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

1998 ◽  
Vol 274 (2) ◽  
pp. G299-G305
Author(s):  
Kenjiro Otani ◽  
Yoshihisa Yano ◽  
Tadayoshi Hasuma ◽  
Tetsuo Arakawa ◽  
Kenzo Kobayashi ◽  
...  

Oral administration of 1 ml of 3.42 M NaCl solution to rats induced spermidine/spermine N 1-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, α-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.

Mutagenesis ◽  
1991 ◽  
Vol 6 (1) ◽  
pp. 3-9 ◽  
Author(s):  
Håkan Larsson ◽  
Jan Fryklund ◽  
Herbert F. Helander ◽  
Björn Wallmark

1994 ◽  
Vol 72 (11) ◽  
pp. 1308-1312 ◽  
Author(s):  
B. L. Tepperman ◽  
B. D. Soper

The present study determined the effects of nitric oxide (NO) synthase induction on ethanol-mediated damage to rat gastric mucosa. NO synthase activity was determined by [14C]arginine conversion to radiolabeled citrulline. Ca2+-independent NO synthase activity was determined by citrulline formation in the presence of EGTA (1 mM) in the incubation mixture. Intraluminal ethanol administration (2 mL; 40% w/v) to control rats resulted in an increase in mucosal damage characterized as vasocongestion and hemorrhagic necrosis and a reduction in Ca2+-dependent NO synthase activity. Administration of Escherichia coli lipopolysaccharide (LPS; 3 mg/kg i.v.) augmented Ca2+-independent NO synthase activity (determined 4 h later) and reduced damage in response to intraluminal ethanol instillation. Ethanol treatment did not significantly affect induction of NO synthase activity. Dexamethasone pretreatment (1 mg/kg i.v. 2 h before LPS administration) reduced both Ca2+-independent NO synthase activity and the gastroprotective effect of LPS against ethanol-mediated mucosal injury. Likewise, concurrent administration of the NO synthase inhibitor NG-nitro-L-arginine methyl ester (10 mg/kg s.c.) inhibited the gastroprotection associated with LPS treatment, an effect abolished by pretreatment with the NO substrate L-arginine (300 mg/kg s.c.). Indomethacin (5 mg/kg i.v.) was ineffective in suppressing LPS-mediated gastroprotection. These results suggest that while Ca2+-dependent NO formation is inhibited by ethanol treatment, the inducible Ca2+-independent NO synthase plays a role in LPS-mediated gastroprotection against ethanol-mediated damage to the gastric mucosa.Key words: nitric oxide, lipopolysaccharide, ethanol, gastroprotection, dexamethasone.


2012 ◽  
Vol 2012 ◽  
pp. 1-9 ◽  
Author(s):  
Woo-Young Jeon ◽  
Mee-Young Lee ◽  
In-Sik Shin ◽  
Hye-Sun Lim ◽  
Hyeun-Kyoo Shin

This study was performed to evaluate the protective effect and safety of Oryeongsan water extract (OSWE) on ethanol-induced acute gastric mucosal injury and an acute toxicity study in rats. Acute gastric lesions were induced via intragastric oral administration of absolute ethanol at a dose of 5 mL/kg. OSWE (100 and 200 mg/kg) was administered to rats 2 h prior to the oral administration of absolute ethanol. The stomach of animal models was opened and gastric mucosal lesions were examined. Gastric mucosal injuries were evaluated by measuring the levels of malondialdehyde (MDA), glutathione (GSH), and the activity of antioxidant enzymes. In the acute toxicity study, no adverse effects of OSWE were observed at doses up to 2000 mg/kg/day. Administration of OSWE reduced the damage by conditioning the gastric mucosa against ethanol-induced acute gastric injury, which included hemorrhage, hyperemia, and loss of epithelial cells. The level of MDA was reduced in OSWE-treated groups compared with the ethanol-induced group. Moreover, the level of GSH and the activity of antioxidant enzymes were significantly increased in the OSWE-treated groups. Our findings suggest that OSWE has a protective effect on the gastric mucosa against ethanol-induced acute gastric injury via the upregulation of antioxidant enzymes.


