Résumé
Objective To explore the inhibitory effects and mechanisms of benzodiazepines on Helicobacter pylori (Hp).Methods The Hp international standard strain ATCC43504 was treated with benzodiazepines diazepam,midazolam,and remimazolam,respectively.The treatments with amoxicillin and clarithromycin were taken as the positive controls,and that with water for injection as the negative control.The inhibition zone of each drug was measured by the disk diffusion method.The minimum inhibitory concentration(MIC)and minimum bactericidal concentration(MBC)of each drug against Hp were determined.Hp suspension was configured and treated with diazepam and midazolam,respectively.The bacterial suspension without drug added was used as the control group.The concentration of K+ in each bacterial suspension was measured by an automatic biochemical analyzer before drug intervention(T0)and 1(T1),2(T2),3(T3),4(T4),5(T5),6(T6),and 7 h(T7)after intervention.Hp urease was extracted and treated with 1/2 MIC diazepam,1 MIC diazepam,2 MIC diazepam,1/2 MIC midazolam,1 MIC midazolam,2 MIC midazolam,1 mg/ml acetohydroxamic acid,and water for injection,respectively.The time required for the rise from pH 6.8 to pH 7.7 in each group was determined by the phenol red coloring method.Results The inhibition zones of diazepam,midazolam,remimazolam,amoxicillin,clarithromycin,and water for injection against Hp were 52.3,42.7,6.0,72.3,60.8,and 6.0 mm,respectively.Diazepam and midazolam showed the MIC of 12.5 μg/ml and 25.0 μg/ml and the MBC of 25 μg/ml and 50 μg/ml,respectively,to Hp.The concentrations of K+ in the diazepam,midazolam,and control groups increased during T1-T7 compared with those at T0(all P<0.01).The concentration of K+ in diazepam and midazolam groups during T1-T4 was higher than that in the control group(all P<0.01).The time of inhibiting urease activity in the 1/2 MIC diazepam,1 MIC diazepam,2 MIC diazepam,1/2 MIC midazolam,1 MIC midazolam,and 2 MIC midazolam groups was(39.86±5.11),(36.52±6.65),(38.58±4.83),(39.25±6.19),(36.36±4.61),and(35.81±6.18)min,respectively,which were shorter than that in the acetohydroxamic acid group(all P<0.01)and had no significance differences from that in the water for injection group(all P>0.05).Conclusion Diazepam and midazolam exerted inhibitory effects on Hp,which may be related to the cleavage of Hp cells rather than inhibiting urease.
Sujets)
Midazolam , Helicobacter pylori , Urease , Clarithromycine/pharmacologie , Benzodiazépines/pharmacologie , Diazépam/pharmacologie , Amoxicilline , Eau , Antibactériens/pharmacologieRésumé
In the 1960s, modern science began involving the essence of heat syndrome, but there have still no in-depth systematic studies on pathological mechanisms of heat syndrome and action mechanisms of cold and cool herbs. In this study, the animal model with heat syndrome was set up by feeding herbs with hot property, and then cold and cool herbs was applied in the experimental therapy. The two-dimensional electrophoresis and mass spectrometry technologies were adopted to compare the liver mitochondria proteome of the rats of the heat syndrome model and the ones treated with cold and cool herbs, so as to discover specificity-related proteins after heat syndrome and treatment with cold and cool herbs.
Sujets)
Animaux , Mâle , Rats , Métabolisme glucidique , Basse température , Médicaments issus de plantes chinoises , Pharmacologie , Métabolisme énergétique , Température élevée , Métabolisme lipidique , Mitochondries du foie , Métabolisme , Protéome , Métabolisme , Rat Sprague-DawleyRésumé
<p><b>OBJECTIVE</b>To investigate the status of controllable risk factors of cardiovascular disease in Chinese pilots.</p><p><b>METHODS</b>Pilots in seven regions of China were selected with cluster sampling. The rates of hypertension, diabetes mellitus,smoking and abnormal body mass index (BMI) as well as levels of total cholesterol, triglyceride and high density lipoprotein-cholesterol were obtained.</p><p><b>RESULTS</b>(1) A total of 5012 pilots were selected and 4684 pilots whose data were effective were studied. (2) The prevalence rates of hypertension, high total cholesterol, triglyceride, low high density lipoprotein-cholesterol and diabetes mellitus were 8.07%, 7.47%, 14. 45%, 27.63% and 0.43%, respectively. The rate of smoking was 66.45%. The rat of increased BMI was 49.64%. (3) Significant difference existed on the rates of hypertension, total cholesterol, triglyceride, low high density lipoprotein-cholesterol, smoking and abnormal BMI among pilots from different regions (all P < 0.01). There was also a significant difference between the rates of hypertension, total cholesterol, triglyceride, smoking and abnormal BMI in different age groups (all P < 0.01). The rate of low high density lipoprotein-cholesterol was similar in different age groups (P > 0.05). (4) 88.96% of the participants had at least one controllable risk factor. 54.46% of the participants had at least two controllable risk factors. None of the participants had more than seven risk factors. There was a significant difference between the rates of pilots who have more than two controllable risk factors in different regions (P < 0.01). There was a significant difference between the rates of pilots who have more than two risk factors in different age groups (P < 0.01).</p><p><b>CONCLUSIONS</b>There was high prevalence of controllable cardiovascular risk factors in Chinese pilots. Active intervention targeting these cardiovascular disease risk factors needs to be considered to reduce the risk of developing cardiovascular disease in Chinese pilots.</p>
