Utsumi Hiroyoshi, Iwakiri Ryuichi, Wu Bin, Fujise Takehiro, Sakata Hiroyuki, Shimoda Ryo, Amemori Sadahiro, Tsunada Seiji, Ootani Akifumi, Fujimoto Kazuma
Department of Internal Medicine, Saga Medical School, 5-1-1 Nabeshima, Saga 849-8501, Japan.
Exp Biol Med (Maywood). 2003 Nov;228(10):1239-44. doi: 10.1177/153537020322801022.
The localization of leptin and leptin receptors in the stomach and small intestine has been reported. Their function is still unknown, although leptin is a hormone that regulates appetite and fat-related metabolism. The small intestine is one of the important organs for regulating metabolism. The purpose of the present study was to investigate whether leptin regulates apoptosis in the small intestinal mucosa. Intestinal apoptosis was evaluated by percent fragmented DNA, electrophoresis, TUNEL staining, and western blotting analysis of caspase-3. Mucosal apoptosis in the rat jejunum and ileum was evaluated at 0, 3, 6, 12, and 24 hrs after injection. Rats were tested after ad libitum feeding and 24-hr fasting to exclude the anorectic effect of leptin. Leptin was injected intraperitoneally (ip) at a dose of 200 microg/rat and infused into the rat third cerebroventricle (icv) at a dose of 8 microg/rat. Leptin at a dose of 8 microg/rat significantly induced intestinal apoptosis in the small intestine at 3 and 6 hrs after icv administration in both ad libitum feeding and 24-hr fasted rats. This increase in apoptosis was not attenuated by vagotomy. Intestinal apoptosis increased 12 and 24 hrs after ip injection of leptin at a dose of 200 microg/rat. The peak of the increase in apoptosis in icv rats appeared earlier than that in ip rats. Leptin induced jejunal and ileal mucosal apoptosis in the rat, indicating that leptin might control intestinal function through the regulation of intestinal apoptosis.
已有报道称瘦素及其受体在胃和小肠中的定位情况。尽管瘦素是一种调节食欲和脂肪相关代谢的激素,但其功能仍不明确。小肠是调节新陈代谢的重要器官之一。本研究的目的是探讨瘦素是否调节小肠黏膜中的细胞凋亡。通过DNA片段化百分比、电泳、TUNEL染色以及半胱天冬酶-3的蛋白质免疫印迹分析来评估肠道细胞凋亡情况。在注射后0、3、6、12和24小时评估大鼠空肠和回肠的黏膜细胞凋亡。在大鼠自由进食和禁食24小时后进行测试,以排除瘦素的食欲抑制作用。以200微克/只的剂量腹腔注射瘦素,并以8微克/只的剂量注入大鼠第三脑室。在自由进食和禁食24小时的大鼠中,以8微克/只的剂量向第三脑室注射瘦素后3和6小时,显著诱导小肠中的肠道细胞凋亡。这种细胞凋亡的增加并未因迷走神经切断术而减弱。以200微克/只的剂量腹腔注射瘦素后12和24小时,肠道细胞凋亡增加。向第三脑室注射瘦素的大鼠中细胞凋亡增加的峰值比腹腔注射的大鼠出现得更早。瘦素诱导大鼠空肠和回肠黏膜细胞凋亡,表明瘦素可能通过调节肠道细胞凋亡来控制肠道功能。