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Diazepam enhances production of diazepam-binding inhibitor (DBI), a negative saliva secretion regulator, localized in rat salivary gland.
- Source :
-
Journal of pharmacological sciences [J Pharmacol Sci] 2011; Vol. 115 (2), pp. 221-9. Date of Electronic Publication: 2011 Jan 26. - Publication Year :
- 2011
-
Abstract
- Peripheral-type benzodiazepine receptor (PBR) and central-type benzodiazepine receptor (CBR) in salivary gland play a role in the inhibitory regulation of salivary secretion in rodents. Diazepam-binding inhibitor (DBI), an endogenous ligand for PBR, produces neurosteroids, which modulate CBR activity. In this study, we investigated the effect of repetitive administration of diazepam (DZP) on salivary secretion and expression of DBI mRNA and peptide. Moreover, mRNA expression of PBR and pituitary adenylate cyclase-activating polypeptide (PACAP), a transcriptional regulator for DBI promoter, was evaluated after repetitive administration of DZP. Repetitive administration, but not single administration, of 0.4 mg/kg DZP caused inhibition of salivary secretion and enhanced expression of DBI, PACAP, and PBR mRNA in rat salivary gland, with an increase in production of DBI peptide. These results suggest that repetitive administration of DZP stimulates DBI production, which may result in an increase in the suppressive effect of DZP on salivary secretion.
- Subjects :
- Animals
Carrier Proteins metabolism
Diazepam administration & dosage
Dose-Response Relationship, Drug
Drug Evaluation, Preclinical
Male
Pituitary Adenylate Cyclase-Activating Polypeptide metabolism
Random Allocation
Rats
Rats, Wistar
Receptors, GABA-A metabolism
Diazepam pharmacology
Diazepam Binding Inhibitor metabolism
Saliva metabolism
Salivary Glands drug effects
Salivary Glands metabolism
Salivation drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1347-8648
- Volume :
- 115
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Journal of pharmacological sciences
- Publication Type :
- Academic Journal
- Accession number :
- 21282931
- Full Text :
- https://doi.org/10.1254/jphs.10282fp