抗组胺药
化学
止痒药
药理学
组胺
体内
西替利嗪
镇静剂
药效团
立体化学
医学
生物
生物技术
作者
Ioanna Antoniadou,Maria Georgiou,Yannis Dotsikas,Alexandra Lamprou,Nikolaos Lougiakis,Nicole Pouli,Nikolaos Karousis,Yannis L. Loukas,Ioulia Tseti,Panagiotis Marakos,Andreas Papapetropoulos
标识
DOI:10.1021/acs.jmedchem.3c00321
摘要
Hydrogen sulfide (H2S) is an endogenous gasotransmitter with anti-inflammatory actions that also reduces itching. To test whether a combination of an antihistamine with a H2S donor has improved antipruritic efficacy, bifunctional molecules with antihistamine and H2S-releasing pharmacophores were synthesized and tested in vitro and in vivo. H2S release from the hybrid molecules was evaluated with the methylene blue and lead acetate methods, and H1-blocking activity was assessed by determining tissue factor expression inhibition. All new compounds released H2S in a dose-dependent manner and retained histamine blocking activity. Two compounds with the highest potency were evaluated in vivo for their antipruritic as well as sedative action; they proved to possess higher efficacy in inhibiting histamine-induced pruritus and decreased sedative effects compared to the parent compounds (hydroxyzine and cetirizine), suggesting that they exhibit superior antipruritic action and limited side effects that likely arise from the H2S-releasing moiety.
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