Wald A, Back C, Bayless T M
Gastroenterology. 1976 Nov;71(5):738-42.
Methylxanthines produce intracellular accumulation of cyclic 3'5'-AMP (cAMP) by inhibition of phosphodiesterase and mucosal cAMP accumulation. Cyclic AMP is thought to mediate small intestinal secretion caused by some enterotoxins, hormones, and methylxanthines. These studies were designed to evaluate the effect of caffeine on small intestinal net fluid movement and transit times. The administration of caffeine in amounts ordinarily contained in many beverages and medications (75 to 300 mg) resulted in striking net secretion in the jejunum which lasted at least 15 minutes. This occurred in six of seven studies. Baseline net absorption of 0.5 ml per cm per hr was reversed to net secretion of 6.0 +/- 2.2 ml per cm per hr after oral caffeine ingestion (P less than 0.01). Net secretion also occurred in the ileum in seven of eight studies, but the onset of secretion appeared 35 min later than in the jejunum. These patterns of secretion correlated best with the passage of the intestinal bolus of caffeine rather than plasma caffeine levels. In contrast to other net secretory conditions, which increase the speed of transit, small intestinal transit times, as determined by dye dilution methods, were unchanged by caffeine. It is possible that methylxanthine-induced small intestinal secretion may play a role in the symptoms experienced by some patients with functional diarrhea.
甲基黄嘌呤通过抑制磷酸二酯酶和黏膜环磷酸腺苷(cAMP)积累,使细胞内cAMP蓄积。环磷酸腺苷被认为介导了由某些肠毒素、激素和甲基黄嘌呤引起的小肠分泌。这些研究旨在评估咖啡因对小肠净液体移动和转运时间的影响。给予许多饮料和药物中通常含有的咖啡因量(75至300毫克),导致空肠出现显著的净分泌,且持续至少15分钟。七项研究中有六项出现这种情况。口服咖啡因后,每厘米每小时0.5毫升的基线净吸收转变为每厘米每小时6.0±2.2毫升的净分泌(P<0.01)。八项研究中有七项回肠也出现了净分泌,但分泌开始时间比空肠晚35分钟。这些分泌模式与咖啡因肠内食团的通过情况相关性最佳,而非与血浆咖啡因水平相关。与其他增加转运速度的净分泌情况不同,通过染料稀释法测定,咖啡因并未改变小肠转运时间。甲基黄嘌呤诱导的小肠分泌可能在一些功能性腹泻患者所经历的症状中起作用。