Differential effectiveness of selected non-psychotropic phytocannabinoids on human sebocyte functions implicates their introduction in dry/seborrhoeic skin and acne treatment

被引:87
作者
Olah, Attila [1 ]
Markovics, Arnold [1 ]
Szabo-Papp, Judit [1 ]
Szabo, Palma Timea [1 ]
Stott, Colin [2 ]
Zouboulis, Christos C. [3 ,4 ,5 ,6 ]
Biro, Tamas [1 ,7 ]
机构
[1] Univ Debrecen, Dept Physiol, DE MTA Lendulet Cellular Physiol Res Grp, Fac Med, Debrecen, Hungary
[2] GW Pharmaceut, Cambridge, England
[3] Dessau Med Ctr, Dept Dermatol, Dessau, Germany
[4] Dessau Med Ctr, Dept Venereol, Dessau, Germany
[5] Dessau Med Ctr, Dept Allergol, Dessau, Germany
[6] Dessau Med Ctr, Dept Immunol, Dessau, Germany
[7] Univ Debrecen, Dept Immunol, Fac Med, Debrecen, Hungary
关键词
acne vulgaris; cutaneous inflammation; dry skin; phytocannabinoid; SEBACEOUS GLAND; PSYCHIATRIC COMORBIDITIES; CANNABIDIOL; MITOCHONDRIA; CANNABIGEROL; PSORIASIS; APOPTOSIS; UPDATE; CELLS;
D O I
10.1111/exd.13042
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Acne is a common skin disease characterized by elevated sebum production and inflammation of the sebaceous glands. We have previously shown that a non-psychotropic phytocannabinoid ((-)-cannabidiol [CBD]) exerted complex anti-acne effects by normalizing 'pro-acne agents'-induced excessive sebaceous lipid production, reducing proliferation and alleviating inflammation in human SZ95 sebocytes. Therefore, in this study we aimed to explore the putative anti-acne effects of further non-psychotropic phytocannabinoids ((-)-cannabichromene [CBC], (-)-cannabidivarin [CBDV], (-)-cannabigerol [CBG], (-)-cannabigerovarin [CBGV] and (-)-Delta(9) -tetrahydrocannabivarin [THCV]). Viability and proliferation of human SZ95 sebocytes were investigated by MTT and CyQUANT assays; cell death and lipid synthesis were monitored by DilC(1)(5)-SYTOX Green labelling and Nile Red staining, respectively. Inflammatory responses were investigated by monitoring expressions of selected cytokines upon lipopolysaccharide treatment (RT-qPCR, ELISA). Up to 10 mu M, the phytocannabinoids only negligibly altered the viability of the sebocytes, whereas high doses (>= 50 mu M) induced apoptosis. Interestingly, basal sebaceous lipid synthesis was differentially modulated by the substances: CBC and THCV suppressed it, and CBDV had only minor effects, whereas CBG and CBGV increased it. Importantly, CBC, CBDV and THCV significantly reduced arachidonic acid (AA)-induced 'acne-like' lipogenesis. Moreover, THCV suppressed proliferation, and all phytocannabinoids exerted remarkable anti-inflammatory actions. Our data suggest that CBG and CBGV may have potential in the treatment of dry-skin syndrome, whereas CBC, CBDV and especially THCV show promise to become highly efficient, novel anti-acne agents. Moreover, based on their remarkable anti-inflammatory actions, phytocannabinoids could be efficient, yet safe novel tools in the management of cutaneous inflammations.
引用
收藏
页码:701 / 707
页数:7
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