Page last updated: 2024-08-18

pyridostigmine bromide and Disease Models, Animal

pyridostigmine bromide has been researched along with Disease Models, Animal in 63 studies

Research

Studies (63)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's9 (14.29)29.6817
2010's37 (58.73)24.3611
2020's17 (26.98)2.80

Authors

AuthorsStudies
Abrams, RPM; Bachani, M; Balasubramanian, A; Brimacombe, K; Dorjsuren, D; Eastman, RT; Hall, MD; Jadhav, A; Lee, MH; Li, W; Malik, N; Nath, A; Padmanabhan, R; Simeonov, A; Steiner, JP; Teramoto, T; Yasgar, A; Zakharov, AV1
Bishay, AE; Carabelli, B; Chinthirla, DB; Currás-Collazo, MC; Denys, ME; Hsiao, A; Kozlova, EV; Tran, JD; Zur Nieden, NI1
Bishay, AE; Carabelli, B; Crawford, MS; Curras-Collazo, MC; Denys, ME; Hsiao, A; Kozlova, EV; Liu, R; Macbeth, JC; McCole, DF; Piamthai, V; Zur Nieden, NI1
Iannucci, J; Nizamutdinov, D; Shapiro, LA1
Abdullah, L; Ait-Ghezala, G; Browning, M; Crawford, F; Ferguson, S; Gratkowski, A; Hahn-Townsend, C; McCartan, R; Morin, A; Mouzon, B; Mullan, M; Ojo, J; Sullivan, K1
Harrison, K; Klaunig, JE; Koyama, S; Meng, F; Shetty, AK; Slevin, E; Wan, Y; Wu, C1
Carreras, I; Dedeoglu, A; Jung, Y; Lopez-Benitez, J; Tognoni, CM1
Ayala, KE; Burzynski, HE; Dufala, HA; Eberl, BR; Fadel, JR; Frick, MA; Grillo, CA; Hollis, F; Macht, VA; McQuail, JA; Reagan, LP; Woodruff, JL1
Beeson, D; Cetin, H; Cheung, J; Cossins, J; Liu, WW; Maxwell, S; Palace, J; Ramjattan, H; Rodriguez Cruz, PM; Vanhaesebrouck, AE; Webster, R; Wickens, J1
Bose, D; Chatterjee, S; Holland, LA; Horner, RD; Janulewicz Lloyd, P; Kimono, D; Klimas, N; Lim, ES; Maqsood, R; Mondal, A; Seth, RK; Sullivan, K1
Agarwal, H; Banerjee, S; Chand, HS; Raizada, V; Roy, S; Singh, SP; Sopori, M1
Pai, YC; Yu, LC1
Carpenter, JM; Filipov, NM; Gordon, HE; Harn, DA; Ludwig, HD; Norberg, T; Wagner, JJ1
Arcanjo, DDR; Cavalcante, GL; da Silva, MTB; Ferreira, FN; Filho, ALMM; Sabino, JPJ; Soriano, RN1
Fried, D; Grubišić, V; Gulbransen, BD; Hernandez, S; Morales-Soto, W1
Lenina, OA; Masson, P; Petrov, KA; Semenov, VE; Zobov, VV; Zueva, IV1
Gerzanich, V; Ivanova, S; Keledjian, K; Kim, K; Moyer, M; Negoita, S; Semick, S; Simard, JM; Tsymbalyuk, O1
Ali, MA; Issotina Zibrila, A; Kang, Y; Li, C; Liu, J; Liu, K; Osei, JA; Sun, Y; Wang, Z; Zafar, S1
Clark, JD; Goba, L; Huang, TT; Nguyen, H; Sahbaie, P; Sul, J; Suzaki, A1
Kelly, KA; Locker, AR; Michalovicz, LT; Miller, DB; Miller, JV; O'Callaghan, JP1
Amancio, GCS; Barcellos, NMS; Cazorla, O; Grabe-Guimarães, A; Haikel, D; Lacampagne, A; Matecki, S; Moreau, J1
Bezerra, OC; Consolim-Colombo, FM; de Angelis, K; Dourado, PM; França, CM; Irigoyen, MCC; Llesuy, S; Loleiro, TCA; Malfitano, C; Neves, GA; Rocha, JA; Souza, PRM; Teixeira Gomes, M; Ulloa, L1
Bogaard, HJ; Casali, AG; Casali, KR; da Silva Gonçalves Bós, D; de Man, FS; Dorfmüller, P; Dos Remedios, C; Goumans, MJ; Guignabert, C; Handoko, ML; Humbert, M; Kurakula, K; Kuster, DWD; Rol, N; Sun, XQ; Szulcek, R; Tu, L; Van Der Bruggen, CEE; van der Velden, J; Vonk-Noordegraaf, A; Wijnker, PJM1
Aytan, N; Blusztajn, JK; Carreras, I; Choi, JK; Crabtree, L; Dedeoglu, A; Jenkins, BG; Lehar, M; Leite-Morris, K; Mellott, T1
Cooper, BY; Flunker, LD; Johnson, RD; Nutter, TJ1
Grillo, CA; Macht, VA; Reagan, LP; Wilson, MA; Wood, CS; Woodruff, JL1
