Department of Pharmacology, Tokyo Dental College, Chiba 261-8502, Japan.
J Pharmacol Sci. 2011;115(2):221-9. doi: 10.1254/jphs.10282fp. Epub 2011 Jan 26.
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.
外周型苯二氮䓬受体(PBR)和中枢型苯二氮䓬受体(CBR)在唾液腺中发挥作用,抑制啮齿动物唾液分泌。地西泮结合抑制剂(DBI)是 PBR 的内源性配体,可产生神经甾体,调节 CBR 活性。本研究探讨了重复给予地西泮(DZP)对唾液分泌以及 DBI mRNA 和肽表达的影响。此外,还评估了重复给予 DZP 后 PBR 和垂体腺苷酸环化酶激活肽(PACAP)mRNA 的表达,PACAP 是 DBI 启动子的转录调节因子。重复给予而非单次给予 0.4mg/kg DZP 可抑制唾液分泌,并增强大鼠唾液腺中 DBI、PACAP 和 PBR mRNA 的表达,同时增加 DBI 肽的产生。这些结果表明,重复给予 DZP 可刺激 DBI 的产生,从而可能增加 DZP 对唾液分泌的抑制作用。