Effect of Cinnamaldehyde Chalcone on Behavior in Adult Zebrafish (Danio rerio): In Silico Approach

被引:0
作者
Romao, Ivana Carneiro [1 ]
Siqueira, Sonia Maria Costa [1 ]
Ferreira, Maria Kueirislene Amancio [1 ]
da Silva, Antonio Wlisses [1 ]
Marinho, Marcia Machado [2 ,3 ,4 ,5 ]
Ribeiro, Walber Henrique Ferreira [4 ,5 ]
Gomes, Andreia Ferreira de Castro [6 ,7 ]
de Menezes, Jane Eire Silva Alencar [1 ]
dos Santos, Helcio Silva [1 ,4 ,5 ]
机构
[1] Univ Estadual Ceara, Programa Posgrad Ciencias Nat, Lab Bioensaios Quim Farmacol & Ambiental LabQFAm, Campus Itaperi, BR-60714242 Fortaleza, Ceara, Brazil
[2] Univ Estadual Ceara, Grp Quim Teor & Eletroquim GQTE, Programa Posgrad Ciencias Nat, Campus Itaperi, BR-60714242 Fortaleza, Ceara, Brazil
[3] Univ Estadual Ceara, Programa Posgrad Ciencias Nat, Fortaleza, Ceara, Brazil
[4] Univ Estadual Vale Acarau, Ctr Ciencias & Tecnol, Curso Quim, BR-62040370 Sobral, Ceara, Brazil
[5] Univ Estadual Vale Acarau, Curso Quim, Sobral, Ceara, Brazil
[6] Univ Minho, Dept Biol, Ctr Mol & Environm Biol CBMA, Aquat Res Network ARNET Associate Lab, Campus Gualtar, P-4710057 Braga, Portugal
[7] Univ Minho, Escola Ciencias, Ctr Biol Mol & Ambiental, Dept Biol, Braga, Portugal
关键词
Chalcone; GABAergic; Anxiety; Zebrafish; ANXIOLYTIC-LIKE; PREDICTION; DOCKING; PERMEABILITY; INVOLVEMENT; PERFORMANCE; METABOLISM; SYSTEM;
D O I
10.1002/cbdv.202400935
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The study focuses on the anxiolytic potential of chalcone (2E,4E)-1-(2-hydroxyphenyl)-5-phenylpenta-2,4-dien-1-one (CHALCNM) in adult zebrafish. Successfully synthesized in 58 % yield, CHALCNM demonstrated no toxicity after 96 h of exposure. In behavioral tests, CHALCNM (40 mg/kg) reduced locomotor activity and promoted less anxious behavior in zebrafish, confirmed by increased permanence in the light zone of the aquarium. Flumazenil reversed its anxiolytic effect, indicating interaction with GABAA receptors. Furthermore, CHALCNM (4 and 20 mg/kg) preserved zebrafish memory in inhibitory avoidance tests. Virtual screening and ADMET profile studies suggest high oral bioavailability, access to the CNS, favored by low topological polarity (TPSA <= 75 & Aring;2) and low incidence of hepatotoxicity, standing out as a promising pharmacological agent against the GABAergic system. In molecular coupling, CHALCNM demonstrated superior affinity to diazepam for the GABAA receptor. These results reinforce the therapeutic potential of CHALCNM in the treatment of anxiety, highlighting its possible future clinical application.
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页数:13
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