;53:716-22. https://doi.org/10.1016/j.archoralbio.2008.02.002
*ref*/Yáñez M, Fraiz N, Cano E, Orallo F. Inhibitory effects of cis- and trans-resveratrol on noradrenaline and 5-hydroxytryptamine uptake and on monoamine oxidase activity. Biochem Biophys Res Commun. 2006;344:688-95. https://doi.org/10.1016/j.bbrc.2006.03.190
*ref*/Colpaert F. Pharmacological characteristics of tremor, rigidity and hypokinesia induced by reserpine in rats. Neuropharmacology. 1987;26:1431-40.
*ref*/Kaur S, Starr M. Antiparkinsonian action of dextramethorphan in the reserpine-treated mouse. Eur J Pharmacol. 1995;280:159-66.
*ref*/Menzaghi F, Whelan K, Risbrough V, Rao T, Lloyd G. Interactions between a novel cholinergic ion channel agonist, SIB-1765F and L-DOPA in the reserpine model of Parkinson’s disease in rats. J. Pharmacol Exp Ther. 1997;280:393-401.
*ref*/Foley P, Gerlach M, Youdim M, Riederer P. MAO-B inhibitors: Multiple roles in the therapy of neurodegenerative disorders? Parkinsonism Relat Disord. 2000;6;25-47. https://doi.org/10.1016/S1353-8020(99)00043-7
*ref*/Fernández H, Chen J. Monoamine oxidase-B inhibition in the treatment of Parkinson’s disease. Pharmacotherapy. 2007;27:174S-85S. https://doi.org/10.1592/phco.27.12part2.174S
*ref*/Fisher A, Biggs C, Eradiri O, Starr M. Dual effects of L-3,4-dihydroxyphenylalanine on aromatic L-amino acid decarboxylase, dopamine release and motor stimulation in the reserpine-treated rat: Evidence that behavior is dopamine independent. Neuroscience. 2000;95:97-111. https://doi.org/10.1016/S0306-4522(99)00406-6
*ref*/Haleem DJ, Inam QU, Haleem MA. Effects of clinically relevant doses of methyphenidate on spatial memory, behavioral sensitization and open field habituation: A time related study. Behav Brain Res. 2015;281:208-14. https://doi.org/10.1016/j.bbr.2014.12.031
*ref*/Deacon RM, Koros E, Bornemann KD, Rawlins JN. Aged Tg2576 mice are impaired on social memory and open field habituation tests. Behav Brain Res. 2009;197:466-8. https://doi.org/10.1016/j.bbr.2008.09.042
*ref*/Wang X, Han C, Xu Y, Wu K, Chen S, Hu M, et al. Synthesis and evaluation of phenylxanthine derivatives as potential dual A2AR antagonists/MAO-B inhibitors for Parkinson’s disease. Molecules. 2017;22:1-13. https://doi.org/10.3390/molecules22061010
*ref*/Duty S, Jenner P. Animal models of Parkinson´s disease: A source of novel treatments and clues to the cause of the disease. Br J Pharmacol. 2011;164:1357-91. https://doi.org/10.1111/j.1476-5381.2011.01426.x
*ref*/Bishnoi M, Chopra K, Kulkarni S. Involvement of adenosinergic receptor system in an animal model of tardive dyskinesia and associated behavioural, biochemical and neurochemical changes. Eur J Pharmacol. 2006;552:55-66. https://doi.org/10.1016/j.ejphar.2006.09.010
*ref*/Bishnoi M, Chopra K, Kulkarni S. Possible anti-oxidant and neuroprotective mechanisms of zolpidem in attenuating typical anti-psychotic-induced orofacial dyskinesia -A biochemical and neurochemical study. Prog Neuropsychopharmacol Biol Psychiatry. 2007;31:1130-8. https://doi.org/10.1016/j.pnpbp.2007.04.007
*ref*/Martins M, Petronilho F, Gomes K, Dai-Pizzol F, Streck E, Quevedo J. Antipsychotic induced oxidative stress in rat brain. Neurotox Res. 2008;13:63-9. https://doi.org/10.1007/BF03033368
*ref*/Naidu P, Singh A, Kulkarni S. Quercetin, a bioflavonoid attenuated haloperidol induced orofacial dyskinesia. Neuropharmacology. 2003;44:1100-6. https://doi.org/10.1016/S0028-3908(03)00101-1
*ref*/Singh A, Naidu P, Kulkarni S. Possible antioxidant and neuroprotective mechanisms of FK506 in attenuating haloperidol-induced orofacial dyskinesia. Eur J Pharmacol. 2003;477:87-94. https://doi.org/10.1016/S0014-2999(03)02124-1
*ref*/Pavshintsev VV, Podshivalova LS, Frolova OY, Belopolskaya OA, Averina OA, Kushnir EA, et al. Effects of mitochondrial antioxidant SkQ1 on biochemical and behavioural parameters in a Parkinsonism model in mice. Biochemistry (Mosc). 2003;82:1513-20. https://doi.org/10.1134/S0006297917120100
*ref*/Molina-Jiménez M F, Sánchez-Reus M I, Benedi J. Effect of fraxetin and myricetin on rotenone-induced cytotoxicity in SH-SY5Y cells: Comparison with N-acetylcysteine. Eur J Pharmacol. 2003;472:81-7. https://doi.org/10.1016/S0014-2999(03)01902-2
*ref*/Kong LD, Tan RX, Woo AY, Cheng CH. Inhibition of rat brain monoamine oxidase activities by psoralen and isopsoralen: Implications for the treatment of affective disorders. Pharmacol Toxicol. 2001;88:75-80. -
8Academic Journal
Alternate Title: Análogo de cumarina 3-metil-7H-furo[3,2-g]cromen-7-ona, un posible agente antiparquinsoniano.
