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1.
Bioinspir Biomim ; 19(1)2023 11 29.
Article in English | MEDLINE | ID: mdl-37976540

ABSTRACT

Inspired by the capillary transport function of plant leaf veins, this study proposes three typical leaf vein features by observing a large number of leaves, including wedge shape, branch asymmetry, as well as hierarchical arrangement, and investigates their capillary transport mechanism. Not only a preliminary theoretical analysis of capillary flow in the bio-inspired channels was carried out, but the COMSOL Multiphysics simulation software was also used to simulate gas-liquid two-phase flow in biomimetic channels. The results reveal the efficient transport mechanism of the leaf vein inspired structure and provide insight into the design of capillary transmission channels.


Subject(s)
Plant Leaves , Software , Plant Leaves/anatomy & histology , Computer Simulation
2.
J Am Chem Soc ; 145(36): 20141-20148, 2023 Sep 13.
Article in English | MEDLINE | ID: mdl-37639692

ABSTRACT

Chemodivergent synthesis has been achieved in asymmetric photocatalysis. Under a dual catalyst system consisting of a chiral phosphoric acid and DPZ as a photosensitizer, different inorganic bases enabled the formation of two sets of valuable products from the three-component radical tandem transformations of 2-bromo-1-arylenthan-1-ones, styrenes, and quinoxalin-2(1H)-ones. The key to success was the distinct pKa environment, in which the radicals that formed on the quinoxalin-2(1H)-one rings after two radical addition processes underwent either single-electron oxidation or single-electron reduction. In addition, this work represents the first use of quinoxalin-2(1H)-ones in asymmetric photoredox catalysis.

3.
Bioinspir Biomim ; 17(6)2022 10 20.
Article in English | MEDLINE | ID: mdl-36103869

ABSTRACT

Topological motifs in pore architecture can profoundly influence the structural properties of that architecture, such as its mass, porosity, modulus, strength, and surface permeability. Taking the irregular cellular structure of the tri-spine horseshoe crab as a research model, we present a new approach to the quantitative description and analysis of structure-property-function relationships. We employ a robust skeletonization method to construct a curve-skeleton that relies on high-resolution 3D tomographic data. The topological motifs and mechanical properties of the long-range cellular structure were investigated using the Grasshopper plugin and uniaxial compression test to identify the variation gradient. Finite element analysis was conducted for the sub-volumes to obtain the variation in effective modulus along the three principal directions. The results show that the branch length and node distribution density varied from the tip to the base of the sharp corner. These node types formed a low-connectivity network, in which the node types 3-N and 4-N tended to follow the motifs of ideal planar triangle and tetrahedral configurations, respectively, with the highest proportion of inter-branch angles in the angle ranges of 115-120° and 105-110°. In addition, mapping the mechanical gradients to topological properties indicated that narrower profiles with a given branch length gradient, preferred branch orientation, and network connectedness degree are the main factors that affect the mechanical properties. These factors suggest significant potential for designing a controllable, irregularly cellular structure in terms of both morphology and function.


Subject(s)
Horseshoe Crabs , Animals
4.
J Mech Behav Biomed Mater ; 125: 104954, 2022 01.
Article in English | MEDLINE | ID: mdl-34741983

ABSTRACT

Horseshoe crab (order Xiphosura) has a large and thick carapace that has evolved as a protective tool to defend against predators and resist impacts from surf-zone turbulence. The naturally occurring spatial variation in the mechanical properties of the carapace cuticle need to be investigated to understand their regulatory mechanism and the underlying design strategies. In this work, we used a combination of high-resolution optical microscopy, scanning electron microscopy, (SEM) and energy-dispersive X-ray spectroscopy (EDS) to evaluate the multiscale microstructure and elemental composition of the cuticle of tri-spine horseshoe crab (Tachypleus tridentatus). The moduli, ultimate strengths, and failure strains of the three individual layers and the entire cuticle were systematically characterized in both the dry and hydrated states. The failure behaviors and energy absorption of the cuticle involved stress stiffening, toughness mechanism and environmental adaptation were analyzed qualitatively and quantitatively and then correlated with the morphological features in different cuticle regions. The mechanical properties are primarily influenced by the endocuticle thickness ratio; a higher thickness ratio corresponds to more stacking of the vertical lamellae, leading to a lower modulus, weaker strength, and greater elongation of the endocuticle. Radial energy is absorbed primarily by the endocuticle, with the energy absorbed in the radial direction being nearly twice that absorbed in the circumferential direction. This is attributed to the larger failure strain and relatively small decrease in the stress plateau in the radial direction. The findings provide a deeper understanding of how nature modulates the cuticle's mechanical properties and inspiration for developing high-performance synthetic composites.


