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Извлечено: 997 / 997 (100.0%) Средняя confidence: 0.13
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Neuroprotective and neuromodulatory role of agmatine in mitigating simulated microgravity-induced cognitive and behavioral deficits in rats.

PMID: 41565415 · DOI: 10.1016/j.lssr.2025.09.005 · Life sciences in space research, 2026 · Pankaj Neje, Sayli Kulkarni, Shalakha Dabhekar, Brijesh Taksande, Milind Umekar, Shubhada Mangrulkar
📄 Abstract

Extended periods of microgravity during orbital flights can impair astronauts' cognitive abilities, including learning and memory, posing a persistent health concern in the field of aerospace medicine. The study examined the pharmacological effects of agmatine and its influence on simulated neurobehavioral changes in rats under microgravity conditions. Rats were exposed to simulated microgravity (SMG) conditions using the hindlimb unloading (HU) model for 28 days and evaluated for behavioural alterations using the open field test, elevated plus maze, and forced swim test, and cognitive deficits using the novel object recognition test and Morris water maze. Further, brain agmatine levels, neurochemical and structural alterations in the hippocampus, and prefrontal cortex were examined. Chronic agmatine treatment dose-dependently (40 and 80mg/kg) and its endogenous modulation by l-arginine, and aminoguanidine prevented behavioral and cognitive deficits by improving exploratory behaviour, reducing anxiety-depressive-like symptoms, and enhancing cognitive performance. Our findings reported a significant reduction in agmatine levels in the hippocampus and prefrontal cortex in SMG conditions. Agmatine administration and its modulation normalized neurotransmitter imbalances, especially by restoring the reduced levels of gamma-aminobutyric acid, dopamine, and serotonin, along with a reduction of elevated levels of glutamate in SMG conditions. Moreover, agmatine decreased reactive oxygen species production, enhanced hippocampal antioxidant enzyme activities, suppressed pro-inflammatory cytokines (TNF-α, IL-6), and improved IL-10 and brain-derived neurotrophic factor levels in HU rats. Moreover, agmatine and its endogenous modulation preserved neuronal cells of the hippocampus and prefrontal cortex. In conclusion, the present study suggests that agmatine administration and modulation of endogenous agmatine levels effectively mitigate SMG-induced neurological dysregulation through neuroprotection and neuromodulation. Understanding the neurobiological mechanisms underlying these effects opens up new possibilities for creating novel interventions targeting agmatinergic signaling in spaceflight conditions and associated complications.

Confidence: 0.26 · 13 полей извлечено
Идентификация (6 полей)
Target
agmatine
1.00
Alt. target
0.00
Protein family
0.00
Functional class
0.00
Subcellular loc.
0.00
Isoforms (metab/obesity)
0.00
Механизм действия (21 полей)
Mechanism
Agmatine is an endogenous neuromodulator that binds to imidazoline and alpha2-adrenergic receptors, blocks NMDA receptors, and inhibits nitric oxide synthase. It modulates neurotransmitter systems (GABA, dopamine, serotonin, glutamate), reduces oxidative stress, suppresses pro-inflammatory cytokines (TNF-α, IL-6), and increases BDNF and IL-10.
0.90
Mutations (obesity/lean)
0.00
Activity (obesity)
0.00
Activity temporal
0.00
Energy balance
0.00
Appetite
0.00
Fat metabolism
0.00
Lipolysis
0.00
Thermogenesis
0.00
Muscle metabolism
0.00
Inflammation
Agmatine suppresses pro-inflammatory cytokines (TNF-α, IL-6) and increases anti-inflammatory IL-10.
0.90
Glucose metabolism
0.00
AA metabolism
Agmatine is synthesized from L-arginine by arginine decarboxylase and can be degraded by agmatinase. Its endogenous modulation by L-arginine and aminoguanidine (an inhibitor of diamine oxidase) affects agmatine levels.
0.80
Hormonal pathways
0.00
Cell death
Agmatine preserved neuronal cells in the hippocampus and prefrontal cortex under simulated microgravity, suggesting neuroprotection against cell death.
0.80
Adipocyte fibrosis
0.00
Upstream (biochem)
L-arginine (precursor for agmatine synthesis), aminoguanidine (inhibitor of agmatine degradation)
0.80
Upstream (physiol)
0.00
Downstream (biochem)
Neurotransmitters (GABA, dopamine, serotonin, glutamate), reactive oxygen species, antioxidant enzymes, pro-inflammatory cytokines (TNF-α, IL-6), IL-10, BDNF
0.90
Downstream (physiol)
Behavioral and cognitive functions (exploratory behavior, anxiety, depression, learning and memory), neuronal preservation
0.90
PTMs
0.00
Экспрессия (8 полей)
Tissue expression
agmatine levels in hippocampus and prefrontal cortex
0.90
In vitro
0.00
In vivo
Rats exposed to simulated microgravity using hindlimb unloading model for 28 days; behavioral tests: open field test, elevated plus maze, forced swim test, novel object recognition test, Morris water maze; agmatine treatment (40 and 80 mg/kg), l-arginine, aminoguanidine; measured brain agmatine levels, neurochemical and structural alterations in hippocampus and prefrontal cortex
1.00
In silico
0.00
Genetic association
0.00
Ex vivo
0.00
Animal model
Rats, hindlimb unloading model
1.00
Diet/model
Simulated microgravity via hindlimb unloading
1.00
Клиника (11 полей)
Drug
agmatine
1.00
Indication
0.00
Patient subgroups
0.00
Safety concerns
0.00
Off-target
0.00
Trial stage
0.00
Pharma competitors
0.00
AE severity
0.00
MOA weight loss
0.00
Endpoints
0.00
Approved
0.00