1.Clinical Observation on Treatment of 60 Cases of Primary Dysmenorrhea with Modified Shenhua Decoction plus Western Medicine
International Journal of Traditional Chinese Medicine 2009;31(4):338-
Objective To explore the efficacy of treating primary dysmenorrheal with modified Shenghua decoction plus western medicine. Methods 120 patients with primary dysmenorrhea were randomly recruited into a control group and a treatment group, with 60 patients in each group. The control group was treated with prostaglandin synthetic inhibitor, and the treatment group was treated with modified Shenghua decoction on the basis of control group. Results The total effective rate of the treatment group and the control group was 90% and 73.3%, respectively, showing significant difference (X2=4.011, P <0.05 ) . Conclusion Modified Shenghua decoction plus western medicine is effective in treating, primary dysmenorrheal.
2.Determination of 12 Kinds of Organophosphorus Pesticides in Water by Capillary Column Gas Chromatography
Journal of Environment and Health 1992;0(04):-
Objective To establish a method for simultaneous determination of 12 kinds of organophosphorus pesticides in water. Methods Organophosphorus pesticides in the water were extracted by liquid-liquid extraction, then analyzed with DB-1701 capillary column. In the same time, they were determined with GC by controlling the temperature and the speed of nitrogen. Retention time of the peaks was used for qualitative analysis, while external standard method was used for the quantitative analysis. Results The linear ranges of organophosphorus pesticides were 0.2~50.0 ?g/L, r≥0.999 1. The lowest detection limit was 0.009~0.04 ?g/L, the rate of recovery were 78.4%~93.9% and RSDs were 3.4%~7.5%. Conclusion This method is simple, rapid, sensitive and can efficiently separate and determine 12 kinds of organophosphorus pesticides in the water with 32.5 minutes of operation only.
3.Medical management of insulin resistance.
Chinese Journal of Practical Internal Medicine 2001;0(03):-
Insulin resistance induces multiple metabolic disorders and are the common risk factors of diabetes mellitus and cardiovascular diseases.Since the causes are complex,the medical management should be integrated to treat insulin resistance.Lifestyle change is the first choice,and the appropriate agents can be selected if needed.
4.Laparoscopic appendectomy: A report of 162 cases
Jiangtao YUE ; Shiping LIU ; Chao JIANG
Chinese Journal of Minimally Invasive Surgery 2005;0(12):-
Objective To summarize the experience of laparoscopic appendectomy(LA).Methods A retrospective analysis was carried out on clinical data of 162 cases of laparoscopic appendectomy in this hospital from August 2002 to April 2005.Results Laparoscopic operation was completed in all the cases but 1 case of intestinal tuberculosis.The operative time was 30~90 min(mean,42 min) and the intraoperative blood loss was 5~10 ml.No complications were noted.Conclusions Laparoscopic appendectomy has advantages of little invasion,less blood loss,rapid recovery,and fewer complications,being a safe and ideal surgical alternative.
5.Protective Effects of Ginsenosides Rb_1 and Re on Injury of the Neonate Rat Cardiomyocyte Induced by Aconitine Alkaloids
Xi DONG ; Shiping ZHAO ; Yan LIU
Chinese Journal of Information on Traditional Chinese Medicine 2006;0(09):-
Objective To investigate the protective effect of ginsenoside Rb1 and Re on injury of the neonate rat cardiomyocyte induced by aconitine alkaloids.Methods The influence of aconitine and ginsenoside Rb1,Re together in neonate rat cardiomyocyte was observed respectively.The influence of these components in neonate rat cardiomyocyte was examined by myocard zymogram.The expression of Ca2+ channel gene Cav1.2 mRNA of neonate rat cardiomyocyte after treatment was observed by RT-PCR.Results The ginsenoside Rb1 and Re were able to decrease the release of AST and LDH,reverse Cav1.2 mRNA abundance induced by aconitine.Conclusion The ginsenoside Rb1 and Re which together with aconitine can alleviate the side effects and boost up the therapeutic effects of aconitine.The action mechanism may be relation with that the ginsenoside Rb1 and Re can decrease injuries of the neonate rat cardiomyocytes and abundant expression of Cav1.2 mRNA induced by aconitine.
6.Microsurgical treatment of petroclival tumors by transpetrosal presigmoid approach
Fengyi ZHU ; Shiping YANG ; Ning LIU
Chinese Journal of Microsurgery 2000;0(03):-
Objective To explore clinical curative effect of microsurgery of petroclival tumors by transpetrosal presigmoid approach. Methods A series of 23 patients of petroclival tumors resected by microneurosurgery were analyzed retrospectively, including tumors histological types, clinical and preoperative MRI features, operative approaches, surgical technique and common postoperative complications. Results Total resection of the tumor was achieved microsurgically in 16 cases, subtotal resection in 4 cases, partial resection in 3 cases. No patient died in this series. 8 patients presented worsening crainal nerves palsies postoperatively. CSF leaks were uncommon, occuring in 2 patients. Conclusion The tumors in petroclival region can be totally resected by transpetrosal presigmoid approach. The advantages were offered by this approach such as the temporal lobes and cerebellum are minimally retracted; the operative distance of petroclival tumors is shortened with exposure of clivus and juxta-clival region.
