Mourad F H, O'Donnell L J, Andre E A, Bearcroft C P, Owen R A, Clark M L, Farthing M J
Digestive Diseases Research Centre, Medical College of St Bartholomew's Hospital, London.
Gut. 1996 Oct;39(4):539-44. doi: 10.1136/gut.39.4.539.
L-Arginine has been shown to induce fluid secretion in human jejunum. Nitric oxide, a derivative of L-arginine is thought to have an important role as an intestinal secretagogue.
To determine the effect of L-arginine and the nitric oxide synthase inhibitor, nitro L-arginine methyl ester (L-NAME), on fluid and electrolyte movement in rat jejunum.
A 25 cm segment of rat jejunum was perfused in situ with iso-osmotic solutions containing either (1) saline, (2) D-arginine 20, (3) L-arginine 20, (4) L-NAME 0.1, 1, or 20 mmol/l, or (5) a combination of L-arginine 20 and L-NAME 0.1, 1, or 20 mmol/l. In further groups the effect of a subcutaneous injection of L-NAME 100 mg/kg was examined in rats pretreated with either D-or L-arginine 500 mg/kg.
L-Arginine, unlike D-arginine, induced fluid secretion despite being better absorbed (mean -7.3 v 17.0 microliters/min/g; p < 0.01). L-NAME at 0.1 mmol/l had no effect on basal fluid movement but reversed L-arginine induced secretion (7.8; p < 0.05). L-NAME at 1 and 20 mmol/l induced fluid secretion (-15.4 and -28.4, respectively), which was enhanced by the addition of L-arginine (-30.0 and -41.0, respectively; both p < 0.05). A subcutaneous injection of L-NAME resulted in marked fluid secretion (-39.9) and histological evidence of intestinal ischaemia. These changes were attenuated or reversed by pretreatment with subcutaneous L- but not D-arginine.
L-arginine induces intestinal fluid secretion through production of nitric oxide. There is a delicate balance between the effect of nitric oxide as a secretagogue and its effect on maintaining blood flow and thus preventing intestinal ischaemia.
已有研究表明,L-精氨酸可诱导人空肠分泌液体。一氧化氮作为L-精氨酸的衍生物,被认为是一种重要的肠道促分泌素。
确定L-精氨酸和一氧化氮合酶抑制剂硝基-L-精氨酸甲酯(L-NAME)对大鼠空肠液体和电解质转运的影响。
将一段25 cm的大鼠空肠原位灌注等渗溶液,溶液包含以下几种:(1)生理盐水;(2)20 mmol/L的D-精氨酸;(3)20 mmol/L的L-精氨酸;(4)0.1、1或20 mmol/L的L-NAME;(5)20 mmol/L的L-精氨酸与0.1、1或20 mmol/L的L-NAME的组合。在其他组中,研究了皮下注射100 mg/kg的L-NAME对预先注射500 mg/kg的D-精氨酸或L-精氨酸的大鼠的影响。
与D-精氨酸不同,L-精氨酸尽管吸收更好,但仍能诱导液体分泌(平均 -7.3对17.0微升/分钟/克;p<0.01)。0.1 mmol/L的L-NAME对基础液体转运无影响,但可逆转L-精氨酸诱导的分泌(7.8;p<0.05)。1和20 mmol/L的L-NAME可诱导液体分泌(分别为-15.4和-28.4),添加L-精氨酸后分泌增加(分别为-30.0和-41.0;均p<0.05)。皮下注射L-NAME导致明显的液体分泌(-39.9)和肠道缺血的组织学证据。皮下注射L-精氨酸而非D-精氨酸预处理可减轻或逆转这些变化。
L-精氨酸通过产生一氧化氮诱导肠道液体分泌。一氧化氮作为促分泌素的作用与其维持血流从而预防肠道缺血的作用之间存在微妙平衡。