AIM:To evaluate the effect of efflux pump inhibitors (EPIs) on multidrug resistance of Helicobacter pylori (H. pylori).METHODS: H. pylori strains were isolated and cultured on Brucella agar plates with 10% sheep's...AIM:To evaluate the effect of efflux pump inhibitors (EPIs) on multidrug resistance of Helicobacter pylori (H. pylori).METHODS: H. pylori strains were isolated and cultured on Brucella agar plates with 10% sheep's blood. The multidrug resistant (MDR) H. pylori were obtained with the inducer chloramphenicol by repeated doubling of the concentration until no colony was seen, then the susceptibilities of the MDR strains and their parents to 9 antibiotics were assessed with agar dilution tests. The present study included periods before and after the advent of the EPIs, carbonyl cyanide m-chlorophenyl hydrazone (CCCP), reserpine and pantoprazole), and the minimum inhibitory concentrations (MICs) were determined accordingly. In the same way, the effects of 5 proton pump inhibitors (PPIs), used in treatment of H. pylori infection, on MICs of antibiotics were evaluated.RESULTS: Four strains of MDR H. pylori were induced successfully, and the antibiotic susceptibilities of MDR strains were partly restored by CCCP and pantoprazole, but there was little effect of reserpine. Rabeprazole was the most effective of the 5 PPIs which could decrease the MICs of antibiotics for MDR H. pylori significantly.CONCLUSION: In vitro, some EPIs can strengthen the activities of different antibiotics which are the putative substrates of the efflux pump system in H. pylori.展开更多
Context: Glucose-insulin-potassium(GIK) infusion is a widely applicable, low-cost therapy that has been postulated to improve mortality in patients with acute ST segment elevation myocardial infarction(STEMI). Given t...Context: Glucose-insulin-potassium(GIK) infusion is a widely applicable, low-cost therapy that has been postulated to improve mortality in patients with acute ST segment elevation myocardial infarction(STEMI). Given the potential global importance of GIK infusion, a large, adequately powered randomized trial is required to determine the effect of GIK on mortality in patients with STEMI. Objective: To determine the effect of high-dose GIK infusion on mortality in patients with STEMI. Design, Setting, and Participants: Randomized controlled trial conducted in 470 centers worldwide among 20201 patients with STEMI who presented within 12 hours of symptom onset. The mean age of patients was 58.6 years, and evidence based therapies were commonly used. Intervention: Patients were randomly assigned to receive GIK intravenous infusion for 24 hours plus usual care(n=10091) or to receive usual care alone(controls; n=10110). Main Outcome Measures: Mortality, cardiac arrest, cardiogenic shock, and reinfarction at 30 days after randomization. Results: At 30 days, 976 control patients(9.7%) and 1004 GIK infusion patients(10.0%) died(hazard ratio [HR], 1.03; 95%confidence interval [CI], 0.95-1.13; P=.45)-. There were no significant differences in the rates of cardiac arrest(1.5%[151/10107] in control and 1.4%[139/10088] in GIK infusion; HR, 0.93; 95%CI, 0.74-1.17; P=.51), cardiogenic shock(6.3%[640/10107] vs 6.6%[667/10088]; HR, 1.05; 95%CI, 0.94-1.17; P=.38), or reinfarction(2.4%[246/10107] vs 2.3%[236/10088]-; HR, 0.98; 95%CI, 0.82-1.17; P=.81). The rates of heart failure at 7 days after randomization were also similar between the groups(16.9%[1711/10107] vs 17.1%[1721/ 10088]; HR, 1.01; 95%CI, 0,95-1.08; P=.72). The lack of benefit of GIK infusion on mortality was consistent in prespecified subgroups, including in those with and without diabetes, in those presenting with and without heart failure, in those presenting early and later after symptom onset, and in those receiving and not receiving reperfusion therapy(thrombolysis or primary percutaneous coronary intervention). Conclusion: In this large, international randomized trial, high-dose GIK infusion had a neutral effect on mortality, cardiac arrest, and cardiogenic shock in patients with acute STEMI.展开更多
The behaviour of water soluble and monomer soluble inhibitors in emulsion polymerization of monomersfollowing Case Ⅱ kinetics(e.g.styrene)has been investigated.Experimental studies reveal that inhibitors canhave an a...The behaviour of water soluble and monomer soluble inhibitors in emulsion polymerization of monomersfollowing Case Ⅱ kinetics(e.g.styrene)has been investigated.Experimental studies reveal that inhibitors canhave an appreciable effect on both polymer particle nucleation and growth.A mathematical model showingthese effects has been developed and simulation studies have been done.The simulation results imply that theconsequences of these effects of monomer soluble inhibitors for industrial emulsion polymerization may be quiteserious.展开更多
