1.Clinical study on tube moxibustion plus point-toward-point needling method in treating refractory facial paralysis
Zhonghao XIONG ; Xi ZHOU ; Na SONG ; Fengwei TIAN ; Fuqing ZHANG
Journal of Acupuncture and Tuina Science 2022;20(5):399-405
Objective: To evaluate the clinical efficacy of tube moxibustion plus point-toward-point needling method for refractory facial paralysis. Methods: A total of 100 patients with refractory facial paralysis who met the inclusion criteria were randomized into an observation group and a control group, with 50 cases in each group. Both groups were treated with acupuncture by point-toward-point needling method, mainly in the affected eye, cheek and mouth areas. The observation group was given additional tube moxibustion after receiving the point-toward-point needling method, which inserted a tube moxibustion device into the external acoustic meatus 1 cm on the affected side for 20 min. Both groups were treated once a day, 6 times a week, for 4 consecutive weeks. The House-Brackmann scale was scored before and after treatment, and the facial nerve electromyogram data were collected. Results: The total effective rate of the observation group was 93.6%, which was higher than 64.6% of the control group, and the difference between the two groups was statistically significant (P<0.05). The proportion of new-onset facial paralysis complications (facial synkinesis, facial spasm, facial paralysis perversion, and crocodile tears) in the observation group was 6.4%, which was lower than 35.4% in the control group. The difference between the two groups was statistically significant (P<0.05). In the observation group, the numbers of cases after treatment with the ratio of action potential amplitude between the affected side and the healthy side increased by 10%-30% and over 30% were more than those in the control group. And the difference between the two groups was statistically significant (P<0.05). Conclusion: Tube moxibustion plus point-toward-point needling method has a better effect in improving symptoms of refractory facial paralysis, decreasing the incidence of sequelae, and increasing clinical efficacy than the point-toward- point needling method alone.
2.Randomized Controlled Trial on Siege Scheme of Traditional Chinese Medicine to Treat Excess Syndrome of Stroke with Bowel and Visceral Strike
Fengwei TIAN ; Zhuxing WANG ; Ying LI ; Jian ZU ; Ning LI ; Guangyan XU ; Xi ZHOU ; Chengwei WANG
Chinese Journal of Information on Traditional Chinese Medicine 2015;(3):27-31
Objective To evaluate the efficacy of siege scheme of TCM for acute cerebral infarction bowel and visceral strike (block pattern). Methods Totally 110 patients were randomly divided into TCM siege scheme group (55 cases) and control group (55 cases) by randomized parallel controlled study with foresight and multicenter. The control group was treated with the standardized treatment, and TCM siege scheme group was treated with TCM siege scheme, including mild hypothermia TCM pillow therapy, TCM rectal enema, and other multiple treatments based on the standardized treatment. The Glasgow Coma Scale (GCS), the time of pulling out urine tube and nasal feeding tube, and the number of tracheotomy caused by illness changes of the two groups were compared. Results The baseline data of two groups have good comparability (P>0.05). On 10, 15 d of treatment, the number of lucid people in the TCM siege scheme group was significantly more than that in the control group (P<0.05). Compared with the control group, treatment group had less number of tracheotomy, and shorter time of success pulling out urine tube and nasogastric feeding tube (P<0.05). Conclusion TCM siege scheme can improve the consciousness of ischemic stroke in patients with acute cerebral infarction bowel and visceral strike, reduce complications, shows shorter successful pull urine tube and nasogastric feeding, and provides guarantee conditions for further rehabilitation treatment.
3.Characterization of protein secretion based on structural fusion degree.
Cuifang GAO ; Xiaojun WU ; Fengwei TIAN ; Yu XIA ; Wei CHEN
Chinese Journal of Biotechnology 2010;26(5):687-695
Selection of suitable signal peptides is an important factor for efficient secretion of heterologous proteins. We defined structural fusion degree (SFD) as the compatibility degree of target proteins and signal peptides by a bioinformatics approach. We mathematically analyzed the interaction of fused signal peptides and adjacent residues of proteins, and proposed a mathematical model of extended signal region and the protein. SFD Features was extracted from this model to characterize the secretability of heterologous proteins. Simulation tests showed that SFD features can effectively discriminate high secretory proteins from poor ones in the host Bacillus subtilis. Results from this research will be useful in signal peptide selection and have a better guiding significance for the optimization of heterologous protein secretion.
