McCarthy D M, Kim Y S
J Clin Invest. 1973 Apr;52(4):942-51. doi: 10.1172/JCI107259.
In a study of changes in digestive enzymes after massive intestinal resection and the mechanisms by which such changes occur, rats were sacrified 4 wk after removal of the proximal two-thirds of the small intestine. Alterations in the mucosal levels of sucrase, enterokinase, and dipeptide hydrolase (L-leucyl-L-alanine substrate) were examined in the light of associated changes in protein. DNA and wet mucosal weight, measured in standardized gut segments from various regions of intestine. Metabolic studies showed that normal growth patterns were reestablished after the operation but significant elevations in stool weight and fecal nitrogen occurred in the second postoperative week, falling towards normal by the 4th wk. In standard gut segments wet weight of mucosa, protein, and DNA rose, especially in distal segments, DNA increasing disproportionately. Mucosal levels of the proximally distributed and membrane-bound enzymes, sucrase and enterokinase, showed similar patterns of change: when enzyme activity was expressed in terms of the total per segment, proximally there were considerable increases in both enzymes, but, expressed in terms of specific activity, that of sucrase fell and that of enterokinase was unaltered. By contrast, the largely soluble and more distally distributed dipeptide hydrolase increased more in distal segments and the increases in total activity were accompanied by lesser increases in specific activity. However, in spite of increases in total activity, enzyme activity per milligram DNA fell by over 50% in postanastomotic segments. Subcellular distribution studies showed no change in the percentage of the total activity which was membrane-bound and zymograms confirmed that no new dipeptide hydrolase had appeared after resection. It is concluded that increases in the segmental totals of various enzymes seen after resection are achieved by disproportinate increases in the number of mucosal cells per segment and that the greatest change in a particular enzyme occurs in the region where the enzyme is normally found in highest concentration.
在一项关于大规模肠道切除术后消化酶变化及其发生机制的研究中,切除大鼠小肠近端三分之二后4周将其处死。根据蛋白质、DNA和湿黏膜重量的相关变化,检测了蔗糖酶、肠激酶和二肽水解酶(L-亮氨酰-L-丙氨酸底物)的黏膜水平,这些指标是在来自肠道不同区域的标准化肠段中测量的。代谢研究表明,术后正常生长模式得以重建,但术后第二周粪便重量和粪氮显著升高,到第4周时降至正常水平。在标准肠段中,黏膜的湿重、蛋白质和DNA增加,尤其是在远端肠段,DNA增加不成比例。近端分布且与膜结合的酶,即蔗糖酶和肠激酶的黏膜水平呈现相似的变化模式:当以每段总量表示酶活性时,近端两种酶均有相当大的增加,但以比活性表示时,蔗糖酶的比活性下降,肠激酶的比活性未改变。相比之下,主要为可溶性且分布更靠远端的二肽水解酶在远端肠段增加更多,总活性的增加伴随着比活性较小的增加。然而,尽管总活性增加,但吻合口后肠段每毫克DNA的酶活性下降了50%以上。亚细胞分布研究表明,膜结合的总活性百分比没有变化,酶谱证实切除术后没有出现新的二肽水解酶。得出的结论是,切除术后各酶的段总量增加是通过每段黏膜细胞数量不成比例的增加实现的,并且特定酶的最大变化发生在该酶通常浓度最高的区域。