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1.
Neurobiol Learn Mem ; 173: 107224, 2020 09.
Article in English | MEDLINE | ID: mdl-32246991

ABSTRACT

The internal globus pallidus (GPi) is one part of basal ganglion nucleuses which play fundamental role in motor function. Recent studies indicated that GPi could modulate emotional processing and learning, but the possible mechanism remains still unknown. In this study, the effects of endopeduncular nucleus (EP, a rodent homolog of GPi) on fear conditioning were tested in rats. GABAA receptor agonist muscimol was bilaterally delivered into the EP 15 min before or immediately after fear conditioning in rats. We found that EP inactivation impaired the acquisition but not consolidation of fear memory in rats. Furthermore, the long-term potentiation (LTP) in hippocampal CA1 area was impaired, and the learning related phosphorylation of α-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid receptor (AMPAR) subunit 1 (GluA1) at the Ser845 site in hippocampus was decreased in muscimol treated group. These results demonstrated that dysfunction of EP impaired hippocampal dependent learning and memory in rats.


Subject(s)
Conditioning, Classical/physiology , Entopeduncular Nucleus/physiology , Fear/physiology , Hippocampus/physiology , Neuronal Plasticity/physiology , Animals , Conditioning, Classical/drug effects , Entopeduncular Nucleus/drug effects , Fear/drug effects , GABA-A Receptor Agonists/pharmacology , Hippocampus/drug effects , Male , Muscimol/pharmacology , Neuronal Plasticity/drug effects , Rats , Rats, Sprague-Dawley
2.
Neurochem Res ; 42(10): 2869-2880, 2017 Oct.
Article in English | MEDLINE | ID: mdl-28536916

ABSTRACT

Advanced maternal or paternal age is associated with increased risks of cognitive and emotional disorders. Chronic stress is also a common experience in human life that causes psychiatric diseases. However, the synergistic effects of these two factors on offspring are rarely studied. In the present study, the offspring of both young (3-4 months) and old (12-14 months) rat parents were given CUMS for 21 days at the age of 4 weeks. The effects of advanced parental age and chronic unpredictable mild stress (CUMS) on emotional and cognitive behaviors and the related cellular mechanisms were investigated by using behavioral and electrophysiological techniques. We found that CUMS decreased sucrose consumption, increased anxiety, and impaired learning and memory in offspring from both old and young breeders. However, advanced parental age impaired fear memory and spatial memory mainly in female offspring. The serum corticosterone of female offspring was lower than males, but advanced parental age significantly elevated serum corticosterone in female offspring in response to electrical foot shocks. In addition, hippocampal LTD was severely impaired in female offspring from older parents. Our results indicated that female offspring from older breeders might be more sensitive to stress, and the hippocampal function was more vulnerable. These results might provide experimental basis for the prevention and treatment of advanced parental age related psychiatric disorders in future.


Subject(s)
Aging/physiology , Corticosterone/blood , Fear/physiology , Hippocampus/metabolism , Prenatal Exposure Delayed Effects , Animals , Excitatory Postsynaptic Potentials/physiology , Female , Male , Neuronal Plasticity/physiology , Pregnancy , Rats, Sprague-Dawley , Spatial Memory/physiology , Stress, Psychological/psychology
3.
Behav Brain Res ; 321: 61-68, 2017 03 15.
Article in English | MEDLINE | ID: mdl-28025067

ABSTRACT

The Lateral Habenula (LHb) plays an important role in emotion and cognition. Recent experiments suggest that LHb has functional interaction with the hippocampus and plays an important role in spatial learning. LHb is reciprocally connected with midbrain monoaminergic brain areas such as the ventral tegmental area (VTA). However, the role of dopamine type 1 receptor (D1R) in LHb in learning and memory is not clear yet. In the present study, D1R agonist or antagonist were administered bilaterally into the LHb in rats. We found that both D1R agonist and antagonist impaired the acquisition of contextual fear memory in rats. D1R agonist or antagonist also impaired long term potentiation (LTP) in hippocampal CA3-CA1 synapses in freely moving rats and attenuated learning induced phosphorylation of α-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid receptor (AMPAR) subunit 1 (GluA1) at Ser831 and Ser845 in hippocampus. Taken together, our results suggested that dysfunction of D1R in LHb affected the function of hippocampus.


Subject(s)
CA1 Region, Hippocampal/drug effects , Dopamine Agents/pharmacology , Fear/drug effects , Habenula/drug effects , Long-Term Potentiation/drug effects , Memory/drug effects , 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine/pharmacology , Animals , Benzazepines/pharmacology , CA1 Region, Hippocampal/metabolism , Catheters, Indwelling , Fear/physiology , Habenula/metabolism , Implantable Neurostimulators , Learning/drug effects , Learning/physiology , Long-Term Potentiation/physiology , Male , Memory/physiology , Nootropic Agents/pharmacology , Phosphorylation/drug effects , Rats , Receptors, AMPA/metabolism , Receptors, Dopamine D1/metabolism , Synaptosomes/drug effects , Synaptosomes/metabolism
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