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口服苣荬菜提取物可抑制 UVB 诱导的 HR-1 无毛小鼠皮肤损伤和前列腺素 E2 产生。

Oral administration of Jumihaidokuto inhibits UVB-induced skin damage and prostaglandin E2 production in HR-1 hairless mice.

机构信息

Kampo Research Laboratories, Kracie Pharma, Ltd., 3-1 Kanebo-machi, Takaoka, Toyama, 933-0856, Japan.

出版信息

J Nat Med. 2021 Jan;75(1):142-155. doi: 10.1007/s11418-020-01465-y. Epub 2020 Nov 17.

Abstract

This study was conducted to investigate whether and how Jumihaidokuto (JHT), a traditional Chinese medicine, prevents UVB-induced skin damage in male HR-1 hairless mice. JHT has been traditionally prescribed for patients presenting skin disorders with redness and swelling, and, in Japan, it is approved for prescription to patients with acute and/or purulent skin disorders, hives, acute eczema, and athlete's foot. Considering the traditional use of JHT, we hypothesized that oral administration of JHT might emerge as an effective strategy to prevent UVB-induced skin damage, such as edema and erythema. Here, we pretreated mice with JHT (1000 mg/kg, p.o.) for 3 weeks and then administered a single dose of UVB irradiation (250 mJ/cm) on the dorsal skin. UVB irradiation increased the erythema index and transepidermal water loss (TEWL) and decreased the skin water content in the epidermis at 72 h post-irradiation. JHT treatment inhibited the increase of TEWL and the loss of water content in the epidermis, but not the elevation of the erythema index. Moreover, administration of JHT suppressed UVB-induced epidermal hyperplasia by blocking the proliferation of keratinocytes and also inhibited irradiation-triggered reduction of collagen fibers and infiltration of immune cells into the dermis. Lastly, administration of JHT suppressed UVB-induced production of proinflammatory mediators, such as prostaglandin E2 and interleukin-1β. These results suggest that JHT prevents UVB-induced skin damage and that the underlying mechanism involves the inhibition of proinflammatory mediators.

摘要

本研究旨在探讨中药救必应(JHT)是否以及如何预防 UVB 诱导的雄性 HR-1 无毛小鼠皮肤损伤。JHT 传统上用于治疗有红肿症状的皮肤病患者,在日本,它被批准用于治疗急性和/或化脓性皮肤病、荨麻疹、急性湿疹和脚气病患者。考虑到 JHT 的传统用途,我们假设口服 JHT 可能成为预防 UVB 诱导的皮肤损伤(如水肿和红斑)的有效策略。在这里,我们用 JHT(1000mg/kg,口服)预处理小鼠 3 周,然后在背部皮肤单次照射 UVB(250mJ/cm)。UVB 照射在照射后 72 小时增加了红斑指数和经表皮水分流失(TEWL),并降低了表皮中的皮肤水分含量。JHT 治疗抑制了 TEWL 的增加和表皮水分含量的丧失,但没有抑制红斑指数的升高。此外,JHT 通过阻断角质形成细胞的增殖抑制了 UVB 诱导的表皮过度增生,还抑制了照射引发的胶原蛋白纤维减少和免疫细胞浸润真皮。最后,JHT 抑制了 UVB 诱导的促炎介质的产生,如前列腺素 E2 和白细胞介素-1β。这些结果表明 JHT 可预防 UVB 诱导的皮肤损伤,其潜在机制涉及抑制促炎介质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23a3/7788030/dc9db68246f9/11418_2020_1465_Fig1_HTML.jpg

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