Analyses of the Mode of Action of an Alpha-Adrenoceptor Blocker in Substantia Gelatinosa Neurons in Rats.


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
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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Auteurs

Daisuke Uta (D)

Department of Applied Pharmacology, Faculty of Pharmaceutical Sciences, University of Toyama, Toyama 930-0194, Japan.

Tsuyoshi Hattori (T)

Department of Medical Affairs, Asahi Kasei Pharma Corporation, Tokyo 100-0006, Japan.

Megumu Yoshimura (M)

Department of Orthopedic Surgery, Nakamura Hospital, Fukuoka 822-0002, Japan.

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Classifications MeSH