Group I metabotropic glutamate receptors generate two types of intrinsic membrane oscillations in hippocampal oriens/alveus interneurons. (1st September 2018)
- Record Type:
- Journal Article
- Title:
- Group I metabotropic glutamate receptors generate two types of intrinsic membrane oscillations in hippocampal oriens/alveus interneurons. (1st September 2018)
- Main Title:
- Group I metabotropic glutamate receptors generate two types of intrinsic membrane oscillations in hippocampal oriens/alveus interneurons
- Authors:
- Govindaiah, Gubbi
Kang, Young-Jin
Lewis, Hannah Elisabeth Smashey
Chung, Leeyup
Clement, Ethan M.
Greenfield, Lazar John
Garcia-Rill, Edgar
Lee, Sang-Hun - Abstract:
- Abstract: GABAergic interneurons in the hippocampus are critically involved in almost all hippocampal circuit functions including coordinated network activity. Somatostatin-expressing oriens-lacunosum moleculare (O-LM) interneurons are a major subtype of dendritically projecting interneurons in hippocampal subregions (e.g., CA1), and express group I metabotropic glutamate receptors (mGluRs), specifically mGluR1 and mGluR5 . Group I mGluRs are thought to regulate hippocampal circuit functions partially through GABAergic interneurons. Previous studies suggest that a group I/II mGluR agonist produces slow supra-threshold membrane oscillations (<0.1 Hz), which are associated with high-frequency action potential (AP) discharges in O-LM interneurons. However, the properties and underlying mechanisms of these slow oscillations remain largely unknown. We performed whole-cell patch-clamp recordings from mouse interneurons in the stratum oriens/alveus (O/A interneurons) including CA1 O-LM interneurons. Our study revealed that the selective mGluR1/5 agonist (S)-3, 5-dihydroxyphenylglycine (DHPG) induced slow membrane oscillations (<0.1 Hz), which were associated with gamma frequency APs followed by AP-free perithreshold gamma oscillations. The selective mGluR1 antagonist (S)-(+)-α-Amino-4-carboxy-2-methylbenzeneacetic acid (LY367385) reduced the slow oscillations, and the selective mGluR5 antagonist 2-methyl-6-(phenylethynyl)pyridine hydrochloride (MPEP) partially blocked them.Abstract: GABAergic interneurons in the hippocampus are critically involved in almost all hippocampal circuit functions including coordinated network activity. Somatostatin-expressing oriens-lacunosum moleculare (O-LM) interneurons are a major subtype of dendritically projecting interneurons in hippocampal subregions (e.g., CA1), and express group I metabotropic glutamate receptors (mGluRs), specifically mGluR1 and mGluR5 . Group I mGluRs are thought to regulate hippocampal circuit functions partially through GABAergic interneurons. Previous studies suggest that a group I/II mGluR agonist produces slow supra-threshold membrane oscillations (<0.1 Hz), which are associated with high-frequency action potential (AP) discharges in O-LM interneurons. However, the properties and underlying mechanisms of these slow oscillations remain largely unknown. We performed whole-cell patch-clamp recordings from mouse interneurons in the stratum oriens/alveus (O/A interneurons) including CA1 O-LM interneurons. Our study revealed that the selective mGluR1/5 agonist (S)-3, 5-dihydroxyphenylglycine (DHPG) induced slow membrane oscillations (<0.1 Hz), which were associated with gamma frequency APs followed by AP-free perithreshold gamma oscillations. The selective mGluR1 antagonist (S)-(+)-α-Amino-4-carboxy-2-methylbenzeneacetic acid (LY367385) reduced the slow oscillations, and the selective mGluR5 antagonist 2-methyl-6-(phenylethynyl)pyridine hydrochloride (MPEP) partially blocked them. Blockade of nonselective cation-conducting transient receptor potential channels, L-type Ca 2+ channels, or ryanodine receptors all abolished the slow oscillations, suggesting the involvement of multiple mechanisms. Our findings suggest that group I mGluR activation in O/A interneurons may play an important role in coordinated network activity, and O/A interneuron vulnerability to excitotoxicity, in disease states like seizures, is at least in part due to an excessive rise in intracellular Ca 2+ . Highlights: Group I mGluR activation in O/A interneurons produced slow membrane oscillations. Slow oscillations were associated with gamma oscillations. Slow oscillations were mediated by both mGluR1 and mGluR5 . TRP channels and L-type Ca 2+ channels were involved in the slow oscillations. Ryanodine receptors were also involved in the slow oscillations. … (more)
- Is Part Of:
- Neuropharmacology. Volume 139(2018)
- Journal:
- Neuropharmacology
- Issue:
- Volume 139(2018)
- Issue Display:
- Volume 139, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 139
- Issue:
- 2018
- Issue Sort Value:
- 2018-0139-2018-0000
- Page Start:
- 150
- Page End:
- 162
- Publication Date:
- 2018-09-01
- Subjects:
- Somatostatin-expressing interneurons -- Metabotropic glutamate receptors -- Perithreshold membrane oscillations -- Excitotoxicity -- Seizures
ACPD 1S, 3R-1-aminocyclopentane-1, 3-dicarboxylic acid -- ACSF artificial cerebrospinal fluid -- AMPA α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid -- AP action potential -- APV 2-Amino-5-phosphonopentanoic acid -- BAPTA 1, 2-Bis(2-aminophenoxy)ethane-N, N, N′, N′-tetraacetic acid -- CGP55845 (2S)-3-[[(1S)-1-(3, 4-Dichlorophenyl)ethyl]amino-2-hydroxypropyl](phenylmethyl)phosphinic acid hydrochloride -- DHPG (S)-3, 5-dihydroxyphenylglycine -- DIC differential interference contrast -- FFA flufenamic acid -- HEPES 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid -- LY 367385 (S)-(+)-α-Amino-4-carboxy-2-methylbenzeneacetic acid -- mGluR metabotropic glutamate receptor -- MPEP 2-methyl-6-(phenylethynyl)pyridine hydrochloride -- NBQX 2, 3-Dihydroxy-6-nitro-7-sulfamoyl-benzo(F) quinoxaline -- NMDA N-methyl-d-aspartate -- O/A interneurons interneurons in the stratum oriens/alveus -- O-LM interneurons oriens-lacunosum moleculare interneurons -- SR95531 6-Imino-3-(4-methoxyphenyl)-1(6H)-pyridazinebutanoic acid hydrobromide -- TRP channels non-selective transient receptor potential channels -- TTX tetrodotoxin -- 2-APB 2-aminoethoxydiphenylborate
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615.78 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00283908 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.neuropharm.2018.06.035 ↗
- Languages:
- English
- ISSNs:
- 0028-3908
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- Legaldeposit
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