Broshtilova Valentina, Lozanov Valentina, Miteva Ljubka
Departments of Dermatology and Venereology, Faculty of Medicine, Sofia Medical University, Bulgaria.
Indian J Dermatol. 2013 Jul;58(4):306-9. doi: 10.4103/0019-5154.113952.
Polyamines - putrescine, spermidine and spermine are polycationic compounds ubiquitous for all living organisms. They are essential for the cell growth and differentiation, the control of cell cycle progress, apoptosis, and cancerogenesis. Accumulated scientific evidence suggests the central role of polyamines in the process of keratinocytic proliferation, differentiation, and regulation.
To elucidate the polyamine metabolic changes that occur in benign keratinocytic proliferation. Fifty eight patients were enrolled in the study, 31 with plaque-form of psoriasis vulgaris, which had been referred to as a model of benign keratinocytic proliferation, and 27-healthy controls.
An original, innovative chromatographic method was used to detect the levels of putrescine, spermidine, and spermine in all skin samples.
Were significantly proven (P < 0.05). No difference was found between the polyamines levels of non-lesional psoriatic skin and healthy controls. Psoriatic lesions showed a two-time higher concentration of all polyamines in lesional, compared to non-lesional skin. Spermine had the highest concentration and highest proliferation trend, which demonstrated the importance of propylamine synthesis in the pathogenesis of psoriasis. Spermine highest concentrations suggested the leading role of adenosine methionine decarboxylase (AMDC) in the pathogenesis of benign keratinocytic proliferations.
Non-lesional skin in psoriatic patients did not show latent changes in polyamine metabolism. Psoriatic lesions demontrated two-time higher levels of the most essential biogenic polyamines compared to healthy controls. The highest level of spermine proved the crucial role of AMDC in the polyamine metabolism changes in psoriasis. Future therapeutic approaches should be focused on reduction of exogenic spermine intake, utilizing new spermine blockers, and synthesis of AMDC inhibitors.
多胺——腐胺、亚精胺和精胺是所有生物体内普遍存在的聚阳离子化合物。它们对于细胞生长和分化、细胞周期进程的控制、细胞凋亡以及肿瘤发生至关重要。越来越多的科学证据表明多胺在角质形成细胞增殖、分化和调节过程中发挥着核心作用。
阐明良性角质形成细胞增殖过程中发生的多胺代谢变化。58名患者参与了该研究,其中31例为寻常型斑块状银屑病患者,该病被视为良性角质形成细胞增殖的模型,另外27例为健康对照者。
采用一种原创的、创新的色谱方法检测所有皮肤样本中腐胺、亚精胺和精胺的水平。
得到显著证实(P < 0.05)。银屑病非皮损部位皮肤和健康对照者的多胺水平无差异。与非皮损皮肤相比,银屑病皮损部位所有多胺的浓度高出两倍。精胺浓度最高且增殖趋势最强,这表明丙胺合成在银屑病发病机制中具有重要意义。精胺的最高浓度表明腺苷甲硫氨酸脱羧酶(AMDC)在良性角质形成细胞增殖发病机制中起主导作用。
银屑病患者的非皮损皮肤未显示多胺代谢的潜在变化。与健康对照者相比,银屑病皮损部位最主要的生物源性多胺水平高出两倍。精胺的最高水平证明了AMDC在银屑病多胺代谢变化中起关键作用。未来的治疗方法应集中在减少外源性精胺摄入、使用新型精胺阻滞剂以及合成AMDC抑制剂。