نتایج جستجو برای: monoamine oxidase inhibition

تعداد نتایج: 375913  

Journal: :Stroke 1987
N Oka I Akiguchi K Matsubayashi M Kameyama T Maeda J Kawamura

The density of sympathetic nerve terminals in human superficial temporal arteries from 5 cases at intra- and extracranial bypass surgery was examined with two histochemical methods, one with potassium permanganate fixation and the other with the new monoamine oxidase staining technique. By potassium permanganate fixation, small cored vesicles containing fibers of noradrenergic nerve terminals m...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2007
Ema Alves Teresa Summavielle Cecília Juliana Alves Joana Gomes-da-Silva José Custódio Barata Eduarda Fernandes Maria de Lourdes Bastos Maria Amélia Tavares Félix Carvalho

3,4-Methylenedioxymethamphetamine (MDMA)-induced neurotoxicity and the protective role of monoamine oxidase-B (MAO-B) inhibition were evaluated at the mitochondrial level in various regions of the adolescent rat brain. Four groups of adolescent male Wistar rats were used: (1) saline control, (2) exposed to MDMA (4 x 10 mg/kg, i.p.; two hourly), (3) treated with selegiline (2 mg/kg, i.p.) 30 min...

Journal: :The Journal of Experimental Medicine 1962
Michael D. Gershon Leonard L. Ross

Protection against anaphylactic shock in mice by reserpine has been shown to be a delayed phenomenon, probably not dependent upon a direct effect of reserpine. The release and depletion of catechol amines by reserpine show little likelihood of being responsible for protection because these substances are in themselves protective against anaphylactic shock, while beta-TM 10, a drug which interfe...

2014
S. Kavimani Sudha Rani

Oxidative stress plays a vital role in dopaminergic neurodegeneration of Parkinson’s disease (PD). However, an antidiabetic drug, pioglitazone had shown a positive effectagainst oxidative stress to treat nervous unrest. Objective of this study is to evaluate the protective effect of Pioglitazone (25mg/kg/p.o) against 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) mice model of PD. The PD i...

2012
Ji Ho Kim Gun Hee Kim Keum Hee Hwang

This research was designed to determine what components of Gardenia jasminoides play a major role in inhibiting the enzymes related antidepressant activity of this plant. In our previous research, the ethyl acetate fraction of G. jasminosides fruits inhibited the activities of both monoamine oxidase-A (MAO-A) and monoamine oxidase-B (MAO-B), and oral administration of the ethanolic extract slig...

Journal: :Journal of clinical pathology 1981
M Sandler M A Reveley V Glover

The most readily available source of monoamine oxidase in man is the platelet, although only the B form of the enzyme is represented in this site. Platelet activity is higher in women than in men. The enzyme activity is generally stable and is partly under genetic control. There is some evidence that individuals with low activity have a higher psychiatric morbidity than those with high activity...

Journal: :The Journal of biological chemistry 1989
S Ottoboni P Caldera A Trevor N Castagnoli

Kinetic deuterium isotope effects for the noncompetitive, intermolecular monoamine oxidase B-catalyzed oxidation of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) to the corresponding 1-methyl-4-phenyl-2,3-dihydropyridinium species MPDP+ were found to be 3.55 on Vmax and 8.01 on Vmax/Km with MPTP-6,6-d2 as the deuterated substrate. Similar values were obtained with MPTP-2,2,6-d4 and MPTP-C...

2014
Oscar M Bautista-Aguilera Gerard Esteban Mourad Chioua Katarina Nikolic Danica Agbaba Ignacio Moraleda Isabel Iriepa Elena Soriano Abdelouahid Samadi Mercedes Unzeta José Marco-Contelles

The design, synthesis, and biochemical evaluation of donepezil-pyridyl hybrids (DPHs) as multipotent cholinesterase (ChE) and monoamine oxidase (MAO) inhibitors for the potential treatment of Alzheimer's disease (AD) is reported. The 3D-quantitative structure-activity relationship study was used to define 3D-pharmacophores for inhibition of MAO A/B, acetylcholinesterase (AChE), and butyrylcholi...

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