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Anti-Inflammatory and Pain-Relieving Effects of Arnica Extract Hydrogel Patch in Carrageenan-Induced Inflammation and Hot Plate Pain Modelsopen access

Authors
Lee, Sang GilLee, Eun ByulNam, Tack SooYou, SunhoIm, DahyeKim, KyusunGu, BonseungNam, Ga-youngLee, HyerimKwon, Soon JaeKim, Yun SeokKim, Sang Geon
Issue Date
Feb-2025
Publisher
MDPI
Keywords
arnica patch; edema; anti-inflammatory; inhibitory effects; pain relief
Citation
Pharmaceutics, v.17, no.2, pp 1 - 13
Pages
13
Indexed
SCIE
SCOPUS
Journal Title
Pharmaceutics
Volume
17
Number
2
Start Page
1
End Page
13
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/57941
DOI
10.3390/pharmaceutics17020171
ISSN
1999-4923
1999-4923
Abstract
Arnica montana (AM), which belongs to the daisy family Asteraceae, has a longstanding traditional use in Europe and North America for pain and inflammation treatment. This study investigates the inhibitory effects of 'Arnica montana extract hydrogel patch (AHP)' on Carrageenan-induced paw edema and hot plate-induced pain models. AHP exhibited transdermal permeability without the occurrence of issues like crystal precipitation. This study employed two animal model assessments using AHP, in comparison with Arnicare Gel (AG), to evaluate anti-inflammatory and pain relief effects. AHP treatment for 2 days showed a decrease in paw edema thickness in mice as compared to vehicle or AG groups; Carrageenan-induced swelling increased maximally at 1 h with the AHP group demonstrating a higher reduction. Thus, the AHP group exhibited a lower ratio of right/left paw thickness and a superior reduction in swelling, supportive of its ability to diminish edema. A histological analysis showed that AHP treatment reduced inflammatory cell infiltration. Consistently, the mRNA levels of inflammatory markers (tnfa, il1b, and il6) were decreased to a greater extent than the AG group. Particularly, tnfa inhibition was better in the AHP group, and the levels of il1b and il6 transcripts showed similar to 80% and 40% lower. Likewise, AHP reduced pain scores in a hot plate-induced rat model, although AG failed to do so. Together, these results demonstrate that AHP has long-lasting inhibitory effects on fluid effusion and edema formation, the production of inflammatory mediators, and pain-sensation, supporting its anti-inflammatory and pain-relieving pharmacological effects.
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