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雪莲花对小鼠三叉神经脊束尾核胶状质神经元甘氨酸和 GABA 样作用。

Glycine- and GABA-mimetic Actions of Shilajit on the Substantia Gelatinosa Neurons of the Trigeminal Subnucleus Caudalis in Mice.

机构信息

Department of Oral Physiology, School of Dentistry and Institute of Oral Bioscience, Chonbuk National University, Jeonju 561-756, Korea.

出版信息

Korean J Physiol Pharmacol. 2011 Oct;15(5):285-9. doi: 10.4196/kjpp.2011.15.5.285. Epub 2011 Oct 31.

Abstract

Shilajit, a medicine herb commonly used in Ayurveda, has been reported to contain at least 85 minerals in ionic form that act on a variety of chemical, biological, and physical stressors. The substantia gelatinosa (SG) neurons of the trigeminal subnucleus caudalis (Vc) are involved in orofacial nociceptive processing. Shilajit has been reported to be an injury and muscular pain reliever but there have been few functional studies of the effect of Shilajit on the SG neurons of the Vc. Therefore, whole cell and gramicidin-perfotrated patch clamp studies were performed to examine the action mechanism of Shilajit on the SG neurons of Vc from mouse brainstem slices. In the whole cell patch clamp mode, Shilajit induced short-lived and repeatable inward currents under the condition of a high chloride pipette solution on all the SG neurons tested. The Shilajit-induced inward currents were concentration dependent and maintained in the presence of tetrodotoxin (TTX), a voltage gated Na(+) channel blocker, CNQX, a non-NMDA glutamate receptor antagonist, and AP5, an NMDA receptor antagonist. The Shilajit-induced responses were partially suppressed by picrotoxin, a GABA(A) receptor antagonist, and totally blocked in the presence of strychnine, a glycine receptor antagonist, however not affected by mecamylamine hydrochloride (MCH), a nicotinic acetylcholine receptor antagonist. Under the potassium gluconate pipette solution at holding potential 0 mV, Shilajit induced repeatable outward current. These results show that Shilajit has inhibitory effects on the SG neurons of Vc through chloride ion channels by activation of the glycine receptor and GABA(A) receptor, indicating that Shilajit contains sedating ingredients for the central nervous system. These results also suggest that Shilajit may be a potential target for modulating orofacial pain processing.

摘要

喜来芝,一种常用于阿育吠陀医学的草药,据报道含有至少 85 种以离子形式存在的矿物质,这些矿物质对各种化学、生物和物理应激源起作用。三叉神经尾核亚核的胶状质(SG)神经元参与口面部痛觉处理。喜来芝已被报道为一种损伤和肌肉疼痛缓解剂,但对喜来芝对 Vc 的 SG 神经元的影响的功能研究较少。因此,进行了全细胞和短杆菌肽穿孔贴附式膜片钳研究,以检查喜来芝对来自小鼠脑干切片的 Vc 的 SG 神经元的作用机制。在全细胞贴附式膜片钳模式下,喜来芝在高氯管内溶液的条件下,在所有测试的 SG 神经元上诱导短暂且可重复的内向电流。喜来芝诱导的内向电流呈浓度依赖性,在电压门控钠(Na+)通道阻断剂河豚毒素(TTX)、非 NMDA 谷氨酸受体拮抗剂 CNQX 和 NMDA 受体拮抗剂 AP5 的存在下得以维持。喜来芝诱导的反应部分被 GABA(A) 受体拮抗剂荷包牡丹碱抑制,在甘氨酸受体拮抗剂士的宁存在下完全阻断,但不受烟碱型乙酰胆碱受体拮抗剂盐酸美金刚胺(MCH)影响。在保持电位 0 mV 的葡萄糖酸钾管内溶液中,喜来芝诱导可重复的外向电流。这些结果表明,喜来芝通过激活甘氨酸受体和 GABA(A)受体,通过氯离子通道对 Vc 的 SG 神经元产生抑制作用,表明喜来芝含有镇静成分的中枢神经系统。这些结果还表明,喜来芝可能是调节口面部疼痛处理的潜在靶点。

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Phytother Res. 2007 May;21(5):401-5. doi: 10.1002/ptr.2100.
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