1.Pterostilbene Ameliorates Glycemic Control, Dyslipidemia and Liver Injury in Type 2 Diabetes Rats.
Yu Jing ZHANG ; Hua Lei SUN ; Teng WANG ; Xin Xin LIU ; Chang LIU ; Fang SHEN ; Bing Ya WANG ; Run Rong DING ; Yi Ming LIU ; Guo Yu HUANG ; Wen Jie LI ; Xing LI
Biomedical and Environmental Sciences 2020;33(5):365-368
Animals
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Chemical and Drug Induced Liver Injury
;
drug therapy
;
Diabetes Mellitus, Experimental
;
drug therapy
;
Diabetes Mellitus, Type 2
;
drug therapy
;
Dyslipidemias
;
drug therapy
;
Glycemic Load
;
drug effects
;
Male
;
Protective Agents
;
pharmacology
;
Rats
;
Rats, Sprague-Dawley
;
Specific Pathogen-Free Organisms
;
Stilbenes
;
pharmacology
2.Comparison of antigenic mutation during egg and cell passage cultivation of H3N2 influenza virus
Yong Wook PARK ; Yun Hee KIM ; Hwan Ui JUNG ; Oh Seok JEONG ; Eun Ji HONG ; Hun KIM ; Jae Il LEE
Clinical and Experimental Vaccine Research 2020;9(1):56-63
specific pathogen free egg and the MDCK-Sky3851 cell line up to 15 passage, and the changes in the antigen sequence of the influenza viruses were confirmed by gene sequencing and protein structure analysis.RESULTS: In term of the hemagglutination titer of influenza virus, the reactivity to chicken and guinea pig red blood cell showed different results between egg propagated and cell propagated viruses. In the sequence analysis results for hemagglutinin and neuraminidase, no antigenic mutation was observed throughout all passages when cultured in MDCK-Sky3851 cells. On the other hand, mutations occurred in three amino acid sequences (H156R, G186S, S219F) in hemagglutinin up to 15 passages when cultured in eggs.CONCLUSION: H3N2 influenza virus cultured in eggs could lead mutations in amino acid sequence of hemagglutinin, distinct from the corresponding virus cultured in cells for which no antigenic mutation was observed. These findings suggest that cell culture is a more stable and effective way of production with lower risk of antigenic mutations for the manufacture of influenza vaccines.]]>
Amino Acid Sequence
;
Animals
;
Cell Culture Techniques
;
Cell Line
;
Chickens
;
Eggs
;
Erythrocytes
;
Guinea Pigs
;
Hand
;
Hemagglutination
;
Hemagglutinins
;
Humans
;
Influenza Vaccines
;
Influenza, Human
;
Neuraminidase
;
Orthomyxoviridae
;
Ovum
;
Sequence Analysis
;
Specific Pathogen-Free Organisms
3.NMDA Receptor Antagonist MK801 Protects Against 1-Bromopropane-Induced Cognitive Dysfunction.
Lin XU ; Xiaofei QIU ; Shuo WANG ; Qingshan WANG ; Xiu-Lan ZHAO
Neuroscience Bulletin 2019;35(2):347-361
Occupational exposure to 1-bromopropane (1-BP) induces learning and memory deficits. However, no therapeutic strategies are currently available. Accumulating evidence has suggested that N-methyl-D-aspartate receptors (NMDARs) and neuroinflammation are involved in the cognitive impairments in neurodegenerative diseases. In this study we aimed to investigate whether the noncompetitive NMDAR antagonist MK801 protects against 1-BP-induced cognitive dysfunction. Male Wistar rats were administered with MK801 (0.1 mg/kg) prior to 1-BP intoxication (800 mg/kg). Their cognitive performance was evaluated by the Morris water maze test. The brains of rats were dissected for biochemical, neuropathological, and immunological analyses. We found that the spatial learning and memory were significantly impaired in the 1-BP group, and this was associated with neurodegeneration in both the hippocampus (especially CA1 and CA3) and cortex. Besides, the protein levels of phosphorylated NMDARs were increased after 1-BP exposure. MK801 ameliorated the 1-BP-induced cognitive impairments and degeneration of neurons in the hippocampus and cortex. Mechanistically, MK801 abrogated the 1-BP-induced disruption of excitatory and inhibitory amino-acid balance and NMDAR abnormalities. Subsequently, MK801 inhibited the microglial activation and release of pro-inflammatory cytokines in 1-BP-treated rats. Our findings, for the first time, revealed that MK801 protected against 1-BP-induced cognitive dysfunction by ameliorating NMDAR function and blocking microglial activation, which might provide a potential target for the treatment of 1-BP poisoning.