Amino Acid Sequence
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Bacillus subtilis
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genetics
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metabolism
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Bacterial Proteins
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genetics
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metabolism
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Biotechnology
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methods
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Membrane Transport Proteins
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genetics
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metabolism
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Metalloendopeptidases
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genetics
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metabolism
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Molecular Sequence Data
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Protein Sorting Signals
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genetics
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Proteins
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secretion
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Recombinant Fusion Proteins
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genetics
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metabolism
4.Expression and characterization of a new class IIa bacteriocin.
Yan XIE ; Haiqin CHEN ; Qiuxiang ZHANG ; Fengwei TIAN ; Yongquan CHEN ; Hao ZHANG ; Wei CHEN
Chinese Journal of Biotechnology 2011;27(7):976-982
NB-Cl gene is a potential class IIa bacteriocin gene. To obtain its soluble expression, NB-C1 was fused with the green fluorescent protein (GFP) gene and a recombinant expression vector plVEX 2.4d-GFP-NB-C1 was constructed, which was transformed into Escherichia coli BL21(DE3) pLysS. The expressed fusion protein GFP-NB-CI was purified by Ni-NTA affinity chromatography and the bioactivity was examined using Listeria monocytogenes as the indicator bacteria. The results showed that the expressed fusion protein GFP-NB-C1 was soluble and the final concentration of the purified fusion protein was 36.1 mg/L E. coli culture and had the purity above 95%. The antimicrobial assay of GFP-NB-C1 was analyzed and showed its high activity against Listeria monocytogenes.
Amino Acid Sequence
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Anti-Bacterial Agents
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pharmacology
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Bacteriocins
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biosynthesis
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genetics
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Chromatography, Affinity
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Escherichia coli
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genetics
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metabolism
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Genetic Vectors
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genetics
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Green Fluorescent Proteins
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biosynthesis
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genetics
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Listeria monocytogenes
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drug effects
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Molecular Sequence Data
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Recombinant Fusion Proteins
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biosynthesis
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genetics
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pharmacology
5.Ultrasonic imaging research atpoints in neck-type cervical spondylosis.
Xiaoming WU ; Fengwei TIAN ; Zhaopeng XIE ; Guifang DONG ; Jianjun LI ; Xi ZHOU
Chinese Acupuncture & Moxibustion 2017;37(4):395-399
OBJECTIVETo conduct the preliminary positioning and qualitative research of high-frequency ultrasonic imaging atpoints (including tender points and trigger points) in neck-type cervical spondylosis and explore the relevant law so as to provide the evidence for the selection of acupuncture scheme.
METHODSThirty patients in compliance with the diagnostic criteria of neck-type cervical spondylosis were selected. The trigger points, tender points and placebo points were positioned on any of the three available oriented lines. The point-to-point high-frequency real-time dynamic ultrasonic imaging technology was used to scan and position each point and record the changes in ultrasound gradation anatomy and two-dimensional ultrasound in perimysium, two-dimensional and color Doppler ultrasonography and blood flow. The ultrasound characteristics were analyzed.
