1.Development of the genetic transformation system in extremely halophilic archaea.
Mei-Xian ZHOU ; Hua XIANG ; Hua-Rong TAN
Chinese Journal of Biotechnology 2002;18(3):267-271
The development of the genetic transformation systems in extremely halophilic Archaea was reviewed in this paper. Included are the screening of selectable markers for resistance to antibiotics, the development of gene cloning and expression vectors, and the modifications of the host organisms.
Archaea
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genetics
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Cloning, Molecular
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Genetic Vectors
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Transformation, Genetic
2.Pharmacokinetics of ibuprefen and pseudo ephedrine with chlorpheniramine suspension after single and multiple doses in healthy volunteers
Min SONG ; Hong-Yi TAN ; Zhi-Rong TAN ; Chang LIU ; Li YANG ; Hong XIANG ; Zhi-Jun HUANG ; Gui-Xiang ZHANG ; Guo-Ping YANG
The Chinese Journal of Clinical Pharmacology 2010;26(1):28-32,36
Objective To study the pharmacokinetics profiles of ibupro-fen and pseudo ephedrine with chlorpheniramine suspension after single and multiple dosing in healthy volunteers.Methods Three single and one multiple oral doses of ibuprofen and pseudo ephedrine with chlorphe-niramine suspension were given to healthy volunteers respectively.Ibu-profen concentrations in plasma were determined by HPLC-UV method.Pseudo ephedrine and chlorpheniramine concentrations in plasma were determined by HPLC-MS-MS method.The pharmacokinetic parameters were obtained with statistical analysis by DAS Ver 2.0.Results The main pharmacokinetic parameters of 3 single doses(ibuprofen:200,400,600 mg pseudo ephedrine:30,60,90 mg;chlorpheniramine:2,4,6 mg)and multiple dose(ibuprofe,pseudo ephedrine and chlorphe-niramine 200,30,2 mg,respectively)shown that the concentration-time curves of ibuprofen,pseudo ephedrine and chlorpheniramine were described by one-compartment open model and physiological disposi-tions were assumed by linear kinetics characteristics.Conclusion In multiple dosing study,physiological dispositions of ibuprofen,pseudo e-phedrine and chlorpheniramine all existed no induction and inhibition of drug enzyme phenomenon.
5.Establishment of perfusion technique for isolated rat pancreas
Nai-Qian ZHAO ; Ye-Rong YU ; Hui-Wen TAN ; Zhi-Ming LU ; Xiang-Xun ZHANG ; Jun-Jie LI ;
Chinese Journal of Endocrinology and Metabolism 2001;0(05):-
Objective To establish an isolated rat pancreas perfusion technique,a method for the precise measurement of insulin secretion in vitro.Methods An isolated rat pancreas perfusion technique was applied in the study of insulin secretion from?-cells in 10 high-fat diet-induced obese Wistar rats.Results For the assessment of the functional integrity of the perfused pancreas,the isolated pancreas of 6 rats met all the criteria: (1)The constancy of perfusion pressure was kept over the whole experiment time[(70?5)mm Hg,1 mm Hg= 0.133 kPa].(2)The duodenal peristaltic activity of isolated pancreas and duodenum block was present after perfusion experiment.(3)Total insulin response to arginine stimulation was significantly increased as compared with glucose stimulation[maximum insulin secretion rate:(987?100)?U/min vs(545?50)?U/min,P
6.Influence of regulatory peptides on the secretion of interleukins from bronchial epithelial cells of the rabbit.
Yu-Rong TAN ; Xiao-Qun QIN ; Cha-Xiang GUAN ; Chang-Qing ZHANG ; Yang XIANG ; Yan-Hong REN
Acta Physiologica Sinica 2002;54(2):107-110
To explore the role of regulatory peptides in the secretion of bronchial epithelial cells (BECs), we observed the effects of four peptides, i.e.vasoactive intestinal peptide (VIP), epidermal growth factor (EGF), endothelin-1 (ET-1), and calcitonin gene-related peptide (CGRP), on the secretion of ILs from unstimulated or O3-stressed BECs. The results of the experiments showed that VIP exerted an inhibitory effect on the secretion of IL-1 and IL-8 from unstimulated and O3-stressed BECs, VIP also decreased the secretion of IL-5 from O3-stressed BECs; EGF promoted secretion of IL-1 and IL-8 from unstimulated BECs, but decreased the secretion of ILs from O3-stressed BECs; ET-1 and CGRP enhanced the secretion of IL-1, IL-5, and IL-8 from unstimlated BECs, CGRP also increased the secretion of ILs from O3-stressed BECs. The results obtained demonstrate that intrapulmonary regulatory peptides modulate the secretion of ILs from BECs, and may play an important part in transduction of inflammatory signals.
Animals
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Bronchi
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cytology
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Calcitonin Gene-Related Peptide
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pharmacology
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Cells, Cultured
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Endothelin-1
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pharmacology
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Epidermal Growth Factor
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pharmacology
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Epithelial Cells
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drug effects
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secretion
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Female
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Interleukins
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secretion
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Male
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Rabbits
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Vasoactive Intestinal Peptide
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pharmacology
7.Killing effect of sequential Herceptin and adriamycin treatment on breast cancer cell line in vitro.
Ke TAN ; Yi-xiang FAN ; Jing-xia MIAO ; Cheng-wei LÜ ; Xiao YAN ; Rong-cheng LUO
Journal of Southern Medical University 2006;26(2):234-236
OBJECTIVETo observe the killing effect of Herceptin and adriamycin sequentially applied on breast cancer cell line in vitro.