Animals
;
Brain
;
drug effects
;
metabolism
;
pathology
;
Cognitive Dysfunction
;
drug therapy
;
metabolism
;
pathology
;
Disease Models, Animal
;
Dizocilpine Maleate
;
pharmacology
;
Excitatory Amino Acid Antagonists
;
pharmacology
;
Hydrocarbons, Brominated
;
Inflammasomes
;
drug effects
;
metabolism
;
Male
;
Maze Learning
;
drug effects
;
physiology
;
Microglia
;
drug effects
;
metabolism
;
pathology
;
NLR Family, Pyrin Domain-Containing 3 Protein
;
metabolism
;
Neurons
;
drug effects
;
metabolism
;
pathology
;
Nootropic Agents
;
pharmacology
;
Random Allocation
;
Rats, Wistar
;
Receptors, N-Methyl-D-Aspartate
;
antagonists & inhibitors
;
metabolism
;
Spatial Memory
;
drug effects
;
physiology
;
Specific Pathogen-Free Organisms
4.Subchronic Oral Toxicity Evaluation of Lanthanum: A 90-day, Repeated Dose Study in Rats.
Hai Qin FANG ; Zhou YU ; Yuan ZHI ; Jin FANG ; Chen Xi LI ; Yi Mei WANG ; Shuang Qing PENG ; Xu Dong JIA
Biomedical and Environmental Sciences 2018;31(5):363-375
OBJECTIVEThe present study was undertaken to evaluate the subchronic toxicity of lanthanum and to determine the no observed adverse effect level (NOAEL), which is a critical factor in the establishment of an acceptable dietary intake (ADI).
METHODSIn accordance with the Organization for Economic Co-operation and Development (OECD) testing guidelines, lanthanum nitrate was administered once daily by gavage to Sprague-Dawley (SD) rats at dose levels of 0, 1.5, 6.0, 24.0, and 144.0 mg/kg body weight (BW) per day for 90 days, followed by a recovery period of 4 weeks in the 144.0 mg/kg BW per day and normal control groups. Outcome parameters were mortality, clinical symptoms, body and organ weights, serum chemistry, and food consumption, as well as ophthalmic, urinary, hematologic, and histopathologic indicators. The benchmark dose (BMD) approach was applied to estimate a point of departure for the hazard risk assessment of lanthanum.
RESULTSSignificant decreases were found in the 144.0 mg/kg BW group in the growth index, including body weight, organ weights, and food consumption. This study suggests that the NOAEL of lanthanum nitrate is 24.0 mg/kg BW per day. Importantly, the 95% lower confidence value of the benchmark dose (BMDL) was estimated as 9.4 mg/kg BW per day in females and 19.3 mg/kg BW per day in males.
CONCLUSIONThe present subchronic oral exposure toxicity study may provide scientific data for the risk assessment of lanthanum and other rare earth elements (REEs).
