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The Antidepressant Mirtazapine Activates Hepatic Macrophages, Facilitating Pathogen Clearance While Limiting Tissue Damage in Mice.
- Source :
-
Frontiers in immunology [Front Immunol] 2020 Nov 03; Vol. 11, pp. 578654. Date of Electronic Publication: 2020 Nov 03 (Print Publication: 2020). - Publication Year :
- 2020
-
Abstract
- Background and Aims: Mirtazapine is an atypical antidepressant with antagonist activity for serotonin and histamine receptors. Clinical and experimental evidence suggests that, in addition to treating depression, mirtazapine also alters liver innate immunity and suppresses immune-driven hepatic macrophage activation. Liver macrophages, Kupffer cells, represent the largest collection of fixed macrophages in the body and are critical in regulating hepatic immunity. In addition to their capacity to regulate inflammation, Kupffer cells are key sentinels for clearing blood-borne pathogens, preventing their dissemination within the body. This process involves pathogen capture, phagocytosis, and activation-induced killing via reactive oxygen species (ROS) production. Therefore, we speculated that mirtazapine might adversely alter Kupffer cell pathogen-associated activation and killing.<br />Methods: Mice were treated with mirtazapine and time-dependent changes in Kupffer cells were characterized using intravital microscopy. Macrophage and neutrophil responses, bacterial dissemination, and liver damage were assessed following i.v. infection with a pathogenic strain of S. aureus .<br />Results: Mirtazapine rapidly (within 1.5 h) activates Kupffer cells, indicated by a loss of elongated shape with cellular rounding. However, this shape change did not result in impaired pathogen capture function, and, in fact, generated enhanced ROS production in response to S. aureus -induced sepsis. Neutrophil dynamics were altered with reduced cellular recruitment to the liver following infection. Bacterial dissemination post-intravenous administration was not altered by mirtazapine treatment; however, hepatic abscess formation was significantly reduced.<br />Conclusions: Mirtazapine rapidly activates Kupffer cells, associated with preserved bacterial capture functions and enhanced ROS generation capacity. Moreover, these changes in Kupffer cells were linked to a beneficial reduction in hepatic abscess size. In contrast to our initial speculation, mirtazapine may have beneficial effects in sepsis and warrants further exploration.<br /> (Copyright © 2020 Davis, Almishri, Jenne and Swain.)
- Subjects :
- Animals
Disease Models, Animal
Host-Pathogen Interactions
Kupffer Cells metabolism
Kupffer Cells microbiology
Liver metabolism
Liver microbiology
Liver pathology
Liver Abscess metabolism
Liver Abscess microbiology
Liver Abscess pathology
Mice, Inbred C57BL
Neutrophil Infiltration drug effects
Neutrophils drug effects
Neutrophils metabolism
Neutrophils microbiology
Reactive Oxygen Species metabolism
Staphylococcal Infections metabolism
Staphylococcal Infections microbiology
Staphylococcal Infections pathology
Time Factors
Antidepressive Agents pharmacology
Kupffer Cells drug effects
Liver drug effects
Liver Abscess drug therapy
Macrophage Activation drug effects
Mirtazapine pharmacology
Phagocytosis drug effects
Staphylococcal Infections drug therapy
Staphylococcus aureus pathogenicity
Subjects
Details
- Language :
- English
- ISSN :
- 1664-3224
- Volume :
- 11
- Database :
- MEDLINE
- Journal :
- Frontiers in immunology
- Publication Type :
- Academic Journal
- Accession number :
- 33250892
- Full Text :
- https://doi.org/10.3389/fimmu.2020.578654