Publications by authors named "Zhi-Qiang Chang"

The gut microbial communities interact with the host immunity and physiological functions. In this study, we investigated the bacterial composition in Litopenaeus vannamei shrimp's gut and rearing water under different host (developmental stage: juvenile and adult; health status: healthy and diseased) and environmental factors (temperature 25 °C and 28 °C; and light intensity: low and high). The PCoA analysis showed that all water samples were clustered together in a quarter, whereas the gut samples spread among three quarters.

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Objective: To analyze the effect of microRNA-22 on autophagy and proliferation and to investigate the underlying molecular mechanism of osteosarcoma cell chemotherapy sensitivity.

Methods: MG-63 cells were divided into four groups, including a control group, a negative control (NC) group, a cisplatin group, and a cisplatin + miR-22 group. Proliferation of MG-63 cells that had been treated with cisplatin and transfected with miR-22 mimics was determined using MTT assay and colony formation assay.

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Cytochrome P450s (CYPs) are the main catalytic enzymes for metabolism by a variety of endogenous and exogenous substrates in mammals, fish, insects, etc. We evaluated the application of a multidrug cocktail on changes in CYP1, CYP2, and CYP3 activity in Turbot Scophthalmus maximus. The probe drugs were a combination of caffeine (5 mg/kg body weight), dapsone (5 mg/kg), and chlorzoxazone (10 mg/kg).

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The pharmacokinetic profiles of sulfamonomethoxine (SMM) were investigated in flatfish tongue soles in the present study. After a single injection of SMM (40 mg/kg BW) to caudal vein of tongue sole at 20 °C, plasma drug concentration versus time data were best fitted to a three-compartment model, characterized with 0.2, 5.

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The effect of temperature and salinity on the elimination of enrofloxacin (EF) in Manila clams Ruditapes philippinarum was investigated. The clams, cultured under different temperatures and salinities (16 degrees C and 30 per thousand, 22 degrees C and 30 per thousand, or 22 degrees C and 20 per thousand), were exposed to EF at 5 microg/mL of water in a medicated bath. After a 24-h exposure, the concentration of EF in various tissues was measured by high-performance liquid chromatography and the elimination rate of EF in those tissues was investigated by regression analysis.

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Article Synopsis
  • The study aimed to evaluate the mutagenic and teratogenic effects of ammonium dinitramide (ADN) using various toxicity tests.
  • Results from the Ames assay indicated ADN was not mutagenic at low doses, but higher doses led to increased micronucleus rates in mice, suggesting potential mutagenicity.
  • Teratogenic assessments revealed higher rates of fetal malformations and survival issues in mice exposed to higher doses of ADN, implying ADN has teratogenic effects.
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Article Synopsis
  • - The study investigates the toxicity effects of ammonium dinitramide (ADN) over different exposure durations (acute, subacute, and subchronic) to identify affected organs and toxicity levels.
  • - Oral toxicity tests on mice and rats revealed an LDx of about 569 mg/kg and 617 mg/kg respectively, indicating low-level acute toxicity, with liver issues showing significant adverse effects at mid-range doses.
  • - Findings indicate that exposure to 30.8 mg/kg ADN showed no negative effects, confirming the liver as the primary target organ for toxicity at higher doses.
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Drug addiction has been considered as a kind of chronic relapsing brain disease influenced by both genetic and environmental factors. At present, many causative genes and pathways related to diverse kinds of drug addiction have been discovered, while less attention has been paid to common mechanisms shared by different drugs underlying addiction. By applying a co-expression meta-analysis method to mRNA expression profiles of alcohol, cocaine, heroin addicted and normal samples, we identified significant gene co-expression pairs.

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Article Synopsis
  • Researchers investigated the biological activities of Phellinus gilvus (PG) and identified the ethyl acetate extract (Fd) as the most effective for its strong antioxidant properties.
  • The study found that protocatechualdehyde (PCA) is likely the key compound in PG that contributes to its ability to scavenge free radicals and inhibit nitric oxide production in macrophages.
  • Further experiments are planned to explore the molecular mechanisms behind these effects and to assess the biological activities of other extracts from PG.
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Sphingolipids are membrane components and are involved in cell proliferation, apoptosis and metabolic regulation. In this study we investigated whether de novo sphingolipid biosynthesis in macrophages is regulated by inflammatory stimuli. Lipopolysaccharide (LPS) treatment upregulated Sptlc2, a subunit of serine palmitoyltransferase (SPT), mRNA and protein in Raw264.

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In the present study, we confirmed the ability of M. hyopneumoniae to induce the secretion of large amount of proinflammatory cytokine and nitric oxide (NO) in murine macrophage RAW 264.7 cells.

