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体内 11,14,17-二十碳三烯酸对无毛小鼠 UV 诱导皮肤损伤的预防作用。

Prevention of UV-induced skin damages by 11,14,17-eicosatrienoic acid in hairless mice in vivo.

机构信息

Department of Dermatology, Seoul Nationa University College of Medicine, Seoul, Korea.

出版信息

J Korean Med Sci. 2010 Jun;25(6):930-7. doi: 10.3346/jkms.2010.25.6.930. Epub 2010 May 24.

Abstract

Polyunsaturated fatty acids (PUFAs) are known to play important roles in various physiological and pathological processes. Recent studies have shown that some omega-3 (omega-3) PUFAs, such as eicosapentaenoic acid (EPA) and dodecahexaenoic acid (DHA), have protective effects on acute and chronic UV-induced changes. However, the effects of other omega-3 PUFAs including 11,14,17-eicosatrienoic acid (20:3) (ETA) on UV-induced skin damages are poorly understood. In this study, we investigated the cutaneous photoprotective effects of ETA in hairless mice in vivo. Female HR-1 hairless mice were topically treated with vehicle (ethanol:polyethylene glycol=30:70) only, 0.1% ETA, or 1% ETA once a day for 3 successive days after one time UV irradiation (200 mJ/cm(2)) on dorsal skins. Skin biopsy was carried out on the fourth day (72 hr after UV irradiation). We found that topical treatment with ETA attenuated UV-induced epidermal and dermal thickness and infiltration of inflammatory cells, and impairment of skin barrier function. In addition, ETA suppressed the expression of IL-1beta, COX-2, and MMP-13 induced by UV irradiation. Our results show that the topical application of ETA protects against UV-induced skin damage in hairless mice and suggest that ETA can be a potential agent for preventing and/or treating UV-induced inflammation and photoaging.

摘要

多不饱和脂肪酸(PUFAs)在各种生理和病理过程中起着重要作用。最近的研究表明,一些 omega-3(omega-3)PUFAs,如二十碳五烯酸(EPA)和二十二碳六烯酸(DHA),对急性和慢性 UV 诱导的变化具有保护作用。然而,其他 omega-3 PUFAs,包括 11、14、17-二十碳三烯酸(20:3)(ETA)对 UV 诱导的皮肤损伤的影响知之甚少。在这项研究中,我们在体内研究了 ETA 对无毛小鼠皮肤的光保护作用。雌性 HR-1 无毛小鼠背部皮肤单次紫外线照射(200 mJ/cm(2))后,每天用溶剂(乙醇:聚乙二醇=30:70)、0.1% ETA 或 1% ETA 局部治疗 3 天。在第四天(紫外线照射后 72 小时)进行皮肤活检。我们发现,ETA 的局部治疗可减轻 UV 诱导的表皮和真皮厚度增加和炎症细胞浸润,并改善皮肤屏障功能障碍。此外,ETA 抑制了由 UV 照射诱导的 IL-1beta、COX-2 和 MMP-13 的表达。我们的结果表明,ETA 的局部应用可防止无毛小鼠的 UV 诱导皮肤损伤,并表明 ETA 可作为预防和/或治疗 UV 诱导的炎症和光老化的潜在药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4226/2877234/9bcfd1adb9b5/jkms-25-930-g001.jpg

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