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β2和β3肾上腺素能受体激动剂对猪黄体期和妊娠初期子宫肌层收缩活性的影响。

Influence of β2- and β3-adrenoceptor agonists on contractile activity of the porcine myometrium in the luteal phase and the first days of pregnancy.

作者信息

Markiewicz W, Jaroszewski J J

机构信息

.

出版信息

Pol J Vet Sci. 2017 Mar 28;20(1):111-121. doi: 10.1515/pjvs-2017-0015.

Abstract

This study analysed the relaxant properties of salbutamol (β2-adrenoceptors agonist) and BRL 37344 (β3-adrenoceptors agonist) regarding the contractility of porcine myometrium on days 10-14 of the oestrous cycle (cyclic group; n = 10) and on days 3-5 of pregnancy (early pregnant group; n = 6). The activity of myometrial strips (tension, frequency and amplitude) was recorded under isometric conditions using force transducers. The contractility was assessed further following the administration of increasing concentrations of the agonists (10-9-10-4 M), both with and without β-adrenoceptor antagonists (butaxamine - a selective β2- adrenoceptor antagonist, propranolol- a non-selective β1- and β2-adrenoceptor antagonist and bupranolol - a non-selective β1-, β2- and β3-adrenoceptor antagonist) at a concentration of 10-4 M. Although neither salbutamol nor BRL 37344 caused changes in the tension, at the highest concentrations they decreased the frequency and amplitude of contractions. These changes were more evident after salbutamol treatment and in the early pregnant group. Antagonists given alone did not cause changes in the parameters examined but changed some activity of the agonists. Butoxamine reduced the decrease in frequency and amplitude induced by salbutamol and produced a decrease in the tension after BRL 37344 treatment in the early pregnant group. Propranolol reduced the decrease in frequency and amplitude induced by salbutamol in both examined groups and did not cause significant changes in BRL 37344 activity. The administration of bupranolol before salbutamol treatment caused an increase in the tension and reduced the decrease in the frequency in the cyclic group. Moreover, bupranolol eliminated a decrease in frequency and induced an increase in amplitude caused by BRL 37344 in both groups and these changes were more evident in the early pregnant group. The data indicates that both β2- and β3-adenoreceptors are involved in the regulation of the contractility in both groups, but the changes after agonists and antagonists treatment are more evident in the early pregnant myometrium.

摘要

本研究分析了沙丁胺醇(β2肾上腺素能受体激动剂)和BRL 37344(β3肾上腺素能受体激动剂)对发情周期第10 - 14天的猪子宫肌层收缩性的舒张特性(周期组;n = 10)以及妊娠第3 - 5天的猪子宫肌层收缩性的舒张特性(早孕组;n = 6)。使用力传感器在等长条件下记录子宫肌条的活性(张力、频率和幅度)。在给予浓度递增的激动剂(10⁻⁹ - 10⁻⁴ M)后,进一步评估收缩性,同时使用浓度为10⁻⁴ M的β肾上腺素能受体拮抗剂(布他沙明 - 一种选择性β2肾上腺素能受体拮抗剂、普萘洛尔 - 一种非选择性β1和β2肾上腺素能受体拮抗剂以及布普洛尔 - 一种非选择性β1、β2和β3肾上腺素能受体拮抗剂)。尽管沙丁胺醇和BRL 37344均未引起张力变化,但在最高浓度时它们降低了收缩的频率和幅度。这些变化在沙丁胺醇治疗后以及早孕组中更为明显。单独给予拮抗剂未引起所检测参数的变化,但改变了激动剂的一些活性。布他沙明减少了沙丁胺醇诱导的频率和幅度降低,并在早孕组中使BRL 37344治疗后的张力降低。普萘洛尔在两个检测组中均减少了沙丁胺醇诱导的频率和幅度降低,并且未引起BRL 37344活性的显著变化。在沙丁胺醇治疗前给予布普洛尔导致周期组中的张力增加并减少了频率降低。此外,布普洛尔消除了两组中由BRL 37344引起的频率降低并诱导了幅度增加,并且这些变化在早孕组中更为明显。数据表明,β2和β3肾上腺素能受体均参与两组中收缩性的调节,但激动剂和拮抗剂治疗后的变化在早孕子宫肌层中更为明显。

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