<b><span style="font-family:Verdana;">Background and Aims:</span></b><span style="font-family:Verdana;"> Open liver resection requiring an upper abdominal incisio...<b><span style="font-family:Verdana;">Background and Aims:</span></b><span style="font-family:Verdana;"> Open liver resection requiring an upper abdominal incision is associated with significant opioid use due to postoperative pain. We tested the hypothesis that the intraoperative combination of low dose lidocaine and ketamine would reduce opioid consumption when given in conjunction with intrathecal morphine for liver resection surgery. </span><b><span style="font-family:Verdana;">Methods:</span></b><span style="font-family:Verdana;"> In this triple blind, parallel group four-arm placebo-controlled trial, we randomized 124 adult</span><span style="font-family:Verdana;color:#FF0000;"> </span><span style="font-family:Verdana;">ASA 2</span><span style="font-family:Verdana;"> </span><span style="font-family:Verdana;">-</span><span style="font-family:Verdana;"> </span><span style="font-family:Verdana;">4 liver resection patients to receive intraoperative lidocaine 0.33 mg/kg/h (group L), ketamine 70 μg/kg/h (group K), combination of lidocaine 0.33 mg/kg/h and ketamine 70 μg/kg/h (group KL) and saline (group P). All patients received 300 μg intrathecal morphine prior to induction of anesthesia. All infusions were started immediately after intubation and continued until the end of surgery. Primary outcome measurements included opioid consumption at 24-hours. Secondary outcomes included pain scores, opioid consumption at 48 and 72-hours and side effects including nausea, vomiting, dizziness, hallucinations, headaches and signs of local anaesthetic toxicity. Patients were followed up for 12 weeks. </span><b><span style="font-family:Verdana;">Results:</span></b><span style="font-family:Verdana;"> There was no difference in the primary outcome of opioid consumption within all 4 groups at rest or movement at 24-hours. Secondary outcome of 48-hour rest pain score was significantly higher in the L group (p = 0.03) but without any difference in opioid use.</span><b><span style="font-family:Verdana;"> </span></b><span style="font-family:Verdana;">There was no difference in any other outcomes between the groups at any time points. </span><b><span style="font-family:Verdana;">Conclusions:</span></b><span style="font-family:Verdana;"> Low dose lidocaine and its combination with ketamine did not add any analgesic/morphine sparing benefit in the presence</span><b><span style="font-family:Verdana;"> </span></b><span style="font-family:Verdana;">of single dose intrathecal morphine in patients with major liver resection.</span>展开更多
The behaviour of water soluble and monomer soluble inhibitors in the emulsion polymerization for CaseI system(e.g.vinyl acetate and vinyl chloride)has been studied.The behaviour of monomer soluble inhibitorsis shown t...The behaviour of water soluble and monomer soluble inhibitors in the emulsion polymerization for CaseI system(e.g.vinyl acetate and vinyl chloride)has been studied.The behaviour of monomer soluble inhibitorsis shown to be quite different from that observed in Case Ⅱ emulsion polymerization system.Model predictionsof the effect of these inhibitors on polymer particle nucleation and growth rate are shown to be in satisfactoryagreement with experimental results.展开更多
基金Supported by Henan Distinguished Junior Scholar Grant,No.074100510017
文摘AIM:To evaluate the effect of efflux pump inhibitors (EPIs) on multidrug resistance of Helicobacter pylori (H. pylori).METHODS: H. pylori strains were isolated and cultured on Brucella agar plates with 10% sheep's blood. The multidrug resistant (MDR) H. pylori were obtained with the inducer chloramphenicol by repeated doubling of the concentration until no colony was seen, then the susceptibilities of the MDR strains and their parents to 9 antibiotics were assessed with agar dilution tests. The present study included periods before and after the advent of the EPIs, carbonyl cyanide m-chlorophenyl hydrazone (CCCP), reserpine and pantoprazole), and the minimum inhibitory concentrations (MICs) were determined accordingly. In the same way, the effects of 5 proton pump inhibitors (PPIs), used in treatment of H. pylori infection, on MICs of antibiotics were evaluated.RESULTS: Four strains of MDR H. pylori were induced successfully, and the antibiotic susceptibilities of MDR strains were partly restored by CCCP and pantoprazole, but there was little effect of reserpine. Rabeprazole was the most effective of the 5 PPIs which could decrease the MICs of antibiotics for MDR H. pylori significantly.CONCLUSION: In vitro, some EPIs can strengthen the activities of different antibiotics which are the putative substrates of the efflux pump system in H. pylori.