Barnes, Z; Fletcher, MA; Kelly, KA; Klimas, NG; Lasley, SM; Locker, AR; Michalovicz, LT; Miller, DB; Miller, JV; Morris, M; O'Callaghan, JP1
Cui, YL; Li, DL; Wu, Q; Xu, M; Xue, RQ; Yang, S; Yu, XJ; Zang, WJ; Zhao, M1
Barboza, CA; Caperuto, EC; Carrozzi, N; Dourado, PMM; Fukushima, AR; Irigoyen, MC; Machi, JF; Morris, M; Mostarda, CT; Nathanson, L; Rodrigues, B1
Bruun, DA; Guignet, M; Harvey, DJ; Lein, PJ1
Cau, SBA; Lataro, RM; Mestriner, FL; Salgado, HC; Silva, MAB; Tostes, RCA1
Fadel, JR; Grillo, CA; Macht, VA; Maissy, ES; Reagan, LP; Wilson, MA; Woodruff, JL1
Attaluri, S; Gitai, D; Kodali, M; Madhu, LN; Shetty, AK; Shuai, B; Upadhya, R1
Abdullah, L; Crawford, F; Cseresznye, A; Darcey, T; Evans, JE; Hammock, B; Hongsibsong, S; Joshi, U; Keegan, AP; Klimas, N; Langlois, H; Mullan, M; Oberlin, S; Ojo, J; Paris, D; Pearson, A; Raya, B; Saltiel, N; Stern, LJ; Sullivan, K; Vasylieva, N1
Hattiangady, B; Parihar, VK; Shetty, AK; Shuai, B1
da Silva, CA; Fazan, R; Giusti, H; Glass, ML; Sabino, JP; Salgado, HC1
Cheng, XW; Duan, JL; Hao, C; Huang, ZH; Lu, W; Murohara, T; Shi, YQ; Song, SW; Su, DF1
Becari, C; Corrêa, WG; de Oliveira, M; do Carmo, JM; Durand, MT; Fazan, R; Prado, CM; Salgado, HC; Tezini, GC1
Abdullah, L; Ait-Ghezala, G; Crawford, F; Crynen, G; Mathura, V; Mullan, M; Mullan, MJ; Nissanka, N; Reed, J; Tweed, M; Zakirova, Z1
Cooper, BY; Johnson, RD; Nutter, TJ2
Araujo, JE; Blanco, JH; Carvalho, EE; Gardim, CB; Gastaldi, AC; Oliveira, LF; Simões, MV; Souza, HC1
Alves, G; Coelho, O; Consolim-Colombo, FM; França, CM; Irigoyen, MC; Kallás, EG; Lacchini, S; Ribeiro, SP; Rocha, JA1
Clark, ME; Farmer, DM; Kurata, WE; Matsumoto, KW; Pierce, LM1
Bealer, SL; Dudek, FE; Pouliot, W; Roach, B1
Amourette, C; Barbier, L; Diserbo, M; Fauquette, W; Lamproglou, I; Viret, R; Zoppe, A1
Blobner, M; Fink, H; Frick, CG; Helming, M; Martyn, JA1
Kaas, B; Kohn, RE; Leatherman, A; Schleidt, S; Vaidya, AR1
Grubbs, RD; Lucot, JB; Mauck, B; Paton, S1
Al-Diwani, A; Bouzat, C; Buckingham, SD; Hernando, G; Jones, AK; Jones, R; Maynard, TP; Rayes, D; Sattelle, DB1
Abbs, S; Beeson, D; Cullup, T; Dowling, JJ; Feng, L; Jungbluth, H; Knight, RK; Kress, W; Laporte, J; Lees, MM; Lillis, S; Manzur, AY; Mills, KR; Muntoni, F; Pike, MG; Pitt, MC; Robb, SA; Sewry, CA1
Beggs, AH; Buj-Bello, A; Dowling, JJ; Dulin-Smith, AN; Durban, AN; Joubert, R; Li, X; Low, SE; Marshall, JT; Marshall, ML; Messaddeq, N; Pierson, CR; Snyder, AD1
Abdullah, L; Ait-Ghezala, G; Bishop, A; Crawford, FC; Crynen, G; Evans, JE; Ferro, A; Mullan, CM; Mullan, MA; Mullan, MJ; Pelot, R; Phillips, J; Reed, JM1
Joosen, MJ; Kuijpers, WC; Noort, D; van der Schans, MJ; van Helden, HP1
Clarke, NF; Dowling, JJ; Feldman, EL; Gibbs, EM; Oates, EC; Rose, K; Webster, R1
Dudley, A; Eudaly, E; Eudaly, J; Gilkeson, G; Keil, DE; Lee, A; Peden-Adam, MM; Robbs, J; Zeigler, J1
Abdel-Rahman, A; Abou-Donia, M; Abou-Donia, S; El-Masry, E; Shetty, A1
Benjamin, A; McDonough, JH; McMonagle, JD; Rowland, T; Shih, TM1
Adani, R; Amitai, G; Avila, J; Farías, GG; Godoy, JA; Inestrosa, NC; Meshulam, H; Vázquez, MC1
Abraham, S; Cohen, G; Dachir, S; Gilat, E; Herskovitz, M; Kapon, J; Levy, A; Raveh, L; Teitelbaum, Z1
McDonough, JH; Shih, TM1
Beck, KD; Beldowicz, D; Brennan, FX; Moldow, RL; Ottenweller, JE; Servatius, RJ; Zhu, G1
Bressler, J; Pope, CN; Pruett, S; Song, X; Tian, H1

