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吲哚美辛可增强内毒素诱导的大鼠胃黏膜血流减少和组织学损伤。

Indomethacin potentiates endotoxin-induced blood flow reduction and histological injury in rat gastric mucosa.

作者信息

Piqué J M, Yonei Y, Whittle B J, Leung F W, Guth P H

机构信息

West Los Angeles, VA Medical Center, California.

出版信息

Br J Pharmacol. 1988 Apr;93(4):925-31. doi: 10.1111/j.1476-5381.1988.tb11481.x.

Abstract
  1. The effect of the intravenous administration of lipopolysaccharide from Salmonella typhosa endotoxin on arterial blood pressure (BP), gastric mucosal blood flow (GMBF) and gastric damage was studied in anaesthetized rats. The effect of the inhibition of endogenous prostaglandin generation by indomethacin on these parameters was also investigated in this model of endotoxin shock. 2. A similar and dose-dependent percentage of reduction in BP and GMBF was observed 5 min after a bolus injection of 20 or 30 mg kg-1 endotoxin. A transient recovery in GMBF at 15 min was observed followed by a second fall at 30 min, at a time when BP was slowly increasing. 3. Pretreatment with indomethacin (5 mg kg-1, s.c.) one hour before the administration of 30 mg kg-1 endotoxin, significantly augmented the reduction in GMBF without affecting the reduction in BP. 4. The gastric damage, assessed histologically, was similar and confined to the superficial mucosa 30 min after the administration of 20 or 30 mg kg-1 endotoxin. The histologically-assessed damage was significantly greater in indomethacin pretreated rats injected with 30 mg kg-1 endotoxin. 5. These findings suggest that endogenous prostaglandin generation plays a protective role in endotoxin-induced gastric mucosal microcirculatory disturbances and mucosal damage.
摘要
  1. 研究了静脉注射伤寒沙门氏菌内毒素脂多糖对麻醉大鼠动脉血压(BP)、胃黏膜血流量(GMBF)和胃损伤的影响。在该内毒素休克模型中,还研究了吲哚美辛抑制内源性前列腺素生成对这些参数的影响。2. 在静脉推注20或30mg/kg内毒素5分钟后,观察到BP和GMBF出现相似且呈剂量依赖性的降低百分比。在15分钟时观察到GMBF短暂恢复,随后在30分钟时再次下降,此时BP正在缓慢上升。3. 在给予30mg/kg内毒素前1小时用吲哚美辛(5mg/kg,皮下注射)预处理,显著增强了GMBF的降低,而不影响BP的降低。4. 在给予20或30mg/kg内毒素30分钟后,经组织学评估的胃损伤相似,且局限于浅表黏膜。在注射30mg/kg内毒素的吲哚美辛预处理大鼠中,经组织学评估的损伤明显更大。5. 这些发现表明,内源性前列腺素的生成在内毒素诱导的胃黏膜微循环紊乱和黏膜损伤中起保护作用。

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