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1.
China Journal of Chinese Materia Medica ; (24): 326-330, 2004.
Article in Chinese | WPRIM | ID: wpr-256362

ABSTRACT

<p><b>OBJECTIVE</b>To identify Tongren Dahuoluo pills and Tongren Niuhuangqingxin pills respectively by analysis of IR fingerprint.</p><p><b>METHOD</b>Both drugs were extracted with hexane, ethylether and butanone respectively and then the obtained extracts were measured with the ET-IR spectrometer.</p><p><b>RESULT</b>By analyzing IR fingerprint of 25 batches of Tongren Dahuoluo pills and 27 batches of Tongren Niuhuangqingxin pills, we found that different batches of the same drug hadstabile and repeatable fingerprint.</p><p><b>CONCLUSION</b>By using IR fingerprint, either Tongren Dahuoluo pills or Tongren Niuhuangqingxin pills can be exactly identified. It provides a rapid method for drug identification and quality control.</p>


Subject(s)
Drug Combinations , Drug Contamination , Drugs, Chinese Herbal , Chemistry , Plants, Medicinal , Chemistry , Quality Control , Spectrophotometry, Infrared
2.
Journal of Zhejiang University. Medical sciences ; (6): 519-523, 2004.
Article in Chinese | WPRIM | ID: wpr-353269

ABSTRACT

<p><b>OBJECTIVE</b>To determine the effects of lactose inducing on the expression of recombinant Helicobacter pylori rUreB and rhpaA, and Escherichia coli rLTB and rLTKA63.</p><p><b>METHODS</b>BIO-RAD gel image analysis system was applied to detect the outputs of the recombinant proteins. SDS-PAGE was performed to measure the target protein expression of recombinant genes at various periods of growth, different lactose concentrations, various inducing temperatures and times. The results of the target protein expression induced by lactose were compared to those by isopropyl-beta-D-thiogalactoside (IPTG).</p><p><b>RESULTS</b>Lactose showed higher efficiency to induce the expression of rHpaA, rUreB, rLTB and rLTKA63 than IPTG. The expression outputs of target recombinant proteins induced at 37 degrees C were remarkably higher than those at 28 degrees C. The optimal expression parameters were 0.8 of OD600 value, 50 g/L of lactose, 4 hours of inducing time for rHpaA, and 1.2 of OD600 value, 100 g/L of lactose, 5 hours of inducing time for both the rUreB and rLtB,and 0.8 of OD600 value, 100 g/L of lactose, 4 hours for rLTKA63.</p><p><b>CONCLUSION</b>Lactose, a sugar with non-toxicity and low cost, is able to induce the recombinant genes to express the target proteins with higher efficiency than IPTG.</p>


Subject(s)
Humans , Adhesins, Bacterial , Genetics , Bacterial Toxins , Genetics , Bacterial Vaccines , Genetics , Enterotoxins , Genetics , Escherichia coli , Genetics , Metabolism , Escherichia coli Proteins , Genetics , Genetic Engineering , Helicobacter Infections , Helicobacter pylori , Genetics , Metabolism , Lactose , Pharmacology , Recombinant Proteins , Genetics , Urease , Genetics , Vaccines, Synthetic , Genetics
3.
Journal of Zhejiang University. Medical sciences ; (6): 21-23, 2003.
Article in Chinese | WPRIM | ID: wpr-231130