Animals ; Blood Chemical Analysis ; Body Weight ; Dose-Response Relationship, Drug ; Drug Administration Schedule ; Female ; Lanthanum ; administration & dosage ; toxicity ; Male ; No-Observed-Adverse-Effect Level ; Rats ; Rats, Sprague-Dawley ; Specific Pathogen-Free Organisms ; Toxicity Tests, Subchronic ; Urinalysis
5.Hexon and fiber gene changes in an attenuated fowl adenovirus isolate from Malaysia in embryonated chicken eggs and its infectivity in chickens
Norfitriah M SOHAIMI ; Mohd H BEJO ; Abdul R OMAR ; Aini IDERIS ; Nurulfiza M ISA
Journal of Veterinary Science 2018;19(6):759-770
Fowl adenovirus (FAdV) is distributed worldwide and causes economic losses in the poultry industry. The objectives of this study were to determine the hexon and fiber gene changes in an attenuated FAdV isolate from Malaysia in specific pathogen-free chicken embryonated eggs (SPF CEE) and its infectivity in commercial broiler chickens. SPF CEE were inoculated with 0.1 mL FAdV inoculum via the chorioallantoic membrane (CAM) for 20 consecutive passages. The isolate at passage 20 (E20), with a virus titer of 10(8.7)TCID₅₀/mL (TCID₅₀, 50% tissue culture infective dose), was inoculated (0.5 mL) into one-day-old commercial broiler chicks either via oral or intraperitoneal routes. The study demonstrated that 100% embryonic mortality was recorded from E2 to E20 with a delayed pattern at E17 onwards. The lesions were confined to the liver and CAM. Substitutions of amino acids in the L1 loop of hexon at positions 49 and 66, and in the knob of fiber at positions 318 and 322 were recorded in the E20 isolate. The isolate belongs to serotype 8b and is non-pathogenic to broiler chickens, but it is able to induce a FAdV antibody titer. It appears that molecular changes in the L1 loop of hexon and the knob of fiber are markers for FAdV infectivity.
Adenoviridae
;
Amino Acids
;
Chickens
;
Chorioallantoic Membrane
;
Eggs
;
Fowl adenovirus A
;
Liver
;
Malaysia
;
Mortality
;
Ovum
;
Poultry
;
Serogroup
;
Specific Pathogen-Free Organisms
;
Viral Load
6.Pulmonary Toxicity in Rats Caused by Exposure to Intratracheal Instillation of SiO2 Nanoparticles.
Hong YANG ; Qiu Yun WU ; ; Ming Yue LI ; Can Shan LAO ; Ying Jian ZHANG ;
Biomedical and Environmental Sciences 2017;30(4):264-279
OBJECTIVEThe effect of the silica nanoparticles (SNs) on lungs injury in rats was investigated to evaluate the toxicity and possible mechanisms for SNs.
METHODSMale Wistar rats were instilled intratracheally with 1 mL of saline containing 6.25, 12.5, and 25.0 mg of SNs or 25.0 mg of microscale SiO2 particles suspensions for 30 d, were then sacrificed. Histopathological and ultrastructural change in lungs, and chemical components in the urine excretions were investigated by light microscope, TEM and EDS. MDA, NO and hydroxyproline (Hyp) in lung homogenates were quantified by spectrophotometry. Contents of TNF-α, TGF-β1, IL-1β, and MMP-2 in lung tissue were determined by immunohistochemistry staining.
RESULTSThere is massive excretion of Si substance in urine. The SNs lead pulmonary lesions of rise in lung/body coefficients, lung inflammation, damaged alveoli, granuloma nodules formation, and collagen metabolized perturbation, and lung tissue damage is milder than those of microscale SiO2 particles. The SNs also cause increase lipid peroxidation and high expression of cytokines.
CONCLUSIONThe SNs result into pulmonary fibrosis by means of increase lipid peroxidation and high expression of cytokines. Milder effect of the SNs on pulmonary fibrosis comparing to microscale SiO2 particles is contributed to its elimination from urine due to their ultrafine particle size.
