3-nitropropionic acid has been researched along with Neurodegenerative Diseases in 48 studies
3-nitropropionic acid: succinate dehydrogenase inactivator; biosynthesized by FABACEAE plants from ASPARAGINE
3-nitropropanoic acid : A C-nitro compound that is propanoic acid in which one of the methyl hydrogens has been replaced by a nitro group.
Neurodegenerative Diseases: Hereditary and sporadic conditions which are characterized by progressive nervous system dysfunction. These disorders are often associated with atrophy of the affected central or peripheral nervous system structures.
Excerpt | Relevance | Reference |
---|---|---|
"Resveratrol is a naturally occurring stilbene which has shown promising results as treatment for several neurodegenerative diseases." | 7.88 | Alkylated resveratrol prodrugs and metabolites as potential therapeutics for neurodegenerative diseases. ( Adán, N; Belmonte-Reche, E; Caro, M; Delgado, M; González-Rey, E; Mateos-Martín, ML; Morales, JC; Peñalver, P, 2018) |
"Resveratrol is a naturally occurring stilbene which has shown promising results as treatment for several neurodegenerative diseases." | 3.88 | Alkylated resveratrol prodrugs and metabolites as potential therapeutics for neurodegenerative diseases. ( Adán, N; Belmonte-Reche, E; Caro, M; Delgado, M; González-Rey, E; Mateos-Martín, ML; Morales, JC; Peñalver, P, 2018) |
" The injections of MitoTracker Red CM-H(2)XRos revealed generation of mitochondrial free radicals primarily in vulnerable neurons following focal cerebral ischemia as well as administration of Fe(2+) or 3-nitropropionic acid." | 3.71 | Analysis of mitochondrial free radical generation in animal models of neuronal disease. ( Gwag, BJ; Kim, DY; Won, SJ, 2002) |
"The 3-nitropropionic acid animal model is a model where excitotoxicity, mitochondrial dysfunction and oxidative stress, mechanisms common to various neurodegenerative diseases, are involved." | 3.71 | Behavioural correlates of striatal glial fibrillary acidic protein in the 3-nitropropionic acid rat model: disturbed walking pattern and spatial orientation. ( Angevaren, M; Appels, M; de Bruijn, C; de Vente, J; Prickaerts, J; Steinbusch, HW; Teunissen, CE, 2001) |
"Creatine, however, was still neuroprotective in mice, which were deficient in mitochondrial creatine kinase." | 2.47 | Neuroprotective effects of creatine. ( Beal, MF, 2011) |
"Fluconazole was able to prevent neurite retraction and cell death in in vitro and in vivo models of toxicity." | 1.72 | Fluconazole Is Neuroprotective via Interactions with the IGF-1 Receptor. ( Bachani, M; Johnson, TP; Lee, MH; Malik, N; Nath, A; Ruffin, A; Steiner, JP; Toodle, V; Vivekanandhan, S; Wang, T, 2022) |
