Sjöqvist A, Fahrenkrug J, Hemlin M, Jodal M, Lundgren O
Acta Physiol Scand. 1985 Dec;125(4):693-8. doi: 10.1111/j.1748-1716.1985.tb07772.x.
Close i.a. infusions of ATP were made to the stomach, the small intestine or the colon in the cat. The vascular reactions were followed by recording arterial pressure and total venous outflow continuously and the release of VIP was estimated intermittently from arterio-venous concentration differences and blood flow. In all experiments ATP caused a vasodilatation and an increased release of VIP into blood. In control experiments it was shown that evoking a vasodilatation of the same magnitude by close i.a. infusions of isoprenaline or papaverine did not evoke any similar release of VIP. It is concluded that the infused ATP released VIP from the different parts of the gastrointestinal tract. Possible mechanisms underlying this effect are tentatively discussed.
在猫身上,将三磷酸腺苷(ATP)经腹腔内近距离注入胃、小肠或结肠。通过持续记录动脉血压和总静脉流出量来跟踪血管反应,并根据动静脉浓度差和血流量间歇性地估算血管活性肠肽(VIP)的释放量。在所有实验中,ATP均引起血管舒张,并使VIP释放到血液中的量增加。在对照实验中发现,经腹腔内近距离注入异丙肾上腺素或罂粟碱引起相同程度的血管舒张时,并未引发任何类似的VIP释放。得出的结论是,注入的ATP从胃肠道的不同部位释放出VIP。并初步讨论了这种作用潜在的可能机制。