Efficacy of two plant extracts against acne vulgaris: Initial results of microbiological tests and cell culture studies. (9th November 2018)

• Record Type: Journal Article
• Authors: Kılıç, Songül; Okullu, Sinem Öktem; Kurt, Özgür; Sevinç, Hakan; Dündar, Cihat; Altınordu, Fahim; Türkoğlu, Murat
• Is Part Of: Journal of cosmetic dermatology. Volume 18:Number 4(2019:Aug.)
• Page Start: 1061
• Page End: 1065
• Publication Date: 2018-11-09
• Subjects: acne -- broth dilution method -- HaCaT -- IL‐1α -- Propionibacterium acnes -- SRD5A1 -- TNFα; Skin -- Diseases -- Treatment -- Periodicals; Lasers in surgery -- Periodicals; Skin -- Pathophysiology -- Periodicals; Surgery, Plastic -- Periodicals; 616.5
• DOI: 10.1111/jocd.12814
• Languages: English
• ISSNs: 1473-2130

Abstract

Summary: Background: Acne vulgaris is a common skin disease characterized by increased sebum production, inflammation, and colonization of Propionibacterium acnes ( P. acnes ) on pilosebaceous follicles. Aims: To determine the efficacy of two different plant extracts against P. acnes and to analyze the gene expression levels of IL‐1α, SRD5A1, and TNFα in HaCaT cells treated with these plant extracts. Methods: Anti‐acne extract 1 (AE1) consisted of Juglans regia (walnut husk), Myrtus communis (myrtle leaves), Matricaria chamomilla (chamomilla flowers), Urtica dioica (stinging nettle leaves), and Rosa damascena (rose flowers). Anti‐acne extract 2 (AE2) contained Brassica oleracea var. botrytis (broccoli) and B. oleracea var. italica (cauliflower). The antimicrobial activities of the extracts were tested on two different P. acnes strains: the reference strain of P. acnes (ATCC 51277) and the clinical isolate from a patient. The minimum inhibitory concentration (MIC) of the extracts was determined using the broth dilution method. Human keratinocyte cells were used for in vitro tests. Gene expression analyses were performed with RT‐qPCR. Results: The MIC values of the extracts were below 1/2048 µg/mL. In the gene expression analysis, AE1 increased the expression level of TNFα (1.1719, P < 0.0001), suppressed the expression level of IL‐1α, SRD5A1 (0.0588, P = 0.0231; 0.3081, P = 0.0351), respectively. AE2 suppressed gene expression level of IL‐1α, SRD5A1, TNFα (0.3815, P = 0.0254; 0.3418, P = 0.0271; 0.1997, P = 0.0623). Conclusions: Both herbal extracts demonstrated strong antibacterial and anti‐inflammatory activity in this preliminary trial. In conclusion, the topical application of these botanical extracts can be good candidates for local acne treatment.