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GLP-1 and Exendin-4 Transiently Enhance GABAA Receptor-Mediated Synaptic and Tonic Currents in Rat Hippocampal CA3 Pyramidal Neurons
被引:80
|作者:
Korol, Sergiy V.
[1
]
Jin, Zhe
[1
]
Babateen, Omar
[1
]
Birnir, Bryndis
[1
]
机构:
[1] Uppsala Univ, Dept Neurosci, Uppsala, Sweden
来源:
基金:
瑞典研究理事会;
关键词:
GLUCAGON-LIKE PEPTIDE-1;
CENTRAL-NERVOUS-SYSTEM;
ALZHEIMERS-DISEASE;
COGNITIVE IMPAIRMENT;
BRAIN;
INSULIN;
MEMORY;
PLASTICITY;
MODEL;
MICE;
D O I:
10.2337/db14-0668
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Glucagon-like peptide-1 (GLP-1) is a hormone that stimulates insulin secretion. Receptors for GLP-1 are also found in the brain, including the hippocampus, the center for memory and learning. Diabetes is a risk factor for decreased memory functions. We studied effects of GLP-1 and exendin-4, a GLP-1 receptor agonist, on gamma-aminobutyric acid (GABA) signaling in hippocampal CA3 pyramidal neurons. GABA is the main inhibitory neurotransmitter and decreases neuronal excitability. GLP-1 (0.01-1 nmol/L) transiently enhanced synaptic and tonic currents, and the effects were blocked by exendin (9-39). Ten pmol/L GLP-1 increased both the spontaneous inhibitory postsynaptic current (sIPSC) amplitudes and frequency by a factor of 1.8. In 0.1, 1 nmol/L GLP-1 or 10, 50, or 100 nmol/L exendin-4, only the sIPSC frequency increased. The tonic current was enhanced by 0.01-1 nmol/L GLP-1 and by 0.5-100 nmol/L exendin-4. When action potentials were inhibited by tetrodotoxin (TTX), inhibitory postsynaptic currents decreased and currents were no longer potentiated by GLP-1 or exendin-4. In contrast, although the tonic current decreased in TTX, it was still enhanced by GLP-1 or exendin-4. The results demonstrate GLP-1 receptor regulation of hippocampal function and are consistent with GLP-1 receptor agonists enhancing GABA(A) signaling by pre- and postsynaptic mechanisms.
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页码:79 / 89
页数:11
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