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Subacute toxicity and immunopharmacological activities of β-glucan from P. polymyxa JB115 was evaluated in a 28-day feeding study in rats. The white blood cell count, red blood cell count, hematocrit, hemoglobin, thrombocytes (THR) and thrombocytocrit were significantly higher in male fed with β-glucan than control rats and the insignificant lower eosinophil count, mean corpuscular volume, mean cell hemoglobin and uninfected THR (uTHR) levels were observed in male whereas no marked changes in female rats.

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Beta-glucans are heterogeneous groups of glucose polymers found in the cell walls of fungi, plants and some bacteria. Our previous report showed that a novel beta-1,3/1,6-glucan produced from Paenibacillus (P.) polymyxa JB115 can induce nitric oxide (NO) production in RAW264.

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Article Synopsis
  • The study examines how extracellular beta-glucan from Paenibacillus polymyxa JB115 influences nitric oxide (NO) production in RAW264.7 macrophages.
  • Results showed that beta-glucan increases NO production in a way that's dependent on both the concentration of beta-glucan and the duration of exposure.
  • Additionally, beta-glucan boosts the mRNA expression of key inflammatory markers (iNOS, COX-2, and IL-6) in the macrophages, again in a concentration-dependent manner.
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The pharmacokinetics (PK) and pharmacodynamics (PD) of orbifloxacin were studied in beagle dogs after intravenous (i.v.) and intramuscular (i.

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Article Synopsis
  • The study compared the immunomodulating activities of polysaccharides from three types of Phellinus species: P. linteus (PL), P. baumii (PB), and P. gilvus (PG).
  • Results indicated that all three species enhanced the proliferation of murine splenocytes, with PG exhibiting the strongest effect.
  • Additionally, PL and PB increased mixed splenocyte proliferation in a concentration-dependent way, while PG notably boosted phagocytosis in immune cells more effectively than PL and PB.
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Sample's moisture content and granularity would have an important influence on NIR veracity. Preprocesssing methods have been used for NIR analysis to achieve better NIR veracity. With Yunnan flue-cured tobacco as study materials, the authors innovatively applied microwave fast drying technology and home pulverizer to tobacco preprocessing, which could finish the preprocessing in 5 min, faster than the traditional methods such as oven drying and sifting.

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Clinical pharmacokinetic profiles were investigated following intramuscular (i.m.) administration to pigs with a commercial tylosin-florfenicol combination product at a dose of 2.

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The influence of sample annum and the distribution of sample component on NIR veracity was studied with homemade grating diffuse NIR instrument using Yunnan flue-cured tobacco. Results showed that sample annum had an obvious influence on the total sugar and nicotine models, but had an unconspicuous influence on the total-nitrogen model. Models set up by samples, whose component content distribution was normal school, was better than those set up by even distribution.

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The influence of sample test conditions on the NIR veracity was studied with homemade grating diffuse NIR instrument using Yunnan flue-cured tobacco. Deducing analysis error was achieved by model self-emendation when a global NIR model was set up. Without regarding the influence of loading samples and test conditions, the test repetition error, re-loading error and samples tightness error, which were brought by instrument S/N, accounted for 50%, 30% and 20% of the total error, respectively.

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The pharmacokinetics and dosage regimen of norfloxacin-glycine acetate (NFLXGA) was investigated in pigs after a single intravenous (i.v.) or oral (p.

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Intact pathogenic Mycoplasma hyopneumoniae at 100 microg protein ml(-1) induced transcription of proinflammatory cytokines such as cyclooxygenase (COX)-2, tumor necrosis factor (TNF)-alpha, interleukin(IL)-1, IL-6 and inducible nitric oxide synthase (iNOS) in RAW 264.7 cells. After pretreatment with 50 microg surfactin C/ml, purified from Bacillus subtilis, transcription of the COX-2, IL-1beta, IL-6 and iNOS genes induced by M.

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The theory of local partial least square (LPLS) algorithm was described based on locally weighted regression algorithm (LWR). The influence of data processing parameters, such as principal component numbers and local set-up sample number in LPLS mode, on the NIR veracity was studied with homemade grating diffuse NIR instrument using Yunnan flue-cured tobacco. Results showed that for nicotine model, the principal component number decided by cross validation was not the best choice, and better results could be achieved by reducing the principal component number; using 30-50 samples to set up NIR model, the veracity of total sugar, total nitrogen, and nicotine could be improved by 7%, 14% and 10%, respectively.

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In the present study, we analyzed the antioxidant, antiplatelet aggregation, anti-inflammatory, and tyrosinase inhibitory activities of a variety of solvent extracts of Elaeagnus multiflora Thunb. (Family Elaeagnaceae). Among the solvent extracts of E.

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