INT2397
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
Unlike previously reported studies with cultured cells of neuronal origin expressing only MAO A, both of these cell lines were sensitive to MPTP. | |||||||||||||||
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The toxicity of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), its oxidized metabolite, and two recently synthesized 2'-alkyl derivatives of MPTP (methyl and ethyl), found to be more toxic in vivo in mice, have been compared in two neuroblastoma hybrid cell lines (NCB-20 and 140-3) that express the B form of monoamine oxidase (MAO), as tissue culture models for the mode of action of MPTP in the central nervous system. | |||||||||||||||
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The toxicity of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), its oxidized metabolite, and two recently synthesized 2'-alkyl derivatives of MPTP (methyl and ethyl), found to be more toxic in vivo in mice, have been compared in two neuroblastoma hybrid cell lines (NCB-20 and 140-3) that express the B form of monoamine oxidase (MAO), as tissue culture models for the mode of action of MPTP in the central nervous system. | |||||||||||||||
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Toxicity of MPTP and structural analogs in clonal cell lines of neuronal origin expressing B type monoamine oxidase activity. | |||||||||||||||
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MAO activity and MAO protein concentration were therefore measured in platelets since this is the most easily accessible source of MAO. | |||||||||||||||
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It thus appears that MAO inhibition during smoking was compensated by a higher synthesis. | |||||||||||||||
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Therefore, a novel series of 1-thiocarbamoyl-3-substituted phenyl-5-(2-pyrrolyl)-4,5-dihydro-(1H)-pyrazole derivatives as promising MAO-B inhibitors was synthesized and investigated for the ability to inhibit selectively the activity of the A and B isoforms of monoamine oxidase (MAO). | |||||||||||||||
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Unexpectedly however, the platelet MAO protein concentration was also higher in S (Fig. 1D). | |||||||||||||||
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Methadone produced a slight but significant inhibition of whole brain MAO and a 34% inhibition of the striatal enzyme. | |||||||||||||||
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Subclasses of CFS have been associated with polymorphisms in genes that function in the HPA axis NR3C1, TPH2 and MAOA [37-39]. | |||||||||||||||
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We examined the expression of several 5-HT receptors and the enzyme monoamine oxidase (MAO-A) in frontal cortex of Gtf2ird1? | |||||||||||||||
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In contrast, MAOA deficiency in humans [17] and mice [18] leads to increased aggression, despite the resulting increase in 5-HT levels. | |||||||||||||||
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These neurons do not express tryptophan hydroxylase (Tph) or dopa decarboxylase (Aadc), which are required for serotonin synthesis, or the catabolic enzymes monoamine oxidase A and B. | |||||||||||||||
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Moreover, monoamine oxidase-A (MAO-A) expression is regulated by dimer formation of Clock and Bmal1, and MAO-A activity accordingly shows a circadian rhythmicity [118]. | |||||||||||||||
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