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硫酸巴龙霉素治疗人体绦虫病的疗效及其对绦虫的体外药理作用

[Efficacy of paromomycin sulfate against human cestodiasis and its pharmacological action on tapeworm in vitro].

作者信息

Niimura M, Yokogawa M, Hata H, Kobayashi M, Tokita K, Hasunuma Y

出版信息

Jpn J Antibiot. 1983 Mar;36(3):594-601.

PMID:6876366
Abstract

Recently, it has been reported that paromomycin sulfate has marked anthelmintic efficacy against tapeworm infections in man. In the present study this drug was used in the treatment of 14 cases of diphyllobothriasis latum and 1 case of taeniasis saginata. Also, the actions of paromomycin sulfate on Diphyllobothrium ditremum and D. erinacei were examined pharmacologically using Magnus apparatus and biochemical methods. The results obtained were as follows. For the treatment, a total of 50 mg/kg of paromomycin sulfate divided into 2 doses was given orally at intervals of 30 minutes. Two hours after medication, 20 g of magnesium sulfate dissolved in 200--300 ml of water was given as purgative. One or 2 worms were found in the stools of 11 cases with D. latum and 1 case with T. saginata within 24 hours after medication, but scolex was found in only 2 of them. All cases were negative for the eggs or segments in stool examinations at 1 and 3 months after treatment. Except 1 case complained mild and transient vomiting no side effects were noticed. All cases showed no abnormality in blood examination, liver function test and urinalysis. Both of the proglottids of D. ditremum and D. erinacei showed muscle relaxation in Tyrode solution containing 10(-4) g/ml of paromomycin sulfate. In D. ditremum the recovery of muscle tonus was observed within 10--15 minutes after affection of this drug, while the persistence of muscle relaxation was seen in D. erinacei. The activity of phosphoglucose isomerase was slightly inhibited by 10(-3) M paromomycin sulfate while those of hexokinase, phosphofructokinase and glucose-6-phosphate dehydrogenase were not inhibited. In phosphoenolpyruvate-succinate pathway, the activity of fumarate reductase was slightly inhibited 10(-3) M paromomycin sulfate while those of phosphoenolpyruvate carboxykinase and malate dehydrogenase were not inhibited.

摘要

最近,有报道称硫酸巴龙霉素对人体绦虫感染具有显著的驱虫效果。在本研究中,该药物用于治疗14例阔节裂头绦虫病和1例牛肉绦虫病。此外,使用马格努斯装置和生化方法对硫酸巴龙霉素对歧腔吸虫和猬迭宫绦虫的作用进行了药理学研究。获得的结果如下。治疗时,口服总共50mg/kg硫酸巴龙霉素,分为2剂,间隔30分钟给药。用药2小时后,给予20g溶解于200 - 300ml水中的硫酸镁作为泻药。用药后24小时内,11例阔节裂头绦虫病患者和1例牛肉绦虫病患者的粪便中发现1条或2条虫,但仅其中2例发现头节。治疗后1个月和3个月的粪便检查中,所有病例的虫卵或节片均为阴性。除1例患者抱怨有轻微短暂的呕吐外,未观察到副作用。所有病例的血液检查、肝功能检查和尿液分析均未显示异常。在含有10(-4)g/ml硫酸巴龙霉素的台氏液中,歧腔吸虫和猬迭宫绦虫的孕节均表现出肌肉松弛。在歧腔吸虫中,该药物作用后10 - 15分钟观察到肌肉张力恢复,而猬迭宫绦虫则持续肌肉松弛。10(-3)M硫酸巴龙霉素轻微抑制磷酸葡萄糖异构酶的活性,而己糖激酶、磷酸果糖激酶和葡萄糖-6-磷酸脱氢酶的活性未受抑制。在磷酸烯醇丙酮酸-琥珀酸途径中,10(-3)M硫酸巴龙霉素轻微抑制延胡索酸还原酶的活性,而磷酸烯醇丙酮酸羧激酶和苹果酸脱氢酶的活性未受抑制。

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