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1.
Eur Rev Med Pharmacol Sci ; 24(14): 7578, 2020 07.
Article in English | MEDLINE | ID: mdl-32744683

ABSTRACT

Since this article has been suspected of research misconduct and the corresponding authors did not respond to our request to prove originality of data and figures, "MiR-20a regulates fibroblast-like synoviocyte proliferation and apoptosis in rheumatoid arthritis, by X.-J. Wei, X.-W. Li, J.-L. Lu, Z.-X. Long, J.-Q. Liang, S.-B. Wei, C.-X. Lu, W.-Z. Lu, published in Eur Rev Med Pharmacol Sci 2017; 21 (17): 3886-3893-PMID: 28975975" has been withdrawn. The Publisher apologizes for any inconvenience this may cause. https://www.europeanreview.org/article/13351.

2.
Eur Rev Med Pharmacol Sci ; 24(11): 6446-6454, 2020 06.
Article in English | MEDLINE | ID: mdl-32572942

ABSTRACT

OBJECTIVE: Traumatic brain injury (TBI) induced neuroinflammation is featured as excessive glial inflammatory activation and violent neurologic destruction and dysfunction. Massive microglia activation in situ and disrupt of blood-brain barrier contribute to severely collapsed nervous system. Tizoxanide (TIZ), a synthetic thiazolide derivative agent possessing a broad-spectrum anti-infective effect, currently shows a potential resistance against pathogens like bacteria, virus and parasites, while its underlying role in neuroinflammation is elusive. The study aimed to explore the effect of TIZ on neuroinflammation in vitro microglia. MATERIALS AND METHODS: Primary microglia were accepted to neuroinflammatory activation via lipopolysaccharide (LPS) administration. TIZ was conducted to pretreatment of microglia. Cell viability, inflammatory cytokines, chemotaxis, nitric oxide release, inflammation-related enzymes, and mitogen-activated protein kinase (MAPK) pathway activation in microglia were investigated respectively. RESULTS: We demonstrated that TIZ administration attenuates inflammatory cytokines and chemokines through quantitative real-time polymerase chain reaction (qRT-PCR) and enzyme-linked immunosorbent assay (ELISA) of medium supernatant. In addition, TIZ reduces pro-inflammatory mediators and nitric oxide release in microglia. Furtherly, TIZ inhibits the level of p38/MAPK pathway in LPS stimuli, indicating that TIZ negatively regulates neuroinflammation via inhibiting p38/MAPK pathway. CONCLUSIONS: TIZ is verified to be an anti-inflammation effect on neuroinflammation in microglia via downregulation of p38/MAPK pathway, which restrains inflammation by reduced inflammatory cytokines, chemokines and mediators and decreased nitric oxide release. To summarize, TIZ is considered to be a promising reagent to alleviate neuroinflammation targeting microglia in nervous system injury.


Subject(s)
Inflammation/drug therapy , Lipopolysaccharides/antagonists & inhibitors , Microglia/drug effects , Thiazoles/pharmacology , p38 Mitogen-Activated Protein Kinases/antagonists & inhibitors , Animals , Cell Survival/drug effects , Cells, Cultured , Female , Inflammation/chemically induced , Inflammation/pathology , MAP Kinase Signaling System/drug effects , Mice , Mice, Inbred C57BL , Microglia/metabolism , Microglia/pathology , Nitric Oxide/antagonists & inhibitors , Nitric Oxide/biosynthesis , Pregnancy , p38 Mitogen-Activated Protein Kinases/metabolism
3.
Eur Rev Med Pharmacol Sci ; 22(22): 7928-7937, 2018 11.
Article in English | MEDLINE | ID: mdl-30536340

ABSTRACT

OBJECTIVE: The aim of the study was to investigate the influences of micro ribonucleic acid (miR)-21 and downstream Toll-like receptor 4 (TLR4)/nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) pathway on myocardial apoptosis induced by myocardial ischemia-reperfusion (I/R) injury in rats. MATERIALS AND METHODS: Recombinant adeno-associated virus rAAV9-ZsGreen-pre-miR-21 and blank control virus were constructed. A total of 48 Sprague-Dawley (SD) rats were randomly divided into S1 group (open chest only), S2 group (transfection with blank virus + open chest), I/R1 group (transfection with blank virus + 6 d of myocardial I/R), and I/R2 group (transfection with miR-21 + 6 d of myocardial I/R). The cardiac function and myocardial infarct size of rats were evaluated in each group. Quantitative Polymerase Chain Reaction (qPCR) was applied to measure the expression level of miR-21 in the myocardium. The level of myocardial apoptosis in each group was detected through terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate-biotin nick end labeling (TUNEL) staining. Western blotting was performed to determine the protein expression levels of B-cell lymphoma 2 (Bcl-2)/Bcl-2-associated X protein (Bax), Caspase-3, TLR4, and NF-κB in the myocardium. The content of interleukin-6 (IL-6) and IL-10 was measured using enzyme-linked immunosorbent assay (ELISA) kits. RESULTS: The cardiac function of rats in I/R1 and I/R2 groups was significantly lower than that in S1 and S2 groups (p<0.01). Rats in I/R2 group had better cardiac function than those in I/R1 group (p<0.01). In I/R1 group, the level of myocardial apoptosis of rats was overtly increased compared with that in S1, S2, and I/R2 groups (p<0.01), while the expression level of miR-21 in myocardium was evidently lower than that in S1, S2, and I/R2 groups (p<0.01). Compared with S1, S2, and I/R2 groups, I/R1 group had markedly decreased Bcl-2/Bax expression level and IL-10 content and overtly elevated expression levels of Caspase-3, p-TLR4, p-NF-κB, and IL-6 content in the myocardium (p<0.01). CONCLUSIONS: Myocardial I/R injury in rats leads to decreased expression of miR-21. The overexpression of miR-21 is able to effectively inhibit the TLR4/NF-κB pathway and reduce the level of myocardial apoptosis of rats and the release of inflammatory factors.


