TY - JOUR
T1 - Novel H2S-Releasing Bifunctional Antihistamine Molecules with Improved Antipruritic and Reduced Sedative Actions
AU - Antoniadou, Ivi
AU - Georgiou, Maria
AU - Dotsikas, Yannis
AU - Lamprou, Alexandra
AU - Lougiakis, Nikolaos
AU - Pouli, Nicole
AU - Karousis, Nikolaos
AU - Loukas, Yannis
AU - Tseti, Ioulia
AU - Marakos, Panagiotis
AU - Papapetropoulos, Andreas
N1 - Publisher Copyright:
© 2023 American Chemical Society.
PY - 2023/7/27
Y1 - 2023/7/27
N2 - 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.
AB - 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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U2 - 10.1021/acs.jmedchem.3c00321
DO - 10.1021/acs.jmedchem.3c00321
M3 - Article
C2 - 37409873
AN - SCOPUS:85164665433
SN - 0022-2623
VL - 66
SP - 9607
EP - 9621
JO - Journal of medicinal chemistry
JF - Journal of medicinal chemistry
IS - 14
ER -