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Role of serotonin in Alzheimer's disease: a new therapeutic target?5-羟色胺在阿尔茨海默病中的作用:一个新的治疗靶点?
CNS Drugs. 2011 Sep 1;25(9):765-81. doi: 10.2165/11590190-000000000-00000.
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The monoamine neurotransmitter disorders: an expanding range of neurological syndromes.单胺类神经递质紊乱:一系列不断扩大的神经综合征。
Lancet Neurol. 2011 Aug;10(8):721-33. doi: 10.1016/S1474-4422(11)70141-7.
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Large neutral amino acids in the treatment of PKU: from theory to practice.大中性氨基酸在苯丙酮尿症治疗中的应用:从理论到实践。
J Inherit Metab Dis. 2010 Dec;33(6):671-6. doi: 10.1007/s10545-010-9216-1. Epub 2010 Oct 26.
4
Suboptimal outcomes in patients with PKU treated early with diet alone: revisiting the evidence.仅饮食治疗的苯丙酮尿症患者的结局不佳:重新审视证据。
Mol Genet Metab. 2010 Oct-Nov;101(2-3):99-109. doi: 10.1016/j.ymgme.2010.05.017. Epub 2010 Jun 22.
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Adult Polyglucosan Body Disease (APBD): Anaplerotic diet therapy (Triheptanoin) and demonstration of defective methylation pathways.成人多聚醇体病(APBD):生糖氨基酸补充治疗(三庚酸甘油脂)和甲基化途径缺陷的验证。
Mol Genet Metab. 2010 Oct-Nov;101(2-3):246-52. doi: 10.1016/j.ymgme.2010.06.017. Epub 2010 Jul 6.
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Future treatment strategies in phenylketonuria.苯丙酮尿症的未来治疗策略。
Mol Genet Metab. 2010;99 Suppl 1:S90-5. doi: 10.1016/j.ymgme.2009.10.008.
7
Hepatocyte transplantation (HTx) corrects selected neurometabolic abnormalities in murine intermediate maple syrup urine disease (iMSUD).肝细胞移植(HTx)可纠正小鼠中间型枫糖尿症(iMSUD)中某些神经代谢异常。
Biochim Biophys Acta. 2009 Oct;1792(10):1004-10. doi: 10.1016/j.bbadis.2009.08.006. Epub 2009 Aug 19.
8
Dual mechanism of brain injury and novel treatment strategy in maple syrup urine disease.枫糖尿症脑损伤的双重机制及新治疗策略
Brain. 2009 Apr;132(Pt 4):903-18. doi: 10.1093/brain/awp024. Epub 2009 Mar 17.
9
LAT-1 expression in pre- and post-implantation embryos and placenta.植入前和植入后胚胎及胎盘中LAT-1的表达。
Placenta. 2009 Mar;30(3):270-6. doi: 10.1016/j.placenta.2008.12.015. Epub 2009 Feb 4.
10
Effects of feeding individual amino acids upon the distribution of other amino acids between cells and extracellular fluid.喂食单个氨基酸对其他氨基酸在细胞与细胞外液之间分布的影响。
J Biol Chem. 1948 Feb;172(2):515-24.

针对脑苯丙氨酸降低的非生理氨基酸(NPAA)治疗:在 PAHENU2 小鼠中的初步研究。

Non-physiological amino acid (NPAA) therapy targeting brain phenylalanine reduction: pilot studies in PAHENU2 mice.

机构信息

Section of Clinical Pharmacology, College of Pharmacy, Washington State University, Pullman, WA 99164-6510, USA.

出版信息

J Inherit Metab Dis. 2013 May;36(3):513-23. doi: 10.1007/s10545-012-9524-8. Epub 2012 Sep 14.

DOI:10.1007/s10545-012-9524-8
PMID:22976763
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3654543/
Abstract

Transport of large neutral amino acids (LNAA) across the blood brain barrier (BBB) is facilitated by the L-type amino acid transporter, LAT1. Peripheral accumulation of one LNAA (e.g., phenylalanine (phe) in PKU) is predicted to increase uptake of the offending amino acid to the detriment of others, resulting in disruption of brain amino acid homeostasis. We hypothesized that selected non-physiological amino acids (NPAAs) such as DL-norleucine (NL), 2-aminonorbornane (NB; 2-aminobicyclo-(2,1,1)-heptane-2-carboxylic acid), 2-aminoisobutyrate (AIB), and N-methyl-aminoisobutyrate (MAIB), acting as competitive inhibitors of various brain amino acid transporters, could reduce brain phe in Pah (enu2) mice, a relevant murine model of PKU. Oral feeding of 5 % NL, 5 % AIB, 0.5 % NB and 3 % MAIB reduced brain phe by 56 % (p < 0.01), -1 % (p = NS), 27 % (p < 0.05) and 14 % (p < 0.01), respectively, compared to untreated subjects. Significant effects on other LNAAs (tyrosine, methionine, branched chain amino acids) were also observed, however, with MAIB displaying the mildest effects. Of interest, MAIB represents an inhibitor of the system A (alanine) transporter that primarily traffics small amino acids and not LNAAs. Our studies represent the first in vivo use of these NPAAs in Pah (enu2) mice, and provide proof-of-principle for their further preclinical development, with the long-term objective of identifying NPAA combinations and concentrations that selectively restrict brain phe transport while minimally impacting other LNAAs and downstream intermediates.

摘要

氨基酸转运蛋白 L 型(LAT1)促进了大中性氨基酸(LNAA)穿过血脑屏障(BBB)的转运。一种 LNAA(例如苯丙氨酸(phe)在 PKU 中的积累)的外周积累预计会增加摄入的氨基酸,从而损害其他氨基酸,导致大脑氨基酸稳态的破坏。我们假设,选择非生理氨基酸(NPAAs),如 DL-正亮氨酸(NL)、2-氨基降冰片烷(NB;2-氨基双环[2.1.1]庚烷-2-羧酸)、2-氨基异丁酸(AIB)和 N-甲基-氨基异丁酸(MAIB),作为各种脑氨基酸转运蛋白的竞争性抑制剂,可能会降低 Pah(enu2)小鼠(PKU 的相关小鼠模型)的脑中 phe 水平。口服给予 5%的 NL、5%的 AIB、0.5%的 NB 和 3%的 MAIB,与未治疗的对照组相比,分别降低了 56%(p<0.01)、-1%(p=NS)、27%(p<0.05)和 14%(p<0.01)的脑中 phe 水平。此外,还观察到对其他 LNAA(酪氨酸、甲硫氨酸、支链氨基酸)的显著影响,但 MAIB 的影响最小。有趣的是,MAIB 是系统 A(丙氨酸)转运蛋白的抑制剂,该蛋白主要转运小分子氨基酸而不是 LNAA。我们的研究代表了这些 NPAAs 在 Pah(enu2)小鼠体内的首次应用,并为它们在临床前的进一步开发提供了原理证明,长期目标是确定 NPAA 组合和浓度,这些组合和浓度可以选择性地限制脑 phe 转运,同时对其他 LNAA 和下游中间产物的影响最小。