Reviews

3 review(s) available for pyridostigmine bromide and Disease Models, Animal

ArticleYear
Dysbiosis in gastrointestinal pathophysiology: Role of the gut microbiome in Gulf War Illness.
    Journal of cellular and molecular medicine, 2023, Volume: 27, Issue:7

    Topics: Animals; Disease Models, Animal; Dysbiosis; Gastrointestinal Microbiome; Gulf War; Mice; Permethrin; Persian Gulf Syndrome; Pyridostigmine Bromide

2023
Timing of decontamination and treatment in case of percutaneous VX poisoning: a mini review.
    Chemico-biological interactions, 2013, Mar-25, Volume: 203, Issue:1

    Topics: Acetylcholinesterase; Animals; Butyrylcholinesterase; Chemical Warfare Agents; Cholinesterase Inhibitors; Decontamination; Disease Models, Animal; Guinea Pigs; Organophosphate Poisoning; Organothiophosphorus Compounds; Procyclidine; Pyridostigmine Bromide; Scopolamine; Skin; Time Factors

2013
Central nervous system effects from a peripherally acting cholinesterase inhibiting agent: interaction with stress or genetics.
    Annals of the New York Academy of Sciences, 2001, Volume: 933

    Topics: Acetylcholine; Acetylcholinesterase; Animals; Basal Ganglia; Behavior, Animal; Brain Chemistry; Cholinesterase Inhibitors; Disease Models, Animal; Dose-Response Relationship, Drug; Drug Resistance; Electroshock; Genetic Predisposition to Disease; Genetic Variation; Muscle Contraction; Nerve Tissue Proteins; Persian Gulf Syndrome; Prosencephalon; Pyridostigmine Bromide; Rats; Rats, Inbred WKY; Rats, Sprague-Dawley; Salivation; Stress, Physiological

2001

Other Studies

60 other study(ies) available for pyridostigmine bromide and Disease Models, Animal

ArticleYear
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
    Proceedings of the National Academy of Sciences of the United States of America, 2020, 12-08, Volume: 117, Issue:49

    Topics: Animals; Antiviral Agents; Artificial Intelligence; Chlorocebus aethiops; Disease Models, Animal; Drug Evaluation, Preclinical; High-Throughput Screening Assays; Immunocompetence; Inhibitory Concentration 50; Methacycline; Mice, Inbred C57BL; Protease Inhibitors; Quantitative Structure-Activity Relationship; Small Molecule Libraries; Vero Cells; Zika Virus; Zika Virus Infection

2020
Persistent exercise fatigue and associative learning deficits in combination with transient glucose dyshomeostasis in a mouse model of Gulf War Illness.
    Life sciences, 2022, Jan-15, Volume: 289

    Topics: Animals; Disease Models, Animal; Fatigue; Glucose; Humans; Learning Disabilities; Male; Mice; Persian Gulf Syndrome; Pyridostigmine Bromide

2022
Induction of distinct neuroinflammatory markers and gut dysbiosis by differential pyridostigmine bromide dosing in a chronic mouse model of GWI showing persistent exercise fatigue and cognitive impairment.
    Life sciences, 2022, Jan-01, Volume: 288

    Topics: Animals; Biomarkers; Cholinesterase Inhibitors; Cognitive Dysfunction; Disease Models, Animal; Dose-Response Relationship, Drug; Dysbiosis; Endotoxemia; Fatigue; Gastrointestinal Microbiome; Gene Expression Profiling; Gene Expression Regulation; Gliosis; Male; Mice; Mice, Inbred C57BL; Neuralgia; Neuroinflammatory Diseases; Persian Gulf Syndrome; Physical Conditioning, Animal; Pyridostigmine Bromide

2022
Neurogenesis and chronic neurobehavioral outcomes are partially improved by vagus nerve stimulation in a mouse model of Gulf War illness.
    Neurotoxicology, 2022, Volume: 90

    Topics: Animals; Disease Models, Animal; Gulf War; Mice; Neurogenesis; Permethrin; Persian Gulf Syndrome; Pyridostigmine Bromide; Vagus Nerve Stimulation

2022
Impact of gulf war toxic exposures after mild traumatic brain injury.
    Acta neuropathologica communications, 2022, 10-18, Volume: 10, Issue:1

    Topics: Animals; Brain Concussion; Brain Injuries, Traumatic; Disease Models, Animal; Gulf War; Mice; Permethrin; Pesticides; Pharmaceutical Preparations; Pyridostigmine Bromide

2022
Fingolimod mitigates memory loss in a mouse model of Gulf War Illness amid decreasing the activation of microglia, protein kinase R, and NFκB.
    Neurotoxicology, 2023, Volume: 96

    Topics: Amnesia; Animals; Disease Models, Animal; Fingolimod Hydrochloride; Gulf War; Male; Memory Disorders; Mice; Mice, Inbred C57BL; Microglia; Neuroinflammatory Diseases; NF-kappa B; Persian Gulf Syndrome; Protein Kinases; Pyridostigmine Bromide

2023
Delayed cognitive impairments in a rat model of Gulf War Illness are stimulus-dependent.
    Brain, behavior, and immunity, 2023, Volume: 113

    Topics: Acetylcholinesterase; Animals; Cholinesterase Inhibitors; Cognitive Dysfunction; Disease Models, Animal; Gulf War; Lipopolysaccharides; Memory Disorders; Persian Gulf Syndrome; Pyridostigmine Bromide; Rats

2023
β2-Adrenergic receptor agonists ameliorate the adverse effect of long-term pyridostigmine on neuromuscular junction structure.
    Brain : a journal of neurology, 2019, 12-01, Volume: 142, Issue:12

    Topics: Action Potentials; Adrenergic beta-2 Receptor Agonists; Albuterol; Animals; Cholinesterase Inhibitors; Disease Models, Animal; Humans; Mice; Myasthenic Syndromes, Congenital; Neuromuscular Junction; Pyridostigmine Bromide; Synaptic Transmission

2019
Gut DNA Virome Diversity and Its Association with Host Bacteria Regulate Inflammatory Phenotype and Neuronal Immunotoxicity in Experimental Gulf War Illness.
    Viruses, 2019, 10-21, Volume: 11, Issue:10

    Topics: Animals; Antiviral Agents; Bacteria; Cytokines; Disease Models, Animal; DNA; Dysbiosis; Gastrointestinal Microbiome; Immunity, Innate; Inflammation; Male; Mice; Mice, Inbred C57BL; Neurons; Permethrin; Persian Gulf Syndrome; Phenotype; Pyridostigmine Bromide; Ribavirin; Viruses

2019
Acetylcholinesterase Inhibitor Pyridostigmine Bromide Attenuates Gut Pathology and Bacterial Dysbiosis in a Murine Model of Ulcerative Colitis.
    Digestive diseases and sciences, 2020, Volume: 65, Issue:1

    Topics: Acetylcholinesterase; Animals; Anti-Inflammatory Agents; Cholinesterase Inhibitors; Colitis, Ulcerative; Colon; Cytokines; Disease Models, Animal; Dysbiosis; Gastrointestinal Microbiome; GPI-Linked Proteins; Inflammation Mediators; Mucin-2; Pyridostigmine Bromide; Th2 Cells

