Complementary effect of hydroquinone and retinoic acid on corneocyte desquamation with their combination use

J Dermatol Sci. 2017 Aug;87(2):192-200. doi: 10.1016/j.jdermsci.2017.03.023. Epub 2017 Apr 7.

Abstract

Background: Retinoic acid (RA) enhances skin-lightening capabilities of hydroquinone (HQ), at least in part, by facilitating desquamation which leads to increase penetration of HQ. The desquamation also affects skin irritation levels. The mechanism of RA-induced desquamation, however, has not been completely explored and no such data has been available for HQ uses.

Objective: To examine the role of HQ, RA, and their combination in the desquamation.

Methods: Primary cultured normal human keratinocytes, which were treated with HQ and/or RA in presence or absence of serine-specific inhibitor Kazal type5 (SPINK5)/lympho-epithelial Kazal-type-related inhibitor (LEKTI) knockdown or recombinant human SPINK5/LEKTI, and biopsied skin samples applied with HQ or RA were examined. Expression levels of corneodesmosin (CDSN), desmocollin1 (DSC1), kallikrein5 (KLK5), KLK7, and SPINK5/LEKTI, and proteolysis activity against extracted human skin epidermal protein were determined using time-course real-time PCR, Western blotting, ELISA, and immunofluorescence staining.

Results: HQ increased but RA decreased the synthesis of CDSN and DSC1. HQ reduced corneodesmosome degradation by the upregulation of SPINK5/LEKTI, whereas RA showed opposite results without upregulation of SPINK5/LEKTI. The combination of HQ and RA was close to the sum of the individual components.

Conclusions: HQ reduced corneocyte desquamation. However, RA enhanced desquamation. The combination induced more desquamation than HQ but less than RA.

Keywords: Desquamation; HQ+RA combination; Hydroquinone; Retinoic acid; SPINK5/LEKTI.

MeSH terms

  • Adult
  • Cell Adhesion / drug effects*
  • Desmocollins / metabolism
  • Desmosomes / drug effects
  • Desmosomes / metabolism
  • Desmosomes / pathology
  • Drug Synergism
  • Epidermal Cells
  • Epidermis / drug effects
  • Epidermis / physiology
  • Female
  • Glycoproteins / metabolism
  • Healthy Volunteers
  • Humans
  • Hydroquinones / pharmacology
  • Intercellular Signaling Peptides and Proteins
  • Keratinocytes / drug effects*
  • Keratinocytes / physiology
  • Male
  • Middle Aged
  • Primary Cell Culture
  • Proteolysis / drug effects
  • RNA Interference
  • RNA, Small Interfering / metabolism
  • Real-Time Polymerase Chain Reaction
  • Serine Peptidase Inhibitor Kazal-Type 5 / genetics
  • Serine Peptidase Inhibitor Kazal-Type 5 / metabolism*
  • Skin Absorption / drug effects
  • Skin Lightening Preparations / pharmacology*
  • Skin Physiological Phenomena / drug effects*
  • Tretinoin / pharmacology
  • Up-Regulation

Substances

  • CDSN protein, human
  • DSC1 protein, human
  • Desmocollins
  • Glycoproteins
  • Hydroquinones
  • Intercellular Signaling Peptides and Proteins
  • RNA, Small Interfering
  • SPINK5 protein, human
  • Serine Peptidase Inhibitor Kazal-Type 5
  • Skin Lightening Preparations
  • Tretinoin
  • hydroquinone