المؤلفون: del Pilar Olaya, María1 mpolayao@unal.edu.co, Esperanza Vergel, Nadezdha1, Luis López, José2, Viña, María3, Francisco Guerrero, Mario1
المصدر: Revista Biomedica. 2019, Vol. 39 Issue 3, p2-30. 29p. 6 Graphs.
مصطلحات موضوعية: *ANTIPARKINSONIAN agents, *COUMARINS, *PARKINSON'S disease treatment, *MONOAMINE oxidase, *HALOPERIDOL
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9Academic Journal
Alternate Title: El análogo de cumarina 3-metil-7H-furo[3,2-g]cromen-7-ona, un posible agent antiparkinsoniano. (Spanish)
المؤلفون: del Pilar Olaya, María, Esperanza Vergel, Nadezdha, Luis López, José, Dolores Viña, María, Francisco Guerrero, Mario
المصدر: Biomédica: Revista del Instituto Nacional de Salud; sep2019, Vol. 39 Issue 3, p491-501, 11p
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10
المؤلفون: Giraldo, Sara E., Rincón, Javier, Guerrero, Mario F., López, Isabel, Jiménez, Ignacio, Marder, Nora Mariel, Wasowski, Cristina Lucia N., Vergel, Nadezdha E.
مصطلحات موضوعية: Otras Ciencias de la Salud, ANTICONVULSANT, CIENCIAS MÉDICAS Y DE LA SALUD, GABA A RECEPTOR, TONIC-CLONIC-EPILEPSY, Ciencias de la Salud, VALERIANA
وصف الملف: application/pdf
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11Academic Journal
المؤلفون: Giraldo, Sara Emilia, Rincón, Javier, Puebla, Pilar, Marder, Mariel, Wasowski, Cristina, Vergel, Nadezdha, Guerrero, Mario Francisco
المصدر: Biomedica; Vol. 30 No. 2 (2010); 245-50 ; Biomédica; Vol. 30 Núm. 2 (2010); 245-50 ; 2590-7379 ; 0120-4157 ; 10.7705/biomedica.v30i2
مصطلحات موضوعية: valerian, medicine, traditional, valproic acid, anticonvulsants, epilepsy, tonic-clonic, valeriana, medicina tradicional, ácido valproico, anticonvulsivos, epilepsia, epilepsia tónico-clónica
وصف الملف: application/pdf
Relation: https://revistabiomedica.org/index.php/biomedica/article/view/187/178; https://revistabiomedica.org/index.php/biomedica/article/view/187/368; Eadie MJ. Could Valerian have been the first anticonvulsant? Epilepsia. 2004;45:1338-43. 2. Houghton PJ. The scientific basis for the reputed activity of Valerian. J Pharm Pharmacol.1999;51:505-12. 3. Fernández S, Wasowski C, Paladini AC, Marder M. Sedative and sleep-enhancing properties of linarin, a flavonoid-isolated from Valeriana officinalis. Pharmacol Biochem Behav. 2004;77:399-04. 4. García H. Flora medicinal de Colombia, Botánica Médica. Instituto de Ciencias Naturales, Universidad Nacional de Colombia, Bogotá: Mundo Editores; 1992. Tomo 3. p. 254-62. 5. Arévalo D, Martínez C, Rincón J, Guerrero MF. Fracción alcaloidal obtenida de Valeriana pavonii Poepp con actividad anticonvulsivante. Rev Colomb Ciencias Quím Farm. 2006;35:168-76. 6. Célis CT, Rincón J, Guerrero MF. Actividad farmacológica sobre el sistema nervioso central del extracto etanólico y de la fracción alcaloidal de Valeriana pavonii. Rev Colomb Ciencias Quím Farm. 2007;36:11-22. 7. Pradilla G, Vesga B, León-Sarmiento F, Grupo Geneco. Estudio neuroepidemiológico nacional (EPINEURO) colombiano. Rev Panam Salud Pública. 2003;14:104-11. 8. Burneo J, Tellez-Zenteno J, Wiebe S. Understanding the burden of epilepsy in Latin America: a systematic review of its prevalence and incidence. Epilepsy Res. 2005; 66:63-74. 9. Löscher W. Current status and future directions in the pharmacotherapy of epilepsy. Trends Pharmacol Sci. 2002;23:113-8. 10. Schachter SC. Botanicals and herbs: a traditional approach to treating epilepsy. Neurotherapeutics. 2009;6:415-20. 11. Giardina WJ. Models of epilepsy: Electroshock and chemical induced convulsions in the mouse. En: Current Protocols in Pharmacology. New York: John Wiley & Sons; 2000. Volume 5. p. 1-22. 12. Wolf P. Basic principles of the ILAE syndrome classification. Epilepsy Res. 2006;70(Suppl.1):S20-6. 13. Swinyard EA, Woodhead JH. Experimental detection, quantification, and evaluation of anticonvulsants. En: Woodbury DM, Penry JK, Pippenger CE. Antiepileptic Drugs. 2nd edition. New York: Raven Press; 1982. p. 111-26. 14. Bialer M, Johannessenb SI, Kupferbergc HJ, Levyd RH, Perucca E, Tomson T. Progress report on new antiepileptic drugs: a summary of the seventh EILAT conference (EILAT VII). Epilepsy Res. 2004;61:1-48. 15. Pollard JR, French J. Antiepileptic drugs in development. Lancet Neurol. 2006;5:1064-7. 16. America´s Pharmaceutical Research Companies. Pharmaceutical companies researching and developing more than 500 medicines for neurological disorders. En: Report, medicines in development for neurological disorders. Washington, D.C.: Pharma, New Medicines, New Hope; 2008. p. 37. 17. Bialer M, Yagen B. Valproic acid: second generation. Neurotherapeutics. 2007;4:130-7. 18. Isoherranen N, Yagen B, Bialer M. New CNS-active drugs which are second-generation valproic acid: can they lead to the development of a magic bullet? Curr Opin Neurol. 2003;16:203-11. 19. Nau H, Siemens H. Differentiation between valproate-induced antiepileptic effect, teratogenicity and hepatotoxicity. Pharm Weekbl Sci. 1992;14:101-5. 20. Bucková A, Grznár K, Haladová M, Eisenreichová E. Active principles in Valeriana officinalis L. Cesk Farm. 1977;26:308-9.; https://revistabiomedica.org/index.php/biomedica/article/view/187
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12Academic Journal
المؤلفون: Vergel, Nadezdha E., López, José L., Orallo, Francisco, Viña, Dolores, Buitrago, Diana M., del Olmo, Esther, Mico, Juan A., Guerrero, Mario F.
