ibotenic acid has been researched along with Inflammation in 14 studies
Ibotenic Acid: A neurotoxic isoxazole (similar to KAINIC ACID and MUSCIMOL) found in AMANITA mushrooms. It causes motor depression, ataxia, and changes in mood, perceptions and feelings, and is a potent excitatory amino acid agonist.
Inflammation: A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function.
Excerpt | Relevance | Reference |
---|---|---|
"Patients with an orofacial pain history appear to be more susceptible to occlusal interference pain in dental practice for unknown reasons." | 1.43 | Inflammatory pain memory facilitates occlusal interference-induced masticatory muscle hyperalgesia in rats. ( Cao, Y; Ding, TT; Gan, YH; Liu, CR; Xie, QF; Xu, XX, 2016) |
"The persistent hyperalgesia and neuronal hyperexcitability may be mediated in part by a descending pain facilitatory system involving NGC." | 1.30 | Nucleus reticularis gigantocellularis and nucleus raphe magnus in the brain stem exert opposite effects on behavioral hyperalgesia and spinal Fos protein expression after peripheral inflammation. ( Dubner, R; Ren, K; Wei, F, 1999) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (7.14) | 18.2507 |
2000's | 6 (42.86) | 29.6817 |
2010's | 6 (42.86) | 24.3611 |
2020's | 1 (7.14) | 2.80 |
Authors | Studies |
---|---|
Saunders, MJ | 1 |
Edwards, BS | 1 |
Zhu, J | 1 |
Sklar, LA | 1 |
Graves, SW | 1 |
Yang, X | 1 |
Ji, J | 1 |
Liu, C | 1 |
Zhou, M | 1 |
Li, H | 1 |
Ye, S | 1 |
Hu, Q | 1 |
Degos, V | 2 |
Peineau, S | 2 |
Nijboer, C | 1 |
Kaindl, AM | 2 |
Sigaut, S | 1 |
Favrais, G | 3 |
Plaisant, F | 2 |
Teissier, N | 1 |
Gouadon, E | 2 |
Lombet, A | 2 |
Saliba, E | 1 |
Collingridge, GL | 2 |
Maze, M | 1 |
Nicoletti, F | 1 |
Heijnen, C | 1 |
Mantz, J | 2 |
Kavelaars, A | 2 |
Gressens, P | 7 |
Ding, TT | 1 |
Xu, XX | 1 |
Cao, Y | 1 |
Liu, CR | 1 |
Gan, YH | 1 |
Xie, QF | 1 |
Doverhag, C | 1 |
Keller, M | 2 |
Karlsson, A | 1 |
Hedtjarn, M | 1 |
Nilsson, U | 1 |
Kapeller, E | 1 |
Sarkozy, G | 2 |
Klimaschewski, L | 1 |
Humpel, C | 1 |
Hagberg, H | 1 |
Simbruner, G | 2 |
Savman, K | 1 |
Adén, U | 1 |
Winerdal, M | 1 |
Felderhoff-Mueser, U | 1 |
Lampa, J | 1 |
Lelièvre, V | 2 |
Ahmed, T | 1 |
Gilani, AH | 1 |
Chhor, V | 1 |
Loron, G | 1 |
Le Charpentier, T | 1 |
Josserand, J | 1 |
Ali, C | 1 |
Vivien, D | 1 |
Issa, L | 1 |
Rene, F | 1 |
Loeffler, JP | 1 |
Verney, C | 1 |
Morimoto, K | 1 |
Murasugi, T | 1 |
Oda, T | 1 |
Couvineau, A | 1 |
Laburthe, M | 1 |
Griesmaier, E | 1 |
Auer, M | 1 |
Schlager, G | 1 |
Urbanek, M | 1 |
Wei, F | 1 |
Dubner, R | 1 |
Ren, K | 1 |
Askovic, S | 1 |
Favara, C | 1 |
McAtee, FJ | 1 |
Portis, JL | 1 |
Patkai, J | 1 |
Mesples, B | 1 |
Dommergues, MA | 1 |
Fromont, G | 1 |
Thornton, EM | 1 |
Renauld, JC | 1 |
Evrard, P | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Phase II Multicenter 16-Week Randomized Double Blind Placebo-Controlled Evaluation of the Efficacy, Tolerability and Safety of Memantine Hydrochloride on Enhancing the Cognitive Abilities of Adolescents and Young Adults With Down Syndrome[NCT02304302] | Phase 2 | 160 participants (Actual) | Interventional | 2014-10-31 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
This is a measure of adaptive functioning that integrates information from 13 different domains (e.g., gross motor, social interaction, eating, toileting, dressing, personal self-care, etc.). It is in a questionnaire format, which a caregiver can complete while the participant is being tested. Standard scores for all indices will be derived from age norms that extend from birth to age 80, as these were used as dependent variables. We report here on the Broad Independence Score recorded as change in score from baseline (T1) to after the treatment (T2). The minimum value of the SIB-R Score Scale in this study was -24 (this number is below 0 because -24 was the minimum value for the worst performing participant in the trial) and the maximum value of this scale is 153; higher scores mean better outcomes. (NCT02304302)
Timeframe: baseline and 16 weeks from start of treatment
Intervention | score on a scale (Mean) |
---|---|
Placebo | 6.88 |
Memantine | 3.23 |