"Treatment with naringin ameliorated the reduced glutathione/oxidized glutathione ratio with concomitant decrease in the levels of hydroxyl radical, hydroperoxide and nitrite in 3-NP-induced rats." | 1.38 | Naringin modulates oxidative stress and inflammation in 3-nitropropionic acid-induced neurodegeneration through the activation of nuclear factor-erythroid 2-related factor-2 signalling pathway. ( Gopinath, K; Sudhandiran, G, 2012) |
"Quinolinic acid (QUIN) was used as a typical excitotoxic/pro-oxidant inducer, 3-nitropropionic acid (3-NP) was employed as a mitochondrial function inhibitor, and their combination (QUIN + 3-NP) was also evaluated in in vitro studies." | 1.36 | Antioxidant strategy to rescue synaptosomes from oxidative damage and energy failure in neurotoxic models in rats: protective role of S-allylcysteine. ( Elinos-Calderón, D; Galván-Arzate, S; Maldonado, PD; Pedraza-Chaverrí, J; Pérez-De La Cruz, V; Robledo-Arratia, Y; Santamaría, A, 2010) |
"Several human neurodegenerative disorders are characterized by the accumulation of 8-oxo-7,8-dihydroguanine (8-oxodG) in the DNA of affected neurons." | 1.35 | A role for oxidized DNA precursors in Huntington's disease-like striatal neurodegeneration. ( Bignami, M; Crescenzi, M; De Luca, G; Degan, P; Mattei, E; Meccia, E; Nakabeppu, Y; Pepponi, R; Pèzzola, A; Popoli, P; Russo, MT; Tiveron, C; Ventura, I; Zijno, A, 2008) |
"5 h after each dose were exposed to microwave radiation at a whole body averaged specific absorption rate (SAR) of 0 (sham exposure), 0." | 1.33 | Acute effects of pulsed microwaves and 3-nitropropionic acid on neuronal ultrastructure in the rat caudate-putamen. ( Phelix, CF; Seaman, RL, 2005) |
" These results indicate that antagonists of NMDA-type glutamate receptors are protective during the toxic outcome associated with mitochondrial dysfunction." | 1.33 | 3-Nitropropionic acid toxicity in hippocampus: protection through N-methyl-D-aspartate receptor antagonism. ( Bahr, BA; Baude, AS; Brown, QB; Karanian, DA; Parsons, CG, 2006) |
"Striatal gliosis induced by 3-NP treatment was prevented by (+/-)-huprine Y pretreatment, as demonstrated by the attenuation of both the increase in [(3)H]PK 11195 specific binding indicative of microgliosis and the expression of hsp27 kDa, a chaperone expressed mainly in astrocytes." | 1.32 | Neuroprotective effects of (+/-)-huprine Y on in vitro and in vivo models of excitoxicity damage. ( Camins, A; Camps, P; Canudas, AM; Jiménez, A; Muñoz-Torrero, D; Pallàs, M; Pubill, D; Sureda, FX; Verdaguer, E, 2003) |
"The precise cause of neuronal death in Huntington's disease (HD) is unknown." | 1.32 | Histone deacetylase inhibition by sodium butyrate chemotherapy ameliorates the neurodegenerative phenotype in Huntington's disease mice. ( Beesen, A; Ferrante, RJ; Hersch, SM; Kowall, NW; Kubilus, JK; Lee, J; Luthi-Carter, R; Ratan, RR; Ryu, H; Smith, K; Zucker, B, 2003) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (4.17) | 18.2507 |
2000's | 27 (56.25) | 29.6817 |
2010's | 15 (31.25) | 24.3611 |
2020's | 4 (8.33) | 2.80 |
Authors | Studies |
