Vatta M S, Presas M, Bianciotti L G, Zarrabeitia V, Fernández B E
Cátedra de Fisiopatología, Facultad de Farmacia y Bioquimíca, Universidad de Buenos Aires, Argentina.
Regul Pept. 1996 Sep 16;65(3):175-84. doi: 10.1016/0167-0115(96)00090-0.
We previously reported that atrial natriuretic factor (ANF) regulates catecholamine metabolism in the central nervous system. ANF, B and C types natriuretic peptides (BNP and CNP) also play a regulatory role in body fluid homeostasis, cardiovascular activity and hormonal and neuro-hormonal secretions. The aim of the present work was to investigate BNP and CNP effects on the uptake and release of norepinephrine (NE) in rat hypothalamic slices incubated in vitro. Results showed that BNP (100 nM) and CNP (1, 10 and 100 nM) enhanced total and neuronal [3H]NE uptake but did not modify non-neuronal uptake. BNP (100 nM) and CNP (1 nM) caused a rapid increase in NE uptake (1 min), which was sustained for 60 min. BNP (100 nM) did not modify the intracellular distribution of NE; however, 1 nM CNP increased the granular store and decreased the cytosolic pool of NE. BNP (100 nM) and CNP (1, 10 and 100 nM), diminished spontaneous NE release. In addition, BNP (1, 10, 100 nM) and CNP (1, 10 and 100 pM, as well as 1, 10 and 100 nM) reduced NE output induced by 25 mM KCl. These results suggest that BNP and CNP may be involved in the regulation of several central as well as peripheral physiological functions through the modulation of noradrenergic neurotransmission at the presynaptic neuronal level. Present results provide evidence to consider CNP as the brain natriuretic peptide since physiological concentrations of this peptide (pM) diminished NE evoked release.
我们之前报道过,心房利钠因子(ANF)可调节中枢神经系统中的儿茶酚胺代谢。ANF、B型和C型利钠肽(BNP和CNP)在体液平衡、心血管活动以及激素和神经激素分泌方面也发挥着调节作用。本研究的目的是探讨BNP和CNP对体外培养的大鼠下丘脑切片中去甲肾上腺素(NE)摄取和释放的影响。结果显示,BNP(100 nM)和CNP(1、10和100 nM)可增强总的和神经元的[3H]NE摄取,但不改变非神经元摄取。BNP(100 nM)和CNP(1 nM)可使NE摄取迅速增加(1分钟),并持续60分钟。BNP(100 nM)不改变NE的细胞内分布;然而,1 nM CNP可增加颗粒储存并减少NE的胞质池。BNP(100 nM)和CNP(1、10和100 nM)可减少NE的自发释放。此外,BNP(1、10、100 nM)和CNP(1、10和100 pM以及1、10和100 nM)可降低由25 mM KCl诱导的NE释放。这些结果表明,BNP和CNP可能通过在突触前神经元水平调节去甲肾上腺素能神经传递,参与多种中枢和外周生理功能的调节。目前的结果为将CNP视为脑利钠肽提供了证据,因为该肽的生理浓度(pM)可减少NE诱发的释放。