Suppr超能文献

川陈皮素,一种柑橘多甲氧基黄酮,对培养的牛肾上腺嗜铬细胞瘤细胞儿茶酚胺分泌的双重作用。

Dual effects of nobiletin, a citrus polymethoxy flavone, on catecholamine secretion in cultured bovine adrenal medullary cells.

机构信息

Department of Pharmacology, University of Occupational and Environmental Health, School of Medicine, Yahatanishi-ku, Kitakyushu, Japan.

出版信息

J Neurochem. 2010 Aug;114(4):1030-8. doi: 10.1111/j.1471-4159.2010.06840.x. Epub 2010 Jun 1.

Abstract

Nobiletin, a compound of polymethoxy flavones found in citrus fruits, possesses a wide range of pharmacological activities. Here we report the effects of nobiletin on catecholamine secretion in cultured bovine adrenal medullary cells. Nobiletin (1.0-100 microM) concentration-dependently stimulated catecholamine secretion and (45)Ca(2+) influx. Its stimulatory effect of nobiletin on catecholamine secretion was abolished by deprivation of extracellular Ca(2+) and partially inhibited by specific inhibitors of voltage-dependent Ca(2+) channels and Na(+)/Ca(2+) exchangers. On the other hand, nobiletin suppressed catecholamine secretion and (22)Na(+) and (45)Ca(2+) influx induced by acetylcholine, an agonist of nicotinic acetylcholine receptors, in a concentration-dependent manner. It also inhibited catecholamine secretion, (22)Na(+) influx and/or (45)Ca(2+) influx induced by veratridine, an activator of voltage-dependent Na(+) channels, and 56 mM K(+), an activator of voltage-dependent Ca(2+) channels. In Xenopus oocytes expressing alpha3beta4 neuronal acetylcholine receptors, nobiletin directly inhibited the current evoked by acetylcholine in a concentration-dependent manner similar to that observed in catecholamine secretion. The present findings suggest that nobiletin, by itself, stimulates catecholamine secretion via activation of voltage-dependent Ca(2+) channels or Na(+)/Ca(2+) exchangers, whereas it inhibits catecholamine secretion induced by acetylcholine through the suppression of Na(+) influx and Ca(2+) influx in cultured bovine adrenal medullary cells.

摘要

川陈皮素是柑橘类水果中多甲氧基黄酮类化合物的一种,具有广泛的药理活性。本研究报告了川陈皮素对培养的牛肾上腺髓质细胞儿茶酚胺分泌的影响。川陈皮素(1.0-100 μM)浓度依赖性地刺激儿茶酚胺分泌和(45)Ca(2+)内流。川陈皮素对儿茶酚胺分泌的刺激作用被剥夺细胞外 Ca(2+)所消除,被电压依赖性 Ca(2+)通道和 Na(+)/Ca(2+)交换体的特异性抑制剂部分抑制。另一方面,川陈皮素浓度依赖性地抑制乙酰胆碱(烟碱型乙酰胆碱受体激动剂)诱导的儿茶酚胺分泌和(22)Na(+)和(45)Ca(2+)内流。它还抑制veratridine(电压依赖性 Na(+)通道激活剂)和 56 mM K+(电压依赖性 Ca(2+)通道激活剂)诱导的儿茶酚胺分泌、(22)Na(+)内流和/或(45)Ca(2+)内流。在表达α3β4 神经元烟碱型乙酰胆碱受体的非洲爪蟾卵母细胞中,川陈皮素以类似于儿茶酚胺分泌的方式直接浓度依赖性地抑制乙酰胆碱诱导的电流。本研究结果表明,川陈皮素本身通过激活电压依赖性 Ca(2+)通道或 Na(+)/Ca(2+)交换体刺激儿茶酚胺分泌,而通过抑制 Na(+)内流和 Ca(2+)内流抑制乙酰胆碱诱导的儿茶酚胺分泌在培养的牛肾上腺髓质细胞中。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验