The primary efficacy measure is focused on episodic memory. The CVLT-II short form assesses supraspan word learning ability as an index of episodic verbal long-term memory. We hypothesize that treatment with memantine will produce significant improvements in this test. The main dependent variable selected, based on prior literature was the total number of target items correct summed across learning trials 1-4. The values for this measure have been recorded as change in score from baseline (T1) to after the treatment (T2). Scale Range: from 0 to 36; higher scores represent better outcomes. (NCT02304302)
Timeframe: baseline and 16 weeks from start of treatment
Intervention | score on a scale (Mean) |
---|---|
Placebo | 3.3 |
Memantine | 3.49 |
This is a measure of non-verbal memory that requires the participant to learn associations between an abstract visual pattern and its location. Two dependent variables have been selected: Total number of items correct on the first trial of each stage, and total number of stages completed. The values for this measure have been recorded as change in score from baseline (T1) to after the treatment (T2). The minimum value of the PAL Memory Score Scale is 0 and the maximum value is 21; higher scores mean better outcomes. (NCT02304302)
Timeframe: baseline and 16 weeks from start of treatment
Intervention | score on a scale (Mean) |
---|---|
Placebo | 1 |
Memantine | 0.67 |
This is a measure of non-verbal memory. Total number correct across the two series of items presented was used as the dependent variable. We used the PRM total scale in this study, which represents the sum of the PRM correct scores (ranging from 0 to 24) and the PRM delayed scores (ranging from 0 to 24). Therefore, the range of the PRM total scale is from 0 to 48; higher values mean better outcomes. (NCT02304302)
Timeframe: baseline and 16 weeks from start of treatment
Intervention | score on a scale (Mean) |
---|---|
Placebo | 0.45 |
Memantine | -0.05 |
This is a measure of rote short-term verbal memory. Total number of items correct were used as the dependent variable. The values for this measure have been recorded as change in score from baseline (T1) to after the treatment (T2). The minimum value for this scale is 0 and the maximum value is 38; higher scores mean a better outcome. (NCT02304302)
Timeframe: baseline and 16 weeks from start of treatment
Intervention | score on a scale (Mean) |
---|---|
Placebo | 0.03 |
Memantine | -0.01 |
This measure is a computerized version of the Corsi Blocks task, a long-standing neuropsychological test. The main dependent variables selected for this test was the span length, which is the longest sequence of numbers recalled accurately. The minimum value of the Spatial Span Length Score Scale is 0 and the maximum value is 9; higher scores mean better outcomes. The values for this measure have been recorded as change in score from baseline (T1) to after the treatment (T2). (NCT02304302)
Timeframe: baseline and 16 weeks from start of treatment
Intervention | score on a scale (Mean) |
---|---|
Placebo | 0.13 |
Memantine | 0.03 |
"The test requires participants to search under a series of colored boxes to locate a blue token hidden underneath one of them. During a series of trials, the participant is told that the token will be in a new location each time and that they should not go back to a location he or she has looked in previously. The main dependent variable was the total number of errors (between errors), which indexes the number of times a participant went back to a box where a token had already been found, lower scores mean better performance. The minimum value of the Spatial Working Memory scale is 0 and the maximum value is 137 (which was computed as the equivalent to -4 standard deviations from the mean of this measure); higher scores mean worse outcomes. The values for this measure have been recorded as change in score from baseline (T1) to after the treatment (T2)." (NCT02304302)
Timeframe: baseline and 16 weeks from start of treatment
Intervention | score on a scale (Mean) |
---|---|
Placebo | -0.09 |
Memantine | -1.4 |
