Objective To investigate the effect and underlying mechanism of nocodazole on the inhibition of rVSMCs proliferation. Methods rVSMCs were divided into four groups, group A (normal culture), group B (serum-free culture for 24 h) , group C ( 18 h normal culture after 48 h of serum-free culture ) , and group D ( nocodazole treatment for 12 h after thymidine treatment for 12 h) . Flow cytometry, transmission electron microscopy, and metabolism measurements were performed and mitofusin-2 ( Mfn-2 ) expression was detected. Results Flow cytometry analysis showed rVSMCs of group B、C、D were arrested to G0/G1 , S and G2/M phases, respectively. Less and smaller mitochondria were observed in group D by transmission electron microscopy in nocodazole-treated rVSMCs. Compared with groups A and C, there were significant decreases in glucose and L-amino acid metabolism, levels of ATP, and marked increase in NADH in group D(P<0. 05). Western Blot showed that G2/M cell cycle arrest and nocodazole could induce up-regulation of Mfn-2 in rVSMCs(P<0. 05). Conclusion Nocodazole can block the energy metabolism and proliferation in rVSMCs, which is probably associated with the role of Mfn-2 on anti-atherosclerosis.

Objective To explore a new electrodiagnostic approach using the H reflex elicited by magnetic stimulation of the S1 nerve root and F waves to evaluate sensory nerve root function in patients with S1 radiculopathy.Methods Thirty normal subjects and 30 patients with unilateral S1 radiculopathy were recruited in this study.H reflex and M response were recorded from the bilateral soleus of all the subjects by magnetic stimulation of S1 nerve roots.F and M wave responses elicited by electrical stimulation of bilateral tibial nerves at the popliteal fossa were also recorded.The sensory root conduction time (SRCT) was calculated.Correlations of age and body height with SRCT in the healthy subjects,and between SRCT and pain in the patients with S1 radiculopathy were analyzed.Results The mean values of normal subjects were 3.10 ± 0.44 ms for SRCT,and 0.13 ± 0.19 ms for inter-side SRCT differences.In the 30 patients with S1 radiculopathy,H reflex could not be elicited from 4 patients.Among the remaining patients,the SRCT of the affected side was prolonged significantly (3.90 ±0.65 ms),and the mean value of the inter-side difference increased significantly (0.90 ±0.50 ms).A regression equation correlating SRCT with height was developed,but no significant correlation between SRCT and age in the normal subjects was revealed.There was positive correlation between SRCT and the severity of pain among the patients.Conclusion SRCT can be used as a new electrodiagnostic index in estimating sensory nerve root function in patients with S1 radiculopathy.

Objective To explore the value of a new electrodiagnostic approach for evaluating motor nerve root function in patients with S1 radiculopathy. Methods Thirty healthy subjects and 30 patients with clinical mani-festations of unilateral S1 radiculopathy were recruited. Bilateral compound muscle action potentials evoked by magnetic stimulation of the first sacral nerve root were recorded from the soleus of all the subjects. F wave and M responses to electrical stimulation of the bilateral tibial nerves at the popliteal fossa were also recorded. The peripheral motor conduction time (PMCT) and the motor root conduction time (MRCT) were calculated and compared between the two groups. In addition, needle electromyographic examination (NEE) was performed on the affected side to detect any possible EMG abnormalities. Results The norm established with the normal subjects was 3.45±0.39 ms for the MRCT, and 0.28±0.15 ms for the inter-side difference in the MRCT. In the 30 patients, the mean MRCT and PMCT values on the affected side were prolonged. Of the 23 patients who received NEE, 6 had EMG abnormalities. The agreement between the NEE and MRCT diagnoses was 82.6%. Conclusion MRCT can be used reliably for non-invasive estimation of motor nerve root function and to help diagnose the S1 radiculopathy.

Objective To study the effects of two fungal elicitors on the growth of Dendrobium candidum protocorms cultured on the solid medium.Methods The medium for propagation of protocorms was selected and the growth curve on that medium was obtained.According to the curve,the two fungal elicitors were added at the different growth stages of protocorms.The fresh weight(FW) and dry weight(DW) of protocorms were measured.Results The medium for propagation of protocorms was 1/2MS+20% potato extract+3% sucrose+0.8% agar.Compared with the control MF23 elicitor added at weeks 11 and 13 could significantly increase the FW by 16.4%(P

Objective To establish a method for determining the content of Naringin and Hesperidin in Zengshi Keli by HPLC. Methods The Kromasil C18 column with acetonitrile-water-phosphoric acid (20∶80∶0.02) as the mobile phase was used. The flow rate was 1.0 mL/min, the detective wavelength was 283 nm, the temperature of column is 35 ℃. Results The calibration curve were linear in the range of 0.178 5～0.892 5 ?g for Naringin and 0.073 68～0.368 4 ?g for Hesperidin (r=0.999 9) respectively. The average recovery was 97.24% (RSD=1.21%) and 96.95% (RSD=1.49%) respectively. Conclusion The method was simple, accurate, reproducible and can be used for quality control of Zengshi Keli.