Subject(s)
Animal Shells , Horseshoe Crabs , Animals
5.
Anal Chem ; 91(10): 6815-6819, 2019 05 21.
Article in English | MEDLINE | ID: mdl-31050286

ABSTRACT

The ability to sort and dispense droplets accurately is essential to droplet-based single-cell analysis. Here, we describe a fluorescence-activated single-droplet dispenser (FASD) that is analogous to a conventional fluorescence-activated cell sorter, but sorts droplets containing single cells within an oil emulsion. The FASD system uses cytometric detection and electrohydrodynamic actuation-based single-droplet manipulation, allowing droplet isolation and dispensing with high efficiency and accuracy. The system is compatible with multiwell plates and can be integrated with existing microfluidic devices and large-scale screening systems. By enabling sorting based on single-cell reactions such as PCR, this platform will help expand the basis of cell sorting from mainly protein biomarkers to nucleic acid sequences and secreted biomolecules.


Subject(s)
Cell Separation/instrumentation , Flow Cytometry/instrumentation , Single-Cell Analysis/instrumentation , Fluorescence , Humans , K562 Cells , Lab-On-A-Chip Devices
6.
Eur J Pharmacol ; 714(1-3): 83-8, 2013 Aug 15.
Article in English | MEDLINE | ID: mdl-23791614

ABSTRACT

Parkinson's disease (PD) is a progressive neurodegenerative disorder affecting predominantly the dopaminergic mesotelencephalic system. Enormous progress has been made in the treatment of PD. Our previous study has shown that hydroxysafflor yellow A (HSYA) could attenuate the neurotoxicity induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine in mice. In the present work, we examined whether HSYA had the neuroprotective effect on dopaminergic neurons of substantia nigra in a rat model of PD. Adult Sprague-Dawley rats were unilaterally injected with 6-hydroxydopamine (6-OHDA) into the medial forebrain bundle. The PD rats were treated with HSYA (2 or 8 mg/kg) via caudal vein injection daily for 4 weeks. Rotational tests showed that HSYA significantly attenuated apomorphine-induced turns in 6-OHDA-induced PD rats. HSYA treatment resulted in a significant protection against the loss of tyrosine hydroxylase-positive cells. Our data showed that HSYA also increased the levels of dopamine and its metabolites, glial cell line-derived neurotrophic factor and brain-derived neurotrophic factor in striatum of PD rats. In conclusion, these results supported a role for HSYA in preserving dopamine neuron integrity and motor function in a rodent model of PD, and implied a potential neuroprotective role for HSYA in this disease.


Subject(s)
Chalcone/analogs & derivatives , Neuroprotective Agents/pharmacology , Oxidopamine , Parkinson Disease/prevention & control , Quinones/pharmacology , 3,4-Dihydroxyphenylacetic Acid/metabolism , Animals , Apomorphine/pharmacology , Behavior, Animal/drug effects , Chalcone/pharmacology , Gene Expression Regulation, Enzymologic/drug effects , Homovanillic Acid/metabolism , Male , Neostriatum/drug effects , Neostriatum/metabolism , Parkinson Disease/metabolism , Rats , Rats, Sprague-Dawley , Rotation , Substantia Nigra/drug effects , Substantia Nigra/metabolism , Tyrosine 3-Monooxygenase/metabolism
7.
Food Chem Toxicol ; 51: 137-42, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23036454

ABSTRACT

We conducted a 90-day feeding study to investigate subchronic toxicity of rice hull fiber. Sprague Dawley rats were randomly divided into four groups; each received a diet containing 0%, 2.5%, 3.75% and 5.0% (w/w) rice hull fiber for 90days. Clinical observations were carried out daily, with weekly measurements of body weight and food consumption. We performed ophthalmic and histological examinations at termination. Blood and urine samples were collected to measure hematology and clinical chemistry parameters. No mortality, ophthalmic abnormalities, or adverse treatment-related effects were seen during clinical observations, hematological tests, or analyses of urine. Macroscopic or microscopic examinations of organs revealed no treatment related abnormalities. The only treatment related significant changes were reduced concentrations of fasting blood glucose (up to 17.6%) and cholesterol (up to 22.0%), typical benefits of dietary fiber, in males treated with 3.75 and 5% rice hull fiber. The no-observed-adverse-effect-level (NOAEL) for rice hull fiber was 5.0% for both genders (females, 3.80g/kg body weight/day; males, 4.11g/kg body weight/day).


