Szabo S
Department of Pathology, University of California, Irvine, USA.
Ann N Y Acad Sci. 1998 Jun 30;851:19-27. doi: 10.1111/j.1749-6632.1998.tb08972.x.
Hans Selye has a historic role in the development of the stress concept. Before his short article in Nature in 1936, the neuroendocrine response to nonspecific injury was thought to be restricted to the release of catecholamines, as recognized by Cannon. Selye was the first to appreciate the crucial role of the adrenal cortex/hypophysis axis in the stress response. He also insisted on the nonspecificity of this neuroendocrine response, and he named the stress-causing agent "stressors". His last major contribution was the distinction between negative, that is, distress, and positive, that is, eustress reactions. The "triad of stress" (adrenal hypertrophy, gastrointestinal ulcers, thymolymphatic atrophy) was also first described by Selye, who was fascinated by the fact that in stressed rodents only gastric and not duodenal ulcers would develop. It was not until the recognition of duodenal ulcerogenic properties of propionitrile and cysteamine as well as the subsequent quantitative structure-activity studies predicting the duodenal ulcerogenic action of complex molecules that pathogenetic investigations allowed a molecular and mechanistic approach for studying the etiology and pathogenesis of duodenal ulceration. Recent studies on the role of sulfhydryls, TRH, ET, and growth factors provide new insights into central and peripheral pre-ulcer pathways. We were surprised to learn that an organ-specific ET-1 release may play a role both in ulcer induction and healing, which seems to start with the expression of immediate early genes such as egr-1 and stimulation of the local synthesis of growth factors such as bFGF and PDGF. Thus, a historic review originating with Hans Selye and extending through the next 60 years allows a cellular and molecular approach to the better understanding of stress-related disorders such as gastroduodenal ulceration.
汉斯·塞尔耶在应激概念的发展中具有历史性作用。在他1936年发表于《自然》杂志的短文之前,人们认为对非特异性损伤的神经内分泌反应仅限于释放儿茶酚胺,这一点已为坎农所认识。塞尔耶是第一个认识到肾上腺皮质/垂体轴在应激反应中关键作用的人。他还坚持这种神经内分泌反应的非特异性,并将引起应激的因素命名为“应激源”。他的最后一项重大贡献是区分了消极的即痛苦的反应和积极的即良性应激反应。“应激三联征”(肾上腺肥大、胃肠道溃疡、胸腺淋巴萎缩)也是塞尔耶首先描述的,他对在应激的啮齿动物中仅会发生胃溃疡而不是十二指肠溃疡这一事实很感兴趣。直到认识到丙腈和半胱胺的致十二指肠溃疡特性以及随后的定量构效关系研究预测了复杂分子的致十二指肠溃疡作用,病因学研究才得以采用分子和机制方法来研究十二指肠溃疡的病因和发病机制。最近关于巯基、促甲状腺激素释放激素、内皮素和生长因子作用的研究为溃疡前期的中枢和外周途径提供了新的见解。我们惊讶地发现,器官特异性的内皮素-1释放可能在溃疡的诱导和愈合中都起作用,这似乎始于早期即刻基因如egr-1的表达以及对局部生长因子如碱性成纤维细胞生长因子和血小板衍生生长因子合成的刺激。因此,从汉斯·塞尔耶开始并延续至接下来60年的历史回顾,使得我们能够采用细胞和分子方法更好地理解诸如胃十二指肠溃疡等与应激相关的疾病。