The Tiger Milk Medicinal Mushroom TM02®, Lignosus rhinocerus (Agaricomycetes), Water-Soluble Sclerotial Extract (xLr®) Induces Vasorelaxation in Rat Isolated Aortae.

IF 1.4
Mei-Kee Lee, Kayatri Govindaraju, Shin Yee Fung, Yvonne Mbaki, Szu-Ting Ng, Chon-Seng Tan, Hwei-San Loh, Suresh Kumar Mohankumar, Kang-Nee Ting
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Abstract

Lignosus rhinocerus (Cooke) Ryvarden, a traditional medicinal mushroom in Southeast Asia, is utilized for various health conditions. Although there is evidence that L. rhinocerus sclerotia supplementation had decreased systolic blood pressure and improved acetylcholine-induced vasorelaxation, the underlying mechanism remains poorly understood. Therefore, this study investigated the vasorelaxant effect and possible mechanism of action of L. rhinocerus TM02® sclerotial cold water extract (xLr®) on rat-isolated aortae using an organ bath technique. Aortic rings removed from Sprague Dawley rats were pre-contracted with phenylephrine (PE) prior to the construction of the cumulative concentration-response curve to xLr®. Exposure to increasing concentrations of xLr® significantly relaxed the pre-contracted aorta [maximum tissue contraction or relaxation response (Emax): 97.70 ± 5.21%; P = 0.0005]. Furthermore, our findings revealed that the xLr®-induced vasorelaxation is independent of endothelium and muscarinic receptor-mediated pathways. The attenuation of PE-induced contractions by SKF96365 and nifedipine suggests the possible effect of xLr®-induced vasorelaxation on the inhibition of external calcium influx through membrane calcium channels. This is the first study detailing the endothelium-independent vasorelaxant effects of xLr® in isolated blood vessels. These findings have enhanced our understanding of the pharmacological effects of xLr® on vasculature.

虎乳药菇TM02®、木耳菌、水溶性硬化剂提取物(xLr®)诱导大鼠离体主动脉血管舒张。
Lignosus rhinocerus (Cooke) Ryvarden是东南亚的一种传统药用蘑菇,用于各种健康状况。尽管有证据表明,补充L. rhinocerus菌核可以降低收缩压,改善乙酰胆碱诱导的血管松弛,但其潜在机制尚不清楚。因此,本研究采用器官浴技术研究了L. rhinocerus TM02®硬化冷水提取物(xLr®)对大鼠离体主动脉的血管松弛作用及其可能的作用机制。在构建xLr®的累积浓度-反应曲线之前,先用苯肾上腺素(PE)预收缩Sprague Dawley大鼠的主动脉环。暴露于浓度增加的xLr®显著放松预收缩的主动脉[最大组织收缩或舒张反应(Emax): 97.70±5.21%;P = 0.0005]。此外,我们的研究结果表明,xLr®诱导的血管松弛不依赖于内皮细胞和毒蕈碱受体介导的途径。SKF96365和硝苯地平对pe诱导的收缩的衰减表明xLr®诱导的血管松弛可能对通过膜钙通道的外钙流入的抑制有作用。这是第一个详细描述xLr®在分离血管中内皮不依赖性血管松弛作用的研究。这些发现增强了我们对xLr®对血管系统药理作用的理解。
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