Widdowson P S, Masten T, Halaris A E
Department of Psychiatry, Case Western Reserve University, Cleveland, OH.
Peptides. 1991 Jan-Feb;12(1):71-5. doi: 10.1016/0196-9781(91)90169-p.
Neuropeptide Y significantly reduced the potassium-stimulated release of [3H]norepinephrine [( 3H]NE) from slices of rat hippocampus, hypothalamus and frontal cortex but not from slices of parieto-occipital cortex. The NPY-induced inhibition of [3H]NE release from frontal cortical slices was concentration dependent, reaching statistical significance at 10 nM. The alpha 2-adrenoceptor partial agonist, clonidine, also reduced the potassium-stimulated release of [3H]NE. The combination of NPY and clonidine in hippocampal slices produced a greater reduction of stimulated [3H]NE release than either of the two compounds alone, suggesting a potentiation of their activity, whereas in frontal cortical slices, the effect was additive. When NPY and clonidine were added to frontal cortical slices, they independently produced a significant concentration-dependent reduction in forskolin-stimulated cAMP accumulation. However, NPY and clonidine combined did not produce a further reduction in forskolin-induced cAMP accumulation than either compound when used alone. These results suggest that the ability of NPY to potentiate alpha 2-adrenoceptor-induced inhibition of [3H]NE release in discrete brain regions does not depend on the reductions in cAMP.
神经肽Y能显著降低钾离子刺激引起的大鼠海马、下丘脑和额叶皮质切片中[3H]去甲肾上腺素([3H]NE)的释放,但对顶枕叶皮质切片中[3H]NE的释放没有影响。神经肽Y对额叶皮质切片中[3H]NE释放的抑制作用呈浓度依赖性,在10 nM时具有统计学意义。α2 -肾上腺素能受体部分激动剂可乐定也能降低钾离子刺激引起的[3H]NE释放。在海马切片中,神经肽Y和可乐定联合使用比单独使用这两种化合物中的任何一种对刺激的[3H]NE释放的降低作用更大,表明它们的活性具有增强作用;而在额叶皮质切片中,二者的作用是相加的。当将神经肽Y和可乐定添加到额叶皮质切片中时,它们各自独立地引起福斯高林刺激的环磷酸腺苷(cAMP)积累显著的浓度依赖性降低。然而,神经肽Y和可乐定联合使用时,对福斯高林诱导的cAMP积累的降低作用并不比单独使用任何一种化合物时更大。这些结果表明,神经肽Y在离散脑区增强α2 -肾上腺素能受体诱导的对[3H]NE释放的抑制作用的能力并不依赖于cAMP的降低。