神经毒素
肽
化学
神经递质
毒液
毒性
合理设计
毒素
作用机理
皮肤刺激
神经毒性
药理学
生物
生物化学
体外
医学
受体
有机化学
遗传学
皮肤病科
作者
Clara Blanes‐Mira,José C. Clemente,G. Jodas,Anabel Gil,Gregorio Fernández‐Ballester,Berta Ponsati,Luis M. Gutiérrez,Enríque Pérez‐Payá,Antonio Ferrer‐Montiel
标识
DOI:10.1046/j.1467-2494.2002.00153.x
摘要
Synopsis Botulinum neurotoxins (BoNTs) represent a revolution in cosmetic science because of their remarkable and long‐lasting antiwrinkle activity. However, their high neurotoxicity seriously limits their use. Thus, there is a need to design and validate non‐toxic molecules that mimic the action of BoNTs. The hexapeptide Ac‐EEMQRR‐NH 2 (coined Argireline) was identified as a result of a rational design programme. Noteworthy, skin topography analysis of an oil/water (O/W) emulsion containing 10% of the hexapeptide on healthy women volunteers reduced wrinkle depth up to 30% upon 30 days treatment. Analysis of the mechanism of action showed that Argireline significantly inhibited neurotransmitter release with a potency similar to that of BoNT A, although as expected, it displayed much lower efficacy than the neurotoxin. Inhibition of neurotransmitter release was due to the interference of the hexapeptide with the formation and/or stability of the protein complex that is required to drive Ca 2+ ‐dependent exocytosis, namely the vesicular fusion (known as SNARE) complex. Notably, this peptide did not exhibit in vivo oral toxicity nor primary irritation at high doses. Taken together, these findings demonstrate that Argireline is a non‐toxic, antiwrinkle peptide that emulates the action of currently used BoNTs. Therefore, this hexapetide represents a biosafe alternative to BoNTs in cosmetics.
科研通智能强力驱动
Strongly Powered by AbleSci AI