Evidence map›Paper›PMID 42057627›Full record

ArticleVeterinary medicine and science2026

A Botanical Mixture of Boswellia serrata, Commiphora myrrha, Propolis and Scutellaria baicalensis Reduces Expression of Inflammatory Chemokines in Canine Keratinocytes In Vitro.

Danbee Ha, Kyungsook Jung, Hyungyeong Choi, Ji-Seon Yoon

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Article in Veterinary medicine and science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Danbee HaBiosafety Research Institute and College of Veterinary Medicine, Jeonbuk National University, Iksan, Republic of Korea.
Kyungsook JungFunctional Biomaterials Research Center, Korea Research Institute of Bioscience and Biotechnology, Jeongeup, Republic of Korea.
Hyungyeong ChoiK Pharms, Incheon, Republic of Korea.
Ji-Seon YoonBiosafety Research Institute and College of Veterinary Medicine, Jeonbuk National University, Iksan, Republic of Korea.ORCID https://orcid.org/0000-0002-7354-3255

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBotanical ingredients can function as adjunctive therapies for managing inflammatory skin diseases.

objectivesThis study aimed to investigate the anti-inflammatory effects of a mixture of Boswellia serrata, Commiphora myrrha, propolis and Scutellaria baicalensis (YSK-AB) on canine keratinocytes in vitro.

methodsHigh-performance liquid chromatography (HPLC) was used to identify major components of YSK-AB. In addition, to evaluate nitric oxide (NO) production, RAW 264.7 cells were treated with YSK-AB (25, 50, 100 and 200 µg/mL) for 24 h, subsequently stimulated with lipopolysaccharide (1 µg/mL). To analyse the cytotoxic effects of YSK-AB, canine progenitor epidermal keratinocytes (CPEKs) were incubated with YSK-AB for 48 h. To investigate the effects of YSK-AB on cytokine expression, CPEKs were incubated with YSK-AB for 24 h and then stimulated with a mixture of interferon-γ and tumour necrosis factor-α (30 ng/mL each) for 24 h. The enzyme-linked immunosorbent assay (ELISA) was performed to measure chemokine (C-C motif) ligand 2 (CCL2) and CCL5. Real-time polymerase chain reaction (PCR) was used to quantify CCL17 mRNA expression.

resultsHPLC analysis identified four components in YSK‑AB, including 6‑hydroxy‑2,6‑dimethylhepta‑2,4‑dienal, baicalin, galangin and AKBA. CPEKs treated with 100, 150, 200 and 250 µg/mL of YSK‑AB exhibited significantly higher viability than that of the control group. In addition, YSK‑AB treatment (50, 100 and 200 µg/mL) significantly reduced NO production in RAW 264.7 cells. Furthermore, CCL17 mRNA expression and CCL2 and CCL5 protein levels were significantly reduced in YSK‑AB‑treated CPEKs compared with the control.

conclusionsYSK-AB downregulates the expression of chemokines produced by canine keratinocytes and could be a potential novel natural product-derived therapeutic agent for alleviating inflammatory skin diseases in dogs.

Indexed as

Anti-Inflammatory AgentsBoswelliaChemokinesCommiphoraKeratinocytesPlant ExtractsScutellaria baicalensisAnimalsChromatography, High Pressure LiquidDogsMiceRAW 264.7 CellsAnti-Inflammatory AgentsChemokinesPlant Extractsbotanical ingredientschemokinedogkeratinocyteskin

Identifiers

PMID42057627
PMCPMC13129499

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.