7.SYNTHESIS AND ANTICANCER ACTIVITY OF 3-[(3′-METHYL-4′-(SUBSTITUTED PHENYL)-1′,3′-BUTADIENYL] INDOLE DERIVATIVES
Li XU ; Jie LIU ; Shiping XU
Acta Pharmaceutica Sinica 2001;36(1):29-33
AIM To study the synthesis and anticancer activity of 3-[(3′-methyl-4′-(substituted phenyl)-1′,3′-butadienyl] indole derivatives. METHODS Electrophilic-substitution, aldol-condensation, selective-reduction, phase-transfer Wittig reaction and hydrolysis reaction were used in the synthesis of the title compounds. RESULTS Eleven compounds of 3-[(3′-methyl-4′-(substituted phenyl)-1′,3′-butadienyl] indole were synthesized. They are new compounds. Compound 8 showed different inhibitory effects on HL-60, HCT-8 and Bel7402 cell lines in vitro, and its inhibitory rate of antiinflammation was 100% at 10-5 mol*L-1 concentration. CONCLUSION Compound 8 showed high anticancer and antiinflammatory activities, and is worth further studying.
8.STUDIES ON MILK SUBSTITUTES——X. The Role of Egg Yolk Powder on the Growth Promoting Effect of Soybean Milk Substitute 5410
Shengjie LIU ; Shiping GUO ; Chiyuan CHOU
Acta Nutrimenta Sinica 1956;0(01):-
It has been demonstrated by animal and human experiments that the growth promoting effect of soybean milk substitute formula 5410 is comparable with that of human milk or cow's milk formula commonly used in infant feeding. It was assumed that such a favorable effect is due in part to the inclusion of 5% of egg yolk powder in the formula. However, such an assumption remains to be confirmed.In the present animal experiment, the 5% egg yolk powder was either removed (diet 5700), or substituted with 5% whole egg powder (diet 5411), 5% whole cow's milk powder (diet 5720), 10% whole cow's milk powder (diet 5721).It was fouad that the growth promoting effect of diet 5411 is the, same as that of 5410, while that of the other, diets are all significantly inferior than that of 5410. The role played by the definite amount of egg yolk in the soybean milk substitute is postulated.
9.Effects of different dose proportioning the danggui-shaoyao powder on learning and memory and the content of NO in brain in mice
Hong LIU ; Yu ZENG ; Shiping MA
Chinese Journal of Clinical Pharmacology and Therapeutics 2004;0(09):-
AIM: To study the effects of different dose proportioning the danggui-shaoyao powder (DS) on learning and memory and the content of NO in brain in mice. METHODS: The ability of learning and memory was measured by the step-through task and the water maze task. The content of NO in brain was determined referring to the reagent manual. RESULTS: All different dose proportion of DS promoted the memory of normal mice. And only DS 1 (1 5.4) and DS 3 (1 1.34) obviously improved the scopolamine-induced mice passive avoidance handicap, prolonged the latency, and decreased number of errors. DS 3(1 1.34) obviously improved reserpine-induced mice spatial orientation handicap and prolonged the latency; others had no remarkable effect on spatial orientation handicap of mice. And all different dose proportions of DS could reduce the content of NO in the brain of passive avoidance disruption mice induced by scopolamine. CONCLUSION: DS 3 (1 1.34) improves passive avoidance handicap and spatial orientation handicap of mice, and reduced the content of NO in the brain of passive avoidance handicap mice induced by scopolamine. The effect of DS 3(1 1.34) is the best on benefiting memory.
10.Preparation and Physicochemical Properties of Phloroglucinol Phospholipids Complex
Yilei ZHAO ; Yongxi SONG ; Shiping LIU
China Pharmacy 2005;0(19):-
OBJECTIVE: To optimize the preparation technology of phloroglucinol phospholipids complex and study its physicochemical properties.METHODS: The preparation technology for phloroglucinol phospholipids complex was optimized taking the molar ratio of phloroglucinol to phospholipids(A),reaction temperature(B) and reaction time(C) as factors and complex ratio of phloroglucinol and phospholipid as index.The dissolubility and oil/water partition coefficient of the complex in different solvents were determined and compared with crude drug,and the new complex's physicochemical properties were validated by UV and IR(infrared spectra).RESULTS: The optimized preparation conditions for phloroglucinol phospholipids complex were obtained as follows: A was 1∶2;B was 60 ℃ and C was 2 h.The complex ratio remained at above 98%.Compared with phloroglucinol crude drug,the phloroglucinol phospholipids complex in water or chloroform showed increase in both dissolubility and oil/water partition coefficient.UV and IR confirmed that no new complex had been formed from phloroglucinol and phospholipids.CONCLUSION: The optimized technology greatly enhanced the dissolubility and lipotropy of the phloroglucinol phospholipids complex.