人子宫颈管中的东莨菪碱-N-丁基溴化物和双氯芬酸钠的体外效应。

IF 2.7 4区 医学 Q2 PHARMACOLOGY & PHARMACY Basic & Clinical Pharmacology & Toxicology Pub Date : 2024-05-27 DOI:10.1111/bcpt.14038
Mustafa Sengul, Baris Karadas, Selin Acar-Sahan, Ozan Ozturk, Huseyin Yılmaz, Fatma Simsek, Tijen Kaya-Temiz
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引用次数: 0

摘要

引言目的:研究双氯芬酸对输卵管平滑肌的体外影响,以替代子宫输卵管造影术(HSG)前用药的溴化东莨菪碱:材料和方法:从七名双侧输卵管结扎术后的健康女性身上取回输卵管,使用组织浴和免疫组化方法进行体外收缩力和组织学研究:结果:双氯芬酸钠和东莨菪碱-N-丁基溴化物对基础平均张力无明显改变,但可降低氯化钾(KCl)诱导的收缩。双氯芬酸钠和东莨菪碱-N-丁基溴化物的松弛作用在统计学上没有明显差异。免疫组化研究表明,输卵管中存在环氧化酶(COX)-2:结论:双氯芬酸钠对输卵管的体外松弛作用与溴化透明质酸丁酯相似。双氯芬酸钠有可能替代溴化透明质酸丁酯用于 HSG 的预处理。
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In vitro effect of hyoscine-N-butyl bromide and diclofenac sodium in human tuba uterina

Introduction

To investigate the in vitro effect of diclofenac on tubal smooth muscle as an alternative to hyoscine-N-butyl bromide, which is used for premedication before hysterosalpingography (HSG).

Material and Methods

Fallopian tubes were retrieved from seven healthy women after bilateral tubal ligation and in vitro contractility and histological studies were conducted using tissue bath and immunohistochemistry.

Results

Diclofenac sodium and hyoscine-N-butyl bromide did not significantly change the basal mean tension; however, they decreased the contractions induced by potassium chloride (KCl). The relaxant effect of diclofenac sodium and hyoscine-N-butyl bromide was not statistically significantly different. The presence of cyclooxygenase (COX)-2 enzyme in the fallopian tube was demonstrated by immunohistochemical studies.

Conclusions

The in vitro relaxant effect of diclofenac sodium on the fallopian tube is similar to hyoscine-N-butyl bromide. Diclofenac may have the potential to be used as an alternative to hyoscine-N-butyl bromide in premedication in HSG.

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来源期刊
CiteScore
5.60
自引率
6.50%
发文量
126
审稿时长
1 months
期刊介绍: Basic & Clinical Pharmacology and Toxicology is an independent journal, publishing original scientific research in all fields of toxicology, basic and clinical pharmacology. This includes experimental animal pharmacology and toxicology and molecular (-genetic), biochemical and cellular pharmacology and toxicology. It also includes all aspects of clinical pharmacology: pharmacokinetics, pharmacodynamics, therapeutic drug monitoring, drug/drug interactions, pharmacogenetics/-genomics, pharmacoepidemiology, pharmacovigilance, pharmacoeconomics, randomized controlled clinical trials and rational pharmacotherapy. For all compounds used in the studies, the chemical constitution and composition should be known, also for natural compounds.
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