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Effect of alpha 2-adrenoceptor agonists on gastric pepsin and acid secretion in the rat.

机译:α2肾上腺素受体激动剂对大鼠胃蛋白酶和胃酸分泌的影响。

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摘要

1. The purpose of the present study was to analyze the effects of the alpha 2-adrenoceptor agonists clonidine, guanabenz, detomidine and medetomidine on pepsin secretion in conscious rats provided with gastric chronic fistula and to compare this with acid secretion. 2. Basal interdigestive gastric secretion, which is mainly neurally driven in the rat, and the secretion directly stimulated by the two main stimulants of chief cells, cholecystokinin octapeptide (CCK8) and methacholine, were studied. 3. Basal secretion of pepsin and acid was inhibited by all four drugs with comparable EC50S. 4. CCK-stimulated pepsin and acid secretion was less sensitive than basal pepsin and acid secretion to alpha 2-adrenoceptor inhibition. 5. Methacholine-stimulated pepsin and acid secretion was not changed by clonidine and guanabenz; methacholine-stimulated acid was even marginally increased by clonidine. 6. These results do not favour the presence of alpha 2-receptors on chief cells in the rat stomach. They rather suggest that pepsin inhibition by alpha 2-adrenoceptor agonists is indirect and due to central or peripheral inhibition of the discharge of nerve fibres activating pepsin secretion.
机译:1.本研究的目的是分析α2-肾上腺素受体激动剂可乐定,瓜纳本斯,地托米定和美托咪定对患有胃慢性瘘的清醒大鼠胃蛋白酶分泌的影响,并将其与酸分泌进行比较。 2.研究了大鼠消化道胃底分泌物,其主要是神经驱动的,并研究了主要细胞的两种主要刺激物胆囊收缩素八肽(CCK8)和乙酰甲胆碱直接刺激的分泌。 3.所有四种具有相似EC50S的药物均抑制了胃蛋白酶和胃酸的基础分泌。 4. CCK刺激的胃蛋白酶和胃酸分泌对α2-肾上腺素受体的抑制作用不如基础胃蛋白酶和胃酸分泌。 5.可乐定和瓜纳贝斯不改变甲胆碱刺激的胃蛋白酶和酸的分泌。可乐定甚至会稍微增加乙酰甲胆碱刺激的酸。 6.这些结果不利于大鼠胃中主要细胞上存在α2受体。他们宁愿暗示α2肾上腺素受体激动剂对胃蛋白酶的抑制作用是间接的,并且是由于中枢或外周抑制了激活胃蛋白酶分泌的神经纤维的释放。

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