Mózsik G, Király A, Sütö G, Vincze A
First Department of Medicine, Medical University, Pécs, Hungary.
Acta Physiol Hung. 1992;80(1-4):39-80.
The changes in membrane-bound ATP systems (breakdown and resynthesis) were analyzed in different experimental ulcer models (such as ETOH, HCl, NaOH, 25% NaCl-induced, pyloric ligated + epinephrine treated, stress, reserpine treated, indomethacin treated rat models) and chronic antral, duodenal and jejunal ulcers in patients. The energy system parameters (adenosine triphosphate (ATP), adenosine diphosphate (ADP), adenosine monophosphate (AMP), cyclic AMP (cAMP), lactate) were measured from different sites of gastrointestinal mucosa, and values of ATP/ADP, adenylate pool (ATP + ADP + AMP) and energy charge ((ATP + 0.5 ADP)/(ATP + ADP + AMP)) were calculated. The biochemical measurements were done at different times during the development of gastrointestinal mucosal lesions, without and with application of different drugs (PGI2, atropine, cimetidine) and bilateral surgical vagotomy. The aims of our present paper were: 1.) To summarize the main directions of ATP breakdown during the development of gastrointestinal lesions or ulcers in different experimental models and human beings: 2.) To summarize the biochemical steps of defense of gastrointestinal mucosa against chemicals, drugs or unknown pathogenic factors; 3.) To analyze the importance of membrane-bound ATP-dependent energy systems in order to understand the mucosal lesions and their prevention; 4.) To evaluate the real values of changes in these parameters from the point of view of ulcerogenesis and its prevention; 5.) To find some correlation between the energy parameters during mucosal damage and its prevention: 6.) To understand better the types of tissue reactions (metabolic) due to development of mucosal lesions and prevention.(ABSTRACT TRUNCATED AT 400 WORDS)
在不同的实验性溃疡模型(如乙醇、盐酸、氢氧化钠、25%氯化钠诱导、幽门结扎+肾上腺素处理、应激、利血平处理、吲哚美辛处理的大鼠模型)以及患者的慢性胃窦、十二指肠和空肠溃疡中,分析了膜结合ATP系统(分解和再合成)的变化。从胃肠道黏膜的不同部位测量能量系统参数(三磷酸腺苷(ATP)、二磷酸腺苷(ADP)、一磷酸腺苷(AMP)、环磷酸腺苷(cAMP)、乳酸),并计算ATP/ADP、腺苷酸池(ATP+ADP+AMP)和能荷((ATP+0.5ADP)/(ATP+ADP+AMP))的值。在胃肠道黏膜损伤发展的不同时间进行生化测量,测量时未使用和使用了不同药物(前列环素I2、阿托品、西咪替丁)以及双侧手术切断迷走神经。本文的目的是:1.)总结不同实验模型和人类胃肠道病变或溃疡发展过程中ATP分解的主要方向;2.)总结胃肠道黏膜抵御化学物质、药物或未知致病因素的生化步骤;3.)分析膜结合ATP依赖能量系统的重要性,以了解黏膜损伤及其预防机制;4.)从溃疡发生及其预防的角度评估这些参数变化的实际价值;5.)寻找黏膜损伤及其预防过程中能量参数之间的某些相关性;6.)更好地理解由于黏膜损伤及其预防而产生的组织反应(代谢)类型。(摘要截断于400字)