Subject(s)
Oryza/adverse effects , Toxicity Tests, Subchronic , Administration, Oral , Animal Feed , Animals , Blood Chemical Analysis , Blood Glucose/analysis , Body Weight/drug effects , Cholesterol/blood , Diet , Dietary Fiber/adverse effects , Female , Male , No-Observed-Adverse-Effect Level , Organ Size/drug effects , Rats , Rats, Sprague-Dawley
8.
Food Chem Toxicol ; 50(5): 1432-8, 2012 May.
Article in English | MEDLINE | ID: mdl-22343037

ABSTRACT

The aim of the study was to determine the effects of Asperosaponin VI (ASA VI), a triterpene saponin isolated from Dipsacus asper Wall, on chronic myocardial infarction (MI) and possible mechanisms in rats. MI was induced by permanent ligation of the left coronary artery. Twenty-four hours after MI, the rats were administered the extract by gavage (once a day). Six weeks after MI/sham surgery, cardiac dysfunction, infarct size (IS), cardiac fibrosis, hydroxyproline concentration, the oxidative stress parameter and inflammation mediators were examined. The results indicated that ASA VI improved left ventricular systolic pressure (LVSP), left ventricular end-diastolic pressure (LVEDP), ±dP/dt, heart weight/body weight, right ventricular weight/body weight and lung weight/body weight (P<0.01, P<0.05). These were accompanied by the attenuation of cardiac fibrosis, IS and hydroxyproline concentration (P<0.01, P<0.05). ASA VI could decrease the levels of tumor necrosis factor-α (TNF-α) and interleukin 6 (IL-6), but increase IL-10 content (P<0.01, P<0.05). Furthermore, it also could raise the activities of catalase, superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px), but reduce malonyldialdehyde (MDA) level (P<0.01, P<0.05). The results indicated that ASA VI improved cardiac function and myocardial fibrosis from myocardial ischemia injury, and this cardioprotection might be attributed to reduce oxidative stress and regulate inflammation mediators.


Subject(s)
Myocardial Infarction/physiopathology , Saponins/pharmacology , Administration, Oral , Animals , Body Weight , Disease Models, Animal , Fibrosis , Interleukin-10/metabolism , Interleukin-6/metabolism , Male , Myocardial Infarction/metabolism , Myocardial Infarction/pathology , Organ Size , Oxidative Stress , Rats , Rats, Sprague-Dawley , Tumor Necrosis Factor-alpha/metabolism
9.
Environ Toxicol Pharmacol ; 33(2): 304-11, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22301160

ABSTRACT

Fucoidan is a complex sulfated polysaccharide, derived from marine brown seaweed. In the present study, we investigated the effects of fucoidan on improving learning and memory impairment in rats induced by infusion of Aß (1-40), and its possible mechanisms. The results indicated that fucoidan could ameliorate Aß-induced learning and memory impairment in animal behavioral tests. Furthermore, fucoidan reversed the decreased activity of choline acetyl transferase (ChAT), superoxide dismutase (SOD), glutathione peroxidase (GSH-Px) and content of acetylcholine (Ach), as well as the increased activity of acetylcholine esterase (AchE) and content of malondialdehyde (MDA) in hippocampal tissue of Aß-injected rats. Moreover, these were accompanied by an increase of Bcl-2/Bax ratio and a decrease of caspase-3 activity. These results suggested that fucoidan could ameliorate the learning and memory abilities in Aß-induced AD rats, and the mechanisms appeared to be due to regulating the cholinergic system, reducing oxidative stress and inhibiting the cell apoptosis.