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El-Shamarka, ME | 1 |
El-Sahar, AE | 1 |
Saad, MA | 1 |
Assaf, N | 1 |
Sayed, RH | 1 |
Toodle, V | 1 |
Lee, MH | 1 |
Bachani, M | 1 |
Ruffin, A | 1 |
Vivekanandhan, S | 1 |
Malik, N | 1 |
Wang, T | 1 |
Johnson, TP | 1 |
Nath, A | 1 |
Steiner, JP | 1 |
Okada, N | 1 |
Nakamura, S | 1 |
Shimazawa, M | 1 |
Ranganayaki, S | 1 |
Jamshidi, N | 1 |
Aiyaz, M | 1 |
Rashmi, SK | 1 |
Gayathri, N | 1 |
Harsha, PK | 1 |
Padmanabhan, B | 1 |
Srinivas Bharath, MM | 1 |
Peñalver, P | 1 |
Belmonte-Reche, E | 1 |
Adán, N | 1 |
Caro, M | 1 |
Mateos-Martín, ML | 1 |
Delgado, M | 1 |
González-Rey, E | 1 |
Morales, JC | 1 |
Cho, KJ | 2 |
Kim, HW | 1 |
Cheon, SY | 2 |
Lee, JE | 1 |
Kim, GW | 3 |
Brouillet, E | 3 |
Ayyappan, P | 1 |
Palayyan, SR | 1 |
Kozhiparambil Gopalan, R | 1 |
Qi, L | 1 |
Sun, X | 1 |
Li, FE | 1 |
Zhu, BS | 1 |
Braun, FK | 1 |
Liu, ZQ | 1 |
Tang, JL | 1 |
Wu, C | 1 |
Xu, F | 1 |
Wang, HH | 1 |
Velasquez, LA | 1 |
Zhao, K | 1 |
Lei, FR | 1 |
Zhang, JG | 1 |
Shen, YT | 1 |
Zou, JX | 1 |
Meng, HM | 1 |
An, GL | 1 |
Yang, L | 2 |
Zhang, XD | 1 |
Calderón Guzmán, D | 1 |
Brizuela, NO | 1 |
Ortíz Herrera, M | 1 |
Hernández García, E | 1 |
Barragán Mejía, G | 1 |
Juárez Olguín, H | 1 |
Valenzuela Peraza, A | 1 |
Attilus, J | 1 |
Labra Ruíz, N | 1 |
Mu, S | 1 |
Li, Y | 1 |
Liu, B | 1 |
Wang, W | 1 |
Chen, S | 1 |
Wu, J | 1 |
OuYang, L | 1 |
Zhu, Y | 1 |
Li, K | 1 |
Zhan, M | 1 |
Liu, Z | 1 |
Jia, Y | 1 |
Ma, Y | 1 |
Lei, W | 1 |
Chen, SD | 1 |
Wu, CL | 1 |
Hwang, WC | 1 |
Yang, DI | 1 |
De Luca, G | 1 |
Russo, MT | 1 |
Degan, P | 1 |
Tiveron, C | 1 |
Zijno, A | 1 |
Meccia, E | 1 |
Ventura, I | 1 |
Mattei, E | 1 |
Nakabeppu, Y | 2 |
Crescenzi, M | 1 |
Pepponi, R | 1 |
Pèzzola, A | 1 |
Popoli, P | 1 |
Bignami, M | 1 |
Crespo-Biel, N | 1 |
Camins, A | 3 |
Gutiérrez-Cuesta, J | 1 |
Melchiorri, D | 1 |
Nicoletti, F | 1 |
Pallàs, M | 3 |
Canudas, AM | 2 |
Kumar, P | 1 |
Kumar, A | 1 |
Elinos-Calderón, D | 1 |
Robledo-Arratia, Y | 1 |
Pérez-De La Cruz, V | 2 |
Maldonado, PD | 1 |
Galván-Arzate, S | 1 |
Pedraza-Chaverrí, J | 1 |
Santamaría, A | 2 |
Beal, MF | 5 |
Duran-Vilaregut, J | 1 |
Manich, G | 1 |
Del Valle, J | 1 |
Vilaplana, J | 1 |
Pelegrí, C | 1 |
Gopinath, K | 1 |
Sudhandiran, G | 1 |
Sheng, Z | 1 |
Oka, S | 1 |
Tsuchimoto, D | 1 |
Abolhassani, N | 1 |
Nomaru, H | 1 |
Sakumi, K | 1 |
Yamada, H | 1 |
Kim, DY | 1 |
Won, SJ | 1 |
Gwag, BJ | 1 |
Ryu, JK | 1 |
Nagai, A | 1 |
Kim, J | 1 |
Lee, MC | 1 |
McLarnon, JG | 1 |
Kim, SU | 1 |
Pubill, D | 1 |
Sureda, FX | 1 |
Verdaguer, E | 1 |
Camps, P | 1 |
Muñoz-Torrero, D | 1 |
Jiménez, A | 1 |
Bizat, N | 2 |
Hermel, JM | 1 |
Humbert, S | 1 |
Jacquard, C | 1 |
Créminon, C | 1 |
Escartin, C | 1 |
Saudou, F | 1 |
Krajewski, S | 1 |
Hantraye, P | 2 |
Gasche, Y | 1 |
Grzeschik, S | 1 |
Copin, JC | 1 |
Maier, CM | 1 |
Chan, PH | 1 |
Hellweg, R | 1 |
von Arnim, CA | 1 |
Büchner, M | 1 |
Huber, R | 1 |