0.05),while there was significant difference among other groups(P

Objective To study inhibitory activity of anthraquinone in Polygonum Cillinerve(Nakai) Ohwi (anthraquinone in PCO) to nitrosation. Methods Anthraquinone was extracted from Polygonum Cillinerve(Nakai) Ohwi with sulfuric acid and chloroform as solvents. The capability of scavenging sodium nitrite and disconnecting nitrosamine synthesis with anthraquinone in PCO were determined by spectrophotometry under simulated human gastric juice. Results Both the sodium nitrite scavenging rate and the nitrosamine synthesis disconnecting rate showed the positive correlation with the concentration of anthraquinone in PCO. The strongest capability of scavenging sodium nitrite was 53.5%, and the strongest capability of disconnecting nitrosamine synthesis was 71.3%. Conclusion Anthraquinone in PCO had strong capability of scavenging sodium nitrite and disconnecting nitrosamine synthesis.

The role of lipid-regulating capsule in the regulation of experimental dislipidemia was studied in SD rats. The SD rats were divided into 6 groups: group A (normal control)，group B to F (experimental hyperlipidemia). The rats in the groups C，D and E received the capsule in a daily dose of 2.5 g，5 g and 10 g/kg respectively for 3 weeks，while the rats in the group F received Simvastatin in a daily dose of 7.5 mg/kg for 3 weeks. By comparison with the group B after 3 weeks，the levels of plasma total cholesterol (TC) and low density lipoprotein (LDL-C) were very significantly decreased in the groups C，D，E and F(P<0.01)，the value of plasma total triglyceride (TG) was very significantly decreased in the groups D，E and F (<0.01)，and the level of high density lipoprotein was significantly increased in the groups C，D and E (P<0.05)，but very significantly increased in the group F (P<0.01). It was suggested that the therapeutic efficiency of the lipid-regulating capsule in low，middle and high dosage was the same as that in high dose of simvastatin for the SD rats with high plasma TC and LDL-C，and middle and high doses of the capsule had the same effect of simvastatin on the plasma TG.

Objective To analyse the effect of progesterone on peripheral blood corticotropin releasing hormone ( CRH ) and delivery time in women with premature rupture of membranes ( PROM ) .Methods 80 patients who were diagnosed with PROM in Department of Obstetrics and Gynecology, China Medical University were collected.Randomly divided into dexamethasone (DEX) group, dexamethasone plus progesterone (DEX+P) group, progesterone ( P) group and control group, three groups were detected on admission, admission 24 h, 48 h on peripheral white blood cell count, C-reaction protein, CRH level and time of delivery, neonatal weight, and analysis of CRH the level of the correlation and delivery time.Results Compared with the other three groups, the level of CRH in peripheral blood of DEX group were higher (P<0.05);CRH (P<0.05) increased faster;shorter delivery time (P<0.05); the level of CRH was negatively correlated with delivery time (r=-0.832, P<0.05).The results were statistically significant.Conclusion Dexamethasone treatment can make the premature rupture of fetal membranes of peripheral blood CRH levels rise, shorten the delivery time, progesterone can inhibit this process.

Objective To evaluate the effect of hydrogen on the endoplasmic reticulum stress during liver cold ischemia-reperfusion (I/R) in rats.Methods Twenty-four SPF healthy adult male Sprague-Dawley rats,weighing 200-250 g,were divided into 3 groups (n=8 each) using a random number table:sham operation group (group S),liver cold I/R group (group I/R) and hydrogen-saturated lactated Ringer's solution group (group HL).After occlusion of the liver blood flow,livers were perfused through the portal vein with 4 ℃ hydrogen-saturated lactated Ringer's solution 6-8 ml/min for 30 min.The liver blood flow was restored after the end of perfusion.At 6 h of reperfusion in I/R and HL groups or at 6 h after peritoneum closure in group S,blood samples from the inferior vena cava were collected for determination of serum alanine transaminase (ALT) and aspartate transaminase (AST) concentrations.After blood sampling,liver tissues were obtained for examination of pathological changes and for determination of cell apoptosis (using TUNEL),malondialdehyde (MDA) content (by thiobarbituric acid method),superoxide dismutase (SOD) activity (using xanthine oxidase method),expression of endoplasmic reticulum protein 46 (ERP46),immunoglobulin heavy chain binding protein (BiP) and caspase-12 (by immunohistochemistry),and expression of ERP46,BiP and caspase-12 mRNA (using quantitative real-time polymerase chain reaction).The pathological changes were scored.Apoptosis rate was calculated.Results Compared with group S,the serum ALT and AST concentrations,pathological scores,apoptosis rate and MDA content were significantly increased,the SOD activity was decreased,and the expression of ERP46,BiP and caspase-12 protein and mRNA was up-regulated in I/R and HL groups (P＜0.05).Compared with group I/R,the serum ALT and AST concentrations,pathological scores,apoptosis rate and MDA content were significantly decreased,the SOD activity was increased,and the expression of ERP46,BiP and caspase-12 protein and mRNA was down-regulated in group HL (P＜0.05).Conclusion The mechanism by which hydrogen reduces cell apoptosis may be related to inhibition of endoplasmic reticulum stress during liver cold I/R in rats.