Subject(s)
Amyloid beta-Peptides , Behavior, Animal/drug effects , Cognition Disorders/drug therapy , Cognition/drug effects , Neuroprotective Agents/pharmacology , Nootropic Agents/pharmacology , Peptide Fragments , Phaeophyceae/chemistry , Polysaccharides/pharmacology , Acetylcholine/metabolism , Acetylcholinesterase/metabolism , Animals , Apoptosis/drug effects , Avoidance Learning/drug effects , Caspase 3/metabolism , Choline O-Acetyltransferase/metabolism , Cognition Disorders/chemically induced , Cognition Disorders/metabolism , Cognition Disorders/psychology , Disease Models, Animal , Dose-Response Relationship, Drug , Female , GPI-Linked Proteins/metabolism , Glutathione Peroxidase/metabolism , Hippocampus/drug effects , Hippocampus/metabolism , Male , Malondialdehyde/metabolism , Memory/drug effects , Motor Activity/drug effects , Neuroprotective Agents/isolation & purification , Nootropic Agents/isolation & purification , Oxidative Stress/drug effects , Polysaccharides/isolation & purification , Proto-Oncogene Proteins c-bcl-2/metabolism , Rats , Rats, Sprague-Dawley , Reaction Time/drug effects , Superoxide Dismutase/metabolism , bcl-2-Associated X Protein/metabolism
10.
Cell Mol Neurobiol ; 32(4): 523-9, 2012 May.
Article in English | MEDLINE | ID: mdl-22222440

ABSTRACT

One of the plausible ways to prevent the reactive oxygen species (ROS)-mediated cellular injury is dietary or pharmaceutical augmentation of endogenous antioxidant defense capacity. In this study, we investigated the neuroprotective effect of fucoidan on H(2)O(2)-induced apoptosis in PC12 cells and the possible signaling pathways involved. The results showed that fucoidan inhibited the decrease of cell viability, scavenged ROS formation and reduced lactate dehydrogenase release in H(2)O(2)-induced PC12 cells. These changes were associated with an increase in superoxide dismutase and glutathione peroxidase activity, and reduction in malondialdehyde. In addition, fucoidan treatment inhibited apoptosis in H(2)O(2)-induced PC12 cells by increasing the Bcl-2/Bax ratio and decreasing active caspase-3 expression, as well as enhancing Akt phosphorylation (p-Akt). However, the protection of fucoidan on cell survival, p-Akt, the Bcl-2/Bax ratio and caspase-3 activity were abolished by pretreating with phosphatidylinositol-3-kinase (PI3K) inhibitor LY294002. In consequence, fucoidan might protect the neurocytes against H(2)O(2)-induced apoptosis via reducing ROS levels and activating PI3K/Akt signaling pathway.


Subject(s)
Apoptosis/drug effects , Neuroprotective Agents/pharmacology , Phosphatidylinositol 3-Kinases/metabolism , Polysaccharides/pharmacology , Proto-Oncogene Proteins c-akt/metabolism , Signal Transduction/physiology , Animals , Antineoplastic Agents/pharmacology , Apoptosis/physiology , Hydrogen Peroxide/toxicity , Oxidants/toxicity , PC12 Cells , Rats , Signal Transduction/drug effects
11.
Toxicol In Vitro ; 26(1): 1-6, 2012 Feb.
Article in English | MEDLINE | ID: mdl-21978812

ABSTRACT

Sophocarpine, a tetracyclic quinolizidine alkaloid, is one of the most abundant active ingredients in Sophora alopecuroides L. Our previous studies have showed that sophocarpine exerts anti-inflammatory activity in animal models. In the present study, anti-inflammatory mechanisms of sophocarpine were investigated in lipopolysaccharide (LPS)-induced responses in RAW 264.7 cells. Furthermore, the cytotoxicity of sophocarpine was tested. The results indicated that sophocarpine could increase the LDH level and inhibit cell viability up to 800µg/ml, and which was far higher than that of the plasma concentration of sophocarpine in clinical effective dosage. The results also demonstrated that sophocarpine (50 and 100µg/ml) suppressed LPS-stimulated NO production and pro-inflammatory cytokines secretion, including tumor necrosis factor alpha (TNF-α) and interleukin-6 (IL-6). These were associated with the decrease of the expression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2). Furthermore, sophocarpine inhibited LPS-mediated nuclear factor-κB (NF-κB) activation via the prevention of inhibitor κB (IκB) phosphorylation. Sophocarpine had no effect on the LPS-induced phosphorylation of extracellular signal-regulated kinase 1/2 (Erk1/2), whereas it attenuated the phosphorylation of p38 mitogen-activated protein (MAP) kinase and c-Jun NH(2)-terminal kinase (JNK). Our data suggested that sophocarpine exerted anti-inflammatory activity in vitro, and it might attribute to the inhibition of iNOS and COX-2 expressions via down-regulation of the JNK and p38 MAP kinase signal pathways and inhibition of NF-κB activation.