Riepe, MW | 1 |
Ferrante, RJ | 3 |
Kubilus, JK | 1 |
Lee, J | 2 |
Ryu, H | 2 |
Beesen, A | 1 |
Zucker, B | 1 |
Smith, K | 1 |
Kowall, NW | 1 |
Ratan, RR | 3 |
Luthi-Carter, R | 1 |
Hersch, SM | 1 |
Klivenyi, P | 2 |
Starkov, AA | 1 |
Calingasan, NY | 1 |
Gardian, G | 1 |
Browne, SE | 1 |
Bubber, P | 1 |
Gibson, GE | 1 |
Patel, MS | 1 |
Rosenstock, TR | 1 |
Carvalho, AC | 1 |
Jurkiewicz, A | 1 |
Frussa-Filho, R | 1 |
Smaili, SS | 1 |
Chin, PC | 1 |
Liu, L | 1 |
Morrison, BE | 1 |
Siddiq, A | 1 |
Bottiglieri, T | 1 |
D'Mello, SR | 1 |
Seaman, RL | 1 |
Phelix, CF | 1 |
Lian, XY | 1 |
Zhang, Z | 1 |
Stringer, JL | 1 |
Canonaco, M | 1 |
Madeo, M | 1 |
Alò, R | 1 |
Giusi, G | 1 |
Granata, T | 1 |
Carelli, A | 1 |
Canonaco, A | 1 |
Facciolo, RM | 1 |
Ueberham, U | 1 |
Ueberham, E | 1 |
Brückner, MK | 1 |
Seeger, G | 1 |
Gärtner, U | 1 |
Gruschka, H | 1 |
Gebhardt, R | 1 |
Arendt, T | 1 |
Kim, CH | 1 |
Simon, DK | 1 |
Aminova, LR | 1 |
Andreyev, AY | 1 |
Kushnareva, YE | 1 |
Murphy, AN | 1 |
Lonze, BE | 1 |
Kim, KS | 1 |
Ginty, DD | 1 |
Karanian, DA | 1 |
Baude, AS | 1 |
Brown, QB | 1 |
Parsons, CG | 1 |
Bahr, BA | 1 |
Bjugstad, KB | 1 |
Crnic, LS | 1 |
Goodman, SI | 1 |
Freed, CR | 1 |
Ayala, A | 1 |
Venero, JL | 1 |
Cano, J | 1 |
Machado, A | 1 |
Lee, ST | 1 |
Park, JE | 1 |
Kim, DH | 1 |
Kim, S | 1 |
Im, WS | 1 |
Kang, L | 1 |
Jung, SH | 1 |
Kim, MW | 1 |
Chu, K | 1 |
Kim, M | 1 |
Silva-Adaya, D | 1 |
Herrera-Mundo, MN | 1 |
Mendoza-Macedo, K | 1 |
Villeda-Hernández, J | 1 |
Binienda, Z | 1 |
Ali, SF | 1 |
Schulz, JB | 1 |
Matthews, RT | 1 |
Klockgether, T | 1 |
Dichgans, J | 1 |
Nishino, H | 1 |
Nakajima, K | 1 |
Kumazaki, M | 1 |
Fukuda, A | 1 |
Muramatsu, K | 1 |
Deshpande, SB | 1 |
Inubushi, T | 1 |
Morikawa, S | 1 |
Borlongan, CV | 1 |
Sanberg, PR | 1 |
Seidel, B | 1 |
Jiang1, L | 1 |
Wolf, G | 1 |
Dautry, C | 1 |
Vaufrey, F | 1 |
Henry, PG | 1 |
Condé, F | 1 |
Bloch, G | 1 |
Andreassen, OA | 1 |
Dedeoglu, A | 1 |
Albers, DW | 1 |
Carlson, EJ | 1 |
Epstein, CJ | 1 |
Teunissen, CE | 1 |
Steinbusch, HW | 1 |
Angevaren, M | 1 |
Appels, M | 1 |
de Bruijn, C | 1 |
Prickaerts, J | 1 |
de Vente, J | 1 |
4 reviews available for 3-nitropropionic acid and Neurodegenerative Diseases
Article | Year |
---|---|
More Insight into BDNF against Neurodegeneration: Anti-Apoptosis, Anti-Oxidation, and Suppression of Autophagy.
Topics: Animals; Apoptosis; Autophagy; Brain-Derived Neurotrophic Factor; Cells, Cultured; Disease Models, A | 2017 |
Neuroprotective effects of creatine.
Topics: 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine; Animals; Creatine; Humans; Neurodegenerative Diseases; | 2011 |
Mitochondrial toxins and neurodegenerative diseases.
Topics: Animals; Disease Models, Animal; Humans; Huntington Disease; Mitochondria; MPTP Poisoning; Neurodege | 2007 |
The role of mitochondrial dysfunction and neuronal nitric oxide in animal models of neurodegenerative diseases.