المصدر: Life Sciences ; volume 86, issue 21-22, page 819-824 ; ISSN 0024-3205
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13
المؤلفون: OSPINA G, Luis F, ARAGÓN N, Diana M, VERGEL, Nadezdha E, ISAZA M, Gustavo, PÉREZ C, Jorge E
المصدر: Vitae, Volume: 18, Issue: 1, Pages: 49-55, Published: APR 2011
مصطلحات موضوعية: Tabebuia chrysantha, reactive oxygen species, inflammation, inflamación, Phenax rugosus, especies de oxígeno reactivas
وصف الملف: text/html
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14
المؤلفون: Giraldo, Sara Emilia, Rincón, Javier, Puebla, Pilar, Marder, Mariel, Wasowski, Cristina, Vergel, Nadezdha, Guerrero, Mario Francisco
المصدر: Biomédica, Volume: 30, Issue: 2, Pages: 245-250, Published: JUN 2010
مصطلحات موضوعية: medicina tradicional, valeriana, epilepsia tónico-clónica, valproic acid, epilepsy, tonic-clonic, anticonvulsants, epilepsy, valerian, ácido valproico, epilepsia, anticonvulsivos, medicine, traditional
وصف الملف: text/html
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15
المؤلفون: Muñoz, Carol E, Vergel, Nadezdha E, Cabral, Pablo, Aragón, Diana Marcela, Ospina, Luis Fernando
المصدر: Revista Colombiana de Ciencias Químico-Farmacéuticas, Volume: 38, Issue: 1, Pages: 31-41, Published: JAN 2009
مصطلحات موضوعية: contorsiones abdominales, Salvia rubescens, Acetic acid induced writhing, Formalin Test, Placa caliente, Hot Plate, Critoniella acuminata, Physalis peruviana, formalina
وصف الملف: text/html
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16Electronic Resource
Additional Titles: Isovaleramida, principio anticonvulsivo aislado de Valeriana pavonii
المؤلفون: Giraldo, Sara Emilia, Rincón, Javier, Puebla, Pilar, Marder, Mariel, Wasowski, Cristina, Vergel, Nadezdha, Guerrero, Mario Francisco
المصدر: Biomedica; Vol. 30 No. 2 (2010); 245-50; Biomédica; Vol. 30 Núm. 2 (2010); 245-50; 2590-7379; 0120-4157; 10.7705/biomedica.v30i2
مصطلحات الفهرس: valerian, medicine, traditional, valproic acid, anticonvulsants, epilepsy, tonic-clonic, valeriana, medicina tradicional, ácido valproico, anticonvulsivos, epilepsia, epilepsia tónico-clónica, info:eu-repo/semantics/article, info:eu-repo/semantics/publishedVersion
URL:
https://revistabiomedica.org/index.php/biomedica/article/view/187 https://revistabiomedica.org/index.php/biomedica/article/view/187/178 https://revistabiomedica.org/index.php/biomedica/article/view/187/368 https://revistabiomedica.org/index.php/biomedica/article/view/187/178 https://revistabiomedica.org/index.php/biomedica/article/view/187/368
