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Effect of Hataedock Treatment on Epidermal Structure Maintenance through Intervention in the Endocannabinoid System

Hee-Yeon Kim, Sang-Hyun Ahn, In-Jun Yang, Sun-Young Park, Kibong Kim. Evid Based Complement Alternat Med. 2020;2020:3605153.

Laboratory studyOther animalsWith Douchi (fermented soybean) extract used as Hataedock; genistein and PEA compared in a separate involucrin assay

This study tested palmitoylethanolamide together with Douchi (fermented soybean) extract used as Hataedock; genistein and PEA compared in a separate involucrin assay. Its results cannot be assigned to palmitoylethanolamide alone. More combination studies.

Design
Laboratory study
Subjects
NC/Nga mice with Dermatophagoides farinae-induced atopic dermatitis (numbers not stated in the abstract)
Dose used in the study
Douchi extract 20 mg/kg by mouth; PEA used in an involucrin expression test, concentration not stated
Duration
Mite extract applied in weeks 4 to 6 and 8 to 10
What was measured
Clinical scores, skin histology, CB1, CB2 and GPR55 expression, barrier proteins (filaggrin, involucrin, loricrin, Lass2), E-cadherin, GPx4, CD1A, apoptosis, p-ERK, p-JNK, p-mTOR and epidermal thickness; involucrin after genistein or PEA.

What the authors reported

Hataedock treatment reduced clinical scores (p<0.01) and histological signs, raised cannabinoid receptor and barrier protein expression, raised E-cadherin and GPx4, lowered CD1A, and reduced p-ERK, p-JNK, p-mTOR and epidermal thickness. In the involucrin test, genistein produced a greater lipid barrier effect than PEA.

Limits of this study

A mouse model of atopic dermatitis testing a fermented soybean preparation; PEA was only a comparator in one assay and performed less well than genistein. It cannot show effect in people. The authors declare no conflicts of interest.

Source

PubMed 32063982 · doi:10.1155/2020/3605153

Entry checked against the abstract on PubMed on 2026-09-22. The dose shown is the dose the researchers used. It is not a recommendation. How to read this page.