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Am J Physiol Gastrointest Liver Physiol 274: G299-G305, 1998;
0193-1857/98 $5.00
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Vol. 274, Issue 2, G299-G305, February 1998

Polyamine metabolism of rat gastric mucosa after oral administration of hypertonic sodium chloride solution

Kenjiro Otani1, Yoshihisa Yano1, Tadayoshi Hasuma1, Tetsuo Arakawa2, Kenzo Kobayashi2, Isao Matsui-Yuasa3, and Shuzo Otani1

1 Department of Biochemistry and 2 Third Department of Internal Medicine, Osaka City University Medical School; and 3 Department of Food and Nutrition, Faculty of Human Life Science, Osaka City University, Osaka 545, Japan

Oral administration of 1 ml of 3.42 M NaCl solution to rats induced spermidine/spermine N1-acetyltransferase (SSAT) activity in gastric mucosa as well as ornithine decarboxylase (ODC) activity. SSAT activity increased and peaked at 5 h and again at 7 h, whereas ODC activity peaked at 6 h. SSAT mRNA also increased after 3.42 M NaCl administration to an extent similar to the increase in SSAT activity at 5 h. Intracellular putrescine level and DNA synthesis were increased by NaCl administration. A polyamine oxidase inhibitor, N,N'-bis(2,3-butadienyl)-1,4-butanediamine (MDL-72527), but not an ODC inhibitor, alpha -difluoromethylornithine (DFMO), inhibited the increases in putrescine level and DNA synthesis at 5 h. The inhibition of DNA synthesis by MDL-72527 was reversed by putrescine administration. In contrast, both MDL-72527 and DFMO inhibited the increase in putrescine level and DNA synthesis at 16.5 h. These findings suggest that putrescine produced from preexistent spermidine by SSAT is responsible for the initial DNA synthesis after mucosal injury induced by NaCl and that both SSAT and ODC are involved in formation of putrescine, which is required for subsequent DNA synthesis.

spermidine/spermine N1-acetyltransferase; putrescine; ornithine decarboxylase





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