Ventimiglia María S, Rodríguez Myrian R, Elverdín Juan C, Davio Carlos A, Vatta Marcelo S, Bianciotti Liliana G
Cátedras de Fisiopatología, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires Junin 956 Piso 5 (1113AAD) Buenos Aires, Argentina.
Regul Pept. 2008 Oct 9;150(1-3):43-9. doi: 10.1016/j.regpep.2008.03.003. Epub 2008 Mar 25.
We previously reported that intravenously administered atrial natriuretic factor (ANF) induced no salivation but enhanced agonist-evoked secretion in submandibular glands. The gene expression of ANF and natriuretic peptide receptors (NPR) was later reported in the glands. In the present study we sought to establish the intracellular signalling mechanisms underlying ANF modulation of salivary secretion. Fasted rats were prepared with submandibular duct and femoral cannulation. Dose-response curves to methacholine (MC) and norepinephrine (NE) were performed in the presence of cANP (4-23 amide) (selective NPR-C agonist) and ANF. Local injection of the agonist or ANF-induced no salivation, but enhanced MC and NE-evoked secretion. ANF and cANP (4-23 amide) enhanced phosphoinositide turnover being the effect abolished by U73122 (PLC inhibitor). Further ANF and cANP (4-23 amide) decreased basal cAMP content but failed to affect isoproterenol or forskolin-evoked cAMP. ANF response was inhibited by pertussis toxin and mimicked by cANP (4-23 amide) strongly supporting NPR-C activation. ANF-induced cAMP reduction was abolished by PLC and PKC inhibitors. The content of cGMP was dose dependently stimulated by ANF but not modified by cANP (4-23 amide). These findings support that ANF through NPR-C receptors coupled to PLC activation and adenylyl cyclase inhibition interacts with sialogogic agonists in the submandibular gland to potentiate salivation.
我们之前报道过,静脉注射心钠素(ANF)不会引起唾液分泌,但会增强下颌下腺中激动剂诱发的分泌。随后有报道称该腺体中存在ANF和利钠肽受体(NPR)的基因表达。在本研究中,我们试图确立ANF调节唾液分泌的细胞内信号传导机制。对禁食大鼠进行下颌下腺导管和股动脉插管制备。在存在cANP(4 - 23酰胺)(选择性NPR - C激动剂)和ANF的情况下,进行对乙酰甲胆碱(MC)和去甲肾上腺素(NE)的剂量反应曲线实验。局部注射激动剂或ANF不会引起唾液分泌,但会增强MC和NE诱发的分泌。ANF和cANP(4 - 23酰胺)增强了磷酸肌醇的周转,而U73122(磷脂酶C抑制剂)可消除该效应。此外,ANF和cANP(4 - 23酰胺)降低了基础cAMP含量,但未能影响异丙肾上腺素或福斯高林诱发的cAMP。百日咳毒素可抑制ANF反应,而cANP(4 - 23酰胺)可模拟该反应,这有力地支持了NPR - C的激活。PLC和PKC抑制剂可消除ANF诱导的cAMP降低。ANF可剂量依赖性地刺激cGMP含量,但cANP(4 - 23酰胺)不会改变其含量。这些发现支持ANF通过与PLC激活和腺苷酸环化酶抑制偶联的NPR - C受体,在下颌下腺中与促唾液分泌激动剂相互作用以增强唾液分泌。