Topics: 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine; Animals; Disease Models, Animal; Dopamine Agents; Hydr | 1997 |
44 other studies available for 3-nitropropionic acid and Neurodegenerative Diseases
Article | Year |
---|---|
Inosine attenuates 3-nitropropionic acid-induced Huntington's disease-like symptoms in rats via the activation of the A2AR/BDNF/TrKB/ERK/CREB signaling pathway.
Topics: Animals; Brain-Derived Neurotrophic Factor; Complement Factor B; Cyclic AMP Response Element-Binding | 2022 |
Fluconazole Is Neuroprotective via Interactions with the IGF-1 Receptor.
Topics: Animals; Antifungal Agents; D-Aspartic Acid; Fluconazole; Insulins; Neurodegenerative Diseases; Neur | 2022 |
3-Nitropropionic Acid Enhances Ferroptotic Cell Death via NOX2-Mediated ROS Generation in STHdhQ111 Striatal Cells Carrying Mutant Huntingtin.
Topics: Animals; Caspases; Huntington Disease; Mice; Mice, Transgenic; Nerve Tissue Proteins; Neurodegenerat | 2023 |
Inhibition of mitochondrial complex II in neuronal cells triggers unique pathways culminating in autophagy with implications for neurodegeneration.
Topics: 1-Methyl-4-phenylpyridinium; Animals; Autophagy; Cell Death; Cell Line; Cell Survival; Cells, Cultur | 2021 |
Alkylated resveratrol prodrugs and metabolites as potential therapeutics for neurodegenerative diseases.
Topics: Alkylation; Animals; Cell Survival; Cytokines; Dose-Response Relationship, Drug; Humans; Inflammatio | 2018 |
Apoptosis signal-regulating kinase-1 aggravates ROS-mediated striatal degeneration in 3-nitropropionic acid-infused mice.
Topics: Animals; Apoptosis; Corpus Striatum; Male; MAP Kinase Kinase Kinase 5; Mice; Mice, Inbred C57BL; Mic | 2013 |
The 3-NP Model of Striatal Neurodegeneration.
Topics: Animals; Corpus Striatum; Disease Models, Animal; Huntington Disease; Male; Neurodegenerative Diseas | 2014 |
Attenuation of Oxidative Damage by Boerhaavia diffusa L. Against Different Neurotoxic Agents in Rat Brain Homogenate.
Topics: Animals; Antioxidants; Brain; DNA Damage; Edetic Acid; Ferrous Compounds; Free Radicals; Lipid Perox | 2016 |
HMGB1 Promotes Mitochondrial Dysfunction-Triggered Striatal Neurodegeneration via Autophagy and Apoptosis Activation.
Topics: Animals; Apoptosis; Autophagy; Caspase 3; Cell Proliferation; Cells, Cultured; Corpus Striatum; Dise | 2015 |
Apoptosis signal-regulating kinase 1 mediates striatal degeneration via the regulation of C1q.
Topics: Animals; Astrocytes; Cell Death; Complement C1q; Corpus Striatum; Dendrites; Disease Models, Animal; | 2016 |
Effect of cerebrolysin on dopaminergic neurodegeneration of rat with oxidative stress induced by 3-nitropropionic acid.
Topics: Amino Acids; Animals; Antioxidants; Calcium; Cerebellar Cortex; Cerebellum; Cerebrum; Convulsants; D | 2016 |
Dihydromyricetin Ameliorates 3NP-induced Behavioral Deficits and Striatal Injury in Rats.
Topics: Animals; Apoptosis; Corpus Striatum; Flavonols; Locomotion; Male; Malondialdehyde; Maze Learning; Ne | 2016 |
A role for oxidized DNA precursors in Huntington's disease-like striatal neurodegeneration.
Topics: 8-Hydroxy-2'-Deoxyguanosine; Animals; Corpus Striatum; Deoxyguanosine; DNA Damage; DNA Repair Enzyme | 2008 |
Regulation of GSK-3beta by calpain in the 3-nitropropionic acid model.
Topics: Amino Acid Chloromethyl Ketones; Aminophenols; Animals; Calpain; Caspases; Cell Survival; Cells, Cul | 2010 |
Protective effects of epigallocatechin gallate following 3-nitropropionic acid-induced brain damage: possible nitric oxide mechanisms.
