首页> 外文期刊>The Journal of Physiology >Characterization of 5-HT-sensitive potassium conductances in neonatal rat facial motoneurones in vitro.
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Characterization of 5-HT-sensitive potassium conductances in neonatal rat facial motoneurones in vitro.

机译:体外对新生大鼠面部运动神经元中5-HT敏感性钾电导的表征。

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1. The properties of the 5-HT-sensitive K+ conductance of neonatal rat facial motoneurones were examined in brainstem slices using whole-cell patch-clamp techniques. 2. In a small proportion of motoneurones, 5-hydroxytryptamine (5-HT) evoked an inward current mediated solely by a decrease in K+ conductance. The reversal potential (V5-HT) was dependent on the external K+ concentration and the 5-HT-evoked current (I5-HT) displayed a linear current-voltage (I-V) relationship. 3. In the remaining motoneurones, the 5-HT-evoked decrease in K+ conductance could only be observed in isolation once a concomitant 5-HT-mediated enhancement of the hyperpolarization-activated current, Ih, had been abolished with the Ih blocker, ZD-7288. 4. External Cs+ also abolished the Ih-mediated component of I5-HT but, in addition, blocked part of the 5-HT-sensitive K+ current. At potentials hyperpolarized to V5-HT, Cs+ voltage dependently blocked I5-HT while at potentials depolarized to V5-HT, I5-HT was largely unaffected. Ba2+ and Rb+ had identical actions to Cs+ on the 5-HT-sensitive K+ current. 5. The Ba2+-, Rb+- and Cs+-sensitive component of the 5-HT-sensitive K+ current inwardly rectified with a reversal potential that was dependent on the K+ equilibrium potential (EK). 6. Replacing external Na+ with N-methyl-D-glucamine, blocking Ca2+ entry, or preventing an increase in intracellular [Ca2+] with BAPTA, all failed to alter I5-HT at potentials depolarized to EK. 7. I5-HT at depolarized potentials was reversibly blocked by 4-aminopyridine (4 mM) but not tetraethylammonium chloride (30 mM) and did not show inactivation during depolarizing voltage pulses (1.5 s duration). 8. The results suggest that, in addition to enhancing Ih, 5-HT modulates two distinct K+ conductances in neonatal rat facial motoneurones. The actions of Cs+, Ba2+ and Rb+ support the involvement of a member of the inwardly rectifying family of K+ channels while the other K+ channel may belong to the voltage-gated family.
机译:1.使用全细胞膜片钳技术在脑干切片中检测新生大鼠面部运动神经元对5-HT敏感的K +电导的特性。 2.在一小部分的运动神经元中,5-羟色胺(5-HT)引起仅由K +电导降低介导的内向电流。反向电位(V5-HT)取决于外部K +浓度,并且5-HT诱发电流(I5-HT)显示出线性电流-电压(I-V)关系。 3.在其余的运动神经元中,只有通过Ih阻滞剂ZD消除了伴随5-HT介导的超极化激活电流Ih的增强,才能单独观察到5-HT引起的K +电导降低。 -7288。 4.外部Cs +也取消了Ih介导的I5-HT成分,但此外,还阻止了部分5-HT敏感的K +电流。在对V5-HT超极化的电势下,Cs +电压依赖地阻断了I5-HT,而在对V5-HT反极化的电势下,I5-HT基本上不受影响。 Ba2 +和Rb +在对5-HT敏感的K +电流上具有与Cs +相同的作用。 5. 5-HT敏感的K +电流的Ba2 +,Rb +和Cs +敏感成分向内整流,其反向电位取决于K +平衡电位(EK)。 6.用N-甲基-D-葡糖胺代替外部Na +,阻断Ca2 +的进入或用BAPTA阻止细胞内[Ca2 +]的增加,所有这些都无法在去极化至EK的电位下改变I5-HT。 7.在去极化电势下的I5-HT被4-氨基吡啶(4 mM)可逆地阻断,但未被四乙基氯化铵(30 mM)阻断,并且在去极化电压脉冲期间(1.5 s持续时间)未显示失活。 8.结果表明,除了增强Ih外,5-HT还调节新生大鼠面部运动神经元中的两种不同的K +电导。 Cs +,Ba2 +和Rb +的作用支持K +通道向内整流家族成员的参与,而另一个K +通道可能属于电压门控家族。

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