Subject(s)
Apoptosis/physiology , MicroRNAs/biosynthesis , Myocardial Reperfusion Injury/metabolism , Myocardium/metabolism , NF-kappa B/metabolism , Toll-Like Receptor 4/metabolism , Animals , Male , MicroRNAs/antagonists & inhibitors , Myocardial Reperfusion Injury/pathology , Myocardial Reperfusion Injury/prevention & control , Myocardium/pathology , Rats , Rats, Sprague-Dawley , Signal Transduction/physiology
4.
Eur Rev Med Pharmacol Sci ; 22(21): 7240-7250, 2018 11.
Article in English | MEDLINE | ID: mdl-30468467

ABSTRACT

OBJECTIVE: Chemo-resistance of colon cancer remains a major problem in therapy. The role of miR-215-3p in the chemo-sensitivity of colon cancer remains unidentified. PATIENTS AND METHODS: Here, we constructed a 5-Fluoracil (5-Fu) resistant HCT116 cell line (HCT116/5-Fu) and miR-215-3p expression levels were measured in 56 cases of colon cancer tissues and 23 cases of normal tissues by quantitative real-time polymerase chain reaction (qRT-PCR). The effects of miR-215-3p on colon cancer cell growth and apoptosis were investigated using cell counting kit-8 (CCK-8) and apoptosis assay, respectively. In addition, CXC-chemokine receptor type1 (CXCR1) was identified as a target of miR-215-3p by using luciferase reporter assay. RESULTS: miR-215-3p was down-expressed in the 5-FU resistant cell compared to the parent cell. The level of miR-215-3p was correlated with the 5-Fu sensibility of colorectal cancer cell and the alteration of miR-215-3p affected the sensibility of colorectal cancer cells toward 5-Fu. Furthermore, miR-215-3p accelerated the apoptosis of colorectal cancer cell which was treated with 5-Fu. Mechanically, miR-215-3p regulated the level of endogenous CXCR1 in HCT116 cell and alternation of CXCR1 affected the 5-Fu sensibility mediated by miR-215-3p. Finally, overexpression of miR-215-3p restrained the growth of HCT116/5-Fu cells in the xenograft model. CONCLUSIONS: MiR-215-3p improved the 5-Fu sensibility via regulating the expression of CXCR1 in the colorectal cancer cell.


Subject(s)
Antimetabolites, Antineoplastic/pharmacology , Apoptosis/drug effects , Colorectal Neoplasms/drug therapy , Fluorouracil/pharmacology , MicroRNAs/metabolism , Receptors, Interleukin-8A/metabolism , Animals , Colorectal Neoplasms/genetics , Colorectal Neoplasms/metabolism , Colorectal Neoplasms/pathology , Dose-Response Relationship, Drug , Drug Resistance, Neoplasm , Female , Gene Expression Regulation, Neoplastic , HCT116 Cells , Humans , Mice, Nude , MicroRNAs/genetics , Receptors, Interleukin-8A/genetics , Signal Transduction , Tumor Burden/drug effects , Up-Regulation , Xenograft Model Antitumor Assays
5.
Eur Rev Med Pharmacol Sci ; 22(18): 6063-6071, 2018 09.
Article in English | MEDLINE | ID: mdl-30280792

ABSTRACT

OBJECTIVE: Multilocus sequence typing (MLST) was applied to investigate the genetic diversity of Candida albicans in the intestinal tract of cirrhosis patients. PATIENTS AND METHODS: We used CHROM agar Candida medium to obtain 105 Candida sp. isolates from fecal samples (276 subjects), including 63 isolates from the cirrhosis group (141 subjects) and 42 isolates from the healthy control group (135 subjects). RESULTS: Among the 105 Candida strains isolated, 60 strains were identified as Candida albicans. Patients with cirrhosis had significantly higher rates of colonization by Candida sp. (44.68% vs. 31.11%, p < 0.05) and C. albicans (27.66% vs. 15.56%, p < 0.05) relative to healthy controls. In the cirrhosis group, the rate of colonization further increased with disease progression and antibiotic treatment (p < 0.01). Sixty C. albicans isolates were analyzed by MLST. Fifty diploid sequence types (DST) were observed, and 26 new DSTs and 3 novel alleles were found. The majority of isolates were distributed among three clades, clade 8 (31.67%), clade 14 (15.00%) and clade 18 (21.67%). Among 39 strains from the cirrhosis group, 16 strains (41.02%) belonged to clade 8, while only 3 strains (14.29%) from healthy group belonged to clade 8 (p < 0.05). In addition, concatenated sequences of the 7 housekeeping gene fragments were analyzed for all the different DSTs in clade 8 to evaluate the loss of heterozygosity (LOH), which indicates C. albicans microvariation in the gut of cirrhosis patients. CONCLUSIONS: This study suggests that cirrhosis disease progression and antibiotic treatment is associated with increased colonization by Candida sp. and C. albicans. We are the first to provide MLST-based genotype profiles for C. albicans Guizhou China, and to identify clade 8 as the potential main clade of C. albicans colonization in the gut of cirrhosis patients.


