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Fast adaptation in mouse olfactory sensory neurons does not require the activity of phosphodiesterase

机译:快速适应小鼠嗅觉感觉神经元不需要磷酸二酯酶的活性

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Vertebrate olfactory sensory neurons rapidly adapt to repetitive odorant stimuli. Previous studies have shown that the principal molecular mechanisms for odorant adaptation take place after the odorant-induced production of cAMP, and that one important mechanism is the negative feedback modulation by Ca2+-calmodulin (Ca2+-CaM) of the cyclic nucleotide-gated (CNG) channel. However, the physiological role of the Ca2+-dependent activity of phosphodiesterase (PDE) in adaptation has not been investigated yet. We used the whole-cell voltage-clamp technique to record currents in mouse olfactory sensory neurons elicited by photorelease of 8-Br-cAMP, an analogue of cAMP commonly used as a hydrolysis-resistant compound and known to be a potent agonist of the olfactory CNG channel. We measured currents in response to repetitive photoreleases of cAMP or of 8-Br-cAMP and we observed similar adaptation in response to the second stimulus. Control experiments were conducted in the presence of the PDE inhibitor IBMX, confirming that an increase in PDE activity was not involved in the response decrease. Since the total current activated by 8-Br-cAMP, as well as that physiologically induced by odorants, is composed not only of current carried by Na+ and Ca2+ through CNG channels, but also by a Ca2+-activated Cl(-)current, we performed control experiments in which the reversal potential of Cl- was set, by ion substitution, at the same value of the holding potential, - 50 mV. Adaptation was measured also in these conditions of diminished Ca2+-activated Cl- current. Furthermore, by producing repetitive increases of ciliary's Ca2+ with flash photolysis of caged Ca2+, we showed that Ca2+- activated Cl- channels do not adapt and that there is no Cl- depletion in the cilia. All together, these results indicate that the activity of ciliary PDE is not required for fast adaptation to repetitive stimuli in mouse olfactory sensory neurons.
机译:脊椎动物的嗅觉感觉神经元迅速适应重复的气味刺激。先前的研究表明,气味适应的主要分子机制发生在气味诱导的cAMP产生之后,而一个重要的机制是环状核苷酸门控(CNG)的Ca2 +-钙调蛋白(Ca2 + -CaM)负反馈调制。 )频道。但是,尚未研究磷酸二酯酶(PDE)的Ca2 +依赖性活性的生理作用。我们使用全细胞电压钳技术来记录小鼠释放出来的8-Br-cAMP(一种通常用作抗水解化合物的cAMP类似物,已知是嗅觉的有效激动剂)的类似物引起的嗅觉神经元中的电流。 CNG频道。我们测量了响应cAMP或8-Br-cAMP的重复光释放的电流,并且观察到了对第二刺激的类似适应。在PDE抑制剂IBMX的存在下进行了对照实验,证实了PDE活性的增加不参与响应的降低。由于8-Br-cAMP激活的总电流以及加味剂生理诱导的总电流不仅由Na +和Ca2 +通过CNG通道携带的电流组成,而且还由Ca2 +激活的Cl(-)电流组成。进行了控制实验,其中通过离子取代将Cl-的反向电位设置为保持电位的相同值-50 mV。在Ca2 +激活的Cl-电流减少的这些条件下也测量了适应性。此外,通过笼状Ca2 +的快速光解产生睫状体Ca2 +的重复增加,我们表明Ca2 +-活化的Cl-通道不适应,纤毛中没有Cl-耗竭。总之,这些结果表明,睫状PDE的活性对于快速适应小鼠嗅觉感觉神经元中的重复刺激不是必需的。

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