The vasodilator effect of Eugenol on uterine artery - potential therapeutic applications in pregnancy-associated hypertension.

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Receptors and Signal Transduction Pub Date : 2024-08-26 DOI:10.1080/10799893.2024.2395301
Harithalakshmi Jandhyam, Bimal Prasanna Mohanty, Subas Chandra Parija
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Abstract

Preeclampsia, a gestational associated hypertension, has been reported in 6-8% of pregnant women worldwide leading to premature delivery and low birth weight of newborn due to reduced blood flow to placenta. Although several vasodilators (Methyl dopa, hydralazine, β-blockers and diuretics) are currently in use to treat preeclampsia, still there is a search for safer drugs with better efficacy. Lately, antihypertensive vasodilators from natural sources are gaining importance in treating preeclampsia. Eugenol (Eug), a natural essential oil, has been traditionally used in health and food products without any risk. In the present study, ex vivo experiments were designed to examine the vasorelaxation effect of Eug and its signaling pathways in a middle uterine artery (MUA) of pregnant Capra hircus (Ch). In presence of different blockers (L-NAME, indomethacin, ODQ, Ouabain, glibenclamide, 4-AP, Ba2, Carbenoxolone and 18β Glycyrrhetinic acid), Eug-induced concentration-dependent vasorelaxation response was elicited. The results showed that Eug caused a greater vasorelaxation effect in the MU of pregnant animals, which is mediated by potential activation of eNOS, KATP channels, and Kir channels with moderate activation of Na+- K+- ATPase and sGC and MEGJ. These findings provide a strong basis for developing Eug as a therapeutic candidate in the treatment of pregnancy-associated hypertension.

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丁香酚对子宫动脉的血管扩张作用--在妊娠相关性高血压中的潜在治疗应用。
据报道,全世界有 6-8% 的孕妇患有子痫前期(一种妊娠高血压),由于胎盘血流量减少,导致早产和新生儿体重不足。尽管目前有几种血管扩张剂(甲基多巴、肼屈嗪、β-受体阻滞剂和利尿剂)可用于治疗子痫前期,但人们仍在寻找更安全、疗效更好的药物。最近,来自天然来源的降压血管扩张剂在治疗子痫前期方面的作用越来越重要。丁香酚(Eug)是一种天然精油,历来被用于保健品和食品中,没有任何风险。本研究设计了体内外实验,以检测丁香酚及其信号通路对妊娠貘(Capra hircus,Ch)子宫中动脉(MUA)的血管舒张作用。在不同阻滞剂(L-NAME、吲哚美辛、ODQ、欧阿巴因、格列本脲、4-AP、Ba2、卡贝诺酮和18β甘草次酸)的作用下,Eug诱导了浓度依赖性血管舒张反应。结果表明,Eug对妊娠动物中枢神经系统的血管舒张作用更强,这种作用是由eNOS、KATP通道和Kir通道的潜在激活以及Na+- K+- ATP酶、sGC和MEGJ的适度激活介导的。这些发现为开发 Eug 作为治疗妊娠相关高血压的候选药物提供了坚实的基础。
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来源期刊
Journal of Receptors and Signal Transduction
Journal of Receptors and Signal Transduction 生物-生化与分子生物学
CiteScore
6.60
自引率
0.00%
发文量
19
审稿时长
>12 weeks
期刊介绍: Journal of Receptors and Signal Tranduction is included in the following abstracting and indexing services: BIOBASE; Biochemistry and Biophysics Citation Index; Biological Abstracts; BIOSIS Full Coverage Shared; BIOSIS Previews; Biotechnology Abstracts; Current Contents/Life Sciences; Derwent Chimera; Derwent Drug File; EMBASE; EMBIOLOGY; Journal Citation Reports/ Science Edition; PubMed/MedLine; Science Citation Index; SciSearch; SCOPUS; SIIC.
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