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In this study nikethamide was administered to aged patients with respiratory failure and its effect on arterial blood gas was evaluated.

本研究使用尼可刹米治疗老年人呼衰,评估呼吸兴奋剂对呼衰患者动脉血气的影响。

Methods 100 patients chronic cor pulmonale with heart failure were divided randomly into the intervention group (50 cases) and the control group (50 cases), for the basic routine treatment,the intervention group was administered 100mg amrinone and nikethamide 1.5g each day for 7 days, while the control group was treated with 10mg phentolamine for 7 days, the clinical therapeutic effect and side effects were compared.

将100例慢性肺心病合并心衰的患者随机分为观察组和对照组,各50例,观察组在基础治疗的同时每天加用氨力农100mg和尼可刹米1.5g,对照组在基础治疗的同时每天加用酚妥拉明10mg。目的探讨氨力农联合尼可刹米治疗慢性肺心病合并心衰的临床疗效。

Methods 100 patients chronic cor pulmonale with heart failure were divided randomly into the intervention group (50 cases) and the control group (50 cases), for the basic routine treatment,the intervention group was administered 100mg amrinone and nikethamide 1.5g each day for 7 days, while the control group was treated with 10mg phentolamine for 7 days, the clinical therapeutic effect and side effects were compared.

目的 探讨氨力农联合尼可刹米治疗慢性肺心病合并心衰的临床疗效。方法将100例慢性肺心病合并心衰的患者随机分为观察组和对照组,各50例,观察组在基础治疗的同时每天加用氨力农100mg和尼可刹米1.5g,对照组在基础治疗的同时每天加用酚妥拉明10mg。两组疗程均为7d。

METHODS: A dose-response relationship of 8-OH-DPAT, spontaneousphrenic nerve activity and a nociceptive C-fiber reflexwere established simultaneously in an in situ perfused, nonanesthetized,rat brainstem-spinal cord preparation. Fentanyl was administered in situ to investigate the interaction with 8-OH-DPAT on phrenicnerve activity and nociceptive CFR.

在准备好的原位灌注,未麻醉的大鼠脑干-脊髓上同时建立8-OH-DPAT 的量效关系,自发膈神经活动和疼痛 C -纤维反射原位给予芬太尼观察其与8-OH-DPAT 对膈神经活动和疼痛 C -纤维反射的相互影响。

Methods: Thirty ASA I nulliparous women were administered 10 ml bolus of epidural ropivacaine in the first stage of labor. A concentration of 0.5% ropivacaine was applied to the first woman, and the dosage to the next one was up-regulated or down-regulated one level in accordance to the previous woman's response to the concentration.

选择30例单胎足月初产妇,在进入第一产程活跃期时行硬膜外给予罗哌卡因10ml,第1例罗哌卡因的浓度为0.5%,下一产妇的药物浓度根据前一产妇有无运动阻滞情况来上调或下调1个浓度级。

These changes were prevented by genistein (a protein tyrosine kinase inhibitor) and antioxidant N-acetyl-L-cysteine, but promoted by sodium orthovanadate (a protein phosphatase inhibitor), which were administered to the SD rats 20 min before ischemia.

进一步的研究表明,缺血前20 min腹腔注射给药,然后缺血30 min,发现蛋白酪氨酸激酶抑制剂染料木黄酮和抗氧化剂N-乙酰半胱氨酸能显著地抑制核内STAT3的磷酸化水平及DNA结合活性的增加(磷酸化水平从2.3和2.5倍分别降为1.2和1.4倍, DNA结合活性则从2.8和3.7倍分别降为1.1和1.5倍),而蛋白酪氨酸磷酸酶抑制剂矾酸钠则能明显地促进他们的增高(磷酸化水平从2.0倍增到3.4倍, DNA结合活性从3.1倍增为5.1倍)。

MethodsFrom March 2005 to December 2007, 120 patients with ovarial cancer of our department who would receive cisdiaminodichloroplatinum treatment were classified randomly into two groups. Group A (n=60) was administered with allactin by intravenous infusion at 10 mg/kg, and Group B (n=60) with allactin for intravenous infusion at 40 mg/kg.

方法将我院2005年3月—2007年12月间,120例卵巢癌顺铂化疗患者,随机分成两组:A组(60例),给予大蒜素10 mg/kg 静脉输注;B组(60例),给予大蒜素40 mg/kg 静脉输注。

One of these compounds, 2-diethyl- aminoethyl-5--(4-methoxybenzylidene) cyclo- pentanone hydrochloride (T81) possessed sig- nificant antiinflammatory and analgesic ac- tivity when administered orally.

Ⅲ类化合物完全无抗癌活性,对其中一个化合物2-二乙胺乙基-5--(4-甲氧基苯亚甲基)环戊酮盐酸盐(T81)试验结果表明,它经口给药时具有显著的抗炎、镇痛活性。

In a rat model,RTX was administered percutaneously to the sciatic and saphenousnerves before the plantar incision.

在一个大鼠模型中,在切割足背前将 RTX 经皮注射至坐骨神经和隐神经。

The survival,growth and development as well as reproduction of Boettcherisca peregrina(Diptera: Sarcophagidae) in the parental generation were significantly influenced as newly oviposited larvae were exposed to various concentration of Cd~(2+) administered in the artificial diet until pupation.

棕尾别麻蝇Boettcherisca peregrina初产幼虫喂饲含不同浓度Cd2+的饲料直至化蛹时,其亲代的生存、生长发育与繁殖受到了显著的影响。

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