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Solid lipid nanoparticles loading with curcumin and dexanabinol to treat major depressive disorder

Dexanabinol (HU-211) is an artificially synthesized cannabinoid derivative that exerts neuroprotective effects through anti-inflammatory and antioxidant effects. Curcumin exhibits antidepressant effects in the treatment of major depressive disorder. To investigate the antidepressant effects of solid...

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Autores principales: He, Xiao-Lie, Yang, Li, Wang, Zhao-Jie, Huang, Rui-Qi, Zhu, Rong-Rong, Cheng, Li-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7996013/
https://www.ncbi.nlm.nih.gov/pubmed/32985484
http://dx.doi.org/10.4103/1673-5374.293155
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author He, Xiao-Lie
Yang, Li
Wang, Zhao-Jie
Huang, Rui-Qi
Zhu, Rong-Rong
Cheng, Li-Ming
author_facet He, Xiao-Lie
Yang, Li
Wang, Zhao-Jie
Huang, Rui-Qi
Zhu, Rong-Rong
Cheng, Li-Ming
author_sort He, Xiao-Lie
collection PubMed
description Dexanabinol (HU-211) is an artificially synthesized cannabinoid derivative that exerts neuroprotective effects through anti-inflammatory and antioxidant effects. Curcumin exhibits antidepressant effects in the treatment of major depressive disorder. To investigate the antidepressant effects of solid lipid nanoparticles loaded with both curcumin and dexanabinol, and the underlying mechanisms associated with this combination, we established wild-type (CBR1(+/+)) and cannabinoid receptor 1 (CBR1) knockout (CBR1(–/–)) mouse models of major depressive disorder, through the intraperitoneal injection of corticosterone, for 3 successive days, followed by treatment with intraperitoneal injections of solid lipid nanoparticles loading with curcumin (20 mg/kg) and dexanabinol (0.85 mg/kg), for 2 successive days. Our results revealed that solid lipid nanoparticle loading with curcumin and dexanabinol increased the mRNA and protein expression levels of the mature neuronal markers neuronal nuclei, mitogen-activated protein 2, and neuron-specific beta-tubulin III, promoted the release of dopamine and norepinephrine, and increased the mRNA expression of CBR1 and the downstream genes Rasgef1c and Egr1, and simultaneously improved rat locomotor function. However, solid lipid nanoparticles loaded with curcumin and dexanabinol had no antidepressant effects on the CBR1(–/–) mouse models of major depressive disorder. This study was approved by the Institutional Ethics Committee of Tongji Hospital of Tongji University, China (approval No. 2017-DW-020) on May 24, 2017.
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spelling pubmed-79960132021-06-02 Solid lipid nanoparticles loading with curcumin and dexanabinol to treat major depressive disorder He, Xiao-Lie Yang, Li Wang, Zhao-Jie Huang, Rui-Qi Zhu, Rong-Rong Cheng, Li-Ming Neural Regen Res Research Article Dexanabinol (HU-211) is an artificially synthesized cannabinoid derivative that exerts neuroprotective effects through anti-inflammatory and antioxidant effects. Curcumin exhibits antidepressant effects in the treatment of major depressive disorder. To investigate the antidepressant effects of solid lipid nanoparticles loaded with both curcumin and dexanabinol, and the underlying mechanisms associated with this combination, we established wild-type (CBR1(+/+)) and cannabinoid receptor 1 (CBR1) knockout (CBR1(–/–)) mouse models of major depressive disorder, through the intraperitoneal injection of corticosterone, for 3 successive days, followed by treatment with intraperitoneal injections of solid lipid nanoparticles loading with curcumin (20 mg/kg) and dexanabinol (0.85 mg/kg), for 2 successive days. Our results revealed that solid lipid nanoparticle loading with curcumin and dexanabinol increased the mRNA and protein expression levels of the mature neuronal markers neuronal nuclei, mitogen-activated protein 2, and neuron-specific beta-tubulin III, promoted the release of dopamine and norepinephrine, and increased the mRNA expression of CBR1 and the downstream genes Rasgef1c and Egr1, and simultaneously improved rat locomotor function. However, solid lipid nanoparticles loaded with curcumin and dexanabinol had no antidepressant effects on the CBR1(–/–) mouse models of major depressive disorder. This study was approved by the Institutional Ethics Committee of Tongji Hospital of Tongji University, China (approval No. 2017-DW-020) on May 24, 2017. Wolters Kluwer - Medknow 2020-09-22 /pmc/articles/PMC7996013/ /pubmed/32985484 http://dx.doi.org/10.4103/1673-5374.293155 Text en Copyright: © 2021 Neural Regeneration Research http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Research Article
He, Xiao-Lie
Yang, Li
Wang, Zhao-Jie
Huang, Rui-Qi
Zhu, Rong-Rong
Cheng, Li-Ming
Solid lipid nanoparticles loading with curcumin and dexanabinol to treat major depressive disorder
title Solid lipid nanoparticles loading with curcumin and dexanabinol to treat major depressive disorder
title_full Solid lipid nanoparticles loading with curcumin and dexanabinol to treat major depressive disorder
title_fullStr Solid lipid nanoparticles loading with curcumin and dexanabinol to treat major depressive disorder
title_full_unstemmed Solid lipid nanoparticles loading with curcumin and dexanabinol to treat major depressive disorder
title_short Solid lipid nanoparticles loading with curcumin and dexanabinol to treat major depressive disorder
title_sort solid lipid nanoparticles loading with curcumin and dexanabinol to treat major depressive disorder
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7996013/
https://www.ncbi.nlm.nih.gov/pubmed/32985484
http://dx.doi.org/10.4103/1673-5374.293155
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