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多胺与表皮生长因子在应激性胃损伤后胃黏膜恢复中的作用

Polyamines and epidermal growth factor in the recovery of gastric mucosa from stress-induced gastric lesions.

作者信息

Konturek P C, Brzozowski T, Konturek S J, Szlachcic A, Hahn E G

机构信息

Department of Medicine I, University Nuremberg-Erlangen, Erlangen, Germany.

出版信息

J Clin Gastroenterol. 1998;27 Suppl 1:S97-104. doi: 10.1097/00004836-199800001-00016.

Abstract

Polyamines such as spermine or putrescine, resulting from increased activity of ornithine decarboxylase (ODC), are known for gastroprotective and mucosal growth-promoting effects. EGF exhibits similar effects, but little is known about the involvement of polyamines in acceleration of the healing of stress-induced gastric lesions by epidermal growth factor (EGF). In this study, rats with intact or suppressed ODC activity by alpha-difluoromethy-ornithine (DFMO, 400 mg/kg i.p.) were subjected to 3.5 h of water immersion and restraint stress (WRS) without or with addition of spermine or EGF. At 0, 2, 6, 12, or 24 h after stress, rats were sacrificed. The number of gastric lesions was determined and gastric blood flow (GBF) was recorded by the H2 gas clearance technique. Stress produced gastric lesions (mean number 18+/-2 per stomach) and decreased GBF (by approximately 43%), but at 2, 6, 12, and 24 h after stress, these lesions and the decrease in GBF were gradually attenuated. Pretreatment with DFMO or removal of an endogenous source of EGF by salivectomy resulted in a marked decrease in mucosal DNA synthesis and significantly delayed the healing of stress lesions. EGF or spermine significantly accelerated ulcer healing and increased the GBF in rats with intact or removed salivary glands. DFMO significantly reduced the enhancement of healing and the increase in GBF induced by EGF, but failed to influence those induced by exogenous spermine. We conclude that polyamines play an important role in mucosal recovery from stress lesions due to acceleration of mucosal repair and increase in gastric microcirculation and that increased ODC activity and resulting excessive polyamine release appear to act as primary mediators of EGF-induced acceleration of the healing of stress lesions.

摘要

鸟氨酸脱羧酶(ODC)活性增加所产生的多胺,如精胺或腐胺,具有胃保护和促进黏膜生长的作用。表皮生长因子(EGF)也有类似作用,但关于多胺在表皮生长因子(EGF)加速应激性胃损伤愈合过程中的作用知之甚少。在本研究中,用α-二氟甲基鸟氨酸(DFMO,400mg/kg腹腔注射)使大鼠ODC活性保持完整或受到抑制,然后对其进行3.5小时的水浸束缚应激(WRS),应激过程中不添加或添加精胺或EGF。应激后0、2、6、12或24小时处死大鼠。测定胃损伤数量,并采用氢气清除技术记录胃血流量(GBF)。应激导致胃损伤(平均每个胃18±2个损伤)并使GBF降低(约43%),但在应激后2、6、12和24小时,这些损伤和GBF的降低逐渐减轻。用DFMO预处理或通过唾液腺切除去除内源性EGF来源,导致黏膜DNA合成显著减少,并显著延迟应激性损伤的愈合。EGF或精胺显著加速完整或切除唾液腺大鼠的溃疡愈合并增加GBF。DFMO显著降低EGF诱导的愈合增强和GBF增加,但不影响外源性精胺诱导的这些作用。我们得出结论,多胺在应激性损伤的黏膜恢复中起重要作用,这是由于其加速了黏膜修复并增加了胃微循环,并且ODC活性增加及由此导致的多胺过度释放似乎是EGF诱导应激性损伤愈合加速的主要介质。

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