2020
Is "Cholinergic" Stimulus Useful for Ulcerative Colitis Treatment?
    Digestive diseases and sciences, 2020, Volume: 65, Issue:1

    Topics: Acetylcholinesterase; Animals; Colitis, Ulcerative; Disease Models, Animal; Dysbiosis; Gastrointestinal Microbiome; Mice; Pyridostigmine Bromide

2020
Neurochemical and neuroinflammatory perturbations in two Gulf War Illness models: Modulation by the immunotherapeutic LNFPIII.
    Neurotoxicology, 2020, Volume: 77

    Topics: Amino Sugars; Animals; Biogenic Monoamines; Brain; Brain Chemistry; DEET; Disease Models, Animal; Encephalitis; Humans; Immunotherapy; Male; Mice, Inbred C57BL; Permethrin; Persian Gulf Syndrome; Pesticides; Polysaccharides; Pyridostigmine Bromide; Spleen

2020
Acetylcholinesterase inhibition prevents alterations in cardiovascular autonomic control and gastric motility in L-NAME-induced hypertensive rats.
    Life sciences, 2020, Sep-01, Volume: 256

    Topics: Acetylcholinesterase; Animals; Arterial Pressure; Autonomic Nervous System; Baroreflex; Cardiovascular System; Cholinesterase Inhibitors; Disease Models, Animal; Donepezil; Heart Rate; Hypertension; Male; NG-Nitroarginine Methyl Ester; Protective Agents; Pyridostigmine Bromide; Rats; Rats, Wistar; Stomach; Stroke Volume

2020
Pyridostigmine bromide exposure creates chronic, underlying neuroimmune disruption in the gastrointestinal tract and brain that alters responses to palmitoylethanolamide in a mouse model of Gulf War Illness.
    Neuropharmacology, 2020, 11-15, Volume: 179

    Topics: Amides; Animals; Anti-Inflammatory Agents, Non-Steroidal; Brain; Cholinesterase Inhibitors; Chronic Disease; Disease Models, Animal; Ethanolamines; Female; Gastrointestinal Tract; Male; Mice; Mice, Inbred C57BL; Neuroimmunomodulation; Palmitic Acids; Persian Gulf Syndrome; Pyridostigmine Bromide

2020
Slow-binding reversible inhibitor of acetylcholinesterase with long-lasting action for prophylaxis of organophosphate poisoning.
    Scientific reports, 2020, 10-06, Volume: 10, Issue:1

    Topics: Animals; Benzylammonium Compounds; Bromides; Cholinesterase Inhibitors; Delayed-Action Preparations; Disease Models, Animal; Mice; Organophosphate Poisoning; Organophosphorus Compounds; Paraoxon; Pyridostigmine Bromide; Time Factors

2020
The peroxisome proliferator-activated receptor gamma (PPARγ) agonist, rosiglitazone, ameliorates neurofunctional and neuroinflammatory abnormalities in a rat model of Gulf War Illness.
    PloS one, 2020, Volume: 15, Issue:11

    Topics: Animals; Anxiety; Astrocytes; Brain; Cognition; Disease Models, Animal; Female; Hippocampus; Lipopolysaccharides; Male; Persian Gulf Syndrome; PPAR gamma; Pyridostigmine Bromide; Rats; Rats, Wistar; Rosiglitazone; Stress, Psychological

2020
Pyridostigmine ameliorates preeclamptic features in pregnant rats by inhibiting tumour necrosis factor-α synthetsis and antagonizing tumour necrosis factor-α-related effects.
    Journal of hypertension, 2021, 09-01, Volume: 39, Issue:9

    Topics: Acetylcholinesterase; Animals; Blood Pressure; Disease Models, Animal; Endothelial Cells; Female; Humans; Ischemia; Placenta; Pre-Eclampsia; Pregnancy; Pyridostigmine Bromide; Rats; Rats, Sprague-Dawley; Tumor Necrosis Factor-alpha

2021
Exposure to Gulf War Illness-related agents leads to the development of chronic pain and fatigue.
    Life sciences, 2021, Oct-15, Volume: 283

    Topics: Animals; Chlorpyrifos; Chronic Pain; DEET; Disease Models, Animal; Fatigue; Humans; Mice; Permethrin; Persian Gulf Syndrome; Pyridostigmine Bromide

2021
Corticosterone primes the neuroinflammatory response to Gulf War Illness-relevant organophosphates independently of acetylcholinesterase inhibition.
    Journal of neurochemistry, 2017, Volume: 142, Issue:3

    Topics: Acetylcholinesterase; Animals; Brain; Cholinesterase Inhibitors; Corticosterone; Disease Models, Animal; Gulf War; Male; Mice, Inbred C57BL; Organophosphates; Persian Gulf Syndrome; Pyridostigmine Bromide

2017
Effect of pyridostigmine on in vivo and in vitro respiratory muscle of mdx mice.
    Respiratory physiology & neurobiology, 2017, Volume: 243

    Topics: Age Factors; Animals; Cholinesterase Inhibitors; Disease Models, Animal; Drug Delivery Systems; In Vitro Techniques; Liposomes; Male; Mice; Mice, Inbred C57BL; Mice, Inbred mdx; Muscle Contraction; Muscular Dystrophy, Duchenne; Plethysmography; Pyridostigmine Bromide; Respiration Disorders; Respiratory Muscles; Respiratory Rate; Spectrophotometry, Ultraviolet; Tidal Volume

2017
Cholinergic Stimulation Improves Oxidative Stress and Inflammation in Experimental Myocardial Infarction.
    Scientific reports, 2017, 10-20, Volume: 7, Issue:1

    Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Antioxidants; Cardiotonic Agents; Cholinesterase Inhibitors; Cytokines; Disease Models, Animal; Hemodynamics; Inflammation; Male; Myocardial Infarction; Oxidative Stress; Pyridostigmine Bromide; Random Allocation; Rats, Wistar

