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β-桉叶醇,一种氧化倍半萜烯,通过 TRPA1 和自主神经系统刺激食欲。

β-Eudesmol, an oxygenized sesquiterpene, stimulates appetite via TRPA1 and the autonomic nervous system.

机构信息

Research Laboratories for Health Science and Food Technologies, Kirin Company, Limited, Yokohama, Kanagawa, 236-0004, Japan.

Central Laboratories for Key Technologies, Kirin Company, Limited., Yokohama, Kanagawa, 236-0004, Japan.

出版信息

Sci Rep. 2017 Nov 17;7(1):15785. doi: 10.1038/s41598-017-16150-6.

Abstract

Transient receptor potential ankyrin 1 (TRPA1) is a calcium-permeable non-selective cation channel, which is activated by various noxious or irritant substances in nature. TRPA1 activators have been generally recognized as noxious, however, foods and beverages containing TRPA1 activators are preferably consumed; the reasons for this discrepancy are not well understood. We demonstrate that TRPA1 is involved in the stimulatory appetite control mechanism. β-Eudesmol is an oxygenated sesquiterpene contained in medicinal or edible plants which activates TRPA1. Oral administration of β-eudesmol brought significant increments in food intake in rats and elevated plasma ghrelin levels. Gastric vagal nerve activity (GVNA) has been reported to affect feeding behavior. In vivo electrophysiological measurement of GVNA revealed that oral-ingestion of β-eudesmol significantly increased GVNA. This GVNA elevation was eliminated by TRPA1 inhibitor (HC-030031) treatment prior to β-eudesmol administration. The physiological effects of β-eudesmol, for example, incremental increase in food intake, ghrelin elevation and activation of GVNA, were significantly reduced in TRPA1 knockout rats. Our results indicated that β-eudesmol stimulates an increase in appetite through TRPA1, and suggests why TRPA1 activator containing foods and beverages are preferably consumed.

摘要

瞬时受体电位锚蛋白 1(TRPA1)是一种钙通透性非选择性阳离子通道,可被自然界中的各种有害或刺激性物质激活。TRPA1 激活剂通常被认为是有害的,然而,含有 TRPA1 激活剂的食物和饮料却更受欢迎;这种差异的原因尚不清楚。我们证明 TRPA1 参与了食欲刺激的控制机制。β-桉叶醇是一种存在于药用或食用植物中的含氧倍半萜,可激活 TRPA1。β-桉叶醇的口服给药可显著增加大鼠的食物摄入量,并升高血浆胃饥饿素水平。胃迷走神经活动(GVNA)已被报道会影响摄食行为。体内电生理测量 GVNA 显示,β-桉叶醇的口服摄入可显著增加 GVNA。在给予β-桉叶醇之前,用 TRPA1 抑制剂(HC-030031)处理可消除这种 GVNA 升高。β-桉叶醇的生理作用,例如食物摄入量的增加、胃饥饿素水平的升高和 GVNA 的激活,在 TRPA1 敲除大鼠中显著降低。我们的结果表明,β-桉叶醇通过 TRPA1 刺激食欲增加,并解释了为什么含有 TRPA1 激活剂的食物和饮料更受欢迎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed38/5693998/75fe43865262/41598_2017_16150_Fig1_HTML.jpg

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