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Alternative targets within the endocannabinoid system for future treatment of gastrointestinal diseases.内源性大麻素系统内用于未来胃肠道疾病治疗的替代靶点。
Can J Gastroenterol. 2011 Jul;25(7):377-83. doi: 10.1155/2011/953975.
2
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The endocannabinoid system in the physiology and pathophysiology of the gastrointestinal tract.内源性大麻素系统在胃肠道生理与病理生理中的作用
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Endocannabinoids and the Digestive Tract and Bladder in Health and Disease.内源性大麻素与健康和疾病状态下的消化道及膀胱
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本文引用的文献

1
The atypical cannabinoid O-1602 protects against experimental colitis and inhibits neutrophil recruitment.非典型大麻素 O-1602 可预防实验性结肠炎并抑制中性粒细胞募集。
Inflamm Bowel Dis. 2011 Aug;17(8):1651-64. doi: 10.1002/ibd.21538. Epub 2010 Nov 15.
2
Preliminary efficacy and safety of an oromucosal standardized cannabis extract in chemotherapy-induced nausea and vomiting.口腔黏膜标准化大麻素提取物治疗化疗诱导性恶心呕吐的初步疗效和安全性。
Br J Clin Pharmacol. 2010 Nov;70(5):656-63. doi: 10.1111/j.1365-2125.2010.03743.x.
3
The cannabinoid receptor agonist delta-9-tetrahydrocannabinol does not affect visceral sensitivity to rectal distension in healthy volunteers and IBS patients.大麻素受体激动剂 Δ9-四氢大麻酚不会影响健康志愿者和 IBS 患者对直肠扩张的内脏敏感性。
Neurogastroenterol Motil. 2011 Jan;23(1):30-5, e2. doi: 10.1111/j.1365-2982.2010.01587.x. Epub 2010 Aug 16.
4
The effects of Delta-tetrahydrocannabinol and cannabidiol alone and in combination on damage, inflammation and in vitro motility disturbances in rat colitis.Delta-四氢大麻酚和大麻二酚单独及联合作用对大鼠结肠炎损伤、炎症和体外运动障碍的影响。
Br J Pharmacol. 2010 Jun;160(3):712-23. doi: 10.1111/j.1476-5381.2010.00791.x.
5
A one-year study to assess the safety and efficacy of the CB1R inverse agonist taranabant in overweight and obese patients with type 2 diabetes.一项为期一年的研究,旨在评估 CB1R 反向激动剂 taranabant 在超重和肥胖 2 型糖尿病患者中的安全性和有效性。
Diabetes Obes Metab. 2010 Jun;12(6):517-31. doi: 10.1111/j.1463-1326.2009.01188.x.
6
Cannabinoid receptor 1 gene polymorphism and irritable bowel syndrome in the Korean population: a hypothesis-generating study.大麻素受体 1 基因多态性与韩国人群肠易激综合征:一项假说生成研究。
J Clin Gastroenterol. 2011 Jan;45(1):45-9. doi: 10.1097/MCG.0b013e3181dd1573.
7
Plasma cytokine profiles in females with irritable bowel syndrome and extra-intestinal co-morbidity.肠易激综合征伴肠外共病女性的血浆细胞因子谱。
Am J Gastroenterol. 2010 Oct;105(10):2235-43. doi: 10.1038/ajg.2010.159. Epub 2010 Apr 20.
8
N-arachidonoyl glycine, an abundant endogenous lipid, potently drives directed cellular migration through GPR18, the putative abnormal cannabidiol receptor.N-花生四烯酰甘氨酸是一种丰富的内源性脂质,通过假定的异常大麻素受体 GPR18 强烈驱动定向细胞迁移。
BMC Neurosci. 2010 Mar 26;11:44. doi: 10.1186/1471-2202-11-44.
9
The cannabinoid 1 receptor (CNR1) 1359 G/A polymorphism modulates susceptibility to ulcerative colitis and the phenotype in Crohn's disease.大麻素 1 型受体(CNR1)1359 G/A 多态性与溃疡性结肠炎易感性及克罗恩病表型相关。
PLoS One. 2010 Feb 26;5(2):e9453. doi: 10.1371/journal.pone.0009453.
10
Endocannabinoid control of gastric sensorimotor function in man.内源性大麻素系统对人类胃感觉运动功能的调控。
Aliment Pharmacol Ther. 2010 May;31(10):1123-31. doi: 10.1111/j.1365-2036.2010.04259.x. Epub 2010 Feb 8.

内源性大麻素系统内用于未来胃肠道疾病治疗的替代靶点。

Alternative targets within the endocannabinoid system for future treatment of gastrointestinal diseases.

作者信息

Schicho Rudolf, Storr Martin

机构信息

Medical University of Graz, Austria.

出版信息

Can J Gastroenterol. 2011 Jul;25(7):377-83. doi: 10.1155/2011/953975.

DOI:10.1155/2011/953975
PMID:21876860
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3174079/
Abstract

Many beneficial effects of herbal and synthetic cannabinoids on gut motility and inflammation have been demonstrated, suggesting a vast potential for these compounds in the treatment of gastrointestinal disorders. These effects are based on the so-called 'endocannabinoid system' (ECS), a cooperating network of molecules that regulate the metabolism of the body's own and of exogenously administered cannabinoids. The ECS in the gastrointestinal tract quickly responds to homeostatic disturbances by de novo synthesis of its components to maintain homeostasis, thereby offering many potential targets for pharmacological intervention. Of major therapeutic interest are nonpsychoactive cannabinoids or compounds that do not directly target cannabinoid receptors but still possess cannabinoid-like properties. Drugs that inhibit endocannabinoid degradation and raise the level of endocannabinoids are becoming increasingly promising alternative therapeutic tools to manipulate the ECS.

摘要

草药和合成大麻素对肠道蠕动和炎症具有许多有益作用,这表明这些化合物在治疗胃肠道疾病方面具有巨大潜力。这些作用基于所谓的“内源性大麻素系统”(ECS),这是一个由分子组成的协作网络,可调节体内自身和外源性大麻素的代谢。胃肠道中的ECS通过从头合成其成分来快速响应体内稳态紊乱,以维持体内平衡,从而提供了许多药理学干预的潜在靶点。具有重大治疗意义的是非精神活性大麻素或不直接靶向大麻素受体但仍具有类大麻素特性的化合物。抑制内源性大麻素降解并提高内源性大麻素水平的药物正日益成为操纵ECS的有前景的替代治疗工具。