2017
Contribution of Impaired Parasympathetic Activity to Right Ventricular Dysfunction and Pulmonary Vascular Remodeling in Pulmonary Arterial Hypertension.
    Circulation, 2018, 02-27, Volume: 137, Issue:9

    Topics: Animals; Cells, Cultured; Cholinesterase Inhibitors; Disease Models, Animal; Endothelium, Vascular; Humans; Hypertension, Pulmonary; Male; Organ Culture Techniques; Parasympathetic Nervous System; Pulmonary Artery; Pyridostigmine Bromide; Rats; Rats, Sprague-Dawley; Vascular Remodeling; Ventricular Dysfunction, Right; Ventricular Function, Right

2018
Anxiety, neuroinflammation, cholinergic and GABAergic abnormalities are early markers of Gulf War illness in a mouse model of the disease.
    Brain research, 2018, 02-15, Volume: 1681

    Topics: Acetylcholine; Animals; Anxiety; Astrocytes; Brain; DEET; Disease Models, Animal; Encephalitis; Female; gamma-Aminobutyric Acid; Male; Mice, Transgenic; Microglia; Permethrin; Persian Gulf Syndrome; Pyridostigmine Bromide; Stress, Psychological

2018
Behavioral, cellular and molecular maladaptations covary with exposure to pyridostigmine bromide in a rat model of gulf war illness pain.
    Toxicology and applied pharmacology, 2018, 08-01, Volume: 352

    Topics: Adaptation, Physiological; Animals; Behavior, Animal; Chlorpyrifos; DEET; Disease Models, Animal; Ganglia, Spinal; KCNQ Potassium Channels; Male; Muscle, Skeletal; NAV1.9 Voltage-Gated Sodium Channel; Pain Perception; Pain Threshold; Permethrin; Persian Gulf Syndrome; Pyridostigmine Bromide; Rats, Sprague-Dawley; Receptors, Muscarinic; Signal Transduction; Time Factors; TRPA1 Cation Channel

2018
Pathophysiology in a model of Gulf War Illness: Contributions of pyridostigmine bromide and stress.
    Psychoneuroendocrinology, 2018, Volume: 96

    Topics: Animals; Brain; Cholinesterases; Corticosterone; Cytokines; Disease Models, Animal; Gulf War; Male; Memory Disorders; Persian Gulf Syndrome; Pyridostigmine Bromide; Rats; Rats, Sprague-Dawley; Stress, Psychological; Time Factors

2018
Corticosterone and pyridostigmine/DEET exposure attenuate peripheral cytokine expression: Supporting a dominant role for neuroinflammation in a mouse model of Gulf War Illness.
    Neurotoxicology, 2019, Volume: 70

    Topics: Animals; Cholinesterase Inhibitors; Corticosterone; Cytokines; DEET; Disease Models, Animal; Gene Expression; Inflammation; Inflammation Mediators; Insect Repellents; Male; Mice; Mice, Inbred C57BL; Persian Gulf Syndrome; Pyridostigmine Bromide

2019
Pyridostigmine alleviates cardiac dysfunction via improving mitochondrial cristae shape in a mouse model of metabolic syndrome.
    Free radical biology & medicine, 2019, Volume: 134

    Topics: Animals; Cholinesterase Inhibitors; Diet, High-Fat; Disease Models, Animal; Heart Diseases; Insulin Resistance; Male; Metabolic Syndrome; Mice; Mitochondria, Heart; Mitochondrial Membranes; Mitochondrial Proteins; Organelle Shape; Pyridostigmine Bromide

2019
Cholinergic Stimulation by Pyridostigmine Bromide Before Myocardial Infarction Prevent Cardiac and Autonomic Dysfunction.
    Scientific reports, 2019, 02-21, Volume: 9, Issue:1

    Topics: Animals; Autonomic Nervous System; Blood Pressure; Cholinesterase Inhibitors; Disease Models, Animal; Gene Expression Regulation; Interferon-gamma; Interleukin-10; Interleukin-1beta; Interleukin-6; Male; Myocardial Infarction; Pyridostigmine Bromide; Rats; Rats, Wistar; Ventricular Function, Left

2019
Pretreatment with pyridostigmine bromide has no effect on seizure behavior or 24 hour survival in the rat model of acute diisopropylfluorophosphate intoxication.
    Neurotoxicology, 2019, Volume: 73

    Topics: Acetylcholinesterase; Animals; Brain; Cholinesterase Inhibitors; Disease Models, Animal; GPI-Linked Proteins; Isoflurophate; Male; Neurotoxicity Syndromes; Organophosphate Poisoning; Pyridostigmine Bromide; Rats, Sprague-Dawley; Seizures; Time Factors

2019
Chronic Treatment With Acetylcholinesterase Inhibitors Attenuates Vascular Dysfunction in Spontaneously Hypertensive Rats.
    American journal of hypertension, 2019, 05-09, Volume: 32, Issue:6

    Topics: Acetylcholinesterase; Animals; Antihypertensive Agents; Arterial Pressure; Cholinesterase Inhibitors; Disease Models, Animal; Donepezil; GPI-Linked Proteins; Hemodynamics; Hypertension; Mesenteric Arteries; NADPH Oxidases; Nitric Oxide; Nitric Oxide Synthase Type III; Pyridostigmine Bromide; Rats, Inbred SHR; Rats, Inbred WKY; Reactive Oxygen Species; Vascular Resistance; Vasoconstriction; Vasodilation

2019
Pyridostigmine bromide and stress interact to impact immune function, cholinergic neurochemistry and behavior in a rat model of Gulf War Illness.
    Brain, behavior, and immunity, 2019, Volume: 80

    Topics: Acetylcholine; Animals; Behavior, Animal; C-Reactive Protein; Cholinesterase Inhibitors; Conditioning, Classical; Disease Models, Animal; Fear; Hippocampus; Inflammation; Lipopolysaccharides; Male; Persian Gulf Syndrome; Prefrontal Cortex; Pyridostigmine Bromide; Rats, Sprague-Dawley; Stress, Psychological