"This is a measure of inhibitory control, often used as a marker for prefrontal-striatal function integrity. Specifically, it measures the participant's ability to inhibit pre-potent behavioral responses that have been established by provision of prior go or no-go cues in a classical conditioning paradigm. The main dependent variables selected was speed of response of execution to Go targets. The minimum value of the speed of response of execution to Go targets is 280 milliseconds (ms) and the maximum value is 1000 ms; higher scores mean worse outcomes. The values for this measure have been recorded as change in score from baseline (T1) to after the treatment (T2)." (NCT02304302)
Timeframe: baseline and 16 weeks from start of treatment
Intervention | ms (Mean) |
---|---|
Placebo | -2.52 |
Memantine | 0.22 |
This test provides a measure of non-verbal reasoning ability that requires subjects to visually inspect a matrix of 4 or 9 pictures that has a missing piece. Participants have to infer a rule or pattern in the stimuli and select the appropriate response from a range of 4-6 possibilities. Since age norms are not available for individuals older than 17y11m, the ability score will be used as the dependent variable. This is an intermediate score based on Rasch modeling that corrects for different items set being administered to participants. The minimum value of the DAS-II Rasch Score Scale is 0 and the maximum value is 153; higher scores mean better outcomes. The values for this measure have been recorded as change in score from baseline (T1) to after the treatment (T2). (NCT02304302)
Timeframe: baseline and 16 weeks from start of treatment
Intervention | score on a scale (Mean) |
---|---|
Placebo | 0.75 |
Memantine | 2.66 |
This is a measure of receptive semantics, whereby the participant is asked to point to a picture (out of 4) that corresponds to a word spoken by the examiner. As this test has a 0.85 correlation with composite measures of Verbal IQ (i.e. from the Wechsler Intelligence Scale series), it can be used in conjunction with the Matrices subtest to estimate overall intellectual functioning. The total number of items correct was used as the dependent variable, following the administration manual's rules for basals and ceilings. The values for this measure have been recorded as change in score from baseline (T1) to after the treatment (T2). The minimum value for this scale is 0 and the maximum value is 192, higher scores mean a better outcome. (NCT02304302)
Timeframe: baseline and 16 weeks from start of treatment
Intervention | score on a scale (Mean) |
---|---|
Placebo | 4.46 |
Memantine | 5.63 |
This is a measure of receptive syntax skills (Bishop, 1983). Participants are asked to point to a picture (out of 4) that corresponds to a phrase or sentence spoken by the examiner. The total number of items correct (rather than blocks passed) will be used as the dependent variable, following the administration manual's ceiling rule. The values for this measure have been recorded as change in score from baseline (T1) to after the treatment (T2). The minimum value of the scores is 0 and the maximum value is 40; with higher scores considered to be a better outcome. (NCT02304302)
Timeframe: baseline and 16 weeks from start of treatment
Intervention | score on a scale (Mean) |
---|---|
Placebo | 0.49 |
Memantine | 0.89 |
Incidence of adverse events was monitored by clinical history, physical examinations, electrocardiograms (ECGs), clinical laboratory tests, the Screen for Childhood Anxiety Related Emotional Disorders (SCARED). Here, we report the analysis of the effect of memantine treatment on QTc intervals because of its clinical importance for this analysis for potential drug toxicity. QTc intervals ≥ 450 ms are generally considered long, and drug-induced QTc interval prolongations ≥ 60 ms are generally considered clinically relevant. (NCT02304302)
Timeframe: baseline and 16 weeks from start of treatment
Intervention | ms (Mean) |
---|---|
Placebo | -1.30 |
Memantine | -0.11 |
14 other studies available for ibotenic acid and Inflammation
Article | Year |
---|---|
Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
Topics: Animals; Biotinylation; Flow Cytometry; Fluorescence Resonance Energy Transfer; Green Fluorescent Pr | 2010 |
HJ22, a Novel derivative of piperine, Attenuates ibotenic acid-induced cognitive impairment, oxidativestress, apoptosis and inflammation via inhibiting the protein-protein interaction of Keap1-Nrf2.