*ref*/Eadie MJ. Could Valerian have been the first anticonvulsant? Epilepsia. 2004;45:1338-43.2. Houghton PJ. The scientific basis for the reputed activity of Valerian. J Pharm Pharmacol.1999;51:505-12.3. Fernández S, Wasowski C, Paladini AC, Marder M. Sedative and sleep-enhancing properties of linarin, a flavonoid-isolated from Valeriana officinalis. Pharmacol Biochem Behav. 2004;77:399-04.4. García H. Flora medicinal de Colombia, Botánica Médica. Instituto de Ciencias Naturales, Universidad Nacional de Colombia, Bogotá: Mundo Editores; 1992. Tomo 3. p. 254-62.5. Arévalo D, Martínez C, Rincón J, Guerrero MF. Fracción alcaloidal obtenida de Valeriana pavonii Poepp con actividad anticonvulsivante. Rev Colomb Ciencias Quím Farm. 2006;35:168-76.6. Célis CT, Rincón J, Guerrero MF. Actividad farmacológica sobre el sistema nervioso central del extracto etanólico y de la fracción alcaloidal de Valeriana pavonii. Rev Colomb Ciencias Quím Farm. 2007;36:11-22.7. Pradilla G, Vesga B, León-Sarmiento F, Grupo Geneco. Estudio neuroepidemiológico nacional (EPINEURO) colombiano. Rev Panam Salud Pública. 2003;14:104-11.8. Burneo J, Tellez-Zenteno J, Wiebe S. Understanding the burden of epilepsy in Latin America: a systematic review of its prevalence and incidence. Epilepsy Res. 2005; 66:63-74.9. Löscher W. Current status and future directions in the pharmacotherapy of epilepsy. Trends Pharmacol Sci. 2002;23:113-8.10. Schachter SC. Botanicals and herbs: a traditional approach to treating epilepsy. Neurotherapeutics. 2009;6:415-20.11. Giardina WJ. Models of epilepsy: Electroshock and chemical induced convulsions in the mouse. En: Current Protocols in Pharmacology. New York: John Wiley & Sons; 2000. Volume 5. p. 1-22.12. Wolf P. Basic principles of the ILAE syndrome classification. Epilepsy Res. 2006;70(Suppl.1):S20-6.13. Swinyard EA, Woodhead JH. Experimental detection, quantification, and evaluation of -
17Academic Journal
المؤلفون: Pilar Olaya, María del, Vergel, Nadezdha Esperanza, López, Jose Luis, Viña Castelao, María Dolores
المساهمون: Universidade de Santiago de Compostela. Centro de Investigación en Medicina Molecular e Enfermidades Crónicas, Universidade de Santiago de Compostela. Departamento de Farmacoloxía, Farmacia e Tecnoloxía Farmacéutica
مصطلحات موضوعية: Parkinson’s disease, Monoamine oxidase B, Coumarin, Mice, Reserpine, Levodopa, Carbidopa
وصف الملف: application/pdf
Relation: https://doi.org/10.1590/s2175-97902019000317609; OLAYA, María del Pilar et al. 8-Propyl-6H-[1,3]dioxolo[4,5-g]chromen-6-one: A new coumarin with monoamine oxidase B inhibitory activity and possible anti-parkinsonian effects. Braz. J. Pharm. Sci. [online]. 2020, vol.56 [cited 2020-04-23], e17609. Available from: . Epub Mar 16, 2020. ISSN 2175-9790. https://doi.org/10.1590/s2175-97902019000317609; http://hdl.handle.net/10347/21693
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18Academic Journal
المؤلفون: Giraldo, Sara E., Rincón, Javier, Guerrero, Mario F., López, Isabel, Jiménez, Ignacio, Marder, Nora Mariel, Wasowski, Cristina Lucia N., Vergel, Nadezdha E.