Topics: Animals; Antioxidants; Behavior, Animal; Catechin; Disease Models, Animal; Dose-Response Relationshi | 2009 |
Antioxidant strategy to rescue synaptosomes from oxidative damage and energy failure in neurotoxic models in rats: protective role of S-allylcysteine.
Topics: Animals; Antioxidants; Brain; Corpus Striatum; Cysteine; Disease Models, Animal; Dyskinesia, Drug-In | 2010 |
Expression pattern of ataxia telangiectasia mutated (ATM), p53, Akt, and glycogen synthase kinase-3β in the striatum of rats treated with 3-nitropropionic acid.
Topics: Animals; Ataxia Telangiectasia Mutated Proteins; Cell Cycle Proteins; Convulsants; Corpus Striatum; | 2012 |
Naringin modulates oxidative stress and inflammation in 3-nitropropionic acid-induced neurodegeneration through the activation of nuclear factor-erythroid 2-related factor-2 signalling pathway.
Topics: Administration, Oral; Analysis of Variance; Animals; Convulsants; Corpus Striatum; Cyclooxygenase 2; | 2012 |
8-Oxoguanine causes neurodegeneration during MUTYH-mediated DNA base excision repair.
Topics: Animals; Apoptosis Inducing Factor; Benzamides; Calpain; Cell Nucleus; Corpus Striatum; Dipeptides; | 2012 |
Analysis of mitochondrial free radical generation in animal models of neuronal disease.
Topics: Adenosine Triphosphate; Animals; Brain Ischemia; Disease Models, Animal; Fluorescent Dyes; Free Radi | 2002 |
Microglial activation and cell death induced by the mitochondrial toxin 3-nitropropionic acid: in vitro and in vivo studies.
Topics: Animals; Antigens, CD; Antigens, Neoplasm; Antigens, Surface; Apoptosis; Avian Proteins; Basigin; Bl | 2003 |
Neuroprotective effects of (+/-)-huprine Y on in vitro and in vivo models of excitoxicity damage.
Topics: Aminoquinolines; Animals; Binding, Competitive; Calcium; Cell Death; Cells, Cultured; Cerebellum; Co | 2003 |
In vivo calpain/caspase cross-talk during 3-nitropropionic acid-induced striatal degeneration: implication of a calpain-mediated cleavage of active caspase-3.
Topics: Amino Acid Sequence; Animals; Blotting, Western; Brain; Calpain; Caspase 3; Caspase 9; Caspases; Cel | 2003 |
Neurodegeneration in striatum induced by the mitochondrial toxin 3-nitropropionic acid: role of matrix metalloproteinase-9 in early blood-brain barrier disruption?
Topics: Animals; Behavior, Animal; Blood-Brain Barrier; Brain Edema; Corpus Striatum; Guanosine; Immunohisto | 2003 |
Neuroprotection and neuronal dysfunction upon repetitive inhibition of oxidative phosphorylation.
Topics: Action Potentials; Amyloid beta-Protein Precursor; Animals; Cell Survival; Drug Administration Sched | 2003 |
Histone deacetylase inhibition by sodium butyrate chemotherapy ameliorates the neurodegenerative phenotype in Huntington's disease mice.
Topics: Acetylation; Animals; Body Weight; Brain; Butyrates; Disease Models, Animal; Dose-Response Relations | 2003 |
Mice deficient in dihydrolipoamide dehydrogenase show increased vulnerability to MPTP, malonate and 3-nitropropionic acid neurotoxicity.
Topics: 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine; Animals; Caudate Nucleus; Cell Count; Cerebral Cortex; | 2004 |
Mitochondrial calcium, oxidative stress and apoptosis in a neurodegenerative disease model induced by 3-nitropropionic acid.
Topics: Animals; Antioxidants; Apoptosis; Astrocytes; Behavior, Animal; Calcium; Cell Survival; Cells, Cultu | 2004 |
The c-Raf inhibitor GW5074 provides neuroprotection in vitro and in an animal model of neurodegeneration through a MEK-ERK and Akt-independent mechanism.
Topics: Animals; Cell Death; Cells, Cultured; Disease Models, Animal; Enzyme Inhibitors; Farnesol; Huntingto | 2004 |
Acute effects of pulsed microwaves and 3-nitropropionic acid on neuronal ultrastructure in the rat caudate-putamen.
