Niel J P, Miolan J P
Département de Physiologie et Neurophysiologie, U.R.A. CNRS 205, Faculté des Sciences et Techniques, St Jérome, Marseille, France.
Neuroscience. 1990;36(3):803-9. doi: 10.1016/0306-4522(90)90023-w.
Membrane potentials were recorded in vitro with intracellular electrodes from the circular muscle cells of the cat lower oesophageal sphincter and oesophageal body. In addition, the tension of lower oesophageal sphincter and oesophageal body strips was recorded isotonically. Under the experimental conditions, no spontaneous electrical activity or variation in the tension of the strips occurred. The resting membrane potential of the circular muscle cells was significantly lower in the lower oesophageal sphincter (-51.0 +/- 0.3 mV) than in the circular muscle cells of the oesophageal body (-57.1 +/- 0.4 mV). These values were not affected by infusion of tetrodotoxin 3.1 x 10(-6) M. In the presence of atropine (3.5 x 10(-7) M), the resting membrane potential of the circular muscle cells of the lower oesophageal sphincter increased significantly (-57.6 +/- 0.4 mV), whereas the resting membrane potential of the circular muscle cells of the oesophageal body was not significantly affected (-57.8 +/- 0.6 mV). In the presence of atropine, no significant difference in the values of the resting membrane potential of the circular muscle cells was observed between the lower oesophageal sphincter and the oesophageal body. Hyoscine (2.9 x 10(-7) M) significantly increased the resting membrane potential of the circular muscle cells of the lower oesophageal sphincter, whereas eserine (3.6 x 10(-6) M) significantly decreased it. Atropine induced a significant decrease in the membrane resistance of the circular muscle cells of the lower oesophageal sphincter. Atropine decreased the resting tension of lower oesophageal sphincter strips whereas eserine increased it, but no such effects were recorded on oesophageal body strips.(ABSTRACT TRUNCATED AT 250 WORDS)
采用细胞内电极在体外记录猫下食管括约肌和食管体环形肌细胞的膜电位。此外,等张记录下食管括约肌和食管体条带的张力。在实验条件下,条带未出现自发电活动或张力变化。下食管括约肌环形肌细胞的静息膜电位(-51.0±0.3mV)显著低于食管体环形肌细胞(-57.1±0.4mV)。这些值不受3.1×10⁻⁶M河豚毒素灌注的影响。在存在阿托品(3.5×10⁻⁷M)的情况下,下食管括约肌环形肌细胞的静息膜电位显著升高(-57.6±0.4mV),而食管体环形肌细胞的静息膜电位未受显著影响(-57.8±0.6mV)。在存在阿托品的情况下,下食管括约肌和食管体环形肌细胞静息膜电位值之间未观察到显著差异。东莨菪碱(2.9×10⁻⁷M)显著升高下食管括约肌环形肌细胞的静息膜电位,而毒扁豆碱(3.6×10⁻⁶M)则使其显著降低。阿托品导致下食管括约肌环形肌细胞膜电阻显著降低。阿托品降低下食管括约肌条带的静息张力,而毒扁豆碱则使其升高,但对食管体条带未记录到此类作用。(摘要截断于250字)