Department of Biochemistry, Adeleke University Ede, Ede, Nigeria.
School of Public Health and Interdisciplinary Studies, Auckland University of Technology, Auckland, New Zealand.
Cell Biochem Funct. 2024 Jul;42(5):e4095. doi: 10.1002/cbf.4095.
This study aimed to investigate the effects of the n-hexane fraction of the ethanolic seed extract of PG (NFESEPG) on hypertension induced by Nω-nitro-L-arginine methyl ester (L-NAME) in rats. Specifically, the study examined the impact of NFESEPG on blood pressure, oxidative stress markers, NO concentration, angiotensin-converting enzyme (ACE) and arginase activities, and cardiac biomarkers in hypertensive rats. The study involved collecting, identifying, and processing the PG plant to obtain the ethanolic seed extract. The extract was then partitioned with solvents to isolate the n-hexane fraction. Hypertension was induced in rats by oral administration of L-NAME for 10 days, while concurrent treatment with NFESEPG at two doses (200 and 400 mg/kg/day) was administered orally. Blood pressure was measured using a noninvasive tail-cuff method, and various biochemical parameters were assessed. Treatment with both doses of NFESEPG significantly reduced systolic and diastolic blood pressure in L-NAME-induced hypertensive rats. Additionally, NFESEPG administration increased NO concentration and decreased ACE and arginase activities, malondialdehyde (MDA) levels, and cardiac biomarkers in hypertensive rats. The findings indicate that NFESEPG effectively lowered blood pressure in hypertensive rats induced by L-NAME, potentially through mechanisms involving the modulation of oxidative stress, NO bioavailability, and cardiac biomarkers. These results suggest the therapeutic potential of NFESEPG in managing hypertension and related cardiovascular complications.
本研究旨在探讨 PG 植物乙醇种子提取物的正己烷部分(NFESEPG)对 Nω-硝基-L-精氨酸甲酯(L-NAME)诱导的高血压大鼠的影响。具体而言,本研究考察了 NFESEPG 对高血压大鼠血压、氧化应激标志物、NO 浓度、血管紧张素转换酶(ACE)和精氨酸酶活性以及心脏生物标志物的影响。研究涉及收集、鉴定和处理 PG 植物以获得乙醇种子提取物。然后,提取物用溶剂进行分配以分离正己烷部分。通过给大鼠口服 L-NAME 10 天诱导高血压,同时口服给予 NFESEPG 两种剂量(200 和 400mg/kg/天)进行治疗。使用非侵入性尾套法测量血压,并评估各种生化参数。两种剂量的 NFESEPG 治疗均显著降低了 L-NAME 诱导的高血压大鼠的收缩压和舒张压。此外,NFESEPG 给药增加了高血压大鼠的 NO 浓度,并降低了 ACE 和精氨酸酶活性、丙二醛(MDA)水平和心脏生物标志物。这些发现表明,NFESEPG 可有效降低 L-NAME 诱导的高血压大鼠的血压,其机制可能涉及调节氧化应激、NO 生物利用度和心脏生物标志物。这些结果表明 NFESEPG 具有治疗高血压和相关心血管并发症的潜力。