Subject(s)
Candida albicans/classification , Candidiasis/microbiology , Liver Cirrhosis/microbiology , Multilocus Sequence Typing/methods , Anti-Bacterial Agents/therapeutic use , Candida albicans/drug effects , Candida albicans/genetics , Candidiasis/drug therapy , Case-Control Studies , Disease Progression , Feces/microbiology , Fungal Proteins/genetics , Genes, Essential , Humans , Mycological Typing Techniques , Phylogeny
6.
Eur Rev Med Pharmacol Sci ; 22(17): 5627-5634, 2018 09.
Article in English | MEDLINE | ID: mdl-30229838

ABSTRACT

OBJECTIVE: To investigate the relationship between microRNA-203 (miR-203) and diabetic nephropathy and its potential mechanism. MATERIALS AND METHODS: The expression of microRNA-203 in mice with diabetic nephropathy and M4200 cells cultured with high glucose was detected by quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR). Toll-like receptor 4 (TLR4), the target gene of microRNA-203, was predicted and screened by bioinformatics method. Real-time quantitative PCR and Western blot were used to detect the endogenous TLR4 level in renal cortex of db/db mice with diabetic nephropathy and glomerular mesangial cells cultured in high glucose or low glucose. The expression of microRNA-203 and TLR4 mRNA were evaluated by RT-PCR after treatment of miR-203 mimics and inhibitor. The protein of TLR4 level was detected by Western blot. Additionally, the proliferation ability of cells was evaluated by Cell Counting Kit-8 (CCK8). The target relationship between microRNA-203 and TLR4 3' UTR was confirmed by luciferase reporter assay RESULTS: The expression of miR-203 was significantly decreased in the kidney of mice with diabetic nephropathy and M4200 cells cultured in high glucose. On the contrary, TLR4 expression was significantly increased. Results of in vitro experiments showed that miR-203 could bind to 3'UTR region of TLR4. Overexpression of microRNA-203 significantly decreased the levels of TLR4 mRNA and protein. Meanwhile, low expression of miR-203 leaded to increased TLR4 expression, resulting in an enhanced proliferation of M4200 cells. CONCLUSIONS: The downregulation of microRNA-203 leaded to an increased level of TLR4, thus promoting proliferation of M4200 cells in the pathogenesis of diabetic nephropathy.


Subject(s)
Diabetic Nephropathies/etiology , MicroRNAs/physiology , Toll-Like Receptor 4/physiology , Animals , Cells, Cultured , Diabetic Nephropathies/genetics , Mesangial Cells/pathology , Mice
7.
Eur Rev Med Pharmacol Sci ; 21(17): 3886-3893, 2017 Oct.
Article in English | MEDLINE | ID: mdl-28975975

ABSTRACT

OBJECTIVE: STAT3 expression is elevated in the synovial tissue of patients with rheumatoid arthritis (RA). MiR-20a plays a role in mediating synovial inflammation in RA. Bioinformatics analysis has identified a binding site between miR-20 and the 3'-UTR of STAT3 mRNA. This study aimed to investigate the role of miR-20a in the regulation of STAT3 expression and synovial cell proliferation as well as apoptosis. PATIENTS AND METHODS: Synovial tissues were collected from RA patients and osteoarthritis (OA) patients to measure miR-20a, STAT3, p-STAT3, and Ki-67 expressions. Fibroblast-like synoviocytes (FLS) were treated with IL-17 (10 ng/ml) and then Ki-67 expression and cell cycle were evaluated by flow cytometry. The targeting relationship between miR-20a and STAT3 was assessed by dual luciferase reporter gene assay. FLS cells were divided into five groups: miR-NC, miR-20a mimic, si-NC, si-STAT3, and miR-20a mimic + si-STAT3 groups. RESULTS: In RA patients, significantly lower MiR-20a expression, and substantially higher STAT3, p-STAT3, and Ki-67 expression were found in the synovial tissues compared with those in OA patients. IL-17A treatment markedly promoted FLS cell proliferation, inhibited cell apoptosis, reduced miR-20a expression, as well as upregulated levels of STAT3, p-STAT3, and Bcl-2. MiR-20a played a regulatory function on the expression of STAT3. MiR-20a mimic and/or si-STAT3 transfection apparently downregulated STAT3, p-STAT3, and Bcl-2 expression, attenuated IL-17A-induced cell proliferation promotive and enhanced cell apoptosis in FLS cells. CONCLUSIONS: The expression of miR-20a was reduced in synovial tissue of RA patients with the increased level of STAT3. Downregulation of miR-20a promoted the expression of STAT3, p-STAT3, and Bcl-2, facilitated FLS cell proliferation, reduced apoptosis and, thereby, played a critical role in RA.


