Institute for Pharmacology and Toxicology, Medical Faculty, Martin Luther University Halle-Wittenberg, Magdeburger Straße 4, 06097, Halle (Saale), Germany.
Normandie Univ, UNICAEN CERMN (Centre d'Etudes Et de Recherche Sur Le Médicament de Normandie), 14032, Caen, France.
Naunyn Schmiedebergs Arch Pharmacol. 2024 Nov;397(11):8893-8902. doi: 10.1007/s00210-024-03226-0. Epub 2024 Jun 10.
MR33317 was synthesized as an acetylcholinesterase-inhibitor and an agonist at brain 5-HT-receptors. MR33317 might be used to treat Morbus Alzheimer. This therapeutic action of MR33317 might be based on MR33317´s dual synergistic activity. We tested the hypothesis that MR33317 also stimulates 5-HT-receptors in the heart. MR33317 (starting at 10 nM) increased force of contraction and beating rate in isolated atrial preparations from mice with cardiac confined overexpression of the human 5-HT-serotonin receptor (5-HT-TG) but was inactive in wild type mouse hearts (WT). Only in the presence of the phosphodiesterase III-inhibitor cilostamide, MR33317 raised force of contraction under isometric conditions in isolated paced (1 Hz) human right atrial preparations (HAP). This increase in force of contraction in human atrium by MR33317 was attenuated by 10 µM tropisetron or GR125487. These data suggest that MR33317 is an agonist at human 5-HT-serotonin receptors in the human atrium. Clinically, one would predict that MR33317 may lead to atrial fibrillation.
MR33317 被合成作为乙酰胆碱酯酶抑制剂和脑 5-HT 受体激动剂。MR33317 可能用于治疗阿尔茨海默病。MR33317 的这种治疗作用可能基于其双重协同活性。我们测试了这样一个假设,即 MR33317 也会刺激心脏中的 5-HT 受体。MR33317(从 10 nM 开始)增加了在心脏中过表达人类 5-HT 血清素受体(5-HT-TG)的小鼠的分离心房制剂的收缩力和搏动率,但在野生型小鼠心脏(WT)中无活性。只有在磷酸二酯酶 III 抑制剂西洛酰胺存在的情况下,MR33317 才会在分离的起搏(1 Hz)人心房制备物(HAP)中增加等长条件下的收缩力。MR33317 在心房中增加收缩力的作用被 10 µM 曲昔派特或 GR125487 减弱。这些数据表明,MR33317 是人心房 5-HT 血清素受体的激动剂。临床上,人们可能会预测 MR33317 可能导致心房颤动。