The New Zealand Institute for Plant and Food Research Limited, Palmerston North, New Zealand.
PLoS One. 2022 May 6;17(5):e0267567. doi: 10.1371/journal.pone.0267567. eCollection 2022.
The benefits of lowering blood pressure (BP) are well established for the prevention of cardiovascular disease. While there are a number of pharmaceuticals available for lowering BP, there is considerable interest in using dietary modifications, lifestyle and behaviour changes as alternative strategies. Kukoamines, caffeic acid derivatives of polyamines present in solanaceous plants, have been reported to reduce BP. We investigated the effect of orally administered synthetic kukoamine A on BP in the Spontaneously Hypertensive Rat (SHR) laboratory animal model of hypertension. Prior to the hypertension study, we determined the safety of the synthetic kukoamine A in a single oral dose (5 or 10 mg kg-1 bodyweight) 14-day observational study in mice. No negative effects of the oral administration of kukoamine A were observed. We subsequently investigated the effect of daily oral doses of kukoamine A (0, 5, 10 mg kg-1 bodyweight) for 35 days using the SHR rat model of hypertension. The normotensive control Wistar Kyoto (WKY) strain was used to provide a baseline for normal BP in rats. We observed no effect of orally administered synthetic kukoamine A on arterial hypertension in this laboratory animal model of hypertension.
降低血压(BP)对预防心血管疾病的益处已得到充分证实。虽然有许多药物可用于降低血压,但人们对使用饮食改变、生活方式和行为改变作为替代策略非常感兴趣。在茄科植物中存在的多胺的咖啡酸衍生物 kukoamines 已被报道可降低血压。我们研究了口服合成 kukoamine A 对高血压实验动物模型自发性高血压大鼠(SHR)血压的影响。在进行高血压研究之前,我们在小鼠中进行了为期 14 天的单次口服剂量(5 或 10 mg kg-1 体重)观察研究,以确定合成 kukoamine A 的安全性。口服 kukoamine A 没有观察到任何不良影响。随后,我们使用高血压 SHR 大鼠模型研究了每天口服 kukoamine A(0、5、10 mg kg-1 体重)35 天的效果。使用正常血压大鼠的 Wistar Kyoto(WKY)品系作为对照,提供大鼠正常血压的基线。我们在该高血压实验动物模型中未观察到口服合成 kukoamine A 对动脉高血压的影响。