Peters J H, Karpiel A B, Ritter R C, Simasko S M
Department of Veterinary and Comparative Anatomy, College of Veterinary Medicine, Washington State University, Pullman, Washington 99164-6520, USA.
Endocrinology. 2004 Aug;145(8):3652-7. doi: 10.1210/en.2004-0221. Epub 2004 Apr 22.
To test the hypothesis that leptin can directly activate vagal afferent neurons, we used fluorescence imaging to detect acute changes in cytosolic calcium after leptin application to primary cultures of vagal afferent neurons dissociated from adult rat nodose ganglia. We found that approximately 40% of vagal afferent neurons exposed to leptin (40 ng/ml) responded with rapid and reversible increases in cytosolic calcium. These responses were dependent upon extracellular calcium. As previously reported, about 35% of vagal afferents increase cytosolic calcium in response to the gut-peptide cholecystokinin (CCK). A majority (74%) of neurons that responded to CCK also exhibited increases in cytosolic calcium in response to leptin. In addition, synergistic increases in cytosolic calcium were observed when leptin and CCK were applied in combination. These results demonstrate that leptin acts directly on vagal afferent neurons to trigger acute influxes of extracellular calcium. Our results also suggest cooperation between leptin and CCK in the activation of some vagal afferent neurons. Acute activation of vagal afferents by leptin alone and in combination with CCK may contribute to modulation of visceral reflexes and control of food intake.
为了验证瘦素可直接激活迷走神经传入神经元这一假说,我们运用荧光成像技术,检测了将瘦素作用于从成年大鼠结状神经节分离出的迷走神经传入神经元原代培养物后,胞质钙的急性变化。我们发现,约40%暴露于瘦素(40纳克/毫升)的迷走神经传入神经元,其胞质钙会迅速且可逆地增加。这些反应依赖于细胞外钙。如先前报道,约35%的迷走神经传入纤维会因肠肽胆囊收缩素(CCK)而使胞质钙增加。大多数(74%)对CCK有反应的神经元,对瘦素也表现出胞质钙增加。此外,当联合应用瘦素和CCK时,观察到胞质钙有协同增加。这些结果表明,瘦素直接作用于迷走神经传入神经元,引发细胞外钙的急性内流。我们的结果还提示,瘦素与CCK在激活某些迷走神经传入神经元方面存在协同作用。瘦素单独以及与CCK联合对迷走神经传入纤维的急性激活,可能有助于调节内脏反射和控制食物摄入。