Bardocz S, Brown D S, Grant G, Pusztai A
Rowett Research Institute, Aberdeen, U.K.
Biochim Biophys Acta. 1990 Apr 23;1034(1):46-52. doi: 10.1016/0304-4165(90)90151-l.
Luminal and basolateral uptake of polyamines by the rat small intestine was studied in vivo. In the concentration range studied (0.1-5 mg per rat) 23-47% of the individual polyamines given intragastrically were found in the body after 1 h, with the small intestine retaining 4-12% of the dose. With spermidine or spermine, labelled polyamines accounted for 85-96% of the counts in the small intestine and between 72-82% were in the form given. However, with putrescine only 29-39% of the label found in the tissue remained in polyamine form and even less, 11-15%, as putrescine. Luminal uptake of polyamines was linear, non-saturable and was not stimulated when small intestinal growth was stimulated by phytohaemagglutinin (PHA). On the basolateral side of the gut, polyamine uptake was stimulated by PHA in a time-dependent way in advance of detectable growth. Overall polyamine recoveries were high (89-99%) with intraperitoneally administered spermidine and spermine. Moreover, a large proportion of the counts in the tissue (63-89%) were still in the original form. Even with putrescine, total recoveries of polyamines (72-88%) and putrescine (24-33%) were elevated in comparison with those from the lumen. Treatment of rats with alpha-difluoromethylornithine (DFMO), an inhibitor of ornithine decarboxylase, reduced tissue polyamine content, although it had slight effects only on basolateral polyamine transport. The PHA-stimulated increase of polyamine uptake was not abolished in the presence of DFMO.
在体内研究了大鼠小肠对多胺的肠腔和基底外侧摄取情况。在所研究的浓度范围内(每只大鼠0.1 - 5毫克),灌胃给予的单个多胺在1小时后有23 - 47%存在于体内,小肠保留了剂量的4 - 12%。对于亚精胺或精胺,标记的多胺占小肠中计数的85 - 96%,其中72 - 82%为给予的形式。然而,对于腐胺,组织中发现的标记物仅有29 - 39%仍以多胺形式存在,而以腐胺形式存在的更少,仅为11 - 15%。多胺的肠腔摄取是线性的、非饱和的,并且在植物血凝素(PHA)刺激小肠生长时不会被刺激。在肠道的基底外侧,PHA以时间依赖性方式在可检测到的生长之前刺激多胺摄取。腹腔注射亚精胺和精胺后,多胺的总体回收率很高(89 - 99%)。此外,组织中很大一部分计数(63 - 89%)仍为原始形式。即使是腐胺,与肠腔来源相比,多胺的总回收率(72 - 88%)和腐胺的回收率(24 - 33%)也有所提高。用鸟氨酸脱羧酶抑制剂α-二氟甲基鸟氨酸(DFMO)处理大鼠,可降低组织多胺含量,尽管它对基底外侧多胺转运仅有轻微影响。在DFMO存在的情况下,PHA刺激的多胺摄取增加并未被消除。