板黄口服液治疗牛呼吸道疾病的疗效和安全性。

Bing Li, Xu-Zheng Zhou, Jian-Rong Niu, Xiao-Juan Wei, Jian-Yong Li, Ya-Jun Yang, Xi-Wang Liu, Fu-Sheng Cheng, Ji-Yu Zhang
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引用次数: 1

摘要

背景:班黄口服液是由中国农业科学院兰州畜牧与药物研究所研制的兽药复方制剂。本研究的目的是确定中药班黄口服液制剂治疗牛呼吸道疾病是否安全有效。材料与方法:对Wistar大鼠和昆明小鼠进行急性口服毒性实验。双倍稀释法对牛支原体的最低体外抑制浓度为500 mg/mL,具有良好的敏感性。结合实验室病原菌检测、临床症状分析和病理解剖分析,对147头西门塔尔牛由牛分枝杆菌、牛呼吸道合胞病毒、牛副流感病毒3型和溶血性曼海姆病混合感染引起的牛呼吸道疾病进行了诊断。将牛随机分为药物治疗组1(替尔米科星注射液)、药物治疗组2(双黄连口服液联合替尔米科星注射液)、药物治疗组3(班黄口服液联合替尔米科星注射液)。7 d内观察治疗效果。结果:无毒性,最大耐受剂量大于20 g/kg BW。药物治疗组87头牛,治愈率为90.80%,有效率为94.25%。药物治疗组的治愈率较药物对照组1提高14.13%,较药物对照组2提高7.47%(均P < 0.05)。结论:班黄口服液是一种安全有效的治疗牛呼吸道疾病的药物,尤其对牛支原体、细菌和病毒混合感染有较好的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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EFFICACY AND SAFETY OF BAN HUANG ORAL LIQUID FOR TREATING BOVINE RESPIRATORY DISEASES.

Background: Ban Huang oral liquid was developed as a veterinary compound preparation by the Lanzhou Institute of Husbandry and Pharmaceutical Sciences of the Chinese Academy of Agricultural Sciences (CAAS). The purpose of this study was to determine whether the oral liquid preparation of traditional Chinese medicine, Ban Huang, is safe and effective for treating respiratory diseases in cattle.

Materials and methods: Acute oral toxicity experiments were conducted in Wistar rats and Kunming mice via oral administration. The minimum inhibitory concentration of the drug against Mycoplasma bovis in vitro with the double dilution method was 500 mg/mL, indicating good sensitivity. The results of laboratory pathogen testing, analysis of clinical symptoms, and analysis of pathological anatomy were combined to diagnose bovine respiratory diseases in 147 Simmental cattle caused by mixed infections of M. bovis, bovine respiratory syncytial virus, bovine parainfluenza virus type 3, and Mannheimia haemolytica. These cattle were randomly divided into three groups: drug treatment group 1 (treated via Tilmicosin injection), drug treatment group 2 (treated with Shuang Huang Lian oral liquid combined with Tilmicosin injection), and drug treatment group 3 (treated with Ban Huang oral liquid combined with Tilmicosin injection). Treatment effects were observed within 7 days.

Results: The results showed no toxicity and a maximum tolerated dose greater than 20 g/kg BW. For the 87 cattle in drug-treatment group, the cure rate was 90.80%, whereas the response rate was 94.25%. The cure rate of drug treatment group was increased by 14.13% in comparison with that of drug control group 1 and by 7.47% in comparison with that of drug control group 2 (both P < 0.05).

Conclusion: This study demonstrates that Ban Huang oral liquid is a safe and effective treatment for bovine respiratory diseases, especially for mixed infection caused by M. bovis, bacteria, and viruses.

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