Subject(s)
Apoptosis , Arthritis, Rheumatoid/pathology , Cell Proliferation , MicroRNAs/metabolism , 3' Untranslated Regions , Aged , Antagomirs/metabolism , Apoptosis/drug effects , Arthritis, Rheumatoid/genetics , Cell Proliferation/drug effects , Cells, Cultured , Female , Fibroblasts/cytology , Fibroblasts/metabolism , Humans , Interleukin-17/pharmacology , Ki-67 Antigen/metabolism , Male , MicroRNAs/antagonists & inhibitors , MicroRNAs/genetics , Middle Aged , Osteoarthritis/genetics , Osteoarthritis/pathology , RNA Interference , RNA, Small Interfering/metabolism , STAT3 Transcription Factor/antagonists & inhibitors , STAT3 Transcription Factor/genetics , STAT3 Transcription Factor/metabolism , Synoviocytes/cytology , Synoviocytes/metabolism
8.
Transl Psychiatry ; 7(7): e1168, 2017 07 04.
Article in English | MEDLINE | ID: mdl-28675393

ABSTRACT

Many psychiatric diseases such as post-traumatic stress disorder (PTSD) are characterized by abnormal processing of emotional stimuli particularly fear. The medial prefrontal cortex (mPFC) is critically involved in fear expression. However, the molecular mechanisms underlying this process are largely unknown. Neuregulin-1 (NRG1) reportedly regulates pyramidal neuronal activity via ErbB4 receptors, which are abundant in parvalbumin (PV)-expressing interneurons in the PFC. In this study, we aimed to determine how NRG1/ErbB4 signaling in the mPFC modulates fear expression and found that tone-cued fear conditioning increased NRG1 expression in the mPFC. Tone-cued fear conditioning was inhibited following neutralization of endogenous NRG1 and specific inhibition or genetic ablation of ErbB4 in the prelimbic (PL) cortex but not in the infralimbic cortex. Furthermore, ErbB4 deletion specifically in PV neurons impaired tone-cued fear conditioning. Notably, overexpression of ErbB4 in the PL cortex is sufficient to reverse impaired fear conditioning in PV-Cre;ErbB4-/- mice. Together, these findings identify a previously unknown signaling pathway in the PL cortex that regulates fear expression. As both NRG1 and ErbB4 are risk genes for schizophrenia, our study may shed new light on the pathophysiology of this disorder and help to improve treatments for psychiatric disorders such as PTSD.


Subject(s)
Fear/physiology , Neuregulin-1/metabolism , Prefrontal Cortex/metabolism , Receptor, ErbB-4/metabolism , Animals , Behavior, Animal , Conditioning, Classical , Interneurons/metabolism , Mice , Mice, Knockout , Parvalbumins/metabolism , Receptor, ErbB-4/genetics , Signal Transduction
9.
Bull Entomol Res ; 107(1): 77-84, 2017 Feb.
Article in English | MEDLINE | ID: mdl-27444230

ABSTRACT

Green leaf volatiles (GLVs) have been reported to play an important role in the host-locating behavior of several folivores that feed on angiosperms. However, next to nothing is known about how the green leafhopper, Empoasca vitis, chooses suitable host plants and whether it detects differing emission levels of GLV components among genetically different tea varieties. Here we found that the constitutive transcript level of the tea hydroperoxide lyase (HPL) gene CsiHPL1, and the amounts of (Z)-3-hexenyl acetate and of total GLV components are significantly higher in tea varieties that are susceptible to E. vitis (Enbiao (EB) and Banzhuyuan (BZY)) than in varieties that are resistant to E. vitis (Changxingzisun (CX) and Juyan (JY)). Moreover, the results of a Y-tube olfactometer bioassay and an oviposition preference assay suggest that (Z)-3-hexenyl acetate and (Z)-3-hexenol offer host and oviposition cues for E. vitis female adults. Taken together, the two GLV components, (Z)-3-hexenol and especially (Z)-3-hexenyl acetate, provide a plausible mechanism by which tea green leafhoppers distinguish among resistant and susceptible varieties. Future research should be carried out to obtain the threshold of the above indices and then assess their reasonableness. The development of practical detection indices would greatly improve our ability to screen and develop tea varieties that are resistant to E. vitis.


