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口服那可丁对咪喹莫特诱导的银屑病样皮肤损伤有显著疗效。

A promising impact of oral administration of noscapine against imiquimod-induced psoriasis-like skin lesions.

作者信息

Nourbakhsh Fahimeh, Mousavi Seyed Hadi, Rahmanian-Devin Pouria, Baradaran Rahimi Vafa, Rakhshandeh Hassan, Askari Vahid Reza

机构信息

Medical Toxicology Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.

Pharmacological Research Center of Medicinal Plants, Mashhad University of Medical Sciences, Mashhad, Iran.

出版信息

Avicenna J Phytomed. 2023 Jul-Aug;13(4):412-428. doi: 10.22038/AJP.2023.21828.

Abstract

OBJECTIVE

Psoriasis is a chronic inflammatory autoimmune disease. The effectiveness of noscapine has been employed as a helpful treatment for various disorders and subjected to recent theoretical breakthroughs.

MATERIALS AND METHODS

Psoriasis-like lesions were induced by topical application of 5% imiquimod (IMQ) (10 mg/cm of skin) in male mice and then medicated with a single oral dose of methotrexate (MET) as a positive control or daily oral treatment of noscapine (5, 15 and 45 mg/kg). In this way, skin inflammation intensity, psoriatic itchiness, psoriasis area severity index (PASI) score, ear length, thickness, and organ weight were daily measured. At the end of the study, histological and immunohistochemical and enzyme-linked immunosorbent assays (ELISA, for pro-/anti-inflammatory factors) were performed in each ear.

RESULTS

IMQ caused psoriasis-like lesions. Noscapine markedly alleviated macroscopic parameters, namely ear thickness, ear length, skin inflammation, itching, and organ weight, as well as microscopic parameters including, pathology and Ki67 and p53, and tissue immunological mediators, such as tumour necrosis factor (TNF-α), interleukin (IL)-10, transforming growth factor (TGF-β), interferon- (IFN-), IL-6, IL-17, and IL-23p19 in the psoriatic skin in a concentration manner (p<0.05-<0.001).

CONCLUSION

Therefore, noscapine with good pharmacological properties has considerable effects on psoriasis inflammation.

摘要

目的

银屑病是一种慢性炎症性自身免疫性疾病。那可丁的有效性已被用于多种疾病的治疗,并取得了近期的理论突破。

材料与方法

通过在雄性小鼠皮肤局部涂抹5%咪喹莫特(IMQ)(10mg/cm皮肤)诱导银屑病样病变,然后以单剂量口服甲氨蝶呤(MET)作为阳性对照,或每日口服那可丁(5、15和45mg/kg)进行治疗。通过这种方式,每天测量皮肤炎症强度、银屑病瘙痒程度、银屑病面积严重程度指数(PASI)评分、耳长、耳厚度和器官重量。在研究结束时,对每只耳朵进行组织学、免疫组织化学和酶联免疫吸附测定(ELISA,用于检测促炎/抗炎因子)。

结果

IMQ诱发了银屑病样病变。那可丁显著减轻了宏观参数,即耳厚度、耳长、皮肤炎症、瘙痒和器官重量,以及微观参数,包括病理学、Ki67和p53,以及组织免疫介质,如银屑病皮肤中的肿瘤坏死因子(TNF-α)、白细胞介素(IL)-10、转化生长因子(TGF-β)、干扰素(IFN)-、IL-6、IL-17和IL-23p19,且呈浓度依赖性(p<0.05-<0.001)。

结论

因此,具有良好药理特性的那可丁对银屑病炎症有显著疗效。

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