Subject(s)
Alkaloids/pharmacology , Anti-Inflammatory Agents/pharmacology , Cyclooxygenase 2 Inhibitors/pharmacology , Mitogen-Activated Protein Kinases/metabolism , NF-kappa B/metabolism , Animals , Cell Line , Cell Survival/drug effects , Cyclooxygenase 2/metabolism , I-kappa B Proteins/metabolism , Interleukin-6/metabolism , L-Lactate Dehydrogenase/metabolism , Lipopolysaccharides , Mice , NF-KappaB Inhibitor alpha , Nitric Oxide/metabolism , Nitric Oxide Synthase Type II/metabolism , Signal Transduction/drug effects , Tumor Necrosis Factor-alpha/metabolism
12.
Food Chem Toxicol ; 49(9): 2090-5, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21645579

ABSTRACT

The aim of the study was to determine the effects of fucoidan on rat myocardial ischemia-reperfusion (I/R) model and elucidate the potential mechanisms. Myocardial I/R injury was induced by the occlusion of left anterior descending coronary artery for 30 min followed by reperfusion for 2h. After 2h reperfusion, hemodynamics parameters were detected. Blood samples were collected to determine serum levels of tumor necrosis factor-α (TNF-α) and interleukin 6, 10 (IL-6, 10). Hearts were harvested to assess histopathological changes, infarct size (IS), and the content of myeloperoxidase (MPO). The expression of high-mobility group box 1 (HMGB1), phosphor-IκB-α and phosphor-nuclear factor kappa B (NF-κB) were assayed by western blot. Compared with control group, treatment with fucoidan improved left ventricular systolic pressure (LVSP), left ventricular end-diastolic pressure (LVEDP) and the contractility index (P<0.05, P<0.01). Fucoidan reduced the myocardial IS, the levels of TNF-α and IL-6, and the activity of MPO (P<0.05, P<0.01). Fucoidan down-regulated the expression of HMGB1, phosphor-IκB-α and NF-κB, but increased the content of IL-10 when compared with control (P<0.05, P<0.01). Besides, the infiltration of polymorph nuclear leukocytes (PMNs) and histopathological damages in myocardium were decreased in fucoidan treated groups (PMNs, P<0.05, P<0.01). These findings revealed that the administration of fucoidan could regulate the inflammation response via HMGB1 and NF-κB inactivation in I/R-induced myocardial damage.


Subject(s)
Inflammation/prevention & control , Myocardial Reperfusion Injury/prevention & control , Phaeophyceae/chemistry , Polysaccharides/pharmacology , Animals , Blotting, Western , Cytokines/blood , HMGB1 Protein/metabolism , Hemodynamics , Inflammation/physiopathology , Myocardial Reperfusion Injury/physiopathology , NF-kappa B/metabolism , Peroxidase/metabolism , Polysaccharides/isolation & purification , Rats , Rats, Sprague-Dawley
13.
J Ethnopharmacol ; 135(3): 620-5, 2011 Jun 01.
Article in English | MEDLINE | ID: mdl-21459139

ABSTRACT

ETHNOPHARMACOLOGICAL RELEVANCE: Sophora alopecuroides L. (the clinical usefulness of compound Kudouzi injection) has been used mainly for the treatment of fever, inflammation, edema and pain. Sophocarpine, a tetracyclic quinolizidine alkaloid, is one of the most abundant active ingredients in Sophora alopecuroides L. Sophocarpine injection (called the Kangke injection) has been demonstrated to have significant antivirus effects against coxsackievirus B3 and therapeutic effects for viral myocarditis in clinical. AIM OF THE STUDY: The present study was to evaluate the protective effect of sophocarpine on the inhibition of NF-kappaB (NF-κB) and effect on inflammatory markers during myocardial ischemia-reperfusion (I/R) injury in rat. MATERIALS AND METHODS: Myocardial I/R injury was induced by the occlusion of left anterior descending coronary artery for 30 min followed by reperfusion for 2 h. 2 h after reperfusion was established, the hemodynamics and infarct size were examined. Blood samples were collected for biochemical analysis. Expression of NF-κB and mitogen-activated protein kinases (MAPKs) in ischemic myocardial tissue were assayed by western blot. RESULTS: Administration of sophocarpine significantly improved cardiac function and reduced infarct size in I/R rat heart in vivo. Furthermore, sophocarpine ameliorated the contents of inflammatory mediators (tumor necrosis factor-alpha, TNF-α; interleukin-6, IL-6; IL-10), neutrophil infiltration and myeloperoxidase (MPO) activity. Interestingly, sophocarpine also significantly inhibited translocation of NF-κB, which was associated with attenuated phosphorylations of p38 and c-Jun NH2-terminal protein kinase (JNK). CONCLUSIONS: Inflammatory mediators, infiltration of neutrophil, and MPO were ameliorated via down-regulation of JNK and p38, and inactivation of NF-κB. This might be one of the important mechanisms of sophocarpine that protected myocardial injury from I/R.