Sujets)
Adulte , Humains , Mâle , Adulte d'âge moyen , Jeune adulte , Médecine aérospatiale , Asiatiques , Maladies cardiovasculaires , Épidémiologie , Chine , Épidémiologie , Facteurs de risqueRésumé
The fusion protein (F) gene of Newcastle disease virus was amplified by polymerase chain reaction (PCR) from the recombinant plasmid pVAX1-F, and subcloned into eukaryotic expression vector pmcDNA3. 1+. The F gene was identified by sequencing. The recombinant plasmid was transformed into attenuated Salmonella typhimurium SL7207, and the recombinant was designated as SL7207 (pmcDNA3. 1-F). In vitro and in vivo experiments showed that the plasmid stability of pmcDNA3. 1-F was apparently higher than that of pcDNA3. 1-F in SL7207. In order to compare the immune response induced by these two re combinant bacteria, BALB/c mice were immunized orally with them at the dosage of 2 x 10(9) CFU respectively. Both SL7207(pcDNA3. 1-F) and SL7207(pmcDNA3. 1-F) initiated F-specific serum and mucosal antibodies in immunized mice. Furthermore, 4-day-old SPF chickens were immunized with SL7207(pcDNA3. 1-F) and SL7207(pmcDNA3. 1-F) at the dosage of 5 x 10(9) CFU and boosted two weeks later with the same dosage. Humoral and intestinal mucosal immune responses were observed and their levels were significantly higher than that of negative and positive controls. The result of protective efficacy showed that the chickens immunized with SL7207(pmcDNA3. 1-F) had the protective rate of 70.0%, higher than that of the SL7207 (pcDNA3. 1-F) with 50.0%. In summary, the DNA vaccine delivered by attenuated Salmonella typhimurium has good immunogenicity. A novel mucosal DNA vaccine has been developed and could be useful for controlling the infection and epidemic of Newcastle disease in the poultry.
Sujets)
Animaux , Femelle , Souris , Poulets , Immunisation , Souris de lignée BALB C , Virus de la maladie de Newcastle , Allergie et immunologie , Plasmides , Salmonella typhimurium , Génétique , Vaccins atténués , Allergie et immunologie , Vaccins à ADN , Allergie et immunologie , Vaccins antiviraux , Allergie et immunologieRésumé
To improve the rescue efficiency of measles virus cDNA clone, the cell line that stably expressed the T7 RNA polymerase was established. Firstly, the T7 RNA polymerase gene was amplified by PCR and then the PCR product was inserted into pcDNA3 to obtain plasmid pcDNA3-T7. Vero cell was transfected with the plasmid and G418 was added to the cell 24h later to kill the cells without the plasmid. Western blotting analysis showed that the Vero/pcDNA3-T7 cell could express T7 RNA polymerase. To analyze the gene function of T7 RNA polymerase, the pT7IP-EGFP plasmid was transfected into the Vero/pcDNA3 T7 cell and EGFP was analized by fluorescence. The result suggested that T7 RNA polymerase expressed in the Vero/pcDNA3-T7 cell could transcribe the gene under control of the T7 promoter. Moreover, the minigenome PminiEGFP inserted reversely with report gene EGFP was established. After trans fection with the plasmid and infection with measles virus, EGFP was expressed, indicating the Vero/pcDNA3-T7 cell could rescue the minigenome.
Sujets)
Animaux , Technique de Western , Lignée cellulaire , Chlorocebus aethiops , DNA-directed RNA polymerases , Génétique , Métabolisme , Protéines à fluorescence verte , Génétique , Métabolisme , Virus de la rougeole , Génétique , Microscopie de fluorescence , Protéines de fusion recombinantes , Génétique , Métabolisme , Transfection , Cellules Vero , Protéines virales , Génétique , Métabolisme , Réplication viraleRésumé
In order to detect the nucleic acid of Puumala hantavirus, RNA was extracted from lungs of bank voles captured in Northeast China, and partial S and M genome segments of Puumala virus were amplified by RT-PCR and sequenced. Phylogenetic analysis suggested that Chinese Puumala virus had diverged from the common node of PUUV, with accumulating nucleotide substitutions and formed a distinct lineage from other Puumala viruses. Newly found Puumala virus was most closely related to the Kamiiso-8Cr-95 and Tobetsu-60Cr-93 strains which came from Japan and the muju strains which came from South Korea. By analysis of S and M genome segments of Puumala virus, we deduced a new Puumala virus subtype did exist in Northeast China.