文摘Context: Glucose-insulin-potassium(GIK) infusion is a widely applicable, low-cost therapy that has been postulated to improve mortality in patients with acute ST segment elevation myocardial infarction(STEMI). Given the potential global importance of GIK infusion, a large, adequately powered randomized trial is required to determine the effect of GIK on mortality in patients with STEMI. Objective: To determine the effect of high-dose GIK infusion on mortality in patients with STEMI. Design, Setting, and Participants: Randomized controlled trial conducted in 470 centers worldwide among 20201 patients with STEMI who presented within 12 hours of symptom onset. The mean age of patients was 58.6 years, and evidence based therapies were commonly used. Intervention: Patients were randomly assigned to receive GIK intravenous infusion for 24 hours plus usual care(n=10091) or to receive usual care alone(controls; n=10110). Main Outcome Measures: Mortality, cardiac arrest, cardiogenic shock, and reinfarction at 30 days after randomization. Results: At 30 days, 976 control patients(9.7%) and 1004 GIK infusion patients(10.0%) died(hazard ratio [HR], 1.03; 95%confidence interval [CI], 0.95-1.13; P=.45)-. There were no significant differences in the rates of cardiac arrest(1.5%[151/10107] in control and 1.4%[139/10088] in GIK infusion; HR, 0.93; 95%CI, 0.74-1.17; P=.51), cardiogenic shock(6.3%[640/10107] vs 6.6%[667/10088]; HR, 1.05; 95%CI, 0.94-1.17; P=.38), or reinfarction(2.4%[246/10107] vs 2.3%[236/10088]-; HR, 0.98; 95%CI, 0.82-1.17; P=.81). The rates of heart failure at 7 days after randomization were also similar between the groups(16.9%[1711/10107] vs 17.1%[1721/ 10088]; HR, 1.01; 95%CI, 0,95-1.08; P=.72). The lack of benefit of GIK infusion on mortality was consistent in prespecified subgroups, including in those with and without diabetes, in those presenting with and without heart failure, in those presenting early and later after symptom onset, and in those receiving and not receiving reperfusion therapy(thrombolysis or primary percutaneous coronary intervention). Conclusion: In this large, international randomized trial, high-dose GIK infusion had a neutral effect on mortality, cardiac arrest, and cardiogenic shock in patients with acute STEMI.
文摘The behaviour of water soluble and monomer soluble inhibitors in emulsion polymerization of monomersfollowing Case Ⅱ kinetics(e.g.styrene)has been investigated.Experimental studies reveal that inhibitors canhave an appreciable effect on both polymer particle nucleation and growth.A mathematical model showingthese effects has been developed and simulation studies have been done.The simulation results imply that theconsequences of these effects of monomer soluble inhibitors for industrial emulsion polymerization may be quiteserious.
文摘<b><span style="font-family:Verdana;">Background and Aims:</span></b><span style="font-family:Verdana;"> Open liver resection requiring an upper abdominal incision is associated with significant opioid use due to postoperative pain. We tested the hypothesis that the intraoperative combination of low dose lidocaine and ketamine would reduce opioid consumption when given in conjunction with intrathecal morphine for liver resection surgery. </span><b><span style="font-family:Verdana;">Methods:</span></b><span style="font-family:Verdana;"> In this triple blind, parallel group four-arm placebo-controlled trial, we randomized 124 adult</span><span style="font-family:Verdana;color:#FF0000;"> </span><span style="font-family:Verdana;">ASA 2</span><span style="font-family:Verdana;"> </span><span style="font-family:Verdana;">-</span><span style="font-family:Verdana;"> </span><span style="font-family:Verdana;">4 liver resection patients to receive intraoperative lidocaine 0.33 mg/kg/h (group L), ketamine 70 μg/kg/h (group K), combination of lidocaine 0.33 mg/kg/h and ketamine 70 μg/kg/h (group KL) and saline (group P). All patients received 300 μg intrathecal morphine prior to induction of anesthesia. All infusions were started immediately after intubation and continued until the end of surgery. Primary outcome measurements included opioid consumption at 24-hours. Secondary outcomes included pain scores, opioid consumption at 48 and 72-hours and side effects including nausea, vomiting, dizziness, hallucinations, headaches and signs of local anaesthetic toxicity. Patients were followed up for 12 weeks. </span><b><span style="font-family:Verdana;">Results:</span></b><span style="font-family:Verdana;"> There was no difference in the primary outcome of opioid consumption within all 4 groups at rest or movement at 24-hours. Secondary outcome of 48-hour rest pain score was significantly higher in the L group (p = 0.03) but without any difference in opioid use.</span><b><span style="font-family:Verdana;"> </span></b><span style="font-family:Verdana;">There was no difference in any other outcomes between the groups at any time points. </span><b><span style="font-family:Verdana;">Conclusions:</span></b><span style="font-family:Verdana;"> Low dose lidocaine and its combination with ketamine did not add any analgesic/morphine sparing benefit in the presence</span><b><span style="font-family:Verdana;"> </span></b><span style="font-family:Verdana;">of single dose intrathecal morphine in patients with major liver resection.</span>
文摘The behaviour of water soluble and monomer soluble inhibitors in the emulsion polymerization for CaseI system(e.g.vinyl acetate and vinyl chloride)has been studied.The behaviour of monomer soluble inhibitorsis shown to be quite different from that observed in Case Ⅱ emulsion polymerization system.Model predictionsof the effect of these inhibitors on polymer particle nucleation and growth rate are shown to be in satisfactoryagreement with experimental results.