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肝性脑病中苯二氮䓬受体的天然内源性配体。

Natural endogenous ligands for benzodiazepine receptors in hepatic encephalopathy.

作者信息

Baraldi M, Avallone R, Corsi L, Venturini I, Baraldi C, Zeneroli M L

机构信息

Department of Biomedical Sciences (Section of Pharmacology), University of Modena and Reggio Emilia, Via Campi 287, 41100 Modena, Italy.

出版信息

Metab Brain Dis. 2009 Mar;24(1):81-93. doi: 10.1007/s11011-008-9111-8. Epub 2008 Dec 11.

Abstract

Benzodiazepines of natural origin (NBZDs) have been found in human blood and brains as well as in medicinal plants and foods. In plasma and brain tissue there are i.e. diazepam and nordiazepam equal to commercial drugs but there are also other benzodiazepine-like compounds termed "endozepines", which act as agonists at the benzodiazepine receptors of central type (CBR). A synthetic pathway for the production of NBZDs has not yet been found, but it has been suggested that micro-organisms may synthesize molecules with benzodiazepine-like structures. Hence NBZDs could be of both endogenous and exogenous source and be considered as natural anxyolitic and sedative. Interestingly there are also natural compounds, such as the polypeptide Diazepam Binding Inhibitor (DBI) acting as an "inversive agonist" implicated in fair and panic disorders. It has been suggested that NBZDs may play a role in the pathogenesis of hepatic encephalopathy (HE). Multidirectional studies evaluated NBZDs levels (1) in the blood of normal subjects, of cirrhotic with or without HE and in commercial benzodiazepine consumers; (2) in the blood of cirrhotic treated or not with a non-absorbable antibiotic; (3) in several constituents of our diet. In conclusion, NBZDs increase sometime in cirrhotics with or without HE but they reach concentrations not higher than those found in commercial benzodiazepines consumers. Hence NBZDs must be considered as occasional precipitating factor of HE and benzodiazepine antagonists only symptomatic drugs. The finding that NBZDs may be in part synthesized by intestinal bacterial flora and in part constituent of our diet underlines the importance to feed cirrhotic patients with selected food.

摘要

天然来源的苯二氮䓬类药物(NBZDs)已在人体血液和大脑以及药用植物和食物中被发现。在血浆和脑组织中,存在与市售药物相当的地西泮和去甲地西泮,但也存在其他被称为“内源性苯二氮䓬类化合物”的苯二氮䓬样化合物,它们作为中枢型苯二氮䓬受体(CBR)的激动剂发挥作用。尚未发现NBZDs的合成途径,但有人提出微生物可能合成具有苯二氮䓬样结构的分子。因此,NBZDs可能既有内源性来源也有外源性来源,可被视为天然的抗焦虑和镇静剂。有趣的是,也有天然化合物,如多肽地西泮结合抑制剂(DBI),作为“反向激动剂”与惊恐障碍有关。有人提出NBZDs可能在肝性脑病(HE)的发病机制中起作用。多方向研究评估了NBZDs水平:(1)在正常受试者、有或无HE的肝硬化患者以及市售苯二氮䓬类药物使用者的血液中;(2)在接受或未接受不可吸收抗生素治疗的肝硬化患者的血液中;(3)在我们饮食的几种成分中。总之,NBZDs在有或无HE的肝硬化患者中有时会增加,但它们达到的浓度不高于市售苯二氮䓬类药物使用者中发现的浓度。因此,NBZDs必须被视为HE的偶尔诱发因素,而苯二氮䓬类拮抗剂只是对症药物。NBZDs可能部分由肠道细菌菌群合成且部分是我们饮食成分的这一发现强调了为肝硬化患者提供特定食物的重要性。

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