Subject(s)
Acetates/metabolism , Aldehydes/metabolism , Camellia sinensis/metabolism , Hemiptera/physiology , Herbivory , Hexanols/metabolism , Animals , Cues , Food Chain , Plant Proteins/genetics , Plant Proteins/metabolism
10.
Eur Rev Med Pharmacol Sci ; 20(9): 1829-33, 2016 05.
Article in English | MEDLINE | ID: mdl-27212176

ABSTRACT

OBJECTIVE: To analyze the effects of intravascular embolization on adult vein of Galen aneurysmal dilatation (VGAD) patients. PATIENTS AND METHODS: Five consecutively selected patients (median age of 56.4 years) were diagnosed with VGAD in our hospital from February 2010 to February 2015 and treated with intravascular embolization. RESULTS: 2 cases were confirmed with malformed vessels in cerebellum, 2 cases in basal ganglia region and 1 case in brain stem; 3 cases with single branch artery blood supply and 2 cases with multiple branch artery blood supply; malformed vessel was 2.5-5.5 cm in diameter, on average 4.3 (±1.2) cm; 3 cases were dominated by intracranial hemorrhage, 1 case by a headache and 1 case by seizure; GCS scores ranged from 8-12, on average 10.5 (±1.6); intraoperative blood loss ranged from 20-80 ml, on average (55.8±15.9) ml; 1 case died after operation, 1 case was disabled, and the remainder were normal. CONCLUSIONS: Intravascular embolization was safe and effective for adult VGAD patients.


Subject(s)
Embolization, Therapeutic , Vein of Galen Malformations , Adult , Cerebellum , Dilatation, Pathologic , Humans , Middle Aged
11.
Neuroscience ; 307: 151-9, 2015 Oct 29.
Article in English | MEDLINE | ID: mdl-26318331

ABSTRACT

Identifying novel neuroprotectants that can halt or even reverse the effects of stroke is of interest to both clinicians and scientists. Neuregulin 1 (NRG1) is an effective neuroprotectant, but its molecular mechanisms are largely unclear. In this study, NRG1 rescued cortical neurons from oxygen-glucose deprivation (OGD) model, but the effect was blocked by neutralizing NRG1 and ErbB4 inhibition. In addition, γ-Aminobutyric acid (GABA) receptor agonists had no synergistic effect with NRG1, and the neuroprotective effect of NRG1 against OGD was partly blocked by GABA receptor antagonists. Importantly, NRG1 neuroprotection against brain ischemia was abolished in the mice with specific deletion of ErbB4 in parvalbumin (PV)-positive interneurons. In summary, NRG1 protects against ischemic brain injury via ErbB4 receptors by enhancing GABAergic transmission.


Subject(s)
Brain Injuries/metabolism , Brain Injuries/prevention & control , Neuregulin-1/therapeutic use , Neuroprotective Agents/therapeutic use , Receptor, ErbB-4/metabolism , Synaptic Transmission/drug effects , gamma-Aminobutyric Acid/metabolism , Animals , Apoptosis/drug effects , Apoptosis/physiology , Brain Injuries/etiology , Cell Hypoxia/drug effects , Cells, Cultured , Disease Models, Animal , GABA Agonists/pharmacology , Infarction, Middle Cerebral Artery/complications , Infarction, Middle Cerebral Artery/genetics , Male , Mice , Mice, Transgenic , Neuregulin-1/pharmacology , Neurons/drug effects , Neuroprotective Agents/pharmacology , Parvalbumins/metabolism , Rats , Receptor, ErbB-4/genetics , Synaptic Transmission/genetics
12.
Genet Mol Res ; 14(1): 2608-16, 2015 Mar 30.
Article in English | MEDLINE | ID: mdl-25867408

ABSTRACT

The aim of this study was to analyze the results of two crossing systems between wild boars and different domesticated pig breeds. Hybrid wild boars were produced by crossing captured wild boars with Meishan pigs and LY sows according to the traditional production system. The resultant commercial hybrids were black and white in coat color, respectively. Significant differences were found in the carcass and meat quality traits and nutritional values between these two hybrid wild boars. Compared with the white hybrid wild boars, at the age of 300 days, the body weight of black hybrid wild boars was 9.41 kg lower, while percent lean was 2.51% less and percent fat 2.45% higher (P < 0.05). The black hybrid wild boars had higher pH2 (6.17 vs 6.09) and intramuscular fat (3.34 vs 2.52%), lower drip loss (2.21 vs 2.68%) and shear force (44.00 vs 52.23) (P < 0.05), and more unsaturated fatty acids and essential amino acids (P < 0.05). In conclusion, cross breeding was shown to be an effective method to improve the overall production performance of wild boars, but crossing with different dam line breeds caused different responses. Compared with the white hybrid wild boars, the black hybrid wild boars had worse growth rate and carcass traits, but better meat quality traits and nutritional values.


Subject(s)
Body Weight/genetics , Hybridization, Genetic , Meat/analysis , Nutritive Value , Sus scrofa/genetics , Adipose Tissue/metabolism , Amino Acids, Essential/metabolism , Animals , Body Composition/genetics , Breeding/methods , Crosses, Genetic , Fatty Acids, Unsaturated/metabolism , Female , Hair Color/genetics , Male , Meat/standards , Quantitative Trait Loci/genetics , Swine
13.
Spinal Cord ; 53(8): 604-7, 2015 Aug.
Article in English | MEDLINE | ID: mdl-25687518