Topics: Acute Disease; Animals; Corpus Striatum; Dose-Response Relationship, Radiation; Male; Microwaves; Ne | 2005 |
Protective effects of ginseng components in a rodent model of neurodegeneration.
Topics: Animals; Behavior, Animal; Body Weight; Energy Metabolism; Enzyme Inhibitors; Ginsenosides; Heat-Sho | 2005 |
The histaminergic signaling system exerts a neuroprotective role against neurodegenerative-induced processes in the hamster.
Topics: Animals; Cricetinae; Mesocricetus; Neurodegenerative Diseases; Nitro Compounds; Propionates; Rats; R | 2005 |
Inducible neuronal expression of transgenic TGF-beta1 in vivo: dissection of short-term and long-term effects.
Topics: Animals; Anti-Bacterial Agents; Apolipoproteins E; Benzothiazoles; Brain; Doxycycline; Gene Expressi | 2005 |
Mitochondrial cyclic AMP response element-binding protein (CREB) mediates mitochondrial gene expression and neuronal survival.
Topics: Animals; Base Sequence; Brain; Cell Survival; Cerebral Cortex; Cyclic AMP; Cyclic AMP Response Eleme | 2005 |
3-Nitropropionic acid toxicity in hippocampus: protection through N-methyl-D-aspartate receptor antagonism.
Topics: Animals; Animals, Newborn; Cytoskeleton; Dose-Response Relationship, Drug; Excitatory Amino Acid Ant | 2006 |
Infant mice with glutaric acidaemia type I have increased vulnerability to 3-nitropropionic acid toxicity.
Topics: Animals; Animals, Newborn; Brain; Brain Diseases, Metabolic, Inborn; Disease Models, Animal; Dose-Re | 2006 |
Granulocyte-colony stimulating factor attenuates striatal degeneration with activating survival pathways in 3-nitropropionic acid model of Huntington's disease.
Topics: Animals; Corpus Striatum; Disease Models, Animal; Drug Interactions; Fluoresceins; Gene Expression R | 2008 |
Excitotoxic damage, disrupted energy metabolism, and oxidative stress in the rat brain: antioxidant and neuroprotective effects of L-carnitine.
Topics: Animals; Antioxidants; Brain; Carnitine; Convulsants; Disease Models, Animal; Dose-Response Relation | 2008 |
Estrogen protects against while testosterone exacerbates vulnerability of the lateral striatal artery to chemical hypoxia by 3-nitropropionic acid.
Topics: Animals; Animals, Newborn; Antihypertensive Agents; Antineoplastic Agents, Hormonal; Astrocytes; Blo | 1998 |
Differentially displayed genes in neuroblastoma cells treated with a mitochondrial toxin: evidence for possible involvement of ICAM-1 in 3-nitropropionic acid-mediated neurodegeneration.
Topics: Animals; Blotting, Northern; Cyclic AMP-Dependent Protein Kinases; DNA, Complementary; Gene Expressi | 2000 |
Early N-acetylaspartate depletion is a marker of neuronal dysfunction in rats and primates chronically treated with the mitochondrial toxin 3-nitropropionic acid.
Topics: Animals; Aspartic Acid; Biomarkers; Cerebral Cortex; Corpus Striatum; Dyskinesia, Drug-Induced; In S | 2000 |
Limited-time exposure to mitochondrial toxins may lead to chronic progressive neurodegenerative diseases.
Topics: Animals; Cebus; Chronic Disease; Humans; Mitochondria; Neurodegenerative Diseases; Neurotoxins; Nitr | 2000 |
Mice with a partial deficiency of manganese superoxide dismutase show increased vulnerability to the mitochondrial toxins malonate, 3-nitropropionic acid, and MPTP.
Topics: 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine; 3,4-Dihydroxyphenylacetic Acid; Animals; Carrier Prote | 2001 |
Behavioural correlates of striatal glial fibrillary acidic protein in the 3-nitropropionic acid rat model: disturbed walking pattern and spatial orientation.
Topics: Animals; Behavior, Animal; Discrimination Learning; Disease Models, Animal; Gait Disorders, Neurolog | 2001 |