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从车前子这一汉方药“葛根汤”的原料药中寻找抗痛觉过敏化合物。

Search of anti-allodynic compounds from Plantaginis Semen, a crude drug ingredient of Kampo formula "Goshajinkigan".

机构信息

Division of Pharmacognosy, Institute of Natural Medicine, University of Toyama, 2630 Sugitani, Toyama, Toyama, 930-0194, Japan.

Department of Applied Pharmacology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, 2630 Sugitani, Toyama, Toyama, 930-0194, Japan.

出版信息

J Nat Med. 2019 Sep;73(4):761-768. doi: 10.1007/s11418-019-01327-2. Epub 2019 Jun 12.

Abstract

Chemotherapy-induced peripheral neuropathy (CIPN) is one of the dose-limiting side effects of cancer chemotherapy. Although the control of CIPN is important, it is difficult to manage with currently available therapeutic drugs. Therefore, there is a need for novel therapeutic agents for treating CIPN. Goshajinkigan (GJG) is a Kampo formula composed of ten crude drugs. While GJG has been used for the treatment of CIPN, the active constituents of GJG and their underlying mechanisms of pharmacological effects are still unknown. Our previous study revealed that repetitive oral administration of the water extract of Plantaginis Semen, a crude drug ingredient of GJG, inhibited the mechanical allodynia induced by an intraperitoneal injection of paclitaxel in mice. To elucidate the active compounds of Plantaginis Semen, activity-guided separation of the water extract of Plantaginis Semen was performed. From the active fraction, four iridoids (1-4) were identified. Repetitive oral administration of aucubin (1) at 100 or 30 mg/kg and 100 mg/kg of the fraction crude 3 [primarily comprised of pedicularis-lactone (3)], showed anti-allodynic activity, suggesting 1 and 3 could be some of the active compounds responsible for the anti-allodynic property of Plantaginis Semen and GJG. Our study establishes that oral administration of 1 has potent anti-allodynic effect in addition to the activity of intraperitoneally administered 1 reported previously. Identification of active anti-allodynic compounds found in Kampo formulations will support the development of novel therapies for the management of CIPN in cancer patients.

摘要

化疗引起的周围神经病(CIPN)是癌症化疗的剂量限制副作用之一。尽管 CIPN 的控制很重要,但目前可用的治疗药物很难对此进行管理。因此,需要新型治疗剂来治疗 CIPN。贯众(GJG)是一种由十种粗药组成的汉方配方。虽然 GJG 已被用于治疗 CIPN,但 GJG 的活性成分及其药理作用的潜在机制仍不清楚。我们之前的研究表明,贯众中一种粗药成分车前子水提取物的重复口服给药可抑制紫杉醇腹腔注射引起的小鼠机械性痛觉过敏。为了阐明车前子的活性化合物,对车前子水提取物进行了基于活性的分离。从活性部分中鉴定出四个环烯醚萜(1-4)。重复口服给药 100 或 30mg/kg 的桃叶珊瑚苷(1)和 100mg/kg 的粗 3 馏分[主要由马兜铃内酰胺(3)组成]表现出抗痛觉过敏活性,表明 1 和 3 可能是车前子和 GJG 抗痛觉过敏特性的一些活性化合物。我们的研究确立了口服 1 除了先前报道的腹腔内给药 1 具有潜在的抗痛觉过敏作用之外,还具有很强的抗痛觉过敏作用。鉴定出汉方制剂中具有活性的抗痛觉过敏化合物将支持开发用于管理癌症患者 CIPN 的新型疗法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a59/7176603/743f4a45fe4c/11418_2019_1327_Fig1_HTML.jpg

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