ABSTRACT

STUDY DESIGN: This is an interventional training session. OBJECTIVE: The objective of this study was to investigate the difference in response to self-assessment questions in the original and an adjusted version for a submodule of www.elearnSCI.org for student nurses. SETTING: The study was conducted in a teaching hospital affiliated to Peking University, China. METHODS: In all, 28 student nurses divided into two groups (groups A and B; 14 in each) received a print-out of a Chinese translation of the slides from the 'Maintaining skin integrity following spinal cord injury' submodule in www.elearnSCI.org for self-study. Both groups were then tested using the 10 self-assessment multiple-choice questions (MCQs) related to the same submodule. Group A used the original questions, whereas group B received an adjusted questionnaire. RESULTS: The responses to four conventional single-answer MCQs were nearly all correct in both groups. However, in three questions, group A, with the option 'All of the above', had a higher number of correct answers than group B, with multiple-answer MCQs. In addition, in another three questions, group A, using the original multiple-answer MCQs, had fewer correct answers than group B, where it was only necessary to tick a single incorrect answer. CONCLUSION: Variations in design influence the response to questions. The use of conventional single-answer MCQs should be reconsidered, as they only examine the recall of isolated knowledge facts. The 'All of the above' option should be avoided because it would increase the number of correct answers arrived at by guessing. When using multiple-answer MCQs, it is recommended that the questions asked should be in accordance with the content within the www.elearnSCI.org.


Subject(s)
Education, Nursing/methods , Educational Measurement , Internet , Personal Satisfaction , Self-Assessment , Surveys and Questionnaires , China , Education, Medical , Educational Measurement/methods , Female , Humans , Male , Pilot Projects , Spinal Cord Injuries
14.
J Fish Dis ; 37(4): 319-25, 2014 Apr.
Article in English | MEDLINE | ID: mdl-23962282

ABSTRACT

KHV ORF25 fragments were cloned from Koi Herpes Virus-CJ (KHV-CJ) strains isolated in our laboratory. The amplified products were inserted into the eukaryotic expression vector pIRES-neo, forming recombinant plasmid pIRES-ORF25. The recombinant plasmid pIRES-ORF25 at 1 µg per koi, 10 µg per koi and 50 µg per koi was intramuscularly injected into healthy kois, respectively. The results showed that the recombinant pIRES-ORF25 could induce the production of specific antibodies in koi determined by indirect ELISA. The differences of immune effect between three doses were not significant (P > 0.05), but all of them could induce the production of neutralizing antibodies. The immune challenge test showed that the mortality of koi injected with PBS, blank pIRES-neo vector and nothing was 90%, 92.5% and 85% at 25 days. While the mortalities of koi injected with eukaryotic expression plasmid pIRES-ORF25 were 20%, 17.5% and 12.5%. Differences in comparison with the control group were highly significant (P < 0.01). Histopathological staining revealed that the tissues of the immunized koi did not change apparently. In conclusion, the DNA vaccine pIRES-ORF25 construct could well protect koi against KHV and had the potential to be applied in practice.


Subject(s)
Carps , DNA Virus Infections/veterinary , DNA Viruses/immunology , Fish Diseases/prevention & control , Viral Vaccines/immunology , Animals , DNA Virus Infections/prevention & control , DNA Virus Infections/virology , Fish Diseases/virology , Open Reading Frames , Plasmids/genetics , Polymerase Chain Reaction , Viral Vaccines/genetics
15.
Genet Mol Res ; 12(3): 4003-8, 2013 Sep 27.
Article in English | MEDLINE | ID: mdl-24089089

ABSTRACT

To study the impact of cold ischemia on tumor necrosis factor-alpha (TNF-α) and interleukin-10 (IL-10) expression after liver transplantation, a stable model of partial liver transplantation in rats was established. The experimental animals were divided into the following groups: a partial hepatectomy control group, a group that received partial liver transplantation after 30 min of cold ischemia (experimental group A), and a group that received a partial liver transplantation after 10 h of cold ischemia (experimental group B). The survival rate was observed in each group. The liver tissue was sampled 1, 2, and 4 days after surgery, and immunohistochemical detection of proliferating cell nuclear antigen TNF-α and IL-10 was performed. The correlation between liver regeneration and TNF-α and IL-10 expression was analyzed, and the impact of the 2 cytokines on rat liver regeneration after liver transplantation was evaluated. The survival rates of rats in the partial hepatectomy control group, in the group that received a partial liver transplantation after 30 min of cold ischemia, and the group that received a partial liver transplantation after 10 h of cold ischemia were 100, 70, and 33.3%, respectively. The expression of proliferating cell nuclear antigen and TNF-α was decreased (P < 0.05), and IL-10 expression was increased (P < 0.05) in animals that received a partial liver transplant after 10 h of cold ischemia compared with that in the animals that received a partial liver transplant after 30 min of cold ischemia. We conclude that with the extension of cold ischemic time, liver regeneration and survival rate after liver transplantation decreased. TNF-α and IL-10 play important regulatory roles in the regeneration process of transplanted livers.