مصطلحات موضوعية: Anticonvulsant, Gaba a Receptor, Tonic-Clonic-Epilepsy, Valeriana, https://purl.org/becyt/ford/3.3, https://purl.org/becyt/ford/3
وصف الملف: application/pdf
Relation: info:eu-repo/semantics/altIdentifier/url/http://www.latamjpharm.org/previous_issue.php?vol=32&num=8; http://hdl.handle.net/11336/8514; Giraldo, Sara E.; Rincón, Javier; Guerrero, Mario F.; López, Isabel; Jiménez, Ignacio; et al.; Valepotriate Hydrines Isolated from an Anticonvulsant Fraction of Valeriana pavonii Poepp. & Endl; Colegio Farmaceuticos Provincia de Buenos Aires; Latin American Journal of Pharmacy; 32; 8-2013; 1224-1230
الاتاحة: http://hdl.handle.net/11336/8514
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19Academic Journal
المؤلفون: Giraldo, Sara Emilia, Bedoya, Mauricio, Peña Varas, Carlos, Santana, Paula A., Bazzocchi, Isabel L., Jiménez, Ignacio A., Marder, Nora Mariel, Vergel, Nadezdha E., Guerrero, Mario F., Ramírez, David
مصطلحات موضوعية: ENSEMBLE MOLECULAR DOCKING, GABAA MODULATORS, GABAA RECEPTOR, IRIDOIDS, VALERIAN, https://purl.org/becyt/ford/1.4, https://purl.org/becyt/ford/1
وصف الملف: application/pdf
Relation: info:eu-repo/semantics/altIdentifier/url/https://jppres.com/jppres/iridoid-esters-from-valeriana-pavonii-as-gabaa-modulators/; http://hdl.handle.net/11336/227836; Giraldo, Sara Emilia; Bedoya, Mauricio; Peña Varas, Carlos; Santana, Paula A.; Bazzocchi, Isabel L.; et al.; Iridoid esters from Valeriana pavonii Poepp. & Endl. as GABAA modulators: Structural insights in their binding mode and structure-activity relationship; Asociación Académica de Ciencias Farmacéuticas de Antofagasta; Journal of Pharmacy and Pharmacognosy Research; 11; 3; 5-2023; 367-380; CONICET Digital; CONICET
الاتاحة: http://hdl.handle.net/11336/227836
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20Academic Journal
المؤلفون: Giraldo, Sara Emilia, Rincón, Javier, Puebla, Pilar, Marder, Nora Mariel, Wasowski, Cristina Lucia N., Vergel, Nadezdha, Guerrero, Mario Francisco
مصطلحات موضوعية: Valeriana, Medicina tradicional, Ácido valproico, Anticonvulsivos, Epilepsia, Epilepsia tónico clónica, https://purl.org/becyt/ford/1.4, https://purl.org/becyt/ford/1
وصف الملف: application/pdf
Relation: info:eu-repo/semantics/altIdentifier/url/http://www.revistabiomedica.org/index.php/biomedica/article/view/187; info:eu-repo/semantics/altIdentifier/url/http://ref.scielo.org/d39vnv; http://hdl.handle.net/11336/18247; Giraldo, Sara Emilia; Rincón, Javier; Puebla, Pilar; Marder, Nora Mariel; Wasowski, Cristina Lucia N.; et al.; Isovaleramida, principio anticonvulsivo aislado de Valeriana pavonii; Instituto Nacional de Salud; Biomédica; 30; 2; 4-2010; 245-250; CONICET Digital; CONICET
الاتاحة: http://hdl.handle.net/11336/18247