Anselmi Laura, Stella Salvatore L, Brecha Nicholas C, Sternini Catia
CURE Digestive Diseases Research Center, Digestive Diseases Division, Veterans Administration Greater Los Angeles Healthcare System, Los Angeles, California 90073, USA.
J Neurosci Res. 2009 Apr;87(5):1107-14. doi: 10.1002/jnr.21923.
Galanin activates three receptors, the galanin receptor 1 (GalR1), GalR2, and GalR3. In the gastrointestinal tract, GalR1 mediates the galanin inhibition of cholinergic transmission to the longitudinal muscle and reduction of peristalsis efficiency in the small intestine. Galanin has also been shown to inhibit depolarization-evoked Ca2+ increases in cultured myenteric neurons. Because GalR1 immunoreactivity is localized to cholinergic myenteric neurons, we hypothesized that this inhibitory action of galanin on myenteric neurons is mediated by GalR1. We investigated the effect of galanin 1-16, which has high affinity for GalR1 and GalR2, in the presence or absence of the selective GalR1 antagonist, RWJ-57408, and of galanin 2-11, which has high affinity for GalR2 and GalR3, on Ca2+ influx through voltage-dependent Ca2+ channels in cultured myenteric neurons. Myenteric neurons were loaded with fluo-4 and depolarized by high K+ concentration to activate voltage-dependent Ca2+ channels. Intracellular Ca2+ levels were quantified with confocal microscopy. Galanin 1-16 (0.01-1 microM) inhibited the depolarization-evoked Ca2+ increase in a dose-dependent manner with an EC(50) of 0.172 microM. The selective GalR1 antagonist, RWJ-57408 (10 microM), blocked the galanin 1-16 (1 microM)-mediated inhibition of voltage-dependent Ca2+ channel. By contrast, the GalR2/GalR3 agonist, galanin 2-11 did not affect the K+-evoked Ca2+ influx in myenteric neurons. GalR1 immunoreactivity was localized solely to myenteric neurons in culture, as previously observed in intact tissue. These findings indicate that the inhibition of depolarization-evoked Ca2+ influx in myenteric neurons in culture is mediated by GalR1 and confirm the presence of functional GalR1 in the myenteric plexus. This is consonant with the hypothesis that GalR1 mediates galanin inhibition of transmitter release from myenteric neurons.
甘丙肽激活三种受体,即甘丙肽受体1(GalR1)、GalR2和GalR3。在胃肠道中,GalR1介导甘丙肽对胆碱能传递至纵行肌的抑制作用以及小肠蠕动效率的降低。甘丙肽还被证明可抑制培养的肠肌间神经元中去极化诱发的Ca2+升高。由于GalR1免疫反应性定位于胆碱能肠肌间神经元,我们推测甘丙肽对肠肌间神经元的这种抑制作用是由GalR1介导的。我们研究了对GalR1和GalR2具有高亲和力的甘丙肽1-16在存在或不存在选择性GalR1拮抗剂RWJ-57408的情况下,以及对GalR2和GalR3具有高亲和力的甘丙肽2-11对培养的肠肌间神经元中通过电压依赖性Ca2+通道的Ca2+内流的影响。肠肌间神经元用fluo-4加载,并通过高钾浓度去极化以激活电压依赖性Ca2+通道。用共聚焦显微镜对细胞内Ca2+水平进行定量。甘丙肽1-16(0.01-1 microM)以剂量依赖性方式抑制去极化诱发的Ca2+升高,EC(50)为0.172 microM。选择性GalR1拮抗剂RWJ-57408(10 microM)阻断了甘丙肽1-16(1 microM)介导的对电压依赖性Ca2+通道的抑制作用。相比之下,GalR2/GalR3激动剂甘丙肽2-11对肠肌间神经元中钾离子诱发的Ca2+内流没有影响。如先前在完整组织中观察到的那样,GalR1免疫反应性仅定位于培养的肠肌间神经元。这些发现表明,培养的肠肌间神经元中去极化诱发的Ca2+内流的抑制作用是由GalR1介导的,并证实了肠肌丛中存在功能性GalR1。这与GalR1介导甘丙肽对肠肌间神经元递质释放的抑制作用这一假设一致。