The effects of acetylcholine, noradrenaline and pentagastrin on the action potential of canine antral circular muscle were determined using the intracellular micro-electrode technique. 2. Acetylcholine increased the amplitude and duration of the plateau potential of the action potential. Since these effects were blocked by atropine but not by hexamethonium, the effects of acetylcholine were on muscarinic receptors, probably located on the smooth muscle cell. 3. Pentagastrin 2 x 10(-10) M increased the size of the plateau potential and the frequency of the action potential; pentagastrin 1 x 10(-9) M increased the frequency of the action potential complex and produced a marked diastolic depolarization between action potentials. The effect on the size of the plateau potential was biphasic. The amplitude and half-time duration of the plateau potential increased in the first 3 min, but thereafter, during steady-state conditions, they were the same as or slightly greater than those obtained in Krebs solution. 4. All the effects produced by pentagastrin were due to a direct action on the smooth muscle cell. 5. Noradrenaline decreased the size of the plateau potential but increased its frequency; high concentrations (greater than 10(-5) M) additionally produced a diastolic depolarization between action potentials. These effects were mediated primarily by alpha-adrenoceptors presumably located on the smooth muscle cell. 6. It was concluded that the substances studied primarily alter the size of the plateau potential in antral circular muscle. Since phasic contractions are associated with the plateau potential, it is suggested that agents which increase the size of the plateau potential increase the force of the contraction whereas agents which decrease the size of the plateau potential have the opposite effect.
摘要
采用细胞内微电极技术测定了乙酰胆碱、去甲肾上腺素和五肽胃泌素对犬胃窦环行肌动作电位的影响。2. 乙酰胆碱增加了动作电位平台期电位的幅度和持续时间。由于这些作用可被阿托品阻断而不能被六甲铵阻断,所以乙酰胆碱的作用是通过毒蕈碱受体介导的,这些受体可能位于平滑肌细胞上。3. 2×10⁻¹⁰ M 的五肽胃泌素增加了平台期电位的大小和动作电位的频率;1×10⁻⁹ M 的五肽胃泌素增加了动作电位复合波的频率,并在动作电位之间产生明显的舒张期去极化。对平台期电位大小的影响是双相的。平台期电位的幅度和半衰期在最初 3 分钟增加,但此后在稳态条件下,它们与在 Krebs 溶液中获得的相同或略大。4. 五肽胃泌素产生的所有作用都是由于其对平滑肌细胞的直接作用。5. 去甲肾上腺素减小了平台期电位的大小但增加了其频率;高浓度(大于 10⁻⁵ M)还在动作电位之间产生舒张期去极化。这些作用主要由可能位于平滑肌细胞上的α-肾上腺素能受体介导。6. 得出的结论是,所研究的物质主要改变胃窦环行肌平台期电位的大小。由于相性收缩与平台期电位相关,因此表明增加平台期电位大小的药物会增加收缩力,而减小平台期电位大小的药物则有相反的作用。