Subject(s)
Alkaloids/therapeutic use , Anti-Inflammatory Agents/therapeutic use , Myocardial Infarction/prevention & control , Myocardial Reperfusion Injury/prevention & control , NF-kappa B/antagonists & inhibitors , Phytotherapy , Sophora/chemistry , Alkaloids/isolation & purification , Alkaloids/pharmacology , Animals , Anti-Inflammatory Agents/isolation & purification , Anti-Inflammatory Agents/pharmacology , Biological Transport/drug effects , Coronary Occlusion , Heart/drug effects , Heart/physiopathology , Inflammation Mediators/metabolism , Mitogen-Activated Protein Kinases/metabolism , Myocardial Infarction/metabolism , Myocardial Infarction/pathology , Myocardial Reperfusion Injury/metabolism , Myocardial Reperfusion Injury/pathology , Myocardium/metabolism , Myocardium/pathology , Neutrophils/metabolism , Peroxidase/metabolism , Plant Extracts/chemistry , Plant Extracts/pharmacology , Plant Extracts/therapeutic use , Rats , Rats, Sprague-Dawley , Seeds
14.
J Food Sci ; 76(6): T125-9, 2011 Aug.
Article in English | MEDLINE | ID: mdl-22417523

ABSTRACT

UNLABELLED: Tartrazine is an artificial azo dye commonly used in human food and pharmaceutical products. The present study was conducted to evaluate the toxic effect of tartrazine on the learning and memory functions in mice and rats. Animals were administered different doses of tartrazine for a period of 30 d and were evaluated by open-field test, step-through test, and Morris water maze test, respectively. Furthermore, the biomarkers of the oxidative stress and pathohistology were also measured to explore the possible mechanisms involved. The results indicated that tartrazine extract significantly enhanced active behavioral response to the open field, increased the escape latency in Morris water maze test and decreased the retention latency in step-through tests. The decline in the activities of catalase, glutathione peroxidase (GSH-Px), and superoxide dismutase (SOD) as well as a rise in the level of malonaldehyde (MDA) were observed in the brain of tartrazine-treated rats, and these changes were associated with the brain from oxidative damage. The dose levels of tartrazine in the present study produced a few adverse effects in learning and memory functions in animals. The mechanisms might be attributed to promoting lipid peroxidation products and reactive oxygen species, inhibiting endogenous antioxidant defense enzymes and the brain tissue damage. PRACTICAL APPLICATION: Tartrazine is an artificial azo dye commonly used in human food and pharmaceutical products. Since the last assessment carried out by the Joint FAO/WHO Expert Committee on Food Additives in 1964, many new studies have been conducted. However, there is a little information about the effects on learning and memory performance. The present study was conducted to evaluate the toxic effect of tartrazine on the learning and memory functions in animals and its possible mechanism involved. Based on our results, we believe that more extensive assessment of food additives in current use is warranted.


Subject(s)
Brain/drug effects , Food Coloring Agents/adverse effects , Learning/drug effects , Memory/drug effects , Neurons/drug effects , Tartrazine/adverse effects , Animals , Behavior, Animal/drug effects , Biomarkers/metabolism , Brain/metabolism , Brain/pathology , Dose-Response Relationship, Drug , Escape Reaction/drug effects , Exploratory Behavior/drug effects , Female , Food Coloring Agents/administration & dosage , Male , Malondialdehyde/metabolism , Mice , Mice, Inbred Strains , Neurons/metabolism , Neurons/pathology , Oxidative Stress/drug effects , Oxidoreductases/metabolism , Random Allocation , Rats , Rats, Sprague-Dawley , Tartrazine/administration & dosage
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