Sujets)
Animaux , Séquence nucléotidique , Chlorocebus aethiops , Chine , Évolution moléculaire , Génome viral , Orthohantavirus , Génétique , Données de séquences moléculaires , Phylogenèse , Virus Puumala , Classification , Génétique , RT-PCR , Rodentia , Virologie , Analyse de séquence d'ADN , Cellules VeroRésumé
<p><b>AIM</b>To perpare and identify irisquinone hydroxypropyl-beta-cyclodextrin inclusion complex (irisquinone-HP-beta-CD), as well as to study the inclusion mechanism and molecule stoichiometry between irisquinone and hydroxypropyl-beta-cyclodextrin.</p><p><b>METHODS</b>Irisquinone-HP-beta-CD was prepared by freeze-drying technique. The ratio of host and guest was also studied in inclusion process by mol gradient and continuing variational methods. At the same time, the inclusion complex was identified by X-ray diffraction (XRD) and differential scanning calorimetry (DSC).</p><p><b>RESULTS</b>It was demonstrated that the solubility of irisquinone was enhanced markedly by inclusion with HP-beta-CD when stoichiometry was 2:1 of host and guest at 25 degrees C, 35 degrees C and 45 degrees C.</p><p><b>CONCLUSION</b>The solubility and stability of irisquinone could be increased by preparing the inclusion complex with hydroxypropyl-beta-cyclodextrin.</p>
Sujets)
2-Hydroxypropyl-beta-cyclodextrin , Benzoquinones , Chimie , Calorimétrie différentielle à balayage , Préparation de médicament , Méthodes , Stabilité de médicament , Lyophilisation , Solubilité , Diffraction des rayons X , Cyclodextrines bêta , ChimieRésumé
<p><b>AIM</b>To investigate the permeation mechanism of paclitaxel by enhancers and preparation factors.</p><p><b>METHODS</b>The fluidity of mucous membrane and membrane protein conformation changes were determined by using electron spin resonance (ESR) when mucous membrane was treated by several enhancers. At the same time, the factors of penetration of lower dissolution drug across the intestinal mucous membrane were studied in three formulas inclusion complex, microemulsion and injection.</p><p><b>RESULTS</b>Polyethylene glycol (PEG) 1500, hydroxypropyl-beta-cyclodextrin (HP-beta-CD) and phospholipid as enhancers could reinforce the permeation of paclitaxle because of loosening of protein conformation in intestinal mucous membrane. Paclitaxel-HP-beta-CD inclusion complex and paclitaxel microemulsion as vehicle could significantly increased permeation kinetic rate of paclitaxel with fluid diffuse method.</p><p><b>CONCLUSION</b>Characteristics of enhancing intestinal absorption of poor dissolution drug had been provided with enhancer the change of membrane fluid.</p>
Sujets)
Animaux , Rats , 2-Hydroxypropyl-beta-cyclodextrin , Antinéoplasiques d'origine végétale , Pharmacocinétique , Synergie des médicaments , Spectroscopie de résonance de spin électronique , Émulsions , Injections , Absorption intestinale , Muqueuse intestinale , Fluidité membranaire , Paclitaxel , Pharmacocinétique , Véhicules pharmaceutiques , Pharmacologie , Phospholipides , Pharmacologie , Polyéthylène glycols , Pharmacologie , Rat Sprague-Dawley , Cyclodextrines bêta , PharmacologieRésumé
The high-copy-number plasmid pcDNA3.1+ is unstable within S almonella typhimurium. A novel plasmid pmcDNA3.1+ was constructed by removin g the promoter sequence of ampicillin resistance gene (bla gene) in plasmid pcDNA3.1+. In contrast to pcDNA3.1+, pmcDNA3.1+ was stable within Salmonel la typhimurium SL7207 in LB medium with or without ampicillin. Further experi ments showed the ?-lactamase activity of Salmonella typhimurium SL7207(pmc DNA3.1+) was apparently lowered than that of Salmonella typhimurium SL7207( pcDNA3.1+) and the high ampicillin concentration was maintained longer in LB me dium culturing Salmonella typhimurium SL7207(pmcDNA3.1+). When mice were a dministered with Salmonella typhimurium SL7207(pmcDNA3.1+) intraperitoneall y, more than 95% of Salmonella cells separated from the spleen still harbore d the plasmid pmcDNA3.1+ 7 days later; but 99% of Salmonella cells lost the plasmid pcDNA3.1+ at day 3 in mice innoculated with Salmonella typhimurium SL7207(pcDNA3.1+). By lowering the expression of bla gene, the rapid deco mposition of ampicillin in LB medium was avoided and the metabolic pressure was relieved for the host cells. This method offers a solution for the problem of t he instability of high-copy-number plasmid within Salmonella typhimurium.