Air Pollutants ; toxicity ; Animals ; Dose-Response Relationship, Drug ; Lung ; drug effects ; pathology ; ultrastructure ; Male ; Microscopy, Electron, Transmission ; Nanoparticles ; toxicity ; Pulmonary Fibrosis ; chemically induced ; metabolism ; pathology ; Random Allocation ; Rats ; Rats, Wistar ; Silicon Dioxide ; toxicity ; Specific Pathogen-Free Organisms ; Spectrometry, X-Ray Emission ; Urine ; chemistry
7.Assessment of the safety and efficacy of low pathogenic avian influenza (H9N2) virus in inactivated oil emulsion vaccine in laying hens.
Jeong Hwa SHIN ; Jong Seo MO ; Jong Nyeo KIM ; In Pil MO ; Bong Do HA
Journal of Veterinary Science 2016;17(1):27-34
In Korea, several outbreaks of low pathogenic AI (H9N2) viral infections leading to decreased egg production and increased mortality have been reported on commercial farms since 1996, resulting in severe economic losses. To control the H9N2 LPAI endemic, the Korea Veterinary Authority has permitted the use of the inactivated H9N2 LPAI vaccine since 2007. In this study, we developed a killed vaccine using a low pathogenic H9N2 AI virus (A/chicken/Korea/ADL0401) and conducted safety and efficacy tests in commercial layer farms while focusing on analysis of factors that cause losses to farms, including egg production rate, egg abnormality, and feed efficiency. The egg production rate of the control group declined dramatically 5 days after the challenge. There were no changes in feed consumption of all three groups before the challenge, but rates of the control declined afterward. Clinical signs in the vaccinated groups were similar, and a slight decline in feed consumption was observed after challenge; however, this returned to normal more rapidly than the control group and commercial layers. Overall, the results of this study indicate that the safety and efficacy of the vaccine are adequate to provide protection against the AI field infection (H9N2) epidemic in Korea.
Animals
;
Chickens
;
Emulsions
;
Female
;
Influenza A Virus, H9N2 Subtype/*immunology
;
Influenza Vaccines/*immunology/*standards
;
Influenza in Birds/immunology/prevention & control
;
Oviparity
;
Specific Pathogen-Free Organisms
;
Vaccines, Inactivated/immunology
8.Improved immunogenicity of Newcastle disease virus inactivated vaccine following DNA vaccination using Newcastle disease virus hemagglutinin-neuraminidase and fusion protein genes.
Masoumeh FIROUZAMANDI ; Hassan MOEINI ; Davood HOSSEINI ; Mohd Hair BEJO ; Abdul Rahman OMAR ; Parvaneh MEHRBOD ; Aini IDERIS
Journal of Veterinary Science 2016;17(1):21-26
The present study describes the development of DNA vaccines using the hemagglutinin-neuraminidase (HN) and fusion (F) genes from AF2240 Newcastle disease virus strain, namely pIRES/HN, pIRES/F and pIRES-F/HN. Transient expression analysis of the constructs in Vero cells revealed the successful expression of gene inserts in vitro. Moreover, in vivo experiments showed that single vaccination with the constructed plasmid DNA (pDNA) followed by a boost with inactivated vaccine induced a significant difference in enzyme-linked immunosorbent assay antibody levels (p < 0.05) elicited by either pIRES/F, pIRES/F+ pIRES/HN or pIRES-F/HN at one week after the booster in specific pathogen free chickens when compared with the inactivated vaccine alone. Taken together, these results indicated that recombinant pDNA could be used to increase the efficacy of the inactivated vaccine immunization procedure.
Animals
;
Antibodies, Viral/blood
;
Cercopithecus aethiops
;
Chickens
;
*HN Protein/genetics/immunology
;
Immunogenicity, Vaccine/*immunology
;
Newcastle Disease/immunology
;
Newcastle disease virus/enzymology/*genetics/immunology
;
Specific Pathogen-Free Organisms
;
Vaccines, DNA/genetics/*immunology
;
Vaccines, Inactivated/immunology
;
Vero Cells
;
*Viral Fusion Proteins/genetics/immunology
;
Viral Vaccines/genetics/*immunology/*standards
9.Effect of Low Dose of Chicken Infectious Anemia Virus in Attenuated Vaccine on SPF Chicken Body Weight and Vaccine Immune Antibody.
