Analyses of the Mode of Action of an Alpha-Adrenoceptor Blocker in Substantia Gelatinosa Neurons in Rats.
Adrenergic alpha-Antagonists
/ pharmacology
Animals
Excitatory Postsynaptic Potentials
/ drug effects
Inhibitory Postsynaptic Potentials
/ drug effects
Male
Membrane Potentials
/ drug effects
Naphthalenes
/ pharmacology
Neurons
/ drug effects
Norepinephrine
/ pharmacology
Patch-Clamp Techniques
/ methods
Piperazines
/ pharmacology
Prazosin
/ pharmacology
Rats, Sprague-Dawley
Serotonin
/ pharmacology
Substantia Gelatinosa
/ cytology
Synaptic Transmission
/ drug effects
5-HT
blind patch-clamp recording
inhibitory postsynaptic currents
micturition
naftopidil
noradrenaline
substantia gelatinosa
α1-adrenoceptor
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
06 Sep 2021
06 Sep 2021
Historique:
received:
30
07
2021
revised:
24
08
2021
accepted:
03
09
2021
entrez:
10
9
2021
pubmed:
11
9
2021
medline:
26
10
2021
Statut:
epublish
Résumé
To elucidate why naftopidil increases the frequency of spontaneous synaptic currents in only some substantia gelatinosa (SG) neurons, post-hoc analyses were performed. Blind patch-clamp recording was performed using slice preparations of SG neurons from the spinal cords of adult rats. Spontaneous inhibitory and excitatory postsynaptic currents (sIPSCs and sEPSCs, respectively) were recorded. The ratios of the frequency and amplitude of the sIPSCs and sEPSCs following the introduction of naftopidil compared with baseline, and after the application of naftopidil, serotonin (5-HT), and prazosin, compared with noradrenaline (NA) were evaluated. First, the sIPSC analysis indicated that SG neurons reached their full response ratio for NA at 50 μM. Second, they responded to 5-HT (50 μM) with a response ratio similar to that for NA, but prazosin (10 μM) did not change the sEPSCs and sIPSCs. Third, the highest concentration of naftopidil (100 μM) led to two types of response in the SG neurons, which corresponded with the reactions to 5-HT and prazosin. These results indicate that not all neurons were necessarily activated by naftopidil, and that the micturition reflex may be regulated in a sophisticated manner by inhibitory mechanisms in these interneurons.
Identifiants
pubmed: 34502543
pii: ijms22179636
doi: 10.3390/ijms22179636
pmc: PMC8431806
pii:
doi:
Substances chimiques
Adrenergic alpha-Antagonists
0
Naphthalenes
0
Piperazines
0
Serotonin
333DO1RDJY
naftopidil
R9PHW59SFN
Norepinephrine
X4W3ENH1CV
Prazosin
XM03YJ541D
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Japan Society for the Promotion of Science
ID : JP19K09323, JP15K08667, JP25860431, and JP21600005
Organisme : Japan Science and Technology Agency
ID : JPMJTM20DN
Organisme : Asahi Kasei Pharma Corporation
ID : Asahi Kasei Pharma Corporation
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