METHODSBT-474 human breast cancer cells in exponential growth phase were treated with Herceptin alone, adriamycin alone and their sequential administration (Herceptin before adriamycin and vice versa), respectively. Under optical microscope, the morphological changes of the cells were observed before and after drug administration. The expression rate and mean fluorescence intensity (MFI) of HER-2/neu and cell death rate were detected by flow cytometry.
RESULTSMicroscopically, the cells treated with different protocols all exhibited such changes as darkening and increase of cellular debris with irregular cell morphology. Flow cytometry revealed no significant difference in the expression rate of HER-2/neu in each group before and after treatment, but the MFI of HER-2/neu and death rate of the treated cells were significant different from those of the control group (P<0.05). The cell death rate of Herceptin-pretreated cells was significantly higher than that of adriamycin-pretreated ones (P<0.05).
CONCLUSIONHerceptin pretreatment enhances the killing effect of adriamycin on breast cancer cell line BT-474, which provides experimental evidence for designing clinical sequential biochemotherapy of breast cancer.
Antibiotics, Antineoplastic ; pharmacology ; Antibodies, Monoclonal ; pharmacology ; Antibodies, Monoclonal, Humanized ; Antineoplastic Agents ; pharmacology ; Breast Neoplasms ; metabolism ; pathology ; Cell Death ; drug effects ; Cell Line, Tumor ; Doxorubicin ; pharmacology ; Drug Synergism ; Female ; Flow Cytometry ; Humans ; Receptor, ErbB-2 ; biosynthesis ; Trastuzumab
8.TCM colleges and universities laboratory standardization management practice based on the experimental teaching quality monitoring
Huiping LIU ; Guomin ZHANG ; Rong YU ; Ling LI ; Yi XIAO ; Xia WU ; Qin XIANG ; Shanshan HUANG ; Feng TAN ; Hongbao WANG ; Kun PAN ; Lijuan HU
International Journal of Traditional Chinese Medicine 2015;(3):205-208
TCM experimental teaching has a very important position in university training process, in which the laboratory standardized management and the strengthening of the teaching quality monitoring play important roles. According to the the experimental teaching reforms and requirements enacted in recent years by the Ministry of Education of the People’s Republic of China, Hunan TCM University has conducted a series of standardized management of exploration and practice in the laboratory.
9.Analysis of the adult penis 3D digitized image.
Hua CHEN ; Shi-rong LI ; Xiang-dong QI ; Xia TAN ; Jü-long WU ; Chuan CAO
Chinese Journal of Plastic Surgery 2007;23(4):300-303
OBJECTIVETo analyze 3D digitized image of the adult penis, providing morphological data for plastic plerosis of the adult penis diagnosis and the surgery planning.
METHODS200 adult penis were measured at the length and perimeter of the resting state and erection, and the relation among the erectile angle and length, perimeter were analyzed by the Angel Digital Image Studio software.
RESULTSPenis increase with the age and stature growing. But the length increases in not the same ratio with the stature . With the erectile angle increasing, penile hardness is becoming strong, but penile volume do not marked change.
CONCLUSIONSThe digitized model of the penis and adjacent structure offer unique insights into the complex penis anatomy, providing morphological data for preoperative design and postoperative effective evaluation of the penile plastic plerosis.
Adolescent ; Adult ; Humans ; Imaging, Three-Dimensional ; Male ; Middle Aged ; Penis ; anatomy & histology ; Young Adult
10.Preliminary study on hepatotoxicity induced by dioscin and its possible mechanism.
Ya-xin ZHANG ; Yu-guang WANG ; Zeng-chun MA ; Xiang-lin TANG ; Qian-de LIANG ; Hong-ling TAN ; Cheng-rong XIAO ; Yong-hong ZHAO ; Yue GAO
China Journal of Chinese Materia Medica 2015;40(14):2748-2752
Dioscin has a wide range of biological effects and broad application prospects. However the studies concerning the toxicology and mechanism of dioscin is small. This article is to study the hepatotoxicity of dioscin and the effect of dioscin treatment on expression of aryl hydrocarbon receptor (AhR) mRNA and CYP1A mRNA and protein in HepG2 cells in vitro. Dioscin 0.5-32 µmol · L(-1) exposed to HepG2 cells for 12 h, cell viability was examined by CCK-8 assay and the release rate of lactate dehydrogenase (LDH) was to evaluate cell membrane damage. HepG2 cells morphologic changes were quantified by inverted Microscope, and the effect on production of reactive oxygen species (ROS) was detected by flow cytometry. The mRNA expression of CYP1A and AhR was evaluated by RT-RCR. The protein expression of CYP1A1 was detected by western blot. The cell viability was significantly inhibited after HepG2 cells were exposed to dioscin 0.5-32 µmol · L(-1). Compared with the control, the LDH release rate and ROS were significantly increased. The expression of CYPlA and AhR mRNA was increased. The expression of CYP1Al protein was increased after dioscin treatment, and resveratrol, an AhR antagonist, could downregulate the expression of CYP1A1. It follows that large doses dioscin has potential hepatotoxicity. The possible mechanism may be dioscin can active aryl hydrocarbon receptor (AhR) and induce the expression of CYP1A.
Cell Survival
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drug effects
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Chemical and Drug Induced Liver Injury
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etiology
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Cytochrome P-450 CYP1A1
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genetics
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Diosgenin
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analogs & derivatives
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toxicity
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Hep G2 Cells
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Humans
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L-Lactate Dehydrogenase
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secretion
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RNA, Messenger
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analysis
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Reactive Oxygen Species
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metabolism
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Receptors, Aryl Hydrocarbon
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genetics