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1.
Dis Esophagus ; 31(2)2018 Feb 01.
Article in English | MEDLINE | ID: mdl-29077856

ABSTRACT

As a hallmark of platelet activation, mean platelet volume (MPV) has been identified to be associated with various malignancies. However, the correlation between MPV, mean platelet volume/platelet count ratio (MPR), and esophageal squamous cell carcinoma (ESCC) remains unclear. The aim of this study is to clarify the relevance of MPV and MPR in patients with locally advanced ESCC. Four hundred and fifty-seven cases with newly diagnosed locally advanced ESCC followed by radical surgery and 240 healthy subjects matched for age and gender were included in this study. We retrospectively compared various hematological variables between groups and analyzed the correlation between MPV, MPR, and patients' clinicopathologic characteristics. Preoperative MPV and MPR were found to be significantly decreased in locally advanced ESCC when compared to healthy controls, they were (8.14 ± 1.09 fL vs. 10.23 ± 0.78 fL, P < 0.0001) and (0.03875 ± 0.02645 vs. 0.04463 ± 0.00972, P = 0.001), respectively. In addition, patients with advanced tumor length (≥4 cm) tended to have lower MPV levels (8.03 ± 1.11 fL versus 8.33 ± 1.21 fL, P = 0.005), while there was no difference between other subgroups. Moreover, decreased MPR was significantly correlated with advanced tumor length (P < 0.001) when divided at a median of 0.03420. Decreased MPV and MPR were significantly associated with locally advanced ESCC. Thus, they might be helpful in screening and risk stratification for locally advanced ESCC in combination with other approaches.


Subject(s)
Carcinoma, Squamous Cell , Esophageal Neoplasms , Mean Platelet Volume/methods , Platelet Count/methods , Carcinoma, Squamous Cell/blood , Carcinoma, Squamous Cell/diagnosis , Carcinoma, Squamous Cell/epidemiology , Carcinoma, Squamous Cell/pathology , Case-Control Studies , China/epidemiology , Esophageal Neoplasms/blood , Esophageal Neoplasms/diagnosis , Esophageal Neoplasms/epidemiology , Esophageal Neoplasms/pathology , Esophageal Squamous Cell Carcinoma , Esophagectomy/methods , Esophagectomy/statistics & numerical data , Female , Humans , Male , Middle Aged , Neoplasm Staging , Prognosis , Risk Assessment
2.
Biosens Bioelectron ; 42: 177-85, 2013 Apr 15.
Article in English | MEDLINE | ID: mdl-23202349

ABSTRACT

Transgenic zebrafish are a common vertebrate model system for the study of addictive behavior. In the present study, plasmid constructs containing green fluorescent protein (GFP) and the promoter of tyrosine hydroxylase (TH), a key synthetic enzyme for catecholamines, were produced. The TH-GFP constructs were microinjected into zebrafish embryonic cells. Three days post-fertilization, GFP began expressing in distinct catecholaminergic areas. The TH-GFP transgenic zebrafish were employed as live biosensors to test the effects of the commonly abused drugs nicotine and ketamine. First, locomotion assays were used to study the general excitatory effects of the drugs. Maximal locomotor activity was obtained after treatment with a high concentration of nicotine (10 µM), but with a much lower concentration of ketamine (0.1 µM). Second, TH protein levels in zebrafish brains were assessed by Western blot. TH protein levels were significantly increased, with maximal protein levels found after treatment with the same drug concentrations that gave maximal locomotor activity. Importantly, analysis of GFP in the zebrafish catecholaminergic areas revealed the same expression patterns as was obtained by Western blot. The present results indicate that increased locomotor activity can be correlated to TH protein expression, as indicated by Western blot and expression of TH-GFP. We have shown that TH-GFP expression is a reliable method to show the effects of drugs on TH expression that may be employed as a novel high-throughput live biosensor for screening drugs of abuse.


Subject(s)
Biosensing Techniques/methods , Green Fluorescent Proteins/chemistry , Locomotion/drug effects , Tyrosine 3-Monooxygenase/chemistry , Animals , Animals, Genetically Modified , Illicit Drugs , Ketamine/administration & dosage , Nicotine/administration & dosage , Promoter Regions, Genetic , Zebrafish/embryology , Zebrafish/genetics
3.
Biosens Bioelectron ; 31(1): 548-53, 2012 Jan 15.
Article in English | MEDLINE | ID: mdl-22024592