2019
Neuroinflammation in Gulf War Illness is linked with HMGB1 and complement activation, which can be discerned from brain-derived extracellular vesicles in the blood.
    Brain, behavior, and immunity, 2019, Volume: 81

    Topics: Animals; Astrocytes; Brain; Complement Activation; Cytokines; DEET; Disease Models, Animal; Encephalitis; Extracellular Vesicles; Gulf War; HMGB1 Protein; Inflammation; Male; Neuroimmunomodulation; Neurons; Permethrin; Persian Gulf Syndrome; Pyridostigmine Bromide; Rats

2019
A permethrin metabolite is associated with adaptive immune responses in Gulf War Illness.
    Brain, behavior, and immunity, 2019, Volume: 81

    Topics: Adaptive Immunity; Adult; Animals; Benzoates; Brain; Central Nervous System; Disease Models, Animal; Female; Gulf War; Humans; Male; Mice; Mice, Inbred C57BL; Middle Aged; Permethrin; Persian Gulf Syndrome; Pyridostigmine Bromide; Veterans

2019
Mood and memory deficits in a model of Gulf War illness are linked with reduced neurogenesis, partial neuron loss, and mild inflammation in the hippocampus.
    Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2013, Volume: 38, Issue:12

    Topics: Animals; Anxiety; Cell Death; Cholinesterase Inhibitors; DEET; Depression; Disease Models, Animal; Hippocampus; Inflammation; Insect Repellents; Insecticides; Memory Disorders; Mood Disorders; Neurogenesis; Neurons; Permethrin; Persian Gulf Syndrome; Pyridostigmine Bromide; Rats; Rats, Sprague-Dawley; Stress, Psychological; Swimming

2013
Parasympathetic activation by pyridostigmine on chemoreflex sensitivity in heart-failure rats.
    Autonomic neuroscience : basic & clinical, 2013, Volume: 179, Issue:1-2

    Topics: Animals; Cholinesterase Inhibitors; Disease Models, Animal; Heart Failure; Heart Rate; Hypercapnia; Hypoxia; Male; Parasympathetic Nervous System; Pulmonary Ventilation; Pyridostigmine Bromide; Rats; Rats, Wistar

2013
Arterial baroreflex dysfunction impairs ischemia-induced angiogenesis.
    Journal of the American Heart Association, 2014, May-12, Volume: 3, Issue:3

    Topics: Animals; Arteries; Baroreflex; Cholinesterase Inhibitors; Disease Models, Animal; Extremities; Hypoxia-Inducible Factor 1, alpha Subunit; Ischemia; Male; Mice, Inbred C57BL; Mice, Knockout; Neovascularization, Physiologic; Pyridostigmine Bromide; Rats, Sprague-Dawley; Signal Transduction; Vascular Endothelial Growth Factor A

2014
Pyridostigmine prevents haemodynamic alterations but does not affect their nycthemeral oscillations in infarcted mice.
    Autonomic neuroscience : basic & clinical, 2015, Volume: 187

    Topics: Animals; Arterial Pressure; Cholinesterase Inhibitors; Circadian Rhythm; Disease Models, Animal; Heart Rate; Hemodynamics; Male; Mice; Mice, Inbred C57BL; Myocardial Infarction; Myocardium; Pyridostigmine Bromide; Telemetry

2015
Gulf War agent exposure causes impairment of long-term memory formation and neuropathological changes in a mouse model of Gulf War Illness.
    PloS one, 2015, Volume: 10, Issue:3

    Topics: Animals; Astrocytes; Cerebral Cortex; Cognition; Disease Models, Animal; Gene Expression; Gulf War; Hippocampus; Humans; Male; Memory, Long-Term; Memory, Short-Term; Mice; Mice, Inbred C57BL; Permethrin; Persian Gulf Syndrome; Pyridostigmine Bromide; Synaptophysin; Time Factors

2015
A delayed chronic pain like condition with decreased Kv channel activity in a rat model of Gulf War Illness pain syndrome.
    Neurotoxicology, 2015, Volume: 51

    Topics: Animals; Chlorpyrifos; Cholinesterase Inhibitors; Chronic Pain; Delayed Rectifier Potassium Channels; Disease Models, Animal; Ganglia, Spinal; KCNQ1 Potassium Channel; Male; Membrane Potentials; Nociceptors; Pain Threshold; Permethrin; Persian Gulf Syndrome; Potassium Channels, Voltage-Gated; Pyridostigmine Bromide; Rats; Rats, Sprague-Dawley

2015
Chronic cholinergic stimulation promotes changes in cardiovascular autonomic control in spontaneously hypertensive rats.
    Autonomic neuroscience : basic & clinical, 2015, Volume: 193

    Topics: Animals; Autonomic Nervous System; Baroreflex; Blood Pressure; Cholinesterase Inhibitors; Disease Models, Animal; Heart Rate; Hypertension; Male; Pyridostigmine Bromide; Rats, Inbred SHR; Rats, Inbred WKY; Stroke Volume; Vagus Nerve

2015
Increase in cholinergic modulation with pyridostigmine induces anti-inflammatory cell recruitment soon after acute myocardial infarction in rats.
    American journal of physiology. Regulatory, integrative and comparative physiology, 2016, Apr-15, Volume: 310, Issue:8

    Topics: Animals; Anti-Inflammatory Agents; Biomarkers; Blood Pressure; CD8-Positive T-Lymphocytes; Chemotaxis, Leukocyte; Cholinergic Neurons; Cholinesterase Inhibitors; Disease Models, Animal; Forkhead Transcription Factors; Heart Rate; Interleukin-2 Receptor alpha Subunit; Macrophage Activation; Macrophages; Male; Myocardial Infarction; Myocardium; Phenotype; Pyridostigmine Bromide; Rats, Inbred WKY; Spleen; T-Lymphocytes, Regulatory; Time Factors; Ventricular Function, Left