ABSTRACT

<p><b>OBJECTIVE</b>To establish a stable and reliable model of Helicobacter pylori infection in Mongolian gerbil and to observe pathological changes in gastric mucosa from the infected animals.</p><p><b>METHODS</b>Mongolian gerbils were randomly divided into six groups infected with H.pylori strain NCTC11637 (n=6, group N), six groups infected with H.pylori clinical strain Y06 (n=6, group Y) and six groups as negative control (n=4, group C). H.pylori suspensions at the concentrations of 2 X 10(8)CFU/ml and 2 X 10(9) CFU/ml of strain NCTC11637 and strain Y06 were prepared with Brucella broth from Columbia agar containing sheet blood. The animals in one group N and in one group Y were orally challenged once with 0.5 ml of 2 X 10(8) CFU/ml H.pylori suspension. The animals in another group N and in another group Y were orally challenged with 0.5 ml of 2 X 10(9) CFU/ml H.pylori suspension for three times at the intervals of 24 hours, respectively. The animals were killed after 2nd, 4th and 6th week of the last infection and the gastric mucosal samples were taken for urease test, bacterial isolation, routine pathological and H.pylori histochemical examinations.</p><p><b>RESULTS</b>Infection rates of the animals in group N and group Y at the 2nd, 4th and 6th week after one challenge were 0%, 0%, 66.7% and 0%, 16.7%, 16.7%, respectively. Infection rates of the animals in groups N and Y at the 2nd, 4th and 6th week after three challenges were 66.7%, 100%, 100% and 66.7%, 66.7%, 100%, respectively. In animals with positive bacterial isolation H.pylori was found to colonized on the surface of gastric mucosal cells and in the gastric pits, and the lamina propria of gastric mucosal was infiltrated with chronic inflammatory cells.</p><p><b>CONCLUSION</b>By using H.pylori suspension at high concentration of 1 X 10(9) CFU for multiple times, the orally challenged Mongolian gerbils can be prepared as a stable and reliable H.pylori infection model. H.pylori can colonize in gastric mucosa of the infected animals, and mild inflammation reactions can be seen.</p>


Subject(s)
Animals , Female , Disease Models, Animal , Gastric Mucosa , Microbiology , Gerbillinae , Helicobacter Infections , Microbiology , Pathology , Helicobacter pylori , Immunohistochemistry
4.
Journal of Zhejiang University. Medical sciences ; (6): 192-196, 2003.
Article in Chinese | WPRIM | ID: wpr-231088

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the cardiac effect of interleukin-2 (IL-2) and to explore the underlying mechanism.</p><p><b>METHODS</b>The video tracking system and spectrofluorometric method were used to measure the cell contraction and intracellular calcium. Fura-2/AM was used as a calcium fluorescence probe. Langendorff perfusion technique was used to determine the effect of IL-2 on the intact heart.</p><p><b>RESULTS</b>Compared with the control group, IL-2 5 U/ml, 50 U/ml significantly decreased cell contraction amplitude [(74.95+/-4.79) vs (98.09+/-5.02)%, (64.30+/-5.24) vs (97.38+/-4.05)%], peak velocity of cell shortening [(70.23+/-4.85)% vs (98.09+/-5.46)%, (61.15+/-5.20)% vs (97.38+/-6.85)%], peak velocity of cell relengthening [(71.22+/-4.79)% vs (98.32+/-6.08)%, (68.16+/-5.24)% vs (97.55+/-5.00)%] and end- diastolic cell length [(88.28+/-5.84)% vs (97.95+/-5.52)%, (84.18+/-6.52)% vs (98.94+/-6.76)%]. IL-2 (5 U/ml, 50 U/ml) also markedly inhibited intracellular calcium transient [(74.94+/-4.90)% vs (98.09+/-3.74)%,(71.00+/-5.28)% vs (97.38+/-5.52)%], and elevated end-diastolic calcium level of ventricular myocytes [(113.91+/-5.93)% vs (100.10+/-3.02)%, (119.09+/-7.12)% vs (100.52+/-6.00)%], which were attenuated by the opioid receptor antagonist naloxone (Nal,10 nmol/L). In the isolated perfused rat heart,when compared with the control group, IL-2 50 U/ml markedly decreased left ventricular developed pressure [(79.91+/-2.18) vs (93.84+/-2.94)mmHg], maximal rate of rise of left ventricular pressure [(2370.7358.29) vs (2591.50+/-62.81)mmHg] maximal rate of fall of left ventricular [-(1460.95+/-38.6) vs -(1634.24+/-54.05) mmHg/s] and heart rate [(217.35+/-10.56) vs (244.52+/-11.23) beats/min], but increased left ventricular end-diastolic pressure (11.44+/-1.02 vs 9.23+/-0.46). Pretreatment with Nal (10 nmol/L) antagonized the cardiac depression and left ventricular end-diastolic pressure elevation induced by IL-2.</p><p><b>CONCLUSION</b>The cardiac effect of IL-2 is mediated by opioid receptors on the membrane of cardiomyocytes.</p>


Subject(s)
Animals , Male , Rats , Calcium , Metabolism , Depression, Chemical , In Vitro Techniques , Interleukin-2 , Pharmacology , Myocardial Contraction , Naloxone , Pharmacology , Rats, Sprague-Dawley , Receptors, Opioid, kappa , Physiology
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