ABSTRACT

Cytochrome P450 (CYPs) is significant in degradation of endogenous substrates and detoxification of carcinogens, therefore it is a biomarker for assessment of polycyclic aromatic hydrocarbons (PAHs) level in aquatic environment. In the present study, a transgenic line of zebrafish had been generated using a CYP-green fluorescence protein (CYP-GFP) construct, driven by CYP1A1 promoter. Polychlorinated biphenyls (PCBs) were used as toxicant, in concentrations of 0.02 µg/ml, 0.04 µg/ml, 0.08 µg/ml, 0.4 µg/ml, and 0.8 µg/ml. The transgenic control fish showed low intensity of fluorescence in the liver. After exposed to PCBs, zebrafish had morphological changes such as expansion of yolk, contortion of tails and inflation of pericardial area. Green fluorescence signals were found to express according to concentrations and time. The green fluorescence signal was most intense after treatment with 0.08 µg/ml PCBs. However, the maximum area of green fluorescent signal was found at 0.04 µg/ml PCBs. GFP started to express at 3h exposure to PCBs, increasing its intensity until 6 h exposure, and then level off. Since the GFP expression is fast responding and is sensitive to low PAHs concentrations, transgenic fish is a good tool for live imaging and monitoring of aquatic contamination.


Subject(s)
Biological Assay/instrumentation , Biosensing Techniques/instrumentation , Cytochrome P-450 Enzyme System/analysis , Environmental Monitoring/instrumentation , Toxicity Tests/instrumentation , Water Pollutants, Chemical/toxicity , Zebrafish/physiology , Animals , Animals, Genetically Modified , Dose-Response Relationship, Drug , Equipment Design , Equipment Failure Analysis , Reproducibility of Results , Sensitivity and Specificity , Water Pollutants, Chemical/analysis
4.
Neurosignals ; 15(6): 322-31, 2006.
Article in English | MEDLINE | ID: mdl-18437031

ABSTRACT

Methamphetamine (MA), a commonly abused psychostimulant, induces the drug dependence by enhancing the dopamine-mediated neurotransmission. Ketamine (KET) is a non-competitive N-methyl-D-aspartate receptor antagonist, which can be actually mixed with MA for polydrug abuse. In the present study, the individual and combined effects of KET (10 mg/kg, i.p.) and MA (1 mg/kg, i.p.) on conditioned place preference in rats were investigated. The alterations of serine 897 phosphorylations of NR1 receptors in the striatum and ventral tegmental area of after-conditioning rats were measured immunochemically. The results showed repeated administrations of MA, KET and their combination, at the doses studied, all could induce psychological dependences evaluated by conditioned place preference. KET was not able to suppress the MA-induced place preference. The modulations of NR1 phosphorylations in basal ganglia were partly responsible to place preference. Although the alterations induced by KET were not significant in most areas we studied, MA showed a significant increase in the ventral tegmental area but a marked decrease in caudate putamen and nucleus accumbens. Such alterations were much more significant when KET and MA were combined. These results have important implications for public awareness of harm with combined drug abuse. Further investigations toward the specific interaction of the two drugs are necessary.


Subject(s)
Basal Ganglia/drug effects , Conditioning, Classical/drug effects , Ketamine/pharmacology , Methamphetamine/pharmacology , Receptors, N-Methyl-D-Aspartate/drug effects , Spatial Behavior/drug effects , Substance-Related Disorders/physiopathology , Animals , Basal Ganglia/physiology , Basal Ganglia/ultrastructure , Conditioning, Classical/physiology , Male , Neurons/drug effects , Neurons/metabolism , Nucleus Accumbens/cytology , Nucleus Accumbens/drug effects , Nucleus Accumbens/physiology , Organ Specificity , Phosphorylation/drug effects , Phosphoserine/analysis , Protein Processing, Post-Translational/drug effects , Rats , Rats, Wistar , Receptors, N-Methyl-D-Aspartate/chemistry , Receptors, N-Methyl-D-Aspartate/physiology , Spatial Behavior/physiology , gamma-Aminobutyric Acid/physiology
5.
Neurochem Res ; 16(6): 687-92, 1991 Jun.
Article in English | MEDLINE | ID: mdl-1791915

ABSTRACT

A model of incomplete cerebral ischemia involving bilateral ligation of the common carotid arteries in rats, was used to examine the potential of a Chinese herbal preparation and of nifedipine to reduce cell damage following cerebral ischemia. The herbal preparation contained ginsengosides and extracts of Panax notoginseng, Ligusticum chuanxiong Hort., Carthamus tinctorius L. and Salvia militorrhiza Bge. Histological evidence of cell damage and the formation of peroxidation products were both reduced in rats pretreated with the herbal preparation or with nifedipine. It has been suggested that the free radical reaction is involved in tissue damage, particularly in the pathological neurocyte injury of cerebral ischemia. The results show that in this model of incomplete cerebral ischemia, the degree of lipid peroxidation can be lowered by the pretreatment with Chinese herbs containing ginsengosides or with nifedipine. These drugs maybe beneficial in the treatment of cerebral ischemia in humans.


Subject(s)
Brain Ischemia/pathology , Drugs, Chinese Herbal/pharmacology , Neurons/drug effects , Nifedipine/pharmacology , Animals , Cell Survival/drug effects , Female , Male , Neurons/ultrastructure , Rats , Rats, Inbred Strains
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