Endothelium-Independent Vasodilatory Effects of Isodillapiolglycol Isolated from <i>Ostericum citriodorum</i>

• Main Authors: Tengshuo Luo, Zewei Chen, Fengyun Wang, Shanshan Yin, Pan Liu, Jun Zhang, Zhonghua Yang
• Format: Article
• Language: English
• Published: MDPI AG 2020-02-01
• Series: Molecules
• Subjects: <i>ostericum citriodorum</i>; isodillapiolglycol; vasodilation; endothelium-independent; ca²⁺ channels
• Online Access: https://www.mdpi.com/1420-3049/25/4/885
• ISSN: 1420-3049

<i>Ostericum citriodorum</i> is a plant with a native range in China used in herbal medicine for treating angina pectoris. In this study, we investigated the vasodilatory effects of isodillapiolglycol (IDG), which is one of the main ingredients isolated from <i>O. citriodorum</i> ethyl acetate extract, in Sprague&#8722;Dawley rat aortic rings, and measured intracellular Ca²⁺ ([Ca²⁺]_in) using a molecular fluo-3/AM probe. The results show that IDG dose-dependently relaxed endothelium-intact or -denuded aortic rings pre-contracted with noradrenaline (NE) or potassium chloride (KCl), and inhibited CaCl₂-induced contraction in high K⁺ depolarized aortic rings. Tetraethyl ammonium chloride (a Ca²⁺-activated K⁺ channel blocker) or verapamil (an L-type Ca²⁺ channel blocker) significantly reduced the relaxation of IDG in aortic rings pre-contracted with NE. In vascular smooth muscle cells, IDG inhibited the increase in [Ca²⁺]_in stimulated by KCl in Krebs solution; likewise, IDG also attenuated the increase in [Ca²⁺]_in induced by NE or subsequent supplementation of CaCl₂. These findings demonstrate that IDG relaxes aortic rings in an endothelium-independent manner by reducing [Ca²⁺]_in, likely through inhibition of the receptor-gated Ca²⁺ channel and the voltage-dependent Ca²⁺ channel, and through opening of the Ca²⁺-activated K⁺ channel.