RESULTS①Regarding the changes in ultrasound gradation anatomy and two-dimensional ultrasound in perimysium, the anatomic gradation at trigger points and tender points was in the sequence as cutaneous layer, subcutaneous fat layer, shallow muscular tissue layer, deep muscular tissue layer and vertebrae. The linear high echo presented in cutaneous layer; the low echo in subcutaneous fat layer; the linear high echo in muscular fasciae; the low echo in muscular layer and the clear linear echo in its perimysium; the high echo and declined posterior echo in vertebrae. Compared with the placebo points, 93.3% of trigger points (28/30) presented enhanced or thickened perimysium echo (<0.05), and 96.7% of tender points (29/30) presented enhanced or thickened perimysium echo (<0.05). The differences were not significant between the trigger points and the tender points (>0.05). ②In the two-dimensional ultrasonography, the clear linear echo presented in perimysium, the enhanced or thickened echo in perimysium of trigger points and tender points. In the color Doppler ultrasonography, the blinking unstable dotted blood flow signal or stable short rod-like blood flow signal presented in the trigger points and tender points. ③Regarding the condition of blood flow, 56.7% of trigger points (17/30) presented Ⅱ degree of color blood flow signal and 83.3% of tender points (25/30) presented Ⅱ degree of color blood flow signal; 0% of placebo points presented Ⅱ degree of color blood flow signal. Compared with the placebo points, the differences in the rate of Ⅱ degree of color blood flow signal were significant statistically at both the trigger points and the tender points (both<0.05). The difference was not significant between the trigger points and tender points (>0.05).
CONCLUSIONSIn the high-frequency ultrasound imaging at trigger points and tender points in neck-type cervical spondylosis, the ultrasound imaging characteristics present, which are similar between the trigger points and the tender points. The high-frequency ultrasound imaging is valuable in positioning and quantitative research ofpoints in cervical spondylosis and has a certain significance to guide treatment.
6.Pharmacokinetic Study on Single and Multiple Administration of Gefitinib Emulsion in Rats
Ying LI ; Zhou WEN ; Fengwei MA ; Zhigang LIU ; Chi TIAN ; Zhifang LIU ; Zeneng CHENG
China Pharmacy 2020;31(1):48-52
ABSTRACT OBJECTIVE:To study pharmacokinetic characteristics of single dose and multiple dose administration of Gefitinib emulsion in rats. METHODS:The rats were divided into single administration group and multiple administration group. Single administration group was subdivided into Gefitinib raw medicine group(50 mg/kg,i.g.)and Gefitinib emulsion group(50 mg/kg,i.g.),with 6 rats in each group,gavage once. Multiple administration group were subdivided into Gefitinib raw medicine group (50 mg/kg)and Gefitinib emulsion group(50 mg/kg),with 8 rats in each group;they were given relevant medicine intragastricaly for consecutive 7d,once a day. 0.3 mL blood of rats in Gefitinib raw medicine group was taken before medication and 1,2,2.5, 3,3.5,3.75,4,4.25,4.5,6,8,12 and 24 h after medication;0.3 mL blood of rats in Gefitinib emulsion group was taken before medication and 2,4,6,8,9,10,11,12,13,14,16,24,36 and 48 h after administration(Multiple administration group is after 7 d of administration). HPLC method was used to determine the plasma concentration of gefitinib in rat,and plasma concentration-time curves were drawn. Pharmacokinetic parameters were fitted by using DAS 2.0 software. RESULTS:After single administration,compared with the tmax([ 2.67±0.75)h],MRT0-24 h ([ 8.68±0.91)h],MRT0- ∞ ([ 14.20±3.45)h] of Gefitinib raw medicine group,tmax ([ 8.33±4.41)h],MRT0-48 h ([ 15.00±1.60)h],MRT0-∞ ([ 17.60±2.66)h] of Gefitinib emulsion group were increased significantly(P<0.05). After multiple administration,compared with the tmax ([ 6.79±3.75)h],AUC0-48 h ([ 41.10±8.92) mg·h/L],Vz/F [(16.30±5.45)L/kg],CLz/F [(0.94±0.19) L/(h·kg)],MRT0-48 h ([ 10.10 ± 0.36) h] of Gefitinib raw medicine group,Vz/F [(44.20±30.3)L/kg],CLz/F[(1.89± 1.56) L/(h·kg)],MRT0-48 h ([ 16.20 ± 2.52) h] of Gefitinib emulsion group were increased significantly (P<0.05) AUC0-48 h ([ 38.70±26.20)mg·h/L] was decreased significantly (P<0.05),and tmax ([ 10.40±3.25)h] was increased,without statistical significance. CONCLUSIONS: Compared with Gefitinib raw medicine,single and multiple administration of Gefitinib emulsion can effectively prolong the peak time,the results of this study can provide reference for new delivery system study of Gefitinib.