不同杀菌剂对草坪草病原菌毒力的作用测定

采用生长速率法测定了不同杀菌剂对3种主要引起坪草病害的褐斑病菌、腐霉枯萎菌、夏季斑枯病菌的毒力。结果表明,烯唑醇、甲基硫菌灵、代森锰锌、咪鲜胺对立枯丝核菌的EC50值分别为0.078 3,5.968 4,7.181 2和11.386 8 mg/L,以烯唑醇对立枯丝核菌的毒力最高。烯唑醇、咪鲜胺、代森锰锌、甲基硫菌灵对夏季斑枯病菌的EC50值分别为0.016 2,0.554 4,6.035 3,1 218.497 8 mg/L,以烯唑醇抑菌效果显著优于其它3种杀菌剂。采用菌丝干重测定法测定了阿米西达、霜脲氰、霜克、咪鲜胺、代森锰锌对腐霉枯萎病菌的毒力,其EC50值依次为0.053 3,7.837 4,13.310 7,19.715 1,29.771 5 mg/L,以阿米西达的抑菌效果最好。     

黄花补血草醇提物对小鼠急性毒性试验

采用改良寇氏法测定黄花补血草醇提物对小鼠腹腔注射的急性毒性试验,评价其安全性。实验组小鼠灌服不同浓度的黄花补血草醇提物,观察给药后小鼠的临床表现与死亡情况。结果黄花补血草醇提物最大剂量一次性给8 g/kg,1周后未见明显中毒症状,并测得最大耐受量（MTD）试验值为15 g/kg（〉10 g/kg）。结果提示,黄花补血草醇提物的毒性较低,临床用药安全可靠,为黄花补血草的临床前和临床研究提供安全的实验数据,并进一步了解了黄花补血草的生物学活性,为将其更好地应用于制药业和临床治疗提供科学依据。     

红蓼提取物对13种农业害虫触杀活性的研究

关于红蓼提取物对农业害虫的触杀活性,国内外研究甚少。研究红蓼提取物对害虫的触杀活性,可为利用该植物研制新型植物源杀虫剂提供理论依据。本研究采用浸渍法测定了红蓼提取物对害虫的触杀活性,结果表明,红蓼种子乙酸乙酯萃取物对粘虫、菜粉蝶、棉铃虫、甘蓝夜蛾、甜菜夜蛾和小地老虎4~5龄幼虫具有很强的触杀活性,在16.80 g/L浓度下的校正死亡率在87.50%~100%;对小菜蛾3龄幼虫也具有很强的触杀活性,在21.00 g/L浓度下的校正死亡率为92.85%;秋季茎秆乙酸乙酯萃取物对菜粉蝶4龄幼虫和粘虫5龄幼虫具有很强和较强的触杀活性,在33.60 g/L浓度下的校正死亡率分别为100%和59.20%。盛花期茎秆石油醚粗提物对棉蚜具有较强的触杀活性,在0.27 g/L浓度下的校正死亡率为51.65%。盛花期花石油醚和甲醇粗提物对朱砂叶螨具有很强的触杀活性,在0.13和1.15 g/L浓度下的校正死亡率均高达100%。     

茶粕渣急性毒性评价

采用急性经口毒性试验方法对茶粕渣的毒性进行了评价,为茶粕渣能否作为一种新型饲料原料被养殖所利用奠定了基础。试验证明,茶粕渣在5500mg/kg体重的剂量下具有极低毒性反应,并且无死亡。根据剂量进行毒性分级,属于实际无毒的毒性等级,初步认为茶粕渣有用做饲料原料的潜力。     

玉米赤霉烯酮的代谢、毒性及其预防措施

玉米赤霉烯酮(ZEA)是由镰孢属真菌产生的类雌激素毒素.由于气候条件不同,食品和饲料中ZEA浓度差异很大(从几个mg/kg至几千个mg/kg).本文综述了ZEA的吸收、代谢和生物转化机制,ZEA的生殖毒性、细胞毒性、免疫毒性和遗传毒性,并且从预防土壤中镰孢菌及其相关霉菌的污染、收获和收获后真菌毒素的控制、污染颗粒的物理...     

青霉菌毒素的某些毒性机理

用标准和从饲料中提取的青霉素（桔青霉素毒素和青霉酸）对家兔，蟾蜍进行了某些毒性机理的研究，结果表明，青霉菌毒素具有促进胃肠蠕动，增绳子宫收缩和减慢心率的毒性作用。     

铜中毒对雏鸭某些血液指标的影响

选用1日龄天府肉鸭210只,随机分为3组,分别喂以对照日粮(Cu12.16mg/kg)、铜中毒日粮(Cu850mg/kg)和铜中毒日粮(Cu1050mg/kg)。试验期7周。以血液病理学方法观察了铜中毒对雏鸭某些血液学指标的影响。结果显示铜中毒组、组雏鸭分别于2周龄和3周龄开始出现临床症状,死亡18只和5只。血液病理学变化表现为,红细胞大小不等、变形变性、坏死溶解;红细胞数量和血红蛋白含量显著降低(P<0.01),血清谷丙转氨酶、谷草转氨酶活性显著升高(P<0.05或P<0.01),血清铜蓝蛋白活性下降。结果表明,铜中毒对雏鸭的生长发育和上述血液指标影响明显。     

ROUTE DEVELOPMENT,ANTIVIRAL STUDIES,FIELD EVALUATION AND TOXICITY OF AN ANTIVIRAL PLANT PROTECTANT NK0238

• Developed a two-step synthetic route to anti-plant-virus candidate NK0238. • NK0238 exhibited a broad antivirus spectrum in greenhouse. • NK0238 showed comparable antivirus activities as controls in field trials. • NK0238 was safe to birds, fish, bees and silkworms. • NK0238 has a very good prospect in commercial development. It has previously been shown that tryptophan, the biosynthesis precursor of Peganum harmala alkaloids, and its derivatives have anti-TMV activity both in vitro and in vivo. Further exploration of this led to the identification of NK0238 as a highly effective agent for the prevention and control of diseases caused by plant viruses, but the existing routes are unsuitable for its large-scale synthesis. This study optimized a route for two-step synthesis of this virucide candidate via reaction of l-tryptophan with triphosgene to produce l-tryptophan-N-carboxylic anhydride, which then reacts with n-octylamine to give NK0238 at up to 94% yield and nearly 97% HPLC purity. In addition, the route was used for the preparation of NK0238 on a>40 g scale permitting further assessment of its antivirus activity in the greenhouse and field experiments, and toxicity tests. NK0238 exhibited useful antiviral activities against a variety of viruses both in greenhouse and field experiments. The toxicity tests showed that NK0238 was not acutely toxic to birds, fish, honey bees and silkworms. The optimized route provides a solid foundation for its large-scale synthesis and subsequent efficacy and toxicity studies, its excellent activity and safety make NK0238 a promising drug candidate for further development.