Magistretti P J, Hof P, Schorderet M
Département de Pharmacologie, Centre Médical Universitaire, 1211 Geneva Switzerland.
Neurochem Int. 1984;6(6):751-3. doi: 10.1016/0197-0186(84)90006-8.
We have recently observed that noradrenaline potentiates, via the activation of specific ?-receptors, the stimulatory effects of vasoactive intestinal peptide on cyclic-AMP levels. We report here that certain ergot derivatives of the ergopeptine class, such as bromocriptine, ergotamine and codergocrine known to interact with alpha-adrenergic receptors, will also potentiate the effects of VIP on cyclic-AMP levels, without increasing directly the levels of the cyclic nucleotide. To our knowledge, these results demonstrate for the first time the existence of an interaction between a neuropeptide and ergot alkaloids within the cerebral cortex.
我们最近观察到,去甲肾上腺素通过激活特定的β受体,增强了血管活性肠肽对环磷酸腺苷水平的刺激作用。我们在此报告,某些麦角肽类的麦角衍生物,如已知与α-肾上腺素能受体相互作用的溴隐亭、麦角胺和氢化麦角碱,也会增强血管活性肠肽对环磷酸腺苷水平的作用,而不会直接提高环核苷酸的水平。据我们所知,这些结果首次证明了大脑皮层中神经肽与麦角生物碱之间存在相互作用。