Johnson L R, Brockway P D, Madsen K, Hardin J A, Gall D G
Department of Physiology and Biophysics, University of Tennessee College of Medicine, Memphis 38163.
Am J Physiol. 1995 Mar;268(3 Pt 1):G416-23. doi: 10.1152/ajpgi.1995.268.3.G416.
Polyamines are required for the growth of all eukaryotic cells. Enterocytes respond to luminal nutrients with large increases in polyamine synthesis, even though they are mature, nonproliferating cells. The role of polyamines in these cells is unknown. The current experiments examined whether polyamines affected intestinal transport of glucose, since absorption is the primary activity of enterocytes and since polyamines are known to affect membrane function and stability. Glucose transport was examined in rabbit brush-border membrane vesicles (BBMV). BBMV from rabbits given 5% alpha-difluoromethylornithine (DFMO) in their drinking water 24 h before they were killed transported significantly less glucose than control vesicles [38% decrease in maximal transport rate (Jmax)]. Orogastric administration of spermine, spermidine, or putrescine to DFMO-treated animals 24 h before they were killed prevented the decrease. In rabbits receiving only orogastric spermine, glucose transport was significantly increased (64% increase in Jmax), whereas in vivo spermidine and putrescine decreased Jmax. This increase in Jmax caused by in vivo administration of spermine was not dependent on protein synthesis. Addition of polyamines whether in vivo or in vitro decreased Michaelis constant in vesicles from control and DFMO-treated animals. The change in glucose transport induced by DFMO or polyamines was not related to altered membrane lipid composition or fluidity.(ABSTRACT TRUNCATED AT 250 WORDS)
多胺是所有真核细胞生长所必需的。肠上皮细胞对肠腔营养物质的反应是多胺合成大幅增加,尽管它们是成熟的、不增殖的细胞。多胺在这些细胞中的作用尚不清楚。当前的实验研究了多胺是否影响葡萄糖的肠道转运,因为吸收是肠上皮细胞的主要活动,而且已知多胺会影响膜功能和稳定性。在兔刷状缘膜囊泡(BBMV)中检测葡萄糖转运。在处死前24小时给兔子饮用含5%α-二氟甲基鸟氨酸(DFMO)的水,其BBMV转运的葡萄糖明显少于对照囊泡[最大转运速率(Jmax)降低38%]。在处死前24小时给DFMO处理的动物经口胃管给予精胺、亚精胺或腐胺可防止这种降低。在仅经口胃管给予精胺的兔子中,葡萄糖转运显著增加(Jmax增加64%),而体内给予亚精胺和腐胺则降低Jmax。体内给予精胺引起的Jmax增加不依赖于蛋白质合成。无论在体内还是体外添加多胺,均可降低对照和DFMO处理动物囊泡中的米氏常数。DFMO或多胺诱导的葡萄糖转运变化与膜脂质组成或流动性改变无关。(摘要截短于250字)