Morley J E, Flood J F
Geriatric Research, Education and Clinical Center, Sepulveda Veterans Administration Medical Center, CA 91343.
Brain Res. 1989 Aug 7;494(1):129-37. doi: 10.1016/0006-8993(89)90151-0.
Neuropeptide Y (NPY) when administered intracerebroventricularly is a potent stimulator of feeding and drinking in rats. In these studies we demonstrated that, in contrast, in mice NPY inhibits drinking induced by water deprivation and that associated with food intake. In addition, we found that mice failed to respond to the rat dipsogen angiotensin II. Old mice demonstrated hypodipsia compared to young mice and NPY failed to inhibit drinking in older mice. Monosodium glutamate (MSG) administered neonatally produces lesions of the arcuate nucleus, an area rich in NPY cell bodies. NPY inhibited drinking and enhanced feeding in MSG treated mice. NPY also significantly inhibited the intake of water flavored with 8% sucrose and 0.1% quinine. NPY failed to alter ingestion of 0.2% or 5% saline. These studies support the contention that marked species differences exist in the regulation of water intake between rats and mice.
当脑室内注射神经肽Y(NPY)时,它是大鼠进食和饮水的有力刺激物。然而,在这些研究中我们证明,与之相反,在小鼠中NPY会抑制因缺水诱导的饮水以及与食物摄入相关的饮水。此外,我们发现小鼠对大鼠的致渴剂血管紧张素II没有反应。与年轻小鼠相比,老年小鼠表现出低渗性多饮,并且NPY无法抑制老年小鼠的饮水。新生期给予的谷氨酸钠(MSG)会导致富含NPY细胞体的弓状核损伤。NPY抑制了MSG处理小鼠的饮水并增加了其进食。NPY还显著抑制了添加8%蔗糖和0.1%奎宁的水的摄入量。NPY未能改变0.2%或5%盐水的摄入量。这些研究支持了大鼠和小鼠在水摄入调节方面存在显著物种差异这一观点。