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来自仙人掌的 indicaxanthin 可穿过血脑屏障,并以与饮食一致的量调节大鼠海马体中的神经元生物电活动。

Indicaxanthin from Opuntia ficus-indica Crosses the Blood-Brain Barrier and Modulates Neuronal Bioelectric Activity in Rat Hippocampus at Dietary-Consistent Amounts.

作者信息

Allegra Mario, Carletti Fabio, Gambino Giuditta, Tutone Marco, Attanzio Alessandro, Tesoriere Luisa, Ferraro Giuseppe, Sardo Pierangelo, Almerico Anna Maria, Livrea Maria Antonia

机构信息

Dipartimento di Scienze e Tecnologie Biologiche, Chimiche e Farmaceutiche, University of Palermo , Via M. Cipolla 74, 90121 Palermo, Italy.

Dipartimento di Biomedicina Sperimentale e Neuroscienze Cliniche, Sezione di Fisiologia Umana "G. Pagano", University of Palermo , Corso Tukory 129, 90134 Palermo, Italy.

出版信息

J Agric Food Chem. 2015 Aug 26;63(33):7353-60. doi: 10.1021/acs.jafc.5b02612. Epub 2015 Aug 13.

Abstract

Indicaxanthin is a bioactive and bioavailable betalain pigment from the Opuntia ficus-indica fruits. In this in vivo study, kinetic measurements showed that indicaxanthin is revealed in the rat brain within 1 h from oral administration of 2 μmol/kg, an amount compatible with a dietary consumption of cactus pear fruits in humans. A peak (20 ± 2.4 ng of indicaxanthin per whole brain) was measured after 2.5 h; thereafter the molecule disappeared with first order kinetics within 4 h. The potential of indicaxanthin to affect neural activities was in vivo investigated by a microiontophoretic approach. Indicaxanthin, administered in a range between 0.085 ng and 0.34 ng per neuron, dose-dependently modulated the rate of discharge of spontaneously active neurons of the hippocampus, with reduction of the discharge and related changes of latency and duration of the effect. Indicaxanthin (0.34 ng/neuron) showed inhibitory effects on glutamate-induced excitation, indicating activity at the level of glutamatergic synapses. A molecular target of indicaxanthin is suggested by in silico molecular modeling of indicaxanthin with N-methyl-D-aspartate receptor (NMDAR), the most represented of the glutamate receptor family in hippocampus. Therefore, at nutritionally compatible amounts indicaxanthin (i) crosses the rat BBB and accumulates in brain; (ii) can affect the bioelectric activity of hippocampal neurons locally treated with amounts comparable with those measured in the brain; and (iii) modulates glutamate-induced neuronal excitation. The potential of dietary indicaxanthin as a natural neuromodulatory agent deserves further mechanistic and neurophysiologic investigation.

摘要

紫茉莉黄素是一种来自仙人掌果实的具有生物活性且可生物利用的甜菜色素。在这项体内研究中,动力学测量表明,口服2 μmol/kg的紫茉莉黄素后1小时内,大鼠脑中就能检测到该物质,这一剂量与人类食用仙人掌果的饮食摄入量相当。2.5小时后测得峰值(每全脑20±2.4 ng紫茉莉黄素);此后,该分子在4小时内以一级动力学消失。通过微离子电泳法在体内研究了紫茉莉黄素影响神经活动的潜力。以每神经元0.085 ng至0.34 ng的剂量范围施用紫茉莉黄素,可剂量依赖性地调节海马体自发活动神经元的放电速率,同时降低放电频率以及相关的潜伏期和效应持续时间的变化。紫茉莉黄素(0.34 ng/神经元)对谷氨酸诱导的兴奋具有抑制作用,表明其在谷氨酸能突触水平具有活性。通过紫茉莉黄素与N-甲基-D-天冬氨酸受体(NMDAR)的计算机模拟分子建模,提示了紫茉莉黄素的一个分子靶点,NMDAR是海马体中谷氨酸受体家族中最具代表性的受体。因此,可以得出,在营养兼容量下紫茉莉黄素(i)可穿过大鼠血脑屏障并在脑中蓄积;(ii)能够影响局部处理的海马神经元的生物电活动,其处理剂量与在脑中测得的剂量相当;(iii)调节谷氨酸诱导的神经元兴奋。膳食紫茉莉黄素作为一种天然神经调节剂的潜力值得进一步进行机制和神经生理学研究。

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