Muller Arnaud, Glattard Elise, Taleb Omar, Kemmel Véronique, Laux Alexis, Miehe Monique, Delalande François, Roussel Guy, Van Dorsselaer Alain, Metz-Boutigue Marie-Hélène, Aunis Dominique, Goumon Yannick
Inserm, U575, Physiopathologie du Système Nerveux, Strasbourg, France.
PLoS One. 2008 Feb 20;3(2):e1641. doi: 10.1371/journal.pone.0001641.
Morphine, the principal active agent in opium, is not restricted to plants, but is also present in different animal tissues and cell types, including the mammalian brain. In fact, its biosynthetic pathway has been elucidated in a human neural cell line. These data suggest a role for morphine in brain physiology (e.g., neurotransmission), but this hypothesis remains a matter of debate. Recently, using the adrenal neuroendocrine chromaffin cell model, we have shown the presence of morphine-6-glucuronide (M6G) in secretory granules and their secretion products, leading us to propose that these endogenous alkaloids might represent new neuroendocrine factors. Here, we investigate the potential function of endogenous alkaloids in the central nervous system.
Microscopy, molecular biology, electrophysiology, and proteomic tools were applied to human neuroblastoma SH-SY5Y cells (i) to characterize morphine and M6G, and (ii) to demonstrate the presence of the UDP-glucuronyltransferase 2B7 enzyme, which is responsible for the formation of M6G from morphine. We show that morphine is secreted in response to nicotine stimulation via a Ca(2+)-dependent mechanism involving specific storage and release mechanisms. We also show that morphine and M6G at concentrations as low as 10(-10) M are able to evoke specific naloxone-reversible membrane currents, indicating possible autocrine/paracrine regulation in SH-SY5Y cells. Microscopy and proteomic approaches were employed to detect and quantify endogenous morphine in the mouse brain. Morphine is present in the hippocampus, cortex, olfactory bulb, and cerebellum at concentration ranging from 1.45 to 7.5 pmol/g. In the cerebellum, morphine immunoreactivity is localized to GABA basket cells and their termini, which form close contacts on Purkinje cell bodies.
CONCLUSIONS/SIGNIFICANCE: The presence of morphine in the brain and its localization in particular areas lead us to conclude that it has a specific function in neuromodulation and/or neurotransmission. Furthermore, its presence in cerebellar basket cell termini suggests that morphine has signaling functions in Purkinje cells that remain to be discovered.
吗啡是鸦片中的主要活性成分,并非植物所特有,在包括哺乳动物大脑在内的不同动物组织和细胞类型中也有存在。事实上,其生物合成途径已在一种人类神经细胞系中得到阐明。这些数据表明吗啡在大脑生理学(如神经传递)中发挥作用,但这一假说仍存在争议。最近,我们利用肾上腺神经内分泌嗜铬细胞模型,在分泌颗粒及其分泌产物中发现了吗啡 -6- 葡萄糖醛酸苷(M6G),这使我们提出这些内源性生物碱可能代表新的神经内分泌因子。在此,我们研究内源性生物碱在中枢神经系统中的潜在功能。
运用显微镜、分子生物学、电生理学和蛋白质组学工具对人神经母细胞瘤 SH - SY5Y 细胞进行研究,(i)以表征吗啡和 M6G,(ii)证明负责从吗啡形成 M6G 的 UDP - 葡萄糖醛酸基转移酶 2B7 酶的存在。我们发现,吗啡通过涉及特定储存和释放机制的 Ca(2+) 依赖性机制响应尼古丁刺激而分泌。我们还表明,低至 10(-10) M 的吗啡和 M6G 浓度能够引发特定的纳洛酮可逆膜电流,表明在 SH - SY5Y 细胞中可能存在自分泌/旁分泌调节。采用显微镜和蛋白质组学方法检测和定量小鼠大脑中的内源性吗啡。吗啡存在于海马体、皮质、嗅球和小脑中,浓度范围为 1.45 至 7.5 pmol/g。在小脑中,吗啡免疫反应性定位于 GABA 篮状细胞及其终末,它们在浦肯野细胞体上形成紧密接触。
结论/意义:大脑中吗啡的存在及其在特定区域的定位使我们得出结论,它在神经调节和/或神经传递中具有特定功能。此外,它在小脑篮状细胞终末的存在表明吗啡在浦肯野细胞中具有尚待发现的信号功能。