Contractility Measurements of Human Uterine Smooth Muscle to Aid Drug Development

被引:21
作者
Arrowsmith, Sarah [1 ]
Keov, Peter [2 ]
Muttenthaler, Markus [3 ,4 ]
Gruber, Christian W. [2 ,5 ]
机构
[1] Univ Liverpool, Inst Translat Med, Dept Cellular & Mol Physiol, Harris Wellbeing Preterm Birth Res Ctr, Liverpool, Merseyside, England
[2] Univ Queensland, Sch Biomed Sci, Brisbane, Qld, Australia
[3] Univ Vienna, Inst Biol Chem, Fac Chem, Vienna, Austria
[4] Univ Queensland, Inst Mol Biosci, Brisbane, Qld, Australia
[5] Med Univ Vienna, Ctr Physiol & Pharmacol, Vienna, Austria
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2018年 / 131期
基金
欧洲研究理事会; 澳大利亚研究理事会; 奥地利科学基金会;
关键词
Medicine; Issue; 131; Physiology; pharmacology; myometrium; human uterus; contraction; organ bath; peptide; oxytocin; vasopressin; drug discovery; OXYTOCIN ANTAGONIST ATOSIBAN; HUMAN MYOMETRIAL CELLS; ISOLATED RAT UTERUS; PRETERM LABOR; INTRACELLULAR PH; PREGNANT-WOMEN; IN-VITRO; CALCIUM; CHANNELS; IMMORTALIZATION;
D O I
10.3791/56639
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Discovery and characterization of novel pharmaceutical compounds or biochemical probes rely on robust and physiologically relevant assay systems. We describe methods to measure ex vivo myometrium contractility. This assay can be used to investigate factors and molecules involved in the modulation of myometrial contraction and to determine their excitatory or inhibitory actions, and hence their therapeutic potential in vivo. Biopsies are obtained from women undergoing cesarean section delivery with informed consent. Fine strips of myometrium are dissected, clipped and attached to a force transducer within 1 mL organ baths superfused with physiological saline solution at 37 degrees C. Strips develop spontaneous contractions within 2-3 h under set tension and remain stable for many hours (>6 h). Strips can also be stimulated to contract such as by the endogenous hormones, oxytocin and vasopressin, which cause concentration-dependent modulation of contraction frequency, force and duration, to more closely resemble contractions in labor. Hence, the effect of known and novel drug leads can be tested on spontaneous and agonist-induced contractions. This protocol specifically details how this assay can be used to determine the potency of known and novel agents by measuring their effects on various parameters of human myometrial contraction. We use the oxytocin-and V-1a receptor antagonists, atosiban and SR49059 as examples of known compounds which inhibit oxytocin-and vasopressin-induced contractions, and demonstrate how this method can be used to complement and validate pharmacological data obtained from cell-based assays to aid drug development. The effects of novel agonists in comparison to oxytocin and vasopressin can also be characterized. Whilst we use the example of the oxytocin/vasopressin system, this method can also be used to study other receptors and ion channels that play a role in uterine contraction and relaxation to advance the understanding of human uterine physiology and pathophysiology.
引用
收藏
页数:12
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