2016
Exposure to Gulf War Illness chemicals induces functional muscarinic receptor maladaptations in muscle nociceptors.
    Neurotoxicology, 2016, Volume: 54

    Topics: Animals; Chemical Warfare Agents; Chlorpyrifos; Chronic Pain; Disease Models, Animal; Ganglia, Spinal; Gene Expression Regulation; Male; Membrane Potentials; Muscarinic Agonists; Muscle, Skeletal; Neurons; Nociceptors; Pain Threshold; Permethrin; Potassium Channel Blockers; Potassium Channels; Pyridostigmine Bromide; Rats; Receptors, Muscarinic

2016
Long-term epigenetic alterations in a rat model of Gulf War Illness.
    Neurotoxicology, 2016, Volume: 55

    Topics: Animals; Apoptosis; Brain; Cytokines; Disease Models, Animal; DNA Methylation; Enzyme-Linked Immunosorbent Assay; Epigenesis, Genetic; Fluoresceins; Gene Expression Regulation; In Situ Nick-End Labeling; Male; MicroRNAs; Permethrin; Persian Gulf Syndrome; Pyridostigmine Bromide; Rats; Rats, Sprague-Dawley; RNA, Messenger

2016
A rodent model of human organophosphate exposure producing status epilepticus and neuropathology.
    Neurotoxicology, 2016, Volume: 56

    Topics: Animals; Antidotes; Atropine; Central Nervous System Diseases; Cholinesterase Inhibitors; Disease Models, Animal; Dose-Response Relationship, Drug; Electroencephalography; Male; Organophosphates; Phosphoric Triester Hydrolases; Pralidoxime Compounds; Pyridostigmine Bromide; Rats; Rats, Sprague-Dawley; Status Epilepticus

2016
Gulf War illness: Effects of repeated stress and pyridostigmine treatment on blood-brain barrier permeability and cholinesterase activity in rat brain.
    Behavioural brain research, 2009, Nov-05, Volume: 203, Issue:2

    Topics: Acetylcholinesterase; Animals; Autoradiography; Avoidance Learning; Blood-Brain Barrier; Brain; Cholinesterase Inhibitors; Chromatography, High Pressure Liquid; Disease Models, Animal; Erythrocytes; Male; Permeability; Persian Gulf Syndrome; Pyridostigmine Bromide; Radioimmunoassay; Rats; Stress, Physiological

2009
Continuous administration of pyridostigmine improves immobilization-induced neuromuscular weakness.
    Critical care medicine, 2010, Volume: 38, Issue:3

    Topics: Animals; Atracurium; Cholinesterase Inhibitors; Disease Models, Animal; Hindlimb; Immobilization; Infusion Pumps; Infusions, Subcutaneous; Male; Muscle Contraction; Muscle Strength; Muscle Weakness; Muscular Atrophy; Neuromuscular Junction; Neuromuscular Nondepolarizing Agents; Pyridostigmine Bromide; Rats; Rats, Sprague-Dawley; Receptors, Cholinergic

2010
Technical report: exploring the basis of congenital myasthenic syndromes in an undergraduate course, using the model organism, Caenorhabditis elegans.
    Invertebrate neuroscience : IN, 2010, Volume: 10, Issue:1

    Topics: Animals; Caenorhabditis elegans; Caenorhabditis elegans Proteins; Cholinesterase Inhibitors; Disease Models, Animal; Education, Medical, Undergraduate; Mutation; Myasthenic Syndromes, Congenital; Pyridostigmine Bromide; Receptors, Nicotinic

2010
Cholinesterase inhibitors and stress: effects on brain muscarinic receptor density in mice.
    Neurotoxicology, 2010, Volume: 31, Issue:5

    Topics: Animals; Brain; Cholinesterase Inhibitors; Cholinesterases; Disease Models, Animal; Dose-Response Relationship, Drug; Male; Mice; Mice, Inbred C57BL; Physostigmine; Protein Binding; Pyridostigmine Bromide; Receptors, Muscarinic; Stress, Psychological

2010
A Cys-loop mutation in the Caenorhabditis elegans nicotinic receptor subunit UNC-63 impairs but does not abolish channel function.
    The Journal of biological chemistry, 2011, Jan-28, Volume: 286, Issue:4

    Topics: 4-Aminopyridine; Amifampridine; Animals; Caenorhabditis elegans; Caenorhabditis elegans Proteins; Cholinesterase Inhibitors; Disease Models, Animal; Gene Expression Regulation; Humans; Muscles; Mutation; Myasthenic Syndromes, Congenital; Neuromuscular Junction; Potassium Channel Blockers; Protein Structure, Secondary; Pyridostigmine Bromide; Receptors, Nicotinic; Swimming

2011
Impaired neuromuscular transmission and response to acetylcholinesterase inhibitors in centronuclear myopathies.
    Neuromuscular disorders : NMD, 2011, Volume: 21, Issue:6

    Topics: Adolescent; Animals; Biopsy; Child; Cholinesterase Inhibitors; Disease Models, Animal; Electromyography; Female; Gene Knockout Techniques; Humans; Infant; Male; Muscle, Skeletal; Myopathies, Structural, Congenital; Neuromuscular Junction; Protein Tyrosine Phosphatases, Non-Receptor; Pyridostigmine Bromide; Synaptic Transmission; Treatment Outcome; Zebrafish; Zebrafish Proteins

2011
Myotubular myopathy and the neuromuscular junction: a novel therapeutic approach from mouse models.
    Disease models & mechanisms, 2012, Volume: 5, Issue:6

    Topics: Animals; Cell Membrane; Disease Models, Animal; Gene Expression Regulation; Mice; Mice, Knockout; Motor Activity; Myopathies, Structural, Congenital; Neuregulin-1; Neuromuscular Junction; Phenotype; Pyridostigmine Bromide; Receptors, Cholinergic; Signal Transduction; Synaptic Transmission

