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1.
Biosens Bioelectron ; 247: 115912, 2024 Mar 01.
Article in English | MEDLINE | ID: mdl-38096721

ABSTRACT

The monitoring of acetylcholinesterase (AChE) activity and the screening of its inhibitors are significance of the diagnosis and drug therapy of nervous diseases. A metal ions-mediated signal amplification strategy was developed for the highly sensitive and multicolor assay of AChE activity and visually screening its drug inhibitors. After the specific reaction between AChE and acetylthiocholine (ATCh), the hydrolysis product thiocholine (TCh) can directly and decompose the α-FeOOH nanorods (NRs) to release amounts of Fe2+, which was regarded as Fenton reagent to efficiently catalyze H2O2 to produce ·OH. Then, the as-formed ·OH can further largely shorten the gold nanobipyramids (Au NBPs), generating a series of palpable color variations. The linear range for AChE activity was 0.01-500.0 U/L with the limit of detection as low as 0.0074 U/L. The vivid visual effects could be easily distinguished for the multicolor assay of AChE activity by naked eye in visible light. To achieve the point-of-care testing, Au NBPs were further assembled on polymeric electrospun nanofibrous films (ENFs) surface as test strips for the easy-to-use test of AChE activity by RGB values with a smartphone. Fascinatingly, this proposed strategy can be used for the visual screening AChE inhibitors or non-inhibitors. Comparing with the clinical drugs (rivastigmine tartrate, and donepezil), some natural alkaloids such as evodiamine, caffeine, camptothecin, and berberine hydrochloride were selected as inhibitor modes to confirm the drug screening capability of this method. This proposed strategy may have great potential in the other disease-related enzymatic biomarkers assay and the rapid screening of drug therapy.


Subject(s)
Biosensing Techniques , Metal Nanoparticles , Acetylcholinesterase , Hydrogen Peroxide , Drug Evaluation, Preclinical/methods , Biosensing Techniques/methods , Cholinesterase Inhibitors/pharmacology , Cholinesterase Inhibitors/analysis , Point-of-Care Testing
2.
Int J Biol Macromol ; 58: 127-32, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23567289

ABSTRACT

Sargassum fusiforme is a kind of brown algae that has been widely consumed not only as food, but also as herbal medicine for thousands of years. The purpose of this study was to investigate the antioxidant activities and intestinal functions of polysaccharides extracted from S. fusiforme (SFP) in normal and cyclophosphamide-induced immunosuppressed mice. The experiment was performed on six groups of ICR mice, which treated with cyclophosphamide (CY, 200 mg/kg) or different dosages of SFP for 14 days. The results showed that administration of SFP was able to overcome the immunosuppression, and significantly increased the spleen index and antioxidant activities in mice (P<0.05). It also remarkably improved the numbers of jejunal intraepithelial lymphocytes (IELs) and goblet cells in immunosuppressed mice (P<0.05). For normal mice, SFP increased both thymus index and intestinal function parameters such as villus length/crypt depth ratio and intestinal IELs and goblet cells (P<0.05). The results suggested that SFP, possessing pronounced antioxidant activities, may play an important role in the improvement of intestinal function in mice. This might be one of the possible mechanisms of SFP for the immunomodulatory effects.


Subject(s)
Antioxidants/pharmacology , Immunologic Factors/pharmacology , Jejunum/drug effects , Plant Extracts/pharmacology , Polysaccharides/pharmacology , Sargassum/chemistry , Animals , Glutathione/metabolism , Jejunum/cytology , Jejunum/immunology , Liver/enzymology , Lymphocytes/drug effects , Lymphocytes/immunology , Malondialdehyde/metabolism , Mice, Inbred ICR , Spleen/drug effects , Spleen/immunology , Superoxide Dismutase/metabolism , Thymus Gland/drug effects , Thymus Gland/immunology
3.
Food Chem Toxicol ; 48(2): 620-5, 2010 Feb.
Article in English | MEDLINE | ID: mdl-19944127

ABSTRACT

Phorbol esters are the main toxins in Jatropha curcas seed and oil. The aim of this study was to assess the acute toxicity of phorbol esters given by intragastric administration and to determine the LD50 for Swiss Hauschka mice. The LD50 and 95% confidence limits for male mice were 27.34 mg/kg body mass and 24.90-29.89 mg/kg body mass; and the LD5 and LD95 were 18.87 and 39.62 mg/kg body mass, respectively. The regression equations between the probits of mortalities (Y) and the log of doses (D) was Y=-9.67+10.21 log (D). Histopathological studies on the organs from the dead mice showed: (1) no significant abnormal changes in the organs at the lowest dose (21.26 mg/kg body mass) studied, (2) prominent lesions mainly found in lung and kidney, with diffused haemorrhages in lung, and glomerular sclerosis and atrophy in kidney at doses > or = 32.40 mg/kg body mass, and (3) multiple abruption of cardiac muscle fibres and anachromasis of cortical neurons at the highest dose of 36.00 mg/kg body mass. The results obtained would aid in developing safety measures for the Jatropha based biofuel industry and in exploiting the pharmaceutical and agricultural applications of phorbol esters.


Subject(s)
Jatropha/chemistry , Phorbol Esters/toxicity , Administration, Oral , Animal Feed , Animals , Cerebral Cortex/drug effects , Cerebral Cortex/pathology , Glomerulosclerosis, Focal Segmental/chemically induced , Glomerulosclerosis, Focal Segmental/pathology , Heart/drug effects , Hemorrhage/chemically induced , Hemorrhage/pathology , Lethal Dose 50 , Lung Diseases/chemically induced , Lung Diseases/pathology , Male , Mice , Myocytes, Cardiac/drug effects , Myocytes, Cardiac/pathology , Plant Extracts/toxicity , Specific Pathogen-Free Organisms
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