Subject(s)
Cold Ischemia/adverse effects , Interleukin-10/metabolism , Liver Transplantation/methods , Proliferating Cell Nuclear Antigen/metabolism , Tumor Necrosis Factor-alpha/metabolism , Animals , Hepatectomy , Interleukin-10/genetics , Liver/pathology , Liver Regeneration , Male , Proliferating Cell Nuclear Antigen/genetics , Rats , Rats, Wistar , Tumor Necrosis Factor-alpha/genetics
16.
Genet Mol Res ; 12(3): 3383-90, 2013 Sep 04.
Article in English | MEDLINE | ID: mdl-24065679

ABSTRACT

This study analyzed the effect of muscle-fiber type composition on glycogenin-1 (GYG) gene expression and its impact on pH. The longissimus dorsi (LD) muscle contains more type IIB fibers (75.10%) than does the psoas major (PM) muscle (41.58%), while the PM has more type I (3.65 vs 0.94%), type IIA (34.15 vs 10.63%), and type IIX (20.62 vs 13.33%) fibers. Compared with PM, glycolytic potential (GP), pH45 min, and ΔpH from 45 min to 24 h post-mortem were all relatively higher in LD. Glycogen metabolites (lactate and GP) were negatively correlated with pH24 h and positively correlated with ΔpH. Expression of GYG was generally higher in LD. GYG expression was positively correlated with glycogen metabolite (lactate and GP) content and ΔpH, and was negatively correlated with pH24 h. These data confirm that the muscle-fiber type and GP have significant effects on ultimate pH and pH decline, and suggest that expression of GYG in muscles is related to the metabolism of glycogen and may impact GP, ΔpH, and ultimate pH. High expression of GYG was associated with a high glycogen content, large pH decline, and low ultimate pH in muscles post-mortem.


Subject(s)
Glucosyltransferases/biosynthesis , Glycogen/metabolism , Glycoproteins/biosynthesis , Muscle Fibers, Skeletal/metabolism , Swine/genetics , Animals , Gene Expression Regulation , Glucosyltransferases/genetics , Glycoproteins/genetics , Hydrogen-Ion Concentration , Male , Meat , Muscle Fibers, Skeletal/classification , Swine/growth & development
17.
Cancer Gene Ther ; 20(6): 366-74, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23703473

ABSTRACT

STAT1 has a key role in exerting the antiproliferative and proapoptotic effects of interferon (IFN)-α on tumors, and its defects in expression is associated with IFN-α resistance. In this study we want to investigate whether aspirin can improve the antitumor efficiency of IFN-α on hepatocellular carcinoma (HCC) through the activation of STAT1. We found that aspirin not only significantly enhanced IFN-α-induced antiproliferation and apoptosis of HCC in vitro study but also enhanced tumor growth inhibition in nude mice. Although IFN-α alone resulted in significant phosphorylation of both STAT1 and STAT3, aspirin only prompted the IFN-α-induced phosphorylation of STAT1. Further study revealed that aspirin-prompted phosphorylation of STAT1 was activated through phosphorylation of JAK1. Furthermore, aspirin-activated STAT1 upregulated the transcription of proapoptotic IFN-stimulated gene (ISG) of X-linked inhibitor of apoptosis-associated factor-1 and downregulated the transcription of antiapoptotic ISG of G1P3, which in turn promoted the expression of Bax and activation of caspase-9 and caspase-3, thereby sensitizing HCC cells to IFN-α-induced apoptosis. Taken together, our findings suggest a novel strategy of using aspirin to overcome tumor resistance and enhance the effectiveness of IFN-α in HCC treatment through activating STAT1 gene, and have potential implications for improving future IFN-α protein and gene therapy.


Subject(s)
Aspirin/administration & dosage , Carcinoma, Hepatocellular/pathology , Janus Kinase 1/biosynthesis , Liver Neoplasms/pathology , STAT1 Transcription Factor/biosynthesis , Animals , Apoptosis/drug effects , Carcinoma, Hepatocellular/drug therapy , Carcinoma, Hepatocellular/metabolism , Cell Proliferation/drug effects , Drug Resistance, Neoplasm/drug effects , Drug Synergism , Gene Expression Regulation, Neoplastic/drug effects , Humans , Interferon-alpha/administration & dosage , Interferon-alpha/metabolism , Liver Neoplasms/drug therapy , Liver Neoplasms/metabolism , Mice , Signal Transduction
18.
Eur Rev Med Pharmacol Sci ; 17(24): 3291-5, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24379058

ABSTRACT

BACKGROUND: Inflammatory bowel disease (IBD) is a common disease in human resulted from a various of factors including genetic background, immune system and environment factors. OBJECTIVES: Recent studies suggest pro-inflammatory cytokine IL-17 producing cell subset was involved in the disease development and the maintenance of IBD. And the differentiated and activation of IL-17 producing cells were mostly dependent on the cytokines profile secreted by innate cells in intestinal tissues. In this study, we examined the functions of IL-6 signal in regulatory of IL-17 production in acute IBD model. MATERIALS AND METHODS: Wildtype mice were treated with anti-IL-6 neutralizing antibodies to block IL-6 signal And then treated with DSS to induce acute IBD. RESULTS: Mice treated with anti-IL-6 neutralizing antibodies show severe colitis and high level of pro-inflammatory cytokine IL-17 production in DSS-induced acute IBD model when compared with control group. Our research suggested blockade of IL-6 signal pathways in acute colitus model resulted in specific activation of IL-17 producing cell population. Furthermore, CD44+ activated Th17 cell population and CD44- IL-17 producing T cells exhibited different susceptibility to IL-6 signal in our model. CONCLUSIONS: Blockade of IL-6 signal in DSS-induced acuted IBD model increased IL-17 production level specifically in CD44- T cells and reduced CD44+ Th17 cell population.


