4.6 Article

Oxymatrine therapy inhibited epidermal cell proliferation and apoptosis in severe plaque psoriasis

Journal

BRITISH JOURNAL OF DERMATOLOGY
Volume 181, Issue 5, Pages 1028-1037

Publisher

WILEY
DOI: 10.1111/bjd.17852

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Funding

  1. Natural Science Foundation of Ningxia [NZ17154] Funding Source: Medline

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Background Psoriasis is a chronic skin disorder that manifests as epidermal keratinocyte hyperplasia. Objectives We examined the effect of oxymatrine treatment on cell proliferation and apoptosis in skin lesions of psoriasis. Patients and methods Patients with severe plaque psoriasis were treated with oxymatrine or with acitretin. The skin lesions were stained with proliferating cell nuclear antigen (PCNA), Ki-67 and Bcl-2, as well as examined by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labelling (TUNEL). We performed correlations of the Psoriasis Area and Severity Index (PASI) and the proliferation and apoptosis index. Results Oxymatrine significantly reduced the psoriasis lesions as demonstrated by the reduced PASI score after treatment [6 center dot 91; 95% confidence interval (CI) 5 center dot 00-8 center dot 81, P < 0 center dot 001]. In the oxymatrine group, the mitotic index was 26 center dot 15 (95% CI 24 center dot 80-27 center dot 49) before oxymatrine treatment, decreasing to 14 center dot 52 (95% CI 13 center dot 82-15 center dot 25; P < 0 center dot 001) after treatment, but remained higher than the normal group (6 center dot 24; 95% CI 5 center dot 87-6 center dot 61, P < 0 center dot 001). Oxymatrine also inhibited the proliferation of epidermal cells in the skin lesion as indicated by the reduced proliferation index after treatment (P < 0 center dot 01). In addition, oxymatrine treatment reduced cellular apoptosis as shown by increased Bcl-2 expression and a decrease in TUNEL-positive cells. The PASI score was positively correlated with mitotic index, proliferation index and apoptotic index (TUNEL), but negatively correlated with Bcl-2 expression. Conclusions Oxymatrine treatment reduced proliferation but inhibited apoptosis of cells in the skin lesion. The balance between cell proliferation and turnover may contribute to the significant alleviation of psoriasis by oxymatrine. What's already known about this topic? Psoriasis manifests as epidermal keratinocyte hyperplasia with proliferation, keratinocyte maturation and turnover rates. Current drugs for psoriasis may inhibit cell proliferation but could not adjust the balance of cell division, differentiation and apoptosis. What does this study add? We studied the efficacy of oxymatrine in the treatment of psoriasis and analysed the correlation of skin lesions, proliferation and apoptosis index before and after oxymatrine treatment. What is the translational message? Our study has demonstrated that oxymatrine is effective in the treatment of severe plaque psoriasis. It has comparable efficacy with acitretin. Because acitretin treatment was sometimes associated with metabolic abnormalities, our study suggests oxymatrine therapy as an alternative treatment for psoriasis in the context of acitretin allergy or adverse reactions.

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