A selanylimidazopyridine (3-SePh-IP) reverses the prodepressant- and anxiogenic-like effects of a high-fat/high-fructose diet in mice

Author:

Veloso Izolene Corrêa1,Delanogare Eslen1,Machado Adriano Emanuel1,Braga Sara Pereira2,Rosa Giovana Karoline3,De Bem Andreza Fabro4,Rafique Jamal5ORCID,Saba Sumbal6,da Trindade Roberth Nascimento7,Galetto Fábio Zazyki7,Moreira Eduardo Luiz Gasnhar312ORCID

Affiliation:

1. Programa de Pós-Graduação em Neurociências, Universidade Federal de Santa Catarina, Florianópolis, SC, Brazil

2. Programa de Pós-Graduação Multicêntrico em Ciências Fisiológicas, Universidade Federal de Santa Catarina, Florianópolis, SC, Brazil

3. Departamento de Ciências Fisiológicas, Universidade Federal de Santa Catarina, Florianópolis, SC, Brazil

4. Departamento de Ciências Fisiológicas, Instituto de Ciências Biológicas, Universidade de Brasília, Brasília, DF, Brazil

5. Instituto de Química, Universidade Federal do Mato Grosso do Sul, Campo Grande, MS, Brazil

6. Centro de Ciências Naturais e Humanas – CCNH, Universidade Federal do ABC, Santo André, SP, Brazil

7. Departamento de Química, Universidade Federal de Santa Catarina, Florianópolis, SC, Brazil

Abstract

Abstract Objective While chronic feeding with high-fat or high-sugar diets is known related to obesity and type 2 diabetes, later data have indicated that it is also related to depression and anxiety appearance. In this regard, multi-target drugs raise considerable interest as promising therapeutic solutions to complex diseases. Considering the pharmacological effects of the imidazopyridine-derivative moiety imidazo[1,2-a]pyridine and the organoselenium molecules, the combination of both could be a feasible strategy to develop efficient drugs to handle obesity and related comorbidities, for example dyslipidemia and mood disorders. Methods The antidepressant- and anxiolytic-like properties of a selanylimidazopyridine compound, 2-Phenyl-3-(phenylselanyl)imidazo[1,2-a]pyridine (3-SePh-IP), were evaluated on high-fat/high-fructose diet (HFFD)-fed female Swiss mice. Key findings Our results showed that a short-term HFFD (16 days) could promote a significant body weight gain, hypercholesterolemia, glucose intolerance, and anxiety- and depressive-like behaviour in mice. Concomitant treatment with 3-SePh-IP (10 mg/kg; i.p.) attenuated the HFFD-induced increase in cholesterol levels and blunted the anxiety- and depressive-like behaviour in mice. Conclusions 3-SePh-IP holds multimodal pharmacological properties, which provide a rationale for further studies, for example to assess the underlying mechanisms linked to its anxiolytic- and antidepressive-like activities.

Funder

Brazilian Council for Scientific and Technological

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

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