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The results showed that FW, DW, root activity, POD activity and CAT activity of Vallisneria natans L and Elodea nuttallii were improved when ammonia concentrations were less than 50mg?kg^(-1) and 500mg?kg^(-1), respectively.

kg^(-1)和＜500mg？kg^(-1)时可以分别促进苦草和伊乐藻鲜物质量、干物质量和根系活力的增加，大于此范围则会抑制苦草为Vallisneria natans L和伊乐藻Elodea nuttallii的生长。

The endermic LD50 to rat and mouse were 926 mg/Kg and 1210 mg/Kg respectively. The results of subscute toxicity test in rats showed that the content of blood urea nitrogen in exposure groups was higher than that in control group, the histopathological changes of testis observed in exposure groups were obvious. Mutagenic tests including bacillus subtilis DNA rec-assay, micronucleus ...

其大、小鼠经皮LD_(50)分别为926mg/kg和1210mg/kg；大鼠90天经皮染毒，试验组BUN含量高于对照组，光镜下，试验组睾丸的组织学结构有明显改变；枯草杆菌DNA重组试验、小鼠骨髓多染红细胞微核试验和小鼠睾丸染色体畸变分析试验均获得阳性结果。

Unsaturated fatty acid EPA and DHA content respectively was 170 mg/kg and 150 mg/kg.

不饱和脂肪酸EPA、DHA的含量分别为170 mg/kg和150 mg/kg。

METHODS: Sixty Sprague-Dawley male rats were randomly divided into four groups(n = 15), four methods were designed on rats models of sciatic nerve compression. There were simple decompression as group A, internal neurolysis after decompression as group B, lemithason(0.5 mg/kg) injected in the epineurium after decompression as group C, and lemithason(0.5 mg/kg) injected around the epineurium after decompression and internal neurolysis as group D.

在大鼠坐骨神经卡压模型基础上，将60只SD成年雄性大鼠随机等分为四组。A组：仅去除卡压；B组：去除卡压后切开神经外膜；C组：去除卡压后神经外膜下周围注射利美达松(0.5mg/kg)；D组：去除卡压后切开神经外膜，然后在神经周围注射利美达松(0.5mg/kg)。

The results showed that under different doses the hemolytic index of the gelatin microspheres was lower than 5%, so it did not have significant toxicity; primary skin irritation test showed there were no erythema, eschar and edema of 10% florfenicol gelatin microspheres injection; the LD50 of the microspheres was 2.226 7 g/kg and its 95% credibility limit was 1.950 2~2.635 6 g/kg.

实验结果显示，不同剂量的肺靶向氟苯尼考明胶微球注射剂的溶血指数均小于5%，无明显毒性；10%氟苯尼考明胶微球注射剂对受试动物皮肤无明显刺激作用；肺靶向氟苯尼考明胶微球对小鼠的LD50为2.226 7 g/kg，LD50 95%的可信限为1.950 2 ~2.635 6 g/kg。

Lung concentration-time data after oral administration of 50mg/kg body weight we re also best d escribed by a two-compartment open model. The parameter of male chicken were as following: t1/2 a 为 2.28S±0.657h , t1/2Ka1.090±0.193h, t1/2B 为 37.606±4.474h, AUC530.797±48.050*h, CL 0.095±0.008mg/kg/h/, Tmax 5.256±0.442h, Cmax 9.044±0.016ug/g.

