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α-红没药醇对妊娠人子宫的抗炎及子宫松弛作用。

Anti-inflammatory and utero-relaxant effect of α-bisabolol on the pregnant human uterus.

作者信息

Muñoz-Pérez Victor Manuel, Ortiz Mario I, Ponce-Monter Héctor A, Monter-Pérez Vicente, Barragán-Ramírez Guillermo

机构信息

Área Académica de Medicina del Instituto de Ciencias de la Salud. Universidad Autónoma del Estado de Hidalgo, Pachuca, Hidalgo, México.

Hospital General de los SSH, Pachuca, Hidalgo, Mexico.

出版信息

Korean J Physiol Pharmacol. 2018 Jul;22(4):391-398. doi: 10.4196/kjpp.2018.22.4.391. Epub 2018 Jun 25.

Abstract

The aim of this study was to evaluate the anti-inflammatory and utero-relaxant effect of α-bisabolol on the pregnant human myometrium. Samples from the pregnant human myometrium were used in functional tests to evaluate the inhibitory effect of α-bisabolol (560, 860, 1,200 and 1,860 µM) on spontaneous myometrial contractions. The intracellular cyclic adenosine monophosphate (cAMP) levels generated in response to α-bisabolol in human myometrial homogenates were measured by ELISA. The anti-inflammatory effect of α-bisabolol was determined through the measurement of two pro-inflammatory cytokines, tumor necrosis factor-α (TNFα) and interleukin (IL)-1β, and the anti-inflammatory cytokine IL-10, in pregnant human myometrial explants stimulated with lipopolysaccharide (LPS). Forskolin was used as a positive control to evaluate the cAMP and cytokine levels. α-Bisabolol was found to induce a significant inhibition of spontaneous myometrial contractions at the highest concentration level (p<0.05). α-Bisabolol caused a concentration-dependent decrease in myometrial cAMP levels (p<0.05) and a concentration-dependent decrease in LPS-induced TNFα and IL-1β production, while IL-10 production did not increase significantly (p>0.05). The anti-inflammatory and utero-relaxant effects induced by α-bisabolol were not associated with an increase in cAMP levels in pregnant human myometrial samples. These properties place α-bisabolol as a potentially safe and effective adjuvant agent in cases of preterm birth, an area of pharmacological treatment that requires urgent improvement.

摘要

本研究的目的是评估α-红没药醇对妊娠人类子宫肌层的抗炎和子宫舒张作用。从妊娠人类子宫肌层获取的样本用于功能测试,以评估α-红没药醇(560、860、1200和1860µM)对子宫肌层自发收缩的抑制作用。通过酶联免疫吸附测定法测量人类子宫肌层匀浆中α-红没药醇刺激后产生的细胞内环磷酸腺苷(cAMP)水平。通过测量脂多糖(LPS)刺激的妊娠人类子宫肌层外植体中两种促炎细胞因子肿瘤坏死因子-α(TNFα)和白细胞介素(IL)-1β以及抗炎细胞因子IL-10,来确定α-红没药醇的抗炎作用。使用福斯高林作为阳性对照来评估cAMP和细胞因子水平。发现α-红没药醇在最高浓度水平时可显著抑制子宫肌层的自发收缩(p<0.05)。α-红没药醇导致子宫肌层cAMP水平呈浓度依赖性下降(p<0.05),并使LPS诱导的TNFα和IL-1β产生呈浓度依赖性下降,而IL-10的产生没有显著增加(p>0.05)。α-红没药醇诱导的抗炎和子宫舒张作用与妊娠人类子宫肌层样本中cAMP水平的升高无关。这些特性使α-红没药醇成为早产情况下潜在安全有效的辅助药物,早产是一个急需改进的药物治疗领域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cfb/6019870/400f01d1ac2b/kjpp-22-391-g001.jpg

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