Braekow Pauline, Neumann Joachim, Kirchhefer Uwe, Gergs Ulrich
Institute for Pharmacology and Toxicology, Medical Faculty, Martin Luther University Halle-Wittenberg, 06097 Halle, Germany.
Institute of Pharmacology and Toxicology, University of Münster, 48149 Münster, Germany.
Pharmaceuticals (Basel). 2025 Jul 6;18(7):1009. doi: 10.3390/ph18071009.
: Hallucinogenic substances such as psilocybin, psilocin, ergometrine, ergotamine, and lysergic acid diethylamide (LSD) have been demonstrated to enhance the force of contraction (FOC), in part due to the phosphorylation of phospholamban in human atrial preparations via 5-HT serotonin receptors and/or H histamine receptors. However, whether psilocybin or psilocin acts at isolated mammalian ventricular preparations and whether they increase protein phosphorylation in the mammalian ventricle remains to be elucidated. : To this end, the FOC and phospholamban phosphorylation in isolated perfused hearts from transgenic mice with cardiomyocyte-specific overexpression of either human 5-HT receptors (5-HT-TG) or human H receptors (H-TG) and their wild-type littermates (WT) were examined. Furthermore, the ergot alkaloids ergometrine, ergotamine, and LSD were used as references. : Psilocybin and psilocin enhanced the FOC to 137% and to 152%, respectively, and elevated the phospholamban phosphorylation in isolated perfused hearts from 5-HT-TG. In H-TG hearts, psilocybin and psilocin increased the FOC to a much lesser extent but had no effect on the phospholamban phosphorylation. In contrast, LSD increased the FOC and phosphorylation state of phospholamban in isolated hearts of both 5-HT-TG and H-TG. On the other hand, ergometrine and ergotamine increased the FOC only in H-TG. Ergometrine increased the phosphorylation state of phospholamban in perfused hearts from H-TG, but not from 5-HT-TG. Ergotamine failed to increase the phospholamban phosphorylation in both H-TG and 5-HT-TG. Psilocybin, psilocin, ergotamine, ergometrine, and LSD were unable to increase FOC and phospholamban phosphorylation in perfused hearts from WT. : The increase in the phosphorylation state of phospholamban could provide a partial explanation for the positive inotropic effects and the relaxant effects of not only psilocybin and psilocin but also ergometrine and LSD in the isolated hearts of the animals used in this study.
诸如裸盖菇素、脱磷酸裸盖菇素、麦角新碱、麦角胺和麦角酸二乙胺(LSD)等致幻物质已被证明可增强收缩力(FOC),部分原因是通过5-羟色胺血清素受体和/或H组胺受体使人心房标本中的受磷蛋白发生磷酸化。然而,裸盖菇素或脱磷酸裸盖菇素是否作用于分离的哺乳动物心室标本,以及它们是否会增加哺乳动物心室中的蛋白质磷酸化,仍有待阐明。为此,研究了来自心肌细胞特异性过表达人5-羟色胺受体(5-HT-TG)或人H受体(H-TG)的转基因小鼠及其野生型同窝小鼠(WT)的分离灌注心脏中的FOC和受磷蛋白磷酸化。此外,使用麦角生物碱麦角新碱、麦角胺和LSD作为对照。裸盖菇素和脱磷酸裸盖菇素分别将5-HT-TG分离灌注心脏中的FOC提高到137%和152%,并提高了受磷蛋白的磷酸化水平。在H-TG心脏中,裸盖菇素和脱磷酸裸盖菇素在较小程度上增加了FOC,但对受磷蛋白磷酸化没有影响。相比之下,LSD增加了5-HT-TG和H-TG分离心脏中的FOC和受磷蛋白的磷酸化状态。另一方面,麦角新碱和麦角胺仅在H-TG中增加了FOC。麦角新碱增加了H-TG灌注心脏中受磷蛋白的磷酸化状态,但未增加5-HT-TG灌注心脏中受磷蛋白的磷酸化状态。麦角胺未能增加H-TG和5-HT-TG中受磷蛋白的磷酸化。裸盖菇素、脱磷酸裸盖菇素、麦角胺、麦角新碱和LSD均无法增加WT灌注心脏中的FOC和受磷蛋白磷酸化。受磷蛋白磷酸化状态的增加可以部分解释本研究中使用的动物分离心脏中,不仅裸盖菇素和脱磷酸裸盖菇素,而且麦角新碱和LSD的正性肌力作用和舒张作用。