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Repeated Levonorgestrel Administration Impairs Cognitive Function via Glutamatergic Transmission and CaMKII-PKA-BDNF Signaling in the Hippocampus of Female Wistar Rats.

PMID: 41446780 · DOI: 10.2147/JEP.S559477 · Journal of experimental pharmacology, 2025 · Halimat Amin Abdulrahim, Noah Adavize Omeiza, Ganiu Jimoh Akorede, Oluwadamilare Iyapo, John Olabode Fatoki, Ben-Azu Ben
📄 Abstract

Levonorgestrel (LNG), a synthetic progestin widely used in emergency contraception, is increasingly taken frequently and often without medical supervision. With rising concerns that repeated exposure to such hormones may adversely affect brain function, this study investigated whether chronic LNG administration impairs cognitive-like behavior and alters key neurochemical pathways in female Wistar rats. Experimental rats were assigned to three groups receiving normal saline (control) or LNG (4 or 8 µg/kg) every alternate day for 60 days. Cognitive performance was assessed using the Morris water maze (MWM) and novel object recognition (NOR) tests. Hippocampal tissues were subsequently analyzed for glutamatergic markers and downstream signaling molecules involved in learning and memory. Chronic LNG exposure (4 and 8 µg/kg) impaired both spatial and non-spatial memory, evidenced by prolonged escape latency and reduced path efficiency in the MWM, along with a decreased discrimination index in the NOR test. Neurochemically, LNG significantly reduced hippocampal levels of glutamate, N-methyl-D-aspartate (NMDA) and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor ligands, protein kinase A (PKA), calcium/calmodulin-dependent kinase II (CaMKII), and brain-derived neurotrophic factor (BDNF), with the 8 µg/kg dose exerting more pronounced effects. Repeated LNG administration leads to notable cognitive deficits, likely mediated by impairments in glutamatergic signaling and downstream molecular pathways essential for synaptic plasticity. These findings underscore potential neurocognitive risks associated with prolonged LNG exposure.

Confidence: 0.21 · 9 полей извлечено
Идентификация (6 полей)
Механизм действия (21 полей)
Mechanism
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Mutations (obesity/lean)
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Activity (obesity)
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Activity temporal
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Energy balance
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Appetite
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Fat metabolism
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Lipolysis
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Thermogenesis
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Muscle metabolism
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Inflammation
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Glucose metabolism
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AA metabolism
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Hormonal pathways
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Cell death
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Adipocyte fibrosis
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Upstream (biochem)
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Upstream (physiol)
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Downstream (biochem)
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Downstream (physiol)
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PTMs
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Экспрессия (8 полей)
Tissue expression
Hippocampus
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In vitro
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In vivo
Female Wistar rats administered levonorgestrel (4 or 8 µg/kg) every alternate day for 60 days; cognitive tests (Morris water maze, novel object recognition) and hippocampal tissue analysis performed.
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In silico
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Genetic association
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Ex vivo
Hippocampal tissues analyzed for glutamatergic markers and signaling molecules (glutamate, NMDA, AMPA, PKA, CaMKII, BDNF).
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Animal model
Female Wistar rats
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Diet/model
Levonorgestrel administration (4 or 8 µg/kg) every alternate day for 60 days
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Клиника (11 полей)
Drug
Levonorgestrel
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Indication
emergency contraception
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Patient subgroups
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Safety concerns
cognitive deficits, impaired spatial and non-spatial memory, reduced hippocampal glutamate, NMDA and AMPA receptor ligands, PKA, CaMKII, BDNF
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Off-target
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Trial stage
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Pharma competitors
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AE severity
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MOA weight loss
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Endpoints
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Approved
True
0.90