2012
Lipidomic profiling of phosphocholine-containing brain lipids in mice with sensorimotor deficits and anxiety-like features after exposure to Gulf War agents.
    Neuromolecular medicine, 2012, Volume: 14, Issue:4

    Topics: Animals; Anxiety; Ataxia; Brain Chemistry; Cerebral Cortex; DEET; Dentate Gyrus; Disease Models, Animal; Exploratory Behavior; Fatty Acids; Female; Gliosis; Male; Maze Learning; Mice; Mice, Inbred C57BL; Nerve Tissue Proteins; Permethrin; Peroxisomes; Persian Gulf Syndrome; Phosphatidylcholines; Psychomotor Performance; Pyridostigmine Bromide; Random Allocation; Rotarod Performance Test; Sensation Disorders; Sphingomyelins; Stearoyl-CoA Desaturase

2012
Neuromuscular junction abnormalities in DNM2-related centronuclear myopathy.
    Journal of molecular medicine (Berlin, Germany), 2013, Volume: 91, Issue:6

    Topics: Adult; Animals; Child; Cholinesterase Inhibitors; Disease Models, Animal; Dynamin II; Female; Humans; Male; Motor Activity; Muscle Weakness; Muscle, Skeletal; Myopathies, Structural, Congenital; Neuromuscular Junction; Pyridostigmine Bromide; Young Adult; Zebrafish

2013
Evaluation of immunotoxicity induced by single or concurrent exposure to N,N-diethyl-m-toluamide (DEET), pyridostigmine bromide (PYR), and JP-8 jet fuel.
    Toxicology and industrial health, 2001, Volume: 17, Issue:5-10

    Topics: Animals; Cholinesterase Inhibitors; DEET; Disease Models, Animal; Drug Interactions; Female; Hydrocarbons; Hypersensitivity, Delayed; Immune System; Insect Repellents; Mice; Persian Gulf Syndrome; Pyridostigmine Bromide

2001
Stress and combined exposure to low doses of pyridostigmine bromide, DEET, and permethrin produce neurochemical and neuropathological alterations in cerebral cortex, hippocampus, and cerebellum.
    Journal of toxicology and environmental health. Part A, 2004, Jan-23, Volume: 67, Issue:2

    Topics: Animals; Cerebellum; Cerebral Cortex; Cholinesterase Inhibitors; Cognition Disorders; DEET; Disease Models, Animal; Dose-Response Relationship, Drug; Hippocampus; Humans; Insect Repellents; Movement Disorders; Persian Gulf Syndrome; Pyridostigmine Bromide; Rats; Rats, Sprague-Dawley; Stress, Psychological

2004
Effects of fosphenytoin on nerve agent-induced status epilepticus.
    Drug and chemical toxicology, 2004, Volume: 27, Issue:1

    Topics: Animals; Anticonvulsants; Atropine; Chemical Warfare Agents; Diazepam; Disease Models, Animal; Dose-Response Relationship, Drug; Drug Therapy, Combination; Electroencephalography; Guinea Pigs; Injections, Intraperitoneal; Male; Phenytoin; Pralidoxime Compounds; Pyridostigmine Bromide; Soman; Status Epilepticus

2004
The anti-inflammatory and cholinesterase inhibitor bifunctional compound IBU-PO protects from beta-amyloid neurotoxicity by acting on Wnt signaling components.
    Neurobiology of disease, 2005, Volume: 18, Issue:1

    Topics: Alzheimer Disease; Amyloid beta-Peptides; Amyloid beta-Protein Precursor; Animals; Anti-Inflammatory Agents, Non-Steroidal; beta Catenin; Brain; Cells, Cultured; Cholinesterase Inhibitors; Cytoskeletal Proteins; Disease Models, Animal; Down-Regulation; Drug Compounding; Glycogen Synthase Kinase 3; Glycogen Synthase Kinase 3 beta; Ibuprofen; Intercellular Signaling Peptides and Proteins; Mice; Mice, Transgenic; Neuroprotective Agents; Peptide Fragments; Pyridinium Compounds; Pyridostigmine Bromide; Rats; Rats, Sprague-Dawley; Signal Transduction; Trans-Activators; Wnt Proteins

2005
Extrapolating from animal studies to the efficacy in humans of a pretreatment combination against organophosphate poisoning.
    Archives of toxicology, 2007, Volume: 81, Issue:5

    Topics: Animals; Chemical Warfare Agents; Cholinergic Antagonists; Cyclopentanes; Disease Models, Animal; Dogs; Dose-Response Relationship, Drug; Drug Evaluation, Preclinical; Drug Therapy, Combination; Female; Humans; Infusions, Intravenous; Infusions, Parenteral; Lethal Dose 50; Male; Metabolic Clearance Rate; Organophosphate Poisoning; Organophosphates; Papio anubis; Poisoning; Pyridostigmine Bromide; Sarin; Species Specificity; Treatment Outcome

2007
Efficacy of biperiden and atropine as anticonvulsant treatment for organophosphorus nerve agent intoxication.
    Archives of toxicology, 2000, Volume: 74, Issue:3

    Topics: Animals; Anticonvulsants; Atropine; Biperiden; Cholinesterase Inhibitors; Cholinesterase Reactivators; Disease Models, Animal; Drug Therapy, Combination; Electroencephalography; Guinea Pigs; Lethal Dose 50; Male; Organophosphates; Organophosphorus Compounds; Pralidoxime Compounds; Pyridostigmine Bromide; Sarin; Seizures; Soman

2000
Neither forced running nor forced swimming affect acute pyridostigmine toxicity or brain-regional cholinesterase inhibition in rats.
    Toxicology, 2002, Jul-01, Volume: 176, Issue:1-2

    Topics: Administration, Oral; Animals; Blood-Brain Barrier; Brain; Cholinesterase Inhibitors; Cholinesterases; Corticosterone; Disease Models, Animal; Exercise Test; Horseradish Peroxidase; Male; Physical Exertion; Pyridostigmine Bromide; Rats; Rats, Sprague-Dawley; Running; Stress, Physiological; Swimming

2002