首页> 外文期刊>American Journal of Physiology >Polyamine metabolism of rat gastric mucosa after oral administration of hypertonic sodium chloride solution.
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Polyamine metabolism of rat gastric mucosa after oral administration of hypertonic sodium chloride solution.

机译:口服高渗氯化钠溶液后大鼠胃黏膜的多胺代谢。

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摘要

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.
机译:向大鼠口服1 ml 3.42 M NaCl溶液可诱导胃粘膜的亚精胺/亚精胺N1-乙酰基转移酶(SSAT)活性以及鸟氨酸脱羧酶(ODC)活性。 SSAT活性增加并在5 h达到峰值,然后在7 h再次达到峰值,而ODC活性在6 h达到峰值。施用3.42 M NaCl后,SSAT mRNA也增加,其程度类似于5 h SSAT活性的增加。 NaCl给药可增加细胞内腐胺水平和DNA合成。多胺氧化酶抑制剂N,N'-双(2,3-丁二烯基)-1,4-丁二胺(MDL-72527)而非ODC抑制剂α-二氟甲基鸟氨酸(DFMO)抑制了腐胺水平的升高和5小时DNA合成。 MDL-72527对DNA合成的抑制作用可通过腐胺给药逆转。相反,MDL-72527和DFMO均在16.5 h抑制了腐胺水平和DNA合成的增加。这些发现表明,由SSAT从先前存在的亚精胺产生的腐胺负责由NaCl引起的粘膜损伤后的初始DNA合成,并且SSAT和ODC都参与了腐胺的形成,这是后续DNA合成所必需的。

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