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Aggressive behaviors are one of the most important negative behaviors that seriously endangers human health. Also, the central para-inflammation of microglia triggered by stress can affect neurological function, plasticity, and behavior. NLRP3 integrates stress-related signals and is a key driver of this neural para-inflammation. However, it is unclear whether the NLRP3 inflammasome is implicated in the development of aggressive behaviors. First, aggressive behavior model mice were established using the resident intruder paradigm. Then, aggressive behaviors were determined with open-field tests (OFT), elevated plus-maze (EPM), and aggressive behavior tests (AT). Moreover, the expression of P2X7R and NLRP3 inflammasome complexes were assessed by immunofluorescence and Western blot. The levels of NLRP3 and inflammatory cytokines were evaluated using enzyme-linked immunosorbent assay (ELISA) kits. Finally, nerve plasticity damage was observed by immunofluorescence, transmission electron microscope, and BrdU staining. Overall, the resident intruder paradigm induced aggressive behaviors, activated the hippocampal P2X7R and NLRP3 inflammasome, and promoted the release of proinflammatory cytokines IL-1β in mice. Moreover, NLRP3 knockdown, administration of P2X7R antagonist (A804598), and IL-1β blocker (IL-1Ra) prevented NLRP3 inflammasome-driven inflammatory responses and ameliorated resident intruder paradigm-induced aggressive behaviors. Also, the resident intruder paradigm promoted the activation of mouse microglia, damaging synapses in the hippocampus, and suppressing hippocampal regeneration in mice. Besides, NLRP3 knockdown, administration of A804598, and IL-1Ra inhibited the activation of microglia, improved synaptic damage, and restored hippocampal regeneration. The NLRP3 inflammasome-driven inflammatory response contributed to resident intruder paradigm-induced aggressive behavior, which might be related to neuroplasticity. Therefore, the NLRP3 inflammasome can be a potential target to treat aggressive behavior-related mental illnesses.
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http://dx.doi.org/10.3389/fphar.2023.974905 | DOI Listing |
Yakugaku Zasshi
August 2025
Department of Neurophysiology & Brain Science, Graduate School of Medical Sciences, Nagoya City University.
Monosodium glutamate (MSG), an umami substance, activates the gut-brain axis via vagus nerves. However, the brain mechanism involved in the effect of MSG on aggression during the developmental period has not been clarified. SHR/Izm, a known model of attention-deficit hyperactivity disorder (ADHD), was used to investigate the effect of MSG oral ingestion (60 mM solution) on aggression.
View Article and Find Full Text PDFCell Rep
July 2025
Department of Neuroscience, Zuckerman Mind Brain Behavior Institute, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY 10027, USA; Department of Pharmacology, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY 10027, USA.
Social aggression, a fundamental motivated behavior, is driven by external stimuli and internal states. Since early ethological studies, social novelty has been recognized as a key external trigger, with strangers eliciting increased aggression compared with familiar conspecifics. While progress has been made in identifying the neural bases of aggression and social novelty recognition (SNR) memory, the mechanisms linking social novelty detection to aggression remain unknown.
View Article and Find Full Text PDFPharmacol Biochem Behav
September 2025
Hebei Key Laboratory of Early Life Health Promotion (SZX202419), Hebei Medical University, Shijiazhuang 050031, China; Neuroscience Research Center, Institute of Medical and Health Science, Hebei Medical University, Shijiazhuang 050017, China. Electronic address:
Chronic stress has been widely reported to be related to alterations in emotional behaviors of individuals, yet the potential effects of post-weaning stress (PWS) and the associated mechanisms are still poorly understood. Mitochondria-associated endoplasmic reticulum membranes (MAM) play crucial roles in cellular energy metabolism, calcium homeostasis, lipid synthesis, and have been highlighted in recent studies for their importance in the nervous system. This study aims to explore how PWS affects behaviors, especially aggressive behavior and social hierarchy, and whether MAM plays a role in this process in ICR mice.
View Article and Find Full Text PDFSci Rep
July 2025
Medical Plants Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran.
Social isolation stress can alter liver function. This study examined the effects of N-acetylcysteine (NAC) on biochemical and genetic liver changes in mice under social isolation stress. Ten male and ten female mice were individually placed in Plexiglas cages for mating.
View Article and Find Full Text PDFSci Rep
July 2025
Department of Behavioral Neuroscience and Drug Development, Maj Institute of Pharmacology, Polish Academy of Sciences, 12 Smetna Street, 31-343, Kraków, Poland.
Serotonin is a crucial neurotransmitter implicated in various physiological processes. Dysregulation of the serotonergic system, particularly in early life, may be associated with neuropsychiatric disorders, including autism spectrum disorder. This study utilises a rat model lacking the central serotonin-synthesising enzyme tryptophan hydroxylase 2 (TPH2) to investigate the effects of brain serotonin depletion on core autism-related behaviours.
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