Widdowson P S, Halaris A E
Department of Psychiatry, Case Western Reserve University, Cleveland, OH.
Peptides. 1990 Jul-Aug;11(4):661-5. doi: 10.1016/0196-9781(90)90176-6.
Neuropeptide Y (NPY) (1 microM) significantly reduced the basal cAMP concentration in slices of rat frontal cortex. However, NPY (10(-9)-10(-6)M) did not alter the isoproterenol-stimulated (10(-9)-10(-5) M) accumulation of cAMP in the frontal cortical slices, showing that Y2 NPY receptors do not modulate the beta-adrenoceptor-stimulated adenylase cyclase activity. NPY (10(-8)-2.5 x 10(-5) M) was also demonstrated to stimulate inositol phosphate accumulation in rat frontal cortex slices in a dose-dependent manner. However, NPY (1 microM) did not potentiate the ability of phenylephrine (5 X 10(-8)-10(-4) M), an alpha 1-adrenoceptor agonist, to stimulate inositol phosphate hydrolysis. The combined effects of phenylephrine and NPY (1 microM) on inositol phosphate hydrolysis were additive, suggesting that the alpha 1-adrenoceptor and NPY Y1 receptor sites are located on different postsynaptic sites in rat frontal cortex. This study demonstrates the existence of both Y2 and Y1 NPY receptors in the rat frontal cortex based on second messenger systems, but there does not appear to be an interaction of NPY with either alpha 1- or beta-adrenoceptors.
神经肽Y(NPY)(1微摩尔)显著降低了大鼠额叶皮质切片中的基础环磷酸腺苷(cAMP)浓度。然而,NPY(10⁻⁹ - 10⁻⁶摩尔/升)并未改变异丙肾上腺素刺激(10⁻⁹ - 10⁻⁵摩尔/升)的额叶皮质切片中cAMP的积累,表明Y2 NPY受体不会调节β - 肾上腺素能受体刺激的腺苷酸环化酶活性。NPY(10⁻⁸ - 2.5×10⁻⁵摩尔/升)也被证明以剂量依赖的方式刺激大鼠额叶皮质切片中肌醇磷酸的积累。然而,NPY(1微摩尔)并未增强苯肾上腺素(5×10⁻⁸ - 10⁻⁴摩尔/升)(一种α1 - 肾上腺素能受体激动剂)刺激肌醇磷酸水解的能力。苯肾上腺素和NPY(1微摩尔)对肌醇磷酸水解的联合作用是相加的,表明α1 - 肾上腺素能受体和NPY Y1受体位点位于大鼠额叶皮质的不同突触后位点。本研究基于第二信使系统证明了大鼠额叶皮质中存在Y2和Y1 NPY受体,但NPY似乎与α1 - 或β - 肾上腺素能受体均无相互作用。