环核苷酸门控通道激活是不需要的活动依赖的标记斑马鱼嗅觉受体神经元的氨基酸。

W C Michel
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引用次数: 22

摘要

鱼的嗅觉上皮在存在的受体细胞类型和在这些细胞中表达的气味受体家族方面都是异质的。由于这种多样性,由气味剂激活的传导级联尚未明确建立。在目前的研究中,电生理和活动依赖的标记技术被用于评估环核苷酸门控通道在斑马鱼嗅觉转导中的作用。氨基酸和胆汁盐气味剂都引起了强烈的电生理反应,但只有氨基酸气味剂才能刺激活性碳的活性依赖性标记。腺苷酸环化酶(AC)激活剂(forskolin)和磷酸二酯酶抑制剂(3-异丁基-1-甲基黄嘌呤,IBMX)也引起了强烈的电生理反应;通常比氨基酸或胆汁盐气味引起的反应更大。然而,无论是单独使用福斯高林还是福斯高林和IBMX的混合物都不能刺激活性依赖性标记。用福斯可林浸泡嗅觉上皮,可能会增加细胞内cAMP的浓度,比氨基酸气味剂明显更大程度地降低了对胆盐气味剂的反应。总的来说,这些发现表明氨基酸输入的转导并不主要依赖于环核苷酸门控(CNG)通道的激活,而CNG通道的激活可能是胆盐输入转导所必需的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cyclic nucleotide-gated channel activation is not required for activity-dependent labeling of zebrafish olfactory receptor neurons by amino acids.

The olfactory epithelium of fish is heterogeneous both with respect to the types of receptor cells (ORNs) present and the families of odorant receptors expressed in these cells. As a consequence of this diversity, the transduction cascade(s) activated by odorants has yet to be unambiguously established. In the current study, electrophysiological and activity-dependent labeling techniques were used to assess the role of the cyclic nucleotide-gated channel in zebrafish olfactory transduction. Both amino acid and bile salt odorants elicited robust electrophysiological responses, however, activity-dependent labeling of ORNs could be stimulated only by the amino acid odorants. An adenylate cyclase (AC) activator (forskolin) and a phosphodiesterase inhibitor (3-isobutyl-1-methylxanthine, IBMX) also elicited robust electrophysiological responses; generally larger than the responses elicited by either the amino acid or bile salt odorants. However, neither forskolin alone or a mixture of forskolin and IBMX stimulated activity-dependent labeling. Bathing the olfactory epithelium with forskolin, which presumably increased the intracellular concentration of cAMP, reduced the responses to bile salt odorants to a significantly greater extent than amino acid odorants. Collectively, these findings suggest that the transduction of amino acid input does not rely primarily on cyclic nucleotide-gated (CNG) channel activation and that CNG channel activation may be required for the transduction of bile salt input.

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