Lichun FANG ; Xiaohan LI ; Zhihao REN ; Yang LI ; Yixin WANG ; Zhizhong CUI ; Shuang CHANG ; Peng ZHAO
Chinese Journal of Virology 2016;32(2):190-194
In order to observe the effect of the immune and weight of chickens after use the attenuated vaccine with low dose of chicken infectious anemia virus (CIAV). In this study, the effects of low dose of CIAV on the weight of SPF chickens and NDV antibody production were observed by simulated experiments. The results showed that 10 EID50 and 5 EID50 CIAV per plume attenuated NDV vaccines were used to cause the weight loss of SPF chickens. Compared with the use of the non contaminated vaccine group, it has significant difference. And NDV antibody levels compared with the use of the non contaminated groups also decreased after use the vaccine with two doses of CIAV contaminated. It has significant difference. A certain proportion of CIAV antibody positive was detected at the beginning of the second week after use the NDV vaccine with two doses of CIAV contaminated. The detection of a high proportion of CIAV nucleic acid was detected in the first week after the use of a contaminated vaccine. The results of the study demonstrate the effects of CIAV pollution on the production and immune function of SPF chickens, and it is suggested that increasing the detection of viral nucleic acid can help save time and improve the detection rate in the detection of exogenous virus contamination by SPF chicken test method.
Animals
;
Antibodies, Viral
;
immunology
;
Chicken anemia virus
;
genetics
;
immunology
;
physiology
;
Chickens
;
Circoviridae Infections
;
immunology
;
veterinary
;
virology
;
Poultry Diseases
;
immunology
;
virology
;
Specific Pathogen-Free Organisms
;
Vaccines, Attenuated
;
administration & dosage
;
genetics
;
immunology
10.Protective effects of shikonin on brain injury induced by carbon ion beam irradiation in mice.
Lu GAN ; ; Zhen Hua WANG ; Hong ZHANG ; ; Rong ZHOU ; ; Chao SUN ; ; Yang LIU ; ; Jing SI ; ; Yuan Yuan LIU ; ; Zhen Guo WANG
Biomedical and Environmental Sciences 2015;28(2):148-151
Radiation encephalopathy is the main complication of cranial radiotherapy. It can cause necrosis of brain tissue and cognitive dysfunction. Our previous work had proved that a natural antioxidant shikonin possessed protective effect on cerebral ischemic injury. Here we investigated the effects of shikonin on carbon ion beam induced radiation brain injury in mice. Pretreatment with shikonin significantly increased the SOD and CAT activities and the ratio of GSH/GSSG in mouse brain tissues compared with irradiated group (P<0.01), while obviously reduced the MDA and PCO contents and the ROS levels derived from of the brain mitochondria. The shikonin also noticeably improved the spatial memory deficits caused by carbon ion beam irradiation. All results demonstrated that shikonin could improve the irradiated brain injury which might resulted from its modulation effects on the oxidative stress induced by the 12C6+ ion beam.
Animals
;
Antioxidants
;
pharmacology
;
Brain Injuries
;
prevention & control
;
Catalase
;
metabolism
;
Heavy Ion Radiotherapy
;
Male
;
Malondialdehyde
;
metabolism
;
Mice
;
Naphthoquinones
;
pharmacology
;
Protein Carbonylation
;
Radiation Injuries, Experimental
;
prevention & control
;
Radiation-Protective Agents
;
pharmacology
;
Random Allocation
;
Specific Pathogen-Free Organisms
;
Superoxide Dismutase
;
metabolism

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