Lasmiditan Ameliorates Serotonergic Itch in Mice: Possible Involvement of 5-Ht1f Receptors Publisher Pubmed



Afrooghe A^{1, 2} ; Ahmadi E^{1, 2} ; Babaei M^{1, 2} ; Soltani ZE¹ ; Elahi M^{1, 3} ; Shayan M^{1, 4} ; Jafari RM^{1, 5} ; Dehpour AR^{1, 5}
Source: Naunyn-Schmiedeberg's Archives of Pharmacology Published:2025

Abstract

Previously, some allergic conditions involving pruritus have been linked to migraine, raising the possibility that migraine and itching may be governed by similar underlying mechanisms. We aimed to investigate the efficacy of Lasmiditan, a highly selective agonist of the 5-hydroxytryptamine 1F (5-HT1F) receptor and a recently approved medication for the treatment of migraine headaches, in ameliorating serotonergic itching. Forty animals were employed in the present study (n = 40). Eight animals were randomly assigned to each of the following study groups (n = 8, in each group): (1) “Normal Saline”: This group was given intradermal injections of normal saline (2) “5-HT”: The animals were injected with intradermal 5-HT, which was used to induce itching. (3) “Lasmiditan 0.3”, “Lasmiditan 1”, and “Lasmiditan 3” groups: injected with 5-HT as well as intraperitoneal Lasmiditan at different dose levels (0.3, 1, and 3 mg/kg, respectively). Scratching behavior was recorded for 60 min, and the skin tissue of three mice was sampled at the end of the behavioral experiment to assess the levels of TLR-4, IL-31, 5-HT1F receptor, CGRP & TRPV4. In the present study, we found that Lasmiditan when administered at 1 mg/kg effectively reduced serotonin-induced itching compared to the “5-HT” group (P < 0.0001). Following the administration of Lasmiditan (1 mg/kg), the expression levels of the 5-HT1F receptor significantly increased (P < 0.01). Further, the levels of TLR-4, IL-31, CGRP & TRPV4 were substantially reduced upon the administration of Lasmiditan (1 mg/kg). We found that Lasmiditan is effective in reducing serotonergic itch in mice through its interaction with the 5-HT1F receptor in the skin tissue of mice. © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2024.