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©2012 Baishideng Publishing Group Co.
World J Gastroenterol. Feb 14, 2012; 18(6): 522-531
Published online Feb 14, 2012. doi: 10.3748/wjg.v18.i6.522
Published online Feb 14, 2012. doi: 10.3748/wjg.v18.i6.522
Figure 3 Ih recorded under whole-cell voltage and current clamp from DiI labeled dissociated dorsal root ganglia and nodose ganglia neurons innervating the jejunum.
A: DiI labeled dissociated dorsal root ganglia neurons; B: Representative current traces of Ih current (top trace); Current recorded in the presence of 5 mmol/L CsCl (middle trace); voltage clamp protocal: Ih was induced from a holding potential of -60 mV in 1 s pulses from -60 mV to -120 mV in steps of 10 mV, followed by a final step to -80 mV to record the tail current (bottom trace); C: Voltage response to test current pulse before (black) and after (grey) application of 5 mmol/L CsCl (top trace); bottom trace shows the current clamp protocol, i.e., hyperpolarizing current pulses ranging from 0 pA to -200 pA in steps of 50 pA. Note that the current elicited an instantaneous hyperpolarization that was followed by depolarization (named “sag”) of membrane potential. DRG: Dorsal root ganglia; NG: Nodose ganglia.
- Citation: Wang YP, Sun BY, Li Q, Dong L, Zhang GH, Grundy D, Rong WF. Hyperpolarization-activated cyclic nucleotide-gated cation channel subtypes differentially modulate the excitability of murine small intestinal afferents. World J Gastroenterol 2012; 18(6): 522-531
- URL: https://www.wjgnet.com/1007-9327/full/v18/i6/522.htm
- DOI: https://dx.doi.org/10.3748/wjg.v18.i6.522