Bitran M, Tapia W, Eugenín E, Orio P, Boric M P
Departamento de Ciencias Fisiológicas, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
Brain Res. 1999 Dec 18;851(1-2):87-93. doi: 10.1016/s0006-8993(99)02123-x.
We aimed at characterizing the receptor subtype and the signaling pathway involved in the inhibitory effect of neuropeptide Y on the release of endogenous noradrenaline from rat hypothalamus. Slices of hypothalamus were stimulated with two trains of electrical pulses, and the release of noradrenaline and nitric oxide was measured. The electrical stimulation of hypothalamic slices induced a consistent release of both endogenous noradrenaline and NO. Neuropeptide Y inhibited concentration dependently the stimulated noradrenaline release. Similarly, agonists for neuropeptide Y Y1, Y2 and Y5 receptors inhibited noradrenaline release, albeit with a potency lower than neuropeptide Y. GW1229, a selective neuropeptide Y Y1 receptor antagonist counteracted the effect of neuropeptide Y, but not that of PYY-(3-36), an agonist active at neuropeptide Y Y5 and Y2 receptors. These results indicate that the inhibitory effect of neuropeptide Y is likely mediated by several receptor subtypes, including neuropeptide Y Y1, Y5 and possibly Y2 receptors. One microM NPY significantly enhanced NO release induced by the electrical stimulation. NG-monomethyl-L-arginine, an inhibitor of nitric oxide synthase, abolished NO release and blocked the inhibitory effect of neuropeptide Y on noradrenaline release. We conclude that nitric oxide participates in the signaling pathway of neuropeptide Y in the rat hypothalamus.
我们旨在确定神经肽Y对大鼠下丘脑内源性去甲肾上腺素释放的抑制作用所涉及的受体亚型和信号通路。用两串电脉冲刺激下丘脑切片,并测量去甲肾上腺素和一氧化氮的释放。下丘脑切片的电刺激诱导了内源性去甲肾上腺素和一氧化氮的一致释放。神经肽Y浓度依赖性地抑制刺激引起的去甲肾上腺素释放。同样,神经肽Y Y1、Y2和Y5受体的激动剂也抑制去甲肾上腺素释放,尽管其效力低于神经肽Y。选择性神经肽Y Y1受体拮抗剂GW1229可抵消神经肽Y的作用,但不能抵消PYY-(3-36)(一种对神经肽Y Y5和Y2受体有活性的激动剂)的作用。这些结果表明,神经肽Y的抑制作用可能由几种受体亚型介导,包括神经肽Y Y1、Y5以及可能的Y2受体。1微摩尔神经肽Y显著增强了电刺激诱导的一氧化氮释放。一氧化氮合酶抑制剂NG-甲基-L-精氨酸消除了一氧化氮释放,并阻断了神经肽Y对去甲肾上腺素释放的抑制作用。我们得出结论,一氧化氮参与了大鼠下丘脑神经肽Y的信号通路。