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Besides, effect of sweet stimulability and bitter stimulability on vagus nerve maybe is identical after CTA established, zhe two stimulate may have no difference in coordinating taste information and gut information.3 FLI neurons of SON and DMV in the CTA rats had much more expressions than that in the control rats., but after vagotomy, expressions are lowwer.

建立CTA后,苦味刺激与甜味刺激在味觉信息与内脏信息的整合作用效果类似,两者对迷走神经的调节趋于一致。3 CTA大鼠在SON和DMV内FLI神经元的表达高于正常组大鼠,而切断迷走神经后,表达却低于正常组大鼠

Methods: Myocardial ischemia-reperfusion injury model was established through accluding the left anterior descending branch of coronary artery for 60 min and removing the ligation tater to reperfuse for 30 min.

结扎大鼠冠状动脉左前降支60min,再灌注90min复制大鼠心肌缺血再灌注损伤模型,观察心安灵对大鼠心肌缺血再灌注损伤的保护作用。

Models were established by rats of stress ulcer,observe the ulcerous index,the contents of GAS and TSH were measured in serum.

用束缚水浸应激法复制大鼠应激性胃溃疡模型,观察模型大鼠胃黏膜病损情况和溃疡指数的变化,检测模型大鼠血清胃泌素和促甲状腺激素含量的变化。

Methods Twenty-two adolescent SD female rats were selected. All rats were killed by dislocation of cervical vertebra, the eyeballs were in paraffin imbedding and made to a series of sections, using immunohistochemical method; ERα and ERβ distribution were investigated in uvea tissue of rats; and quantitied by Tanaka scores analytical method. The uteri of rats was used as positive control and PBS as negative control.

选择青春期SD雌性大鼠22只,采用颈椎脱臼处死大鼠,取眼球作常规石蜡包埋,连续切片, SP免疫组织化学方法显示ERα、ERβ在葡萄膜组织的表达;采用Tanaka记分法对ERα、ERβ进行定量分析,并设正常大鼠子宫作阳性对照;PBS代替一抗作阴性对照。

Methods OECs were cultured in the olfactory bulb of newborn wistar rat. OECs suspension was infused into the lateral cerebral ventriculus of AE rats, intraperitoneal methyl-vitamine B12 associated with above OECs suspension in combined transpiantion group, and the saline with the same quantity was infused in pseudo-operation group. Afterwards, sport-function grade, histo pathological change were observed.

用新生wistar大鼠嗅球培养OEC,移植组将OECs悬液注入实验性变态反应性脑脊髓炎大鼠的侧脑室;联合移植组在侧脑室注入OECs的基础上,腹腔注入甲基维生素B12;假手术组按以上方法注入等量生理盐水;观察两组大鼠运动功能评分、组织病理学变化。

The rest SD rats were injected abdominally to induce chronic-kindling models by PTZ 35mg/kg for 28 days,then 30 having build-up model rats were divided randomly completely into three groups: model, YXL, VPA.

将SD大鼠随机取10只作为正常组,其余大鼠以PTZ 35mg/kg腹腔注射28天作慢性点燃造模,再取造模成功大鼠随机分为3组:模型组、丙戊酸钠组和愈痫灵颗粒剂组。

Gelatin zymography was used to detect the activation and secretion of MMP-2 and MMP-9 in gastroenemius、soleus、plantaris during early、intermediate and final stage of experimental group. Picric- sirius red polarized light was used to detect the accrementition and reconstitution of mesenchymal fibers in the muscle specimens from the operated group and normal controls.

3采用RT-PCR和Western blot及免疫组化的方法分别检测不同时期的大鼠骨骼肌中核因子κB、MMP-2、MMP-9的表达;采用明胶酶谱的方法检测实验组大鼠早、中、晚期腓肠肌、比目鱼肌、跖肌MMP-2、MMP-9活化、分泌情况;天狼猩红-偏振光法检测大鼠骨骼肌间质纤维增生及成分改变。

Adult male Wistar rats were randomLy allocated to 3 groups:control group, stone-forming group, Alisma Orientalis group. Reverse transcription polymerase chain reaction technique was used to examine bikunin mRNA expression levels in rat renal tissue.

将Wistar大鼠随机分成对照组、结石模型组、泽泻组,采用半定量逆转录聚合酶链反应检测大鼠肾组织bikunin mRNA的表达水平、镜下观察肾组织草酸钙晶体分布,同时检测大鼠血生化、肾钙含量、24h尿钙和尿草酸的分泌量。

It showed similar pattern with that in lung tissues. Conclusion: There were TGF-β1 mRNA expression in both normal rats and pulmonary fibrosis rats. AMs seemed to be the main source of TGF-β1 mRNA in lung tissues, especially at stage of alveolitis.

TGF-β1 mRNA在正常大鼠及肺纤维化大鼠中均有表达,后者表达明显高于前者;肺纤维化大鼠肺内TGF-β1 mRNA 可能主要来源于AM。

Methods: 60 SD rats were divided into 4 groups randomly, the nomal group, the model group, QZHJ group, and the hydrocortisone group. Rats were sacrificed in bdtch on the 3rd, 7th and 21st day after treatment, then the concentration of interleukin-8(IL-8) in bronchoalveolar lavage fluid and the content of transforming growth factor-β1 (TGF-β1) of lung tissue were deected, while the severity of alveolitis and fibrosis were measured.

将60只健康SD大鼠随机分为正常组、模型组、芪术合剂组和强的松组,经气管滴入博莱霉素复制肺纤维化大鼠模型,并分组予以治疗,于治疗后第3、7、21日分批处死大鼠,每组每次6只;用免疫组化法观察肺组织转化生长因子-β1的表达,并测定支气管肺泡灌洗液中中性粒细胞和白介素-8的水平。

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