Subject(s)
Antibodies, Monoclonal/toxicity , Colitis/immunology , Colon/drug effects , Interleukin-17/metabolism , Interleukin-6/antagonists & inhibitors , Lymphocyte Activation/drug effects , Signal Transduction/drug effects , Th17 Cells/drug effects , Animals , Biomarkers/metabolism , Colitis/chemically induced , Colitis/genetics , Colitis/metabolism , Colon/immunology , Colon/metabolism , Dextran Sulfate , Disease Models, Animal , Female , Hyaluronan Receptors/metabolism , Interleukin-6/genetics , Interleukin-6/metabolism , Mice , Severity of Illness Index , Th17 Cells/immunology , Th17 Cells/metabolism , Time Factors
19.
Eur Rev Med Pharmacol Sci ; 16(10): 1409-13, 2012 Oct.
Article in English | MEDLINE | ID: mdl-23104658

ABSTRACT

BACKGROUND: Epilepsy is a recurrent chronic nervous system disease. A correct choice of antiepileptic drug is the key to control seizures and improve patient's life quality. AIM: To study the effectiveness and safety of lamotrigine monotherapy for treatment of epilepsy, systemic evaluation was carried out on published comparative trials between lamotrigine and carbamazepine. METHODS: The retrieval method referred to the search strategy developed by Cochrane Epilepsy Group and software Rev.Man 5 was used for META analysis and forest plots. The Odds ratio (OR) was selected as the effect size and funnel plot was used to analyze the publication bias. RESULTS: A total of 9 studies and 2269 cases of patients were included in the analysis. There was no significant difference between lamotrigine and carbamazepine for treatment of epilepsy as the OR was 1.17, 95% confidence interval (CI) [0.88, 1.54]. However, lamotrigine had advantages in the overall withdrawal rate and withdrawal rate due to side effects as the ORs were 0.57, 95% CI [0.47, 0.69] and 0.41, 95% CI [0.32, 0.52]. CONCLUSIONS: Lamotrigine has certain advantages over carbamazepine for treatment of epilepsy as it has less side effects and higher tolerability. In addition, the quality of such clinical trials should be further improved to have a more comprehensive understanding.


Subject(s)
Anticonvulsants/therapeutic use , Epilepsy/drug therapy , Triazines/therapeutic use , Humans , Lamotrigine , Publication Bias , Triazines/adverse effects
20.
Genet Mol Res ; 11(1): 166-73, 2012 Jan 27.
Article in English | MEDLINE | ID: mdl-22370883

ABSTRACT

The Yanan (YN) pig is a traditional Chinese indigenous breed that is raised in southwest China in the Sichuan Province, but there is little data on the germplasm characteristics of this breed. To evaluate carcass characteristics and meat quality of the YN pig, we compared carcass and meat quality of YN pigs and Landrace × Yanan (CY) hybrid pigs; 30 YN pigs and 30 CY pigs weighing 20 ± 2 kg were reared and slaughtered at the normal slaughter weight (100-120 kg). The carcasses were chilled and the left carcass side was dissected into bone, lean meat, fat, and skin; meat quality parameters were measured. Carcasses of YN pigs were lighter (88.85 vs 90.05 kg, P < 0.05) and shorter (71.88 vs 77.61 cm, P < 0.001); they contained less lean meat (41.60 vs 49.25%, P < 0.001), less ham and breech (25.93 vs 27.53%, P < 0.001) and less carcass bone (9.83 vs 10.53%, P < 0.01) than did carcasses of CY pigs. On the other hand, YN pigs had more carcass subcutaneous fat and skin (48.58 vs 40.23%, P < 0.001), thicker backfat (3.67 vs 3.43 cm, P < 0.001) and smaller loin muscle area (9.83 vs 26.91 cm(2), P < 0.001) compared with CY pigs. Among meat quality parameters, YN pigs had higher pH(1) (6.41 vs 6.17, P < 0.001), higher color score(u) (3.86 vs 3.36, P < 0.001) and lower Minolta L(u) values (40.89 vs 45.32, P < 0.01) than CY pigs. On the other hand, YN pigs had lower drip loss (1.31 vs 2.26%, P < 0.05) and lesser fiber area (2351.34 vs 3025.43 µm(2), P < 0.01) than CY pigs. Both breeds had high intramuscular fat (4.46% in YN and 4.45% in CY). No significant differences in other carcass traits and meat quality were found in the two populations. We conclude that YN pigs could be used in commercial pig production to provide good tasting and high-quality niche products.


Subject(s)
Body Composition/physiology , Meat Products/analysis , Meat/analysis , Subcutaneous Fat , Animals , Body Weight/physiology , China , Livestock , Meat-Packing Industry , Muscle, Skeletal/physiology , Swine
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