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胰腺腺泡细胞:乙酰胆碱、促胰酶素、胃泌素和促胰液素对体内及体外膜电位和电阻的影响

Pancreatic acinar cells: effect of acetylcholine, pancreozymin, gastrin and secretin on membrane potential and resistance in vivo and in vitro.

作者信息

Petersen O H, Ueda N

出版信息

J Physiol. 1975 May;247(2):461-71. doi: 10.1113/jphysiol.1975.sp010941.

Abstract
  1. Intracellular recordings of membrane potential and input resistance have been made in vivo and in vitro from the exocrine acinar cells of rat pancreas using indwelling glass micro-electrodes. 2. The resting cell membrane potential and input resistance in the in vivo experiments were not markedly different from the values obtained in the in vitro experiments. The effect of both acetylcholine (ACh) and pancreozymin (CCK-Pz) on the pancreas in vivo as well as in vitro was to reduce both the acinar cell membrane potential and the input resistance narkedly. The amplitude of the evoked depolarization and the change in input resistance evoked by supramaximal stimuli were of the same magnitude in both types of preparations. 3. Gastrin had an effect on the acinar cell potential and resistance which was indistinguishable from that of CCK-Pz or ACh. The effect of gastrin or CCK-Pz was, in contrast to that of ACh, not influenced by the presence of atropine. The reversal potential for the gastrin evoked potential change was about -20 mV. 4. Secretin in doses producing maximal volume secretion in vivo had no effect on acinar cell membrane potential and input resistance. 5. Dibutyryl cyclic AMP (5mM) and cyclic GMP (1mM) had no effect on cell membrane potential or resistance. 6. It is concluded that the in vitro superfused pancreas segment preparation is a useful model system in electrophysiological studies since it functions essentially as the in vivo preparation. In contrast to both gastrin and CCK-Pz, secretin has no effect on the bioelectrical properties of the acinar cells, indicating that there are no physiologically important secretin receptors in rat acinar cells.
摘要
  1. 采用留置玻璃微电极,在体内和体外对大鼠胰腺外分泌腺泡细胞进行了膜电位和输入电阻的细胞内记录。2. 体内实验中静息细胞膜电位和输入电阻与体外实验所得值无明显差异。乙酰胆碱(ACh)和促胰酶素(CCK - Pz)在体内和体外对胰腺的作用均是显著降低腺泡细胞膜电位和输入电阻。在两种类型的制备物中,由超强刺激诱发的去极化幅度和输入电阻变化幅度相同。3. 胃泌素对腺泡细胞电位和电阻的作用与CCK - Pz或ACh的作用无法区分。与ACh不同,胃泌素或CCK - Pz的作用不受阿托品存在的影响。胃泌素诱发电位变化的反转电位约为 - 20 mV。4. 在体内产生最大容量分泌剂量的促胰液素对腺泡细胞膜电位和输入电阻无影响。5. 二丁酰环磷腺苷(5mM)和环磷鸟苷(1mM)对细胞膜电位或电阻无影响。6. 得出结论:体外灌流胰腺段制备物是电生理研究中一个有用的模型系统,因为其功能与体内制备物基本相同。与胃泌素和CCK - Pz不同,促胰液素对腺泡细胞的生物电特性无影响,表明大鼠腺泡细胞中不存在生理上重要的促胰液素受体。

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