Suzuki A G, Kameyama J, Tsukamoto M, Kaneko K, Suzuki Y
Department of Surgery, Yamagata University School of Medicine, Japan.
Am J Physiol. 1993 Jan;264(1 Pt 1):G118-25. doi: 10.1152/ajpgi.1993.264.1.G118.
Regulation of Cl- and HCO3- secretion by intramural cholinergic neurons was investigated in guinea pig antrum in vitro. Sheet preparations composed of the mucosa and the submucosa were mounted between Ussing chambers and bathed with buffer-free solution on the luminal surface and with HCO3(-)-CO2 solution on the serosal side. Short-circuit current (Isc), unidirectional fluxes of 36Cl and 22Na, and the luminal alkalinization rate (JOHSL) were determined. Electrical stimulation of the preparations elicited increases in both JOHSL and Isc, which were inhibited by tetrodotoxin (TTX) and atropine. Physostigmine also evoked TTX- and atropine-sensitive increases in JOHSL and Isc. Similar increases in JOHSL and Isc were observed when the muscarinic agonist bethanechol chloride (BCh) was added to the serosal side. The responses to BCh were not affected by TTX. The BCh-induced increase in JOHSL was largely abolished by removal of HCO3- or Na+ and addition of ouabain (serosal side) but was neither sensitive to Cl- removal nor associated with 22Na secretion. The increase in Isc induced by BCh was associated with the increase in 36Cl secretion and was inhibited by removal of Cl- or Na+ and by addition of bumetanide or ouabain (both, serosal side). These results suggest that the submucosal cholinergic neurons are involved via muscarinic receptors in the stimulation of epithelial HCO3- and Cl- secretion. For both HCO3- and Cl-, the cellular and membrane mechanisms of secretion induced by muscarinic stimulation, although not entirely clear, appear to be different from those occurring under baseline conditions.
在体外对豚鼠胃窦中壁内胆碱能神经元对氯离子(Cl⁻)和碳酸氢根离子(HCO₃⁻)分泌的调节进行了研究。由黏膜和黏膜下层组成的薄片标本安装在尤斯灌流小室之间,腔面用无缓冲溶液冲洗,浆膜侧用含HCO₃⁻-CO₂的溶液冲洗。测定了短路电流(Isc)、³⁶Cl和²²Na的单向通量以及腔面碱化速率(JOHSL)。对标本进行电刺激会引起JOHSL和Isc增加,这两种增加都被河豚毒素(TTX)和阿托品抑制。毒扁豆碱也能引起JOHSL和Isc的增加,且这种增加对TTX和阿托品敏感。当向浆膜侧加入毒蕈碱激动剂氯化贝胆碱(BCh)时,观察到JOHSL和Isc有类似的增加。对BCh的反应不受TTX影响。去除HCO₃⁻或Na⁺并在浆膜侧加入哇巴因后,BCh诱导的JOHSL增加大部分被消除,但对去除Cl⁻不敏感,也与²²Na分泌无关。BCh诱导的Isc增加与³⁶Cl分泌增加有关,去除Cl⁻或Na⁺以及在浆膜侧加入布美他尼或哇巴因可抑制Isc增加。这些结果表明,黏膜下胆碱能神经元通过毒蕈碱受体参与刺激上皮细胞HCO₃⁻和Cl⁻的分泌。对于HCO₃⁻和Cl⁻,毒蕈碱刺激诱导分泌的细胞和膜机制虽然不完全清楚,但似乎与基线条件下发生的机制不同。