نتایج جستجو برای: acetylcholinesterase inhibitor

تعداد نتایج: 217751  

Journal: :The Journal of biological chemistry 1981
P B Taylor F Rieger M L Shelanski L A Greene

The cellular localization of the molecular forms of acetylcholinesterase was explored in chick sympathetic neurons and in mouse T28 cells (neuroblastoma X sympathetic ganglion cell hybrids) using the reversible, poorly lipid-soluble inhibitor of acetylcholinesterase, BW284C51, to protect cell surface activity while inactivating cytoplasmic activity with DFP, an irreversible, lipid-soluble inhib...

Journal: :Expert review of neurotherapeutics 2001
Norifumi Tsuno

Alzheimer's disease (AD) is the most common cause of dementia and is characterized by an insidious onset and slow deterioration in cognition, activities of daily living (ADL), mood stability and social functioning. The cholinesterase inhibitors (ChEIs), developed based on the cholinergic hypothesis, are currently considered to be the best established treatment for AD, although the significant a...

Journal: :iranian journal of pharmaceutical research 0
aa moshtaghie m afrang m mesripour

the short and long term effects of chromium toxicity on brain catecholamines and acetylcholinesterase levels were investigated. rats were injected daily with varying amounts of chromium. the short term (2 h) administration of chromium (8 mmol/kg) reduced catecholamines level of cerebellum, mid-brain and brain-cortex by 22.8, 19.4 and 21.2% respectively. acetylcholinesterase activity was also re...

Journal: :Psychiatria Danubina 2009
Ninoslav Mimica Paola Presecki

The aim of this review is to describe side effects of five antidementives which are approved by the United States Food and Drug Administration (FDA); four acetylcholinesterase inhibitors and one glutamate - or N-metyl-D-aspartat receptor antagonist - memantine. The antidementives are well tolerated and undesired effects are rare; except hepatotoxicity of tacrine and gastrointestinal side effect...

Journal: :Journal of bacteriology 1969
L L Simpson H Morimoto

An attempt has been made to replicate an earlier finding that type A botulinum toxin can inhibit the in vitro activity of acetylcholinesterase. Two methods of enzyme assay were employed, but with neither technique were we able to reproduce the finding of in vitro enzyme inhibition. In fact, an examination of the data from the previous report leads us to question the possibility of the observati...

Journal: :Molecules 2017
Jingqian Su Huiying Liu Kai Guo Long Chen Minhe Yang Qi Chen

Acetylcholinesterase inhibitors (AChEIs) are an attractive research subject owing to their potential applications in the treatment of neurodegenerative diseases. Fungi and bacteria are major producers of AChEIs. Their active ingredients of fermentation products include alkaloids, terpenoids, phenylpropanoids, and steroids. A variety of in vitro acetylcholinesterase inhibitor assays have been de...

2000
P. KASA

In the symptomatic treatment of mild to moderately severe dementia associated with Alzheimer’s disease, donepezil (E2020) has been introduced for the inhibition of acetylcholinesterase activity in the human brain. However, there is no morphological evidence as to how this chemical agent affects the acetylcholinesterase-positive structures in the various areas of the human and the rat CNS. This ...

Journal: :Research, Society and Development 2022

Polar extracts of Tapirira guianensis Aubl. were prepared for evaluation biological activities. Identification and quantification phenolic compounds, antioxidant activity, inhibition acetylcholinesterase enzyme antifungal potential performed in all extracts. High contents total phenols detected the ethanolic aqueous leaves (237.10±5.39 mg EAG/g 346.46±5.67 EAG) respectively. The same had a free...

Journal: :El-cezeri 2021

In this study, new fumarate compounds (I-IV) containing some natural phenols (eugenol, guaiacol, isoeugenol and vanillin) were synthesized characterized. The single crystal X-ray diffraction technique was used to determine the structures of all compounds. All evaluated as acetylcholinesterase (AChE) inhibitory, especially compound IV (IC50 =5.25±0.51 µg/mL), can be identified a promising anti-a...

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