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Intranasal Nanotransferosomal Gel for Quercetin Brain Targeting: II. Antidepressant Effect in an Experimental Animal Model

Authors :
Mohammed H. Elkomy
Fatma I. Abo El-Ela
Randa Mohammed Zaki
Omar A. Alsaidan
Mohammed Elmowafy
Ameeduzzafar Zafar
Khaled Shalaby
Mohamed A. Abdelgawad
Hany A. Omar
Rania Salama
Hussein M. Eid
Source :
Pharmaceutics, Vol 15, Iss 8, p 2095 (2023)
Publication Year :
2023
Publisher :
MDPI AG, 2023.

Abstract

Depression is a serious mental disorder and the most prevalent cause of disability and suicide worldwide. Quercetin (QER) demonstrated antidepressant effects in rats exhibiting anxiety and depressive-like behaviors. In an attempt to improve QER’s antidepressant activity, a QER-loaded transferosome (QER-TFS) thermosensitive gel for intranasal administration was formulated and optimized. The therapeutic effectiveness of the optimized formulation was assessed in a depressed rat model by conducting a behavioral analysis. Behavioral study criteria such as immobility, swimming, climbing, sucrose intake, number of crossed lines, rearing, active interaction, and latency to feed were all considerably enhanced by intranasal treatment with the QER-TFS in situ gel in contrast to other formulations. A nasal histopathological study indicated that the QER-TFS thermosensitive gel was safe for the nasal mucosa. An immunohistochemical analysis showed that the animals treated with the QER-TFS thermosensitive gel had the lowest levels of c-fos protein expression, and brain histopathological changes in the depressed rats were alleviated. According to pharmacodynamic, immunohistochemical, and histopathological experiments, the intranasal administration of the QER-TFS thermosensitive gel substantially alleviated depressive symptoms in rats. However, extensive preclinical investigations in higher animal models are needed to anticipate its effectiveness in humans.

Details

Language :
English
ISSN :
19994923
Volume :
15
Issue :
8
Database :
Directory of Open Access Journals
Journal :
Pharmaceutics
Publication Type :
Academic Journal
Accession number :
edsdoj.4d5c625e62942779049c7c73f7187e3
Document Type :
article
Full Text :
https://doi.org/10.3390/pharmaceutics15082095