Yokoyama Takuya, Yamamoto Yoshio, Saino Tomoyuki
Department of Anatomy (Cell Biology), Iwate Medical University, Yahaba, Japan.
Laboratory of Veterinary Anatomy and Cell Biology, Faculty of Agriculture, Iwate University, Morioka, Japan.
Neurosci Lett. 2017 Mar 22;644:114-120. doi: 10.1016/j.neulet.2017.02.048. Epub 2017 Feb 22.
We examined serotonin (5-HT)-mediated modulation of acetylcholine (ACh)-induced intracellular Ca ([Ca]) responses in rat adrenal chromaffin cells using calcium imaging. 5-HT did not induce any [Ca] response in clustered chromaffin cells. However, the magnitude of ACh-induced [Ca] increases in the same specimens was inhibited in the presence of 5-HT. ACh-induced [Ca] increases in chromaffin cells were also inhibited by the 5-HT1A receptor agonist, 8-hydroxy-2-(dipropylamino) tetralin hydrobromide, but were not changed by the 5-HT1B, 5-HT2, or 5-HT3 receptor agonists, CP93129, α-methyl-5-HT, or 1-(m-chlorophenyl) biguanide, respectively. RT-PCR analysis detected the expression of all 5-HT receptor subtype mRNAs, except for 5-HT5 receptors, in extracts of the adrenal medulla. Immunohistochemistry revealed that immunoreactivity for 5-HT1A receptor was located in the chromaffin cells immunoreactive for the biosynthetic enzyme for noradrenaline, dopamine β-hydroxylase. These results suggest that 5-HT inhibits ACh-induced excitability in adrenal chromaffin cells via the 5-HT1A receptor in order to reduce catecholamine release during preganglionic sympathetic stimuli.
我们运用钙成像技术,研究了5-羟色胺(5-HT)介导的对大鼠肾上腺嗜铬细胞中乙酰胆碱(ACh)诱导的细胞内钙离子([Ca])反应的调节作用。5-HT在聚集的嗜铬细胞中未诱导出任何[Ca]反应。然而,在存在5-HT的情况下,相同标本中ACh诱导的[Ca]升高幅度受到抑制。嗜铬细胞中ACh诱导的[Ca]升高也受到5-HT1A受体激动剂8-羟基-2-(二丙基氨基)四氢溴化萘的抑制,但分别未被5-HT1B、5-HT2或5-HT3受体激动剂CP93129、α-甲基-5-HT或1-(间氯苯基)双胍改变。逆转录聚合酶链反应(RT-PCR)分析在肾上腺髓质提取物中检测到了除5-HT5受体外所有5-HT受体亚型mRNA的表达。免疫组织化学显示,5-HT1A受体的免疫反应性位于对去甲肾上腺素生物合成酶多巴胺β-羟化酶呈免疫反应性的嗜铬细胞中。这些结果表明,5-HT通过5-HT1A受体抑制肾上腺嗜铬细胞中ACh诱导的兴奋性,以便在节前交感神经刺激期间减少儿茶酚胺释放。