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Study on Promoting Cabbage Growth with Diethy Amioethyl Hexanoate 5% AS
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作者 Xu Weisong Huang Yilin +2 位作者 Zhou Zhenbiao Wen Shuheng Zhuang Zhimin 《Plant Diseases and Pests》 CAS 2014年第6期34-35,共2页
Field efficacy trials showed that Diethy Amioethyl Hexanoate 5% AS could promote growth and increase yield of cabbage. The cabbage yield increase rate was up to 40.37% by using reagent dilution 2 000 -2 500 times twic... Field efficacy trials showed that Diethy Amioethyl Hexanoate 5% AS could promote growth and increase yield of cabbage. The cabbage yield increase rate was up to 40.37% by using reagent dilution 2 000 -2 500 times twice, so Diethy Diethy Amioethyl Hexanoate 5% AS is an ideal agent for regulating cabbage growth and increasing yield. 展开更多
关键词 DiethyAmioethyl Hexanoate CABBAGE Plant growth regulation efficacy trial
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Comparison of Immune Effect of Four Commercial Marek's Disease Vaccines in Wenchang Chicken
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作者 Cao Zongxi Zhang Yan +2 位作者 Tan Shuyi Ye Baoguo Lin Zhemin 《Animal Husbandry and Feed Science》 CAS 2015年第1期18-20,共3页
Marek's disease(MD) is a lymphoproliferative disease of domestic chickens caused by a highly infectious,oncogenic alpha-herpesvirus known as Marek's disease virus(MDV).The aim of this study was to compare the ef... Marek's disease(MD) is a lymphoproliferative disease of domestic chickens caused by a highly infectious,oncogenic alpha-herpesvirus known as Marek's disease virus(MDV).The aim of this study was to compare the efficacy of four commercial MDV vaccines in Wenchang chicken.The 1-day old Wenchang chickens tested were injected with one of four different vaccines or not unvaccinated as control;five days later,they were then challenged by virulent MDV strain MD5.The results showed that,in comparison with HVT vaccines,the CVI988 vaccine gave the immunized chickens more potent immunities against challenges of MDV strain MD5. 展开更多
关键词 Marek's disease virus Wenchang chicken Immunity efficacy Comparative trial
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Effectiveness and Safety of Acupoint Application of Guan Xin Su He Pill (冠心苏合丸) for Patients with Chronic Stable Angina Pectoris: A Multi-Center, Randomized Controlled Trial 被引量:2
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作者 LI De-hua XIE Jin +7 位作者 REN Yu-lan ZHENG Hui LYU Jun-ling LENG Jun-yan ZHANG Ling-lin ZHANG Jie FAN Hai-long LIANG Fan-rong 《Chinese Journal of Integrative Medicine》 SCIE CAS CSCD 2021年第11期838-845,共8页
Objective To assess the clinical effectiveness of acupoint application(AP)of Guan Xin Su He Pill(冠心苏合丸,GXSHP)for patients with chronic stable angina pectoris(CSAP).Methods This study was carried out in 3 local ho... Objective To assess the clinical effectiveness of acupoint application(AP)of Guan Xin Su He Pill(冠心苏合丸,GXSHP)for patients with chronic stable angina pectoris(CSAP).Methods This study was carried out in 3 local hospitals in Chengdu,China.After baseline evaluation,eligible patients were randomly assigned to the placebo application for acupoints(PAA)group or the herbal application for acupoints(HAA)group.Patients in the HAA group underwent AP with herbal powder,which was mainly GXSHP,and patients in the PAA group underwent AP with sham drugs.For each treatment session,unilateral acupoints including Neiguan(PC 6),Danzhong(RN 17),Xinshu(BL 15)and Jueyinshu(BL 14),were stimulated for both groups.AP was performed 3 times a week with a 2-day interval for 4 weeks.The primary outcome was the frequency of angina pectoris attacks per week,while the secondary outcomes included angina pain intensity measured by the Visual Analogue Scale(VAS),dose of rescue oral drugs(nitroglycerin),scores on the Seattle Angina Questionnaire(SAQ),Self-Rating Anxiety Scale scores(SAS)and Self-Rating Depression Scale scores(SDS).Clinical outcomes were measured at week 0,4 and 8.The safety of AP of GXSHP treatment for CSAP were assessed.Results A total of 121 patients were enrolled.Baseline characteristics were comparable across the 2 groups.After treatment,the angina attack numbers in the HAA group were significantly reduced from 11.00 to 4.81(P<0.05).While,for PAA group,the angina frequency was not significantly improved(baseline 10.55;post-treatment 11.05).The HAA group had significantly fewer angina attacks than the PAA group(P<0.05).Pain intensity measured by VAS in HAA group was significantly reduced from 4.06 to 3.02(P<0.05).While,for PAA group,the VAS was significantly increased(baseline 3.62;post-treatment 3.96;P<0.05).Clinical outcomes showed better improvement after treatment in the HAA group than in the PAA group in terms of oral administration of rescue drugs,SAS,SDS and SAQ scores(P<0.05).The adverse events were also reported.Conclusion AP of GXSHP is a safe and effective treatment for CSAP patients(Registration No.NCT02029118). 展开更多
关键词 acupoint application chronic stable angina pectoris clinical efficacy randomized controlled trial
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