1989 ◽  
Vol 257 (1) ◽  
pp. G9-G13 ◽  
Author(s):  
T. Faust ◽  
J. S. Redfern ◽  
E. Lee ◽  
M. Feldman

Fundic mucosal content and synthesis of 6-ketoprostaglandin F1 alpha, the major prostanoid in the rat gastric mucosa, were determined after rats had ingested a diet containing 10% fish oil or 10% corn oil for 4 wk. 6-Ketoprostaglandin F1 alpha content and synthesis in rats fed a fish oil-supplemented diet were reduced significantly compared with rats receiving a corn oil-supplemented diet (P less than 0.05). However, rats receiving 10% fish oil for 8 wk sustained significantly less gastric mucosal injury after intragastric challenge with 15% and then with absolute ethanol than rats receiving 10% corn oil or regular chow for 8 wk (P less than 0.05). Thus fish oil ingestion protected the gastric mucosa even though fish oils reduced mucosal prostaglandin synthesis.


1994 ◽  
Vol 71 (01) ◽  
pp. 119-123 ◽  
Author(s):  
Iwao Kurose ◽  
Soichiro Miura ◽  
Dai Fukumura ◽  
Masayuki Suzuki ◽  
Hiroshi Nagata ◽  
...  

SummaryThe roles for the fibrinolytic activation and disorder of coagulation in formation of gastric ulcer induced by microvascular derangement were investigated. The rat stomach was exposed and repeated electrical stimuli (RES) were applied on the small arterial wall close to the lesser curvature to induce mucosal microcirculatory disturbances. The level of tissue-type plasminogen activator (t-PA), a key enzyme for fibrinolytic activity, in the regional blood of the stomach was significantly elevated immediately after RES. At 5 min after RES, the leakage of FITC-labeled albumin and thrombus formation in the mucosal microvasculature were visually demonstrated by using an intravital microscopic system. At 30 min, hemorrhagic erosions and linear ulcers were observed in the gastric mucosa. Pretreatment with human anti-thrombin-III (AT-III) in the range of 0.1–10 U/kg dose-dependently attenuated both the fibrinolytic activation and microvascular alteration promoted by RES. Human AT-III also prevented RES-induced gastric mucosal injury. Thrombin inhibitory activity in the gastric vein decreased (69.0 ± 2.1%) just after RES, and further reduced at 30 min (47.7 ± 5.3%). The present study suggests a hypothesis that human AT-III has a preventive effect on the gastric mucosal hemorrhagic changes via attenuating the fibrinolytic activation and subsequent microcirculatory disturbances.


1993 ◽  
Vol 265 (6) ◽  
pp. G1135-G1140
Author(s):  
G. H. Curtis ◽  
W. K. MacNaughton ◽  
D. G. Gall

We have shown that the rat gastric mucosa takes up antigenically intact protein in vitro. The present study investigated the effect of two cyclooxygenase inhibitors, indomethacin and piroxicam, on gastric transport of BSA. Fasted rats were given indomethacin, piroxicam, or vehicle. After 30 min, the stomach was removed, stripped, and mounted in a Ussing chamber. Each side was bathed with Krebs buffer. Bovine serum albumin (BSA), 125I-labeled BSA (125I-BSA), and 51Cr-labeled EDTA (51Cr-EDTA) were added to the mucosal fluid and equilibrated for 30 min. Serosal fluids were sampled for two subsequent 30-min periods, and mean fluxes for immunologically intact BSA (enzyme-linked immunoabsorbent assay), total BSA (125I-BSA), and 51Cr-EDTA were calculated. Cyclooxygenase inhibition significantly (P < 0.01) reduced tissue prostaglandin E2 synthetic capacity (indomethacin, 97%; piroxicam, 92%) but did not cause either macroscopic or microscopic mucosal injury. Both inhibitors significantly (P < 0.05) decreased uptake of immunologically intact BSA (indomethacin, 91%; piroxicam, 81%) and 51Cr-EDTA. In contrast, the movement of degraded BSA was not altered by indomethacin. These findings suggest that a selective pathway exists for the uptake of intact proteins in gastric mucosa and that the pathway is modulated by cyclooxygenase metabolites.


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