Hegarty J E, Fairclough P D, Clark M L, Dawson A M
Gut. 1981 Feb;22(2):108-13. doi: 10.1136/gut.22.2.108.
In this study a perfusion technique has been used to investigate jejunal secretion in response to the dibasic amino acid L-arginine. L-arginine at 5, 15, and 40 mmol/l in isotonic saline solutions induced net intestinal secretion of water and Na+. The structurally similar dibasic amino acid L-lysine caused net absorption at 5 and 15 mmol/l, and only modest net secretion of water and Na+ at 40 mmol/l, although absorption rates of the two amino acids were similar. D-arginine (15 mmol/l) was without effect on net water and Na+ absorption. L-arginine 15 mmol/l inhibited glucose-stimulated water and Na+ absorption when perfused in the same intestinal segment, but was without effect when perfused in separate jejunal or ileal segments. Parenteral chlorpromazine inhibited L-arginine induced jejunal water and Na+ secretion. Jejunal secretion induced by L-arginine thus appears not to be due to passive osmotic water flow, nor to release of circulating secretagogues. Stimulation of a mucosal secretory process is most likely to be the mechanism.
在本研究中,采用了一种灌注技术来研究空肠对二元氨基酸L-精氨酸的分泌反应。等渗盐溶液中5、15和40 mmol/L的L-精氨酸可诱导肠道净分泌水和Na+。结构相似的二元氨基酸L-赖氨酸在5和15 mmol/L时引起净吸收,在40 mmol/L时仅引起适度的水和Na+净分泌,尽管两种氨基酸的吸收率相似。D-精氨酸(15 mmol/L)对水和Na+的净吸收无影响。当在同一肠段灌注时,15 mmol/L的L-精氨酸会抑制葡萄糖刺激的水和Na+吸收,但在单独的空肠或回肠段灌注时则无影响。胃肠外给予氯丙嗪可抑制L-精氨酸诱导的空肠水和Na+分泌。因此,L-精氨酸诱导的空肠分泌似乎既不是由于被动渗透水流,也不是由于循环促分泌素的释放。最有可能的机制是刺激黏膜分泌过程。