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大麻素:通过抑制血管生成和炎症可能成为治疗银屑病的药物。

Cannabinoids: Possible agents for treatment of psoriasis via suppression of angiogenesis and inflammation.

作者信息

Norooznezhad Amir Hossein, Norooznezhad Fatemeh

机构信息

Medical Biology Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran; Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran.

Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Med Hypotheses. 2017 Feb;99:15-18. doi: 10.1016/j.mehy.2016.12.003. Epub 2016 Dec 14.

Abstract

Psoriasis is a chronic skin disease also affecting other sites such as joints. This disease highly depends on inflammation and angiogenesis as well as other pathways. At each step of the psoriasis molecular pathway, different inflammatory cytokines and angiogenic growth factors are involved such as hypoxia inducible factor-1 α (HIF-1 α), vascular endothelial growth factor (VEGF), matrix metalo proteinases (MMPs), basic fibroblast growth factor (bFGF), Angiopoitin-2, interleukin-8 (IL-8), IL-17, and IL-2. Beside the mentioned growth factors and cytokines, cellular adhesion molecule 1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) which play roles in both angiogenesis and inflammation are also involved in the pathogenesis. Cannabinoids are active compounds of Cannabina Sativa inducing their effects through cannabinoid receptors (CBs). JWH-133 is a synthetic cannabinoid with strong anti-angiogenic and anti-inflammatory activities. This agent is able to inhibit HIF-1 α, VEGF, MMPs, bFGF, IL-8, IL-17, and other mentioned cytokines and adhesion molecules both in vivo and in vitro. Altogether, authors suggest using this cannabinoid for treatment of psoriasis due to its potential in suppressing the two main steps of psoriatic pathogenesis. Of course complementary animal studies and human trials are still required.

摘要

银屑病是一种慢性皮肤病,也会影响其他部位,如关节。这种疾病高度依赖于炎症、血管生成以及其他途径。在银屑病分子途径的每一步,都涉及不同的炎性细胞因子和血管生成生长因子,如缺氧诱导因子-1α(HIF-1α)、血管内皮生长因子(VEGF)、基质金属蛋白酶(MMPs)、碱性成纤维细胞生长因子(bFGF)、血管生成素-2、白细胞介素-8(IL-8)、IL-17和IL-2。除了上述生长因子和细胞因子外,在血管生成和炎症中均起作用的细胞间黏附分子1(ICAM-1)和血管细胞黏附分子-1(VCAM-1)也参与了发病机制。大麻素是大麻的活性化合物,通过大麻素受体(CBs)发挥作用。JWH-133是一种具有强大抗血管生成和抗炎活性的合成大麻素。该药物在体内和体外均能抑制HIF-1α、VEGF、MMPs、bFGF、IL-8、IL-17以及其他上述细胞因子和黏附分子。总之,作者建议使用这种大麻素治疗银屑病,因为它具有抑制银屑病发病机制两个主要步骤的潜力。当然,仍需要补充动物研究和人体试验。

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