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1
Curcumin acts via transient receptor potential vanilloid-1 receptors to inhibit gut nociception and reverses visceral hyperalgesia.姜黄素通过瞬时受体电位香草酸 1 型受体发挥作用,抑制肠道伤害感受,并逆转内脏痛觉过敏。
Neurogastroenterol Motil. 2013 Jun;25(6):e429-40. doi: 10.1111/nmo.12145. Epub 2013 May 3.
2
NERD: an umbrella term including heterogeneous subpopulations.NERD:一个包含异质亚群的伞式术语。
Nat Rev Gastroenterol Hepatol. 2013 Jun;10(6):371-80. doi: 10.1038/nrgastro.2013.50. Epub 2013 Mar 26.
3
Therapeutic roles of curcumin: lessons learned from clinical trials.姜黄素的治疗作用:临床试验获得的经验。
AAPS J. 2013 Jan;15(1):195-218. doi: 10.1208/s12248-012-9432-8. Epub 2012 Nov 10.
4
Comparative absorption of a standardized curcuminoid mixture and its lecithin formulation.标准化姜黄素混合物与其卵磷脂配方的比较吸收。
J Nat Prod. 2011 Apr 25;74(4):664-9. doi: 10.1021/np1007262. Epub 2011 Mar 17.
5
Phase IIa clinical trial of curcumin for the prevention of colorectal neoplasia.姜黄素预防结直肠肿瘤的 IIa 期临床试验。
Cancer Prev Res (Phila). 2011 Mar;4(3):354-64. doi: 10.1158/1940-6207.CAPR-10-0098.
6
Use of complementary and alternative medicine by patients with inflammatory bowel disease.炎症性肠病患者对补充和替代医学的使用。
Inflamm Bowel Dis. 2011 Feb;17(2):655-62. doi: 10.1002/ibd.21360.
7
Tumor necrosis factor-{alpha} suppresses angiotensinogen expression through formation of a p50/p50 homodimer in human renal proximal tubular cells.肿瘤坏死因子-α通过形成人肾近端肾小管细胞中的 p50/p50 同源二聚体抑制血管紧张素原的表达。
Am J Physiol Cell Physiol. 2010 Oct;299(4):C750-9. doi: 10.1152/ajpcell.00078.2010. Epub 2010 Jun 30.
8
A position statement on NAFLD/NASH based on the EASL 2009 special conference.基于欧洲肝脏研究学会(EASL)2009年特别会议的非酒精性脂肪性肝病/非酒精性脂肪性肝炎立场声明。
J Hepatol. 2010 Aug;53(2):372-84. doi: 10.1016/j.jhep.2010.04.008. Epub 2010 May 7.
9
Increased TRPV1 gene expression in esophageal mucosa of patients with non-erosive and erosive reflux disease.非糜烂性和糜烂性反流病患者食管黏膜中 TRPV1 基因表达增加。
Neurogastroenterol Motil. 2010 Jul;22(7):746-51, e219. doi: 10.1111/j.1365-2982.2010.01514.x. Epub 2010 May 6.
10
Safety profile of IBD therapeutics: infectious risks.炎症性肠病治疗药物的安全性概况:感染风险
Med Clin North Am. 2010 Jan;94(1):115-33. doi: 10.1016/j.mcna.2009.08.016.

姜黄素在消化疾病中的治疗潜力。

Therapeutic potential of curcumin in digestive diseases.

机构信息

Pietro Dulbecco, Vincenzo Savarino, Department of Internal Medicine and Medical Specialties, University of Genoa, 16132 Genoa, Italy.

出版信息

World J Gastroenterol. 2013 Dec 28;19(48):9256-70. doi: 10.3748/wjg.v19.i48.9256.

DOI:10.3748/wjg.v19.i48.9256
PMID:24409053
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3882399/
Abstract

Curcumin is a low-molecular-weight hydrophobic polyphenol that is extracted from turmeric, which possesses a wide range of biological properties including anti-inflammatory, anti-oxidant, anti-proliferative and anti-microbial activities. Despite its diverse targets and substantial safety, clinical applications of this molecule for digestive disorders have been largely limited to case series or small clinical trials. The poor bioavailability of curcumin is likely the major hurdle for its more widespread use in humans. However, complexation of curcumin into phytosomes has recently helped to bypass this problem, as it has been demonstrated that this new lecithin formulation enables increased absorption to a level 29-fold higher than that of traditional curcuminoid products. This allows us to achieve much greater tissue substance delivery using significantly lower doses of curcumin than have been used in past clinical studies. As curcumin has already been shown to provide good therapeutic results in some small studies of both inflammatory and neoplastic bowel disorders, it is reasonable to anticipate an even greater efficacy with the advent of this new technology, which remarkably improves its bioavailability. These features are very promising and may represent a novel and effective therapeutic approach to both functional and organic digestive diseases.

摘要

姜黄素是一种低分子量疏水性多酚,从姜黄中提取而来,具有广泛的生物学特性,包括抗炎、抗氧化、抗增殖和抗菌活性。尽管这种分子的靶点多样且安全性高,但它在消化疾病方面的临床应用主要局限于病例系列或小型临床试验。姜黄素的生物利用度差可能是其在人类中更广泛应用的主要障碍。然而,最近将姜黄素复合到植物固醇体中有助于克服这个问题,因为已经证明这种新的卵磷脂配方可以使吸收增加 29 倍,高于传统姜黄素产品的吸收水平。这使得我们能够以比过去临床研究中使用的更低剂量实现更高的组织物质传递。由于姜黄素在一些炎症和肿瘤性肠病的小型研究中已经显示出良好的治疗效果,因此随着这项新技术的出现,我们有理由预期其疗效更大,因为这项新技术显著提高了其生物利用度。这些特点非常有前途,可能代表了一种治疗功能性和器质性消化疾病的新的有效治疗方法。