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肠腔多胺对近端小肠黏膜生长的刺激作用。

Stimulation of proximal small intestinal mucosal growth by luminal polyamines.

作者信息

Wang J Y, McCormack S A, Viar M J, Johnson L R

机构信息

Department of Physiology and Biophysics, University of Tennessee College of Medicine, Memphis 38163.

出版信息

Am J Physiol. 1991 Sep;261(3 Pt 1):G504-11. doi: 10.1152/ajpgi.1991.261.3.G504.

DOI:10.1152/ajpgi.1991.261.3.G504
PMID:1716059
Abstract

The purpose of this study was to determine whether luminal polyamines stimulate intestinal mucosal growth in vivo. Rats received 2% alpha-difluoromethylornithine (DFMO) added to their drinking water throughout the experiment. The polyamines spermidine and spermine (3 mg each/100 g body wt) were given intragastrically in combined doses once at 9:30 A.M. and again at 5:30 P.M. Duodenal and jejunal mucosal ornithine decarboxylase (ODC) activity in the DFMO-treated rats was inhibited significantly for the duration of the study. DFMO also markedly decreased the rate of [3H]thymidine incorporation into DNA of duodenal and jejunal mucosa. The decrease in [3H]thymidine incorporation was significant 4 days and maximal 6 and 8 days after beginning treatment with DFMO. Decreased ODC activity and DNA synthesis were paralleled by decreases in total mucosal DNA, RNA, and protein content. Administration of the polyamines significantly reversed the effects of DFMO except the inhibition of ODC. In fact, there were no significant differences in mucosal growth parameters between the controls (without DFMO) and those treated with DFMO plus polyamines. Oral administration of spermidine and spermine at a dose of 4.5 mg each/100 g body wt for 6 days to rats not treated with DFMO increased the normal rate of mucosal growth in the duodenum and jejunum as well. Polyamine accumulation in IEC-6 cells was measured to determine whether it was altered by DFMO. IEC-6 cells took up [3H]putrescine and [3H]spermidine from their surrounding environment and the uptake was stimulated by serum. DFMO (5 mM) totally inhibited the increase in ODC activity but had no effect on the cellular uptake of polyamines in the presence of putrescine.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究的目的是确定肠腔内的多胺是否能在体内刺激肠黏膜生长。在整个实验过程中,给大鼠的饮用水中添加2%的α-二氟甲基鸟氨酸(DFMO)。在上午9:30和下午5:30分别给大鼠胃内一次性联合给予多胺亚精胺和精胺(各3 mg/100 g体重)。在研究期间,DFMO处理的大鼠十二指肠和空肠黏膜鸟氨酸脱羧酶(ODC)活性受到显著抑制。DFMO还显著降低了[3H]胸腺嘧啶核苷掺入十二指肠和空肠黏膜DNA的速率。在用DFMO开始治疗后4天,[3H]胸腺嘧啶核苷掺入量下降显著,6天和8天时降至最大。ODC活性降低和DNA合成减少伴随着黏膜总DNA、RNA和蛋白质含量的下降。除了对ODC的抑制作用外,多胺的给药显著逆转了DFMO的作用。事实上,对照组(未用DFMO)和用DFMO加polyamines处理的组之间黏膜生长参数没有显著差异。对未用DFMO处理的大鼠,以4.5 mg/100 g体重的剂量口服亚精胺和精胺6天,也增加了十二指肠和空肠黏膜的正常生长速率。测量了IEC-6细胞中的多胺积累,以确定其是否被DFMO改变。IEC-6细胞从周围环境中摄取[3H]腐胺和[3H]亚精胺,摄取受到血清刺激。DFMO(5 mM)完全抑制了ODC活性的增加,但在有腐胺存在的情况下,对多胺的细胞摄取没有影响。(摘要截断于250字)

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