公鸡肺脏主要的药代动力学参数：t1／2 α为2.285±0.657h、t_(1/2Ka)为1.090±0.193h、t_(1/2β)为37.606±4.474h；AUC为530.797±48.050~*h、CL为0.095±0.008mg／kg／h／、T_为5.256±0.442h、C_为9.044±0.016μg／g；母鸡肺脏主要的药代动力学参数：t_(1/2α)为1.556±0.825h、t_(1/2Ka)为0.732±0.101h、t_(1/2β)为23.304±2.320h；AUC为395.073±12.095~*h、CL为0.127±0.004mg／kg／h／、T_为3.584±0.440h、C_为10.691±0.542μg／g。

Another 72 mice were randomly divided into control group,egg yolk model group,Expellant and Cleanning Fat Capsule 0.4 g·kg-1 group,CFB 10.0,5.0,2.5 mL·kg-1 groups (n=12).Mice in each group were exhibited once a day for 10 d.16 h before the last administration,except control group,the mice in other groups were injected with 75% yolk physiological salt solution 0.5mL through the abdominal cavity,and began to starve,1 h after the last administration, the contents of serum TCHO and TG were determined,and liver MDA level was measured.

另取小鼠72只随机分为空白对照组、蛋黄模型组、排毒清脂胶囊0.4 g·kg-1组及CFB 10.0、5.0和2.5 mL·kg-13个剂量组( n=12)，每天给药1次，连续 10 d，末次给药前16 h 除空白对照组外，所有各组小鼠每只均腹腔注射75％蛋黄生理盐水溶液0.5 mL，并且开始饥饿；末次给药后1 h测定血清TCHO及TG含量，取肝脏测MDA含量。

CFB 7.0 mL·kg-1was superior to Kanglishu Capsule in reducin g TCHO,TG and MDA,CFB 10.0 mL·kg-1 was superior to Expellant and Cleanning Fat Capsule.

在降低TCHO和TG含量及小鼠肝脏MDA水平方面CFB 7.0 mL·kg-1组优于康立舒胶囊组，CFB 10.0 mL·kg-1组优于排毒清脂胶囊组。

Methods Animals were randomly and equally divided into five groups: saline control group, positive drug control group, low-dose, medium-dose and high-dose crocetin group. Animals were anesthetized with urethane (1.2 g/kg), then followed by the perfusion of aconitine (10 μg/mL) through caudal vein in rats, or of ouabain (9 μg/mL) through external jugular vain in guinea pigs in a constant velocity of 0.1 mL/min, and the emergence time of ventricular fibrillation, ventricular extrasystole, ventricular tachycanlia and cardiac arrest were then detected and recorded. The recorded time was then translated to the cumulated amount of aconitine and ouabain. Experimental arrhythmia was induced by rapid injection of 4% CaCl2 (140 mg/kg), and the emergence time, persistence time, incidence and death of arrhythmia after the administration were observed.

将实验动物随机分为生理盐水组，阳性药物对照组，藏红花酸高、中、低剂量组，SD大鼠采用1.2 g/kg乌拉坦麻醉后，从尾静脉匀速(0.1 ml/min)灌注10μg/ml乌头碱溶液，豚鼠麻醉后从颈静脉匀速(0.1 ml/min)灌注9μg/ml哇巴因溶液，观察出现室性期前收缩、室性心动过速、室颤和心脏停搏的时间，然后换算成乌头碱和哇巴因的累积量；快速推注4%氯化钙(140 mg/kg)诱导大鼠心律失常，观察给药后心律失常出现时间、持续时间、心律失常发生数及死亡数。

Gelsemium total alkaloids improved some blood and immune function of mice when it less than 0.30mg/kg body weight, but more than 1.5mg/kg body weight, the gelsemium total alkaloids can reduced some blood and immune function of mice; below the dose of 3%, GEB"s power can improve some blood and immune function of broilers, but GEB"s power can reduce some blood and immune function of broilers above the dose of 6%.

结论是：钩吻对小鼠和肉鸡的血液学及免疫功能的影响均存在着剂量差别，钩吻总碱稀释液在0.30mg／kg剂量以下，能够提高小鼠的某些血液指标与免疫功能(p＜0.05)，而在1.5mg／kg以上，则降低小鼠的某些血液指标与免疫功能(p＜0.05)；3％以下的钩吻干粉能够提高肉鸡的某些血液指标与免疫功能，而6％以上的钩吻干粉则降低某些血液指标与免疫功能。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。