Topics: Alkaloids; Animals; Apoptosis; Benzodioxoles; Cells, Cultured; Cognitive Dysfunction; Disease Models | 2020 |
G protein-coupled receptor kinase 2 and group I metabotropic glutamate receptors mediate inflammation-induced sensitization to excitotoxic neurodegeneration.
Topics: Analysis of Variance; Animals; Animals, Newborn; Calcium; Calcium-Calmodulin-Dependent Protein Kinas | 2013 |
Inflammatory pain memory facilitates occlusal interference-induced masticatory muscle hyperalgesia in rats.
Topics: Animals; Carrageenan; Facial Pain; Hyperalgesia; Ibotenic Acid; Inflammation; Male; Masticatory Musc | 2016 |
Pharmacological and genetic inhibition of NADPH oxidase does not reduce brain damage in different models of perinatal brain injury in newborn mice.
Topics: Animals; Animals, Newborn; Apoptosis; Brain Injuries; Excitatory Amino Acid Agonists; Female; Gene E | 2008 |
Systemic inflammation sensitizes the neonatal brain to excitotoxicity through a pro-/anti-inflammatory imbalance: key role of TNFalpha pathway and protection by etanercept.
Topics: Animals; Blotting, Western; Brain; Brain Injuries; Calcium-Binding Proteins; Caspase 3; Enzyme-Linke | 2010 |
A comparative study of curcuminoids to measure their effect on inflammatory and apoptotic gene expression in an Aβ plus ibotenic acid-infused rat model of Alzheimer's disease.
Topics: Alzheimer Disease; Amyloid beta-Peptides; Animals; Anti-Inflammatory Agents, Non-Steroidal; Apoptosi | 2011 |
Activation of microglial N-methyl-D-aspartate receptors triggers inflammation and neuronal cell death in the developing and mature brain.
Topics: Animals; Brain; Brain Injuries; Calcium; Cell Death; Cell Survival; Cells, Cultured; Culture Media, | 2012 |
Acute neuroinflammation exacerbates excitotoxicity in rat hippocampus in vivo.
Topics: Acute Disease; Animals; Excitatory Amino Acid Agonists; Hippocampus; Ibotenic Acid; Inflammation; Li | 2002 |
Involvement of VIP and PACAP in neonatal brain lesions generated by a combined excitotoxic/inflammatory challenge.
Topics: Animals; Animals, Newborn; Brain; Female; Gene Expression; Ibotenic Acid; Inflammation; Interleukin- | 2007 |
Dextromethorphan is protective against sensitized N-methyl-D-aspartate receptor-mediated excitotoxic brain damage in the developing mouse brain.
Topics: Animals; Animals, Newborn; Apoptosis; Brain; Caspase 3; Dextromethorphan; Disease Models, Animal; En | 2008 |
Nucleus reticularis gigantocellularis and nucleus raphe magnus in the brain stem exert opposite effects on behavioral hyperalgesia and spinal Fos protein expression after peripheral inflammation.
Topics: 5,6-Dihydroxytryptamine; Animals; Behavior, Animal; Creatinine; Freund's Adjuvant; Hindlimb; Hyperal | 1999 |
Increased expression of MIP-1 alpha and MIP-1 beta mRNAs in the brain correlates spatially and temporally with the spongiform neurodegeneration induced by a murine oncornavirus.
Topics: Animals; Brain; Cell Death; Chemokine CCL3; Chemokine CCL4; Chemokines, CC; Ibotenic Acid; Immunohis | 2001 |
Deleterious effects of IL-9-activated mast cells and neuroprotection by antihistamine drugs in the developing mouse brain.
Topics: Animals; Animals, Newborn; Behavior, Animal; Brain; Cerebral Palsy; Cromolyn Sodium; Disease Models, | 2001 |