Schulzke J D, Fromm M, Riecken E O, Reutter W
Department of Gastroenterology, Klinikum Steglitz, Berlin, FRG.
Eur J Clin Invest. 1990 Apr;20(2):182-91. doi: 10.1111/j.1365-2362.1990.tb02267.x.
The endogenous opioid enkephalin drives ion transport towards absorption. To determine the site and mechanism of this effect, fractionated stripping of guinea-pig ileum was carried out. The muscularis propria, including myenteric plexus, was removed by partial stripping. The submucosa, including the submucosal plexus, plus the muscularis mucosae were removed by total stripping. For binding studies, epithelial cells were removed by the method of Weiser leaving the lamina propria mucosae with the mucosal plexus. Radio-receptor-assay with (3H)2-D-ala-5-D-leu-enkephalin revealed enkephalin binding sites in the submucosa plus muscularis mucosae (KD = 3.6 nmol l-1; Vmax = 7.3 fmol mg-1) and in the lamina propria mucosae (KD = 4.2 nmol l-1; Vmax = 5.1 fmol mg-1. The binding was stereospecific in both layers. No binding was detected on epithelial cells. In the Ussing chamber, partially stripped ileum exhibited spontaneous ISC which was abolished by addition of tetrodotoxin (TTX) or by total stripping indicating that this ISC was neuronally stimulated by the submucosal plexus. Electrogenic chloride secretion was identified as contributing to this ISC, since the TTX-sensitive part of ISC in the partially stripped ileum was lacking in Cl- and HCO3-free medium, reappeared after addition of Cl consistent with Michaelis-Menten kinetics (Km = 19 nmol l-1) and was reversed by serosal addition of bumetanide. In addition, enkephalin increased electroneutral NaCl-absorption as obtained by Na- and Cl-flux measurements. Enkephalin decreased this spontaneous neuronally stimulated electrogenic Cl-secretion in the partially stripped ileum, but had no effect in totally stripped ileum if ISC was stimulated at the cellular level by theophylline or PGE1. We conclude that ganglia located in the submucosal plexus regulate intestinal ion transport. Enkephalin acts by presynaptic inhibition via receptors on these neurons in the submucosa and/or via receptors on their neurites in the lamina propria mucosae.
内源性阿片肽脑啡肽促使离子转运向吸收方向进行。为确定这种作用的部位和机制,对豚鼠回肠进行了分段剥离实验。通过部分剥离去除包括肌间神经丛在内的固有肌层。通过完全剥离去除包括黏膜下神经丛在内的黏膜下层以及黏膜肌层。对于结合研究,采用韦泽尔的方法去除上皮细胞,留下含有黏膜神经丛的黏膜固有层。用(3H)2-D-丙氨酸-5-D-亮氨酸-脑啡肽进行放射受体分析,结果显示在黏膜下层加黏膜肌层(解离常数KD = 3.6纳摩尔/升;最大结合容量Vmax = 7.3飞摩尔/毫克)以及黏膜固有层(KD = 4.2纳摩尔/升;Vmax = 5.1飞摩尔/毫克)存在脑啡肽结合位点。两层中的结合均具有立体特异性。在上皮细胞上未检测到结合。在尤斯灌流小室中,部分剥离的回肠呈现出自发性短路电流(ISC),添加河豚毒素(TTX)或完全剥离后该电流消失,这表明该ISC是由黏膜下神经丛通过神经方式刺激产生的。确定电致氯分泌对该ISC有贡献,因为在无氯和无碳酸氢根的培养基中,部分剥离回肠中对TTX敏感的ISC部分消失,添加氯离子后重新出现,符合米氏动力学(米氏常数Km = 19纳摩尔/升),且在浆膜侧添加布美他尼后该电流逆转。此外,通过钠和氯通量测量发现脑啡肽增加了电中性氯化钠吸收。脑啡肽减少了部分剥离回肠中这种由神经自发刺激产生的电致氯分泌,但如果通过茶碱或前列腺素E1在细胞水平刺激ISC,则对完全剥离的回肠没有影响。我们得出结论,位于黏膜下神经丛的神经节调节肠道离子转运。脑啡肽通过对这些黏膜下神经元上的受体以及/或者其在黏膜固有层神经突上的受体进行突触前抑制来发挥作用。