Department of Physiology, College of Medicine, Brain Korea 21 PLUS Project for Medical Sciences, Yonsei University, 50 Yeonseiro, Seodaemun-gu, Seoul 03722, Korea.
Department of Food and Biotechnology, Korea University, 145 Anam-ro, Seongbuk-gu, Seoul 02841, Korea.
Molecules. 2020 Jul 10;25(14):3160. doi: 10.3390/molecules25143160.
is a well-known medicinal mushroom that is widely used in Asian countries. In several experimental models, extracts were reported to have various biological effects, including anti-inflammatory, anti-cancer, hepatoprotective, anti-diabetic, neuroprotective, and anti-angiogenic activity. In the present study, several bioactive compounds, including palmitic acid ethyl ester and linoleic acid, were identified in . The intermediate-conductance calcium-activated potassium channel (IK) plays an important role in the regulation of the vascular smooth muscle cells' (VSMCs) contraction and relaxation. The activation of the IK channel causes the hyperpolarization and relaxation of VSMCs. To examine whether extract causes vasodilation in the mesenteric arteries of rats, we measured the isometric tension using a wire myograph. After the arteries were pre-contracted with U46619 (a thromboxane analogue, 1 µM), extract was administered. The extract induced vasodilation in a dose-dependent manner, which was independent of the endothelium. To further investigate the mechanism, we used the non-selective K channel blocker tetraethylammonium (TEA). TEA significantly abolished extract-induced vasodilation. Thus, we tested three different types of K channel blockers: iberiotoxin (BK channel blocker), apamin (SK channel blocker), and charybdotoxin (IK channel blocker). Charybdotoxin significantly inhibited extract-induced relaxation, while there was no effect from apamin and iberiotoxin. Membrane potential was measured using the voltage-sensitive dye bis-(1,3-dibutylbarbituric acid)-trimethine oxonol (DiBAC(3)) in the primary isolated vascular smooth muscle cells (VSMCs). We found that the extract induced hyperpolarization of VSMCs, which is associated with a reduced phosphorylation level of 20 KDa myosin light chain (MLC).
灵芝是一种广为人知的药用蘑菇,在亚洲国家被广泛使用。在几个实验模型中,灵芝提取物被报道具有多种生物活性,包括抗炎、抗癌、保肝、抗糖尿病、神经保护和抗血管生成活性。在本研究中,鉴定出灵芝中的几种生物活性化合物,包括棕榈酸乙酯和亚油酸。中间电导钙激活钾通道(IK)在调节血管平滑肌细胞(VSMCs)收缩和舒张中起着重要作用。IK 通道的激活导致 VSMCs 的超极化和舒张。为了研究灵芝提取物是否引起大鼠肠系膜动脉舒张,我们使用张力换能器测量等长张力。在 U46619(血栓烷类似物,1 μM)预收缩血管后,给予灵芝提取物。灵芝提取物呈剂量依赖性诱导血管舒张,且与内皮无关。为了进一步研究其机制,我们使用非选择性 K 通道阻断剂四乙铵(TEA)。TEA 显著抑制了灵芝提取物诱导的血管舒张。因此,我们测试了三种不同类型的 K 通道阻断剂:iberiotoxin(BK 通道阻断剂)、apamin(SK 通道阻断剂)和 charybdotoxin(IK 通道阻断剂)。Charybdotoxin 显著抑制了灵芝提取物诱导的舒张,而 apamin 和 iberiotoxin 没有作用。在原代分离的血管平滑肌细胞(VSMCs)中,使用电压敏感染料双(1,3-二丁基巴比妥酸)-三嗪甲氧基诺伦(DiBAC(3))测量膜电位。我们发现,灵芝提取物诱导 VSMCs 超极化,这与 20 kDa 肌球蛋白轻链(MLC)的磷酸化水平降低有关。